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2025-05-09 17:13:03, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001030055 9604 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens Rho GTPase activating protein 5 (ARHGAP5), transcript
variant 1, mRNA.
ACCESSION NM_001030055
VERSION NM_001030055.1 GI:71834862
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 9604)
AUTHORS Tripathi,B.K. and Zelenka,P.S.
TITLE Cdk5-dependent regulation of Rho activity, cytoskeletal
contraction, and epithelial cell migration via suppression of Src
and p190RhoGAP
JOURNAL Mol. Cell. Biol. 29 (24), 6488-6499 (2009)
PUBMED 19822667
REMARK GeneRIF: Results link Cdk5 to Rho-ROCK signaling via Src and
p190RhoGAP and implicate Cdk5 in the regulation of cell
contraction, attachment, and migration.
REFERENCE 2 (bases 1 to 9604)
AUTHORS Gen,Y., Yasui,K., Zen,K., Nakajima,T., Tsuji,K., Endo,M.,
Mitsuyoshi,H., Minami,M., Itoh,Y., Tanaka,S., Taniwaki,M., Arii,S.,
Okanoue,T. and Yoshikawa,T.
TITLE A novel amplification target, ARHGAP5, promotes cell spreading and
migration by negatively regulating RhoA in Huh-7 hepatocellular
carcinoma cells
JOURNAL Cancer Lett. 275 (1), 27-34 (2009)
PUBMED 18996642
REMARK GeneRIF: ARHGAP5 (the gene encoding p190-B RhoGAP) is a probable
target for the amplification at 14q12, and p190-B RhoGAP promotes
cells spreading and migration by negatively regulating RhoA
activity in Huh-7 hepatocellular carcinoma cells
REFERENCE 3 (bases 1 to 9604)
AUTHORS Zhan,X. and Desiderio,D.M.
TITLE Nitroproteins from a human pituitary adenoma tissue discovered with
a nitrotyrosine affinity column and tandem mass spectrometry
JOURNAL Anal. Biochem. 354 (2), 279-289 (2006)
PUBMED 16777052
REFERENCE 4 (bases 1 to 9604)
AUTHORS Vargo-Gogola,T., Heckman,B.M., Gunther,E.J., Chodosh,L.A. and
Rosen,J.M.
TITLE P190-B Rho GTPase-activating protein overexpression disrupts ductal
morphogenesis and induces hyperplastic lesions in the developing
mammary gland
JOURNAL Mol. Endocrinol. 20 (6), 1391-1405 (2006)
PUBMED 16469769
REMARK GeneRIF: precise control of p190-B Rho GTPase-activating protein
activity is critical for normal branching morphogenesis during
mammary gland development
REFERENCE 5 (bases 1 to 9604)
AUTHORS Blanchetot,C., Chagnon,M., Dube,N., Halle,M. and Tremblay,M.L.
TITLE Substrate-trapping techniques in the identification of cellular PTP
targets
JOURNAL Methods 35 (1), 44-53 (2005)
PUBMED 15588985
REFERENCE 6 (bases 1 to 9604)
AUTHORS Chakravarty,G., Roy,D., Gonzales,M., Gay,J., Contreras,A. and
Rosen,J.M.
TITLE P190-B, a Rho-GTPase-activating protein, is differentially
expressed in terminal end buds and breast cancer
JOURNAL Cell Growth Differ. 11 (7), 343-354 (2000)
PUBMED 10939588
REFERENCE 7 (bases 1 to 9604)
AUTHORS Zrihan-Licht,S., Fu,Y., Settleman,J., Schinkmann,K., Shaw,L.,
Keydar,I., Avraham,S. and Avraham,H.
TITLE RAFTK/Pyk2 tyrosine kinase mediates the association of p190 RhoGAP
with RasGAP and is involved in breast cancer cell invasion
JOURNAL Oncogene 19 (10), 1318-1328 (2000)
PUBMED 10713673
REFERENCE 8 (bases 1 to 9604)
AUTHORS Burbelo,P.D., Miyamoto,S., Utani,A., Brill,S., Yamada,K.M., Hall,A.
and Yamada,Y.
TITLE p190-B, a new member of the Rho GAP family, and Rho are induced to
cluster after integrin cross-linking
JOURNAL J. Biol. Chem. 270 (52), 30919-30926 (1995)
PUBMED 8537347
REFERENCE 9 (bases 1 to 9604)
AUTHORS Foster,R., Hu,K.Q., Shaywitz,D.A. and Settleman,J.
TITLE p190 RhoGAP, the major RasGAP-associated protein, binds GTP
directly
JOURNAL Mol. Cell. Biol. 14 (11), 7173-7181 (1994)
PUBMED 7935432
REFERENCE 10 (bases 1 to 9604)
AUTHORS Ellis,C., Moran,M., McCormick,F. and Pawson,T.
