Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11601 to 11610 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11601
Scavenger receptor class B member 2
AMRF, CD36L2, EPM4, HLGP85, LGP85, LIMP-2, LIMPII, SR-BII
Myoclonus-renal failure syndrome, Alzheimer disease, Progressive myoclonic epilepsy, Rolandic epilepsy, Focal glomerulosclerosis, Gaucher disease, Hypertension, Parkinson disease, Unverricht-lundborg syndrome

11602
Scavenger receptor class F member 1
SREC, SREC-I, SREC1
Brain aneurysm

11603
Scavenger receptor class F member 2
NSR1, SREC-II, SREC2, SRECRP-1, VDEGS
Obstructive pulmonary disease, Desbuquois syndrome, Open angle glaucoma, Van der woude syndrome

11604
Scavenger receptor family member expressed on T cells 1
-
Hearing loss

11605
Saccharopine dehydrogenase (putative)
CGI-49, CGI49, NET11
Vascular dementia

11606
Stearoyl-CoA desaturase
FADS5, MSTP008, SCD1, SCDOS, hSCD1
Adrenoleukodystrophy, Carcinoma, Hepatocellular carcinoma, Cataract, Congestive heart failure, Congestive ophthalmopathy, Dermatologic disorder, Disorder of eye, Fatty liver, Fatty liver, alcoholic, Graves ophthalmopathy, Heart failure, Insomnia, Lipidoses, Lipoidosis
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11607
Stearoyl-CoA desaturase 5
ACOD4, DFNA79, FADS4, HSCD5, SCD2, SCD4
Deafness, Hearing loss, Schizophrenia, Diabetes mellitus type 2, Venous thromboembolism

11608
Sciellin
-
Gastric cancer, Moyamoya angiopathy

11609
Sec1 family domain containing 1
C14orf163, RA410, SLY1, SLY1P, STXBP1L2
Amyotrophic lateral sclerosis

11610
Sec1 family domain containing 2
STXBP1L1
Alzheimer disease, Androgenetic alopecia, Autism, Breast cancer, Cataract, Insomnia, Open angle glaucoma, Uterine fibroid