Mutagenetix > Incidental Mutation

Incidental Mutation 'R0751:Arhgap17'

70328

Institutional Source

Beutler Lab

Gene Symbol

Arhgap17

Ensembl Gene

ENSMUSG00000030766

Gene Name

Rho GTPase activating protein 17

Synonyms

Rich1, Nadrin2, Nadrin, 5730403H17Rik, WBP15

MMRRC Submission

038931-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0751 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

122878441-122969138 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 122913913 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 199 (Y199C)

Ref Sequence

ENSEMBL: ENSMUSP00000145628 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098060] [ENSMUST00000106442] [ENSMUST00000167309] [ENSMUST00000205262] [ENSMUST00000206117] [ENSMUST00000207010]

AlphaFold

Q3UIA2

Predicted Effect

probably damaging
Transcript: ENSMUST00000098060
AA Change: Y199C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000095668
Gene: ENSMUSG00000030766
AA Change: Y199C

Domain	Start	End	E-Value	Type
BAR	1	239	4.45e-65	SMART
RhoGAP	263	439	1.2e-60	SMART
low complexity region	554	595	N/A	INTRINSIC
low complexity region	624	640	N/A	INTRINSIC
low complexity region	644	664	N/A	INTRINSIC
low complexity region	683	704	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000106442
AA Change: Y199C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000102050
Gene: ENSMUSG00000030766
AA Change: Y199C

Domain	Start	End	E-Value	Type
BAR	1	239	4.45e-65	SMART
RhoGAP	263	439	1.2e-60	SMART
low complexity region	542	557	N/A	INTRINSIC
low complexity region	570	582	N/A	INTRINSIC
low complexity region	632	673	N/A	INTRINSIC
low complexity region	702	718	N/A	INTRINSIC
low complexity region	722	742	N/A	INTRINSIC
low complexity region	761	782	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000167309
AA Change: Y199C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000128447
Gene: ENSMUSG00000030766
AA Change: Y199C

Domain	Start	End	E-Value	Type
BAR	1	239	4.45e-65	SMART
RhoGAP	263	439	1.2e-60	SMART
low complexity region	542	557	N/A	INTRINSIC
low complexity region	570	582	N/A	INTRINSIC
low complexity region	632	673	N/A	INTRINSIC
low complexity region	702	718	N/A	INTRINSIC
low complexity region	722	742	N/A	INTRINSIC
low complexity region	761	782	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000205262
AA Change: Y199C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

probably damaging
Transcript: ENSMUST00000206117
AA Change: Y199C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206294

Predicted Effect

probably damaging
Transcript: ENSMUST00000207010
AA Change: Y199C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Meta Mutation Damage Score

0.8177

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 94.4%

Validation Efficiency

99% (73/74)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] RICH1 is a GTPase-activating protein (GAP). GAPs stimulate the intrinsic GTP hydrolysis of small G proteins, such as RHOA (MIM 165390), RAC1 (MIM 602048), and CDC42 (MIM 116952).[supplied by OMIM, Apr 2004]

