Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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12681 to 12690 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12681
Sperm antigen with calponin homology and coiled-coil domains 1
CYTSB, HCMOGT-1, HCMOGT1, NSP, NSP5
Colorectal cancer, Endometriosis, Obesity, Schizophrenia

12682
Sperm antigen with calponin homology and coiled-coil domains 1 like
CYTSA, GBBB2, OBLFC1, TBHS, TBHS1
Opitz g/bbb syndrome, Commissural facial cleft, Coronary artery disease, Craniosynostosis, Desbuquois syndrome, Intellectual developmental disorder, Major depressive disorder, Kawasaki disease, Myocardial infarction, Teebi syndrome, Tessier facial cleft, Diabetes mellitus type 2

12683
Sperm flagellar 2
CT122, KPL2, SPGF43
Asthma, Eczema, Atrophic macular degeneration, Autoimmune thyroid disease, Biliary cirrhosis, Rhinosinusitis, Ciliary dyskinesia, Congenital impairment of spermatozoa motility, Duchenne muscular dystrophy, Hypothyroidism, Multiple sclerosis, Nasal polyp, Nasal disorder, Biliary cholangitis, Psoriasis
View all (5 more)

12684
Striated muscle enriched protein kinase
APEG-1, APEG1, BPEG, CNM5, MYLK6, SPEGalpha, SPEGbeta
Atrial fibrillation, Centronuclear myopathy, Obstructive pulmonary disease, Oligodendroglioma

12685
Spermatid maturation 1
C17orf83
Asthma

12686
SPEM family member 2
C17orf74
Asthma, Uterine fibroid

12687
Spen family transcriptional repressor
HIAA0929, MINT, RATARS, RBM15C, SHARP
1p36 deletion syndrome, Alzheimer disease, Atrial fibrillation, Autism, Chromosome 1p36 deletion syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Prostate cancer, Prostatic neoplasms

12688
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Obesity

12689
SPG11 vesicle trafficking associated, spatacsin
ALS5, CMT2X, KIAA1840
Alzheimer disease, Amyotrophic lateral sclerosis, Autism, Charcot-marie-tooth disease, Spastic paraplegia, Intellectual developmental disorder, Parkinson disease, Spastic ataxia, Hereditary spastic paraplegia

12690
SPG21 abhydrolase domain containing, maspardin
ABHD21, ACP33, BM-019, GL010, MAST
Spastic paraplegia, Hereditary spastic paraplegia, Spinocerebellar ataxia