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Dataset:
Curated
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Showing genes starting with "U"
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1 to 10 of 184 Genes
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Entrez ID
Gene Symbol
Gene Name
Synonyms
Diseases
1
100130015
URAHP
Urate (hydroxyiso-) hydrolase, pseudogene
URAH
Ciliary dyskinesia
2
100130239
UBA52P6
Ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 6
RPL40_3_969
Glaucoma
3
100131327
UQCRC2P1
Ubiquinol-cytochrome c reductase core protein 2 pseudogene 1
-
Celiac disease
4
100271837
USH1H
-
-
Usher syndrome
5
100286971
UBDP1
Ubiquitin D pseudogene 1
dJ994E9.3
Rheumatoid arthritis
6
100287272
USP8P1
USP8 pseudogene 1
D84394.7, USP8P
Diabetes mellitus
,
Monoclonal gammapathies
,
Multiple myeloma
,
Multiple sclerosis
,
Paraproteinemia
,
Sarcoidosis
7
100288170
UBE2V1P15
UBE2V1 pseudogene 15
-
Leprosy
8
100505877
UBE2E2-DT
UBE2E2 divergent transcript
UBE2E2-AS1
Diabetes mellitus
9
100533179
UBE2F-SCLY
UBE2F-SCLY readthrough (NMD candidate)
-
Ovarian neoplasm
10
10083
USH1C
USH1 protein network component harmonin
AIE-75, DFNB18, DFNB18A, NY-CO-37, NY-CO-38, PDZ-45, PDZ-73, PDZ-73/NY-CO-38, PDZ73, PDZD7C, ush1cpst
Anxiety disorder
,
Cataract
,
Cerebral cortical atrophy
,
Ciliopathies
,
Congenital sensorineural hearing loss
,
Deafness
,
Developmental delay
,
Disorder of eye
,
Hallucinations
,
Hearing loss
,
Hemianopsia
,
Hereditary retinal dystrophy
,
Leukemia
,
Mental depression
,
Mental retardation
,
Motor delay
,
Non-syndromic sensorineural deafness
,
Nonsyndromic deafness
,
Nyctalopia
,
Retinitis pigmentosa
,
Rod-cone dystrophy
,
Schizophrenia
,
Subcortical cerebral atrophy
,
Usher syndrome
View all (9 more)
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