kdm6b Phenotypes

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Phenotypes

Gene Literature (5)

Nucleotides (169)

Interactants (203)

XB-GENEPAGE-6067076

Gene Symbol: kdm6b Gene Name: lysine (K)-specific demethylase 6B

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (31 sources): Abnormal pinna morphology, Abnormality of the dentition, Autistic behavior, Cafe-au-lait spot, Clinodactyly of the 5th finger, Cryptorchidism, Depressed nasal bridge, Dolichocephaly, Epicanthus, Esotropia, Exotropia, Full cheeks, Generalized hypotonia, Global developmental delay, Hemangioma, Hyperactivity, Hypermelanotic macule, Hypoplastic nipples, Joint hypermobility, Macrotia, Mandibular prognathia, Pectus excavatum, Prominent forehead, Round face, Seizure, Speech apraxia, Strabismus, Telecanthus, Thick vermilion border, Wide mouth, Wide nasal bridge [+]
Mouse (25 sources): abnormal cartilage development, abnormal lung development, abnormal osteoblast differentiation, abnormal pre-Botzinger complex morphology, abnormal pre-Botzinger complex physiology, abnormal response to infection, abnormal skeleton development, abnormal spermatogonia morphology, cardiovascular system phenotype, decreased bone mineralization, decreased bone ossification, decreased chondrocyte proliferation, decreased fetal size, decreased fetal weight, decreased width of hypertrophic chondrocyte zone, delayed chondrocyte differentiation, delayed endochondral bone ossification, enhanced fertility, impaired eosinophil recruitment, increased cell proliferation, neonatal lethality, complete penetrance, postnatal lethality, postnatal lethality, complete penetrance, respiratory system phenotype, thick pulmonary interalveolar septum [+]
View all ortholog results at Monarch