ENSDARG00000037060


Danio rerio

Features
Gene ID: ENSDARG00000037060
  
Biological name :kmt2d
  
Synonyms : kmt2d / lysine (K)-specific methyltransferase 2D
  
Possible biological names infered from orthology : Histone-lysine N-methyltransferase 2D / lysine methyltransferase 2D / O14686 / Q6PDK2
  
Species: Danio rerio
  
Chr. number: 23
Strand: 1
Band:
Gene start: 27756984
Gene end: 27793877
  
Corresponding Affymetrix probe sets:
  
Cross references: Ensembl peptide - ENSDARP00000119354
Ensembl peptide - ENSDARP00000121042
Ensembl peptide - ENSDARP00000053862
Ensembl peptide - ENSDARP00000116027
Ensembl peptide - ENSDARP00000119206
swissprot - E7F2F7
swissprot - E9QF90
swissprot - F1R3T7
swissprot - F1R733
swissprot - F1R7I1
ZFIN ID - ZDB-GENE-060223-2
Ensembl - ENSDARG00000037060
  
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 ENSGALG00000035501Gallus gallus
 ENSGALG00000031702Gallus gallus
 KMT2DENSG00000167548Homo sapiens
 Kmt2dENSMUSG00000048154Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
kmt2ca / lysine (K)-specific methyltransferase 2Ca / KMT2C* / Q8NEZ4* / lysine methyltransferase 2C*ENSDARG0000007931228
kmt2cb / lysine (K)-specific methyltransferase 2Cb / KMT2C* / Q8NEZ4* / lysine methyltransferase 2C*ENSDARG0000007556027
kmt2bb / lysine (K)-specific methyltransferase 2Bb / KMT2B* / O08550* / Q9UMN6* / lysine methyltransferase 2B* / Histone-lysine N-methyltransferase 2B *ENSDARG000000606977
kmt2a / lysine (K)-specific methyltransferase 2A / P55200* / Q03164* / lysine methyltransferase 2A* / Mus musculus lysine (K)-specific methyltransferase 2A (Kmt2a), transcript variant 1, mRNA.*ENSDARG000000045377
setd1a / SET domain containing 1A / O15047* / AC149222.1*ENSDARG000000600306
setd1ba / SET domain containing 1B, a / Q9UPS6* / SETD1B* / Q8CFT2* / SET domain containing 1B* / Histone-lysine N-methyltransferase SETD1B *ENSDARG000000608476
kmt2ba / lysine (K)-specific methyltransferase 2Ba / KMT2B* / O08550* / Q9UMN6* / lysine methyltransferase 2B* / Histone-lysine N-methyltransferase 2B *ENSDARG000000629626
setd1bb / SET domain containing 1B, bENSDARG000000772442


Protein motifs (from Interpro)
Interpro ID Name
 IPR001214  SET domain
 IPR001841  Zinc finger, RING-type
 IPR001965  Zinc finger, PHD-type
 IPR003616  Post-SET domain
 IPR003888  FY-rich, N-terminal
 IPR003889  FY-rich, C-terminal
 IPR011011  Zinc finger, FYVE/PHD-type
 IPR013083  Zinc finger, RING/FYVE/PHD-type
 IPR019787  Zinc finger, PHD-finger
 IPR034732  Extended PHD (ePHD) domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003428 chondrocyte intercalation involved in growth plate cartilage morphogenesis IMP
 biological_processGO:0007420 brain development IMP
 biological_processGO:0007507 heart development IMP
 biological_processGO:0032259 methylation IEA
 biological_processGO:0034968 histone lysine methylation IEA
 biological_processGO:0048703 embryonic viscerocranium morphogenesis IMP
 biological_processGO:0051568 histone H3-K4 methylation IEA
 biological_processGO:0060026 convergent extension IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0035097 histone methyltransferase complex IEA
 molecular_functionGO:0008168 methyltransferase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0018024 histone-lysine N-methyltransferase activity IEA
 molecular_functionGO:0042800 histone methyltransferase activity (H3-K4 specific) IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Formation of the beta-catenin:TCF transactivating complex
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 ZFA:0000008 brain brain decreased size , abnormal
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 ZFA:0000009 cardiac ventricle cardiac ventricle orientation atrium , abnormal
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 ZFA:0000029 hindbrain hindbrain decreased size , abnormal
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 ZFA:0000032 hypothalamus hypothalamus decreased thickness , abnormal
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 ZFA:0000054 pericardium pericardium edematous , abnormal
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 ZFA:0000109 forebrain forebrain nucleus elongated , abnormal
forebrain neuron differentiation decreased process quality , abnormal
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 ZFA:0000128 midbrain midbrain nucleus elongated , abnormal
midbrain neuron differentiation decreased process quality , abnormal
Show

 ZFA:0000135 notochord notochord increased width , abnormal
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 ZFA:0000160 tegmentum tegmentum decreased thickness , abnormal
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 ZFA:0000445 optic tectum optic tectum decreased thickness , abnormal
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 ZFA:0000545 medulla oblongata medulla oblongata decreased thickness , abnormal
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 ZFA:0001094 whole organism whole organism anterior-posterior axis shortened , abnormal
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 ZFA:0001114 head head lacks all parts of type cleithrum , abnormal
head lacks all parts of type opercle , abnormal
head lacks all parts of type Meckels cartilage , abnormal
head lacks all parts of type ceratohyal cartilage , abnormal
head lacks all parts of type pharyngeal arch 3-7 , abnormal
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 ZFA:0001205 Meckel s cartilage Meckels cartilage decreased distance ceratohyal cartilage , abnormal
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 ZFA:0001321 neurocranial trabecula neurocranial trabecula truncated , abnormal
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 ZFA:0001400 ceratohyal cartilage ceratohyal cartilage increased width , abnormal
ceratohyal cartilage kinked , abnormal
ceratohyal cartilage shortened , abnormal
ceratohyal cartilage chondrocyte disorganized , abnormal
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 ZFA:0001405 ethmoid cartilage ethmoid cartilage truncated , abnormal
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 ZFA:0009084 chondrocyte chondrocyte filamentous actin position , abnormal
chondrocyte myosin II filament position , abnormal
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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