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

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Gene: Adgrd1 ENSRNOG00000023536

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Description

adhesion G protein-coupled receptor D1 [Source:RGD Symbol;Acc:1594795]

Gene Synonyms

Gpr133, LOC689257

Location

Primary_assembly 12: 33,125,915-33,272,509 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 3 transcripts (splice variants), 197 orthologues and 42 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000058586.7	Adgrd1-201	3912	903aa	ENSRNOP00000055384.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZF17	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000073105.3	Adgrd1-202	3816	871aa	ENSRNOP00000066668.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RAV7	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,
ENSRNOT00000168376.1	Adgrd1-203	3777	858aa	ENSRNOP00000101982.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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