Cloning of the murine Krit1 cDNA reveals novel mammalian 5′ coding exons

Genomics

Volumn 70, Issue 3, 2000, Pages 392-395

  Zhang, Jun ^a   Clatterbuck, Richard E ^a   Rigamonti, Daniele ^a   Dietz, Harry C ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GENE PRODUCT; PROTEIN KRIT1; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BRAIN MALFORMATION; CODON; CONSENSUS SEQUENCE; CONTROLLED STUDY; EXON; GENE AMPLIFICATION; GENE MUTATION; GENETIC CODE; GENETIC SCREENING; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL;

MAMMALIA; MURINAE;

EID: 0034671077     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6410     Document Type: Article

References (9)

1. Hundreds of ankyrin-like repeats in functionally diverse proteins: Mobile modules that cross phyla horizontally?
2. Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton
3. KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation
4. At least six nucleotides preceding the AUG initiator codon enhance translation in mammalian cells
5. Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous anglomas
6. Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)
7. Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22
8. Human-mouse comparative mapping of the genomic region containing CDK6: Localization of an evolutionary breakpoint
9. Mutations in KRIT1 in familial cerebral cavernous malformations