Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Atp6v1dtm1b(EUCOMM)Hmgu
Name:	ATPase, H+ transporting, lysosomal V1 subunit D; targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
MGI ID:	MGI:5513749
Gene:	Atp6v1d  Location: Chr12:78889756-78908810 bp, - strand  Genetic Position: Chr12, 35.51 cM
Alliance:	Atp6v1dtm1b(EUCOMM)Hmgu page
IMPC:	Atp6v1d gene page

Mutant Cell Line:	HEPD0526_6_E08
Germline Transmission:	Earliest citation of germline transmission: J:200814
Parent Cell Line:	JM8.N4 (ES Cell)
Strain of Origin:	C57BL/6N
Project Collection:	EUCOMM

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion     Vector: L1L2_Bact_P   Mutation details: Cre excision of MGI:4434885 tm1a allele removes the promoter-driven neo and critical exon(s) leaving behind the lacZ reporter (J:200814)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

2 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Atp6v1d Mutation:	22 strains or lines available

Original:	J:200814 Toronto Centre for Phenogenomics, Strains and alleles submitted by Toronto Centre for Phenogenomics (NorCOMM2, funded by Genome Canada and Ontario Genomics Institute OGI-051). MGI Direct Data Submission. 2013;
All:	3 reference(s)