Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: FANCL ENSGALG00010017104

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Description

Fanconi anemia complementation group L [Source:NCBI gene (formerly Entrezgene);Acc:421202]

Location

Primary_assembly 3: 1,003,657-1,032,140 reverse strand.

bGalGal1.mat.broiler.GRCg7b:CM028484.1

About this gene

This gene has 4 transcripts (splice variants) and 203 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSGALT00010041286.1	FANCL-204	2514	340aa	ENSGALP00010024173.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSGALT00010041290.1	FANCL-203	1944	397aa	ENSGALP00010024177.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-
ENSGALT00010041278.1	FANCL-201	1859	366aa	ENSGALP00010024167.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	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,
ENSGALT00010041282.1	FANCL-202	1829	419aa	ENSGALP00010024170.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-

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Summary

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