Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: FTCDNL1 ENSBTAG00000031595

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Description

formiminotransferase cyclodeaminase N-terminal like [Source:NCBI gene (formerly Entrezgene);Acc:613365]

Location

Primary_assembly 2: 88,317,925-88,459,779 reverse strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 5 transcripts (splice variants), 142 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000044793.5	FTCDNL1-202	1733	328aa	ENSBTAP00000042254.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BL83	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,
ENSBTAT00000067590.2	FTCDNL1-205	1086	195aa	ENSBTAP00000056659.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LF29	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,
ENSBTAT00000081741.2	FTCDNL1-201	967	195aa	ENSBTAP00000073273.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NLI1	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,
ENSBTAT00000070124.2	FTCDNL1-203	819	189aa	ENSBTAP00000069433.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1ND80	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,
ENSBTAT00000068986.2	FTCDNL1-204	666	138aa	ENSBTAP00000066914.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MDK3	-

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Summary

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