Assignment of KCNK6 encoding the human weak inward rectifier potassium channel TWIK-2 to chromosome band 19q13.1 by radiation hybrid mapping

Cytogenetics and Cell Genetics

Volumn 84, Issue 3-4, 1999, Pages 190-191

  Gray, Andrew T ^a,b   Kindler, C H ^a   Sampson, E R ^a   Yost, C S ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL;

ARTICLE; CHROMOSOME 19Q; GENE ASSIGNMENT; GENE MAPPING; HUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

CHROMOSOMES, HUMAN, PAIR 19; COSMIDS; GENETIC MARKERS; HUMANS; HYBRID CELLS; LOD SCORE; MOLECULAR SEQUENCE DATA; PHYSICAL CHROMOSOME MAPPING; POTASSIUM CHANNELS; POTASSIUM CHANNELS, TANDEM PORE DOMAIN; SEQUENCE HOMOLOGY, NUCLEIC ACID;

EID: 0033017929     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Chavez RA, Gray AT, Zhao BB, Kindler CH, Mazurek MJ, Mehta Y, Forsayeth JR, Yost CS: TWIK-2, a new weak inward rectifying member of the tandem pore domain potassium channel family. J biol Chem 274:7887-7892 (1999).
2. Chen AH, Ni L, Fukushima K, Marietta J, O'Neill M, Coucke P, Willems P, Smith RJ: Linkage of a gene for dominant non-syndromic deafness to chromosome 19. Hum Mol Genet 4:1073-1076 (1995).
3. Kubisch C, Schroeder BC, Friedrich T, Lutjohann B, El-Amraoui A, Marlin S, Petit C, Jentsch TJ: KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell 96:437-446 (1999).
4. + channel TWIK-1 gene to chromosome 1q42 → q43. Genomics 34:153-155 (1996).
5. Lesage F, Lazdunski M: Mapping of human potassium channel genes TREK-1 (KCNK2) and TASK (KCNK3) to chromosomes 1q41 and 2p23. Genomics 51:478-479 (1998).
6. + channel from human kidney. J biol Chem 273:30863-30869 (1998).