Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14201 to 14210 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14201
Tubulin beta 4B class IVb
Beta2, LCAEOD, TUBB2, TUBB2C
Leber congenital amaurosis, Retinitis pigmentosa

14202
Tubulin beta 6 class V
FPVEPD, HsT1601, TUBB-5
Blepharoptosis, Facial nerve disorder, Optic atrophy, Spastic ataxia, Spinocerebellar ataxia

14203
Tubulin beta 8 class VIII
OOMD, OOMD2, OZEMA2, bA631M21.2
Female infertility, Oocyte maturation defect

14204
Tubulin delta 1
TUBD
Crohn disease, Gout, Inflammatory bowel disease, Metabolic syndrome, Polydactyly, Diabetes mellitus type 2, Ulcerative colitis

14205
Tubulin gamma 1
CDCBM4, GCP-1, TUBG, TUBGCP1
15q11.2 microdeletion syndrome, Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Lissencephaly, Cortical development malformation, Microcephaly, Myopathy, Myositis, Diabetes mellitus type 2

14206
Tubulin gamma 2
-
Alzheimer disease, Psoriasis, Diabetes mellitus type 2

14207
Tubulin gamma complex component 2
ALP4, GCP-2, GCP2, Grip103, PAMDDFS, SPBC97, SPC97, Spc97p, h103p, hGCP2, hSpc97
Cortical dysplasia with other brain malformations, Lissencephaly, Cortical development malformation

14208
Tubulin gamma complex component 3
104p, ALP6, GCP3, Grip104, SPBC98, Spc98, Spc98p
Bipolar disorder, Cardiac embolism, Cardioembolic stroke, Cardiovascular disease, Prostate cancer

14209
Tubulin gamma complex component 4
76P, GCP-4, GCP4, Grip76, MCCRP3
Chorioretinopathy with microcephaly, Microcephaly, Optic atrophy, Retinitis pigmentosa

14210
Tubulin gamma complex component 5
GCP5
Bipolar disorder, Obsessive-compulsive disorder