ENSG00000100722


Homo sapiens

Features
Gene ID: ENSG00000100722
  
Biological name :ZC3H14
  
Synonyms : Q6PJT7 / ZC3H14 / zinc finger CCCH-type containing 14
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 14
Strand: 1
Band: q31.3
Gene start: 88562909
Gene end: 88627596
  
Corresponding Affymetrix probe sets: 204216_s_at (Human Genome U133 Plus 2.0 Array)   213063_at (Human Genome U133 Plus 2.0 Array)   213064_at (Human Genome U133 Plus 2.0 Array)   242443_at (Human Genome U133 Plus 2.0 Array)   243948_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000452475
Ensembl peptide - ENSP00000452370
Ensembl peptide - ENSP00000477763
Ensembl peptide - ENSP00000251038
Ensembl peptide - ENSP00000307025
Ensembl peptide - ENSP00000327176
Ensembl peptide - ENSP00000338002
Ensembl peptide - ENSP00000377150
Ensembl peptide - ENSP00000384682
Ensembl peptide - ENSP00000450451
Ensembl peptide - ENSP00000450474
Ensembl peptide - ENSP00000450823
Ensembl peptide - ENSP00000450917
Ensembl peptide - ENSP00000451007
Ensembl peptide - ENSP00000451054
Ensembl peptide - ENSP00000451389
Ensembl peptide - ENSP00000451489
Ensembl peptide - ENSP00000451530
Ensembl peptide - ENSP00000451638
Ensembl peptide - ENSP00000451941
Ensembl peptide - ENSP00000452210
NCBI entrez gene - 79882     See in Manteia.
OMIM - 613279
RefSeq - XM_017021650
RefSeq - NM_001160103
RefSeq - NM_001160104
RefSeq - NM_024824
RefSeq - NM_207660
RefSeq - NM_207661
RefSeq - NM_207662
RefSeq - XM_005268067
RefSeq - XM_005268068
RefSeq - XM_005268069
RefSeq - XM_005268070
RefSeq - XM_005268071
RefSeq - XM_005268073
RefSeq - XM_006720257
RefSeq - XM_011537160
RefSeq - XM_011537161
RefSeq - XM_017021648
RefSeq - XM_017021649
RefSeq Peptide - NP_001153576
RefSeq Peptide - NP_001313224
RefSeq Peptide - NP_001313236
RefSeq Peptide - NP_001153575
RefSeq Peptide - NP_079100
RefSeq Peptide - NP_997543
RefSeq Peptide - NP_997544
RefSeq Peptide - NP_997545
swissprot - G3V473
swissprot - G3V4R5
swissprot - G3V572
swissprot - G3V5I6
swissprot - H0YJ51
swissprot - H0YJ87
swissprot - H0YJA2
swissprot - G3V411
swissprot - A0A087WTC9
swissprot - G3V240
swissprot - G3V256
swissprot - G3V2X4
swissprot - G3V3R9
swissprot - G3V3Y4
swissprot - Q6PJT7
Ensembl - ENSG00000100722
  
Related genetic diseases (OMIM): 617125 - Mental retardation, autosomal recessive 56, 617125
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 Q5TYQ8ENSDARG00000041402Danio rerio
 ZC3H14ENSGALG00000010622Gallus gallus
 Q8BJ05ENSMUSG00000021012Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


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:0043488 regulation of mRNA stability IBA
 biological_processGO:1900364 negative regulation of mRNA polyadenylation IBA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005730 nucleolus IDA
 cellular_componentGO:0005737 cytoplasm IBA
 cellular_componentGO:0016607 nuclear speck IDA
 cellular_componentGO:0032839 dendrite cytoplasm IDA
 cellular_componentGO:1904115 axon cytoplasm IDA
 molecular_functionGO:0003723 RNA binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008143 poly(A) binding IBA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0001249 Mental retardation 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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