AC T04050
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ID T04050
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DT 30.11.2000 (created); rio.
DT 01.08.2013 (updated); mkl.
CO Copyright (C), QIAGEN.
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FA MOX1-isoform2
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SY Meox1a.
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OS human, Homo sapiens
OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; primates
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GE G002119 MEOX1; HGNC: MEOX1.
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CL C0006; homeo.
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SZ 184 AA; 19.6 kDa (cDNA) (calc.).
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SQ MDPAASSCMRSLQPPAPVWGCLRNPHSEGNGASGLPHYPPTPFSFHQKPDFLATATAAYP
SQ DFSASCLAATPHSLPQEEHIFTEQHPAFPQSPNWHFPVSDARRRPNSGPAGGSKEMGTSS
SQ LGLVDTTGGPGDDYGVLGSTANETEKKSSRRRKESSGQSVVPEPKDEVEACEGRSAHLPQ
SQ WAGP
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SC translated from EMBL #U10493
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SF two splice variants Meox1T04046/MOX1-isoform2, MOX1-isoform2 lacks the entire homeo domain [1];
SF linked to the BRCA1 T04074 chromosomal region [1];
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CP (fetus:) predominantly in heart, low expression in brain, lung, liver and kidney, (adult:) spleen, thymus, prostate, ovary, small intestine, colon, leukocyte, low expression in testis [1].
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MX M01443 V$MOX1_01.
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DR TRANSPATH: MO000027959.
DR EMBL: U10493;
DR UniProtKB: P50221-2; MEOX1_HUMAN.
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RN [1]; RE0015388.
RX PUBMED: 7987315.
RA Futreal P. A., Cochran C., Rosenthal J., Miki Y., Swenson J., Hobbs M., Bennett L. M., Haugen-Strano A., Marks J., Barrett J. C.
RT Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture
RL Hum. Mol. Genet. 3:1359-1364 (1994).
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