dym Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (152)

Interactants (16)

XB-GENEPAGE-5729290

Gene Symbol: dym Gene Name: dymeclin

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: dym assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (80 sources): Abnormal hip bone morphology, Abnormal ilium morphology, Abnormality of epiphysis morphology, Abnormality of the metaphysis, Abnormality of the wrist, Atlantoaxial instability, Attention deficit hyperactivity disorder, Autism, Barrel-shaped chest, Beaking of vertebral bodies, Brachydactyly, Broad foot, Broad palm, Camptodactyly, Carpal bone hypoplasia, Clinodactyly of the 5th finger, Coarse facial features, Cone-shaped epiphyses of the phalanges of the hand, Deformed sella turcica, Delayed femoral head ossification, Disproportionate short stature, Disproportionate short-trunk short stature, Dolichocephaly, Enlargement of the costochondral junction, Failure to thrive, Femoral bowing, Flaring of lower rib cage, Flat acetabular roof, Flat glenoid fossa, Genu valgum, Genu varum, Global developmental delay, Hip dislocation, Hyperlordosis, Hypoplasia of the odontoid process, Hypoplastic acetabulae, Hypoplastic facial bones, Hypoplastic iliac wing, Hypoplastic scapulae, Iliac crest serration, Intellectual disability, Irregular epiphyses, Joint stiffness, Kyphosis, Limitation of joint mobility, Lumbar hyperlordosis, Mandibular prognathia, Metaphyseal irregularity, Metaphyseal widening, Microcephaly, Micromelia, Multicentric femoral head ossification, Multicentric ossification of proximal femoral epiphyses, Multicentric ossification of proximal humeral epiphyses, Narrow greater sciatic notch, Neurological speech impairment, Pectus carinatum, Pes planus, Platyspondyly, Prominent calcaneus, Prominent sternum, Rhizomelic arm shortening, Scoliosis, Severe global developmental delay, Shield chest, Short metacarpal, Short metatarsal, Short neck, Short phalanx of finger, Short thorax, Shoulder dislocation, Skeletal dysplasia, Sloping forehead, Spinal canal stenosis, Talipes equinovarus, Thickened calvaria, Thoracic kyphosis, Tibial bowing, Waddling gait, Wide pubic symphysis [+]
Mouse (29 sources): abnormal body length, abnormal bone mineralization, abnormal cell morphology, abnormal chondrocyte morphology, abnormal circulating cholesterol level, abnormal circulating triglyceride level, abnormal exploration in a new environment, abnormal long bone epiphyseal ossification zone morphology, abnormal long bone epiphyseal plate morphology, abnormal long bone hypertrophic chondrocyte zone, abnormal spine curvature, abnormal vesicle-mediated transport, behavior/neurological phenotype, decreased birth body size, decreased body length, decreased bone mineral content, decreased circulating glucose level, decreased cranium length, decreased prepulse inhibition, decreased width of hypertrophic chondrocyte zone, disorganized long bone epiphyseal plate, increased circulating alanine transaminase level, increased circulating alkaline phosphatase level, increased circulating aspartate transaminase level, increased exploration in new environment, increased grip strength, increased startle reflex, preweaning lethality, incomplete penetrance, small cranium [+]
View all ortholog results at Monarch