Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Polr2d ENSRNOG00000016231

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Description

RNA polymerase II subunit D [Source:RGD Symbol;Acc:1308565]

Gene Synonyms

LOC364834

Location

Primary_assembly 18: 23,692,578-23,699,709 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021738.7	Polr2d-201	1115	142aa	ENSRNOP00000021738.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J2P3 D4A259	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000097856.2	Polr2d-202	388	110aa	ENSRNOP00000086996.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GFK4	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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