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GM10565 LCL from B-Lymphocyte

Description:

KALLMANN SYN; HYPOGONADOTROPIC HYPOGONADISM, ANOSMIA- 147950, 244200, 308700
TRANSLOCATED CHROMOSOME

Affected:

Yes

Sex:

Male

Age:

45 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Chromosome Abnormalities
DGAP
dbGaP
Class Disorders of Steroid Metabolism
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Other
Ethnicity AMERICAN INDIAN/FRENCH
Relation to Proband proband
Confirmation Clinical summary/Case history
ISCN 46,XY,t(7;12)(7pter>7q22::12q24.1> 12qter;12pter>12q24.1::7q22>7qter),inv(9)(pter>p11::q13>p11::q13>qter)
Species Homo sapiens
Common Name Human
Remarks Chippewa/French; delayed sexual development; low 17-ketosteroids & gonadotropin levels; delayed mental development; hypogonadotropic hypogonadism; deficiency of olfaction; skeletal anomalies; 46,XY, t(7;12)(q22;q24.1),inv(9); balanced

Characterizations

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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
 
Cytogenetics Chromosome 12: TRANSLOCATION Breakpoint 12q24 t(7;12)12q24
Chromosome 12: TRANSLOCATION Breakpoint 12q24.1
Chromosome 7: TRANSLOCATION Breakpoint 7q22
Chromosome 7: TRANSLOCATION Breakpoint 7q22 t(7;12)7q22

Phenotypic Data

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Remarks Chippewa/French; delayed sexual development; low 17-ketosteroids & gonadotropin levels; delayed mental development; hypogonadotropic hypogonadism; deficiency of olfaction; skeletal anomalies; 46,XY, t(7;12)(q22;q24.1),inv(9); balanced

Publications

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Stamou M, Ng SY, Brand H, Wang H, Plummer L, Best L, Havlicek S, Hibberd M, Khor CC, Gusella J, Balasubramanian R, Talkowski M, Stanton LW, Crowley WF, A balanced translocation in Kallmann Syndrome implicates a long noncoding RNA, RMST, as a GnRH neuronal regulator The Journal of clinical endocrinology and metabolism: 2019
PubMed ID: 31628846
 
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
 
Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GA, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, Kishikawa S, Korf BR, Kulkarni S, Lally E, Leach NT, Lemyre E, Lewis J, Ligon AH, Lu W, Maas RL, MacDonald ME, Moore SD, Peters RE, Quade BJ, Quintero-Rivera F, Saadi I, Shen Y, Shendure J, Williamson RE, Morton CC, Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project American journal of human genetics82:712-22 2007
PubMed ID: 18319076
 
Best LG, Wasdahl WA, Larson LM, Sturlaugson J, Chromosome abnormality in Kallmann syndrome American journal of medical genetics35:306-9 1990
PubMed ID: 2309777

External Links

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dbSNP dbSNP ID: 21246
Gene Cards KAL1
Gene Ontology GO:0004867 serine-type endopeptidase inhibitor activity
GO:0005201 extracellular matrix structural constituent
GO:0005515 protein binding
GO:0005578 extracellular matrix
GO:0005615 extracellular space
GO:0006928 cell motility
GO:0006935 chemotaxis
GO:0007155 cell adhesion
GO:0007411 axon guidance
NCBI Gene Gene ID:3730
NCBI GTR 147950 HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA; HH2
244200 HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3
308700 HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1
OMIM 147950 HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA; HH2
244200 HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3
308700 HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1
Omim Description HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIA
  KALLMANN SYNDROME 2; KAL2
  HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIA
  KALLMANN SYNDROME 3; KAL3
  ANOSMIC HYPOGONADISMADHESION MOLECULE-LIKE, X-LINKED, INCLUDED; ADMLX, INCLUDED
  ANOSMIN 1, INCLUDED
  DYSPLASIA OLFACTOGENITALIS OF DE MORSIER
  HYPOGONADOTROPIC HYPOGONADISM AND ANOSMIA; HHA
  KALLMANN SYNDROME 1; KAL1
  KALLMANN SYNDROME INTERVAL GENE 1; KALIG1
  KMS

Culture Protocols

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Split Ratio 1:2
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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