ENSMUSG00000020770


Mus musculus

Features
Gene ID: ENSMUSG00000020770
  
Biological name :Unk
  
Synonyms : Q8BL48 / Unk / unkempt family zinc finger
  
Possible biological names infered from orthology : Q9C0B0
  
Species: Mus musculus
  
Chr. number: 11
Strand: 1
Band: E2
Gene start: 116030322
Gene end: 116061214
  
Corresponding Affymetrix probe sets: 10382756 (MoGene1.0st)   1426681_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000021116
Ensembl peptide - ENSMUSP00000102060
NCBI entrez gene - 217331     See in Manteia.
MGI - MGI:2442456
RefSeq - XM_017314490
RefSeq - NM_001286006
RefSeq - NM_172569
RefSeq - XM_006533088
RefSeq - XM_006533089
RefSeq Peptide - NP_001272935
RefSeq Peptide - NP_766157
swissprot - Q8BL48
swissprot - Q3UYU7
Ensembl - ENSMUSG00000020770
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 unkENSDARG00000000935Danio rerio
 UNKENSGALG00000002278Gallus gallus
 UNKENSG00000132478Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Unkl / Q5FWH2 / unkempt family like zinc finger / Q9H9P5*ENSMUSG0000001512749
Gm5819 / UNKL* / Q9H9P5* / unkempt family like zinc finger*ENSMUSG000000920979


Protein motifs (from Interpro)
Interpro ID Name
 IPR000571  Zinc finger, CCCH-type
 IPR036855  Zinc finger, CCCH-type superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001764 neuron migration IMP
 biological_processGO:0006417 regulation of translation IEA
 biological_processGO:0048667 cell morphogenesis involved in neuron differentiation ISO
 biological_processGO:2000766 negative regulation of cytoplasmic translation ISO
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005844 polysome ISO
 molecular_functionGO:0003723 RNA binding IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:1990715 mRNA CDS binding ISO


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000520 absent kidney "missing paired organs that excrete urine" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49471]
Show

Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0001015 small superior cervical ganglion "reduced size of the group of neurons that is the largest of the ganglia of the sympathetic trunk; normally lies at the base of the skull and innervates the head and neck" [J:23882]
Show

Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0003722 absent ureter "missing the tube that conducts the urine from the renal pelvis to the bladder" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0009532 decreased parotid gland size "reduced size of either of the largest of the major salivary glands situated below and in front of each ear" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0010977 fused right lung lobes "complete or partial fusion of the right lung lobes, indicative of defective lobar septation during embryonic lung development" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0013835 absent hypoglossal nerve "absence of the motor nerve which innervates all the intrinsic and all but one of the extrinsic muscles of the tongue" [ISBN:0-683-40008-8]
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Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0013840 absent segment of posterior cerebral artery "absence of a portion of one of a pair of blood vessels that supplies oxygenated blood to the posterior aspect of the brain" [UBERON:0001636]
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Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0013848 subcutaneous edema "accumulation of watery or serous fluid in the subcutaneous region below the skin" [MGI:csmith]
Show

Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

 MP:0013978 abnormal carotid artery origin 
Show

Allelic Composition: Smg9tm1b(EUCOMM)Wtsi/Smg9tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Smg9tm1b(EUCOMM)Wtsi/Wtsi

  


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






 

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