Mutagenetix > Incidental Mutation

Incidental Mutation 'R0265:9330182L06Rik'

34839

Institutional Source

Beutler Lab

Gene Symbol

9330182L06Rik

Ensembl Gene

ENSMUSG00000056004

Gene Name

RIKEN cDNA 9330182L06 gene

Synonyms

MMRRC Submission

038491-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0265 (G1)

Quality Score

157

Status

Validated

Chromosome

Chromosomal Location

9266118-9481825 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 9434681 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 486 (L486P)

Ref Sequence

ENSEMBL: ENSMUSP00000120849 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069538] [ENSMUST00000115348] [ENSMUST00000134991] [ENSMUST00000152095] [ENSMUST00000154662] [ENSMUST00000155764]

AlphaFold

Q3UZV7

Predicted Effect

probably damaging
Transcript: ENSMUST00000069538
AA Change: L486P

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000069165
Gene: ENSMUSG00000056004
AA Change: L486P

Domain	Start	End	E-Value	Type
signal peptide	1	47	N/A	INTRINSIC
internal_repeat_1	58	334	1.12e-7	PROSPERO
internal_repeat_1	343	665	1.12e-7	PROSPERO
transmembrane domain	926	948	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000115348

SMART Domains

Protein: ENSMUSP00000111005
Gene: ENSMUSG00000056004

Domain	Start	End	E-Value	Type
signal peptide	1	47	N/A	INTRINSIC
low complexity region	213	224	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000134991
AA Change: L486P

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000121757
Gene: ENSMUSG00000056004
AA Change: L486P

Domain	Start	End	E-Value	Type
signal peptide	1	47	N/A	INTRINSIC
internal_repeat_1	58	334	9.82e-8	PROSPERO
internal_repeat_1	343	665	9.82e-8	PROSPERO
transmembrane domain	926	948	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000152095

SMART Domains

Protein: ENSMUSP00000116440
Gene: ENSMUSG00000056004

Domain	Start	End	E-Value	Type
low complexity region	7	24	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000154662

SMART Domains

Protein: ENSMUSP00000116026
Gene: ENSMUSG00000056004

Domain	Start	End	E-Value	Type
signal peptide	1	47	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000155764
AA Change: L486P

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000120849
Gene: ENSMUSG00000056004
AA Change: L486P

Domain	Start	End	E-Value	Type
signal peptide	1	47	N/A	INTRINSIC
internal_repeat_1	58	180	5.47e-6	PROSPERO
internal_repeat_1	343	476	5.47e-6	PROSPERO

Meta Mutation Damage Score

0.7104

Coding Region Coverage

1x: 98.5%
3x: 97.4%
10x: 95.6%
20x: 92.0%

Validation Efficiency

99% (83/84)

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930452B06Rik	T	G	14: 8,431,667	Y655S	probably damaging	Het
Abca14	A	G	7: 120,223,627	I321V	probably benign	Het
Adcy7	A	G	8: 88,324,763	D837G	probably damaging	Het
Aldh1a1	T	A	19: 20,640,076	Y457*	probably null	Het
Alox5	T	C	6: 116,420,362	Y287C	probably benign	Het
Ano8	T	C	8: 71,480,524		probably benign	Het
Ap3b1	A	G	13: 94,493,681	K815E	unknown	Het
Atp11a	A	T	8: 12,856,930		probably benign	Het
Atp6v0a1	A	T	11: 101,048,515	D702V	possibly damaging	Het
Cacna1b	T	A	2: 24,761,844	N108Y	probably damaging	Het
Ccdc57	G	C	11: 120,921,811	A39G	probably benign	Het
Cdhr1	A	T	14: 37,081,376	V581D	probably benign	Het
Cyp2b23	A	G	7: 26,672,879		probably benign	Het
D430041D05Rik	G	C	2: 104,167,950	P1836R	probably damaging	Het
Ddit4l	C	T	3: 137,624,287		probably benign	Het
Dnah8	A	T	17: 30,690,271	I1024F	probably benign	Het
Edc3	T	A	9: 57,727,338	F213I	probably damaging	Het
Edrf1	G	A	7: 133,657,045	D717N	probably damaging	Het
Efna5	G	A	17: 62,651,073	P63S	probably damaging	Het
Entpd3	A	G	9: 120,558,481	Y248C	probably damaging	Het
Flcn	G	A	11: 59,795,809	Q373*	probably null	Het
Fry	T	C	5: 150,434,776	V1908A	probably damaging	Het
Gabrg3	A	T	7: 57,381,617	Y58*	probably null	Het
Gabrp	A	T	11: 33,552,614	Y417N	probably damaging	Het
Golga2	C	A	2: 32,304,952		probably null	Het
Grip2	C	A	6: 91,773,792		probably null	Het
Gsx2	A	G	5: 75,077,068	Y227C	probably damaging	Het
Hif3a	T	C	7: 17,035,868	*665W	probably null	Het
Hist1h2aa	T	C	13: 23,934,649	V63A	probably benign	Het
Hsd3b1	C	A	3: 98,852,773	V301L	probably damaging	Het
Ifitm5	T	C	7: 140,950,008		probably benign	Het
Inpp4a	A	T	1: 37,378,986	D498V	probably damaging	Het
Itga1	A	T	13: 114,992,459	D554E	probably benign	Het
Itk	G	A	11: 46,389,458		probably benign	Het
Kdm3b	T	A	18: 34,795,663		probably benign	Het
Klhl6	A	G	16: 19,948,234	V470A	probably benign	Het
Lamb3	T	A	1: 193,320,531	W95R	probably damaging	Het
Lbhd2	T	A	12: 111,410,242	I41N	probably damaging	Het
Lrp4	A	T	2: 91,490,670	S1014C	probably damaging	Het
Ltbp2	C	T	12: 84,785,969		probably null	Het
Map3k19	A	G	1: 127,822,182	I1144T	possibly damaging	Het
Mfsd10	T	C	5: 34,635,163		probably benign	Het
Mocos	A	G	18: 24,666,276	D189G	probably benign	Het
Mvb12a	T	A	8: 71,547,010	F224L	probably damaging	Het
Myo15	A	T	11: 60,514,897		probably null	Het
Nos2	A	T	11: 78,937,602	H249L	probably damaging	Het
Notum	A	G	11: 120,658,334	M184T	probably benign	Het
Nvl	C	A	1: 181,134,830	D192Y	probably damaging	Het
Olfr1024	T	A	2: 85,904,247	N269I	probably benign	Het
Olfr1065	C	A	2: 86,445,959	V8L	probably benign	Het
Olfr1308	T	C	2: 111,960,494	Y193C	probably damaging	Het
Olfr204	A	T	16: 59,315,071	F112Y	probably damaging	Het
Olfr218	A	G	1: 173,203,917	K187R	probably benign	Het
Osgin1	A	G	8: 119,445,657	I397V	possibly damaging	Het
Otulin	A	G	15: 27,616,424	V123A	probably damaging	Het
P4ha1	A	G	10: 59,348,259	Y181C	probably damaging	Het
Pcdhgc5	A	T	18: 37,821,350	D559V	probably damaging	Het
Phf2	T	C	13: 48,828,794	N151S	unknown	Het
Plxnc1	C	A	10: 94,813,129	G1263C	probably benign	Het
Rad51ap1	A	G	6: 126,924,197	*338Q	probably null	Het
Raver1	A	G	9: 21,075,659	S676P	probably benign	Het
Rfx8	T	C	1: 39,688,577	E196G	possibly damaging	Het
Rreb1	A	T	13: 37,916,155	K187*	probably null	Het
Rxfp1	T	C	3: 79,667,654	T217A	probably benign	Het
Rxra	T	C	2: 27,752,430	L305P	probably damaging	Het
Sardh	T	C	2: 27,227,066		probably benign	Het
Skor2	A	T	18: 76,876,598	E952D	probably damaging	Het
Slc22a29	A	T	19: 8,169,970	S343T	probably benign	Het
Sorbs2	T	C	8: 45,785,337		probably benign	Het
Supt7l	C	T	5: 31,515,918	V329I	probably benign	Het
Taar2	G	A	10: 23,941,495	R311H	probably benign	Het
Tac1	T	C	6: 7,559,165		probably benign	Het
Tcn2	A	T	11: 3,922,044	V361D	probably damaging	Het
Tm2d3	G	A	7: 65,697,834	A170T	possibly damaging	Het
Tnks	G	A	8: 34,839,970	R1142*	probably null	Het
Ttll7	C	A	3: 146,944,160	Y648*	probably null	Het
Umod	G	T	7: 119,466,073	Q578K	probably benign	Het
Upf2	G	A	2: 6,027,204		probably benign	Het
Vmn2r92	C	T	17: 18,167,957	A408V	probably damaging	Het
Washc5	A	G	15: 59,338,960	I1013T	probably benign	Het
Wdr60	T	C	12: 116,257,406		probably benign	Het
Zfp704	C	A	3: 9,565,157	R48L	probably damaging	Het

