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MEIOB

meiosis specific with OB-fold

HCNC Approved Symbol
MEIOB (HGNC:28569)
Genomic Coordinates
16:1,833,986 - 1,872,164 (16p13.3)
Synonyms
MGC35212, C16orf73
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Premature ovarian failure 23
620686AR
Spermatogenic failure 22
617706AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MEIOB gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results