Human (GRCh37.p13)
Description

family with sequence similarity 78, member B [Source:HGNC Symbol;Acc:13495]

Location

Chromosome 1: 166,026,674-166,136,206 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 5 transcripts (splice variants), 269 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000338353.3FAM78B-2011597261aaENSP00000339681.3
 
Protein coding
CCDS30931Q5VT40 -Ensembl CanonicalGENCODE Basic
ENST00000354422.3FAM78B-0011475261aaENSP00000346404.3
 
Protein coding
CCDS30931Q5VT40 NM_001017961.3GENCODE Basic
ENST00000435676.1FAM78B-0024399254aaENSP00000412766.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000456900.1FAM78B-0042300261aaENSP00000389945.1
 
Nonsense mediated decay
CCDS30931Q5VT40 --
ENST00000441649.1FAM78B-0032264257aaENSP00000393329.1
 
Nonsense mediated decay
--CDS 5' incomplete