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: Pno1 ENSRNOG00000005524

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Description

partner of NOB1 homolog [Source:RGD Symbol;Acc:727882]

Gene Synonyms

LOC289809

Location

Primary_assembly 14: 95,688,125-95,905,881 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 4 transcripts (splice variants), 219 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000007824.8	Pno1-201	1879	323aa	ENSRNOP00000007824.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R9PXS8	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 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,
ENSRNOT00000141007.1	Pno1-204	1802	251aa	ENSRNOP00000108720.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000110369.2	Pno1-202	1474	242aa	ENSRNOP00000088236.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9D6	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,
ENSRNOT00000127205.1	Pno1-203	1110	275aa	ENSRNOP00000108788.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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