Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
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: FAXC ENSBTAG00000044061

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Description

failed axon connections homolog, metaxin like GST domain containing [Source:VGNC Symbol;Acc:VGNC:53792]

Location

Primary_assembly 9: 50,418,762-50,488,815 forward strand.

ARS-UCD2.0:CM008176.2

About this gene

This gene has 5 transcripts (splice variants), 295 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000070448.3	FAXC-203	1926	448aa	ENSBTAP00000072336.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NJI5	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,
ENSBTAT00000061622.4	FAXC-204	1864	432aa	ENSBTAP00000053331.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MQ86	-
ENSBTAT00000120243.2	FAXC-201	1796	417aa	ENSBTAP00000084636.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SH23	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSBTAT00000135609.2	FAXC-205	1709	369aa	ENSBTAP00000087860.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SUM7	-
ENSBTAT00000118454.2	FAXC-202	1703	356aa	ENSBTAP00000102681.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TYU3	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,

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Summary

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