Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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1321 to 1330 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1321
Basic helix-loop-helix family member e40
BHLHB2, Clast5, DEC1, HLHB2, SHARP-2, SHARP2, STRA13, Stra14
Androgenetic alopecia, Eczema, Bipolar disorder, Bipolar depression, Glioblastoma, Hypothyroidism, Myocardial ischemia, Osteoarthritis, Psoriasis vulgaris, Schizophrenia, Sleep disorder

1322
Basic helix-loop-helix family member e41
BHLHB3, DEC2, FNSS1, SHARP1, hDEC2
Bipolar disorder, Lung neoplasms, Major depressive disorder, Mood disorder, Diabetes mellitus type 2

1323
Betaine--homocysteine S-methyltransferase
BHMT1, HEL-S-61p
Ischemic stroke, Obstructive pulmonary disease, Diabetes mellitus type 2, Gastric ulcer, Hepatolenticular degeneration, Neural tube defect, Neural tube defects, x-linked

1324
Betaine--homocysteine S-methyltransferase 2
-
Cleft lip, Cleft palate, Complete unilateral cleft lip, Congenital heart defects

1325
BicC family RNA binding protein 1
BICC
Polycystic kidney disease, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Kidney disease, Colorectal cancer, Renal agenesis, Corneal astigmatism, Coronary artery disease, Major depressive disorder, Developmental disability, Eye disease, Glaucoma, Gout, Hypertension, Hyperuricemia
View all (8 more)

1326
BICD cargo adaptor 1
BICD, bic-D 1
Color vision deficiency, Emphysema, Multiple sclerosis, Obesity, Pancreatic cancer

1327
BICD cargo adaptor 2
SMALED2, SMALED2A, SMALED2B, bA526D8.1
Amyotrophic lateral sclerosis, Arthrogryposis multiplex congenita, Autism, Childhood-onset spinal muscular atrophy, Distal hereditary motor neuropathy, Hereditary axonal motor and sensory neuropathy, Spinal muscular atrophy, Cerebral cortical atrophy, Charcot-marie-tooth disease, Distal muscular dystrophy, Hemorrhoid, Myopathy, Spastic paraplegia, Hereditary spastic paraplegia, Diabetes mellitus type 2

1328
BICD family like cargo adaptor 1
BICDR-1, BICDR1, CCDC64, CCDC64A, H_267D11.1
Colorectal cancer

1329
BRD4 interacting chromatin remodeling complex associated protein
CSS12, GLTSCR1, SMARCK1
Androgenetic alopecia, Atrial fibrillation, Coffin-siris syndrome, Colonic neoplasms, Developmental disability, Intellectual developmental disorder, Alzheimer disease, Neurodevelopmental disorder

1330
BICRA like chromatin remodeling complex associated protein
GLTSCR1L, KIAA0240, SMARCK2
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Stroke, Substance abuse