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KLK8

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Kallikrein-8 is a protein that in humans is encoded by the KLK8 gene.[5][6][7][8][9]

AliasesKLK8, HNP, NP, NRPN, PRSS19, TADG14, kallikrein related peptidase 8
External IDsOMIM: 605644; MGI: 1343327; GeneCards: KLK8
PDBOrtholog search: PDBe RCSB
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KLK8
Identifiers
AliasesKLK8, HNP, NP, NRPN, PRSS19, TADG14, kallikrein related peptidase 8
External IDsOMIM: 605644; MGI: 1343327; GeneCards: KLK8
Available structures
PDBOrtholog search: PDBe RCSB
Enzyme activity
EC #BRENDAExPASyKEGGMetaCyc
3.4.21.118↗↗↗↗
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001281431
NM_007196
NM_144505
NM_144506
NM_144507

NM_008940
NM_001324398

RefSeq (protein)

NP_001268360
NP_009127
NP_653088
NP_653089
NP_653090

NP_001311327
NP_032966

Location (UCSC)Chr 19: 51 – 51 MbChr 7: 43.45 – 43.45 Mb
PubMed search[3][4]
Wikidata
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Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Alternate splicing of this gene results in four transcript variants encoding four different isoforms. The isoforms exhibit distinct patterns of expression that suggest roles in brain plasticity and ovarian cancer.[9]

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