EMBL-EBI User Survey 2024

Do data resources managed by EMBL-EBI and our collaborators make a difference to your work?

Please take 10 minutes to fill in our annual user survey, and help us make the case for why sustaining open data resources is critical for life sciences research.

Survey link: https://www.surveymonkey.com/r/HJKYKTT?channel=[webpage]

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_207644.2Ensembl CanonicalGENCODE 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
---