Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "U"
191 to 200 of 268 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
URI1 prefoldin like chaperone
C19orf2, NNX3, PPP1R19, RMP, URI
Carcinoma, Ovarian neoplasms

192
Ubiquitin related modifier 1
C9orf74
Stomach neoplasms, Diabetes mellitus type 2

193
Urocanate hydratase 1
HMFN0320, UROCD
Anorectal malformation, Ataxia, Hepatocellular carcinoma, Intellectual developmental disorder, Hypertension, Urocanase deficiency, Urocanate hydratase deficiency

194
Uroporphyrinogen decarboxylase
PCT, UPD
Head and neck neoplasms, Hepatoerythropoietic porphyria, Porphyria cutanea tarda, Porphyria

195
Uroporphyrinogen III synthase
Mgu, UROIIIS
Congenital erythropoietic porphyria, Cutaneous porphyria, Porphyria

196
U6 snRNA biogenesis phosphodiesterase 1
C16orf57, HVSL1, Mpn1, PN, hMpn1, hUsb1
Obstructive pulmonary disease, Dyskeratosis congenita

197
Upstream transcription factor 1
FCHL, FCHL1, HYPLIP1, MLTF, MLTFI, UEF, bHLHb11
Cardiovascular disease, Diabetes mellitus type 2, Hyperlipidemia

198
Upstream transcription factor 2, c-fos interacting
FIP, bHLHb12
Insomnia

199
Upstream transcription factor family member 3
KIAA2018
Cowden disease, Schizophrenia

200
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
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Meniere disease, Optic atrophy, Retinitis pigmentosa, Usher syndrome