Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SPRYD7 ENSBTAG00000018829

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Description

SPRY domain containing 7 [Source:VGNC Symbol;Acc:VGNC:35247]

Location

Primary_assembly 12: 19,397,591-19,416,305 reverse strand.

ARS-UCD1.3:CM008179.2

About this gene

This gene has 3 transcripts (splice variants) and 226 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000066562.2	SPRYD7-202	1945	237aa	ENSBTAP00000060952.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LUD2	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,
ENSBTAT00000098319.1	SPRYD7-201	1735	167aa	ENSBTAP00000100673.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000025061.5	SPRYD7-203	779	157aa	ENSBTAP00000025061.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2T9X3	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,

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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data