Template:Sex development genes table: Difference between revisions
From Embryology
mNo edit summary |
mNo edit summary |
||
| Line 128: | Line 128: | ||
| valign="top" | Persistent Müllerian duct syndrome | | valign="top" | Persistent Müllerian duct syndrome | ||
|- | |- | ||
| valign="top" | ''Pax2'' | | valign="top" | [https://www.omim.org/entry/167409 ''Pax2''] | ||
| valign="top" | Transcription factor | | valign="top" | Transcription factor | ||
| valign="top" | Dysgenesis of mesonephric tubules | | valign="top" | Dysgenesis of mesonephric tubules | ||
| valign="top" | <sup>a</sup> | | valign="top" | <sup>a</sup> | ||
|-bgcolor="F5FAFF" | |-bgcolor="F5FAFF" | ||
| valign="top" | ''Lim1'' | | valign="top" | [https://www.omim.org/entry/601999 ''Lim1''] | ||
| valign="top" | Transcription factor | | valign="top" | Transcription factor | ||
| valign="top" | Agenesis of Wolffian and Müllerian ducts | | valign="top" | Agenesis of Wolffian and Müllerian ducts | ||
| valign="top" | <sup>a</sup> | | valign="top" | <sup>a</sup> | ||
|- | |- | ||
| valign="top" | ''Dmrt1'' | | valign="top" | [https://www.omim.org/entry/602424 ''Dmrt1''] | ||
| valign="top" | Transcription factor | | valign="top" | Transcription factor | ||
| valign="top" | Loss of Sertoli and germ cells | | valign="top" | Loss of Sertoli and germ cells | ||
| Line 145: | Line 145: | ||
| colspan="4" valign="top" | '''Ovary-determining pathway''' | | colspan="4" valign="top" | '''Ovary-determining pathway''' | ||
|- | |- | ||
| valign="top" | ''Wnt4'' | | valign="top" | [https://www.omim.org/entry/603490 ''Wnt4''] | ||
| valign="top" | Signaling molecule | | valign="top" | Signaling molecule | ||
| valign="top" | Müllerian duct agenesis, testosterone synthesis, and coelomic vessel formation | | valign="top" | Müllerian duct agenesis, testosterone synthesis, and coelomic vessel formation | ||
| valign="top" | XY female (GOF) | | valign="top" | XY female (GOF) | ||
|-bgcolor="F5FAFF" | |-bgcolor="F5FAFF" | ||
| valign="top" | ''FoxL2'' | | valign="top" | [https://www.omim.org/entry/605597 ''FoxL2''] | ||
| valign="top" | Transcription factor | | valign="top" | Transcription factor | ||
| valign="top" | Premature ovarian failure | | valign="top" | Premature ovarian failure | ||
| valign="top" | BPES | | valign="top" | BPES | ||
|- | |- | ||
| valign="top" | ''Dax1'' | | valign="top" | [https://www.omim.org/entry/300473 ''Dax1''] | ||
| valign="top" | Nuclear receptor | | valign="top" | Nuclear receptor | ||
| valign="top" | XY sex reversal (GOF) | | valign="top" | XY sex reversal (GOF) | ||
Revision as of 13:14, 24 February 2018
| Gene (OMIM) | Protein Function | Gonad Phenotype of Null Mice | Human Syndrome | |
| Bipotential gonad | ||||
| Wt1 | Transcription factor | Blockage in genital ridge development | Denys-Drash, WAGR, Frasier syndrome | |
| Sf1 | Nuclear receptor | Blockage in genital ridge development | Embryonic testicular regression syndrome | |
| Lhx9 | Transcription factor | Blockage in genital ridge development | a | |
| Emx2 | Transcription factor | Blockage in genital ridge development | a | |
| M33 | Transcription factor | Gonadal dysgenesis | a | |
| Testis-determining pathway | ||||
| Gata4/Fog2 | Transcription/cofactor | Reduced Sry levels, XY sex reversal | a | |
| Sry | Transcription factor | XY sex reversal | XY sex reversal (LOF); XX sex reversal (GOF) | |
| Sox9 | Transcription factor | XY sex reversal | Campomelic dysplasia, XX sex reversal (GOF) | |
| Sox8 | Transcription factor | XY sex reversal in combination with partial loss of Sox9 function | a | |
| Fgf9 | Signaling molecule | XY sex reversal | a | |
| Dax1 | Nuclear receptor | Impaired testis cord formation and spermatogenesis | Hypogonadism | |
| Pod1 | Transcription factor | XY sex reversal | a | |
| Dhh | Signaling molecule | Impaired differentiation of Leydig and PM cells | XY gonadal dysgenesis | |
| Pgdra | Receptor | Reduction in mesonephric cell migration | a | |
| Pgds | Enzyme | No phenotype | a | |
| Arx | Transcription factor | Abnormal testicular differentiation | X-linked lissencephaly with abnormal genitalia | |
| Atrx | Helicase | ND | ATRX syndrome | |
| Insl3 | Signaling factor | Blockage of testicular descent | Cryptorchidism | |
| Lgr8 | Receptor | Blockage of testicular descent | Cryptorchidism | |
| Hoxa10 | Transcription factor | Blockage of testicular descent | Cryptorchidism | |
| Hoxa11 | Transcription factor | Blockage of testicular descent | Cryptorchidism | |
| Amh | Hormone | No Müllerian duct degeneration | Persistent Müllerian duct syndrome | |
| Misrl1 | Receptor | No Müllerian duct degeneration | Persistent Müllerian duct syndrome | |
| Pax2 | Transcription factor | Dysgenesis of mesonephric tubules | a | |
| Lim1 | Transcription factor | Agenesis of Wolffian and Müllerian ducts | a | |
| Dmrt1 | Transcription factor | Loss of Sertoli and germ cells | XY femaleb | |
| Ovary-determining pathway | ||||
| Wnt4 | Signaling molecule | Müllerian duct agenesis, testosterone synthesis, and coelomic vessel formation | XY female (GOF) | |
| FoxL2 | Transcription factor | Premature ovarian failure | BPES | |
| Dax1 | Nuclear receptor | XY sex reversal (GOF) | XY sex reversal (GOF) | |
|
a No mutations in human sexual disorders identified to date.
b Candidate gene for 9p deletion, XY sex reversal. | |||
| Table modified from Wilhelm D, Palmer S & Koopman P. (2007). Sex determination and gonadal development in mammals. Physiol. Rev. , 87, 1-28. PMID: 17237341 DOI. | ||||