Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CDC14B ENSPTRG00000021155

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Description

cell division cycle 14B [Source:VGNC Symbol;Acc:VGNC:4654]

Location

Chromosome 9: 74,224,000-74,343,840 reverse strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 4 transcripts (splice variants), 144 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000044963.6	CDC14B-201	5628	498aa	ENSPTRP00000046055.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W7R3 H2R3T7	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,
ENSPTRT00000081634.1	CDC14B-202	5511	459aa	ENSPTRP00000076167.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XAK3 K7CGK4	-
ENSPTRT00000109705.1	CDC14B-203	1974	461aa	ENSPTRP00000084918.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y7N4 K7DNM9	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,
ENSPTRT00000095593.1	CDC14B-204	1458	485aa	ENSPTRP00000075810.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SFQ6 A0A6D2WZ30	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,

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Summary

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