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: Cdip1 ENSRNOG00000003328

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Description

cell death-inducing p53 target 1 [Source:RGD Symbol;Acc:1310686]

Gene Synonyms

LOC360480, MGC94589, RGD1310686

Location

Primary_assembly 10: 11,293,827-11,303,415 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 210 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000100719.2	Cdip1-202	2599	235aa	ENSRNOP00000084999.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A313	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,
ENSRNOT00000004999.6	Cdip1-201	2521	208aa	ENSRNOP00000004999.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K4R2 Q5U2U6	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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