Allele List at MGI

Other mutations in this stock

Total: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahdc1	T	A	4: 132,792,707 (GRCm39)	M1316K	probably benign	Het
Alox12	T	C	11: 70,137,776 (GRCm39)	I455V	probably benign	Het
Ankrd28	A	G	14: 31,486,225 (GRCm39)	L89P	probably damaging	Het
Aqp9	A	T	9: 71,045,487 (GRCm39)	C41S	probably damaging	Het
Aspm	A	T	1: 139,384,636 (GRCm39)		probably benign	Het
Cacfd1	T	C	2: 26,908,993 (GRCm39)		probably null	Het
Cd33	T	C	7: 43,181,545 (GRCm39)	D205G	probably damaging	Het
Chadl	T	C	15: 81,577,258 (GRCm39)	S198G	probably benign	Het
Chtf8	A	G	8: 107,613,109 (GRCm39)		probably null	Het
Clec4a4	G	T	6: 122,989,671 (GRCm39)	W104L	probably benign	Het
Clock	A	T	5: 76,377,208 (GRCm39)	I696K	possibly damaging	Het
Crtc2	T	A	3: 90,169,940 (GRCm39)	Y445*	probably null	Het
Dapk1	A	T	13: 60,844,112 (GRCm39)	I44F	probably damaging	Het
Dcbld2	T	A	16: 58,270,204 (GRCm39)		probably null	Het
Derl2	T	C	11: 70,905,373 (GRCm39)		probably null	Het
Dnah7c	A	G	1: 46,505,065 (GRCm39)	T154A	probably benign	Het
Dnmt3b	T	A	2: 153,516,762 (GRCm39)		probably null	Het
Dusp3	A	T	11: 101,872,554 (GRCm39)	S106T	probably benign	Het
Eftud2	A	G	11: 102,730,079 (GRCm39)	V897A	probably damaging	Het
Eif3l	T	A	15: 78,959,966 (GRCm39)		probably null	Het
Fbxo33	A	C	12: 59,265,878 (GRCm39)	F130V	probably damaging	Het
Ffar3	T	A	7: 30,554,529 (GRCm39)	N264Y	probably damaging	Het
Fig4	T	C	10: 41,148,978 (GRCm39)	D158G	probably damaging	Het
Fyco1	A	G	9: 123,648,218 (GRCm39)	F1239L	probably damaging	Het
Gabra2	A	G	5: 71,249,442 (GRCm39)		probably benign	Het
Gabra6	C	A	11: 42,205,844 (GRCm39)	R336S	probably benign	Het
Hkdc1	T	C	10: 62,234,452 (GRCm39)	D581G	probably damaging	Het
Ift70a2	C	T	2: 75,808,375 (GRCm39)	A46T	probably damaging	Het
Iqgap1	A	G	7: 80,375,321 (GRCm39)		probably benign	Het
Larp4b	T	C	13: 9,216,345 (GRCm39)		probably benign	Het
Lcp1	A	T	14: 75,436,827 (GRCm39)	M58L	probably benign	Het
Lrrc8a	T	C	2: 30,146,362 (GRCm39)	V392A	possibly damaging	Het
Mavs	A	T	2: 131,088,684 (GRCm39)	Y496F	probably damaging	Het
Mpi	A	T	9: 57,457,897 (GRCm39)	S102T	probably damaging	Het
Mroh9	G	A	1: 162,893,693 (GRCm39)	R161W	possibly damaging	Het
Myo1h	A	T	5: 114,458,747 (GRCm39)	S161C	probably damaging	Het
Napg	T	G	18: 63,127,409 (GRCm39)	H204Q	probably benign	Het
