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 blood cell physiology
Accession: MP:0012382
browse the term
Definition: aberrant measurable or observable characteristic related to the function of or processes in any of the cells found in the blood
G
Atm
ATM serine/threonine kinase
IMP
RGD
PMID:28007901
RGD:12879399
NCBI chr 8:53,828,741...53,932,773
Ensembl chr 8:53,831,093...53,932,437
G
Atmem1Kyo
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo
IMP
RGD
PMID:28007901
RGD:12879399
G
Gla
galactosidase, alpha
IMP
RGD
PMID:34320241
RGD:401976418
NCBI chr X:97,769,227...97,780,646
Ensembl chr X:97,768,996...97,780,664
G
Gla
galactosidase, alpha
IMP
RGD
PMID:34320241
RGD:401976418
NCBI chr X:97,769,227...97,780,646
Ensembl chr X:97,768,996...97,780,664
G
Ighm
immunoglobulin heavy constant epsilon
IMP
RGD
PMID:21038471
RGD:150523760
Ensembl chr 6:132,329,269...133,053,426
G
Ighmem1Ang
immunoglobulin heavy constant mu; ZFN induced mutant1, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighmem2Ang
immunoglobulin heavy constant mu; ZFN induced mutant2, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighm
immunoglobulin heavy constant epsilon
IMP
RGD
PMID:21038471
RGD:150523760
Ensembl chr 6:132,329,269...133,053,426
G
Ighmem1Ang
immunoglobulin heavy constant mu; ZFN induced mutant1, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighmem2Ang
immunoglobulin heavy constant mu; ZFN induced mutant2, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighm
immunoglobulin heavy constant epsilon
IMP
RGD
PMID:21038471
RGD:150523760
Ensembl chr 6:132,329,269...133,053,426
G
Ighmem1Ang
immunoglobulin heavy constant mu; ZFN induced mutant1, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighmem2Ang
immunoglobulin heavy constant mu; ZFN induced mutant2, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighm
immunoglobulin heavy constant epsilon
IMP
RGD
PMID:21038471
RGD:150523760
Ensembl chr 6:132,329,269...133,053,426
G
Ighmem1Ang
immunoglobulin heavy constant mu; ZFN induced mutant1, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Ighmem2Ang
immunoglobulin heavy constant mu; ZFN induced mutant2, Ang
IMP
RGD
PMID:21038471
RGD:150523760
G
Prkdc
protein kinase, DNA-activated, catalytic subunit
IMP
RGD
PMID:22981234
RGD:8696027
NCBI chr11:85,040,790...85,258,357
Ensembl chr11:85,040,792...85,257,952
G
Cd247
Cd247 molecule
IMP
compared to wild-type
RGD
PMID:24343121
RGD:13442481
NCBI chr13:78,043,302...78,118,437
Ensembl chr13:78,043,307...78,122,263
G
Cd247em1Mcwi
Cd247 molecule; zinc finger nuclease induced mutant 1, Medical College of Wisconsin
IMP
RGD
PMID:24343121
RGD:13442481
G
Dpp4
dipeptidylpeptidase 4
IAGP
compared to DA/Ztm
RGD
PMID:19327106
RGD:41408336
NCBI chr 3:46,962,233...47,043,870
Ensembl chr 3:46,962,243...47,043,901
G
Dpp4DPPIV
dipeptidylpeptidase 4; DPPIV mutant
IAGP
compared to DA/Ztm
RGD
PMID:19327106
RGD:41408336
G
Atm
ATM serine/threonine kinase
IMP
DNA:deletion:exon:
RGD
PMID:28007901
RGD:12879399
NCBI chr 8:53,828,741...53,932,773
Ensembl chr 8:53,831,093...53,932,437
G
Atmem1Kyo
ATM serine/threonine kinase; ZFN induced mutant 1, Kyo
IMP
RGD
PMID:28007901
RGD:12879399
G
Pon1
paraoxonase 1
IMP
compared to SD
RGD
PMID:30262871
RGD:45073131
NCBI chr 4:33,294,737...33,325,759
Ensembl chr 4:33,294,722...33,321,360
G
Pon1em1Lizh
paraoxonase 1; CRISPR/Cas9 induced mutant 1, Lizh
IMP
compared to SD
RGD
PMID:30262871
RGD:45073131
G
Themis
thymocyte selection associated
IAGP
DNA:frameshift mutation:
RGD
PMID:22275874
RGD:38599149
NCBI chr 1:16,433,906...16,623,889
Ensembl chr 1:16,432,631...16,664,329
G
Themism1Adej
thymocyte selection associated; mutant1, Adej
IAGP
compared to BN
RGD
PMID:22275874
RGD:38599149
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