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Human (GRCh37.p13)
Description

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

Gene Synonyms

CILD6, NM23-H8, SPTRX2, TXNDC3, sptrx-2

Location

Chromosome 7: 37,888,199-37,940,003 forward strand.

GRCh37:CM000669.1

About this gene

This gene has 6 transcripts (splice variants), 9 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000199447.4NME8-0012312588aaENSP00000199447.4
 
Protein coding
CCDS5452Q8N427 NM_016616.4Ensembl CanonicalGENCODE basic
ENST00000440017.1NME8-0021879588aaENSP00000397063.1
 
Protein coding
CCDS5452Q8N427 -GENCODE basic
ENST00000444718.1NME8-004561150aaENSP00000390596.1
 
Protein coding
C9JG62 C9JIT0 -CDS 3' incomplete
ENST00000455500.1NME8-003473115aaENSP00000390047.1
 
Protein coding
C9JIT0 -CDS 3' incomplete
ENST00000426106.1NME8-00549554aaENSP00000408841.1
 
Nonsense mediated decay
F8WEA2 --
ENST00000476435.1NME8-006442No protein-
 
Retained intron
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