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Heritable Phenotypic Marker : htd hair-thyroid deficient

Primary Identifier	MGI:96267	Organism	mouse, laboratory
Chromosome	UN	Mgi Type	heritable phenotypic marker

description

PHENOTYPE: Mice homozygous for a spontaneous allele exhibit partial lethality, decreased body size/weight, reduced fertility, complete hair loss at weaning, abnormal hair growth, rubbery skin, reduced thyroid hormone levels, and abnormal submandibular gland morphology. Mutant males show hypercorticosteronemia. [provided by MGI curators]

synonyms:
htd,
hair-thyroid deficient,
MGD-MRK-10992

earliestPublication:
Maltais LJ, et al. (1984) A new Hypothyroid mutation: Hair-thyroid deficient. The Jackson Laboratory Scientific Report :82-4

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

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Mouse features --> Functions (GO terms)

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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