Human (GRCh38.p14)
Description

C1q and TNF related 9B [Source:HGNC Symbol;Acc:HGNC:34072]

Gene Synonyms

CTRP9B

Location
About this transcript

This transcript has 3 exons, is annotated with 27 domains and features, is associated with 2826 variant alleles and maps to 328 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000713589.1C1QTNF9B-2041402333aaENSP00000518885.1
 
Protein coding
CCDS31947B2RNN3-1 NM_001007537.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000382137.8C1QTNF9B-2011261333aaENSP00000371572.3
 
Protein coding
CCDS31947B2RNN3-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000382145.5C1QTNF9B-20288899aaENSP00000371580.1
 
Protein coding
A0A0C4DFX8 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000556521.1C1QTNF9B-203729No protein-
 
Protein coding CDS not defined
--TSL:1
Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,261 bps, Translation length: 333 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: B2RNN3

CCDS

This transcript is a member of the Human CCDS set: CCDS31947

Transcript Support Level (TSL)

TSL:1

Version

ENST00000382137.8

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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

GENCODE primary gene

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