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Human (GRCh37.p13)
Description

lysine (K)-specific methyltransferase 2E [Source:HGNC Symbol;Acc:18541]

Gene Synonyms

HDCMC04P, MLL5, NKp44L

Location

Chromosome 7: 104,654,626-104,754,808 forward strand.

GRCh37:CM000669.1

About this gene

This gene has 17 transcripts (splice variants), 1 paralogue and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000334877.4KMT2E-20270131816aaENSP00000335599.4
 
Protein coding
C9JNE1 C9JQ68 O95038
Q8IZD2
-GENCODE basic
ENST00000311117.3KMT2E-00168741858aaENSP00000312379.3
 
Protein coding
CCDS34723C9JNE1 C9JQ68 O95038
Q8IZD2
NM_182931
NP_891847
GENCODE basic
ENST00000257745.4KMT2E-20167141858aaENSP00000257745.4
 
Protein coding
CCDS34723C9JNE1 C9JQ68 O95038
Q8IZD2
NM_018682
NP_061152
GENCODE basic
ENST00000334914.7KMT2E-2035139589aaENSP00000333986.7
 
Protein coding
E7ETZ7 -GENCODE basic
ENST00000476671.1KMT2E-0032520609aaENSP00000417888.1
 
Protein coding
C9JNE1 C9JQ68 O95038
Q8IZD2
-GENCODE basic
ENST00000478990.1KMT2E-0091500352aaENSP00000419883.1
 
Protein coding
C9JYI9 -CDS 3' incomplete
ENST00000495267.1KMT2E-0081133230aaENSP00000420415.1
 
Protein coding
C9JNE1 C9JQ68 -CDS 3' incomplete
ENST00000479838.2KMT2E-016883144aaENSP00000473963.1
 
Protein coding
--CDS 5' incomplete
ENST00000474203.1KMT2E-01261771aaENSP00000420206.1
 
Protein coding
C9JQ68 -CDS 3' incomplete
ENST00000473063.1KMT2E-007375125aaENSP00000417156.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000334884.5KMT2E-0046840865aaENSP00000335398.5
 
Nonsense mediated decay
C9JNE1 C9JQ68 O95038
Q8IZD2
--
ENST00000482560.2KMT2E-0101759144aaENSP00000417193.2
 
Nonsense mediated decay
C9JQ68 F8WAU9 --
ENST00000478079.1KMT2E-01859721aaENSP00000419525.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000480368.1KMT2E-011679No protein-
 
Processed transcript
---
ENST00000496191.1KMT2E-015584No protein-
 
Retained intron
---
ENST00000468607.1KMT2E-014558No protein-
 
Retained intron
---
ENST00000485619.1KMT2E-013397No protein-
 
Retained intron
---

Gene-based displays