Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: FSD1L ENSPTRG00000021222

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Description

fibronectin type III and SPRY domain containing 1 like [Source:VGNC Symbol;Acc:VGNC:8887]

Location

Chromosome 9: 83,309,108-83,380,135 forward strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 4 transcripts (splice variants), 198 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000039240.5	FSD1L-202	1374	457aa	ENSPTRP00000036259.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QXM7	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,
ENSPTRT00000098572.1	FSD1L-203	1230	409aa	ENSPTRP00000069968.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S072	-
ENSPTRT00000079171.1	FSD1L-204	1192	311aa	ENSPTRP00000072632.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S6N9 A0A6D2W5H9	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,
ENSPTRT00000079913.1	FSD1L-201	921	306aa	ENSPTRP00000079311.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SQT4	-

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Summary

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