Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
2131 to 2140 of 12229 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2131
Crystallin gamma D
CACA, CCA3, CCP, CRYG4, CTRCT4, PCC, cry-g-D
Cataract, Cataract-microcornea syndrome, Congenital cataract, Congenital coloboma of iris, Coralliform cataract, Corneal dystrophy, Microcornea, Myopia, Nystagmus, Pulverulent cataract

2132
MIB E3 ubiquitin protein ligase 2
ZZANK1, ZZZ5
Left ventricular noncompaction

2133
Solute carrier family 34 member 3
HHRH, NPT2C, NPTIIc
Dwarfism, Frontal bossing, Hereditary hypophosphatemic rickets with hypercalciuria, Hypophosphatemic rickets, Hypophosphatemic rickets with hypercalciuria, hereditary, Renal tubular disorder, Rickets

2134
Ankyrin repeat and SOCS box containing 15
-
Chromophobe carcinoma, Leukemia, Papillary renal carcinoma, Renal carcinoma, Rheumatoid arthritis

2135
Crystallin gamma S
CRYG8, CTRCT20
Cataract, Congenital cataract

2136
Crystallin mu
DFNA40, THBP
Deafness, Hearing loss, Non-syndromic sensorineural deafness, Pelvic organ prolapse

2137
Poly(ADP-ribose) polymerase family member 4
ADPRTL1, ARTD4, PARP-4, PARPL, PH5P, VAULT3, VPARP, VWA5C, p193
Colonic neoplasms, Intracranial hypertension

2138
MAGUK p55 scaffold protein 7
-
Asthma, Glaucoma

2139
Citrate synthase
-
Cardiomyopathy, Congestive heart failure, Heart failure, Myocardial diseases, Myocardial infarction, Obesity, Psoriasis

2140
FERM and PDZ domain containing 2
PDZD5C, PDZK4, PDZK5C
Colorectal cancer, Myopia, Narcolepsy