Your Analysis

Genetic Predisposition

Based on your genetic markers, your predisposition to this trait is shown below

Your Result

Higher Tourette syndrome predisposition

Was this result accurate for you?

Scientific Evidence

Understanding the Data
  • SNP: A specific genetic marker relevant to this trait (e.g., rs2588978)
  • Genotype: Your genetic makeup at the given SNP location (e.g., CC)
  • Variant allele: The alternative DNA sequence at the SNP site
  • Variant allele frequency: Percentage of population carrying this variant
  • Variant found: Whether the variant was detected in your DNA file
104 genes analyzed 2 with detected variants
Variant Detected

FPR1 GeneCards

This gene encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. The protein mediates the response of phagocytic cells to invasion of the host by microorganisms and is important in host defense and inflammation.

Genomic Location
Chr 19 Start: 52,248,425 End: 52,255,131 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status
Variant Detected

LINC01122 GeneCards

Genomic Location
Chr 2 Start: 58,747,888 End: 59,290,901 Build: HG19
Associated SNPs
1 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

AAMDC GeneCards

Genomic Location
Chr 11 Start: 77,532,190 End: 77,611,819 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ABCB9 GeneCards

Genomic Location
Chr 12 Start: 123,405,495 End: 123,451,010 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ADAMTS7P1 GeneCards

Genomic Location
Chr 15 Start: 82,585,621 End: 82,626,915 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

AHCTF1P1 GeneCards

Genomic Location
Chr 2 Start: 162,355,578 End: 162,364,413 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ALG8 GeneCards

This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition of the second glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation of proteins. Mutations in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ih). Alternatively spliced transcript variants encoding different isoforms have been identified.

Genomic Location
Chr 11 Start: 77,811,992 End: 77,850,672 Build: HG19

No SNPs found for this gene in your DNA data.

AP3B2 GeneCards

Adaptor protein complex 3 (AP-3 complex) is a heterotrimeric protein complex involved in the formation of clathrin-coated synaptic vesicles. The protein encoded by this gene represents the beta subunit of the neuron-specific AP-3 complex and was first identified as the target antigen in human paraneoplastic neurologic disorders. The encoded subunit binds clathrin and is phosphorylated by a casein kinase-like protein, which mediates synaptic vesicle coat assembly. Defects in this gene are a cause of early-onset epileptic encephalopathy.

Genomic Location
Chr 15 Start: 83,328,033 End: 83,378,627 Build: HG19

No SNPs found for this gene in your DNA data.

AQP11 GeneCards

Genomic Location
Chr 11 Start: 77,300,998 End: 77,321,401 Build: HG19

No SNPs found for this gene in your DNA data.

ARL6IP4 GeneCards

Genomic Location
Chr 12 Start: 123,464,780 End: 123,467,456 Build: HG19

No SNPs found for this gene in your DNA data.

BAZ2B GeneCards

This gene belongs to the bromodomain gene family. Members of this gene family encode proteins that are integral components of chromatin remodeling complexes. The encoded protein showed strong preference for the activating H3K14Ac mark in a histone peptide screen, suggesting a potential role in transcriptional activation. This gene may be associated with susceptibility to sudden cardiac death (SCD).

Genomic Location
Chr 2 Start: 160,175,490 End: 160,568,953 Build: HG19

No SNPs found for this gene in your DNA data.

CCDC62 GeneCards

coiled-coil domain containing 62

Genomic Location
Chr 12 Start: 123,259,119 End: 123,312,075 Build: HG19

No SNPs found for this gene in your DNA data.

CD276 GeneCards

The protein encoded by this gene belongs to the immunoglobulin superfamily, and thought to participate in the regulation of T-cell-mediated immune response. Studies show that while the transcript of this gene is ubiquitously expressed in normal tissues and solid tumors, the protein is preferentially expressed only in tumor tissues. Additionally, it was observed that the 3' UTR of this transcript contains a target site for miR29 microRNA, and there is an inverse correlation between the expression of this protein and miR29 levels, suggesting regulation of expression of this gene product by miR29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 15 Start: 73,976,724 End: 74,006,855 Build: HG19

No SNPs found for this gene in your DNA data.

CD302 GeneCards

Genomic Location
Chr 2 Start: 160,625,139 End: 160,654,719 Build: HG19

No SNPs found for this gene in your DNA data.

CDK2AP1 GeneCards

cyclin dependent kinase 2 associated protein 1

Genomic Location
Chr 12 Start: 123,745,523 End: 123,756,787 Build: HG19

No SNPs found for this gene in your DNA data.

CLNS1A GeneCards

Genomic Location
Chr 11 Start: 77,325,575 End: 77,348,839 Build: HG19

No SNPs found for this gene in your DNA data.

CPEB1 GeneCards

cytoplasmic polyadenylation element binding protein 1

Genomic Location
Chr 15 Start: 83,211,951 End: 83,317,546 Build: HG19

No SNPs found for this gene in your DNA data.

CSMD3 GeneCards

CUB and Sushi multiple domains 3

Genomic Location
Chr 8 Start: 113,235,157 End: 114,449,168 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

DPP4 GeneCards

dipeptidyl peptidase 4

Genomic Location
Chr 2 Start: 162,848,755 End: 162,930,725 Build: HG19

No SNPs found for this gene in your DNA data.

EPB41 GeneCards

The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Genomic Location
Chr 1 Start: 29,213,612 End: 29,446,553 Build: HG19

No SNPs found for this gene in your DNA data.

ERC2 GeneCards

Genomic Location
Chr 3 Start: 55,542,339 End: 56,502,495 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FLT3 GeneCards

This gene encodes a class III receptor tyrosine kinase that regulates hematopoiesis. This receptor is activated by binding of the fms-related tyrosine kinase 3 ligand to the extracellular domain, which induces homodimer formation in the plasma membrane leading to autophosphorylation of the receptor. The activated receptor kinase subsequently phosphorylates and activates multiple cytoplasmic effector molecules in pathways involved in apoptosis, proliferation, and differentiation of hematopoietic cells in bone marrow. Mutations that result in the constitutive activation of this receptor result in acute myeloid leukemia and acute lymphoblastic leukemia.

Genomic Location
Chr 13 Start: 28,577,411 End: 28,674,713 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

FPR2 GeneCards

formyl peptide receptor 2

Genomic Location
Chr 19 Start: 52,264,433 End: 52,273,784 Build: HG19

No SNPs found for this gene in your DNA data.

FPR3 GeneCards

Genomic Location
Chr 19 Start: 52,298,410 End: 52,329,443 Build: HG19

No SNPs found for this gene in your DNA data.

FSD2 GeneCards

Genomic Location
Chr 15 Start: 83,424,114 End: 83,474,821 Build: HG19

No SNPs found for this gene in your DNA data.

GAB2 GeneCards

This gene is a member of the GRB2-associated binding protein (GAB) gene family. These proteins contain pleckstrin homology (PH) domain, and bind SHP2 tyrosine phosphatase and GRB2 adapter protein. They act as adapters for transmitting various signals in response to stimuli through cytokine and growth factor receptors, and T- and B-cell antigen receptors. The protein encoded by this gene is the principal activator of phosphatidylinositol-3 kinase in response to activation of the high affinity IgE receptor. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.

Genomic Location
Chr 11 Start: 77,926,339 End: 78,128,866 Build: HG19

No SNPs found for this gene in your DNA data.

GDPD4 GeneCards

Genomic Location
Chr 11 Start: 76,927,603 End: 77,012,731 Build: HG19

No SNPs found for this gene in your DNA data.

GOLGA6L10 GeneCards

golgin A6 family like 10

Genomic Location
Chr 15 Start: 82,929,674 End: 82,939,197 Build: HG19

No SNPs found for this gene in your DNA data.

GOLGA6L17P GeneCards

Genomic Location
Chr 15 Start: 82,804,060 End: 82,811,851 Build: HG19

No SNPs found for this gene in your DNA data.

GOLGA6L9 GeneCards

Genomic Location
Chr 15 Start: 82,722,185 End: 82,731,587 Build: HG19

No SNPs found for this gene in your DNA data.

HIP1R GeneCards

huntingtin interacting protein 1 related

Genomic Location
Chr 12 Start: 123,319,295 End: 123,347,508 Build: HG19

No SNPs found for this gene in your DNA data.

HOMER2 GeneCards

This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. The encoded protein is a postsynaptic density scaffolding protein. Alternative splicing results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 14.