Nelfcd	C	A	2: 174,264,807 (GRCm39)	A182D	probably benign	Het
Ntsr2	G	T	12: 16,704,031 (GRCm39)	K91N	probably damaging	Het
Obscn	A	G	11: 58,972,645 (GRCm39)	S2134P	probably damaging	Het
Ogfod2	G	A	5: 124,251,539 (GRCm39)		probably benign	Het
Or13a19	G	A	7: 139,903,238 (GRCm39)	V209I	probably benign	Het
Or1e26	G	T	11: 73,479,970 (GRCm39)	T198K	probably benign	Het
Pcdha8	T	C	18: 37,127,123 (GRCm39)	V535A	probably damaging	Het
Pdlim2	C	T	14: 70,402,228 (GRCm39)	R296H	probably damaging	Het
Pik3r1	T	C	13: 101,822,866 (GRCm39)		probably null	Het
Pimreg	C	A	11: 71,933,939 (GRCm39)	Q22K	probably benign	Het
Pld5	A	G	1: 175,872,462 (GRCm39)	I225T	probably damaging	Het
Plxnc1	T	C	10: 94,667,195 (GRCm39)		probably benign	Het
Ppip5k2	A	T	1: 97,677,377 (GRCm39)	C306*	probably null	Het
Ptprc	A	G	1: 138,020,668 (GRCm39)	Y588H	probably damaging	Het
Rac2	T	G	15: 78,450,145 (GRCm39)	D65A	possibly damaging	Het
Rgl3	A	G	9: 21,888,676 (GRCm39)		probably null	Het
Serpinb1a	T	C	13: 33,027,199 (GRCm39)	K248E	probably benign	Het
Serpinb9e	A	C	13: 33,443,757 (GRCm39)	E259A	probably benign	Het
Slc12a4	A	T	8: 106,678,532 (GRCm39)	V266E	probably damaging	Het
Slc8b1	A	G	5: 120,662,260 (GRCm39)		probably benign	Het
Spink6	T	C	18: 44,204,605 (GRCm39)		probably benign	Het
Spta1	G	A	1: 174,012,256 (GRCm39)	R354H	probably damaging	Het
Ssb	T	A	2: 69,700,909 (GRCm39)	S330T	probably benign	Het
Stard9	G	T	2: 120,527,966 (GRCm39)	V1408F	probably benign	Het
Sumf2	A	T	5: 129,878,846 (GRCm39)	T61S	probably benign	Het
Sypl2	T	C	3: 108,124,072 (GRCm39)	T157A	probably damaging	Het
Tgfbr3	A	T	5: 107,287,749 (GRCm39)	D483E	probably damaging	Het
Tnrc6a	A	G	7: 122,769,563 (GRCm39)	N451S	possibly damaging	Het
Tradd	T	C	8: 105,986,403 (GRCm39)	E123G	probably damaging	Het
Trim36	T	C	18: 46,329,318 (GRCm39)	T41A	probably damaging	Het
Ttll7	C	T	3: 146,645,746 (GRCm39)	P535S	probably damaging	Het
Ubr4	C	T	4: 139,164,509 (GRCm39)		probably benign	Het
Uqcc5	G	T	14: 30,810,953 (GRCm39)		probably benign	Het
Vmn1r195	A	G	13: 22,463,181 (GRCm39)	Y217C	probably damaging	Het
Vmn2r63	A	C	7: 42,577,459 (GRCm39)	F360V	probably damaging	Het
Vmn2r78	G	A	7: 86,603,588 (GRCm39)	V589M	possibly damaging	Het
Vmn2r-ps158	A	G	7: 42,696,833 (GRCm39)	Y630C	probably damaging	Het
Vrk2	A	G	11: 26,433,331 (GRCm39)		probably benign	Het

