Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: TFCP2L1 ENSDARG00000029497

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Description

transcription factor CP2-like 1 [Source:ZFIN;Acc:ZDB-GENE-040704-58]

Location

Chromosome 9: 38,292,919-38,311,750 forward strand.

GRCz11:CM002893.2

About this gene

This gene has 4 transcripts (splice variants), 196 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000146663.2	TFCP2L1-204	2076	468aa	ENSDARP00000118325.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9QJE0	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 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,
ENSDART00000040480.7	TFCP2L1-203	1990	397aa	ENSDARP00000040479.5	Nonsense mediated decay	-	-
ENSDART00000139959.2	TFCP2L1-202	844	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-
ENSDART00000139888.2	TFCP2L1-201	719	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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