Human (GRCh38.p14)
Description

SMAD family member 9 [Source:HGNC Symbol;Acc:HGNC:6774]

Gene Synonyms

MADH6, MADH9, SMAD8, SMAD8/9

Location
About this transcript

This transcript has 7 exons, is annotated with 21 domains and features, is associated with 34486 variant alleles and maps to 559 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000379826.5SMAD9-2025558467aaENSP00000369154.4
 
Protein coding
CCDS45032O15198-1 NM_001127217.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000350148.10SMAD9-2012208430aaENSP00000239885.6
 
Protein coding
CCDS9360O15198-2 -GENCODE basicTSL:1
ENST00000399275.7SMAD9-2031588144aaENSP00000382216.3
 
Nonsense mediated decay
A0A7I2R5A4 -TSL:1
ENST00000483941.2SMAD9-204667No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 7, Coding exons: 6, Transcript length: 5,558 bps, Translation length: 467 residues

MANE

This MANE Select transcript contains ENSP00000369154 and matches to NM_001127217.3 and NP_001120689.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: O15198

CCDS

This transcript is a member of the Human CCDS set: CCDS45032

Transcript Support Level (TSL)

TSL:5

Version

ENST00000379826.5

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.