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
8901 to 8910 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8901
NAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL
H105E3, SDR31E1, XAP104
Arachnodactyly, Byzanthine arch palate, Ck syndrome, Congenital hemidysplasia with ichthyosiform erythroderma and limb defects, Connective tissue disease, Desbuquois syndrome, Hearing impairment, Mitral valve prolapse, Perisylvian polymicrogyria, Scoliosis, Squamous cell carcinoma, Polymicrogyria

8902
N-ethylmaleimide sensitive factor, vesicle fusing ATPase
DEE96, SEC18, SKD2
Alzheimer disease, Androgenetic alopecia, Breast cancer, Cancer, Colorectal cancer, Coronary artery disease, Developmental and epileptic encephalopathy, Estrogen-receptor negative breast cancer, Hypertension, Hypertrophic cardiomyopathy, Lung cancer, Major depressive disorder, Ovarian epithelial cancer, Migraine, Neurotic disorder
View all (8 more)

8903
NSFL1 cofactor
P47, UBX1, UBXD10, UBXN2C, dJ776F14.1
Metabolic syndrome, Sjogren syndrome, Diabetes mellitus type 2

8904
Neuronal vesicle trafficking associated 2
CALY3, HMP19
Duchenne muscular dystrophy, Psychiatric disorders

8905
NSL1 component of MIS12 kinetochore complex
C1orf48, DC8, MIS14
Color vision deficiency, Multiple sclerosis, Diabetes mellitus type 1, Diabetes mellitus type 2

8906
Neutral sphingomyelinase activation associated factor
FAN, GRAMD5
Essential tremor

8907
NSE1 component of SMC5/6 complex
NSE1
Asthma, Eczema, Peripheral arterial disease

8908
NSE2 SUMO ligase component of SMC5/6 complex
C8orf36, MMS21, NSE2, ZMIZ7
Alzheimer disease, Behcet disease, Central nervous system cancer, Obstructive pulmonary disease, Desbuquois syndrome, Glioblastoma, Glioma, Global developmental delay, Metabolic syndrome, Oligodendroglioma, Psoriasis, Seckel syndrome, Diabetes mellitus type 2

8909
NSE3 component of SMC5/6 complex
HCA4, LICS, MAGEG1, MAGEL3, NDNL2, NSE3
Lung disease

8910
NMDA receptor synaptonuclear signaling and neuronal migration factor
HH9, NELF
Carcinoma, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Male infertility single gene azoospermia, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Sheehan syndrome