Stock B6.129S1-Gnas<tm2Kel>/H
FESA Number
1944
Strain Name
B6.129S1-Gnas<tm2Kel>/H
Mutation Strain Type
| Mutation Type | Mutation Subtype | Strain Type |
|---|---|---|
| IMSR - Targeted mutation | IMSR - unclassified |
Attribution
| Institution name | Depositor / Originator | Name |
|---|---|---|
| Babraham Institute | Originator | Retained |
| Babraham Institute | Depositor | Retained |
Gene/Allele Information
| Allele Name | Allele MGI ID | Gene Name | Gene MGI ID | Chromosome |
|---|---|---|---|---|
| Gnas<tm2Kel> | MGI:3579575 | Gnas | MGI:95777 | 2 |
Phenotypic Description
There is a behavioural phenotype, response to novel environments as measured through activity in various tasks.
Orphanet Disorders
| OrphaNet ID | Name | Url |
|---|---|---|
| 562 | McCune-Albright syndrome | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=562 |
| 2 762 | Progressive osseous heteroplasia | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2762 |
| 57 782 | Mazabraud syndrome | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=57782 |
| 93 276 | Polyostotic fibrous dysplasia | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=93276 |
| 93 277 | Monostotic fibrous dysplasia | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=93277 |
| 79 445 | Pseudopseudohypoparathyroidism | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=79445 |
| 79 444 | Pseudohypoparathyroidism type 1C | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=79444 |
| 79 443 | Pseudohypoparathyroidism type 1A | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=79443 |
| 94 089 | Pseudohypoparathyroidism type 1B | http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=94089 |
Publications
Displaying 1 - 1 of 1 Stock Publications
| Pubmed ID | Authors | Title | Journal |
|---|---|---|---|
| 15798190 | Plagge A | Imprinted Nesp55 influences behavioral reactivity to novel environments. | Mol Cell Biol (2 005) 25:3019-26 |
Orphanet Categories
Rare developmental defect during embryogenesis
Rare skin disease
Rare endocrine disease
Rare bone disease
Rare oncologic disease
Rare gynecologic or obstetric disease
Rare renal disease
Rare eye disease
EMMA ID
EM:02392
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