TITLE Phosphorylation of GAP and GAP-associated proteins by transforming
and mitogenic tyrosine kinases
JOURNAL Nature 343 (6256), 377-381 (1990)
PUBMED 1689011
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL161665.5, BC050059.1 and
AL045112.1.
Summary: Rho GTPase activating protein 5 negatively regulates RHO
GTPases, a family which may mediate cytoskeleton changes by
stimulating the hydrolysis of bound GTP. Two transcript variants
encoding different isoforms have been found for this gene.
[provided by RefSeq, Jul 2008].
Transcript Variant: This variant (1) represents the longer
transcript and encodes the longer isoform (a).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
CDS exon combination :: BC050059.1 [ECO:0000331]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-147 AL161665.5 145055-145201 c
148-4032 AL161665.5 128104-131988 c
4033-4462 BC050059.1 3959-4388
4463-4744 AL045112.1 234-515
4745-9604 AL161665.5 62762-67621 c
FEATURES Location/Qualifiers
source 1..9604
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="14"
/map="14q12"
gene 1..9604
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Rho GTPase activating protein 5"
/db_xref="GeneID:394"
/db_xref="HGNC:675"
/db_xref="HPRD:04060"
/db_xref="MIM:602680"
exon 1..147
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 126
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377415600"
exon 148..4032
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 192..194
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace=""
/replace="agg"
/db_xref="dbSNP:373668066"
variation 199
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:55965079"
variation 227
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:186382575"
variation 274
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200677078"
variation 279
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376307600"
misc_feature 295..297
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="upstream in-frame stop codon"
CDS 316..4824
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="isoform a is encoded by transcript variant 1;
growth factor independent 2; rho GTPase-activating protein
5; p105 RhoGAP; p100 RasGAP-associated p105 protein;
rho-type GTPase-activating protein 5"
/codon_start=1
/product="rho GTPase-activating protein 5 isoform a"
/protein_id="NP_001025226.1"
/db_xref="GI:71834863"
/db_xref="CCDS:CCDS32062.1"
/db_xref="GeneID:394"
/db_xref="HGNC:675"
/db_xref="HPRD:04060"
/db_xref="MIM:602680"
/translation="
MMAKNKEPRPPSYTISIVGLSGTEKDKGNCGVGKSCLCNRFVRSKADEYYPEHTSVLSTIDFGGRVVNNDHFLYWGDIIQNSEDGVECKIHVIEQTEFIDDQTFLPHRSTNLQPYIKRAAASKLQSAEKLMYICTDQLGLEQDFEQKQMPEGKLNVDGFLLCIDVSQGCNRKFDDQLKFVNNLFVQLSKSKKPVIIAATKCDECVDHYLREVQAFASNKKNLLVVETSARFNVNIETCFTALVQMLDKTRSKPKIIPYLDAYKTQRQLVVTATDKFEKLVQTVRDYHATWKTVSNKLKNHPDYEEYINLEGTRKARNTFSKHIEQLKQEHIRKRREEYINTLPRAFNTLLPNLEEIEHLNWSEALKLMEKRADFQLCFVVLEKTPWDETDHIDKINDRRIPFDLLSTLEAEKVYQNHVQHLISEKRRVEMKEKFKKTLEKIQFISPGQPWEEVMCFVMEDEAYKYITEADSKEVYGRHQREIVEKAKEEFQEMLFEHSELFYDLDLNATPSSDKMSEIHTVLSEEPRYKALQKLAPDRESLLLKHIGFVYHPTKETCLSGQNCTDIKVEQLLASSLLQLDHGRLRLYHDSTNIDKVNLFILGKDGLAQELANEIRTQSTDDEYALDGKIYELDLRPVDAKSPYFLSQLWTAAFKPHGCFCVFNSIESLSFIGEFIGKIRTEASQIRKDKYMANLPFTLILANQRDSISKNLPILRHQGQQLANKLQCPFVDVPAGTYPRKFNETQIKQALRGVLESVKHNLDVVSPIPANKDLSEADLRIVMCAMCGDPFSVDLILSPFLDSHSCSAAQAGQNNSLMLDKIIGEKRRRIQITILSYHSSIGVRKDELVHGYILVYSAKRKASMGMLRAFLSEVQDTIPVQLVAVTDSQADFFENEAIKELMTEGEHIATEITAKFTALYSLSQYHRQTEVFTLFFSDVLEKKNMIENSYLSDNTRESTHQSEDVFLPSPRDCFPYNNYPDSDDDTEAPPPYSPIGDDVQLLPTPSDRSRYRLDLEGNEYPIHSTPNCHDHERNHKVPPPIKPKPVVPKTNVKKLDPNLLKTIEAGIGKNPRKQTSRVPLAHPEDMDPSDNYAEPIDTIFKQKGYSDEIYVVPDDSQNRIKIRNSFVNNTQGDEENGFSDRTSKSHGERRPSKYKYKSKTLFSKAKSYYRRTHSDASDDEAFTTSKTKRKGRHRGSEEDPLLSPVETWKGGIDNPAITSDQELDDKKMKKKTHKVKEDKKQKKKTKNFNPPTRRNWESNYFGMPLQDLVTAEKPIPLFVEKCVEFIEDTGLCTEGLYRVSGNKTDQDNIQKQFDQDHNINLVSMEVTVNAVAGALKAFFADLPDPLIPYSLHPELLEAAKIPDKTERLHALKEIVKKFHPVNYDVFRYVITHLNRVSQQHKINLMTADNLSICFWPTLMRPDFENREFLSTTKIHQSVVETFIQQCQFFFYNGEIVETTNIVAPPPPSNPGQLVEPMVPLQLPPPLQPQLIQPQLQTDPLGII
"
misc_feature 406..1053
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="P-loop containing Nucleoside Triphosphate
Hydrolases; Region: P-loop_NTPase; cl09099"
/db_xref="CDD:214148"
misc_feature order(406..423,595..597,910..915,919..921,997..1005)
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="GTP/Mg2+ binding site [chemical binding]; other
site"
/db_xref="CDD:206648"
misc_feature 406..420
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="G1 box; other site"
/db_xref="CDD:206648"
misc_feature 490..492
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="G2 box; other site"
/db_xref="CDD:206648"
misc_feature 496..504
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Switch I region; other site"
/db_xref="CDD:206648"
misc_feature order(595..597,784..789)
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Switch II region; other site"
/db_xref="CDD:206648"
misc_feature 910..921
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="G4 box; other site"
/db_xref="CDD:206648"
misc_feature 997..1005
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="G5 box; other site"
/db_xref="CDD:206648"
misc_feature 1126..1290
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Contains two conserved F residues; Region: FF;
smart00441"
/db_xref="CDD:128718"
misc_feature 1417..1575
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Contains two conserved F residues; Region: FF;
smart00441"
/db_xref="CDD:128718"
misc_feature 1600..1758
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Contains two conserved F residues; Region: FF;
smart00441"
