Human (GRCh37.p13)
Description

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

Gene Synonyms

HEL-S-92n, MGC88159, PTX2, SAP

Location

Chromosome 1: 159,557,615-159,558,655 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 1 transcript (splice variant) and 6 paralogues.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000255040.2APCS-001926223aa
 
Protein coding
CCDS1186P02743 NM_001639.3Ensembl CanonicalGENCODE Basic
Name

APCS (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: P02743

CCDS

This gene is a member of the Human CCDS set: CCDS1186.1

Ensembl version

ENSG00000132703.3

Other assemblies

This gene maps to 159,587,825-159,588,865 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000022741 (version 2)

Loading component