SRY is a sex-determining gene on the Y chromosome in the therians.This intronless gene encodes a transcription factor that is a member of the high mobility group (HMG)-box family of DNA-binding proteins. This protein is the testis determining factor (TDF), also referred to as the SRY protein, which initiates male sex determination. Mutations in this gene give rise to XY females with gonadal dysgenesis ; translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome.SRY has been linked to the fact that men are more likely than women to develop dopamine-related diseases such as schizophrenia and Parkinson's disease. makes a protein that controls concentrations of dopamine, the neurotransmitter that carries signals from the brain that control movement and coordination.
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | RPG341Hu01 | Recombinant Sex Determining Region Y (SRY) | Positive Control; Immunogen; SDS-PAGE; WB. |
Antibodies | MAG341Hu21 | Monoclonal Antibody to Sex Determining Region Y (SRY) | WB; IHC; ICC; IP. |
PAG341Hu01 | Polyclonal Antibody to Sex Determining Region Y (SRY) | WB; IHC | |
Assay Kits | SEG341Hu | ELISA Kit for Sex Determining Region Y (SRY) | Enzyme-linked immunosorbent assay for Antigen Detection. |
Organism species: Mus musculus (Mouse)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Sex Determining Region Y (SRY) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Sex Determining Region Y (SRY) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Sex Determining Region Y (SRY) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Sex Determining Region Y (SRY) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Sex Determining Region Y (SRY) | ELISA Kit Customized Service Offer |
Organism species: Rattus norvegicus (Rat)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Sex Determining Region Y (SRY) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Sex Determining Region Y (SRY) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Sex Determining Region Y (SRY) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Sex Determining Region Y (SRY) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Sex Determining Region Y (SRY) | ELISA Kit Customized Service Offer |
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- "Structure of a complex of tandem HMG boxes and DNA."J. Mol. Biol. 360:90-104(2006) [PubMed] [Europe PMC] [Abstract]
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- "Analysis of the SRY gene in 22 sex-reversed XY females identifies four new point mutations in the conserved DNA binding domain."Hum. Mol. Genet. 2:785-789(1993) [PubMed] [Europe PMC] [Abstract]
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- "Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis."Am. J. Hum. Genet. 51:979-984(1992) [PubMed] [Europe PMC] [Abstract]
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- "A new de novo mutation (A113T) in HMG box of the SRY gene leads to XY gonadal dysgenesis."J. Med. Genet. 30:655-657(1993) [PubMed] [Europe PMC] [Abstract]
- "Description and functional implications of a novel mutation in the sex-determining gene SRY."Hum. Mutat. 3:200-204(1994) [PubMed] [Europe PMC] [Abstract]
- "Molecular basis of mammalian sexual determination: activation of Mullerian inhibiting substance gene expression by SRY."Science 266:1494-1500(1994) [PubMed] [Europe PMC] [Abstract]
- "Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers."Am. J. Hum. Genet. 56:862-869(1995) [PubMed] [Europe PMC] [Abstract]
- "True hermaphroditism with 46,XY karyotype and a point mutation in the SRY gene."J. Pediatr. 126:1022-1022(1995) [PubMed] [Europe PMC] [Abstract]
- "Novel missense mutation (P131R) in the HMG box of SRY in XY sex reversal."Hum. Mutat. Suppl. 1:S328-S328(1998)
- "Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations."Cytogenet. Cell Genet. 80:188-192(1998) [PubMed] [Europe PMC] [Abstract]
- "A novel missense mutation (S18N) in the 5' non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives."Hum. Genet. 102:213-215(1998) [PubMed] [Europe PMC] [Abstract]
- "Independent observation of SRY mutation I90M in a patient with complete gonadal dysgenesis."Hum. Mutat. 11:90-91(1998) [PubMed] [Europe PMC] [Abstract]
- "A rare case of 46,XX true hermaphroditism with hidden mosaicism with sex-determining region Y chromosome-bearing cells in the gonads."Intern. Med. 37:467-471(1998) [PubMed] [Europe PMC] [Abstract]
- "A novel sex-determining region on Y (SRY) missense mutation identified in a 46,XY female and also in the father."Endocr. J. 46:735-739(1999) [PubMed] [Europe PMC] [Abstract]
- "Another mutation within the HMG-box of the SRY gene associated with Swyer syndrome."Hum. Mutat. 13:85-85(1999)
- "SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite."Am. J. Med. Genet. 90:25-28(2000) [PubMed] [Europe PMC] [Abstract]
- "Identification of a new missense mutation (Gly95Glu) in a highly conserved codon within the high-mobility group box of the sex-determining region Y gene: report on a 46,XY female with gonadal dysgenesis and yolk-sac tumor."J. Clin. Endocrinol. Metab. 85:2287-2292(2000) [PubMed] [Europe PMC] [Abstract]
- "A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism."J. Clin. Endocrinol. Metab. 85:1908-1911(2000) [PubMed] [Europe PMC] [Abstract]
- "A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversal."J. Hum. Genet. 45:112-114(2000) [PubMed] [Europe PMC] [Abstract]
- "Familial mutation in the testis-determining gene SRY shared by an XY female and her normal father."J. Clin. Endocrinol. Metab. 87:3428-3432(2002) [PubMed] [Europe PMC] [Abstract]
- "True hermaphroditism in an XY individual due to a familial point mutation of the SRY gene."J. Pediatr. Endocrinol. Metab. 16:575-580(2003) [PubMed] [Europe PMC] [Abstract]
- "Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis."Eur. J. Hum. Genet. 15:76-80(2007) [PubMed] [Europe PMC] [Abstract]