All download files including the archive files are now in a publicly accessible Google Storage Bucket. Downloads page links have been updated.

Not found

Our G-nome assistant hasn't been able to find this symbol report. Please check the URL or use our search to find what you are looking for.

Symbol report for CD163

HGNC data for CD163

Approved symbol
CD163
Approved name

CD163 molecule

Locus type
gene with protein product
HGNC ID
HGNC:1631
Symbol status
Approved
Previous names
CD163 antigen
Alias symbols
M130
MM130
SCARI1
Chromosomal location
12p13.31
UCSC
Alliance of Genome Resources
Canis familiaris
CD163 VGNC:38931 VGNC
Equus caballus
CD163 VGNC:16247 VGNC
Felis catus
CD163 VGNC:60586 VGNC
Macaca mulatta
CD163 VGNC:70752 VGNC
Mus musculus
Cd163 MGI:2135946 Curated
Pan troglodytes
CD163 VGNC:57290 VGNC
Rattus norvegicus
Cd163 RGD:1310382
Sus scrofa
CD163 VGNC:112737 VGNC
Genomic organization and chromosomal localization of the human CD163 (M130) gene: a member of the scavenger receptor cysteine-rich superfamily.
Ritter M et al. Biochem Biophys Res Commun 1999 Jul;260(2)466-474
Ritter M, Buechler C, Langmann T, Schmitz G.
Biochem Biophys Res Commun 1999 Jul;260(2)466-474
Abstract: The human protein CD163 (M130) is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, which is exclusively expressed by monocytes and macrophages. Here, we investigated the genomic organization and the chromosomal localization of the human CD163 gene. The CD163 gene is composed of 17 exons and 16 introns and spans over 35 kb. Each of its nine SRCR domains is encoded by a separate exon, which is similar to other members of the group B SRCR subfamily. Two cytoplasmic variants of CD163 arise from alternative splicing of intron 15, while a truncated and an extracellular variant results from alternative splicing of intron 5 or intron 7, respectively. Using fluorescence in situ hybridization we mapped this gene to the human chromosome 12p13. The transcription initiation sites of the CD163 gene were determined and the 5'-flanking region was sequenced. The nucleotide analysis revealed several putative binding sites for transcription factors, which have been shown to play an important role in myeloid specific gene expression. In addition, we identified a L1 element located 1.4 kb upstream of the major transcription initiation site.
A new macrophage differentiation antigen which is a member of the scavenger receptor superfamily.
Law SK et al. Eur J Immunol 1993 Sep;23(9)2320-2325
Law SK, Micklem KJ, Shaw JM, Zhang XP, Dong Y, Willis AC, Mason DY.
Eur J Immunol 1993 Sep;23(9)2320-2325
Abstract: The antibodies Ki-M8, Ber-Mac3, GHI/61 and SM4 define a human macrophage-associated antigen with a relative molecular mass of 130,000 which we designate M130. The protein was purified by immunoaffinity chromatography and an N-terminal and three internal amino acid sequences were obtained. A cDNA fragment was initially obtained by polymerase chain reaction (PCR) using reverse-translated primers. Several variant cDNA clones, derived from alternative spliced messages, were obtained from a lipopolysaccharide-stimulated human monocyte library and were sequenced. The relative abundance of these variants was evaluated by a series of overlapping PCR reactions. The size of the most representative cDNA is 3.7 kb and closely agrees with the mRNA size of 3.8 kb determined by Northern blot analysis. The membrane protein encoded contains a leader peptide of 40 residues, a putative extracellular domain of 1003 residues, followed by a hydrophobic segment of 24 residues and a cytoplasmic domain of 49 residues. The extracellular domain was found to contain nine repeating elements, of about 110 residues, which are similar to those of the scavenger receptor superfamily.