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445 ASS1

445

ASS1

argininosuccinate synthase 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition argininosuccinate synthase 1

研究结论

Date Results Publications
2021-04-13 10:11:00 Neonatal factors related to survival and intellectual and developmental outcome of patients with early-onset urea cycle disorders. 32273051
2019-12-14 11:45:00 The combination of ADI-PEG20 with temozolomide (TMZ) demonstrates enhanced effects in both ASS1 negative and ASS1 positive backgrounds.Our data provide proof of principle for a therapeutic strategy for GBM using peripheral blood arginine depletion that does not require BBB passage of drug and is well tolerated 30546006
2019-12-07 12:28:00 Citrullinemia type I (CTLN1) is a rare autosomal recessive disorder of the urea cycle caused by a deficiency in the argininosuccinate synthetase (ASS1) enzyme due to mutations in the ASS1 gene. 31208364
2019-08-10 11:02:00 Overexpression of ASS1 inhibits hepatocellular carcinoma progression by inactivating the pathway, which subsequently decreases the expression of ID1. 30883650
2019-05-25 11:46:00 Arginine starvation induces p300 dissociation, allowing histone HDAC2 and cofactor Sin3A to deacetylate these histones at the ASS1 promoter, thereby facilitating HIF-1alpha-proteasomal complex, driven by PHD2, to degrade HIF-1alpha in situ. 28883660

名称对应

Type IDs
Synonymous ASS, CTLN1
Gene
UniProtKB-ID: ASSY_HUMAN, Q5T6L4_HUMAN
UniprotKB: P00966, Q5T6L4
UniParc: UPI00000015D6
EMBL: L00079, BC021676, L00083, L00082, L00081, M34903, KU177923, L00080, X01630, AK027126, L00084, AY034076, BC009243, AK315093, GQ891434, CH471090
Ensembl: ENSG00000130707
KO: hsa:445
Nucleutide sequences
EMBL-CDS: AAA51783.1, AAA51782.1, AAH21676.1, AAK67487.1, CAA25771.1, AAH09243.1, ADO22296.1, EAW87935.1, ALQ33381.1, EAW87932.1, BAG37558.1
Gene_ORFName: hCG_31245
Ensembl_TRS: ENST00000352480, ENST00000372394, ENST00000372393
Protein sequencees
Ensembl_PRO: ENSP00000253004, ENSP00000361469, ENSP00000361471
RefSeq: NP_446464.1, NP_000041.2, XP_005272257.1, XP_016870218.1, XP_011517007.1
Others
UniRef100: UniRef100_P00966
UniRef90: UniRef90_P00966
UniRef50: UniRef50_P00966
UniGene: Hs.160786
CCDS: CCDS6933.1

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