Genomic Location
Chr 15 Start: 83,517,735 End: 83,621,472 Build: HG19

No SNPs found for this gene in your DNA data.

INTS4 GeneCards

integrator complex subunit 4

Genomic Location
Chr 11 Start: 77,589,766 End: 77,705,714 Build: HG19

No SNPs found for this gene in your DNA data.

ITGB6 GeneCards

This gene encodes a protein that is a member of the integrin superfamily. Members of this family are adhesion receptors that function in signaling from the extracellular matrix to the cell. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. The encoded protein forms a dimer with an alpha v chain and this heterodimer can bind to ligands like fibronectin and transforming growth factor beta 1. Alternate splicing results in multiple transcript variants.

Genomic Location
Chr 2 Start: 160,956,182 End: 161,056,783 Build: HG19

No SNPs found for this gene in your DNA data.

KCTD14 GeneCards

Genomic Location
Chr 11 Start: 77,726,761 End: 77,757,237 Build: HG19

No SNPs found for this gene in your DNA data.

KCTD21 GeneCards

potassium channel tetramerization domain containing 21

Genomic Location
Chr 11 Start: 77,882,295 End: 77,899,672 Build: HG19

No SNPs found for this gene in your DNA data.

KCTD21-AS1 GeneCards

KCTD21 antisense RNA 1

Genomic Location
Chr 11 Start: 77,850,839 End: 77,885,023 Build: HG19

No SNPs found for this gene in your DNA data.

LMO3 GeneCards

The protein encoded by this gene belongs to the rhombotin family of cysteine-rich LIM domain oncogenes. This gene is predominantly expressed in the brain. Related family members, LMO1 and LMO2 on chromosome 11, have been reported to be involved in chromosomal translocations in T-cell leukemia. Many alternatively spliced transcript variants have been found for this gene.

Genomic Location
Chr 12 Start: 16,701,306 End: 16,761,148 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

LOC101929512 GeneCards

uncharacterized LOC101929512

Genomic Location
Chr 2 Start: 162,079,769 End: 162,111,154 Build: HG19

No SNPs found for this gene in your DNA data.

LOC102724034 GeneCards

Genomic Location
Chr 15 Start: 83,112,062 End: 83,113,589 Build: HG19

No SNPs found for this gene in your DNA data.

LOC727751 GeneCards

Genomic Location
Chr 15 Start: 82,944,750 End: 82,976,258 Build: HG19

No SNPs found for this gene in your DNA data.

LY75 GeneCards

lymphocyte antigen 75

Genomic Location
Chr 2 Start: 160,659,866 End: 160,761,267 Build: HG19

No SNPs found for this gene in your DNA data.

LY75-CD302 GeneCards

LY75-CD302 readthrough

Genomic Location
Chr 2 Start: 160,625,139 End: 160,761,267 Build: HG19

No SNPs found for this gene in your DNA data.

MECR GeneCards

The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy.

Genomic Location
Chr 1 Start: 29,519,169 End: 29,557,446 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MEX3B GeneCards

Genomic Location
Chr 15 Start: 82,334,119 End: 82,338,359 Build: HG19

No SNPs found for this gene in your DNA data.

MIR2053 GeneCards

Genomic Location
Chr 8 Start: 113,655,722 End: 113,655,812 Build: HG19

No SNPs found for this gene in your DNA data.

MIR2113 GeneCards

Genomic Location
Chr 6 Start: 98,472,407 End: 98,472,497 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MIR4304 GeneCards

Genomic Location
Chr 12 Start: 123,495,214 End: 123,495,275 Build: HG19

No SNPs found for this gene in your DNA data.

MIR4785 GeneCards

Genomic Location
Chr 2 Start: 161,264,321 End: 161,264,393 Build: HG19

No SNPs found for this gene in your DNA data.

MIR8072 GeneCards

Genomic Location
Chr 12 Start: 123,849,311 End: 123,849,390 Build: HG19

No SNPs found for this gene in your DNA data.

MPHOSPH9 GeneCards

M-phase phosphoprotein 9

Genomic Location
Chr 12 Start: 123,638,762 End: 123,717,688 Build: HG19

No SNPs found for this gene in your DNA data.

