Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Rprd1b ENSRNOG00000012923

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Description

regulation of nuclear pre-mRNA domain containing 1B [Source:RGD Symbol;Acc:1304782]

Gene Synonyms

Crept, LOC311591, RGD1304782

Location

Primary_assembly 3: 167,102,859-167,206,374 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 220 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000017265.8	Rprd1b-201	3616	326aa	ENSRNOP00000017265.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B5DEK0	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 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,
ENSRNOT00000109927.2	Rprd1b-202	1089	224aa	ENSRNOP00000091603.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AFR9	-

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Summary

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