ENSMUSG00000031995


Mus musculus

Features
Gene ID: ENSMUSG00000031995
  
Biological name :St14
  
Synonyms : P56677 / St14 / suppression of tumorigenicity 14 (colon carcinoma)
  
Possible biological names infered from orthology : Q9Y5Y6 / suppression of tumorigenicity 14
  
Species: Mus musculus
  
Chr. number: 9
Strand: -1
Band: A4
Gene start: 31089402
Gene end: 31131853
  
Corresponding Affymetrix probe sets: 10592001 (MoGene1.0st)   1418076_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000150666
Ensembl peptide - ENSMUSP00000034478
Ensembl peptide - ENSMUSP00000121971
NCBI entrez gene - 19143     See in Manteia.
MGI - MGI:1338881
RefSeq - XM_017313213
RefSeq - NM_011176
RefSeq - XM_006510098
RefSeq - XM_006510099
RefSeq Peptide - NP_035306
swissprot - P56677
swissprot - Q543E3
swissprot - D6RIN3
swissprot - A0A1L1SU89
Ensembl - ENSMUSG00000031995
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 st14aENSDARG00000061173Danio rerio
 st14bENSDARG00000044655Danio rerio
 ST14ENSGALG00000001331Gallus gallus
 ST14ENSG00000149418Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9DBI0 / Tmprss6 / Mus musculus transmembrane serine protease 6 (Tmprss6), transcript variant 2, mRNA. / Q8IU80* / transmembrane serine protease 6*ENSMUSG0000001694229
Q8BIK6 / Tmprss7 / Transmembrane protease serine 7 / Q7RTY8* / transmembrane serine protease 7*ENSMUSG0000003317727
Corin / Q9Z319 / Atrial natriuretic peptide-converting enzyme Atrial natriuretic peptide-converting enzyme, N-terminal propeptide Atrial natriuretic peptide-converting enzyme, activated prot...ENSMUSG0000000522022
P97435 / Tmprss15 / transmembrane protease, serine 15 / P98073* / transmembrane serine protease 15*ENSMUSG0000002285720
Tmprss9 / transmembrane protease, serine 9 / Q7Z410* / transmembrane serine protease 9*ENSMUSG0000005940618
Klkb1 / P26262 / Plasma kallikrein Plasma kallikrein heavy chain Plasma kallikrein light chain / P03952* / kallikrein B1*ENSMUSG0000010976417
F11 / Q91Y47 / Coagulation factor XI Coagulation factor XIa heavy chain Coagulation factor XIa light chain / P03951* / coagulation factor XI*ENSMUSG0000003164517
Q9JIQ8 / Tmprss2 / Transmembrane protease serine 2 Transmembrane protease serine 2 non-catalytic chain Transmembrane protease serine 2 catalytic chain / O15393* / transmembrane serine protease 2*ENSMUSG0000000038516
Q8K1T0 / Tmprss3 / transmembrane protease, serine 3 / P57727* / transmembrane serine protease 3*ENSMUSG0000002403415
Q8VCA5 / Tmprss4 / Transmembrane protease serine 4 / Q9NRS4* / transmembrane serine protease 4*ENSMUSG0000003209115
Tmprss13 / transmembrane serine protease 13 / Q9BYE2*ENSMUSG0000003712915
Q9ER04 / Tmprss5 / transmembrane protease, serine 5 (spinesin) / Q9H3S3* / transmembrane serine protease 5*ENSMUSG0000003226814
Hpn / O35453 / Serine protease hepsin Serine protease hepsin non-catalytic chain Serine protease hepsin catalytic chain / hepsin* / P05981*ENSMUSG0000000124914


