Chromosomal assignment of a gene encoding a new collagen type (COL15A1) to 9q21 → q22

Genomics

Volumn 14, Issue 2, 1992, Pages 220-224

  Huebner, Kay ^a   Cannizzaro, Linda A ^a   Jabs, Ethylin Wang ^b   Kiyirikko, Sirpa ^c   Manzone, Holly ^d   Pihlajaniemi, Taina ^c   Myers, Jeanne C ^d  

^a THOMAS JEFFERSON UNIVERSITY HOSPITAL   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF OULU   (Finland)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN; COLLAGEN TYPE 15; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 9Q; GENE ASSIGNMENT; GENE LOCATION; HUMAN; HUMAN CELL; HYBRID CELL; IN SITU HYBRIDIZATION;

AMINO ACID SEQUENCE; ANIMAL; BLOTTING, SOUTHERN; CHROMOSOMES, HUMAN, PAIR 9; COLLAGEN; ELECTROPHORESIS, AGAR GEL; HUMAN; HYBRID CELLS; IN SITU HYBRIDIZATION; METAPHASE; MOLECULAR SEQUENCE DATA; RESTRICTION MAPPING; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

RODENTIA;

EID: 0026471828     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/S0888-7543(05)80209-5     Document Type: Article

References (30)

1. Cloning of human α1(X) collagen DNA and localization of the COL10A1 gene to the q21 → q22 region of human chromosome 6
2. Localization of the human V preB gene to the 22q11.2 region of chromosome 22 near a cluster of VI1 segments
3. Chromosome localization of human ARH genes, a ras-related gene family
4. Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2
5. Cathepsin L (CTSL) is located in the chromosome 9q21 → q22 region: A related sequence is located on chromosome 10
6. Location of the gene for Gorlin syndrome
7. The COL6A1 and COL6A2 genes exist as a gene cluster and detect highly informative DNA polymorphisms in the telomeric region of human chromosome 21Q
8. Naevoid basal-cell carcinoma syndrome
9. Human collagen gene COL5A1 maps to the q34.2 → 34.3 region of chromosome 9, near the locus for Nail-Patella syndrome
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13. Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering
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