smarcad1 Phenotypes

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Phenotypes

Gene Literature (3)

Nucleotides (153)

Interactants (48)

XB-GENEPAGE-492699

Gene Symbol: smarcad1 Gene Name: SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (28 sources): Abnormal blistering of the skin, Abnormal dermatoglyphics, Abnormality of the nail, Adermatoglyphia, Amniotic constriction ring, Aplasia/Hypoplasia of the skin, Camptodactyly of finger, Clubbing, Cutaneous syndactyly of toes, Dry skin, Ectodermal dysplasia, Epidermal acanthosis, Flexion contracture, Hyperkeratosis, Hypohidrosis, Lack of skin elasticity, Milia, Neoplasm, Palmar hyperkeratosis, Palmoplantar keratoderma, Sclerodactyly, Single transverse palmar crease, Skin rash, Small nail, Tapered finger, Thickened skin, Thin skin, obsolete Congenital palmoplantar keratodermia [+]
Mouse (26 sources): abnormal anxiety-related response, abnormal digestive system morphology, abnormal embryo size, abnormal fertility/fecundity, abnormal locomotor activation, abnormal spine curvature, abnormal sternocostal joint morphology, abnormal thoracic vertebrae morphology, asymmetric sternocostal joints, cardiac hypertrophy, decreased birth body size, decreased body size, decreased fetal size, decreased litter size, decreased oocyte number, decreased thigmotaxis, immune system phenotype, neonatal lethality, incomplete penetrance, no abnormal phenotype detected, perinatal lethality, incomplete penetrance, postnatal lethality, incomplete penetrance, premature death, preweaning lethality, incomplete penetrance, reduced female fertility, reduced male fertility, small thoracic cage [+]
View all ortholog results at Monarch