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:5752257
Description: Allele Detail: Spontaneous This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Spontaneous This is a legacy resource.
Phenotype: increased or absent threshold for auditory brainstem response, hippocampal neuron degeneration, deafness, lethality at weaning, complete penetrance, axonal dystrophy, abnormal hair cycle, neuron degeneration, abnormal cochlear ganglion morphology, weakness, abnormal intestinal mucosa morphology, thymus atrophy, decreased body weight, cachexia, preweaning lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, abnormal stomach wall morphology
Affected Gene: Ctsd
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:', '') }})
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 Ctsdm1J/Ctsdm1J.
No alerts have been found for Ctsdm1J/Ctsdm1J.
Source: MGI
Source Database: MGI, Mouse Genome Informatics MGI