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Human (GRCh37.p13)
Description

family with sequence similarity 86, member B2 [Source:HGNC Symbol;Acc:32222]

Location

Chromosome 8: 12,282,913-12,293,915 reverse strand.

GRCh37:CM000670.1

About this gene

This gene has 6 transcripts (splice variants) and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000262365.4FAM86B2-2011268330aaENSP00000262365.4
 
Protein coding
CCDS59092P0C5J1 NM_001137610
NP_001131082
GENCODE basic
ENST00000393715.3FAM86B2-2041171129aaENSP00000377318.3
 
Protein coding
F6QN85 -GENCODE basic
ENST00000351291.4FAM86B2-2031166296aaENSP00000283479.4
 
Protein coding
E9PQV7 H7BXI9 -GENCODE basic
ENST00000309608.5FAM86B2-202900153aaENSP00000311330.5
 
Protein coding
E9PPT9 -GENCODE basic
ENST00000527331.1FAM86B2-001885295aaENSP00000432491.1
 
Protein coding
E9PQV7 -CDS 3' incomplete
ENST00000532480.1FAM86B2-002447149aaENSP00000436338.1
 
Protein coding
E9PPT9 -CDS 3' incomplete

Gene-based displays