Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
1241 to 1250 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1241
BBSome interacting protein 1
BBIP10, BBS18, NCRNA00081, bA348N5.3
Bardet-biedl syndrome, Hypogonadotropic hypogonadism, Micropenis, Obesity, Retinitis pigmentosa, Rod-cone dystrophy, Specific learning disability, Systemic lupus erythematosus, Diabetes mellitus type 2, Postaxial polydactyly

1242
Basal body orientation factor 1
C14orf45, CCDC176, FBB10
Polycystic ovary syndrome

1243
Gamma-butyrobetaine hydroxylase 1
BBH, BBOX, G-BBH, gamma-BBH
Breast cancer, Liver cirrhosis, Otosclerosis

1244
Bardet-Biedl syndrome 1
BBS2L2
Bardet-biedl syndrome, Ciliopathy, Insomnia, Retinitis pigmentosa, Usher syndrome

1245
Bardet-Biedl syndrome 10
C12orf58
Bardet-biedl syndrome, Ciliopathy, Intellectual developmental disorder, Macular degeneration, Optic atrophy, Polydactyly, Retinitis pigmentosa, Saldino-noonan syndrome, Postaxial polydactyly

1246
Bardet-Biedl syndrome 12
C4orf24
Bardet-biedl syndrome, Ciliopathy, Congenital neurologic anomalies, Polydactyly, Retinitis pigmentosa, Sarcoidosis

1247
Bardet-Biedl syndrome 2
BBS, RP74
Retinitis pigmentosa, Bardet-biedl syndrome, Breast cancer, Ciliopathy, Hearing loss, Insomnia, Metabolic syndrome, Obesity, Diabetes mellitus type 2

1248
Bardet-Biedl syndrome 4
-
Bardet-biedl syndrome, Ciliopathy, Major depressive disorder, Obesity, Retinitis pigmentosa, Diabetes mellitus type 2

1249
Bardet-Biedl syndrome 5
-
Bardet-biedl syndrome, Cone dystrophy, Ocular sarcoidosis, Retinitis pigmentosa

1250
Bardet-Biedl syndrome 7
BBS2L1
Atrial fibrillation, Bardet-biedl syndrome, Breast cancer, Ciliopathy, Intellectual developmental disorder, Optic atrophy, Psoriasis, Retinitis pigmentosa