Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: ptch1 ENSDARG00000016404

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Description

patched 1 [Source:ZFIN;Acc:ZDB-GENE-980526-196]

Location

Chromosome 8: 29,962,635-30,068,277 forward strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues, 12 paralogues and is associated with 56 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000007640.10	ptch1-201	4834	1475aa	ENSDARP00000025418.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R8E2	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, 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,
ENSDART00000148258.2	ptch1-202	4068	1355aa	ENSDARP00000114906.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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