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PMID: 2563353 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Mapping of the human complement factor I gene to 4q25.

Genomics ·Vol. 4 ·No. 1 ·1989-01-00 ·Pages 82-6

Shiang R, Murray JC, Morton CC, Buetow KH, Wasmuth JJ, Olney AH, Sanger WG, Goldberger G

Abstract

A detailed genetic and physical map of human complement factor I (IF) using somatic cell hybrids, in situ hybridization, and genetic linkage is reported. The gene has been localized to band 4q25. The order GC-INP10-ADH3-EGF-IF-IL2-MNS is proposed for genes on 4q on the basis of genetic and physical mapping techniques. A BclI polymorphism found with the IF probe demonstrated a maternal origin for a de novo deletion of chromosome 4 that was used in physically mapping the gene. The genetic and physical distances around band 4q24 suggest that 1 cM is approximately 1.2 million bp of DNA. This work provides a useful addition to the map of 4q.

MeSH Terms
Chromosome Mapping Chromosomes, Human, Pair 4 Complement Factor I Genetic Linkage Humans Hybrid Cells Nucleic Acid Hybridization Polymorphism, Restriction Fragment Length Serine Endopeptidases/genetics
Chemicals
Serine Endopeptidases Complement Factor I
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Shiang R
Department of Pediatrics, University of Iowa, Iowa City 52242.
Murray J C
Morton C C
Buetow K H
Wasmuth J J
Olney A H
Sanger W G
Goldberger G
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1989-01-00
Pages
82-6
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NIGMS NIH HHS · GM 33293 · United States
NICHD NIH HHS · R01-HD20998 · United States
NIGMS NIH HHS · T32-GM07091 · United States
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