ENSMUSG00000084128


Mus musculus

Features
Gene ID: ENSMUSG00000084128
  
Biological name :Esrp2
  
Synonyms : Epithelial splicing regulatory protein 2 / Esrp2 / Q8K0G8
  
Possible biological names infered from orthology : Q9H6T0
  
Species: Mus musculus
  
Chr. number: 8
Strand: -1
Band: D3
Gene start: 106130319
Gene end: 106136974
  
Corresponding Affymetrix probe sets: 10581455 (MoGene1.0st)   1419977_s_at (Mouse Genome 430 2.0 Array)   1433683_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000111639
Ensembl peptide - ENSMUSP00000123114
NCBI entrez gene - 77411     See in Manteia.
MGI - MGI:1924661
RefSeq - XM_011248547
RefSeq - NM_176838
RefSeq - XM_006531492
RefSeq - XM_006531493
RefSeq Peptide - NP_789808
swissprot - D3Z139
swissprot - Q8K0G8
Ensembl - ENSMUSG00000084128
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 esrp2ENSDARG00000018814Danio rerio
 ESRP2ENSGALG00000003374Gallus gallus
 ESRP2ENSG00000103067Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Esrp1 / Q3US41 / Mus musculus epithelial splicing regulatory protein 1 (Esrp1), transcript variant 3, mRNA. / Q6NXG1* / epithelial splicing regulatory protein 1*ENSMUSG0000004072857
O35737 / Hnrnph1 / Mus musculus heteroous nuclear ribonucleoprotein H1 (Hnrnph1), transcript variant 1, mRNA. / P31943* / heterogeneous nuclear ribonucleoprotein H1*ENSMUSG0000000785018
P70333 / Hnrnph2 / Heteroous nuclear ribonucleoprotein H2 Heteroous nuclear ribonucleoprotein H2, N-terminally processed / P55795* / heterogeneous nuclear ribonucleoprotein H2*ENSMUSG0000004542718
Grsf1 / Q8C5Q4 / G-rich sequence factor 1 / Q12849* / G-rich RNA sequence binding factor 1*ENSMUSG0000004422116
Hnrnpf / Q9Z2X1 / Heteroous nuclear ribonucleoprotein F Heteroous nuclear ribonucleoprotein F, N-terminally processed / P52597* / heterogeneous nuclear ribonucleoprotein F*ENSMUSG0000004207916
Q80YR9 / Rbm12b1 / RNA-binding protein 12B-A / RBM12B* / Q8IXT5* / RNA binding motif protein 12B*ENSMUSG0000004666714
Q66JV4 / Rbm12b2 / Mus musculus RNA binding motif protein 12 B2 (Rbm12b2), transcript variant 3, mRNA. / Q8IXT5* / RBM12B* / RNA binding motif protein 12B*ENSMUSG0000005213714
Rbm12 / Q8R4X3 / RNA-binding protein 12 / Q9NTZ6* / RNA binding motif protein 12*ENSMUSG0000008982413
Hnrnph3 / Mus musculus heteroous nuclear ribonucleoprotein H3 (Hnrnph3), transcript variant 3, mRNA. / P31942* / heterogeneous nuclear ribonucleoprotein H3*ENSMUSG0000002006911
Gm28036ENSMUSG000000989503


Protein motifs (from Interpro)
Interpro ID Name
 IPR000504  RNA recognition motif domain
 IPR012337  Ribonuclease H-like superfamily
 IPR034431  Epithelial splicing regulatory protein 2
 IPR035979  RNA-binding domain superfamily
 IPR036397  Ribonuclease H superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000380 alternative mRNA splicing, via spliceosome IGI
 biological_processGO:0006397 mRNA processing IEA
 biological_processGO:0008380 RNA splicing IEA
 biological_processGO:0043484 regulation of RNA splicing IEA
 biological_processGO:0050679 positive regulation of epithelial cell proliferation IGI
 biological_processGO:0060441 epithelial tube branching involved in lung morphogenesis IGI
 biological_processGO:0060445 branching involved in salivary gland morphogenesis IGI
 cellular_componentGO:0005634 nucleus ISO
 cellular_componentGO:0005654 nucleoplasm IEA
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003723 RNA binding IEA
 molecular_functionGO:0003729 mRNA binding IEA


Pathways (from Reactome)
Pathway description
FGFR2 alternative splicing


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000090 absent premaxilla "missing anterior and interior portion of the maxilla" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000103 nasal bone hypoplasia "reduced cell number in the bone which forms the nasal bridge" [J:53370]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000111 cleft palate "congenital fissure of the tissues normally uniting to form the palate" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

