Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: ENSPTRG00000049437

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Location

Chromosome X: 44,227,771-44,229,359 forward strand.

Pan_tro_3.0:CM000336.3

About this gene

This gene has 3 transcripts (splice variants), 279 orthologues and 64 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000076517.1	-	1371	456aa	ENSPTRP00000083924.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T3W6	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,
ENSPTRT00000097144.1	-	1368	455aa	ENSPTRP00000076271.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SGZ2	-
ENSPTRT00000104681.1	-	1314	437aa	ENSPTRP00000086809.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TC41	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,

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Summary

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