Property Summary

NCBI Gene PubMed Count 5
Grant Count 21
R01 Count 5
Funding $8,809,627.75
PubMed Score 69.69
PubTator Score 22.48

Knowledge Summary

Patent

No data available

Expression

Gene RIF (1)

PMID Text
17990594 no indications were found for an association between the MBX gene and microphthalmia with congenital cataract in humans

AA Sequence

MQHYGVNGYSLHAMNSLSAMYNLHQQAAQQAQHAPDYRPSVHALTLAERLAGCTFQDIILEARYGSQHRK      1 - 70
QRRSRTAFTAQQLEALEKTFQKTHYPDVVMRERLAMCTNLPEARVQVWFKNRRAKFRKKQRSLQKEQLQK     71 - 140
QKEAEGSHGEGKAEAPTPDTQLDTEQPPRLPGSDPPAELHLSLSEQSASESAPEDQPDREEDPRAGAEDP    141 - 210
KAEKSPGADSKGLGCKRGSPKADSPGSLTITPVAPGGGLLGPSHSYSSSPLSLFRLQEQFRQHMAATNNL    211 - 280
VHYSSFEVGGPAPAAAAAAAAVPYLGVNMAPLGSLHCQSYYQSLSAAAAAHQGVWGSPLLPAPPAGLAPA    281 - 350
SATLNSKTTSIENLRLRAKQHAASLGLDTLPN                                          351 - 382
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Text Mined References (6)

PMID Year Title
24816252 2014 An atlas of genetic influences on human blood metabolites.
18669648 2008 A quantitative atlas of mitotic phosphorylation.
17990594 Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.
16710414 2006 The DNA sequence and biological annotation of human chromosome 1.
12142024 2002 The homeobox gene mbx is involved in eye and tectum development.
12055180 2002 Identification, tissue expression, and functional characterization of Otx3, a novel member of the Otx family.