Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12771 to 12780 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12771
Spectrin beta, non-erythrocytic 2
GTRAP41, SCA5, SCAR14
Spinocerebellar ataxia, Cerebellar ataxia, Bipolar disorder, Breast cancer, Insomnia, Intellectual developmental disorder, Major depressive disorder, Osteoarthritis, Schizophrenia

12772
Spectrin beta, non-erythrocytic 4
CMND, NEDHND, QV, SPNB4, SPTBN3
Renal cell carcinoma, Global developmental delay, Neurodevelopmental disorder, Polycystic ovary syndrome

12773
Spectrin beta, non-erythrocytic 5
BSPECV, HUBSPECV, HUSPECV
Autism, Candidemia, Cardiovascular disease, Neurodevelopmental disorder

12774
Serine palmitoyltransferase long chain base subunit 1
ALS27, HSAN1, HSN1, LBC1, LCB1, SPT1, SPTI
Alzheimer disease, Amyotrophic lateral sclerosis, Bipolar disorder, Charcot-marie-tooth disease, Dementia, Glaucoma, Hereditary sensory and autonomic neuropathy, Major depressive disorder, Schizophrenia

12775
Serine palmitoyltransferase long chain base subunit 2
HSN1C, LCB2, LCB2A, NSAN1C, SPT2, hLCB2a
Amyotrophic lateral sclerosis, Charcot-marie-tooth disease, Colorectal cancer, Hereditary sensory and autonomic neuropathy, Psychiatric disorders

12776
Serine palmitoyltransferase long chain base subunit 3
C20orf38, LCB 3, LCB2B, LCB3, SPT 3, SPT3, SPTLC2L, dJ718P11, dJ718P11.1, hLCB2b
Cerebral amyloid angiopathy, Peripheral neuropathy, Sensory neuropathy

12777
Serine palmitoyltransferase small subunit A
C14orf147, SPG90A, SPG90B, SSSPTA
Spastic paraplegia

12778
Serine palmitoyltransferase small subunit B
ADMP, C3orf57, SSSPTB
Parkinson disease

12779
SPT2 chromatin protein domain containing 1
Spt2
Breast cancer, Psychiatric disorders

12780
Spermatogenic leucine zipper 1
CILD38, NYD-TSP1, PPP1R148
Breast cancer, Stomach neoplasms