nsdhl Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (149)

Interactants (14)

XB-GENEPAGE-1004922

Gene Symbol: nsdhl Gene Name: NAD(P) dependent steroid dehydrogenase-like

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: nsdhl assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (74 sources): Abnormal cardiac septum morphology, Abnormal cardiovascular system morphology, Abnormal cerebral cortex morphology, Abnormal cortical bone morphology, Abnormal digit morphology, Abnormality of the nail, Adrenal hypoplasia, Aggressive behavior, Almond-shaped palpebral fissure, Aplasia/Hypoplasia involving the central nervous system, Aplasia/hypoplasia of the extremities, Arachnodactyly, Asthenia, Behavioral abnormality, Cleft upper lip, Congenital hip dislocation, Congenital ichthyosiform erythroderma, Delayed speech and language development, Dental crowding, Dysphasia, Elevated 8(9)-cholestenol, Elevated 8-dehydrocholesterol, Epicanthus, Epiphyseal stippling, Erythema, Flexion contracture, Generalized hypotonia, Global developmental delay, Hearing impairment, High palate, Hydronephrosis, Hyperactivity, Hyperkeratosis, Hyperlordosis, Hypoplastic pelvis, Hypoplastic scapulae, Intellectual disability, Intellectual disability, mild, Irritability, Joint hypermobility, Kyphoscoliosis, Kyphosis, Long face, Long toe, Lumbar hyperlordosis, Malar flattening, Microcephaly, Micrognathia, Microretrognathia, Mild intrauterine growth retardation, Narrow face, Pachygyria, Parakeratosis, Polymicrogyria, Posteriorly rotated ears, Prominent nasal bridge, Pulmonary hypoplasia, Renal agenesis, Renal hypoplasia/aplasia, Retrognathia, Scoliosis, Seizure, Short clavicles, Short ribs, Short stature, Single ventricle, Sleep disturbance, Slender build, Strabismus, Thyroid hypoplasia, Umbilical hernia, Upslanted palpebral fissure, Vertebral hypoplasia, obsolete Hypotrichosis [+]
Mouse (41 sources): abnormal Bergmann glial cell morphology, abnormal Purkinje cell dendrite morphology, abnormal auchene hair morphology, abnormal cerebellar granule cell morphology, abnormal cerebral cortex morphology, abnormal dentate gyrus morphology, abnormal guard hair morphology, abnormal hippocampus granule cell morphology, abnormal hippocampus neuron morphology, abnormal limb morphology, abnormal maternal nurturing, abnormal neurite morphology, abnormal neuronal stem cell physiology, abnormal placenta labyrinth morphology, abnormal skin condition, abnormal tail morphology, abnormal vertebral column morphology, abnormal vitelline vascular remodeling, decreased body size, decreased cerebellar granule cell number, decreased embryo size, disheveled coat, disorganized placental labyrinth, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, focal hair loss, irregular coat pigmentation, kinked tail, pale yolk sac, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance, premature death, premature endochondral bone ossification, prenatal lethality, prenatal lethality, complete penetrance, short hair, short tail, small cerebellum, small hippocampus, thin external granule cell layer, thin placenta labyrinth [+]
View all ortholog results at Monarch