Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene 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: FANCL ENSSSCG00000008394

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Description

FA complementation group L [Source:VGNC Symbol;Acc:VGNC:88007]

Location

Primary_assembly 3: 83,337,253-83,436,942 forward strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 3 transcripts (splice variants) and 203 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000059199.3	FANCL-202	1699	378aa	ENSSSCP00000052056.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B7H5 A0A8D1XQA8	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,
ENSSSCT00000066702.2	FANCL-203	1606	347aa	ENSSSCP00000067583.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1W699 A0A5G2RAE5	-
ENSSSCT00000009191.4	FANCL-201	1401	258aa	ENSSSCP00000008958.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1WBP2 A0A8D1LLU0	-

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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