Human (GRCh38.p14)
Description

NME/NM23 family member 8 [Source:HGNC Symbol;Acc:HGNC:16473]

Gene Synonyms

CILD6, DNAI8, NM23-H8, SPTRX2, TXNDC3

Location

Chromosome 7: 37,848,597-37,900,397 forward strand.

GRCh38:CM000669.2

About this gene

This gene has 6 transcripts (splice variants), 123 orthologues, 8 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000199447.9NME8-2012308588aaENSP00000199447.4
 
Protein coding
CCDS5452Q8N427 NM_016616.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000440017.5NME8-2031879588aaENSP00000397063.1
 
Protein coding
CCDS5452Q8N427 -GENCODE basicAPPRIS P1TSL:1
ENST00000444718.5NME8-204561150aaENSP00000390596.1
 
Protein coding
C9JG62 -TSL:3CDS 3' incomplete
ENST00000455500.5NME8-205473115aaENSP00000390047.1
 
Protein coding
C9JIT0 -TSL:5CDS 3' incomplete
ENST00000426106.1NME8-20249554aaENSP00000408841.1
 
Nonsense mediated decay
F8WEA2 -TSL:5
ENST00000476435.1NME8-206442No protein-
 
Retained intron
--TSL:1