/db_xref="CDD:128718"
misc_feature 1765..1914
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Contains two conserved F residues; Region: FF;
smart00441"
/db_xref="CDD:128718"
misc_feature 1963..1965
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Nitrated tyrosine; propagated from
UniProtKB/Swiss-Prot (Q13017.2); modified site"
misc_feature 2608..2610
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature <2809..3114
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="P-loop containing Nucleoside Triphosphate
Hydrolases; Region: P-loop_NTPase; cl09099"
/db_xref="CDD:214148"
misc_feature 2860..2865
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="Switch II region; other site"
/db_xref="CDD:206648"
misc_feature 2974..2985
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="G4 box; other site"
/db_xref="CDD:206648"
misc_feature 3073..3081
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="G5 box; other site"
/db_xref="CDD:206648"
misc_feature 3166..3168
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3217..3219
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3658..3660
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3832..3834
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3841..3843
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3898..3900
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3919..3921
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3919..3921
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 3967..3969
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(Q13017.2); phosphorylation site"
misc_feature 3967..3969
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 4093..4647
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="RhoGAP_p190: RhoGAP (GTPase-activator protein [GAP]
for Rho-like small GTPases) domain of p190-like proteins.
p190, also named RhoGAP5, plays a role in neuritogenesis
and axon branch stability. p190 shows a preference for
Rho, over Rac and Cdc42, and...; Region: RhoGAP_p190;
cd04373"
/db_xref="CDD:63842"
misc_feature 4129..4650
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="GTPase-activator protein for Rho-like GTPases;
Region: RhoGAP; smart00324"
/db_xref="CDD:197653"
misc_feature order(4204..4206,4318..4320,4330..4332,4537..4539,
4546..4551,4618..4620)
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="putative GTPase interaction site [polypeptide
binding]; other site"
/db_xref="CDD:63842"
misc_feature 4204..4206
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/note="catalytic residue [active]"
/db_xref="CDD:63842"
variation 364
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:17386818"
variation 375
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:146791896"
variation 442
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369146124"
variation 465
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:139278127"
variation 474
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201062895"
variation 509
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:373505990"
variation 564
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/db_xref="dbSNP:143497372"
variation 610
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377715761"
variation 657
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/db_xref="dbSNP:377565912"
variation 669
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:370391316"
variation 685
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200755411"
variation 703
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:367805928"
variation 719
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:371747331"
variation 774
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:374638293"
variation 795
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:190485053"
variation 796
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:145904404"
variation 798
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370059505"
variation 809
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200498117"
variation 824
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375076650"
variation 869
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:369503160"
variation 927
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144274970"
variation 956
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:369093762"
variation 1155
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367996747"
variation 1200
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144586464"
variation 1214
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371461440"
variation 1341
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148782993"
variation 1419
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142697641"
variation 1489
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372981423"
variation 1566
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:145993763"
variation 1569
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:61747596"
variation 1625
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:56259828"
variation 1677
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143684972"
variation 1680
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:151276606"
variation 1736
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200111638"
variation 1753
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201986816"
variation 1756
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:200628183"
variation 1780
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:78337553"
variation 1877
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:201351112"
