Gene: NME8 ENSG00000086288

Description

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

Gene Synonyms

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

Location

GRCh37:CM000669.1

About this gene

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

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000199447.4	NME8-001	2312	588aa	ENSP00000199447.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5452	Q8N427	NM_016616.4	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000440017.1	NME8-002	1879	588aa	ENSP00000397063.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS5452	Q8N427	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000444718.1	NME8-004	561	150aa	ENSP00000390596.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9JG62 C9JIT0	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000455500.1	NME8-003	473	115aa	ENSP00000390047.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9JIT0	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000426106.1	NME8-005	495	54aa	ENSP00000408841.1	Nonsense mediated decay		F8WEA2	-	-
ENST00000476435.1	NME8-006	442	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

Summary