Human (GRCh37.p13)
Description

TMEM9 domain family, member B [Source:HGNC Symbol;Acc:1168]

Gene Synonyms

C11orf15

Location
About this transcript

This transcript has 5 exons, is annotated with 8 domains and features, is associated with 7553 variant alleles and maps to 400 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000534025.1TMEM9B-0012083198aaENSP00000433361.1
 
Protein coding
CCDS7796E9PMI7 Q543A1 Q7Z649
Q9NQ34
NM_020644.1GENCODE basic
ENST00000309134.5TMEM9B-0041659124aaENSP00000311842.5
 
Protein coding
CCDS66021E9PMI7 Q7Z649 NM_001286094.1GENCODE basic
ENST00000525069.1TMEM9B-0021433124aaENSP00000431487.1
 
Protein coding
CCDS66021E9PMI7 Q7Z649 -GENCODE basic
ENST00000528117.1TMEM9B-00394995aaENSP00000432373.1
 
Protein coding
E9PMI7 E9PR12 -GENCODE basic
ENST00000530136.1TMEM9B-00562553aaENSP00000434961.1
 
Protein coding
E9PMI7 -CDS 3' incomplete
Statistics

Exons: 5, Coding exons: 5, Transcript length: 2,083 bps, Translation length: 198 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NQ34

CCDS

This transcript is a member of the Human CCDS set: CCDS7796

Version

ENST00000534025.1

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.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000385722 (version 1)
GENCODE basic gene

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