Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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Gene: Dsg4 ENSMUSG00000001804

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Description

desmoglein 4 [Source:MGI Symbol;Acc:MGI:2661061]

Gene Synonyms

CDHF13, lah

Location

Chromosome 18: 20,436,175-20,471,821 forward strand.

GRCm38:CM001011.2

About this gene

This gene has 1 transcript (splice variant), 111 orthologues, 8 paralogues and is associated with 52 phenotypes.

Transcripts

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Name	Transcript ID	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
Dsg4-201	ENSMUST00000019426.4	3478	1041aa	ENSMUSP00000019426.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS29082	Q7TMD7	<p>TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA.</p><p>The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript.</p>TSL:1, The GENCODE set is the gene set for human and mouse. <a href="/Help/Glossary?id=500" class="popup">GENCODE Basic</a> is a subset of representative transcripts (splice variants).GENCODE basic, <p>APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS.</p><p>APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene.</p>APPRIS P1,

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Summary

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Gene-based displays