ripk4 Phenotypes

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Phenotypes

Gene Literature (3)

Nucleotides (183)

Interactants (362)

XB-GENEPAGE-494473

Gene Symbol: ripk4 Gene Name: receptor interacting serine/threonine kinase 4

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: ripk4 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (64 sources): Abnormal cardiovascular system morphology, Abnormal oral frenulum morphology, Absent eyebrow, Absent eyelashes, Absent thumb, Agenesis of maxillary incisor, Agenesis of permanent teeth, Alopecia totalis, Ambiguous genitalia, Anal stenosis, Ankyloblepharon, Anonychia, Aplasia/Hypoplasia of the distal phalanges of the toes, Aplasia/Hypoplasia of the eyebrow, Ataxia, Atelectasis, Axillary pterygium, Bifid tongue, Bilateral cryptorchidism, Cleft palate, Cleft upper lip, Commissural lip pit, Corneal opacity, Cupped ear, Curly hair, Depressed nasal bridge, Dry skin, Eyelid coloboma, Finger syndactyly, Hydroureter, Hypertelorism, Hypohidrosis, Hypoplasia of the maxilla, Hypoplastic labia majora, Hypoplastic male external genitalia, Hypoplastic scapulae, Hypoplastic toenails, Imperforate hymen, Inferiorly positioned umbilicus, Intellectual disability, Intrauterine growth retardation, Low-set ears, Median cleft upper lip, Microcephaly, Micrognathia, Microphthalmia, Nail dysplasia, Narrow mouth, Opacification of the corneal stroma, Popliteal pterygium, Renal hypoplasia/aplasia, Short fifth metatarsal, Short nose, Short phalanx of finger, Skin tags, Small nail, Sparse or absent eyelashes, Syndactyly, Synostosis of joints, Talipes equinovarus, Tessier cleft, Toe syndactyly, Underdeveloped nasal alae, Wide intermamillary distance [+]
Mouse (17 sources): abnormal epidermis suprabasal layer morphology, abnormal hindlimb morphology, abnormal keratinocyte differentiation, abnormal skin appearance, abnormal tail morphology, abnormal vibrissa morphology, absent epidermis stratum corneum, absent vibrissae, craniofacial phenotype, epidermal hyperplasia, hematopoietic system phenotype, immune system phenotype, interdigital webbing, oral atresia, perinatal lethality, complete penetrance, short tail, thick skin [+]
View all ortholog results at Monarch