Human (GRCh38.p14)
Description

family with sequence similarity 156 member B [Source:HGNC Symbol;Acc:HGNC:31962]

Gene Synonyms

TMEM29B

Location

Chromosome X: 52,891,306-52,908,560 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 8 transcripts (splice variants), 52 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000416841.8FAM156B-2013757213aaENSP00000424864.1
 
Protein coding
CCDS43957Q8NDB6 NM_001321178.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000593751.7FAM156B-2032942213aaENSP00000469248.1
 
Protein coding
CCDS43957Q8NDB6 -GENCODE basicAPPRIS P1TSL:2
ENST00000616419.4FAM156B-2072032213aaENSP00000483008.1
 
Protein coding
CCDS43957Q8NDB6 -GENCODE basicAPPRIS P1TSL:2
ENST00000509613.1FAM156B-2021701213aaENSP00000422411.1
 
Protein coding
CCDS43957Q8NDB6 -GENCODE basicAPPRIS P1TSL:2
ENST00000619346.4FAM156B-20899256aaENSP00000478064.1
 
Protein coding
A0A087WZZ1 -TSL:2CDS 3' incomplete
ENST00000610405.4FAM156B-20485849aaENSP00000484983.1
 
Protein coding
A0A087X2H2 -TSL:2CDS 3' incomplete
ENST00000612188.4FAM156B-206776129aaENSP00000482608.1
 
Protein coding
A0A087WZE8 -TSL:2CDS 3' incomplete
ENST00000610609.4FAM156B-2055453aaENSP00000479752.1
 
Protein coding
--TSL:2CDS 3' incomplete