Mutagenetix > Incidental Mutation

Incidental Mutation 'R6020:Rnd2'

478880

Institutional Source

Beutler Lab

Gene Symbol

Rnd2

Ensembl Gene

ENSMUSG00000001313

Gene Name

Rho family GTPase 2

Synonyms

Arhn, Rohn

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6020 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

101464999-101471853 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 101468999 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Phenylalanine at position 57 (L57F)

Ref Sequence

ENSEMBL: ENSMUSP00000001347 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000001347] [ENSMUST00000040430]

AlphaFold

Q9QYM5

Predicted Effect

probably damaging
Transcript: ENSMUST00000001347
AA Change: L57F

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

SMART Domains

Protein: ENSMUSP00000001347
Gene: ENSMUSG00000001313
AA Change: L57F

Domain	Start	End	E-Value	Type
RHO	10	184	5.22e-100	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000040430

SMART Domains

Protein: ENSMUSP00000048350
Gene: ENSMUSG00000034993

Domain	Start	End	E-Value	Type
low complexity region	3	31	N/A	INTRINSIC
low complexity region	41	60	N/A	INTRINSIC
Pfam:ADH_N	89	157	8.8e-11	PFAM
Pfam:ADH_zinc_N	213	355	2.1e-21	PFAM
Pfam:ADH_zinc_N_2	245	398	6.9e-22	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134980

