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

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Gene: CCNB1IP1 ENSDARG00000104639

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Description

si:ch211-212k18.11 [Source:ZFIN;Acc:ZDB-GENE-160728-138]

Location

Chromosome 7: 19,538,425-19,544,575 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants) and 196 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000161549.3	CCNB1IP1-201	999	251aa	ENSDARP00000139067.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M6Z7T5	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,
ENSDART00000181659.1	CCNB1IP1-202	756	251aa	ENSDARP00000156073.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M6Z7T5	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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