Genomic organization and chromosomal localization of the mouse IKBKAP gene

Gene

Volumn 279, Issue 1, 2001, Pages 81-89

  Coli, Rocco ^a   Anderson, Sylvia L ^a   Volpi, Sabrina A ^a   Rubin, Berish Y ^a  

^a FORDHAM UNIVERSITY   (United States)

Author keywords

Exon intron boundaries; Familial dysautonomia; Gene structure; Mapping panels

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; I KAPPA B KINASE ASSOCIATED PROTEIN; MESSENGER RNA; PROTEIN; PROTEIN SERINE THREONINE KINASE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 4; CONTROLLED STUDY; DNA SEQUENCE; DYSAUTONOMIA; ENZYME PHOSPHORYLATION; EXON; GENE LOCATION; GENE MUTATION; GENE STRUCTURE; GENETIC CODE; GENETIC CONSERVATION; GENETIC LINKAGE; GENETIC ORGANIZATION; GENETIC RECOMBINATION; INTRON; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; RABBIT; RAT; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CARRIER PROTEINS; CHROMOSOME MAPPING; DNA; DNA, COMPLEMENTARY; EXONS; FEMALE; GENES; HUMANS; INTRONS; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED STRAINS; MOLECULAR SEQUENCE DATA; MURIDAE; RABBITS; RATS; RATS, SPRAGUE-DAWLEY; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; SEQUENCE HOMOLOGY, AMINO ACID; SEQUENCE HOMOLOGY, NUCLEIC ACID;

ORYCTOLAGUS CUNICULUS;

EID: 0035861181     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(01)00737-5     Document Type: Article

References (14)

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2. Familial dysautonomia is caused by mutations of the IKAP gene
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4. Familial dysautonomia: Diagnosis, pathogenesis and management
5. Familial dysautonomia: A report of genetic and clinical studies, with a review of the literature
6. IKAP is a scaffold protein of the IκB kinase complex
7. Human/mouse homology relationships
8. The IκB kinase (IKK) complex is tripartite and contains IKKγ but not IKAP as a regular component
9. Incidence of familial dysautonomia in Israel 1977-1981
10. Central autonomic dysfunction with defective lacrimation
11. Maps from two interspecific backcross DNA panels available as a community genetic mapping resource
12. A comparative genetic map of rat, mouse and human genomes
13. Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia