KLK7 - kallikrein related peptidase 7 Gene

Also Known as hK7; SCCE; PRSS6

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5650

About KLK7

Cytogenetic location: 19q13.41 Genomic coordinates (GRCh38): 19:50,976,468-50,984,064 (from NCBI)

This gene has 6 transcripts (splice variants), 107 orthologues and 12 paralogues. Biased expression in skin (RPKM 68.1) and esophagus (RPKM 25.3).

Summary

This gene encodes a member of the Kallikrein subfamily of serine proteases. These Enzymes have diverse physiological functions and many Kallikrein genes are biomarkers for Cancer. The encoded protein has chymotrypsin-like activity and plays a role in the proteolysis of intercellular cohesive structures that precedes desquamation, the shedding of the outermost layer of the epidermis. The encoded protein may play a role in Cancer invasion and metastasis, and increased expression of this gene is associated with unfavorable prognosis and progression of several types of Cancer. Polymorphisms in this gene may play a role in the development of atopic dermatitis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, which is one of fifteen Kallikrein subfamily members located in a gene cluster on chromosome 19. [provided by RefSeq, May 2011]

KLK7 Products (4)

mRNA Protein Name
NM_001207053.2 NP_001193982.1 kallikrein-7 isoform 2
NM_001243126.1 NP_001230055.1 kallikrein-7 isoform 3
NM_005046.4 NP_005037.1 kallikrein-7 isoform 1 preproprotein
NM_139277.2 NP_644806.1 kallikrein-7 isoform 1 preproprotein
Molecular Function GO Annotation Evidence References Source
enables peptidase activity IMP
IMP: Inferred from mutant phenotype
17012259 GOA
Biological Process GO Annotation Evidence References Source
involved in positive regulation of antibacterial peptide production IMP
IMP: Inferred from mutant phenotype
17012259 GOA
Cellular Component GO Annotation Evidence References Source
located in epidermal lamellar body IDA
IDA: Inferred from direct assay
15675955 GOA
located in extracellular space IMP
IMP: Inferred from mutant phenotype
17012259 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

KLK7 Protein Structure

Trypsin

Trypsin: Trypsin (30 - 245)

  • 0
  • 100
  • 200
  • 253 a.a.
Protein Preferred Names Protein Names

kallikrein-7

  • kallikrein 7 (chymotryptic, stratum corneum)

Recombinant KLK7 Proteins

Cat. No. Product Name Accession Purity
HY-P70163 Kallikrein-7 Protein, Human (HEK293, His, solution) P49862 (E23-H252) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P76466 Kallikrein-7 Protein, Human (HEK293, His) NP_005037.1 (E23-R253) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Netherton Syndrome
  • NETH

  • Ns

  • Netherton Disease

  • Comel-Netherton Syndrome

  • Erythroderma, Ichthyosiform, With Hypotrichosis And Hyper-Ige

  • Bamboo Hair Syndrome

  • Ichthyosis Linearis Circumflexa

  • Ichthyosiform Erythroderma With Hypotrichosis And Hyper-Ige

  • Ilc

  • Nts

  • N Syndrome

Dermatitis
  • Eczema

  • Skin Inflammation

  • Inflammatory Dermatosis

Dermatitis, Atopic
  • Atopic Dermatitis

  • Atopic Eczema

  • Dermatitis, Atopic, Susceptibility To, 1

  • Atod

  • Eczema, Atopic

  • Dermatitis, Atopic 1

  • Allergic Dermatitis

  • Atopic Neurodermatitis

  • Besnier'S Prurigo

  • Dermatitis, Atopic, 1

  • Dermatitis Atopic

  • Eczema

  • Besnier Prurigo

Skin Disease
  • Skin Diseases

  • Genodermatosis

  • Abnormality Of The Skin

  • Skin Diseases, Genetic

  • Skin And Subcutaneous Tissue Disease

  • Dermatologic Disorders

Ichthyosis
  • Ichthyoses

  • Non-Syndromic Ichthyosis

  • Congenital Ichthyosis

Occupational Dermatitis
  • Dermatitis, Occupational

  • Occupational Allergic Contact Dermatitis

  • Occupational Eczema

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Cancer Of The Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

Psoriasis
Peeling Skin Syndrome
  • Deciduous Skin

  • Familial Continuous Skin Peeling Syndrome

  • Idiopathic Deciduous Skin

  • Keratosis Exfoliativa Congenita

  • Pss

  • Peeling Skin Disease

  • Skin Peeling Syndrome

  • Familial Continuous Skin Peeling

  • Keratolysis Exfoliativa Congenita

  • Exfoliation Syndrome

  • Keratolysis Exfoliativa

Ichthyosis Vulgaris
  • Ichthyosis Simplex

  • Dominant Congenital Ichthyosiform Erythroderma

  • Common Ichthyosis

  • Fish Scale Disease

  • VI

  • Ichthyoses

  • Congenital Ichthyosis

Ichthyosis, Congenital, Autosomal Recessive 4b
  • Harlequin Ichthyosis

  • Autosomal Recessive Congenital Ichthyosis 4b

  • Hi

  • Harlequin Fetus

  • ARCI4B

  • Ichthyosis Congenita, Harlequin Fetus Type

  • Harlequin Type Ichthyosis

  • 'Harlequin Fetus'

  • Harlequin Type Ichthyosis Congenita

  • Harlequin Type Ichthyosis Fetalis

  • Harlequin Baby Syndrome

  • Ichthyosis Congenita, Harlequin Type

  • Ichthyosis Fetalis, Harlequin Type

  • Ichthyosis Congenita Harlequin Fetus Type

  • Ichthyosis, Harlequin

  • Ichthyosis, Congenital, Autosomal Recessive, Type 4b

Autosomal Recessive Congenital Ichthyosis
  • Lamellar Ichthyosis

  • Congenital Ichthyosiform Erythroderma

  • Li

  • Congenital Nonbullous Ichthyosiform Erythroderma

  • Arci

  • Congenital Lamellar Ichthyosis

  • Nonbullous Congenital Ichthyosiform Erythroderma

  • Cie

  • Congenital Non-Bullous Ichthyosiform Erythroderma

  • Erythrodermic Ichthyosis

  • Nbcie

  • Ncie

  • Non-Bullous Congenital Ichthyosiform Erythroderma

  • Collodion Baby

  • Ichthyosis, Lamellar

  • Non Bullous Congenital Ichthyosiform Erythroderma

  • Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form

  • Ichthyosiform Erythroderma, Congenital, Nonbullous, 1

  • Collodion Baby Syndrome

  • Ichthyoses, Lamellar

  • Nbie

  • Nonbullous Ichthyosiform Erythroderma

  • Classic Lamellar Ichthyosis

  • Ichthyosiform Erythroderma Nonbullous Congenital

  • Ichthyosiform Erythroderma Congenital

  • Ichthyosis, Congenital, Autosomal Recessive

  • Ichthyosiform Erythroderma, Congenital

  • Collodion Fetus

  • Non-Bullous Ichthyosiform Erythroderma

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus KLK7 RGD RGD:1306420
Felis catus KLK7 VGNC VGNC:67967
Mus musculus KLK7 MGD MGI:1346336
Macaca mulatta KLK7 VGNC VGNC:74193
Bos taurus KLK7 VGNC VGNC:30681
Others KLK7 NCBI