Protein motifs (from Interpro)
Interpro ID Name
 IPR000082  SEA domain
 IPR000859  CUB domain
 IPR001254  Serine proteases, trypsin domain
 IPR002172  Low-density lipoprotein (LDL) receptor class A repeat
 IPR009003  Peptidase S1, PA clan
 IPR017051  Peptidase S1A, matripase
 IPR018114  Serine proteases, trypsin family, histidine active site
 IPR023415  Low-density lipoprotein (LDL) receptor class A, conserved site
 IPR033116  Serine proteases, trypsin family, serine active site
 IPR035914  Spermadhesin, CUB domain superfamily
 IPR036055  LDL receptor-like superfamily
 IPR036364  SEA domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001843 neural tube closure IGI
 biological_processGO:0006508 proteolysis ISO
 biological_processGO:0016477 cell migration TAS
 biological_processGO:0030216 keratinocyte differentiation IEA
 biological_processGO:0060672 epithelial cell morphogenesis involved in placental branching IGI
 cellular_componentGO:0005576 extracellular region IDA
 cellular_componentGO:0005615 extracellular space IEA
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0005887 integral component of plasma membrane TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0016323 basolateral plasma membrane IEA
 cellular_componentGO:0019897 extrinsic component of plasma membrane IEA
 molecular_functionGO:0004252 serine-type endopeptidase activity EXP
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0008233 peptidase activity IEA
 molecular_functionGO:0008236 serine-type peptidase activity ISO
 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]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0000379 reduced hair follicle number "fewer number of the epidermal invaginations from which the hair shaft develops" [J:15108]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 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]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0000414 alopecia "absence of hair or loss of hair; not usually in reference to primary genetic hairlessness but may be due to dietary, stress, secondary to immune condition" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:30772, J:33796]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0000443 abnormal snout morphology "anomalous structure or development of the anterior facial part of the muzzle" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0000479 abnormal intestinal cell "anomalous structure or development of the cells comprising the intestine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0000489 abnormal large intestine morphology "structural or developmental anomalies of the intestinum crassum " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0000495 abnormal colon morphology "malformation of the portion of the large intestine between the cecum and the rectum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

 MP:0000507 absent digestive secretion "missing the production and/or release of a physiologically active substance (usually but not exclusively in liquid form) from a cell or a gland of the digestive system" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0000623 reduced salivation "decrease flow, secretion, or amount of saliva" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

Allelic Composition: St14tm3Bug/St14tm3Bug
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0000764 abnormal tongue epithelium morphology "malformation of the epithelial layer of the tongue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc]
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Allelic Composition: Abca3tm1Holz/Abca3tm1Holz
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0000914 exencephaly "neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: F2rl1tm1Cgh/F2rl1tm1Cgh,Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae

 MP:0001190 reddish skin "skin has a more intense ruddy appearance than normal, often due to capillary congestion" [J:65038]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0001192 scaly skin "skin covered with shedding scales or flakes" [J:65146]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0001196 shiny skin "skin with a glossy or glistening appearance" [J:56641]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001211 wrinkled skin "irregular folds and/or indentations on the skin" [J:19212]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 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]
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Allelic Composition: Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0001218 thin epidermis "reduced thickness of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790]
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Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0001219 thickened epidermis "increase in the width of the epidermal cell layer in the skin" [J:65146]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0001239 abnormal granular layer morphology "structural or developmental anomaly of the layer of flattened cells containing basophilic granules of keratohyalin and lying just above the stratum spinosum (spiny layer) of the epidermis" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 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]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0001242 hyperkeratosis "increased depth of the corneal layer of the epidermis; thickening of the horny layer of the epidermis" [J:1133]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0001258 decreased body length "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001263 weight loss "progressive reduction of body weight below normal average for age" [J:45400]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

 MP:0001284 absent vibrissae "missing whiskers" [J:18378]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 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]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0001665 chronic diarrhea "prolonged diarrhea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

 MP:0001711 abnormal placenta 
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0001716 abnormal placental labyrinth "malformed structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood" [J:23171]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

 MP:0001874 acanthosis "diffuse hyperplasia of the spinous layer of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0002151 abnormal neural tube morphology/development "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0002656 abnormal keratinocyte differentiation "developmental anomaly of the cells of the epidermis that produce keratin in the process of differentiating into the dead and fully keratinized cells of the stratum corneum " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0002731 megacolon "extreme dilation of the colon" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:40722]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

