Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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- Orthologues
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Ontologies
- GO: Anatomical entity
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Gene: Cdc123 ENSRNOG00000017770

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Description

cell division cycle 123 [Source:RGD Symbol;Acc:619766]

Gene Synonyms

D123

Location

Primary_assembly 17: 77,368,397-77,412,659 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 4 transcripts (splice variants), 203 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000117639.2	Cdc123-204	1865	336aa	ENSRNOP00000089218.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A9Q9 A6JLY4	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,
ENSRNOT00000113414.2	Cdc123-202	1865	336aa	ENSRNOP00000083559.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZX90	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,
ENSRNOT00000024016.8	Cdc123-201	1850	331aa	ENSRNOP00000024016.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QDG3	-
ENSRNOT00000116923.2	Cdc123-203	1521	316aa	ENSRNOP00000096017.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q62834	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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Summary

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