EZH1 - enhancer of zeste 1 polycomb repressive complex 2 subunit Gene

Also Known as KMT6B

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2145

About EZH1

Cytogenetic location: 17q21.2 Genomic coordinates (GRCh38): 17:42,700,275-42,745,040 (from NCBI)

This gene has 24 transcripts (splice variants), 234 orthologues and 19 paralogues. Ubiquitous expression in ovary (RPKM 23.1), fat (RPKM 20.0) and 25 other tissues.

Summary

EZH1 is a component of a noncanonical Polycomb repressive complex-2 (PRC2) that mediates methylation of histone H3 (see MIM 602812) lys27 (H3K27) and functions in the maintenance of embryonic stem cell pluripotency and plasticity (Shen et al., 2008 [PubMed 19026780]).[supplied by OMIM, Mar 2009]

EZH1 Products (7)

mRNA Protein Name
XM_005257145.3 XP_005257202.1 histone-lysine N-methyltransferase EZH1 isoform X2
XM_047435594.1 XP_047291550.1 histone-lysine N-methyltransferase EZH1 isoform X3
NM_001991.5 NP_001982.2 histone-lysine N-methyltransferase EZH1 isoform 1
NM_001321082.2 NP_001308011.1 histone-lysine N-methyltransferase EZH1 isoform 3
NM_001321079.2 NP_001308008.1 histone-lysine N-methyltransferase EZH1 isoform 2
XM_011524517.3 XP_011522819.1 histone-lysine N-methyltransferase EZH1 isoform X1
NM_001321081.2 NP_001308010.1 histone-lysine N-methyltransferase EZH1 isoform 4
Molecular Function GO Annotation Evidence References Source
enables histone H3K27 methyltransferase activity IMP
IMP: Inferred from mutant phenotype
33514705 GOA
enables molecular condensate scaffold activity IMP
IMP: Inferred from mutant phenotype
33514705 GOA
enables nucleosome binding IMP
IMP: Inferred from mutant phenotype
33514705 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
20211142 GOA
Cellular Component GO Annotation Evidence References Source
part of ESC/E(Z) complex IDA
IDA: Inferred from direct assay
20075857 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

EZH1 Protein Structure

EZH2_WD-Binding

EZH2_WD-Binding: WD repeat binding protein EZH2 (39 - 68)

SET

SET: SET domain (615 - 718)

  • 0
  • 200
  • 400
  • 600
  • 738 a.a.
Protein Preferred Names Protein Names

histone-lysine N-methyltransferase EZH1

  • ENX-2

  • enhancer of zeste homolog 1

EZH1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
EZH1 Q92800 EED Homo sapiens O75530 33961781
Intra
EZH1 Q92800 EED Homo sapiens O75530
TAP
24981860
Intra
EZH1 Q92800 EED Homo sapiens O75530
TAP
27705803
Intra
EZH1 Q92800 EED Homo sapiens O75530 20211142
Cross: Cross-species interaction Intra: Intraspecies interaction

EZH1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P84703 EZH1 Antibody (YA4400) WB, FC, ELISA Human
HY-P84703A EZH1 Antibody (YA4400)(PBS only) WB, FC, ELISA Human

Related Diseases

Diseases Alias
Weaver Syndrome
  • Wss

  • Weaver-Smith Syndrome

  • WVS

  • Weaver-Like Syndrome

  • Weaver-Williams Syndrome

  • Camptodactyly-Overgrowth-Unusual Facies Syndrome

  • Camptodactyly - Overgrowth - Unusual Facies

  • Ezh2 Related Overgrowth

  • Overgrowth Syndrome With Accelerated Skeletal Maturation, Unusual Facies, And Camptodactyly

  • Weaver Smith Syndrome

  • Weaver Like Syndrome

  • Weaver Williams Syndrome

  • Camptodactyly-Overgrowth-Unusual Facies

  • Weaver Syndrome 1

  • Weaver Syndrome 2

  • Wvs1

  • Wvs2

Sotos Syndrome
  • Cerebral Gigantism

  • SOTOS

  • Chromosome 5q35 Deletion Syndrome

  • Sotos Syndrome 1, Formerly

  • Sotos1, Formerly

  • Distinctive Facial Appearance, Overgrowth In Childhood, And Learning Disabilities Or Delayed Development

  • Sotos Sequence

  • Sotos' Syndrome

  • Sotos1

  • Sotos Syndrome 1

Meier-Gorlin Syndrome 1
  • Meier-Gorlin Syndrome

  • Ear, Patella, Short Stature Syndrome

  • Microtia, Absent Patellae, Micrognathia Syndrome

  • MGORS1

  • Eps

  • Ear-Patella-Short Stature Syndrome

  • Ear Patella Short Stature Syndrome

  • Microtia Absent Patellae Micrognathia Syndrome

  • Meier-Gorlin Syndrome, Type 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris EZH1 VGNC VGNC:40540
Mus musculus EZH1 MGD MGI:1097695
Bos taurus EZH1 VGNC VGNC:28674
Rattus norvegicus EZH1 RGD RGD:1305028
Felis catus EZH1 VGNC VGNC:62017
Macaca mulatta EZH1 VGNC VGNC:72457
Others EZH1 NCBI