Human (GRCh38.p14)
Description

ermin [Source:HGNC Symbol;Acc:HGNC:29208]

Gene Synonyms

ERMIN, JN, KIAA1189

Location

Chromosome 2: 157,318,631-157,327,713 reverse strand.

GRCh38:CM000664.2

About this gene

This gene has 9 transcripts (splice variants), 173 orthologues and 6 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000410096.6ERMN-2053677284aaENSP00000387047.1
 
Protein coding
CCDS46431Q8TAM6-1 NM_020711.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000397283.6ERMN-2013760297aaENSP00000380453.2
 
Protein coding
CCDS42764Q8TAM6-2 -GENCODE basicTSL:2
ENST00000420719.6ERMN-2091246264aaENSP00000410646.2
 
Protein coding
CCDS77475B4DIZ1 -GENCODE basicTSL:2
ENST00000409216.5ERMN-202746146aaENSP00000387049.1
 
Protein coding
B8ZZ94 -GENCODE basicTSL:4
ENST00000419116.2ERMN-207594111aaENSP00000410934.2
 
Protein coding
C9J8X3 -TSL:4CDS 3' incomplete
ENST00000411762.5ERMN-206590152aaENSP00000389595.1
 
Protein coding
C9JN04 -TSL:4CDS 3' incomplete
ENST00000409925.1ERMN-204556146aaENSP00000387325.1
 
Protein coding
B8ZZ94 -GENCODE basicTSL:4
ENST00000420317.5ERMN-208541160aaENSP00000398149.1
 
Protein coding
C9J6B4 -TSL:4CDS 3' incomplete
ENST00000409395.3ERMN-203146684aaENSP00000387339.3
 
Nonsense mediated decay
F8WAQ2 -TSL:5