| Primary Identifier | IPR026186 | Type | Family |
| Short Name | POF1B |
| description | Proteins in this family may be involved in ovary development. Defects in POF1B are the cause of premature ovarian failure type 2B (POF2B), an ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterised by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol []. |
