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: C4A ENSSSCG00000001427

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Description

complement C4A (Rodgers blood group) [Source:NCBI gene (formerly Entrezgene);Acc:445467]

Gene Synonyms

C4

Location

Primary_assembly 7: 24,068,019-24,083,061 forward strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 3 transcripts (splice variants), 225 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000079853.2	C4A-202	5433	1758aa	ENSSSCP00000061845.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QCL1	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,
ENSSSCT00000001570.6	C4A-201	5400	1747aa	ENSSSCP00000001528.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RQW2	-
ENSSSCT00000102168.1	C4A-203	5393	1752aa	ENSSSCP00000080009.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FKZ4	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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