Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- 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: CD163 ENSSSCG00000033146

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Description

CD163 molecule [Source:NCBI gene (formerly Entrezgene);Acc:397031]

Location

Primary_assembly 5: 63,300,231-63,334,498 forward strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 4 transcripts (splice variants), 167 orthologues, 24 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000044319.3	CD163-203	3779	1155aa	ENSSSCP00000053212.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B9P2	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,
ENSSSCT00000037917.3	CD163-204	4582	1113aa	ENSSSCP00000040119.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A807	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,
ENSSSCT00000049020.2	CD163-202	3803	867aa	ENSSSCP00000049232.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AZE3	-
ENSSSCT00000044540.2	CD163-201	3573	1111aa	ENSSSCP00000056393.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BJR1 A0A8D0WGD6	-

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Summary

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