oculocutaneous albinism type IB

Summary
Synonym
  • Albinism, Yellow Mutant Type
  • OCA1B
Definition
An oculocutaneous albinism that has_material_basis_in an autosomal recessive hypomorphic mutation of TYR on chromosome 11q14.3 with retention of some residual protein activity.
Super Class
digenic disease oculocutaneous albinism
Disease Ontology
DOID:0070095
Mondo Disease Ontology
MeSH
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7299 TYR tyrosinase
Displaying 1 entry
Gene ID Gene Symbol Description Source
22173 Tyr tyrosinase
Displaying 1 entry
Gene ID Gene Symbol Description Source
176105 tyr-1 Putative tyrosinase-like protein tyr-1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024