alx4 Phenotypes

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Phenotypes

Gene Literature (8)

Nucleotides (29)

Interactants (82)

XB-GENEPAGE-853002

Gene Symbol: alx4 Gene Name: ALX homeobox 4

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (50 sources): Abnormality of the dentition, Agenesis of cerebellar vermis, Agenesis of corpus callosum, Anteverted nares, Aplasia cutis congenita of scalp, Bifid nasal tip, Bifid nose, Brachycephaly, Broad columella, Broad philtrum, Calvarial skull defect, Cerebellar vermis hypoplasia, Conical tooth, Coronal craniosynostosis, Craniosynostosis, Cryptorchidism, Decreased lacrimation, Depressed nasal bridge, Depressed nasal ridge, Encephalocele, Fine hair, Frontal bossing, Hirsutism, Hypertelorism, Hypogonadism, Hypohidrosis, Hypoplasia of the corpus callosum, Intellectual disability, Intellectual disability, mild, Intellectual disability, moderate, Intrauterine growth retardation, Low-set ears, Microcephaly, Microphthalmia, Nystagmus, Oligohydramnios, Parietal foramina, Scrotal hypoplasia, Short palpebral fissure, Sparse and thin eyebrow, Sparse eyelashes, Sparse hair, Strabismus, Symmetrical, oval parietal bone defects, Telecanthus, Underdeveloped nasal alae, Upslanted palpebral fissure, Wide nasal bridge, Wide nasal ridge, obsolete Hypotrichosis [+]
Mouse (15 sources): abnormal abdominal wall morphology, abnormal frontal bone morphology, abnormal limb morphology, abnormal neurocranium morphology, abnormal zone of polarizing activity morphology, delayed hair appearance, eyelids open at birth, focal dorsal hair loss, neonatal lethality, incomplete penetrance, no abnormal phenotype detected, perinatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, small parietal bone, small pubis, upturned snout [+]
View all ortholog results at Monarch