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153185

Meta Mutation Damage Score

0.1630

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.8%
20x: 93.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Rho GTPase family, whose members play a key role in the regulation of actin cytoskeleton organization in response to extracellular growth factors. This particular family member has been implicated in the regulation of neuronal morphology and endosomal trafficking. The gene localizes to chromosome 17 and is the centromeric neighbor of the breast-ovarian cancer susceptibility gene BRCA1. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	C	A	11: 110,145,613	V557F	possibly damaging	Het
Abi3	A	T	11: 95,842,025	L41*	probably null	Het
Actn1	C	A	12: 80,174,455		probably null	Het
Adamts15	G	T	9: 30,902,062	R936S	probably benign	Het
Angel2	T	C	1: 190,932,871	S22P	probably benign	Het
Ank2	T	G	3: 126,946,821		probably benign	Het
Astn1	A	G	1: 158,509,993	D423G	probably damaging	Het
Casp9	A	G	4: 141,796,538	D78G	probably damaging	Het
Cbr4	A	G	8: 61,487,853	D2G	probably benign	Het
Ccdc8	T	A	7: 16,996,581	L665H	probably damaging	Het
Cdh23	T	A	10: 60,331,326	N1847I	probably damaging	Het
Cnst	T	C	1: 179,609,875	W335R	probably benign	Het
Ddr2	T	A	1: 170,005,102	I130F	probably benign	Het
Dnah2	C	T	11: 69,500,839	A677T	probably benign	Het
Dzip3	C	A	16: 48,951,842	W488L	probably damaging	Het
Ephb3	T	G	16: 21,222,013	I637S	probably damaging	Het
Etv3	A	G	3: 87,529,364	D142G	probably benign	Het
Fabp5	C	T	3: 10,016,089	T126I	probably benign	Het
Fam13b	A	C	18: 34,494,774	Y125D	probably damaging	Het
Fsip2	C	A	2: 82,992,127	P6068Q	probably damaging	Het
Gm11232	A	G	4: 71,756,668	F199S	possibly damaging	Het
Gm340	G	A	19: 41,583,547	G247D	possibly damaging	Het
Gm5493	A	G	17: 22,748,061	K57E	probably benign	Het
Gm7334	A	G	17: 50,699,237	M184V	probably benign	Het
Gm9894	T	C	13: 67,763,835		noncoding transcript	Het
Gpd2	T	A	2: 57,364,513	N674K	probably benign	Het
H2-M10.6	A	G	17: 36,813,067	Y141C	probably damaging	Het
Heatr5a	C	T	12: 51,884,327	E1796K	probably benign	Het
Hexim2	A	G	11: 103,138,292	T57A	probably benign	Het
Hrg	A	T	16: 22,954,518	N134Y	probably damaging	Het
Hsd17b12	T	C	2: 94,033,977	T262A	probably damaging	Het
Irak3	G	T	10: 120,143,137	P470T	probably damaging	Het
Itgbl1	A	T	14: 123,846,565	D285V	probably damaging	Het
Kcp	A	T	6: 29,502,864	V164E	probably benign	Het
Klhdc7b	T	A	15: 89,388,386	M1157K	probably damaging	Het
Mdc1	G	A	17: 35,848,633	G635D	probably benign	Het
Mdc1	A	G	17: 35,857,572	K1690R	probably benign	Het
Mpp3	A	T	11: 102,018,539		probably benign	Het
Ncor2	G	T	5: 125,020,011	H2285N	probably benign	Het
Neb	T	A	2: 52,257,827	T2727S	probably benign	Het
Nkx6-2	T	C	7: 139,581,567	D234G	possibly damaging	Het
Nlrp9c	T	C	7: 26,384,725	I476M	probably benign	Het
Nrsn1	T	G	13: 25,253,372	Q191P	probably damaging	Het
Olfr116	A	T	17: 37,623,967	S223T	possibly damaging	Het
Olfr390	C	T	11: 73,787,552	L205F	probably benign	Het
Olfr610	T	A	7: 103,506,799	H49L	probably benign	Het
Patl1	T	G	19: 11,937,354	L623R	probably damaging	Het
Pdc	T	C	1: 150,333,366	I200T	probably benign	Het
Pdzk1	A	G	3: 96,868,426	D370G	probably benign	Het
Pglyrp3	A	T	3: 92,031,534	I339F	probably damaging	Het
Plxnb1	T	C	9: 109,116,611	V2070A	probably damaging	Het
Poln	G	A	5: 34,109,431	R461C	probably damaging	Het
Prl2b1	C	A	13: 27,383,508	V218L	probably damaging	Het
Pygl	T	C	12: 70,216,654	D55G	probably damaging	Het
Rif1	C	G	2: 52,095,844	L614V	probably damaging	Het
RP24-351P7.8	T	C	7: 11,610,301	F62S	probably damaging	Het
Rsrp1	T	C	4: 134,924,381	F152S	probably damaging	Het
Sim2	T	C	16: 94,097,251	S115P	probably damaging	Het
Slc17a1	T	A	13: 23,875,610	I108K	possibly damaging	Het
Slc30a8	A	G	15: 52,325,658	D223G	probably damaging	Het
Slc39a4	A	T	15: 76,616,142	N69K	probably benign	Het
Slc51a	T	G	16: 32,479,766	T58P	probably damaging	Het
Slc7a14	T	C	3: 31,224,112	H448R	probably benign	Het
Smc3	G	A	19: 53,625,163		probably null	Het
Sox6	A	T	7: 115,486,628	D659E	probably damaging	Het
Stard9	GCCC	GCC	2: 120,693,715		probably null	Het
Tsr1	C	T	11: 74,900,293		probably null	Het
Ttc12	T	C	9: 49,443,122	K565E	probably damaging	Het
Ube4b	A	T	4: 149,368,311	V386E	probably benign	Het
Ush2a	T	A	1: 188,728,096		probably null	Het
Usp5	C	A	6: 124,817,613		probably benign	Het
Vmn1r216	T	C	13: 23,099,935	F263L	probably benign	Het
Vmn2r88	T	A	14: 51,418,149	L606*	probably null	Het
Wee2	T	A	6: 40,449,620		probably null	Het
Zfhx3	T	C	8: 108,792,527	Y94H	probably damaging	Het
Zfp385c	G	A	11: 100,632,768	P120L	probably benign	Het

Other mutations in Rnd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00596:Rnd2	APN	11	101471191	missense	possibly damaging	0.81
IGL01964:Rnd2	APN	11	101470806	splice site	probably null
Atkins	UTSW	11	101468999	missense	probably damaging	1.00
R1581:Rnd2	UTSW	11	101471196	missense	probably benign
R4606:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R4797:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R4824:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R4825:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R4931:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5005:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5078:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5079:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5402:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5405:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5497:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5498:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5501:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5534:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5619:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5666:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5669:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5670:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5671:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5786:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5788:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5844:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5845:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5857:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5989:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5991:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R5992:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6018:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6019:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6122:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6144:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6148:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6208:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6209:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6226:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6230:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6332:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6333:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6335:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6491:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6541:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6605:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6606:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6607:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6677:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6678:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6726:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6796:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R6797:Rnd2	UTSW	11	101468999	missense	probably damaging	1.00
R8415:Rnd2	UTSW	11	101471185	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCTGTCTAGGGACTGAGCTG -3'
(R):5'- GGCCGATATTAGACTTCCTACGTG -3'

Sequencing Primer
(F):5'- TCTAGGGACTGAGCTGGACCG -3'
(R):5'- GGTTTCTGTCAGGCCTAAGAAACTC -3'

Posted On

2017-06-26