Gene: Ptchd3 ENSMUSG00000039198

Description

patched domain containing 3 [Source:MGI Symbol;Acc:MGI:1921925]

Gene Synonyms

4930451E13Rik, 4933440L20Rik

Location

Chromosome 11: 121,721,073-121,734,249 forward strand.

GRCm39:CM001004.3

About this gene

This gene has 2 transcripts (splice variants), 327 orthologues, 10 paralogues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000036690.7	Ptchd3-201	3194	906aa	ENSMUSP00000035709.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49014	Q0EEE2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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. APPRIS P1, TSL 1: A transcript where all splice junctions 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, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000125199.2	Ptchd3-202	1543	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	TSL 1: A transcript where all splice junctions 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, based on the type and quality of the alignments used to annotate the transcript. TSL:1,

Gene: Ptchd3 ENSMUSG00000039198

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Gene: Ptchd3 ENSMUSG00000039198

Summary

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