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

Configure this page

Share this page

Bookmark this page

.

Gene: ENSGGOG00000012694

.

Description

TGFB induced factor homeobox 1 [Source:HGNC Symbol;Acc:HGNC:11776]

Location

Chromosome 18: 11,578,749-11,589,450 reverse strand.

gorGor4:FR853089.2

About this gene

This gene has 3 transcripts (splice variants), 221 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGGOT00000061344.1	-	1200	399aa	ENSGGOP00000032750.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I2YD71	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,
ENSGGOT00000012741.3	-	1406	272aa	ENSGGOP00000012384.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3RAB7	-
ENSGGOT00000050808.1	-	861	286aa	ENSGGOP00000044046.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I2ZAE1	-

.

Summary

.

.