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: Pym1 ENSRNOG00000058130

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Description

PYM homolog 1, exon junction complex associated factor [Source:RGD Symbol;Acc:1306096]

Gene Synonyms

LOC366790, RGD1306096, Wibg

Location

Primary_assembly 7: 1,759,110-1,783,948 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 6 transcripts (splice variants), 193 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000170837.1	Pym1-206	1538	283aa	ENSRNOP00000110252.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000095627.2	Pym1-202	1864	190aa	ENSRNOP00000097008.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GMC3	-
ENSRNOT00000123007.1	Pym1-205	1848	215aa	ENSRNOP00000099352.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000106303.2	Pym1-203	1485	257aa	ENSRNOP00000095975.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ARN1	-
ENSRNOT00000112561.2	Pym1-204	1373	228aa	ENSRNOP00000094727.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GKW1	-
ENSRNOT00000092037.3	Pym1-201	1253	203aa	ENSRNOP00000071842.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KSI5 D3ZGY1	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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