Human (GRCh37.p13)
Description

family with sequence similarity 177, member B [Source:HGNC Symbol;Acc:34395]

Gene Synonyms

FLJ43505, RP11-452F19.2

Location

Chromosome 1: 222,910,549-222,924,147 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 6 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000445590.2FAM177B-2011345158aaENSP00000414451.2
 
Protein coding
CCDS1535A6PVY1 A6PVY2 A6PVY3
NM_207468.2GENCODE basic
ENST00000360827.2FAM177B-003764158aaENSP00000354070.2
 
Protein coding
CCDS1535A6PVY1 A6PVY2 A6PVY3
-GENCODE basic
ENST00000456298.1FAM177B-00554599aaENSP00000400233.1
 
Protein coding
A6PVY1 -CDS 3' incomplete
ENST00000434700.1FAM177B-002466100aaENSP00000391615.1
 
Protein coding
A6PVY1 A6PVY2 -CDS 3' incomplete
ENST00000391880.2FAM177B-0011994120aaENSP00000375752.2
 
Nonsense mediated decay
A6PVY3 --
ENST00000460763.1FAM177B-004582No protein-
 
Retained intron
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