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ICAAR, a novel member of a new family of transmembrane, tyrosine phosphatase-like proteins.

作者信息

Smith P D, Barker K T, Wang J, Lu Y J, Shipley J, Crompton M R

机构信息

Section of Cell Biology and Experimental Pathology, Haddow Laboratories, Sutton, Surrey, United Kingdom.

出版信息

Biochem Biophys Res Commun. 1996 Dec 13;229(2):402-11. doi: 10.1006/bbrc.1996.1817.

DOI:10.1006/bbrc.1996.1817
PMID:8954911
Abstract

We have isolated a cDNA from human foetal brain cDNA library which encodes a putative transmembrane protein bearing an intracellular protein tyrosine phosphatase (PTPase) like domain. The PTPase like domain contains an alanine to aspartate amino acid change relative to other PTPases in the catalytic core domain. This amino acid change is found in only three other known proteins, islet cell autoantigens; human, murine and rat IA-2, murine IA-2b and its rat orthologue phogrin, which have a similar overall structure to ICAAR, and the recently identified X-linked myotubular myopathy (MTM1) gene. ICAAR, IA-2 and IA-2b clearly represent a new family of PTP-like proteins for which catalytic activity has yet to be demonstrated. An abundant ICAAR mRNA is detectable in the brain and pancreas but not in the other normal human tissues surveyed. We have localised ICAAR to human chromosome 7q36.

摘要

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引用本文的文献

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IA-2beta, but not IA-2, is induced by ghrelin and inhibits glucose-stimulated insulin secretion.胃饥饿素可诱导IA-2β而非IA-2的产生,并抑制葡萄糖刺激的胰岛素分泌。
Proc Natl Acad Sci U S A. 2006 Jan 24;103(4):885-90. doi: 10.1073/pnas.0502470102. Epub 2006 Jan 17.
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Mapping to chromosomes 1 and 12 of mouse homologs of human protein tyrosine phosphatase, receptor-type, related genes encoding pancreatic beta cell autoantigens.
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Mamm Genome. 1997 Dec;8(12):949-50. doi: 10.1007/s003359900619.