Description

desmoglein 4 [Source:HGNC Symbol;Acc:HGNC:21307]

Synonyms

CDHF13, LAH

Location
INSDC coordinates

chromosome:GRCh38:CM000680.2:31376777:31414912:1

About this gene

This gene has 2 transcripts (splice variants), 85 orthologues, 13 paralogues, is a member of 1 Ensembl protein family and is associated with 3 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
DSG4-002ENST0000035974745261059aaENSP00000352785
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS45845Q86SJ6 NM_001134453
NP_001127925
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
DSG4-001ENST0000030812835791040aaENSP00000311859
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS11897Q86SJ6 NM_177986
NP_817123
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays