Mutagenetix > Incidental Mutation

Incidental Mutation 'R5993:Rhov'

480931

Institutional Source

Beutler Lab

Gene Symbol

Rhov

Ensembl Gene

ENSMUSG00000034226

Gene Name

ras homolog family member V

Synonyms

Arhv, A030005A06Rik

MMRRC Submission

044172-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.246) question?

Stock #

R5993 (G1)

Quality Score

99.0078

Status

Not validated

Chromosome

Chromosomal Location

119099682-119101753 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 119100533 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 235 (F235L)

Ref Sequence

ENSEMBL: ENSMUSP00000041411 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037360]

AlphaFold

Q8VDU1

Predicted Effect

probably damaging
Transcript: ENSMUST00000037360
AA Change: F235L

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000041411
Gene: ENSMUSG00000034226
AA Change: F235L

Domain	Start	End	E-Value	Type
low complexity region	2	30	N/A	INTRINSIC
RHO	34	208	3.12e-89	SMART

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.3%
20x: 91.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts20	G	T	15: 94,236,604 (GRCm39)	N805K	probably damaging	Het
Add1	A	C	5: 34,758,877 (GRCm39)	S64R	probably damaging	Het
Alas1	A	G	9: 106,111,328 (GRCm39)	F613L	probably benign	Het
Ankrd17	A	T	5: 90,487,531 (GRCm39)		probably benign	Het
Anks3	C	T	16: 4,776,001 (GRCm39)	G67D	probably damaging	Het
Aspm	C	T	1: 139,407,269 (GRCm39)	T2052I	probably benign	Het
Atp8b4	C	T	2: 126,245,154 (GRCm39)	V332I	probably benign	Het
Bin2	CGGAGCTGA	C	15: 100,542,901 (GRCm39)		probably null	Het
Bpifb3	T	A	2: 153,771,234 (GRCm39)	M382K	probably benign	Het
Ccdc149	C	T	5: 52,560,117 (GRCm39)	R246Q	probably damaging	Het
Ccdc57	T	C	11: 120,785,550 (GRCm39)	K462E	possibly damaging	Het
Cux1	T	C	5: 136,392,125 (GRCm39)	T9A	probably benign	Het
Cyp2c23	A	G	19: 44,000,799 (GRCm39)	Y362H	probably damaging	Het
D430041D05Rik	A	G	2: 103,998,412 (GRCm39)	I998T	probably damaging	Het
Dclre1a	A	C	19: 56,531,169 (GRCm39)	Y726D	probably damaging	Het
Dnah5	T	C	15: 28,299,372 (GRCm39)	V1578A	probably benign	Het
Dppa4	C	T	16: 48,109,709 (GRCm39)	R110*	probably null	Het
Drc7	T	A	8: 95,800,820 (GRCm39)	V614E	probably benign	Het
Garin2	C	A	12: 78,762,210 (GRCm39)	N12K	probably damaging	Het
Gcc1	G	A	6: 28,424,851 (GRCm39)		probably null	Het
Greb1l	G	A	18: 10,544,455 (GRCm39)	D1350N	probably benign	Het
Kcnc1	G	A	7: 46,076,956 (GRCm39)	V253M	probably damaging	Het
Krt78	T	A	15: 101,858,884 (GRCm39)	I323F	probably damaging	Het
Man2b2	A	G	5: 36,978,324 (GRCm39)	V320A	probably benign	Het
Mphosph9	A	T	5: 124,454,161 (GRCm39)	F112Y	probably benign	Het
Mrc1	A	G	2: 14,310,138 (GRCm39)	T800A	probably damaging	Het
Mroh1	C	A	15: 76,330,880 (GRCm39)	A1197E	probably damaging	Het
Nlrp10	A	T	7: 108,526,220 (GRCm39)	H39Q	probably benign	Het
Nop2	C	T	6: 125,120,982 (GRCm39)	T588I	probably benign	Het
Oxld1	A	G	11: 120,347,835 (GRCm39)	S121P	probably benign	Het
Pakap	A	G	4: 57,855,273 (GRCm39)	K444E	possibly damaging	Het
Prox1	T	A	1: 189,894,436 (GRCm39)	D3V	probably damaging	Het
Ptk7	T	C	17: 46,876,296 (GRCm39)	T1052A	probably benign	Het
Rhot2	T	A	17: 26,060,085 (GRCm39)	T299S	probably benign	Het
Runx1t1	A	T	4: 13,841,863 (GRCm39)	R158S	probably damaging	Het
Runx1t1	A	T	4: 13,875,490 (GRCm39)	E431D	probably benign	Het
Sema3e	A	G	5: 14,274,307 (GRCm39)	E186G	probably damaging	Het
Sema5b	T	A	16: 35,466,572 (GRCm39)	L158H	probably damaging	Het
Serpina3j	A	G	12: 104,280,946 (GRCm39)	T40A	probably benign	Het
Shroom3	A	T	5: 93,088,047 (GRCm39)	S185C	probably damaging	Het
Skint6	A	T	4: 112,666,276 (GRCm39)	V1183D	probably benign	Het
Smg1	A	G	7: 117,739,732 (GRCm39)	V3405A	probably benign	Het
Supt16	C	A	14: 52,415,791 (GRCm39)	R357L	probably damaging	Het
Thrap3	A	T	4: 126,069,253 (GRCm39)		probably null	Het
Topaz1	T	C	9: 122,578,104 (GRCm39)	L338S	probably benign	Het
Ttll3	T	A	6: 113,374,992 (GRCm39)	Y139*	probably null	Het
Ttn	T	G	2: 76,626,251 (GRCm39)	D6641A	probably damaging	Het
Wwc1	T	C	11: 35,743,163 (GRCm39)	D886G	probably benign	Het
Zc3h7a	T	A	16: 10,968,526 (GRCm39)	K484N	probably damaging	Het

Other mutations in Rhov

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01871:Rhov	APN	2	119,101,219 (GRCm39)	missense	probably benign	0.15
R0732:Rhov	UTSW	2	119,101,495 (GRCm39)	missense	probably damaging	1.00
R1646:Rhov	UTSW	2	119,101,501 (GRCm39)	missense	probably damaging	1.00
R4997:Rhov	UTSW	2	119,100,949 (GRCm39)	missense	probably damaging	1.00
R5124:Rhov	UTSW	2	119,101,568 (GRCm39)	missense	unknown
R6168:Rhov	UTSW	2	119,101,453 (GRCm39)	missense	probably damaging	1.00
R9380:Rhov	UTSW	2	119,100,604 (GRCm39)	missense	probably benign	0.03
Z1177:Rhov	UTSW	2	119,100,896 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CCTGTGAGTCTTGACCAAAGAAATC -3'
(R):5'- AGGGTCTGGCTGAGAAGATC -3'

Sequencing Primer
(F):5'- ATCCAAATGGGGCAGCC -3'
(R):5'- TGAGAAGATCCGCGCCTG -3'

Posted On

2017-06-26