variation 1960
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139228559"
variation 1991
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149988341"
variation 2012
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:145387405"
variation 2035
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:142620412"
variation 2058
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:199609559"
variation 2062
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146911446"
variation 2098
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:181754222"
variation 2184
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201489307"
variation 2218
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:115598823"
variation 2219
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141762175"
variation 2269
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146396734"
variation 2271
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:377277190"
variation 2275
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148226075"
variation 2282
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:200687781"
variation 2298
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369766568"
variation 2316
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372988874"
variation 2325
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:374179893"
variation 2349
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191278032"
variation 2360
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372956846"
variation 2363
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141134108"
variation 2404
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150293728"
variation 2457
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377117868"
variation 2472
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:367605056"
variation 2493
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:61739165"
variation 2523
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:186741221"
variation 2602
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:189967153"
variation 2615
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:142663482"
variation 2619
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:146041775"
variation 2620
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370267449"
variation 2635
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373593195"
variation 2650
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:139895818"
variation 2658
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:141747142"
variation 2662
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:200248752"
variation 2664
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61737878"
variation 2667
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371137927"
variation 2669
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:148538118"
variation 2694
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:201765085"
variation 2699
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:374527700"
variation 2798
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:142888518"
variation 2833
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:151030401"
variation 2868
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:140758857"
variation 2901
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139734756"
variation 2925
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200739729"
variation 2937
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147957990"
variation 2949
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61737869"
variation 3009
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143191152"
variation 3016
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150461143"
variation 3031
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:368445681"
variation 3063
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:145372823"
variation 3092
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148845374"
variation 3096
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:372850172"
variation 3162
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:372395150"
variation 3169
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:56011706"
variation 3170
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375310953"
variation 3173
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:151151743"
variation 3228
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:61739174"
variation 3239
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140808667"
variation 3252
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144832681"
variation 3264
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138769686"
variation 3295
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141239257"
variation 3322
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:61739181"
variation 3335
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371418384"
variation 3376
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:201859090"
variation 3387
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:138049187"
variation 3405
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:149587473"
variation 3409
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200073853"
variation 3410
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376418547"
variation 3433
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:368781859"
variation 3448
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:374565403"
variation 3478
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:193025304"
variation 3500
