Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: RXFP1 ENSSSCG00000008875

.

Description

relaxin family peptide receptor 1 [Source:VGNC Symbol;Acc:VGNC:92525]

Location

Primary_assembly 8: 47,473,788-47,601,357 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 4 transcripts (splice variants), 197 orthologues and 23 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000062837.3	RXFP1-201	3027	785aa	ENSSSCP00000034653.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZT62 A0A8D0S196	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 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,
ENSSSCT00000079886.2	RXFP1-202	2874	756aa	ENSSSCP00000072907.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R6M5	-
ENSSSCT00000009716.5	RXFP1-203	2847	725aa	ENSSSCP00000009467.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U4X2 F1RW91	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,
ENSSSCT00000072171.2	RXFP1-204	2802	710aa	ENSSSCP00000061079.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U242 A0A5G2QC39	-

.

Summary

.

.