MUC16 GeneCards

This gene encodes a protein that is a member of the mucin family. Mucins are high molecular weight, O-glycosylated proteins that play an important role in forming a protective mucous barrier, and are found on the apical surfaces of the epithelia. The encoded protein is a membrane-tethered mucin that contains an extracellular domain at its amino terminus, a large tandem repeat domain, and a transmembrane domain with a short cytoplasmic domain. The amino terminus is highly glycosylated, while the repeat region contains 156 amino acid repeats unit that are rich in serines, threonines, and prolines. Interspersed within the repeats are Sea urchin sperm protein Enterokinase and Agrin (SEA) modules, leucine-rich repeats and ankyrin (ANK) repeats. These regions together form the ectodomain, and there is a potential cleavage site found near an SEA module close to the transmembrane domain. This protein is thought to play a role in forming a barrier, protecting epithelial cells from pathogens. Products of this gene have been used as a marker for different cancers, with higher expression levels associated with poorer outcomes.

Genomic Location
Chr 19 Start: 8,959,520 End: 9,092,018 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

MYO7A GeneCards

This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

Genomic Location
Chr 11 Start: 76,839,292 End: 76,926,286 Build: HG19

No SNPs found for this gene in your DNA data.

NARS2 GeneCards

This gene encodes a putative member of the class II family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of asparagine to tRNA molecules. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency 24 (COXPD24).

Genomic Location
Chr 11 Start: 78,147,014 End: 78,285,909 Build: HG19

No SNPs found for this gene in your DNA data.

NDUFC2 GeneCards

Genomic Location
Chr 11 Start: 77,779,343 End: 77,790,908 Build: HG19

No SNPs found for this gene in your DNA data.

NDUFC2-KCTD14 GeneCards

NDUFC2-KCTD14 readthrough

Genomic Location
Chr 11 Start: 77,726,761 End: 77,790,908 Build: HG19

No SNPs found for this gene in your DNA data.

NPTN GeneCards

neuroplastin

Genomic Location
Chr 15 Start: 73,852,355 End: 73,925,730 Build: HG19

No SNPs found for this gene in your DNA data.

NPTN-IT1 GeneCards

Genomic Location
Chr 15 Start: 73,859,279 End: 73,861,884 Build: HG19

No SNPs found for this gene in your DNA data.

OGFOD2 GeneCards

Genomic Location
Chr 12 Start: 123,459,273 End: 123,464,589 Build: HG19

No SNPs found for this gene in your DNA data.

OPRD1 GeneCards

opioid receptor delta 1

Genomic Location
Chr 1 Start: 29,138,682 End: 29,197,779 Build: HG19

No SNPs found for this gene in your DNA data.

OTUD1 GeneCards

OTU deubiquitinase 1

Genomic Location
Chr 10 Start: 23,728,004 End: 23,731,306 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

PAK1 GeneCards

This gene encodes a family member of serine/threonine p21-activating kinases, known as PAK proteins. These proteins are critical effectors that link RhoGTPases to cytoskeleton reorganization and nuclear signaling, and they serve as targets for the small GTP binding proteins Cdc42 and Rac. This specific family member regulates cell motility and morphology. Mutations in this gene have been associated with macrocephaly, seizures, and speech delay. Overexpression of this gene is also reported in many cancer types, and particularly in breast cancer. Alternative splicing results in multiple transcript variants.

Genomic Location
Chr 11 Start: 77,033,062 End: 77,185,139 Build: HG19

No SNPs found for this gene in your DNA data.

PITPNM2 GeneCards

Genomic Location
Chr 12 Start: 123,468,027 End: 123,635,637 Build: HG19

No SNPs found for this gene in your DNA data.

PLA2R1 GeneCards

phospholipase A2 receptor 1

Genomic Location
Chr 2 Start: 160,788,517 End: 160,919,126 Build: HG19

No SNPs found for this gene in your DNA data.

PSMD14 GeneCards

proteasome 26S subunit, non-ATPase 14

Genomic Location
Chr 2 Start: 162,164,936 End: 162,268,228 Build: HG19

No SNPs found for this gene in your DNA data.

PTPRU GeneCards

The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP (MAM) domain, Ig-like and fibronectin type III-like repeats. This PTP was thought to play roles in cell-cell recognition and adhesion. Studies of the similar gene in mice suggested the role of this PTP in early neural development. The expression of this gene was reported to be regulated by phorbol myristate acetate (PMA) or calcium ionophore in Jurkat T lymphoma cells. Alternatively spliced transcript variants have been reported.

