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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nmnat2
nicotinamide nucleotide adenylyltransferase 2
MGI:2444155
34 phenotypes from 5 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nmnat2em1(IMPC)Mbp/Nmnat2em1(IMPC)Mbp
C57BL/6N-Nmnat2em1(IMPC)Mbp/Ucd
preweaning lethality, complete penetrance J:211773
Nmnat2Gt(EUCE0262a08)1.1Hmgu/Nmnat2+
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL
axon degeneration J:200901
Nmnat2Gt(EUCE0262a08)1.1Hmgu/Nmnat2Gt(EUCE0262a08)1.1Hmgu
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL
axon degeneration J:200901
Nmnat2Gt(EUCE0262a08)Hmgu/Nmnat2Gt(EUCE0262a08)Hmgu
involves: 129P2/OlaHsd * C57BL/6J
abnormal axon extension J:200901
abnormal diaphragm development J:200901
abnormal innervation J:200901
abnormal nervous system tract morphology J:200901
abnormal neurite morphology J:200901
abnormal olfactory bulb outer nerve layer morphology J:200901
abnormal optic nerve innervation J:200901
abnormal voluntary movement J:200901
absent optic tract J:200901
anuria J:200901
atelectasis J:192196
decreased corticospinal tract size J:200901
decreased muscle weight J:200901
decreased skeletal muscle mass J:192196
distended urinary bladder J:192196, J:200901
dorsal root ganglion degeneration J:200901
hunched posture J:192196, J:200901
neonatal lethality, complete penetrance J:192196, J:200901
paralysis J:192196
respiratory failure J:192196, J:200901
Nmnat2Gt(EUCE0262a08)Hmgu/Nmnat2Gt(RRF238)Byg
involves: 129P2/OlaHsd * C57BL/6J
no abnormal phenotype detected J:200901
Nmnat2Tn(sb-Tyr)2172.P9KK4BOve/Nmnat2Tn(sb-Tyr)2172.P9KK4BOve
involves: FVB/N
abnormal diaphragm development J:192196
abnormal facial motor nucleus morphology J:192196
abnormal kidney development J:192196
abnormal neuron morphology J:192196
abnormal urethra morphology J:192196
atelectasis J:192196
axon degeneration J:192196
decreased fetal weight J:192196
decreased motor neuron number J:192196
decreased sensory neuron number J:192196
decreased skeletal muscle mass J:192196
distended abdomen J:192196
distended urinary bladder J:192196
hunched posture J:192196
neonatal lethality, complete penetrance J:192196
paralysis J:192196
peripheral nervous system degeneration J:192196
respiratory failure J:192196
small dorsal root ganglion J:192196
ureteral reflux J:192196

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
03/24/2020
MGI 6.15
The Jackson Laboratory