Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14451 to 14460 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14451
Ubiquitin related modifier 1
C9orf74
Stomach neoplasms, Diabetes mellitus type 2

14452
Urocanate hydratase 1
HMFN0320, UROCD
Anorectal malformation, Ataxia, Hepatocellular carcinoma, Intellectual developmental disorder, Hypertension, Urocanase deficiency, Urocanate hydratase deficiency

14453
Uroporphyrinogen decarboxylase
PCT, UPD
Head and neck neoplasms, Hepatoerythropoietic porphyria, Porphyria cutanea tarda, Porphyria

14454
Uroporphyrinogen III synthase
Mgu, UROIIIS
Congenital erythropoietic porphyria, Cutaneous porphyria, Porphyria

14455
U6 snRNA biogenesis phosphodiesterase 1
C16orf57, HVSL1, Mpn1, PN, hMpn1, hUsb1
Obstructive pulmonary disease, Dyskeratosis congenita

14456
Upstream transcription factor 1
FCHL, FCHL1, HYPLIP1, MLTF, MLTFI, UEF, bHLHb11
Cardiovascular disease, Diabetes mellitus type 2, Hyperlipidemia

14457
Upstream transcription factor 2, c-fos interacting
FIP, bHLHb12
Insomnia

14458
Upstream transcription factor family member 3
KIAA2018
Cowden disease, Schizophrenia

14459
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

14460
USH1 protein network component sans
ANKS4A, SANS
Colorectal cancer, Deafness, Hearing impairment, Hearing loss, Idiopathic pulmonary fibrosis, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome