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

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Gene: PTCH2 ENSOCUG00000012489

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Description

patched 2 [Source:HGNC Symbol;Acc:HGNC:9586]

Location

Chromosome 13: 121,795,376-121,811,353 forward strand.

OryCun2.0:CM000802.1

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000012495.3	PTCH2-201	3597	1198aa	ENSOCUP00000010757.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1T3F8	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,
ENSOCUT00000036664.1	PTCH2-202	3426	1142aa	ENSOCUP00000037689.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F9CVA1	-

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Summary

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