Human (GRCh38.p14)
Description

LIM domain only 2 [Source:HGNC Symbol;Acc:HGNC:6642]

Gene Synonyms

RBTN2, RBTNL1, RHOM2, TTG2

Location
About this transcript

This transcript has 3 exons, is annotated with 23 domains and features, is associated with 4949 variant alleles and maps to 383 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000257818.3LMO2-2012081227aaENSP00000257818.2
 
Protein coding
CCDS7888P25791-3 NM_005574.4MANE SelectEnsembl CanonicalGENCODE basicTSL:1
ENST00000395833.7LMO2-2021687158aaENSP00000379175.3
 
Protein coding
CCDS44567P25791-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000411482.1LMO2-203151955aaENSP00000401967.1
 
Nonsense mediated decay
P25791-4 -TSL:1
ENST00000493667.1LMO2-206390No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000464025.5LMO2-2041550No protein-
 
Retained intron
--TSL:1
ENST00000465614.1LMO2-205869No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 3, Coding exons: 3, Transcript length: 1,687 bps, Translation length: 158 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P25791

CCDS

This transcript is a member of the Human CCDS set: CCDS44567

Transcript Support Level (TSL)

TSL:1

Version

ENST00000395833.7

Type

Protein coding

Annotation Method

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

GENCODE basic gene

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