Human (GRCh37.p13)
Description

myopalladin [Source:HGNC Symbol;Acc:23246]

Gene Synonyms

CMD1DD, CMH22, MYOP, RCM4

Location

Chromosome 10: 69,865,912-69,971,774 forward strand.

GRCh37:CM000672.1

About this gene

This gene has 4 transcripts (splice variants), 3 paralogues and is associated with 8 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000358913.5MYPN-00160131320aa
 
Protein coding
CCDS7275A5PKT7 Q86TC9 NM_032578.3Ensembl CanonicalGENCODE Basic
ENST00000540630.1MYPN-20156971320aa
 
Protein coding
F5GWA6 -GENCODE Basic
ENST00000354393.2MYPN-00245961045aa
 
Protein coding
Q86TC9 -GENCODE Basic
ENST00000373675.3MYPN-0032126507aa
 
Protein coding
Q86TC9 -GENCODE Basic
Name

MYPN (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q86TC9

CCDS

This gene is a member of the Human CCDS set: CCDS7275.1

LRG

LRG_410 provides a stable genomic reference framework for describing sequence variants for this gene

Ensembl version

ENSG00000138347.11

Other assemblies

This gene maps to 68,106,155-68,212,017 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000018344 (version 1)

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