Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
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- GO: Anatomical entity
Phenotypes
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ID History
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Gene: FANCD2OS ENSBTAG00000010094

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Description

FANCD2 opposite strand [Source:NCBI gene (formerly Entrezgene);Acc:768064]

Gene Synonyms

C22H3orf24, C3orf24

Location

Primary_assembly 22: 16,732,294-16,737,540 forward strand.

ARS-UCD2.0:CM008189.2

About this gene

This gene has 2 transcripts (splice variants) and 124 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000124305.1	FANCD2OS-201	1555	178aa	ENSBTAP00000099295.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32KZ5	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,
ENSBTAT00000013313.5	FANCD2OS-202	958	178aa	ENSBTAP00000013313.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32KZ5	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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