ENSMUSG00000006673


Mus musculus

Features
Gene ID: ENSMUSG00000006673
  
Biological name :Qrich1
  
Synonyms : glutamine rich 1 / Qrich1
  
Possible biological names infered from orthology : Q2TAL8
  
Species: Mus musculus
  
Chr. number: 9
Strand: 1
Band: F2
Gene start: 108516806
Gene end: 108560163
  
Corresponding Affymetrix probe sets: 10589030 (MoGene1.0st)   1426289_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000141215
Ensembl peptide - ENSMUSP00000142233
Ensembl peptide - ENSMUSP00000142211
Ensembl peptide - ENSMUSP00000142027
Ensembl peptide - ENSMUSP00000142025
Ensembl peptide - ENSMUSP00000141716
Ensembl peptide - ENSMUSP00000141691
Ensembl peptide - ENSMUSP00000141267
Ensembl peptide - ENSMUSP00000006851
Ensembl peptide - ENSMUSP00000107782
NCBI entrez gene - 69232     See in Manteia.
MGI - MGI:1916482
RefSeq - XM_006511808
RefSeq - XM_017313560
RefSeq - XM_006511818
RefSeq - XM_006511814
RefSeq - XM_006511813
RefSeq - XM_006511812
RefSeq - XM_006511811
RefSeq - NM_001114119
RefSeq - NM_175143
RefSeq - XM_017313561
RefSeq - XM_006511809
RefSeq - XM_006511810
RefSeq Peptide - NP_780352
RefSeq Peptide - NP_001107591
swissprot - Q8BUN3
swissprot - A0A0A6YY13
swissprot - G3X8R5
swissprot - A0A0A6YVQ2
swissprot - A0A0A6YWT7
swissprot - A0A0A6YWV5
swissprot - A0A0A6YXK0
swissprot - A0A0A6YXK2
swissprot - A0A0A6YXZ6
Ensembl - ENSMUSG00000006673
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 qrich1ENSDARG00000019797Danio rerio
 QRICH1ENSGALG00000006867Gallus gallus
 Q2TAL8ENSG00000198218Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Zmym4 / A2A791 / zinc finger, MYM-type 4 / Q5VZL5* / zinc finger MYM-type containing 4*ENSMUSG0000004244626
Zmym3 / Q9JLM4 / zinc finger, MYM-type 3 / Q14202* / zinc finger MYM-type containing 3*ENSMUSG0000003131023
Zmym2 / Q9CU65 / zinc finger, MYM-type 2 / Q9UBW7* / zinc finger MYM-type containing 2*ENSMUSG0000002194522
Zmym6 / zinc finger, MYM-type 6 / AC114490.2*ENSMUSG0000004240811
Zmym5 / Q3U2E2 / zinc finger, MYM-type 5 / Q9UJ78* / zinc finger MYM-type containing 5*ENSMUSG000000401235


Protein motifs (from Interpro)
Interpro ID Name
 IPR011029  Death-like domain superfamily
 IPR021893  Protein of unknown function DUF3504


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0005654 nucleoplasm IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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]
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Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0000273 overriding aorta "congenitally mispositioned aorta where the origin straddles the ventral septum and so receives ejected blood from the right ventricle as well as the left." [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cml, J:67826]
Show

Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0000284 double outlet right ventricle "both the aorta and the pulmonary trunk originate from the right ventricle, usually in conjunction with a ventricular septal defect" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:67826]
Show

Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0001823 thymus hypoplasia "small size due to reduced cell number in the thymus" [J:23255]
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Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0004056 abnormal myocardial compact layer morphology "malformation of the outer, dense layer of the myocardium " [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0008528 polycystic kidney "the development of innumerable cysts in the kidneys filled with fluid replacing much of the mass of the kidneys leading to reduction in kidney function and frequently kidney failure" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0010402 ventricular septal defect "abnormal communications between the two lower chambers of the heart, including such defects in the perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular regions" [MESH:C14.240.400.560.540]
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Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0010418 perimembraneous ventricular septal defect "abnormal communications between the two lower chambers of the heart, occurring in the membranous septum with defects in the adjacent muscular portion of the septum; it is generally located in the LV outflow tract just below the aortic valve, associated with pouches or aneurysms of the septal leaflet of the tricuspid valve, which may partially or completely close the defect; an LV-to-RA shunt may also be associated with this defect" [http://emedicine.medscape.com]
Show

Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

 MP:0011667 double outlet right ventricle with atrioventricular septal defect "a form of DORV in which there is also a complete atrioventricular canal" [MGI:csmith]
Show

Allelic Composition: Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo
Genetic Background: C57BL/6J-Ccdc39b2b2025.1Clo

  


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






 

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