Human (GRCh37.p13)
Description

Ellis van Creveld syndrome 2 [Source:HGNC Symbol;Acc:19747]

Gene Synonyms

LBN

Location
About this transcript

This transcript has 22 exons, is annotated with 16 domains and features, is associated with 83950 variant alleles and maps to 494 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000310917.2EVC2-00148281228aaENSP00000311683.2
 
Protein coding
CCDS54718Q4W5A4 Q4W5B1 Q86UK5
NM_001166136.1GENCODE basic
ENST00000344408.5EVC2-00343901308aaENSP00000342144.5
 
Protein coding
CCDS3382Q4W5A4 Q4W5B1 Q86UK5
NM_147127.4GENCODE basic
ENST00000344938.1EVC2-20137951246aaENSP00000339954.1
 
Protein coding
Q4W5A4 Q86UK5 -GENCODE basic
ENST00000475313.1EVC2-00244561166aaENSP00000431981.1
 
Nonsense mediated decay
Q4W5A4 Q86UK5 --
ENST00000509670.1EVC2-0044079452aaENSP00000423876.1
 
Nonsense mediated decay
E9PFT2 Q4W5A4 --
Statistics

Exons: 22, Coding exons: 22, Transcript length: 3,795 bps, Translation length: 1,246 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86UK5

Version

ENST00000344938.1

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

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