Stock B6;129P2-Grm1<tm1Dgen>/H

FESA Number

1908

Strain Name

B6;129P2-Grm1<tm1Dgen>/H

Mutation Strain Type

Attribution

Institution name Depositor / Originator Name
Deltagen Originator Retained
Deltagen Depositor Retained

Phenotypic Description

No visible phenotype.

Orphanet Disorders

OrphaNet ID Name Url
324 262 Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=324262

Publications

Orphanet Categories

Inborn errors of metabolism
Rare neurologic disease

EMMA ID

EM:02357

Background Strain Name

C57BL/6J

Background Strain MGI ID

MGI:3028467

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