Results for the protein: NP

Results for the Protein: NP_115885

122939147

64333

ARHGAP9

NCBI

rho GTPase-activating protein 9 isoform 1 [Homo sapiens]

Known Diseases associated with this Protein:
RECLASSIFIED - VARIANT OF UNKOWN SIGNIFICANCE

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Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
PH	cd00821	1.1e-13	325	433
RhoGAP_MgcRacGAP	cd04382	2e-13	511	731
RhoGAP-p50rhoGAP	cd04404	1.7e-14	516	730
RhoGAP_nadrin	cd04386	1.4e-13	517	731
RhoGAP_DLC1	cd04375	1.1e-05	519	730
RhoGAP_srGAP	cd04383	5.5e-11	519	725
RhoGAP_CdGAP	cd04384	1.6e-21	519	727
RhoGAP_ARHGAP22_24_2	cd04390	5.2e-11	519	730
RhoGAP_FAM13A1a	cd04393	4.5e-09	519	725
RhoGAP_ARHGAP18	cd04391	2.8e-11	520	730
RhoGAP-ARHGAP11A	cd04394	4.2e-07	520	723
RhoGAP_ARHGAP21	cd04395	3.8e-24	520	730
RhoGAP_fSAC7_BAG7	cd04396	7.4e-07	520	719
RhoGAP_fBEM3	cd04400	2.4e-11	520	706
RhoGAP_ARHGAP20	cd04402	1.1e-07	520	730
RhoGAP_chimaerin	cd04372	1.1e-34	521	730
RhoGAP_p190	cd04373	1.6e-19	521	729
RhoGAP_myosin_IX	cd04377	4.2e-11	521	725
RhoGAP_GMIP_PARG1	cd04378	5.2e-27	521	725
RhoGAP_SYD1	cd04379	1.8e-14	521	727
RhoGAP_ARAP	cd04385	9.8e-14	521	722
RhoGAP_Bcr	cd04387	7.4e-24	521	728
RhoGAP_KIAA1688	cd04389	1.8e-06	521	725
RhoGAP_fLRG1	cd04397	4.6e-06	521	729
RhoGap_RalBP1	cd04381	1.9e-08	521	726
RhoGAP_ARHGAP27_15_1	cd04403	4e-152	521	725
RhoGAP_myosin_IXA	cd04406	2e-08	521	725
RhoGAP_myosin_IXB	cd04407	3.6e-17	521	725
RhoGAP_GMIP	cd04408	1.7e-22	521	725
RhoGAP_PARG1	cd04409	2.6e-20	521	725
RhoGAP_fRGD1	cd04398	1.4e-36	521	730
RhoGAP_Graf	cd04374	2.4e-12	525	707
RhoGAP_ARHGAP6	cd04376	5.3e-10	527	730
RhoGAP_p85	cd04388	3.2e-06	534	725
RhoGAP_ARHGAP19	cd04392	2.1e-06	534	730
RhoGAP	cd00159	6.3e-53	537	725
SH3_1	pfam00018	0.00033	28	71
PH	pfam00169	4.6e-10	323	435
RhoGAP	pfam00620	2.3e-76	537	707
PH	smart00233	7.6e-10	323	435
RhoGAP	smart00324	3.1e-52	534	726

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
dbSNP	rs33927108	Polymorphism	p.ARG50GLY	N/A
dbSNP	rs11544238	Polymorphism	p.SER370ALA	N/A
OMIM	610576.0001	Disease	p.ALA370SER	RECLASSIFIED - VARIANT OF UNKOWN SIGNIFICANCE

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