Human (GRCh38.p14)
Description

C1q and TNF related 9 [Source:HGNC Symbol;Acc:HGNC:28732]

Gene Synonyms

AQL1, C1QTNF9A, CTRP9, MGC48915

Location
About this transcript

This transcript has 4 exons, is annotated with 20 domains and features, is associated with 7569 variant alleles and maps to 345 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000332018.5C1QTNF9-2011824333aaENSP00000333737.4
 
Protein coding
CCDS9306A0A3B0J259 P0C862 NM_178540.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000382071.6C1QTNF9-2021854333aaENSP00000371503.2
 
Protein coding
CCDS9306A0A3B0J259 P0C862 -GENCODE basicAPPRIS P1TSL:5
Statistics

Exons: 4, Coding exons: 3, Transcript length: 1,854 bps, Translation length: 333 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P0C862

CCDS

This transcript is a member of the Human CCDS set: CCDS9306

Transcript Support Level (TSL)

TSL:5

Version

ENST00000382071.6

Type

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.