dync2h1 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (69)

Interactants (214)

XB-GENEPAGE-5761968

Gene Symbol: dync2h1 Gene Name: dynein, cytoplasmic 2, heavy chain 1

Anatomical Phenotypes Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormal axis elongation (1 source), abnormal bending of tail (1 source), abnormal embryo morphology (1 source), abnormal gastrulation (1 source), abnormal tail morphology (1 source), absent swimming behavior (1 source), decreased length of anterior-posterior axis (1 source), decreased size of the head (1 source)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xtr Wt + dync2h1 MO (2 sources), Xtr Wt + dync2h1 MO (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (87 sources): Abdominal distention, Abnormal cardiovascular system morphology, Abnormal clavicle morphology, Abnormal pelvis bone ossification, Abnormal rib morphology, Abnormal sternum morphology, Abnormality of pelvic girdle bone morphology, Abnormality of retinal pigmentation, Abnormality of the liver, Abnormality of the metaphysis, Absent or minimally ossified vertebral bodies, Acetabular spurs, Agenesis of corpus callosum, Ambiguous genitalia, Anal atresia, Aplasia/Hypoplasia of the lungs, Bifid epiglottis, Bifid tongue, Brachydactyly, Cataract, Cerebellar cyst, Cerebellar hypoplasia, Cleft palate, Cleft upper lip, Cone-shaped epiphysis, Congenital hepatic fibrosis, Cryptorchidism, Dandy-Walker malformation, Depressed nasal bridge, Disproportionate short-limb short stature, Ectopic anus, Enlarged kidney, Epicanthus, Esophageal atresia, Feeding difficulties in infancy, Femoral bowing, Fibular hypoplasia, Frontal bossing, Hamartoma of tongue, Horizontal ribs, Hydronephrosis, Hydrops fetalis, Hypoplasia of penis, Hypoplasia of the ulna, Intestinal malrotation, Lateral clavicle hook, Lethal skeletal dysplasia, Long philtrum, Macrocephaly, Metaphyseal spurs, Metaphyseal widening, Micrognathia, Micromelia, Micropenis, Narrow chest, Nephronophthisis, Nephropathy, Omphalocele, Polycystic kidney dysplasia, Postaxial foot polydactyly, Postaxial hand polydactyly, Postaxial polydactyly, Preaxial hand polydactyly, Preaxial polydactyly, Pulmonary hypoplasia, Renal cyst, Renal dysplasia, Renal hypoplasia, Renal insufficiency, Respiratory insufficiency, Rudimentary to absent tibiae, Scoliosis, Short foot, Short long bone, Short palm, Short ribs, Short stature, Short thorax, Skeletal dysplasia, Talipes equinovarus, Tessier cleft, Thoracic hypoplasia, Toe syndactyly, Urethrovaginal fistula, Uterus didelphys, Ventriculomegaly, Wide nose [+]
Mouse (13 sources): abnormal cell morphology, abnormal cerebral cortex morphology, abnormal coronary vessel morphology, abnormal craniofacial morphology, abnormal direction of heart looping, abnormal forebrain development, abnormal left-right axis patterning, abnormal lung lobe morphology, aorta pulmonary collateral arteries, duplex kidney, embryo phenotype, embryonic lethality during organogenesis, complete penetrance, preweaning lethality, complete penetrance [+]
View all ortholog results at Monarch