sall1 Phenotypes

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Phenotypes

Gene Literature (42)

Nucleotides (313)

Interactants (490)

XB-GENEPAGE-491392

Gene Symbol: sall1 Gene Name: spalt-like transcription factor 1

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: sall1 assayed (9 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (91 sources): 2-3 toe syndactyly, 2-4 finger cutaneous syndactyly, 3-4 finger osseus syndactyly, 3-4 toe syndactyly, Abnormal cardiac septum morphology, Abnormal cardiovascular system morphology, Abnormal foot morphology, Abnormality of the kidney, Abnormality of the uterus, Abnormality of vision, Abnormal pulmonary valve morphology, Abnormal rib morphology, Abnormal tragus morphology, Abnormal vagina morphology, Abnormal vertebral morphology, Agenesis of corpus callosum, Anal atresia, Anal stenosis, Anteriorly placed anus, Aplasia/Hypoplasia of the 3rd toe, Atrial septal defect, Bifid scrotum, Bifid uterus, Blepharophimosis, Bowel incontinence, Broad hallux phalanx, Broad thumb, Cataract, Chiari malformation, Chorioretinal coloboma, Clinodactyly of the 5th finger, Clinodactyly of the 5th toe, Constipation, Cranial nerve paralysis, Cryptorchidism, Delayed puberty, Duane anomaly, Duodenal atresia, Ectopic kidney, Facial asymmetry, Failure to thrive, Finger aplasia, Gastroesophageal reflux, Global developmental delay, Hearing impairment, Hypoplasia of penis, Hypospadias, Hypothyroidism, Intellectual disability, Iris coloboma, Limbal dermoid, Lower limb asymmetry, Macrotia, Metatarsal synostosis, Microcephaly, Microphthalmia, Microtia, Multicystic kidney dysplasia, Multiple renal cysts, obsolete External ear malformation, Overfolded helix, Overfolding of the superior helices, Partial duplication of thumb phalanx, Patent ductus arteriosus, Pes planus, Preauricular pit, Preauricular skin tag, Preaxial hand polydactyly, Pseudoepiphyses of second metacarpal, Rectoperineal fistula, Rectovaginal fistula, Renal dysplasia, Renal hypoplasia, Renal insufficiency, Satyr ear, Sensorineural hearing impairment, Short metatarsal, Short stature, Stahl ear, Strabismus, Subcutaneous nodule, Tetralogy of Fallot, Toe clinodactyly, Toe syndactyly, Triphalangeal thumb, Ulnar deviation of finger, Umbilical hernia, Urethral valve, Ventricular septal defect, Vesicoureteral reflux, Wide mouth [+]
Mouse (28 sources): abnormal digit development, abnormal kidney development, abnormal kidney mesenchyme morphology, abnormal kidney morphology, abnormal metanephric mesenchyme morphology, abnormal proximal convoluted tubule morphology, abnormal renal tubule morphology, abnormal suckling behavior, abnormal ureteric bud invasion, absent triquetrum, absent ureter, conductive hearing loss, deafness, dilated renal tubules, embryonic lethality during organogenesis, incomplete penetrance, impaired branching involved in ureteric bud morphogenesis, increased metanephric mesenchyme apoptosis, increased or absent threshold for auditory brainstem response, limbs/digits/tail phenotype, metacarpal bone hypoplasia, neonatal lethality, complete penetrance, no abnormal phenotype detected, perinatal lethality, incomplete penetrance, premature death, prenatal lethality, complete penetrance, renal glomerulus atrophy, small kidney, triphalangia [+]
View all ortholog results at Monarch