Searching the RRID Resource Information Network
Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
The record is no longer available at this source.
Proper Citation: RRID:MGI:2173367
Description: Allele Detail: Targeted This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Targeted This is a legacy resource.
Phenotype: abnormal salivary gland morphology, abnormal mammary placode morphology, submandibular gland hypoplasia, absent submandibular gland, abnormal rectum morphology, absent lungs, absent forelimb, absent hindlimb, absent rectum, abnormal perineum morphology, hypospadia, curly tail, cecal atresia, abnormal membranous labyrinth morphology, abnormal otic capsule morphology, abnormal semicircular canal morphology, small otic vesicle, absent eyelids, absent lungs, small scapula, premature squamoparietal suture closure, domed cranium, impaired branching involved in trachea morphogenesis, absent Rathke's pouch, abnormal Rathke's pouch apoptosis, absent adenohypophysis, absent hindlimb, translucent skin, small otic capsule, decreased skin pigmentation, abnormal pituitary gland development, abnormal lung development, caudal vertebral fusion, abnormal semicircular canal morphology, abnormal pelvic girdle bone morphology, abnormal stomach morphology, abnormal ilium morphology, abnormal epidermis stratum basale morphology, abnormal clavicle morphology, abnormal endolymphatic duct morphology, absent hypodermis muscle layer, inner ear cysts, abnormal ischium morphology, abnormal limb development, absent pubis, absent acromion, abnormal endolymphatic duct morphology, cleft palate, small stomach, thin dermal layer, thin epidermis, thin skin, abnormal Rathke's pouch development, arrest of tooth development, abnormal cecum development, absent forelimb, decreased body size, perinatal lethality, complete penetrance, curly tail, abnormal cochlea morphology, abnormal vestibulocochlear ganglion morphology, abnormal cochlear sensory epithelium morphology, abnormal epidermis stratum basale morphology, abnormal mammary gland bud morphology, absent mammary gland
Affected Gene: Fgfr2
Expand AllWe found {{ ctrl2.mentions.all_count }} mentions in open access literature.
We have not found any literature mentions for this resource.
We are searching literature mentions for this resource.
Most recent articles:
{{ mention._source.dc.creators[0].familyName }} {{ mention._source.dc.creators[0].initials }}, et al. ({{ mention._source.dc.publicationYear }}) {{ mention._source.dc.title }} {{ mention._source.dc.publishers[0].name }}, {{ mention._source.dc.publishers[0].volume }}({{ mention._source.dc.publishers[0].issue }}), {{ mention._source.dc.publishers[0].pagination }}. (PMID:{{ mention._id.replace('PMID:', '') }})
Check
for all resource mentions.
A list of researchers who have used the resource and an author search tool
A list of researchers who have used the resource and an author search tool. This is available for resources that have literature mentions.
No rating or validation information has been found for Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn.
No alerts have been found for Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn.
Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI