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:147275403"
variation 3508
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:140666572"
variation 3541
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200670818"
variation 3569
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201427084"
variation 3575
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:367744131"
variation 3587
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370569198"
variation 3590
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373639217"
variation 3596
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144640899"
variation 3605
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/db_xref="dbSNP:147527447"
variation 3607
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140177459"
variation 3664
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:202149589"
variation 3680
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:142991621"
variation 3758
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:374422184"
variation 3759
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:139011417"
variation 3823
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:141066701"
variation 3866
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:188144262"
variation 3892
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:201734513"
variation 3896
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149893615"
variation 3960
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:377181913"
variation 3968
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/db_xref="dbSNP:149916368"
variation 4010
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:372091460"
exon 4033..4180
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 4071
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:373330466"
variation 4087
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370086242"
variation 4105
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:146454039"
variation 4117
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:61731183"
exon 4181..4258
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 4191
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:374154091"
variation 4212
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:144611223"
variation 4218
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:188578201"
exon 4259..4390
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 4322
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/db_xref="dbSNP:182392819"
variation 4345
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:371837356"
variation 4378
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:187384396"
exon 4391..4496
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 4397
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:371504762"
variation 4398
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:370895550"
variation 4409
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:112118715"
variation 4411
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:138543554"
variation 4412
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148897080"
variation 4414
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:189213873"
variation 4467
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:143627018"
STS 4483..4610
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/standard_name="Arhgap5"
/db_xref="UniSTS:526932"
exon 4497..9604
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/inference="alignment:Splign:1.39.8"
variation 4531
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:112370244"
STS 4561..4706
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/standard_name="RH18005"
/db_xref="UniSTS:32239"
variation 4582
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:56077784"
variation 4589
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375679512"
variation 4603
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:371504691"
variation 4620
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369772813"
variation 4622
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:11551871"
variation 4627
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:141737585"
variation 4638
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:375933800"
variation 4667
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184170826"
variation 4685
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:377293078"
variation 4694
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:202041549"
variation 4732
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:200577126"
variation 4741
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147264826"
variation 4745
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:139158293"
variation 4764
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375537995"
variation 4786
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:143148346"
variation 4794
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:149811240"
variation 4802
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:200147073"
variation 4805
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:369779328"
variation 4821
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:139279589"
variation 4843
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:192316189"
variation 4864
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:75664073"
variation 5231
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:375721284"
variation 5257
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184009419"
variation 5282
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:188693069"
variation 5316
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:192582867"
variation 5347
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:57976485"
variation 5512
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:114957711"
variation 5534
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:111284027"
variation 5586
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:45441195"
variation 5683
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:184253112"
variation 5696
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="c"
/db_xref="dbSNP:3168895"
variation 5719
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:3178122"
variation 5783
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:368469887"
polyA_signal 5868..5873
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
polyA_site 5894
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
variation 5919
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:45512399"
variation 5992
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:111791064"
variation 6166
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:182088962"
variation 6265
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:186417627"
variation 6314
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:3178124"
variation 6402
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:376437523"
variation 6464
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:188767762"
variation 6508..6509
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace=""
/replace="a"
/db_xref="dbSNP:200396089"
variation 6509
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:45596831"
variation 6522
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:11551870"
variation 6782
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:373353214"
variation 6879
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:185364317"
STS 6929..7052
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/standard_name="RH45106"
/db_xref="UniSTS:10594"
variation 7002
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:115935597"
variation 7033
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191254361"
variation 7038
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:140094713"
polyA_signal 7071..7076
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
polyA_site 7093
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
polyA_signal 7322..7327
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
polyA_site 7341
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/experiment="experimental evidence, no additional details
recorded"
variation 7358
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:372782800"
variation 7415
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:374885208"
variation 7475
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:7152756"
variation 7547
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:143719152"
variation 7554
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:185877684"
STS 7679..7805
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/standard_name="RH104330"
/db_xref="UniSTS:98655"
variation 7705
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:191217442"
variation 7730..7733
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace=""
/replace="taat"
/db_xref="dbSNP:374103451"
variation 7779
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:183338782"
variation 7878
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:187937575"
variation 7894
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:76071667"
variation 7971
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:145507663"
variation 7975
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:191970842"
variation 8108
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:147751698"
variation 8193
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:148788825"
variation 8273
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:183084810"
variation 8364
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:79332474"
variation 8423
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:188790974"
variation 8636
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:150942994"
variation 8786
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:368796055"
variation 8819
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:192638225"
variation 8887
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:144680817"
variation 9003
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:185070121"
variation 9073
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:189125052"
variation 9100
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:146681076"
variation 9239
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="g"
/replace="t"
/db_xref="dbSNP:140352285"
variation 9242
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:376546766"
variation 9281
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="g"
/db_xref="dbSNP:371480073"
variation 9294
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace=""
/replace="t"
/db_xref="dbSNP:374393715"
variation 9299
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:114509182"
variation 9344
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="g"
/db_xref="dbSNP:376045217"
variation 9566
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="c"
/replace="t"
/db_xref="dbSNP:145415255"
variation 9572
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
/replace="a"
/replace="t"
/db_xref="dbSNP:192723174"
polyA_signal 9580..9585
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
polyA_site 9604
/gene="ARHGAP5"
/gene_synonym="GFI2; p190-B; p190BRhoGAP; RhoGAP5"
ORIGIN
ctcggtgagcgcgccgaggaagagaggcgagcggagagtggaggaggaggcggcggcggcgggagcggtccccaggaatgtcgctgccgccgccaccgccggggccgctgccgttgaggaggagacggaggagaccgacgttgttaggaagatgatccctatgatcttgaagatgtttctgcacagaaatgagggaaatacaaagaaccaaatacagttctgaaatttgggatctgtattttgagatgattttattttcagaatgagaagcatatctggttacctttatgaatgtagagacatgagaagagagttatgatggcaaaaaacaaagagcctcgtcccccatcctataccatcagtatagttggactctctgggactgaaaaagacaaaggtaactgtggagttggaaagtcttgtttgtgcaatagatttgtacgctcaaaagcagatgaatattatccagagcatacttctgtgcttagcaccattgactttggaggacgagtagtaaacaatgatcactttttgtactggggtgacataatacaaaatagtgaagatggagtagaatgcaaaattcatgtcattgaacaaacagagttcattgatgaccagactttcttgcctcatcggagtacgaatttgcaaccatatataaaacgtgcagctgcatctaaattgcagtcagcagaaaaactaatgtacatttgcactgatcagctaggcttagaacaagactttgaacagaagcaaatgcctgaagggaagctcaacgtagatggatttttattatgcattgatgtaagtcaaggatgcaataggaagtttgatgatcaacttaaatttgtgaataacctttttgtccagttatcaaaatcaaaaaaacctgtaataatagcagcaactaaatgtgatgaatgcgtggatcattatcttagagaagttcaggcatttgcttcaaataaaaagaaccttcttgtagtggaaacatcagcacgatttaatgtcaacattgaaacatgttttactgcactggtacaaatgttggataaaactcgtagcaagcctaaaattattccctatttggatgcttataaaacacagagacaacttgttgtcacagcaacagataagtttgaaaaacttgtgcagactgtgagagattatcatgcaacttggaaaactgttagtaataaattaaaaaatcatcctgattatgaagaatacatcaacttagagggaacaagaaaggccagaaatacattctcaaaacatatagaacaacttaaacaggaacatataagaaaaaggagagaagagtatataaatactttaccaagagcttttaacactcttttgccaaatctagaagagattgaacatttgaattggtcagaagctttgaagttaatggaaaagagagcagatttccagttatgttttgtggtgctagaaaaaactccttgggatgaaactgaccatatagacaaaattaatgataggcggattccatttgacctcctgagcactttagaagctgaaaaagtctatcagaaccatgtacagcatctgatatccgagaagaggagggtggaaatgaaggaaaaattcaaaaagactttggaaaaaattcaattcatttcaccagggcagccatgggaggaagttatgtgctttgttatggaggatgaagcctacaaatatatcactgaggctgatagcaaagaggtatatggtaggcatcagcgagaaatagttgaaaaagccaaagaagagtttcaagaaatgctttttgagcattctgaacttttttatgatttagatcttaatgcaacacctagttcagataaaatgagtgaaattcatacagttctgagtgaagaacctagatataaagctttacagaaacttgcacctgatagggaatcccttctacttaagcatataggatttgtttatcatcccactaaagaaacatgtcttagtggccaaaattgtacagacattaaagtggagcagttacttgctagtagtcttttacagttggatcatggccgcttaagattatatcacgatagtaccaatatagataaagttaacctttttattttagggaaggatggccttgcccaagaactagcaaatgagataaggacacaatccactgatgatgagtatgccttagatggaaaaatttatgaacttgatcttcggccggttgatgccaaatcgccttactttttgagtcagttatggactgccgcctttaaaccacatgggtgcttctgtgtatttaattccattgagtcattgagttttattggggaatttattgggaaaataagaactgaagcttctcagatcagaaaagataaatacatggctaatcttccatttacattaattctggctaatcagagagattccattagtaagaatctaccaattctcaggcaccaagggcagcagttggcaaacaagttgcaatgtccttttgtagatgtacctgctggtacatatcctcgtaaatttaatgaaacccaaataaagcaagctctcagaggagtattggaatcagttaaacacaatttggatgtggtgagcccaattcctgccaataaggacttatcagaagctgacttgagaattgtcatgtgcgccatgtgtggagatccatttagtgtggatcttattctttcacccttccttgattctcattcttgcagtgctgctcaagctggacagaataattccctaatgcttgataaaatcattggtgaaaaaaggaggcgaatacagatcacaatattatcataccactcttcaattggagtaagaaaagatgaactagttcatgggtatatattagtttactctgcaaaacggaaagcttcgatgggaatgcttcgagcatttctatcagaagttcaagacaccattcctgtacagctggtggcagttactgacagccaagcagatttttttgaaaatgaggctatcaaagagttaatgactgaaggagaacacattgcaactgagatcactgctaaatttacagcactgtattctttatctcagtatcatcggcaaactgaggtctttactctgttttttagtgatgttctagagaaaaaaaatatgatagaaaattcttatttgtctgataatacaagggaatcaacccatcaaagtgaagatgtttttctaccatctcccagagactgttttccctataataactaccctgattcagatgatgacacagaagcaccacctccttatagtccaattggggatgatgtacagttgcttccaacacctagtgaccgttccagatatagattagatttggaaggaaatgagtatcctattcatagtaccccaaactgtcatgaccatgaacgcaaccataaagtgcctccacctattaaacctaaaccagttgtacctaagacaaatgtgaaaaaactcgatccaaaccttttaaaaacaattgaagctggtattggtaaaaatccaagaaagcagacttcccgggtgcctttggcacatcctgaagatatggatccttcagataactatgcggaacccattgatacaattttcaaacagaagggctattctgatgagatttatgttgtcccagatgatagtcaaaatcgtattaaaattcgaaactcatttgtaaataacacccaaggagatgaagaaaatgggttttctgatagaacctcaaaaagtcatggggaacggaggccttcaaaatacaaatataaatctaaaaccttgtttagtaaagccaagtcatactatagaagaacacattcagatgccagtgatgatgaggctttcaccacttctaaaacaaaaagaaaaggaagacatcgtggaagtgaagaagatccacttctttctcctgttgaaacttggaaaggtggtattgataatcctgcaatcacttctgaccaggagttagatgataagaagatgaagaagaaaacccacaaagtgaaagaagataaaaagcagaaaaagaaaactaagaacttcaatccaccaacacgtagaaattgggaaagtaattactttgggatgcccctccaggatctggttacagctgagaagcccataccactatttgttgagaaatgtgtggaatttattgaagatacagggttatgtaccgaaggactctaccgtgtcagcgggaataaaactgaccaagacaatattcaaaagcagtttgatcaagatcataatatcaatctagtgtcaatggaagtaacagtaaatgctgtagctggagcccttaaagctttctttgcagatctgccagatcctttaattccatattctcttcatccagaactattggaagcagcaaaaatcccggataaaacagaacgtcttcatgccttgaaagaaattgttaagaaatttcatcctgtaaactatgatgtattcagatacgtgataacacatctaaacagggttagtcagcaacataaaatcaacctaatgacagcagacaacttatccatctgtttttggccaaccttgatgagacctgattttgaaaatcgagagtttctgtctactactaagattcatcaatctgttgttgaaacattcattcagcagtgtcagtttttcttttacaatggagaaattgtagaaacgacaaacattgtggctcctccaccaccttcaaacccaggacagttggtggaaccaatggtgccacttcagttgccgccaccattgcaacctcagctgatacaaccacaattacaaacggatcctcttggtattatatgagtaggaagtgattgcaaacaggctggatttggacaaaaagcaaatctagacatgcatgtttcagggttcagtagtatacttcatgtttcatacagataattcacattcaaaattacattttctctttgaactagatggtattccttattcacttacattacaaatctaagaccatgtgataagcatgactggagaggtttaatttttataaacaaaaatagctataaagtacaaagctgctgctgcatgcaaccttattgcaatcagtatatcattcctgtggcaatttctgtcaccttatattgtgaataaaatttttctatagaaattaaatgatttaaaaactcacctatatgaaacatttaatgcttttcagcctgctttctggctgattttgttatttgatgtgctaatttgggcaacttaatttacattctggcagtcggtgtagataactaaaagcccagttaagtattttataatttcaggctactgaggccatgcttgggatgttgtttgaaagaaagaaaaaatacacttgacatatttcacatttctgtaccttcatctttacttccaagtaaacccgtggatgatttgatgagggataaatgaacctatttcttttacacacataccaaggacatgcttgtggctaaagtgagttgataatgttgtgcaaaggatagttgtcaccaactcatttctttatggtccataatgaaataaaaattttgtatactgttaattctgtaaacagatgcatgttcaaaagatctatgatggtcttgtaatcttaatctaatatattttagatattttaattttttccctcttggggaacacatttagtatagtgtagaaaatacttccatgacattttcatataaggttatataacttttcatacataaacatgaaatttgttgtagaaaattctttaaaccaaacatttaaatctaggacttcaatttaatttgttccttgaatctatttttatgtggcccttaaaaaatatccaaaaaacccattgctaatatagcaataaaaatactttgggtactgacagactctttggagtgtttatattacaaatttgtattcatattcttttctgtgatgtgttgtactaaaatccaaaatggcttttgcaccatttttaagccaattttttcctttgatgttggtaccagaattactataagtgactgctgcttttgggggtaaacattttgttagtgaagataaaaccagaacactaaattatggataaaattttcagaataggtggcacaggtaaatttcactaggttatattttgtgtagtaaagaaaaaaattatttggtcaatgttatcttaattcatactacaatttaagattatcttatgtgtattatagtaaatagatgattttcagattcaaggctcctaagagtttgatttgctctgttttttcctaaaataaatattgtctctcccaactgttaagttctaggtattgtacttccaattttaacttcagaaccaagatgttggcatgaaccaggctgctgttgaagtacatgtatattataaattatcttatttgtgttatactcttacatgttatcttttctaagaaaacaaagtccctattattcctattgcaaagcacacaggaattaagaaagtacagtaatttttaaaaaaaaatccggtaaatgtagtattcttaacctgttctatattacttatacctattgtctatatagctttaatttatagttgtcagtttaactattggcatgtctggcaaagaaaattaaactttaagagttttataaactgtttctaggttgctaaagaatttatttttctactatatatggtatagacaaagcatcaaactatgtacaggaaaaaagcctgactatttctatttggaagtaggctgaaaagagaattttcaaaactgttcgtgtcttcagttcattctgtcataactttgctattgtaatatgtgaataccagtttatttaagctgttctcttttatactgtattaatttaatgttcatctgcgtttagtaccatttttgttattaaaactggcatttaccgtttttcacattaacccaccttgcaccttcccccaaacttatctccacttttctatgcattctatcattgatttgacacacttcatagtgagtcatttaaatactctacgtttggttcaattaaccagtaggttacagttattgaaaattaaagtacagtttaaagctcagtctgttacactgaattgattgtgtttgtttttgccaagggtttagatatgcttttaaatattagaaacatctaagaacagaataacataattaaacttttttctggtaagttactggaaggtttcactgtttagggacctatcatatgagacttcttaaaggattaaaagaataggatagtctcataattgtgagtaaacatcaaggcattatattttacaatactgaataaaatttcatctacacacatgttgccattgtttcatttaaggttcagtgcttatagttaactacaatattggacctaacaggatctagattagcaatataaagaagcatagtggtactctgtttcacactttcagtagatttattagaagtcaaattctattcaacagacacttattaggatatacaactaatttaagaataaaattccaggcacaatatattttttttaaatggtatttgttagtagtgcttcttccccttaacatttacagtgtaaatactgcaggtaaccgcaatctaagttagccaaaaagcagctttttttcccatactgtatgtaaataatgtagacctgggtttttttgtttatttgggtttgtttttttttttgaggtactggaatctaattaatatctcttaggtatcaacaaaagggaacaattggaatgagaatttaggccttagcttccatggtgatttttagttttttatacagtaataattgtgatgctatttgtcaactggatataaatacacatataattttaaaaagtcaaaagtgcttttgtttctttgtttaatgtaatttttgtgcttcacctacaggatgctgcagtaaattaaatatcagtgaagcttctgatgtataaagaatgctatgaataaaacattaagaagctgtgtaattttaagttatagttgcctctatttttaccatttcattggtaaaaattagctaatttttttcaagtgaaatgaaaaataaaaatataaatttatcaatatgatggaaatcttattaaggagatgtattattgaattttcactgtacctgaaaaggagattcaaaattttttctggggatgtatataggtgaaaatttgattttttaaattatcaggaaaacaagataatgcacagatttctaagactaagatcttacctggatgtgatttttgagctgtggctagacattctttagagccactggaaatattttgaaaactattctagttatagcagagctgctaatattaacgaatatatttgtgtcttcatggtttgtgactattaggccaaattttgtggtatatgttgtcagtctggatctggtgaggtctgttcaacatgaatctttgtgttatcttgaatttagtagtttcaaggtacttaaattcttaacagtttctaatttgtttcaatacatatgggacatggttgatttttttactgtattagaactcttggaagttcttagccttttcaggttatgaaatacctgaaagtaaaattttctaagatttaataagggaagatactattcaaatcattttcttaggatagcatctttacatacaatgagaggattgtacaagcattaatctcatattccaacatccagttacttgatgtgatccaagtaccctggtctttttgaagcagttaaaatctaattaattaactttgggagtcttcactattcaattgatcctcatcattgtcctatttgcatgactccattttttcctccactatatgagttttctttgtcagggggagaggagtgggaagagtcacagaatctcatattcacatcttaattaaattgtgtgaaattagtcttttgtggaaattctgtaggcagtatgattttgaaaagctaaccaatgataattagcattttagttaatactaaatgcataaaattataacccttgaaattaatttggtgctggcagttctggtttagtcatttttaccagtagttagtagtattaagacctgcagtatatgcactttttgagtagctgtcaaataattgtagttgagaaacaacttgtttattctcacaattcagattttctattcagttttgtctcaaatagtaagttattgtgaacaatttaataacggccctcctgttctagtttgcctaatattttagttaagatttagtgttttaacctatttttttaagtttattttttgtattagattttatttgaataagttatgtgggtttagtaattgacctatttattcattgcttcactaattcatccagattagttttaagtgtgtatatgtatttgctcaccagatcattttcttgggaccttgaactgtgaatgttttgtcctaaccatttaatattttctaggtacttgctgcaagttcttgaactattttaccagctttaactttggggctcttagtttcttttctccagattcttgttattttattttatccaaataaatatttaggtgttctaagaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:394 -> Molecular function: GO:0003924 [GTPase activity] evidence: TAS
GeneID:394 -> Molecular function: GO:0005100 [Rho GTPase activator activity] evidence: TAS
GeneID:394 -> Molecular function: GO:0005525 [GTP binding] evidence: IEA
GeneID:394 -> Molecular function: GO:0042169 [SH2 domain binding] evidence: IPI
GeneID:394 -> Biological process: GO:0002053 [positive regulation of mesenchymal cell proliferation] evidence: IEA
GeneID:394 -> Biological process: GO:0006184 [GTP catabolic process] evidence: TAS
GeneID:394 -> Biological process: GO:0007155 [cell adhesion] evidence: TAS
GeneID:394 -> Biological process: GO:0007264 [small GTPase mediated signal transduction] evidence: TAS
GeneID:394 -> Biological process: GO:0007266 [Rho protein signal transduction] evidence: TAS
GeneID:394 -> Biological process: GO:0008361 [regulation of cell size] evidence: IEA
GeneID:394 -> Biological process: GO:0030335 [positive regulation of cell migration] evidence: IEA
GeneID:394 -> Biological process: GO:0032321 [positive regulation of Rho GTPase activity] evidence: TAS
GeneID:394 -> Biological process: GO:0051056 [regulation of small GTPase mediated signal transduction] evidence: TAS
GeneID:394 -> Cellular component: GO:0005737 [cytoplasm] evidence: TAS
GeneID:394 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:394 -> Cellular component: GO:0016020 [membrane] evidence: IEA
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