Description

amyloid P component, serum [Source:HGNC Symbol;Acc:HGNC:584]

Synonyms

MGC88159, PTX2, SAP

INSDC coordinates

chromosome:GRCh38:CM000663.2:159587825:159588865:1

About this gene

This gene has 1 transcript (splice variant), 106 orthologues, 6 paralogues, is a member of 1 Ensembl protein family and is associated with 70 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
APCS-001ENST00000255040926223aaENSP00000255040
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS1186P02743 V9HWP0 NM_001639
NP_001630
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays