ENSMUSG00000023805


Mus musculus

Features
Gene ID: ENSMUSG00000023805
  
Biological name :Synj2
  
Synonyms : Q9D2G5 / Synaptojanin-2 / Synj2
  
Possible biological names infered from orthology : O15056
  
Species: Mus musculus
  
Chr. number: 17
Strand: 1
Band: A1
Gene start: 5941280
Gene end: 6044290
  
Corresponding Affymetrix probe sets: 10441456 (MoGene1.0st)   1425217_a_at (Mouse Genome 430 2.0 Array)   1427652_x_at (Mouse Genome 430 2.0 Array)   1427685_a_at (Mouse Genome 430 2.0 Array)   1431697_at (Mouse Genome 430 2.0 Array)   1431828_a_at (Mouse Genome 430 2.0 Array)   1452344_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000111456
Ensembl peptide - ENSMUSP00000111455
Ensembl peptide - ENSMUSP00000111457
Ensembl peptide - ENSMUSP00000138449
Ensembl peptide - ENSMUSP00000122381
Ensembl peptide - ENSMUSP00000122316
Ensembl peptide - ENSMUSP00000120006
Ensembl peptide - ENSMUSP00000115371
Ensembl peptide - ENSMUSP00000060382
Ensembl peptide - ENSMUSP00000079164
Ensembl peptide - ENSMUSP00000111450
Ensembl peptide - ENSMUSP00000111451
Ensembl peptide - ENSMUSP00000111452
Ensembl peptide - ENSMUSP00000111453
Ensembl peptide - ENSMUSP00000111454
NCBI entrez gene - 20975     See in Manteia.
MGI - MGI:1201671
RefSeq - XM_017317373
RefSeq - NM_001113351
RefSeq - NM_001113352
RefSeq - NM_001113353
RefSeq - NM_001290698
RefSeq - NM_011523
RefSeq - XM_006523202
RefSeq - XM_006523203
RefSeq - XM_006523204
RefSeq - XM_006523205
RefSeq - XM_006523206
RefSeq - XM_006523208
RefSeq - XM_006523212
RefSeq - XM_017317372
RefSeq Peptide - NP_001106824
RefSeq Peptide - NP_001277627
RefSeq Peptide - NP_035653
RefSeq Peptide - NP_001106822
RefSeq Peptide - NP_001106823
swissprot - D3YZB3
swissprot - F6U4I6
swissprot - F7BI35
swissprot - F8WHD8
swissprot - D3YZB2
swissprot - Q9D2G5
swissprot - D3YWM9
swissprot - S4R207
swissprot - E9Q4P5
swissprot - D3Z6E7
swissprot - D3YZB5
swissprot - D3YZB4
Ensembl - ENSMUSG00000023805
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 SYNJ2ENSGALG00000013727Gallus gallus
 SYNJ2ENSG00000078269Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Synj1 / synaptojanin 1 / O43426*ENSMUSG0000002297344
Ocrl / Q6NVF0 / Inositol polyphosphate 5-phosphatase OCRL-1 / Q01968* / OCRL, inositol polyphosphate-5-phosphatase*ENSMUSG0000000117315
Inpp5b / Q8K337 / Type II inositol 1,4,5-trisphosphate 5-phosphatase / P32019* / inositol polyphosphate-5-phosphatase B*ENSMUSG0000002889414
Inpp5d / Q9ES52 / Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 / Q92835* / inositol polyphosphate-5-phosphatase D*ENSMUSG0000002628813
Inpp5j / P59644 / Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A / Q15735* / inositol polyphosphate-5-phosphatase J*ENSMUSG0000003457013
Inppl1 / Q6P549 / Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 / O15357* / inositol polyphosphate phosphatase like 1*ENSMUSG0000003273713
Inpp5e / Q9JII1 / 72 kDa inositol polyphosphate 5-phosphatase / Q9NRR6* / inositol polyphosphate-5-phosphatase E*ENSMUSG000000269259
Inpp5k / Q8C5L6 / inositol polyphosphate 5-phosphatase K / Q9BT40*ENSMUSG000000061277


Protein motifs (from Interpro)
Interpro ID Name
 IPR000300  Inositol polyphosphate-related phosphatase
 IPR000504  RNA recognition motif domain
 IPR002013  SAC domain
 IPR005135  Endonuclease/exonuclease/phosphatase
 IPR015047  Domain of unknown function DUF1866
 IPR034973  Synaptojanin-2, RNA recognition motif
 IPR034974  Synaptojanin-2
 IPR035979  RNA-binding domain superfamily
 IPR036691  Endonuclease/exonuclease/phosphatase superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0046856 phosphatidylinositol dephosphorylation IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030424 axon IEA
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0045121 membrane raft IEA
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003723 RNA binding IEA
 molecular_functionGO:0004439 phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity IDA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0034595 phosphatidylinositol phosphate 5-phosphatase activity IEA
 molecular_functionGO:0042578 phosphoric ester hydrolase activity IEA


Pathways (from Reactome)
Pathway description
Synthesis of PIPs at the plasma membrane
Clathrin-mediated endocytosis


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000043 organ of Corti degeneration "a retrogressive impairment of function or destruction of the highly specialized epithelium in the floor of the ductus cochlearis" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0001260 increased body weight "greater than normal average weight " [J:33400]
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Allelic Composition: Smoc1tm1a(EUCOMM)Wtsi/Smoc1+
Genetic Background: C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi/H

 MP:0002857 cochlear ganglion degeneration "loss of neural cell bodies in the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0004362 cochlear hair cell degeneration "degeneration or loss of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0004398 cochlear inner hair cell degeneration "degeneration or loss of the single row of flask-shaped inner hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0004404 cochlear outer hair cell degeneration "degeneration or loss of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0004528 fused outer hair cell stereocilia "coalescence of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on cochlear outer hair cells, often resulting in giant stereocilia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0004533 fused inner hair cell stereocilia "coalescence of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on cochlear inner hair cells, often resulting in giant stereocilia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0004740 sensorineural hearing loss "a form of progressive hearing loss due to a lesion of the auditory division of cranial nerve VIII or the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

 MP:0006325 impaired hearing "reduced ability to percieve auditory stimuli" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

Allelic Composition: Synj2mozart/Synj2mozart
Genetic Background: involves: C57BL/6 * CBA/H

Allelic Composition: Synj2mozart/Synj2mozart
Genetic Background: involves: BALB/c * C57BL/6

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
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Allelic Composition: Col1a1tm5(tetO-GFP/RNAi:Cdkn2a)Slowe/Col1a1+,Gt(ROSA)26Sortm1(Luc)Kael/Gt(ROSA)26Sortm1(rtTA*M2)Jae,Krastm4Tyj/Kras+,Tg(Scgb1a1-rtTA)1Jaw/0
Genetic Background: involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6

Allelic Composition: Synj2mozart/Synj2mozart
Genetic Background: involves: C57BL/6 * CBA/H

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000033335 Dnm2 / P39054 / Mus musculus dynamin 2 (Dnm2), transcript variant 5, mRNA. / P50570* / dynamin 2*  / complex / reaction






 

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