MAMMALIAN PHENOTYPE - ANNOTATIONS
The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.
Term: abnormal glial cell morphology
Accession: MP:0003634
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Definition: any structural anomaly of non-neuronal cells of the nervous system that form the myelin insulation of nervous pathways, guide neuronal migration during development, and exchange metabolites with neurons
Synonyms: exact_synonym: abnormal glia morphology; abnormal neuroglia morphology
narrow_synonym: glial cell dysplasia
G
Cryba1
crystallin, beta A1
IMP
RGD
PMID:17931883
RGD:2303652
NCBI chr10:62,608,373...62,614,726
G
Cryba1Nuc1Dbsa
crystallin, beta A1;Nuc1 mutant, Dbsa
IMP
RGD
PMID:17931883
RGD:2303652
G
Atm
ATM serine/threonine kinase
IMP
DNA:deletion:exon:
RGD
PMID:28007901
RGD:12879399
NCBI chr 8:62,724,939...62,829,040
G
Atmem1Kyo
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo
IMP
RGD
PMID:28007901
RGD:12879399
G
Crb1
crumbs cell polarity complex component 1
IAGP
RGD
PMID:25878282
RGD:13451131
NCBI chr13:53,352,932...53,540,019
G
Crb1m1
crumbs 1, cell polarity complex component, mutant 1
IAGP
RGD
PMID:25878282
RGD:13451131
G
Bckdk
branched chain ketoacid dehydrogenase kinase
IAGP
DNA:missense mutation:cds:G369E (rat)
RGD
PMID:27472223
RGD:39131293
NCBI chr 1:191,945,809...191,950,480
G
Ercc6
ERCC excision repair 6, chromatin remodeling factor
IMP
RGD
PMID:31644904
RGD:126925983
NCBI chr16:7,771,311...7,841,895
G
Ercc6em1Cgen
ERCC excision repair 6, chromatin remodeling factor; CRISPR/Cas9 induced mutant 1, Cgen
IMP
RGD
PMID:31644904
RGD:126925983
G
Slc9a6
solute carrier family 9 member A6
IMP
RGD
PMID:34928329
RGD:151664747
NCBI chr X:139,468,045...139,524,111
G
Slc9a6 em1Moro
solute carrier family 9 member A6;CRISPR/Cas9 induced mutant1, Moro
IMP
RGD
PMID:34928329
RGD:151664747
G
Zeb2
zinc finger E-box binding homeobox 2
IMP
RGD
PMID:34852714
RGD:155882542
NCBI chr 3:29,214,581...29,344,890
G
Atm
ATM serine/threonine kinase
IMP
RGD
PMID:28007901
RGD:12879399
NCBI chr 8:62,724,939...62,829,040
G
Atmem1Kyo
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo
IMP
RGD
PMID:28007901
RGD:12879399
G
Csf1r
colony stimulating factor 1 receptor
IMP
RGD
PMID:30249809 PMID:33450391
RGD:41404725 , RGD:126781687
NCBI chr18:56,834,152...56,860,804
G
Csf1rtm(EGFP)Tset
colony stimulating factor 1 receptor; target mutant, Tset
IMP
RGD
PMID:33450391 PMID:30249809
RGD:126781687 , RGD:41404725
G
Cyfip1
cytoplasmic FMR1 interacting protein 1
IMP
RGD
PMID:31371763
RGD:14981598
NCBI chr 1:115,842,754...115,935,163
G
Cyfip1em1Sage
cytoplasmic FMR1 interacting protein 1; CRISPR/Cas9 induced mutant 1, Sage
IMP
RGD
PMID:31371763
RGD:14981598
G
Zeb2
zinc finger E-box binding homeobox 2
IMP
RGD
PMID:34852714
RGD:155882542
NCBI chr 3:29,214,581...29,344,890
G
Atm
ATM serine/threonine kinase
IMP
RGD
PMID:28007901
RGD:12879399
NCBI chr 8:62,724,939...62,829,040
G
Atmem1Kyo
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo
IMP
RGD
PMID:28007901
RGD:12879399
G
Slc9a6
solute carrier family 9 member A6
IMP
RGD
PMID:34928329
RGD:151664747
NCBI chr X:139,468,045...139,524,111
G
Slc9a6 em1Moro
solute carrier family 9 member A6;CRISPR/Cas9 induced mutant1, Moro
IMP
RGD
PMID:34928329
RGD:151664747
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