Genomic Location
Chr 1 Start: 29,563,034 End: 29,653,312 Build: HG19

No SNPs found for this gene in your DNA data.

RBMS1 GeneCards

Genomic Location
Chr 2 Start: 161,128,662 End: 161,350,318 Build: HG19

No SNPs found for this gene in your DNA data.

REC114 GeneCards

REC114 meiotic recombination protein

Genomic Location
Chr 15 Start: 73,735,505 End: 73,852,354 Build: HG19

No SNPs found for this gene in your DNA data.

RILPL2 GeneCards

Genomic Location
Chr 12 Start: 123,899,586 End: 123,921,231 Build: HG19

No SNPs found for this gene in your DNA data.

RNF4 GeneCards

Genomic Location
Chr 4 Start: 2,470,833 End: 2,517,584 Build: HG19

No SNPs found for this gene in your DNA data.

RNU6-83P GeneCards

Genomic Location
Chr 13 Start: 99,677,488 End: 99,677,599 Build: HG19

No SNPs found for this gene in your DNA data.

RPS17 GeneCards

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of four RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S17E family of ribosomal proteins and is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia 4. Alternative splicing of this gene results in multiple transcript variants. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.

Genomic Location
Chr 15 Start: 83,205,501 End: 83,209,208 Build: HG19

No SNPs found for this gene in your DNA data.

RSF1 GeneCards

Genomic Location
Chr 11 Start: 77,377,274 End: 77,531,880 Build: HG19

No SNPs found for this gene in your DNA data.

SBNO1 GeneCards

strawberry notch homolog 1

Genomic Location
Chr 12 Start: 123,773,656 End: 123,849,394 Build: HG19

No SNPs found for this gene in your DNA data.

SCARNA15 GeneCards

Genomic Location
Chr 15 Start: 83,424,697 End: 83,424,823 Build: HG19

No SNPs found for this gene in your DNA data.

SGPP2 GeneCards

Genomic Location
Chr 2 Start: 223,288,707 End: 223,427,340 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

SLC4A10 GeneCards

This gene belongs to a small family of sodium-coupled bicarbonate transporters (NCBTs) that regulate the intracellular pH of neurons, the secretion of bicarbonate ions across the choroid plexus, and the pH of the brain extracellular fluid. The protein encoded by this gene was initially identified as a sodium-driven chloride bicarbonate exchanger (NCBE) though there is now evidence that its sodium/bicarbonate cotransport activity is independent of any chloride ion countertransport under physiological conditions. This gene is now classified as a member A10 of the SLC4 family of transmembrane solute carriers. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Genomic Location
Chr 2 Start: 162,480,926 End: 162,841,780 Build: HG19

No SNPs found for this gene in your DNA data.

SNHG21 GeneCards

Genomic Location
Chr 15 Start: 83,419,316 End: 83,425,958 Build: HG19

No SNPs found for this gene in your DNA data.

SRSF4 GeneCards

Genomic Location
Chr 1 Start: 29,474,255 End: 29,508,412 Build: HG19

No SNPs found for this gene in your DNA data.

TANC1 GeneCards

tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1

Genomic Location
Chr 2 Start: 159,825,152 End: 160,089,170 Build: HG19

No SNPs found for this gene in your DNA data.

TANK GeneCards

TRAF family member associated NFKB activator

Genomic Location
Chr 2 Start: 161,993,474 End: 162,092,741 Build: HG19

No SNPs found for this gene in your DNA data.

TBR1 GeneCards

This gene is a member of a conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of numerous developmental processes. In mouse, the ortholog of this gene is expressed in the cerebral cortex, hippocampus, amygdala and olfactory bulb and is thought to play an important role in neuronal migration and axonal projection. In mouse, the C-terminal region of this protein was found to be necessary and sufficient for association with the guanylate kinase domain of calcium/calmodulin-dependent serine protein kinase.

Genomic Location
Chr 2 Start: 162,272,808 End: 162,282,381 Build: HG19

No SNPs found for this gene in your DNA data.