Other mutations in Arhgap17

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01012:Arhgap17	APN	7	122,885,791 (GRCm39)	utr 3 prime	probably benign
IGL02112:Arhgap17	APN	7	122,917,640 (GRCm39)	missense	possibly damaging	0.92
IGL02117:Arhgap17	APN	7	122,885,996 (GRCm39)	utr 3 prime	probably benign
IGL03062:Arhgap17	APN	7	122,921,097 (GRCm39)	splice site	probably null
gensing	UTSW	7	122,913,913 (GRCm39)	missense	probably damaging	1.00
Nightshade	UTSW	7	122,926,467 (GRCm39)	missense	probably damaging	1.00
tuberose	UTSW	7	122,907,600 (GRCm39)	missense	probably damaging	1.00
yam	UTSW	7	122,905,643 (GRCm39)	missense	probably damaging	1.00
P0028:Arhgap17	UTSW	7	122,885,900 (GRCm39)	utr 3 prime	probably benign
R0480:Arhgap17	UTSW	7	122,893,867 (GRCm39)	missense	probably damaging	0.98
R0593:Arhgap17	UTSW	7	122,885,966 (GRCm39)	utr 3 prime	probably benign
R0594:Arhgap17	UTSW	7	122,893,741 (GRCm39)	missense	probably benign	0.00
R0599:Arhgap17	UTSW	7	122,903,013 (GRCm39)	splice site	probably benign
R1184:Arhgap17	UTSW	7	122,913,913 (GRCm39)	missense	probably damaging	1.00
R1791:Arhgap17	UTSW	7	122,885,925 (GRCm39)	missense	probably benign	0.23
R2036:Arhgap17	UTSW	7	122,917,717 (GRCm39)	missense	possibly damaging	0.92
R3428:Arhgap17	UTSW	7	122,922,854 (GRCm39)	missense	probably damaging	1.00
R4032:Arhgap17	UTSW	7	122,879,289 (GRCm39)	utr 3 prime	probably benign
R4119:Arhgap17	UTSW	7	122,906,217 (GRCm39)	missense	probably damaging	1.00
R4652:Arhgap17	UTSW	7	122,885,841 (GRCm39)	utr 3 prime	probably benign
R4687:Arhgap17	UTSW	7	122,920,826 (GRCm39)	missense	probably damaging	1.00
R4910:Arhgap17	UTSW	7	122,907,600 (GRCm39)	missense	probably damaging	1.00
R4960:Arhgap17	UTSW	7	122,886,149 (GRCm39)	utr 3 prime	probably benign
R4963:Arhgap17	UTSW	7	122,907,583 (GRCm39)	missense	possibly damaging	0.91
R5028:Arhgap17	UTSW	7	122,893,896 (GRCm39)	missense	probably benign	0.05
R5253:Arhgap17	UTSW	7	122,902,971 (GRCm39)	missense	probably benign	0.00
R5316:Arhgap17	UTSW	7	122,895,750 (GRCm39)	missense	possibly damaging	0.63
R5410:Arhgap17	UTSW	7	122,896,716 (GRCm39)	critical splice donor site	probably null
R5890:Arhgap17	UTSW	7	122,885,981 (GRCm39)	utr 3 prime	probably benign
R6367:Arhgap17	UTSW	7	122,907,586 (GRCm39)	makesense	probably null
R6376:Arhgap17	UTSW	7	122,899,727 (GRCm39)	missense	probably damaging	1.00
R6513:Arhgap17	UTSW	7	122,891,379 (GRCm39)	missense	possibly damaging	0.87
R6862:Arhgap17	UTSW	7	122,921,124 (GRCm39)	missense	probably damaging	0.98
R6962:Arhgap17	UTSW	7	122,895,655 (GRCm39)	missense	probably damaging	1.00
R7077:Arhgap17	UTSW	7	122,879,231 (GRCm39)	missense	unknown
R7178:Arhgap17	UTSW	7	122,884,581 (GRCm39)	splice site	probably null
R7205:Arhgap17	UTSW	7	122,905,661 (GRCm39)	missense	probably damaging	1.00
R7342:Arhgap17	UTSW	7	122,926,467 (GRCm39)	missense	probably damaging	1.00
R7524:Arhgap17	UTSW	7	122,905,643 (GRCm39)	missense	probably damaging	1.00
R7812:Arhgap17	UTSW	7	122,879,290 (GRCm39)	missense	unknown
R7901:Arhgap17	UTSW	7	122,885,791 (GRCm39)	utr 3 prime	probably benign
R7950:Arhgap17	UTSW	7	122,886,039 (GRCm39)	missense	probably benign	0.23
R7952:Arhgap17	UTSW	7	122,885,914 (GRCm39)	missense	probably benign	0.23
R8842:Arhgap17	UTSW	7	122,893,750 (GRCm39)	missense	probably benign	0.07
R9460:Arhgap17	UTSW	7	122,879,286 (GRCm39)	missense	unknown
R9630:Arhgap17	UTSW	7	122,907,540 (GRCm39)	missense	probably benign	0.02
R9766:Arhgap17	UTSW	7	122,921,148 (GRCm39)	missense	probably benign	0.27
RF009:Arhgap17	UTSW	7	122,886,085 (GRCm39)	small deletion	probably benign
RF015:Arhgap17	UTSW	7	122,886,085 (GRCm39)	small deletion	probably benign

Predicted Primers

PCR Primer
(F):5'- CGAGGGTTACATTACCTTGATGGGC -3'
(R):5'- GGCTACCATCTTGCTGTAGGAATGC -3'

Sequencing Primer
(F):5'- GGCCTTTTCTAAGACTGCTAATG -3'
(R):5'- CATCTTGCTGTAGGAATGCTGAAC -3'

Posted On

2013-09-30