Description:
WILLIAMS-BEUREN SYNDROME; WBS
Repository
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NIGMS Human Genetic Cell Repository
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Subcollection |
Heritable Diseases dbGaP |
Class |
Disorders of Connective Tissue, Muscle, and Bone |
Quantity |
25 µg |
Quantitation Method |
Please see our FAQ |
Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
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Transformant
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Epstein-Barr Virus
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Sample Source
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DNA from LCL
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Race
|
White
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Family Member
|
1
|
Relation to Proband
|
proband
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Confirmation
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Clinical summary/Case history
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ISCN
|
46,XX.ish del(7)(q11.23q11.23)(ELN-).arr 7q11.23(72363696-73780028)x1
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by Nucleoside Phosphorylase, Glucose-6-Phosphate Dehydrogenase, and Lactate Dehydrogenase Isoenzyme Electrophoresis and by Chromosome Analysis |
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ELASTIN |
FISH performed at the CCR with a probe for the elastin gene at 7q11.23 showed one of the chromosomes 7 to be deleted for the elastin gene for this Williams syndrome subject. |
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Cytogenetics |
Chromosome 7: DELETION Aneuploid Segment (-)7q11>7q11 |
Remarks |
Failure to thrive; vomiting; colic; constipation; short attention span; visuo-spatial problems; epicanthal folds; abnormal gait; soft/velvety skin; perfect pitch; preoccupation with spinning; motor and language delay |
Caballero M, Ge T, Rebelo AR, Seo S, Kim S, Brooks K, Zuccaro M, Kanagaraj R, Vershkov D, Kim D, Smogorzewska A, Smolka M, Benvenisty N, West SC, Egli D, Mace EM, Koren A, Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role for MCM10 in replication timing regulation Human molecular genetics: 2021 |
PubMed ID: 35394024 |
|
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
PubMed ID: 23665875 |
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