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

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000452 abnormal mouth morphology "anomalous structure or development of the oral cavity" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000458 abnormal mandible morphology "malformation of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000460 mandible hypoplasia "arrested growth or atrophy of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator, J:54637]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000547 short limbs "reduced average length of the extremities" [MGI:CLS, J:61509]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000550 abnormal forelimb morphology "malformation of the entire anterior extremities" [MGI:tc]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000553 absent radius "missing the short bone of the lateral forearm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54637]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000564 syndactyly "any degree of webbing or fusion of the digits, may involve only soft tissues or also can include bone" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0000596 abnormal liver development "anomalous differentiation of the liver" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cacna1atm1.1Ehess/Cacna1atm1.1Ehess
Genetic Background: C57BL/6-Cacna1atm1.1Ehess

 MP:0000598 abnormal liver morphology "malformation or absence of this bile-secreting exocrine gland, which is important for detoxification; for fat, carbohydrate, and protein metabolism; and for glycogen storage " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:23170]
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Allelic Composition: Cacna1atm1.1Ehess/Cacna1atm1.1Ehess
Genetic Background: C57BL/6-Cacna1atm1.1Ehess

 MP:0000607 abnormal hepatocyte morphology "malformation of the main structural component of the liver; these are specialized epithelial cells normally organize into interconnected plates called lobules" [J:23170, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Cacna1atm1.1Ehess/Cacna1atm1.1Ehess
Genetic Background: C57BL/6-Cacna1atm1.1Ehess

 MP:0000614 absent salivary gland "missing any of the saliva-secreting glands of the oral cavity" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc, J:54637]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0001181 absent lungs "missing organs of respiration" [J:51966, J:50768]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0001196 shiny skin "skin with a glossy or glistening appearance" [J:56641]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0001199 thin skin "reduced thickness of the outer protective layer of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49471]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 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: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 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]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

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

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0002989 small kidney "reduced physical bulk one or both of the organs responsible for urine secretion" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0003704 abnormal hair follicle development "anomalous development of the epidermis from which the hair shaft develops " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 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: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0003893 increased hepatocyte proliferation "anomalous growth and reproduction of hepatocyte cells of the liver" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Cacna1atm1.1Ehess/Cacna1atm1.1Ehess
Genetic Background: C57BL/6-Cacna1atm1.1Ehess

 MP:0004197 abnormal fetal growth/weight/body size "limited or accelerated growth or development apparent during the fetal period (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0004352 absent humerus "missing one or both of the bones of the forelimb that articulates with the scapula above and the radius and ulna below" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0004912 absent mandibular coronoid process "absence of the thin, flattened, triangular eminence that arises from the upper surface of the mandibular ramus (perpendicular portion)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0005170 cleft lip "defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0005419 hypoalbuminemia "blood albumin concentration below the normal range" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Cacna1atm1.1Ehess/Cacna1atm1.1Ehess
Genetic Background: C57BL/6-Cacna1atm1.1Ehess

 MP:0008469 abnormal protein level "anomaly in the amount of any of the macromolecules consisting of long chains of amino acids in peptide linkage" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cacna1atm1.1Ehess/Cacna1atm1.1Ehess
Genetic Background: C57BL/6-Cacna1atm1.1Ehess

 MP:0009431 decreased fetal weight "reduced weight of a fetus compared to controls (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0009883 palatal shelf hypoplasia "reduced size of the palatal projections from the inner part of the maxillary processes that fuse to form the secondary palate, often due to reduced cell number" [PMID:16680722]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0009893 cleft primary palate "congenital fissure of the tissues normally uniting to form the primary palate" [PMID:16680722]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 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: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0012173 short rostral-caudal axis "length reduction or truncation of the axis that runs from the head to the tail of the body" [MGI:anna]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0013545 cleft hard palate "cleft in the anterior portion of the palate consisting of bone and mucous membranes; the hard palate is formed from bony processes of the maxilla, premaxilla and palatine bones" [UBERON:0003216]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

 MP:0013546 cleft soft palate "a cleft in the soft tissue constituting the back of the roof of the mouth; the soft palate is the posterior portion of the palate extending from the posterior edge of the hard palate to the back of the mouth" [UBERON:0001733]
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Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

Allelic Composition: Esrp1tm1.2Rpc/Esrp1tm1.2Rpc,Esrp2tm1(KOMP)Vlcg/Esrp2+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NTac

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

1 s.

 
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