Description

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

Synonyms

SPTRX2, CILD6, NM23-H8, TXNDC3

Location
About this transcript

This transcript has 16 exons, is annotated with 21 domains and features, is associated with 608 variations and maps to 404 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
NME8-201ENST00000199447.82312588aaENSP00000199447
 
Protein coding
CCDS5452Q8N427 NM_016616
NP_057700
TSL:1GENCODE basicAPPRIS P1
NME8-203ENST00000440017.51879588aaENSP00000397063
 
Protein coding
CCDS5452Q8N427 -TSL:1GENCODE basicAPPRIS P1
NME8-204ENST00000444718.5561150aaENSP00000390596
 
Protein coding
-C9JG62 -CDS 3' incompleteTSL:3
NME8-205ENST00000455500.5473115aaENSP00000390047
 
Protein coding
-C9JIT0 -CDS 3' incompleteTSL:5
NME8-202ENST00000426106.149554aaENSP00000408841
 
Nonsense mediated decay
-F8WEA2 -TSL:5
NME8-206ENST00000476435.1442No protein-
 
Retained intron
---TSL:1
Statistics

Exons: 16, Coding exons: 15, Transcript length: 1,879 bps, Translation length: 588 residues

CCDS

This transcript is a member of the Human CCDS set: CCDS5452

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N427

Transcript Support Level (TSL)

TSL:1

Version

ENST00000440017.5

Type

Known protein coding

Annotation Method

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

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript-based displays