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EHMT1 information


EHMT1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEHMT1, EUHMTASE1, Eu-HMTase1, FP13812, GLP, GLP1, KMT1D, bA188C12.1, euchromatic histone lysine methyltransferase 1, EHMT1-IT1, KLEFS1
External IDsOMIM: 607001; MGI: 1924933; HomoloGene: 11698; GeneCards: EHMT1; OMA:EHMT1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001012518
NM_001109686
NM_001109687
NM_172545

RefSeq (protein)

NP_001012536
NP_001103156
NP_001103157
NP_766133

Location (UCSC)Chr 9: 137.62 – 137.87 MbChr 2: 24.79 – 24.92 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Euchromatic histone-lysine N-methyltransferase 1, also known as G9a-like protein (GLP), is a protein that in humans is encoded by the EHMT1 gene.[5]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000181090 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000036893 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Euchromatic histone-lysine N-methyltransferase 1". Retrieved 2012-03-04.

and 6 Related for: EHMT1 information

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EHMT1

Last Update:

G9a-like protein (GLP), is a protein that in humans is encoded by the EHMT1 gene. EHMT1 messenger RNA is alternatively spliced to produce three predicted...

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Histone methyltransferase

Last Update:

encoding proteins with histone methyltransferase activity include: ASH1L DOT1L EHMT1, EHMT2, EZH1, EZH2 MLL, MLL2, MLL3, MLL4, MLL5 NSD1 PRDM2 SET, SETBP1, SETD1A...

Word Count : 2214

Ankyrin repeat

Last Update:

CTTNBP2; DAPK1; DDEF1; DDEF2; DDEFL1; DGKI; DGKZ; DP58; DYSFIP1; DZANK; EHMT1; EHMT2; ESPN; FANK1; FEM1A; FEM1B; GABPB2; GIT1; GIT2; GLS; GLS2; HACE1;...

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SET domain

Last Update:

this domain include: ASH1L, also has an associated with SET domain (AWS) EHMT1 (FP13812), EHMT2 (BAT8), EZH1, EZH2 MLL, MLL2, MLL3, MLL5 NSD1 PRDM1, PRDM2...

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KMT2C

Last Update:

HG, Veltman JA, Schenck A, van Bokhoven H (July 2012). "Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability"...

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List of OMIM disorder codes

Last Update:

245150; MGP Kindler syndrome; 173650; KIND1 Kleefstra syndrome; 610253; EHMT1 Klippel–Feil syndrome, autosomal dominant; 118100; GDF6 Kniest dysplasia;...

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