nin Phenotypes

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Phenotypes

Gene Literature (7)

Nucleotides (184)

Interactants (151)

XB-GENEPAGE-954250

Gene Symbol: nin Gene Name: ninein

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (28 sources): Abnormal carpal morphology, Bilateral breast hypoplasia, Central hypothyroidism, Clinodactyly, Clinodactyly of the 5th finger, Delayed skeletal maturation, Disproportionate short-limb short stature, Global developmental delay, Hip dysplasia, Hypoplasia of the uterus, Hypotelorism, Intellectual disability, severe, Intrauterine growth retardation, Lumbar scoliosis, Madelung deformity, Microcephaly, Microtia, Obesity, Primary amenorrhea, Prominent nose, Seizure, Severe global developmental delay, Severe intrauterine growth retardation, Severe postnatal growth retardation, Severe short stature, Short middle phalanx of the 5th finger, Short stature, Subglottic stenosis [+]
Mouse (24 sources): abnormal corneocyte morphology, abnormal epidermal lamellar body morphology, abnormal exploration in a new environment, abnormal keratinocyte morphology, abnormal mitotic spindle morphology, abnormal skin development, abnormal startle reflex, cardiovascular system phenotype, decreased anxiety-related response, decreased keratohyalin granule number, decreased keratohyalin granule size, decreased prepulse inhibition, decreased startle reflex, delayed skin barrier formation, impaired skin barrier function, improved glucose tolerance, increased exploration in new environment, increased mean corpuscular hemoglobin, postnatal lethality, incomplete penetrance, prenatal lethality, incomplete penetrance, thin epidermis, thin epidermis stratum basale, thin epidermis stratum granulosum, thin epidermis stratum spinosum [+]
View all ortholog results at Monarch