 MP:0002796 impaired skin barrier function "impaired ability of the skin to regulate water loss; frequently leads to dehydration" [J:56641]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14Gt(RST485)Byg/St14+
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: St14Gt(XM184)Byg/St14+
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0002816 colitis "local accumulation of fluid, plasma proteins, and leukocytes in the colon region of the large intestine" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

 MP:0003009 abnormal cytokine secretion "impairment or increase of the cellular release of any of the non-antibody proteins made by inflammatory leukocytes and some non-leukocytic cells that affect the behavior of other cells " [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, smb:Susan M. Bello , Mouse Genome Informatics Curator]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0003051 curly tail "a loop or corkscrew-like curl in the tail" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

 MP:0003054 spina bifida "common congenital midline defect of fusion of the vertebral arch" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

 MP:0003288 intestinal edema "an accumulation of an excessive amount of serous fluid in the intestine or intestinal cells " [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0003403 absent placental labyrinth "malformed structure where embryonic blood vessels are surrounded by trophoblast cells and maternal blood" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:73417]
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Allelic Composition: Spint1tm1Bug/Spint1tm1Bug
Genetic Background: involves: 129S6/SvEvTac

 MP:0003725 increased autoantibody level "elevated level of antibodies to self-antigens present in the sera; often indicative of autoimmune disease" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, acv:Alicia Valenzuela, Genetic Resources Curator]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0003743 abnormal facial morphology "anomalous structure or development of the face" [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0003756 abnormal hard palate "abnormality in the anterior part of the palate that is supported by and includes the palatal extensions of the maxillary and palatine bones " [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Abca3tm1Holz/Abca3tm1Holz
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 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]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0003853 dry skin "skin characterized by the lack of natural or normal moisture" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0004794 increased anti-nuclear antigen antibody level "elevated level of antibodies to nuclear antigens present in the sera" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology "any structural anomaly in the tubular intestinal glands found in the mucosal membranes of the large intestine" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0004974 decreased regulatory T cell number "reduced number of the specialized subpopulation of T cells that act to suppress activation of the immune system and thus maintain immune system homeostasis and prevent pathological self-reactivity" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0005092 decreased double-positive T cell count "less than the expected number of the subset of T cells found in the thymus that express both CD4 and CD8" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0005150 cachexia "general weight loss and wasting occurring in the course of chronic disease" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0005310 abnormal salivary gland physiology "anomalous function of any of the glands in the mouth that secrete saliva" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: St14tm3Bug/St14tm3Bug
Genetic Background: involves: 129S6/SvEvTac

 MP:0008075 decreased CD4-positive T cell number "reduced number of the subset of T lymphocytes that carry the CD4 marker, recognize intravesicular peptides bound to MHC class-II molecules, and turn on antibody production" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0008079 decreased CD8-positive T cell number "reduction in the number of the regulatory subset of T lymphocytes that are involved in MHC class I restricted interactions" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0008722 abnormal chemokine secretion "anomaly in the production or cellular release of any of the class of pro-inflammatory cytokines that attract and activate leukocytes" [MESH:D12.644.276.374.200]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0008879 submandibular gland inflammation "local accumulation of fluid, plasma proteins, and leukocytes in either of the large major salivary glands situated beneath the mandible" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0008880 lacrimal gland inflammation "local accumulation of fluid, plasma proteins, and leukocytes in the glands that secrete tears" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0008882 abnormal enterocyte physiology "any functional anomaly of the epithelial cells that have an apical plasma membrane folded into microvilli to provide ample surface for the absorption of nutrients from the intestinal lumen" [CL:0000584, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0008883 abnormal enterocyte proliferation "anomaly in the ability of the enterocyte cell population to undergo expansion by cell division" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Hrastm1Mok/Hrastm1Mok,Krastm1Mok/Krastm1Mok,Nrastm1Mok/Nrastm1Mok,Tg(HRAS)7Mok/0
Genetic Background: either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * C57BL/6 * DBA/2)

