Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
1171 to 1180 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1171
HBS1 like translational GTPase
EF-1a, ERFS, HBS1, HSPC276, eRF3c
Hodgkin disease

1172
Adenosylhomocysteinase like 1
DCAL, IRBIT, PPP1R78, PRO0233, XPVKONA
Alzheimer disease

1173
Polo like kinase 2
SNK, hPlk2, hSNK
Anaplastic carcinoma, Arthritis, Carcinoma, Juvenile arthritis, Lung adenocarcinoma, Ovarian endometrioid carcinoma, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease

1174
Zinc finger MYND-type containing 11
BRAM1, BS69, MRD30
Autism, Developmental delay, Dysmorphic features, Eosinophilia, Macrostomia, Mental retardation, Multiple congenital anomalies, Non-syndromic intellectual disability, Ptosis

1175
Serine and arginine rich splicing factor 10
FUSIP1, FUSIP2, NSSR, PPP1R149, SFRS13, SFRS13A, SRp38, SRrp40, TASR, TASR1, TASR2
Endometrial neoplasms, Endometrial carcinoma, Ovarian neoplasm, Sclerocystic ovaries, Ovarian cancer, Polycystic ovary syndrome, Schizophrenia

1176
POP4 ribonuclease P/MRP subunit
RPP29
Ovarian neoplasm, Ovarian cancer

1177
CAMP regulated phosphoprotein 21
ARPP-21, R3HDM3, RCS, TARPP
Mental depression, Mood disorder

1178
NIMA related kinase 6
SID6-1512
Hypothyroidism, Vitiligo

1179
WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit
GAMOS6, MIGSB, TRM82, TRMT82, Wuho, hWH
Aqueductal stenosis, Camptodactyly of fingers, Congenital epicanthus, Developmental delay, Dwarfism, Dyssomnia, Galloway-mowat syndrome, Hemiplegia/hemiparesis, Hiatal hernia, High palate, Impaired cognition, Kidney disease, Macrostomia, Macrotia, Mental retardation
View all (12 more)

1180
Solute carrier family 17 member 3
GOUT4, NPT4, UAQTL4
Breast carcinoma, Coronary heart disease, Gout, Gouty arthritis, Schizophrenia