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: ST7 ENSBTAG00000010756

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Description

suppression of tumorigenicity 7 [Source:VGNC Symbol;Acc:VGNC:49974]

Location

Primary_assembly 4: 51,187,824-51,456,320 reverse strand.

ARS-UCD2.0:CM008171.2

About this gene

This gene has 7 transcripts (splice variants), 209 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000069581.2	ST7-205	2698	585aa	ENSBTAP00000068027.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4D7R9-1	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,
ENSBTAT00000056351.3	ST7-206	2629	562aa	ENSBTAP00000047740.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5BIS7	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,
ENSBTAT00000071233.2	ST7-202	2205	531aa	ENSBTAP00000063194.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LS80	-
ENSBTAT00000071071.2	ST7-203	1966	504aa	ENSBTAP00000069517.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MEP5	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,
ENSBTAT00000014243.7	ST7-201	1857	534aa	ENSBTAP00000014243.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DIE4	-
ENSBTAT00000081507.2	ST7-204	1830	523aa	ENSBTAP00000071443.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MKL6	-
ENSBTAT00000053015.5	ST7-207	753	251aa	ENSBTAP00000049962.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6ZJW5	-

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Summary

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