Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Pwwp3a ENSRNOG00000024549

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Description

PWWP domain containing 3A, DNA repair factor [Source:RGD Symbol;Acc:1308340]

Gene Synonyms

LOC362838, MUM-1, Mum1

Location

Primary_assembly 7: 10,115,866-10,130,925 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000060708.4	Pwwp3a-201	2421	698aa	ENSRNOP00000057438.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QRY6 B1H224	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 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,
ENSRNOT00000113234.2	Pwwp3a-202	2088	678aa	ENSRNOP00000079260.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQH5	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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