Other mutations in 9330182L06Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00780:9330182L06Rik	APN	5	9422367	missense	probably damaging	0.99
IGL00909:9330182L06Rik	APN	5	9380282	missense	probably damaging	1.00
IGL01477:9330182L06Rik	APN	5	9437756	missense	probably damaging	1.00
IGL02486:9330182L06Rik	APN	5	9422323	missense	probably benign	0.00
IGL02863:9330182L06Rik	APN	5	9461399	nonsense	probably null
IGL02939:9330182L06Rik	APN	5	9461478	missense	probably damaging	1.00
IGL03039:9330182L06Rik	APN	5	9418055	missense	probably benign	0.12
IGL03395:9330182L06Rik	APN	5	9422359	missense	probably damaging	0.97
R0063:9330182L06Rik	UTSW	5	9440709	intron	probably benign
R0063:9330182L06Rik	UTSW	5	9440709	intron	probably benign
R0193:9330182L06Rik	UTSW	5	9422359	missense	probably damaging	0.97
R0398:9330182L06Rik	UTSW	5	9445367	missense	probably benign	0.00
R0432:9330182L06Rik	UTSW	5	9440966	nonsense	probably null
R0494:9330182L06Rik	UTSW	5	9420723	critical splice donor site	probably null
R0736:9330182L06Rik	UTSW	5	9441745	missense	probably damaging	1.00
R0850:9330182L06Rik	UTSW	5	9417993	missense	probably damaging	1.00
R1398:9330182L06Rik	UTSW	5	9380297	missense	probably damaging	1.00
R1709:9330182L06Rik	UTSW	5	9440726	nonsense	probably null
R1720:9330182L06Rik	UTSW	5	9428407	missense	probably damaging	1.00
R1770:9330182L06Rik	UTSW	5	9418021	missense	probably benign	0.01
R1782:9330182L06Rik	UTSW	5	9421620	missense	possibly damaging	0.62
R1803:9330182L06Rik	UTSW	5	9427832	missense	probably benign	0.05
R1868:9330182L06Rik	UTSW	5	9479251	missense	probably damaging	1.00
R1870:9330182L06Rik	UTSW	5	9418007	missense	probably damaging	0.97
R1871:9330182L06Rik	UTSW	5	9418007	missense	probably damaging	0.97
R1913:9330182L06Rik	UTSW	5	9266275	missense	probably damaging	0.97
R2054:9330182L06Rik	UTSW	5	9463030	missense	possibly damaging	0.81
R2170:9330182L06Rik	UTSW	5	9479206	missense	probably damaging	1.00
R2381:9330182L06Rik	UTSW	5	9380342	missense	probably damaging	1.00
R2396:9330182L06Rik	UTSW	5	9435395	missense	possibly damaging	0.92
R4003:9330182L06Rik	UTSW	5	9440877	missense	probably benign	0.05
R5030:9330182L06Rik	UTSW	5	9428502	missense	probably damaging	1.00
R5049:9330182L06Rik	UTSW	5	9428488	missense	probably damaging	1.00
R5069:9330182L06Rik	UTSW	5	9440897	missense	probably damaging	1.00
R5219:9330182L06Rik	UTSW	5	9461486	missense	probably damaging	1.00
R5400:9330182L06Rik	UTSW	5	9479247	missense	probably damaging	1.00
R5555:9330182L06Rik	UTSW	5	9422296	splice site	probably null
R5593:9330182L06Rik	UTSW	5	9266350	missense	probably benign	0.07
R5681:9330182L06Rik	UTSW	5	9459308	critical splice donor site	probably null
R5707:9330182L06Rik	UTSW	5	9441698	missense	probably damaging	1.00
R5756:9330182L06Rik	UTSW	5	9462995	missense	probably damaging	0.98
R6087:9330182L06Rik	UTSW	5	9399255	missense	probably damaging	1.00
R6252:9330182L06Rik	UTSW	5	9410693	missense	probably damaging	1.00
R7067:9330182L06Rik	UTSW	5	9266295	missense	possibly damaging	0.81
R7078:9330182L06Rik	UTSW	5	9410709	missense	probably benign	0.10
R7079:9330182L06Rik	UTSW	5	9399253	missense	probably damaging	1.00
R7117:9330182L06Rik	UTSW	5	9445384	nonsense	probably null
R7265:9330182L06Rik	UTSW	5	9446975	missense	possibly damaging	0.65
R7996:9330182L06Rik	UTSW	5	9462881	missense	probably damaging	1.00
R8199:9330182L06Rik	UTSW	5	9420657	missense	probably damaging	1.00
R8246:9330182L06Rik	UTSW	5	9446966	missense	probably benign	0.07
R8928:9330182L06Rik	UTSW	5	9446979	missense	possibly damaging	0.86
R8935:9330182L06Rik	UTSW	5	9441764	missense	probably damaging	1.00
R8963:9330182L06Rik	UTSW	5	9437792	missense	probably damaging	1.00
R9140:9330182L06Rik	UTSW	5	9399226	missense	probably benign	0.00
R9244:9330182L06Rik	UTSW	5	9410700	missense	probably damaging	1.00
R9272:9330182L06Rik	UTSW	5	9410699	missense	probably damaging	0.99
R9395:9330182L06Rik	UTSW	5	9427822	missense	probably benign	0.19
R9548:9330182L06Rik	UTSW	5	9440859	missense	probably damaging	1.00
X0019:9330182L06Rik	UTSW	5	9399231	missense	probably damaging	0.97
X0052:9330182L06Rik	UTSW	5	9440908	missense	possibly damaging	0.87
X0063:9330182L06Rik	UTSW	5	9399239	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- TTCCATTGGCTATCAGCAGAGCGG -3'
(R):5'- CAAAGCAGTGCGGTTGTTACAGG -3'

Sequencing Primer
(F):5'- CCACCGTAGTGTGTCAGAATG -3'
(R):5'- GGTTCTCGGAGAGTAATTCCATAGAC -3'

Posted On

2013-05-09