Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Comparative Genomics
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Genetic Variation
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Gene: CYLD FBgn0032210

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Description

Cylindromatosis

Gene Synonyms

CYLD

Location

Primary_assembly 2L: 10,295,859-10,299,847 reverse strand.

BDGP6.54:AE014134.6

About this gene

This gene has 3 transcripts (splice variants) and 455 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0080070	CYLD-RD	2095	639aa	FBpp0079659	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8IPC5 Q8SYF0	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 ALT1: 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 is conserved in at least 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 ALT1,
FBtr0080071	CYLD-RE	2073	639aa	FBpp0079660	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8IPC5	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
FBtr0080072	CYLD-RB	1846	551aa	FBpp0079661	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8IPC3	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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