Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
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Gene: Rwdd4 ENSRNOG00000022500

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Description

RWD domain containing 4 [Source:RGD Symbol;Acc:1564132]

Gene Synonyms

Rwdd4a

Location

Primary_assembly 16: 44,714,699-44,733,098 reverse strand.

mRatBN7.2:CM026989.1

About this gene

This gene has 3 transcripts (splice variants), 214 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000115627.1	Rwdd4-203	1501	199aa	ENSRNOP00000097685.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AT52	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,
ENSRNOT00000077810.2	Rwdd4-202	2954	187aa	ENSRNOP00000073640.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K617	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,
ENSRNOT00000035323.5	Rwdd4-201	1044	188aa	ENSRNOP00000033649.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q569B7	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,

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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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Personal Data