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 urination
Accession: MP:0001756
browse the term
Definition: anomaly in the process in which parasympathetic nerves stimulate the bladder wall muscle to contract resulting in the expulsion of urine from the body
Synonyms: exact_synonym: abnormal micturition
related_synonym: abnormal urine voiding
xref: GO:0060073
G
Ahr
aryl hydrocarbon receptor
sexual_dimorphism
IMP
males compared to Hsd:SD
RGD
PMID:23859880
RGD:13204753
NCBI chr 6:52,234,089...52,271,568
Ensembl chr 6:52,234,089...52,271,568
G
Ahrem2Sage
aryl hydrocarbon receptor; ZFN induced mutant2, Sage
sexual_dimorphism
IMP
males compared to Hsd:SD
RGD
PMID:23859880
RGD:13204753
G
Alms1
ALMS1, centrosome and basal body associated protein
induces
IMP
RGD
PMID:30385718
RGD:151361229
NCBI chr 4:118,125,581...118,226,005
Ensembl chr 4:118,125,607...118,226,005
G
Alms1em1Mcwi
Alstrom syndrome 1 homolog (human); zinc finger nuclease induced mutant 1, Medical College of Wisconsin
induces
IMP
RGD
PMID:30385718
RGD:151361229
G
Gla
galactosidase, alpha
IMP
compared to Wild type males
RGD
PMID:29979634
RGD:401976416
NCBI chr X:97,769,227...97,780,646
Ensembl chr X:97,768,996...97,780,664
G
Glaem2Mcwi
galactosidase, alpha; CRISPR/Cas9 system induced mutant 2, Medical College of Wisconsin
IMP
compared to Wild type males
RGD
PMID:29979634
RGD:401976416
G
Lepr
leptin receptor
IAGP
DNA:mutations:cds: : (rat)
RGD
PMID:10901178
RGD:401965414
NCBI chr 5:116,294,409...116,477,904
Ensembl chr 5:116,289,823...116,475,908
G
Ren
renin
IMP
compared to wild type
RGD
PMID:21242461
RGD:7771614
NCBI chr13:44,796,260...44,807,491
Ensembl chr13:44,796,091...44,807,489
G
Renem1Mcwi
renin; zinc finger nuclease induced mutant 1, Medical College of Wisconsin
IMP
compared to wild type
RGD
PMID:21242461
RGD:7771614
G
Trpc6
transient receptor potential cation channel, subfamily C, member 6
induces
IMP
compared to vehicle-treated wild type and control
RGD
PMID:29923767
RGD:149735534
NCBI chr 8:5,759,387...5,864,000
Ensembl chr 8:5,758,935...5,828,092
G
Trpc6em1Mcwi
transient receptor potential cation channel, subfamily C, member 6; CRISPR/Cas9 induced mutant 1, Medical College of Wisconsin
induces
IMP
compared to vehicle-treated wild type and control
RGD
PMID:29923767
RGD:149735534
G
Avp
arginine vasopressin
IAGP
RGD
PMID:10919858
RGD:2314654
NCBI chr 3:117,793,447...117,805,091
Ensembl chr 3:117,793,457...117,795,425
G
Avpdi
arginine vasopressin; diabetes insipidus mutant
IAGP
RGD
PMID:10919858
RGD:2314654
G
Col4a5
collagen type IV alpha 5 chain
IMP
RGD
PMID:34675305
RGD:329845598
NCBI chr X:105,118,762...105,322,699
Ensembl chr X:105,118,820...105,322,692
G
Col4a5em1Matsu
collagen type IV alpha 5 chain; CRISPR/Cas9 induced mutant 1, Matsu
IMP
RGD
PMID:34675305
RGD:329845598
G
Ctns
cystinosin, lysosomal cystine transporter
IMP
RGD
PMID:35695380
RGD:155630629
NCBI chr10:57,801,551...57,817,213
Ensembl chr10:57,801,456...57,817,120
G
Mc4r
melanocortin 4 receptor
IMP
RGD
PMID:24400148
RGD:13825242
NCBI chr18:60,419,832...60,421,719
Ensembl chr18:60,419,832...60,421,719
G
Mc4rm1Hubr
melanocortin 4 receptor; ENU induced mutation 1, Hubr
IMP
RGD
PMID:24400148
RGD:13825242
Term paths to the root one shortest all shortest one longest all longest one shortest and longest all