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Compound
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Query: UNIPROT:Q86TM3 (
cage
)
29,987
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
ARHGAP1, ARHGAP2, ARHGAP3, ARHGAP4, ARHGAP5, ARHGAP6, ARHGAP7 (DLC1), ARHGAP8, ARHGAP9, ARHGAP10, ARHGAP12, ARHGAP13 (SRGAP1), ARHGAP14 (SRGAP2), ARHGAP15, ARHGAP17 (RICH1), ARHGAP18, ARHGAP19, ARHGAP20, ARHGAP21, ARHGAP22, ARHGAP23, ARHGAP24, ARHGAP25, ARHGAP26, STARD13 (DLC2), HA-1, GMIP, PARG1, RACGAP1, PIK3R1, PIK3R2, and FNBP2 genes encode Rho/Rac/Cdc42-like GTPase activating (RhoGAP) proteins. Here, we characterized human
ARHGAP27
gene by using bioinformatics. Complete coding sequence of
ARHGAP27
isoform 1, encoding a full-length 889-aa protein, was determined by assembling exon 1 (nucleotide position 143440-144096 of AC091132.16) and most part of FLJ43547 cDNA (nucleotide position 69-3628 of AK125535.1). Complete coding sequence of
ARHGAP27
isoform 2, encoding an N-terminally truncated 548-aa protein, was derived from FLJ43547 cDNA.
ARHGAP27
isoform 1 consists of exons 1-17, while
ARHGAP27
isoform 2 consists of exons 1B, and 2-17.
ARHGAP27
gene encoded two isoforms due to alternative splicing of alternative promoter type.
ARHGAP27
mRNA was expressed in germinal center B cell, spleen, chronic lymphocytic leukemia, pancreatic cancer, and lung cancer. LOC303583 (NM_ 198759.1) was the representative rat Arhgap27 cDNA. Human
ARHGAP27
showed 84.3% total-amino-acid identity with rat Arhgap27, and 39.0% total-amino-acid identity with human ARHGAP12.
ARHGAP27
and ARHGAP12 shared the common-domain structure, consisting of SH3, WW, PH, and RhoGAP domains.
ARHGAP27
gene was located at human chromosome 17q21, while ARHGAP12 gene was located at human chromosome 10p11. ARHGAP family genes are
cancer-associated
genes, because their genetic alterations lead to carcinogenesis through the dysregulation of Rho/Rac/ Cdc42-like GTPases. This is the first report on identification and characterization of the
ARHGAP27
gene.
...
PMID:Identification and characterization of ARHGAP27 gene in silico. 1549 70