ENSMUSG00000036131


Mus musculus

Features
Gene ID: ENSMUSG00000036131
  
Biological name :Frmd7
  
Synonyms : A2AD83 / FERM domain-containing protein 7 / Frmd7
  
Possible biological names infered from orthology : FERM domain containing 7 / Q6ZUT3
  
Species: Mus musculus
  
Chr. number: X
Strand: -1
Band: A5
Gene start: 50895180
Gene end: 50942710
  
Corresponding Affymetrix probe sets: 10604508 (MoGene1.0st)   
  
Cross references: Ensembl peptide - ENSMUSP00000126628
Ensembl peptide - ENSMUSP00000057103
NCBI entrez gene - 385354     See in Manteia.
MGI - MGI:2686379
RefSeq - XM_011251013
RefSeq - XM_006541506
RefSeq - XM_006541507
RefSeq - XM_011251012
RefSeq - NM_001190332
RefSeq - XM_006541505
RefSeq Peptide - NP_001177261
swissprot - E9PXK8
swissprot - A2AD83
Ensembl - ENSMUSG00000036131
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 frmd7ENSDARG00000068958Danio rerio
 si:ch211-243g6.3ENSDARG00000070495Danio rerio
 FRMD7ENSGALG00000023843Gallus gallus
 FRMD7ENSG00000165694Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Farp1 / F8VPU2 / FERM, ARHGEF and pleckstrin domain-containing protein 1 / Q9Y4F1* / FERM, ARH/RhoGEF and pleckstrin domain protein 1*ENSMUSG0000002555538
Farp2 / Q91VS8 / FERM, ARHGEF and pleckstrin domain-containing protein 2 / O94887* / FERM, ARH/RhoGEF and pleckstrin domain protein 2*ENSMUSG0000003406636
Nf2 / P46662 / Merlin / P35240* / neurofibromin 2*ENSMUSG0000000907316
Msn / P26041 / Moesin / P26038*ENSMUSG0000003120716
Rdx / P26043 / radixin / P35241*ENSMUSG0000003205016
Ezr / Ezrin / P26040 / P15311*ENSMUSG0000005239715
Mylip / Q8BM54 / E3 ubiquitin-protein ligase MYLIP / Q8WY64* / myosin regulatory light chain interacting protein*ENSMUSG0000003817513


Protein motifs (from Interpro)
Interpro ID Name
 IPR000299  FERM domain
 IPR011993  PH-like domain superfamily
 IPR014352  FERM/acyl-CoA-binding protein superfamily
 IPR014847  FERM adjacent (FA)
 IPR018979  FERM, N-terminal
 IPR018980  FERM, C-terminal PH-like domain
 IPR019747  FERM conserved site
 IPR019748  FERM central domain
 IPR019749  Band 4.1 domain
 IPR029071  Ubiquitin-like domain superfamily
 IPR035963  FERM superfamily, second domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007399 nervous system development IEA
 biological_processGO:0010592 positive regulation of lamellipodium assembly IDA
 biological_processGO:0010975 regulation of neuron projection development IMP
 biological_processGO:0032091 negative regulation of protein binding IDA
 biological_processGO:0051057 positive regulation of small GTPase mediated signal transduction IGI
 biological_processGO:0051497 negative regulation of stress fiber assembly IDA
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0030426 growth cone IEA
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0043005 neuron projection IDA
 cellular_componentGO:0043025 neuronal cell body IDA
 molecular_functionGO:0003674 molecular_function ND
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0004647 decreased lumbar vertebrae number "reduced number of the six bony segments of the spine located anterior to the sacral vertebrae and posterior to the thoracic vertebrae" [MESH:National Library of Medicine_Medical Subject Headings]
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Allelic Composition: Foxo3tm1.1(KOMP)Vlcg/Foxo3tm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Foxo3tm1.1(KOMP)Vlcg/J

 MP:0010101 increased sacral vertebrae number "increase of any or all of the four bony segments of the spine located posterior to the lumbar vertebrae and anterior to the caudal vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Foxo3tm1.1(KOMP)Vlcg/Foxo3tm1.1(KOMP)Vlcg
Genetic Background: C57BL/6N-Foxo3tm1.1(KOMP)Vlcg/J

  


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






 

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