|
Symbol Name ID |
Naa10
N(alpha)-acetyltransferase 10, NatA catalytic subunit MGI:1915255 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Micrognathia |
Microretrognathia |
Small sella turcica |
Microcephaly |
Prominent metopic ridge |
Delayed cranial suture closure |
Wide anterior fontanel |
Large posterior fontanelle |
Short neck |
Clinodactyly of the 5th finger |
Camptodactyly of finger |
Complete duplication of thumb phalanx |
Prominent fingertip pads |
Radial deviation of finger |
Long fingers |
Broad hallux |
Sandal gap |
Clinodactyly |
Syndactyly |
Finger syndactyly |
Metatarsus valgus |
Congenital hip dislocation |
Joint contracture of the hand |
Camptodactyly |
Delayed skeletal maturation |
Abnormal shoulder morphology |
Down-sloping shoulders |
Abnormal clavicle morphology |
Short clavicles |
Long thorax |
Pectus excavatum |
Narrow chest |
Hyperlordosis |
Lumbar hyperlordosis |
Kyphosis |
Kyphoscoliosis |
Scoliosis |
| Disease(s) Associated with NAA10 | ||||||||||||||||||||||||||||||||||||||
| Ogden syndrome | ||||||||||||||||||||||||||||||||||||||
| syndromic microphthalmia 1 |
| Mouse Phenotypes | enhanced osteoblast differentiation |
impaired osteoblast differentiation |
abnormal osteoblast physiology |
abnormal neurocranium morphology |
abnormal fontanelle morphology |
small neurocranium |
thick neurocranium |
thin neurocranium |
abnormal femur morphology |
decreased bone mineral density |
increased bone mineral density |
decreased bone volume |
increased bone volume |
abnormal skeleton development |
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| Availability | Mouse Genotype | ||||||||||||||
| Naa10tm1Jprk/Naa10tm1Jprk | |||||||||||||||
| Tg(CAG-Naa10)10Jprk/0 | |||||||||||||||
| Tg(CAG-Naa10)15Jprk/0 | |||||||||||||||
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 04/30/2024 MGI 6.23 |
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