AC T02778
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ID T02778
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DT 21.06.1999 (created); mpr.
DT 15.05.2007 (updated); apk.
CO Copyright (C), QIAGEN.
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FA Prop-1
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SY PRH1; PROP1; prophet of Pit-1.
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OS human, Homo sapiens
OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; primates
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GE G006593 PROP1; HGNC: PROP1.
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CL 3.1.3.20.1.
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CP pituitary gland.
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MX M01320 V$PROP1_02.
MX M04626 V$PROP1_Q2.
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DR TRANSPATH: MO000026750.
DR PATHODB: MT000010.
DR PATHODB: MT000011.
DR PATHODB: MT000012.
DR PATHODB: MT000013.
DR PATHODB: MT000014.
DR PATHODB: MT000015.
DR PATHODB: MT000017.
DR PATHODB: MT000018.
DR UniProtKB: O75360;
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RN [1]; RE0013691.
RX PUBMED: 9462743.
RA Wu W., Cogan J. D., Pfaeffle R. W., Dasen J. S., Frisch H., O'Connell S. M., Flynn S. E., Brown M. R., Mullis P. E., Parks J. S., Phillips J. A., Rosenfeld M. G.
RT Mutations in PROP1 cause familial combined pituitary hormone deficiency
RL Nat. Genet. 18:147-149 (1998).
RN [2]; RE0013695.
RX PUBMED: 9824293.
RA Duquesnoy P., Roy A., Dastot F., Ghali I., Teinturier C., Netchine I., Cacheux V., Hafez M., Salah N., Chaussain J. L., Goossens M., Bougneres P., Amselem S.
RT Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency
RL FEBS Lett. 437:216-220 (1998).
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