Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6461 to 6470 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6461
Isochorismatase domain containing 1
CGI-111
Peripheral arterial disease

6462
Isochorismatase domain containing 2
-
Cataract, Osteoarthritis

6463
IST1 factor associated with ESCRT-III
CHMP8, OLC1
Breast cancer

6464
Intestine specific homeobox
Pix-1, RAXLX
Alzheimer disease

6465
Inositol-3-phosphate synthase 1
INO1, INOS, IPS, IPS 1, IPS-1
Adenoid cystic carcinoma, Polycystic ovary syndrome, Salivary gland neoplasms

6466
Itchy E3 ubiquitin protein ligase
ADMFD, AIF4, AIP4, NAPP1
Androgenetic alopecia, Autoimmune disease, Coronary artery disease, Endocrine system disease, Metabolic syndrome, Neurotic disorder, Diabetes mellitus type 2, Venous thromboembolism

6467
Integrin alpha FG-GAP repeat containing 1
2310047C21Rik, CDA08, LINKIN, LNKN-1, TIP
Color vision deficiency

6468
Integrin alpha FG-GAP repeat containing 2
FGGAP1, KICS3, MDS028
Neurodevelopmental disorder

6469
Integrin subunit alpha 1
CD49a, VLA1
Attention deficit hyperactivity disorder, Obstructive pulmonary disease, Coronary artery disease, Diabetes mellitus type 2, Hearing loss, Myocardial infarction

6470
Integrin subunit alpha 11
HsT18964
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Dementia, Dupuytren contracture, Major depressive disorder, Diabetes mellitus type 2, Uterine fibroid