 MP:0009541 increased thymocyte apoptosis "increase in the number of immature T cells located in the thymus that are undergoing programmed cell death" [CL:0000893, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0009546 absent gastric milk in neonates "failure of nursing offspring to ingest milk as indicated by stomach content" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 MP:0009595 enlarged corneocyte envelope "increased size of the electron-dense layer of highly transglutaminase cross-linked protein that is deposited on the inner surface of the plasma membrane of corneocytes in the outermost layers of the epidermis" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0009596 abnormal stratum corneum lipid matrix formation "altered lipid composition or intercellular lipid matrix assembly in the stratum corneum, usually resulting in loss of epidermal barrier function; normally, the intercorneocyte lipid matrix consists of a complex lipid mixture of ceramides, cholesterol and long-chain saturated fatty acids that self-assembles into an ordered multilayer structure known as lipid lamellae" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0009597 impaired stratum corneum desquamation "dysregulated shedding of the outermost layer of corneocytes, affecting the integrity and thickness of the stratum corneum; may result in xerotic and ichthyotic conditions" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm2Bug
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd

 MP:0009931 abnormal skin appearance "skin that looks different from the usual state" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0009932 skin fibrosis "invasion of fibrous connective tissue into the skin, often resulting from inflammation or injury" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA

 MP:0010168 increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number "a greater number of the CD4-positive, CD25-positive T cell subset which regulates overall immune responses as well as the responses of other T cell subsets through direct cell-cell contact and cytokine release" [ISBN:0781735149]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0010169 decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number "a reduction in the number of the CD4-positive, CD25-positive T cell subset which regulates overall immune responses as well as the responses of other T cell subsets through direct cell-cell contact and cytokine release" [ISBN:0781735149]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0010234 abnormal vibrissa follicle morphology "any structural anomaly of one of the tubular invaginations of the epidermis enclosing the hair roots and from which grow the vibrissae located on the muzzle and face of many species" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0010844 increased effector memory CD4-positive, alpha-beta T cell number "increased number of CD4-positive, alpha-beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative" [CL:0000905, GO_REF:0000031, GOC:add, GOC:pam, GOC:tfm]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0010850 increased effector memory CD8-positive, alpha-beta T cell number "increased number of CD8-positive, alpha beta memory T cells with the phenotype CCR7-negative, CD127-positive, CD45RO-positive, and CD25-negative" [CL:0000913, GO_REF:0000031, GOC:add, GOC:pam, PMID:20146720]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 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]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

 MP:0011087 complete neonatal lethality "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14Gt(XM184)Byg/St14Gt(XM184)Byg
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14tm1Bug
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss

 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]
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Allelic Composition: Spint1tm1Bug/Spint1tm1Bug,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0011099 complete lethality throughout fetal growth and development "death of all organisms of a given genotype in a population between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)" [MGI:csmith]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

 MP:0011100 complete preweaning lethality "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
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Allelic Composition: Rad9atm1.1(KOMP)Wtsi/Rad9atm1.1(KOMP)Wtsi
Genetic Background: C57BL/6N-Rad9atm1.1(KOMP)Wtsi/Bay

 MP:0011105 partial embryonic lethality between implantation and placentation "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 the point of implantation and the initiation of placentation (Mus: E4.5 to less than E9)" [MGI:csmith]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

 MP:0011108 partial embryonic lethality during organogenesis "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 embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg,St14tm1Bug/St14+
Genetic Background: involves: 129P2/OlaHsd

 MP:0020220 decreased tear production "decreased production of the amount of fluid produced in the eye" [GOC:NV]
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Allelic Composition: St14tm2Bug/St14tm3Bug,Tg(MMTV-cre)4Mam/0
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss

 MP:0030570 abnormal piliary canal morphology "any structural anomaly of the tubular connection that is found between the epidermal surface and the most distal part of the hair follicle inner root sheath and contains the hair shaft" [PMID:19211055, UBERON:0035610]
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Allelic Composition: Becn1tm1Blev/Becn1+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000074155 Klk5 / kallikrein related-peptidase 5 / Q9Y337*  / reaction






 

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