ENSMUSG00000029712


Mus musculus

Features
Gene ID: ENSMUSG00000029712
  
Biological name :Actl6b
  
Synonyms : actin-like 6B / Actl6b / Q99MR0
  
Possible biological names infered from orthology : O94805
  
Species: Mus musculus
  
Chr. number: 5
Strand: 1
Band: G2
Gene start: 137553517
Gene end: 137569582
  
Corresponding Affymetrix probe sets: 10526614 (MoGene1.0st)   1422564_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000117138
Ensembl peptide - ENSMUSP00000143702
Ensembl peptide - ENSMUSP00000123004
Ensembl peptide - ENSMUSP00000121672
Ensembl peptide - ENSMUSP00000119356
Ensembl peptide - ENSMUSP00000117425
Ensembl peptide - ENSMUSP00000031725
NCBI entrez gene - 83766     See in Manteia.
MGI - MGI:1933548
RefSeq - XM_017321187
RefSeq - XM_006504640
RefSeq - XM_006504639
RefSeq - XM_006504638
RefSeq - XM_006504637
RefSeq - NM_031404
RefSeq - XM_006504635
RefSeq - XM_006504636
RefSeq Peptide - NP_113581
swissprot - Q99MR0
swissprot - D3Z5W4
swissprot - F8WI57
swissprot - A0A0G2JGU5
swissprot - A0A1C7ZN05
swissprot - D3Z2E2
swissprot - D3Z4L2
Ensembl - ENSMUSG00000029712
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 actl6bENSDARG00000034107Danio rerio
 ACTL6BENSG00000077080Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Actl6a / Q9Z2N8 / actin-like 6A / O96019*ENSMUSG0000002767183


Protein motifs (from Interpro)
Interpro ID Name
 IPR004000  Actin family
 IPR004001  Actin, conserved site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006325 chromatin organization IEA
 biological_processGO:0006333 chromatin assembly or disassembly IC
 biological_processGO:0006338 chromatin remodeling IEA
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0007399 nervous system development IMP
 biological_processGO:0021510 spinal cord development IEA
 cellular_componentGO:0005634 nucleus ISO
 cellular_componentGO:0005730 nucleolus IEA
 cellular_componentGO:0016514 SWI/SNF complex IEA
 cellular_componentGO:0071565 nBAF complex IDA
 molecular_functionGO:0005515 protein binding IPI


Pathways (from Reactome)
Pathway description
RMTs methylate histone arginines
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000920 abnormal myelination "atypical or altered myelination in axon sheaths" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Ifngtm1Ts/Ifngtm1Ts,Socs1tm1Jni/Socs1tm1Jni
Genetic Background: involves: 129S7/SvEvBrd

 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
Show

Allelic Composition: Ifngtm1Ts/Ifngtm1Ts,Socs1tm1Jni/Socs1tm1Jni
Genetic Background: involves: 129S7/SvEvBrd

 MP:0004998 decreased CNS synapse formation "a reduction in the frequency of the process of generating the initial connections between an axon and effector tissue or neuron" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Ifngtm1Ts/Ifngtm1Ts,Socs1tm1Jni/Socs1tm1Jni
Genetic Background: involves: 129S7/SvEvBrd

 MP:0008143 abnormal dendrite morphology "any structural anomaly of the highly branched tree-like process of a neuron that serves as a receptive field and conducts impulses toward the cell body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Ifngtm1Ts/Ifngtm1Ts,Socs1tm1Jni/Socs1tm1Jni
Genetic Background: involves: 129S7/SvEvBrd

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Ifngtm1Ts/Ifngtm1Ts,Socs1tm1Jni/Socs1tm1Jni
Genetic Background: involves: 129S7/SvEvBrd

  


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






 

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