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Arhgap6/Hccs/Mid1tm1Hzo
Targeted Allele Detail
Nomenclature
Symbol: Arhgap6/Hccs/Mid1tm1Hzo
Name: holocytochrome c synthetase; targeted mutation 1, Huda Y Zoghbi
MGI ID: MGI:3580072
Synonyms: MLS2loxP
Gene: Hccs  Location: ChrX:169250193-169320372 bp, - strand  Genetic Position: ChrX, 78.98 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:80528
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S7/SvEvBrd
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Hccs Mutation:  1 strain or line available
References
Original:  J:80528 Prakash SK, et al., Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant micro-phthalmia with linear skin defects (MLS) syndrome. Hum Mol Genet. 2002 Dec 1;11(25):3237-48
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/19/2014
MGI 5.19
The Jackson Laboratory