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

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Gene: CD200R1 ENSSSCG00000011925

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Description

CD200 receptor 1 [Source:NCBI gene (formerly Entrezgene);Acc:100155169]

Location

Primary_assembly 13: 146,953,149-146,995,323 forward strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 2 transcripts (splice variants), 248 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000032815.4	CD200R1-202	3183	362aa	ENSSSCP00000028917.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SUJ9 K7GM29	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,
ENSSSCT00000013049.5	CD200R1-201	1643	213aa	ENSSSCP00000012706.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1SVZ0 F1SLU1	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,

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Summary

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