ENSMUSG00000030800


Mus musculus

Features
Gene ID: ENSMUSG00000030800
  
Biological name :Prss8
  
Synonyms : protease, serine 8 (prostasin) / Prss8
  
Possible biological names infered from orthology : Q16651 / serine protease 8
  
Species: Mus musculus
  
Chr. number: 7
Strand: -1
Band: F3
Gene start: 127925716
Gene end: 127930104
  
Corresponding Affymetrix probe sets: 10568332 (MoGene1.0st)   1418320_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000146313
Ensembl peptide - ENSMUSP00000032988
Ensembl peptide - ENSMUSP00000145904
NCBI entrez gene - 76560     See in Manteia.
MGI - MGI:1923810
RefSeq - NM_133351
RefSeq - XM_006508306
RefSeq Peptide - NP_579929
swissprot - A0A0U1RQA6
swissprot - Q99L44
Ensembl - ENSMUSG00000030800
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 CU571315.2ENSDARG00000101956Danio rerio
 CU571315.3ENSDARG00000101990Danio rerio
 prss60.1ENSDARG00000070713Danio rerio
 prss60.2ENSDARG00000055644Danio rerio
 prss60.3ENSDARG00000070710Danio rerio
 si:ch73-182e20.4ENSDARG00000102727Danio rerio
 si:dkey-16l2.17ENSDARG00000027196Danio rerio
 si:dkey-32n7.7ENSDARG00000063444Danio rerio
 si:dkey-32n7.9ENSDARG00000071841Danio rerio
 si:dkeyp-93a5.2ENSDARG00000052064Danio rerio
 si:dkeyp-93a5.2ENSDARG00000100953Danio rerio
 si:dkeyp-93a5.3ENSDARG00000096975Danio rerio
 zgc:100868ENSDARG00000004748Danio rerio
 zgc:112038ENSDARG00000046140Danio rerio
 zgc:123217ENSDARG00000059026Danio rerio
 zgc:123295ENSDARG00000056324Danio rerio
 zgc:153968ENSDARG00000061858Danio rerio
 zgc:163079ENSDARG00000056773Danio rerio
 zgc:165423ENSDARG00000052905Danio rerio
 zgc:92313ENSDARG00000040513Danio rerio
 PRSS8ENSG00000052344Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Prss32 / protease, serine 32ENSMUSG0000004899238
Prss33 / Q80WM7 / Serine protease 33 / Q8NF86*ENSMUSG0000004962037
Prss27 / Q8BJR6 / Serine protease 27 / Q9BQR3*ENSMUSG0000005076237
Tpsg1 / tryptase gamma 1 / Q9NRR2*ENSMUSG0000003320037
Prss30 / Q9QYZ9 / Serine protease 30 ENSMUSG0000002412436
Prss48 / Q14B25 / Serine protease 48 / Q7RTY5*ENSMUSG0000004901334
Prss22 / protease, serine 22 / Q9GZN4* / serine protease 22*ENSMUSG0000004502734
Prss21 / Q9JHJ7 / protease, serine 21 / Q9Y6M0* / serine protease 21*ENSMUSG0000002411633
Prss47ENSMUSG0000009065831
Prss44 / Q402U7 / Serine protease 44 ENSMUSG0000003249331
Prss38 / Q3UKY7 / Serine protease 38 / A1L453*ENSMUSG0000004929131
Prss41 / Q920S2 / Serine protease 41 / Q7RTY9*ENSMUSG0000002411431
Prss45 / Q8K4I7 / Inactive serine protease 45 / Q7RTY3* / AC109583.3* / serine protease 45*ENSMUSG0000004725730
Prss42 / Q8VIF2 / Serine protease 42 / Q7Z5A4*ENSMUSG0000004466430
A6H6T1 / Prss40 / Serine protease 40 ENSMUSG0000003752929
O70169 / Prss39 / Inactive serine protease 39 ENSMUSG0000002612529
Prss43 / protease, serine 43ENSMUSG0000005839829


Protein motifs (from Interpro)
Interpro ID Name
 IPR001254  Serine proteases, trypsin domain
 IPR001314  Peptidase S1A, chymotrypsin family
 IPR009003  Peptidase S1, PA clan
 IPR018114  Serine proteases, trypsin family, histidine active site
 IPR033116  Serine proteases, trypsin family, serine active site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006508 proteolysis IEA
 cellular_componentGO:0005886 plasma membrane IEA
 molecular_functionGO:0004252 serine-type endopeptidase activity IEA
 molecular_functionGO:0008233 peptidase activity IEA
 molecular_functionGO:0008236 serine-type peptidase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA


Pathways (from Reactome)
Pathway description
Formation of the cornified envelope


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000377 abnormal hair follicle "malformed invagination of the epidermis from which the hair shaft develops" [J:65031]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

 MP:0000379 reduced hair follicle number "fewer number of the epidermal invaginations from which the hair shaft develops" [J:15108]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

 MP:0000382 underdeveloped hair follicles "arrest of or retarded differentiation of the epidermal invaginations from which the hair shaft develops" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790]
Show

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

 MP:0000416 sparse fur "fur that is significantly less dense" [J:46854]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0000417 short hair "reduced average length of the hairs" [J:64948]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0000914 exencephaly "neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
Show

Allelic Composition: Prss8fr/Prss8+,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

