mesp2 Phenotypes

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Phenotypes

Gene Literature (8)

Nucleotides (22)

Interactants (114)

XB-GENEPAGE-6467361

Gene Symbol: mesp2 Gene Name: mesoderm posterior bHLH transcription factor 2

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: mesp2 assayed (7 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (42 sources): Abnormal cardiovascular system morphology, Abnormal form of the vertebral bodies, Abnormal intervertebral disk morphology, Abnormal morphology of female internal genitalia, Abnormal rib morphology, Abnormality of immune system physiology, Abnormality of the ureter, Anomalous pulmonary venous return, Anteverted nares, Broad forehead, Camptodactyly of finger, Cleft palate, Congenital diaphragmatic hernia, Cryptorchidism, Depressed nasal bridge, Disproportionate short-trunk short stature, Finger syndactyly, Hemivertebrae, Hypospadias, Intellectual disability, Intrauterine growth retardation, Kyphosis, Long philtrum, Low-set, posteriorly rotated ears, Macrocephaly, Meningocele, Microcephaly, Prominent occiput, Recurrent respiratory infections, Respiratory insufficiency, Rib fusion, Rib segmentation abnormalities, Scoliosis, Short neck, Short stature, Short thorax, Spina bifida occulta, Umbilical hernia, Urogenital fistula, Vertebral clefting, Vertebral segmentation defect, obsolete Restrictive deficit on pulmonary function testing [+]
Mouse (38 sources): abnormal axon extension, abnormal cervical vertebrae morphology, abnormal dermomyotome development, abnormal ectoderm development, abnormal endoderm development, abnormal gastrulation, abnormal mesoderm development, abnormal paraxial mesoderm morphology, abnormal primitive streak formation, abnormal rostral-caudal patterning of the somites, abnormal sacral vertebrae morphology, abnormal sclerotome morphology, abnormal somite border morphology, abnormal somite development, abnormal thoracic vertebrae morphology, abnormal vertebrae development, abnormal vertebral lamina morphology, abnormal vertebral transverse process morphology, absent heart, absent intervertebral disk, absent mesoderm, absent paraxial mesoderm, absent somites, decreased body length, decreased body size, decreased embryo size, delayed somite formation, embryonic lethality during organogenesis, complete penetrance, fused dorsal root ganglion, fusion of vertebral arches, incomplete somite formation, integument phenotype, muscle phenotype, neonatal lethality, complete penetrance, no abnormal phenotype detected, short tail, skeleton phenotype, vestigial tail [+]
View all ortholog results at Monarch