Human (GRCh37.p13)
Description

family with sequence similarity 211, member B [Source:HGNC Symbol;Acc:33155]

Gene Synonyms

C22orf36, MGC131773

Location

Chromosome 22: 24,981,588-24,989,175 reverse strand.

GRCh37:CM000684.1

About this gene

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

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000318753.8FAM211B-0011238315aaENSP00000320520.8
 
Protein coding
CCDS42991Q2VPJ9 NM_207644.2GENCODE basic
ENST00000446942.1FAM211B-0051828108aaENSP00000400102.1
 
Nonsense mediated decay
F8WCG9 --
ENST00000404045.2FAM211B-002141774aaENSP00000384130.2
 
Nonsense mediated decay
F8WCZ7 --
ENST00000495297.1FAM211B-007782No protein-
 
Processed transcript
---
ENST00000464490.1FAM211B-008575No protein-
 
Processed transcript
---
ENST00000491910.1FAM211B-0032943No protein-
 
Retained intron
---
ENST00000460524.1FAM211B-0042276No protein-
 
Retained intron
---
ENST00000465334.1FAM211B-006957No protein-
 
Retained intron
---