TENM2 GeneCards

teneurin transmembrane protein 2

Genomic Location
Chr 5 Start: 166,500,247 End: 167,691,162 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

TENM4 GeneCards

The protein encoded by this gene plays a role in establishing proper neuronal connectivity during development. Defects in this gene have been associated with hereditary essential tremor-5.

Genomic Location
Chr 11 Start: 78,363,874 End: 79,152,074 Build: HG19

No SNPs found for this gene in your DNA data.

THRSP GeneCards

thyroid hormone responsive

Genomic Location
Chr 11 Start: 77,774,907 End: 77,779,397 Build: HG19

No SNPs found for this gene in your DNA data.

TMEM200B GeneCards

Genomic Location
Chr 1 Start: 29,445,941 End: 29,450,415 Build: HG19

No SNPs found for this gene in your DNA data.

TSHR GeneCards

The protein encoded by this gene is a membrane protein and a major controller of thyroid cell metabolism. The encoded protein is a receptor for thyrothropin and thyrostimulin, and its activity is mediated by adenylate cyclase. Defects in this gene are a cause of several types of hyperthyroidism. Three transcript variants encoding different isoforms have been found for this gene.

Genomic Location
Chr 14 Start: 81,421,965 End: 81,612,650 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

TSPYL5 GeneCards

TSPY like 5

Genomic Location
Chr 8 Start: 98,285,716 End: 98,290,156 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

UBE2Q2P2 GeneCards

Genomic Location
Chr 15 Start: 83,023,841 End: 83,084,341 Build: HG19

No SNPs found for this gene in your DNA data.

USP35 GeneCards

ubiquitin specific peptidase 35

Genomic Location
Chr 11 Start: 77,899,965 End: 77,926,278 Build: HG19

No SNPs found for this gene in your DNA data.

VPS37B GeneCards

Genomic Location
Chr 12 Start: 123,349,877 End: 123,380,671 Build: HG19

No SNPs found for this gene in your DNA data.

WDSUB1 GeneCards

Genomic Location
Chr 2 Start: 160,092,309 End: 160,143,214 Build: HG19

No SNPs found for this gene in your DNA data.

WHAMM GeneCards

WASP homolog associated with actin, golgi membranes and microtubules

Genomic Location
Chr 15 Start: 83,478,380 End: 83,504,860 Build: HG19

No SNPs found for this gene in your DNA data.

XYLT1 GeneCards

This locus encodes a xylosyltransferase enzyme. The encoded protein catalyzes transfer of UDP-xylose to serine residues of an acceptor protein substrate. This transfer reaction is necessary for biosynthesis of glycosaminoglycan chains. Mutations in this gene have been associated with increased severity of pseudoxanthoma elasticum.

Genomic Location
Chr 16 Start: 17,195,626 End: 17,564,817 Build: HG19
Associated SNPs
0 / 1 detected
SNP Genotype Ref. Allele Variant Allele Frequency Status

ZFYVE28 GeneCards

zinc finger FYVE-type containing 28

Genomic Location
Chr 4 Start: 2,271,324 End: 2,420,372 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF350 GeneCards

zinc finger protein 350

Genomic Location
Chr 19 Start: 52,467,593 End: 52,490,093 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF432 GeneCards

zinc finger protein 432

Genomic Location
Chr 19 Start: 52,534,631 End: 52,552,091 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF577 GeneCards

Genomic Location
Chr 19 Start: 52,307,695 End: 52,391,204 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF613 GeneCards

Genomic Location
Chr 19 Start: 52,430,725 End: 52,449,874 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF614 GeneCards

Genomic Location
Chr 19 Start: 52,516,577 End: 52,531,632 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF615 GeneCards

Genomic Location
Chr 19 Start: 52,494,585 End: 52,511,464 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF616 GeneCards

Genomic Location
Chr 19 Start: 52,616,344 End: 52,643,191 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF649 GeneCards

Genomic Location
Chr 19 Start: 52,392,488 End: 52,408,270 Build: HG19

No SNPs found for this gene in your DNA data.

ZNF841 GeneCards

Genomic Location
Chr 19 Start: 52,561,348 End: 52,599,018 Build: HG19

No SNPs found for this gene in your DNA data.

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Coverage: 3/24 SNPs detected (12%)
Reference: Human Genome Build 37 (HG19)
Generated: March 02, 2026
DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence. Other testing companies may report using the opposite strand, requiring conversion for accurate comparison.