Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13171 to 13180 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13171
TBC1 domain family member 15
RAB7-GAP
Alzheimer disease, Schizophrenia

13172
TBC1 domain family member 16
-
Color vision deficiency, Major depressive disorder, Migraine

13173
TBC1 domain family member 19
-
Cardiovascular disease, Coronary artery disease, Heart failure, Hypertension, Myocardial infarction, Schizophrenia

13174
TBC1 domain family member 2
PARIS-1, PARIS1, TBC1D2A
Duodenitis, Hypertrophic cardiomyopathy, Post-traumatic stress disorder, Prostatic neoplasms

13175
TBC1 domain family member 20
C20orf140, WARBM4
Apert syndrome, Congenital malformation syndromes predominantly affecting facial appearance, Cryptophthalmos syndrome, Cyclocephaly, Goldenhar syndrome, Mobius syndrome, Orofaciodigital syndrome, Warburg micro syndrome

13176
TBC1 domain family member 21
MgcRabGAP
Bipolar disorder, Kidney disease, Color vision deficiency, Conotruncal cardiac defect, Diabetic neuropathy, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Myopathy, Neurotic disorder, Oligodendroglioma, Scoliosis, Diabetes mellitus type 2

13177
TBC1 domain family member 22A
C22orf4, HSC79E021
Colorectal cancer, Ovarian cancer

13178
TBC1 domain family member 22B
C6orf197
Central nervous system cancer, Glioblastoma, Glioma

13179
TBC1 domain family member 23
NS4ATP1, PCH11
Central nervous system cancer, Glioma, Pontocerebellar hypoplasia

13180
TBC1 domain family member 24
DEE16, DFNA65, DFNB86, DOORS, EIEE16, EIM, EPRPDC, FIME, TLDC6
Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies, Deafness, Deafness with congenital onychodystrophy, Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, Developmental and epileptic encephalopathy, Digitrenocerebral syndrome, Doors syndrome, Dysarthria, Epilepsy of infancy with migrating focal seizures, Infantile myoclonic epilepsy
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