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The Reticulocalbin Gene Maps to the WAGR Region in Human and to the Small Eye Harwell Deletion in Mouse
- Source :
- Genomics. 42:260-267
- Publication Year :
- 1997
- Publisher :
- Elsevier BV, 1997.
-
Abstract
- We describe the localization of the gene encoding reticulocalbin, a Ca 2+ -binding protein of the endoplasmic reticulum, on human chromosome 11p13 midway between the WT1 and the PAX6 genes and show that it is hemizygously deleted in WAGR individuals. The mouse reticulocalbin gene is also shown to map to the region of conserved synteny on mouse chromosome 2 and to be deleted in the Small eye Harwell ( Sey H ) mutation. Loss of the reticulocalbin gene could contribute to the early lethality of Sey H and Sey Dey homozygotes.
- Subjects :
- Male
Genes, Wilms Tumor
PAX6 Transcription Factor
Biology
medicine.disease_cause
Polymerase Chain Reaction
Wilms Tumor
Mice
Species Specificity
Gene mapping
Intellectual Disability
Genetics
medicine
Animals
Humans
Paired Box Transcription Factors
Abnormalities, Multiple
Eye Abnormalities
Eye Proteins
Aniridia
Gene
In Situ Hybridization, Fluorescence
DNA Primers
Homeodomain Proteins
Mutation
Base Sequence
Gene map
Chromosomes, Human, Pair 11
Calcium-Binding Proteins
Homozygote
Chromosome Mapping
Chromosome
Syndrome
medicine.disease
Molecular biology
Kidney Neoplasms
DNA-Binding Proteins
Repressor Proteins
Urogenital Abnormalities
PAX6
Reticulocalbin 1
Gene Deletion
Subjects
Details
- ISSN :
- 08887543
- Volume :
- 42
- Database :
- OpenAIRE
- Journal :
- Genomics
- Accession number :
- edsair.doi.dedup.....825667ff498fd2e650e7697c6c5db8cb
- Full Text :
- https://doi.org/10.1006/geno.1997.4706