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
14181 to 14190 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14181
Tweety family member 1
-
Idiopathic pulmonary fibrosis

14182
Tweety family member 2
C17orf29
Hearing loss

14183
Tweety family member 3
-
Cerebral amyloid angiopathy, Schizophrenia

14184
TUB bipartite transcription factor
RDOB, rd5
Autism, Coronary artery disease, Essential tremor, Hearing loss, Lung cancer, Retinitis pigmentosa

14185
Tubulin alpha 1a
B-ALPHA-1, LIS3, TUBA3
Basal cell carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Cerebral palsy, Congenital fibrosis of extraocular muscles, Congenital neurologic anomalies, Cryptorchidism, Dandy-walker syndrome, Myoclonic encephalopathy, Fetal akinesia deformation sequence, Global developmental delay, Lissencephaly, Macrogyria, Cortical development malformation, Microcephaly, Movement disorder
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14186
Tubulin alpha 1b
K-ALPHA-1
Congenital fibrosis of extraocular muscles, Neuromuscular disease, Osteoporosis

14187
Tubulin alpha 1c
OZEMA24, TUBA6, bcm948
Breast cancer, Cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Lung cancer, Oocyte maturation defect, Osteoporosis, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Stomach neoplasms

14188
Tubulin alpha 3c
TUBA2, bA408E5.3
Alzheimer disease, Coronary aneurysm

14189
Tubulin alpha 3d
H2-ALPHA, KTCN9, TUBA2
Keratoconus

14190
Tubulin alpha 3e
-
Neurodevelopmental disorder, Congenital microcephaly, Global developmental delay, Lissencephaly, Non-specific syndromic intellectual disability