bltp1 Phenotypes

Phenotypes

XB-GENEPAGE-5902542

Gene Symbol: bltp1 Gene Name: bridge-like lipid transfer protein family member 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: bltp1 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (48 sources): Abnormal foot morphology, Abnormality of eye movement, Absent speech, Adducted thumb, Anteverted nares, Aplasia/Hypoplasia of the corpus callosum, Arthrogryposis multiplex congenita, Behavioral abnormality, Camptodactyly, Cataract, Cerebellar dysplasia, Cerebellar hypoplasia, Clinodactyly, Cutaneous syndactyly, Cystic hygroma, Depressed nasal bridge, Eczematoid dermatitis, Edema, Generalized hypotonia, Global developmental delay, Gray matter heterotopia, Hand clenching, High palate, Hydrocephalus, Hypermetropia, Hypertelorism, Hypoplasia of the brainstem, Hypotelorism, Intellectual disability, Kinked brainstem, Lissencephaly, Low-set ears, Macrocephaly, Micropenis, Oculomotor apraxia, Overlapping fingers, Overlapping toe, Pericardial effusion, Plagiocephaly, Posteriorly rotated ears, Seizure, Short nose, Small scrotum, Strabismus, Talipes equinovarus, Upslanted palpebral fissure, Ventriculomegaly, Webbed neck [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (48 sources): Abnormal foot morphology, Abnormality of eye movement, Absent speech, Adducted thumb, Anteverted nares, Aplasia/Hypoplasia of the corpus callosum, Arthrogryposis multiplex congenita, Behavioral abnormality, Camptodactyly, Cataract, [+]