Human (GRCh37.p13)
Description

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

Gene Synonyms

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

Location
About this transcript

This transcript has 2 exons, is associated with 1606 variant alleles and maps to 148 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000199447.4NME8-0012312588aaENSP00000199447.4
 
Protein coding
CCDS5452Q8N427 NM_016616.4GENCODE 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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Statistics

Exons: 2, Coding exons: 0, Transcript length: 442 bps,

Version

ENST00000476435.1

Type

Retained intron

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000338091 (version 1)