Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: PRR15L ENSBTAG00000012249

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Description

proline rich 15 like [Source:VGNC Symbol;Acc:VGNC:33394]

Location

Primary_assembly 19: 38,500,545-38,516,837 forward strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 7 transcripts (splice variants), 105 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000071908.2	PRR15L-202	1573	222aa	ENSBTAP00000072637.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MN41	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,
ENSBTAT00000089415.1	PRR15L-206	1860	219aa	ENSBTAP00000080362.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SDG1	-
ENSBTAT00000136018.1	PRR15L-201	1797	100aa	ENSBTAP00000094869.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3T183	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000116819.1	PRR15L-207	1755	184aa	ENSBTAP00000087707.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SMY2	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000016243.4	PRR15L-205	1450	202aa	ENSBTAP00000016243.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6YXE9	-
ENSBTAT00000134095.1	PRR15L-204	1427	123aa	ENSBTAP00000077072.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S181	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000123348.1	PRR15L-203	1346	143aa	ENSBTAP00000092061.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T5Q9	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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