Human (GRCh38.p14)
Description

family with sequence similarity 9 member C [Source:HGNC Symbol;Acc:HGNC:18405]

Gene Synonyms

TEX39C

Location
About this transcript

This transcript has 8 exons, is annotated with 8 domains and features, is associated with 2592 variant alleles and maps to 327 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000380625.8FAM9C-2021077166aaENSP00000369999.3
 
Protein coding
CCDS35203A0A024RBW5 Q8IZT9 NM_174901.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000542843.5FAM9C-2055858128aaENSP00000439185.1
 
Protein coding
G3V1I3 -GENCODE basicTSL:1
ENST00000333995.7FAM9C-2013361166aaENSP00000334430.3
 
Protein coding
CCDS35203A0A024RBW5 Q8IZT9 -GENCODE basicAPPRIS P1TSL:1
ENST00000438997.1FAM9C-203472126aaENSP00000409506.1
 
Protein coding
H7C346 -TSL:3CDS 5' incomplete
ENST00000468287.1FAM9C-2043445No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 8, Coding exons: 6, Transcript length: 1,077 bps, Translation length: 166 residues

MANE

This MANE Select transcript contains ENSP00000369999 and matches to NM_174901.6 and NP_777561.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8IZT9

CCDS

This transcript is a member of the Human CCDS set: CCDS35203

Transcript Support Level (TSL)

TSL:1

Version

ENST00000380625.8

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.