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Human (GRCh37.p13)
Description

ER lipid raft associated 2 [Source:HGNC Symbol;Acc:1356]

Gene Synonyms

C8orf2, Erlin-2, NET32, SPFH2, SPG18

Location
About this transcript

This transcript has 11 exons, is annotated with 7 domains and features, is associated with 6797 variant alleles and maps to 344 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000276461.5ERLIN2-0016073339aaENSP00000276461.5
 
Protein coding
CCDS6095E5RHW4 O94905 NM_007175.6Ensembl CanonicalGENCODE basic
ENST00000518586.1ERLIN2-0072623206aaENSP00000427847.1
 
Protein coding
O94905 -GENCODE basic
ENST00000523887.1ERLIN2-0062347206aaENSP00000429903.1
 
Protein coding
O94905 -GENCODE basic
ENST00000335171.6ERLIN2-0081742152aaENSP00000335220.6
 
Protein coding
CCDS34879O94905 NM_001003790.3GENCODE basic
ENST00000519638.1ERLIN2-0101718339aaENSP00000428112.1
 
Protein coding
CCDS6095E5RHW4 O94905 -GENCODE basic
ENST00000521644.1ERLIN2-0091602338aaENSP00000429621.1
 
Protein coding
E5RHW4 -CDS 3' incomplete
ENST00000397228.2ERLIN2-0021473152aaENSP00000380405.2
 
Protein coding
CCDS34879O94905 NM_001003791.2GENCODE basic
ENST00000523107.1ERLIN2-015771206aaENSP00000473292.1
 
Protein coding
O94905 -GENCODE basic
ENST00000518526.1ERLIN2-014663197aaENSP00000429229.1
 
Protein coding
E5RJ09 -CDS 3' incomplete
ENST00000521993.2ERLIN2-018764No protein-
 
Retained intron
---
ENST00000519872.1ERLIN2-013550No protein-
 
Retained intron
---
Statistics

Exons: 11, Coding exons: 11, Transcript length: 1,718 bps, Translation length: 339 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: O94905

CCDS

This transcript is a member of the Human CCDS set: CCDS6095

Version

ENST00000519638.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000376716 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.