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8492 PRSS12

8492

PRSS12

serine protease 12

protein-coding

Homo sapiens

基因描述

Type Description
Definition serine protease 12

研究结论

Date Results Publications
2010-06-30 22:04:00 Observational study of gene-disease association. (HuGE Navigator) 20332099
2010-01-21 00:00:00 4-base pair deletion in the neurotrypsin gene was associated with autosomal recessive nonsyndromic mental retardation; findings suggest that neurotrypsin-mediated proteolysis is required for normal synaptic function 12459588

名称对应

Type IDs
Synonymous BSSP-3, BSSP3, MRT1
Gene
UniProtKB-ID: NETR_HUMAN, Q96I80_HUMAN
UniprotKB: P56730, Q96I80
UniParc: UPI0000070C6A, UPI000013E34B
EMBL: BC007761, AC096762, AJ001531, AF077298
Ensembl: ENSG00000164099
KO: hsa:8492
Nucleutide sequences
EMBL-CDS: CAA04816.1, AAD25919.1, AAH07761.1
Ensembl_TRS: ENST00000296498
Protein sequencees
Ensembl_PRO: ENSP00000296498
RefSeq: XP_005263375.1, XP_011530689.1, NP_003610.2
Others
UniRef100: UniRef100_Q96I80, UniRef100_P56730
UniRef90: UniRef90_P56730, UniRef90_Q96I80
UniRef50: UniRef50_A0A4W3GXB6, UniRef50_P56730
UniGene: Hs.445857
CCDS: CCDS3709.1

全选

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研究热度

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