tmem79 Phenotypes

Summary

Expression

Phenotypes

XB-GENEPAGE-6461061

Gene Symbol: tmem79 Gene Name: transmembrane protein 79

Anatomical Phenotypes Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormally open neural tube (2 sources), abnormal anterior-posterior axis, curved dorsal (1 source), abnormal convergent extension involved in axis elongation (1 source), abnormal convergent extension involved in notochord morphogenesis (1 source), abnormal gastrulation (1 source), abnormal head morphology (1 source), abnormal incomplete closing of the blastopore (1 source), abnormal neural plate morphology (1 source), absent cement gland (1 source), absent eye (1 source), decreased length of anterior-posterior axis (1 source), decreased pigmentation in the whole organism (1 source), decreased size of the head (1 source), increased size of the cement gland (1 source), increased size of the epidermis (1 source), increased size of the head (1 source)

Anatomical Phenotypes

Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.

abnormally open neural tube (2 sources), abnormal anterior-posterior axis, curved dorsal (1 source), abnormal convergent extension involved in axis elongation (1 source), abnormal convergent extension involved in notochord morphogenesis (1 source), abnormal gastrulation (1 source), abnormal head morphology (1 source), abnormal incomplete closing of the blastopore (1 source), abnormal neural plate morphology (1 source), absent cement gland (1 source), absent eye (1 source), decreased length of anterior-posterior axis (1 source), decreased pigmentation in the whole organism (1 source), decreased size of the head (1 source), increased size of the cement gland (1 source), increased size of the epidermis (1 source), increased size of the head (1 source)

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.
Manual annotations: tmem79 manipulated (3 sources)
Computed annotations: tmem79 assayed (2 sources)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + tmem79 MO (6 sources), Xla Wt + tmem79 (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (25 sources): abnormal adipose tissue amount, abnormal coat appearance, abnormal corneocyte envelope morphology, abnormal epidermis stratum corneum morphology, abnormal hair cortex keratinization, abnormal hair cuticle, abnormal hair cycle, abnormal hair follicle development, abnormal locomotor activation, abnormal skin condition, abnormal sleep behavior, abnormal zigzag hair morphology, acanthosis, darkened coat color, decreased fasting circulating glucose level, decreased locomotor activity, decreased startle reflex, dermatitis, excessive scratching, impaired skin barrier function, increased body length, increased curvature of zigzag hairs, increased lean body mass, matted coat, shiny fur [+]

Monarch Ortholog Phenotypes

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

Mouse (25 sources): abnormal adipose tissue amount, abnormal coat appearance, abnormal corneocyte envelope morphology, abnormal epidermis stratum corneum morphology, abnormal hair cortex keratinization, abnormal hair cuticle, abnormal hair cycle, abnormal hair follicle development, abnormal locomotor activation, abnormal skin condition, [+]