Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
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Phenotypes
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Gene: FSCB ENSBTAG00000031934

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Description

fibrous sheath CABYR binding protein [Source:VGNC Symbol;Acc:VGNC:29125]

Location

Primary_assembly 21: 54,269,490-54,272,713 reverse strand.

ARS-UCD2.0:CM008188.2

About this gene

This gene has 5 transcripts (splice variants) and 49 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000045287.5	FSCB-204	2528	791aa	ENSBTAP00000050184.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MEI0	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 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,
ENSBTAT00000100486.1	FSCB-201	3125	758aa	ENSBTAP00000088299.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SY96	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,
ENSBTAT00000133621.1	FSCB-205	2528	791aa	ENSBTAP00000086045.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MEI0	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,
ENSBTAT00000122071.1	FSCB-202	2463	742aa	ENSBTAP00000087320.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SPN2	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,
ENSBTAT00000098868.1	FSCB-203	2384	743aa	ENSBTAP00000099990.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TNP6	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,

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Summary

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