Allelic Composition: Prss8fr/Prss8fr,Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
Genetic Background: involves: 129P2/OlaHsd * DBA

 MP:0001190 reddish skin "skin has a more intense ruddy appearance than normal, often due to capillary congestion" [J:65038]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001211 wrinkled skin "irregular folds and/or indentations on the skin" [J:19212]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001216 abnormal epidermal layer morphology "anomalous structure or development of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001240 abnormal cornified layer morphology "structural or developmental anomaly of the outer layer of the epidermis, consisting of several layers of flat keratinized non-nucleated cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

Allelic Composition: Prss8Gt(IST10122F12)Tigm/Prss8Gt(IST10122F12)Tigm
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001263 weight loss "progressive reduction of body weight below normal average for age" [J:45400]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001274 curly vibrissae "whiskers twisted into coils or spirals" [J:47620]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001278 kinked vibrissae "sharp bends in the vibrissae" [J:56641]
Show

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001282 short vibrissae "decreased length of the vibrissae" [J:30249]
Show

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001284 absent vibrissae "missing whiskers" [J:18378]
Show

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001429 dehydration "excessive water loss from the body or from an organ or bodily part" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:50053]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Prss8Gt(IST10122F12)Tigm/Prss8Gt(IST10122F12)Tigm
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0001510 abnormal coat appearance "coat that looks different from the usual state " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

Allelic Composition: Prss8fr/Prss8fr,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

 MP:0001511 disheveled coat "coat that looks generally unkempt" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0001547 abnormal lipid level "anomalous concentrations of fat-soluble substances (molecules composed of carbon and hydrogen and are characteristically insoluble in water) in the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001711 abnormal placenta 
Show

Allelic Composition: Prss8fr/Prss8fr,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

 MP:0002073 abnormal hair growth "absence or reduced amount of hair or abnormal onset of hair growth cycle or development" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0002098 abnormal vibrissae morphology "irregular or unusual structure, appearance, or alignment of the vibrissae" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Tgfbr2tm1.1Hlm/Tgfbr2tm1.1Hlm
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

 MP:0002796 impaired skin barrier function "impaired ability of the skin to regulate water loss; frequently leads to dehydration" [J:56641]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Prss8Gt(IST10122F12)Tigm/Prss8Gt(IST10122F12)Tigm
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

Allelic Composition: Prss8tm1.1Bug/Prss8Gt(IST10122F12)Tigm
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0002908 delayed wound healing "longer time requirement for the ability to self-repair and close wounds than normal" [J:63037]
Show

Allelic Composition: Prss8tm1.1Bug/Prss8tm1.1Bug
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0003051 curly tail "a loop or corkscrew-like curl in the tail" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Prss8fr/Prss8+,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

 MP:0003054 spina bifida "common congenital midline defect of fusion of the vertebral arch" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]
Show

Allelic Composition: Prss8fr/Prss8+,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

 MP:0003704 abnormal hair follicle development "anomalous development of the epidermis from which the hair shaft develops " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003809 abnormal hair shaft morphology "irregular or unusual structure of the cuticle, and/or cortex and/or medulla of a hair" [llw2:Linda Washburn , Mouse Genome Informatics Curator]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0003812 abnormal hair medulla "anomalies of hair medullary cell formation and arrangement of the innermost core of the hair shaft " [llw2:Linda Washburn , Mouse Genome Informatics Curator]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0003853 dry skin "skin characterized by the lack of natural or normal moisture" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
Show

Allelic Composition: Prss8fr/Prss8tm1.1Hum
Genetic Background: involves: 129/Sv * FS/EiJ

 MP:0008770 decreased survivor rate "a smaller percentage of organisms than expected survive to adulthood and have a lifespan similar to controls" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Prss8tm1.1Bug/Prss8Gt(IST10122F12)Tigm
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0009675 orthokeratosis "thickening of the stratum corneum of the epidermis (hyperkeratosis) with non-nucleated keratinocytes retained in this layer" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010179 rough coat "coat does not have the usual smooth appearance" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Actbtm1Npa/Actbtm1Npa
Genetic Background: involves: BALB/cJ

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Prss8tm1.1Bug/Prss8Gt(IST10122F12)Tigm
Genetic Background: involves: 129S6/SvEvTac * Black Swiss * C57BL/6J * C57BL/6N

 MP:0011092 complete embryonic lethality "death of all organisms of a given genotype in a population within the embryonic period prior to organogenesis (Mus: prior to E14)" [MGI:csmith]
Show

Allelic Composition: Prss8fr/Prss8+,Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
Genetic Background: involves: 129P2/OlaHsd * DBA

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
Show

Allelic Composition: Prss8fr/Prss8+,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

 MP:0011101 partial prenatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
Show

Allelic Composition: Prss8fr/Prss8fr,Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * DBA

Allelic Composition: Prss8fr/Prss8fr,Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
Genetic Background: involves: 129P2/OlaHsd * DBA

 MP:0013589 thymus medulla hypoplasia "underdevelopment or reduced size, usually due to a reduced cell number, of the inner area of thymus lobules" [MGI:Anna]
Show

Allelic Composition: Wt1tm1Nhsn/Wt1+
Genetic Background: involves: 129S2/SvPas * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000030800 Prss8 / protease, serine 8 (prostasin) / Q16651* / serine protease 8*  / complex






 

0 s.

 
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