Mutagenetix > Incidental Mutation

Incidental Mutation 'R5931:4930590J08Rik'

461841

Institutional Source

Beutler Lab

Gene Symbol

4930590J08Rik

Ensembl Gene

ENSMUSG00000034063

Gene Name

RIKEN cDNA 4930590J08 gene

Synonyms

LOC381798

MMRRC Submission

044126-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5931 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

91879790-91927706 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 91896096 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Tryptophan at position 315 (R315W)

Ref Sequence

ENSEMBL: ENSMUSP00000146101 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000059318] [ENSMUST00000205686]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000059318
AA Change: R315W

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000053778
Gene: ENSMUSG00000034063
AA Change: R315W

Domain	Start	End	E-Value	Type
low complexity region	89	109	N/A	INTRINSIC
Pfam:FAM194	357	561	4.1e-68	PFAM
low complexity region	626	637	N/A	INTRINSIC
transmembrane domain	774	796	N/A	INTRINSIC
low complexity region	891	909	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000205686
AA Change: R315W

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.1%
20x: 94.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Atrn	A	T	2: 130,775,356 (GRCm39)	Y153F	possibly damaging	Het
C4b	A	G	17: 34,948,167 (GRCm39)	V1644A	probably damaging	Het
Carmil3	A	C	14: 55,736,397 (GRCm39)	K654T	probably damaging	Het
Cdh1	T	C	8: 107,392,964 (GRCm39)		probably null	Het
Chrna1	C	T	2: 73,398,444 (GRCm39)	V332M	probably benign	Het
Clca3a2	A	C	3: 144,797,886 (GRCm39)	V193G	possibly damaging	Het
Cyld	A	G	8: 89,456,470 (GRCm39)		probably null	Het
Dbt	A	T	3: 116,317,074 (GRCm39)	E83D	possibly damaging	Het
Deup1	T	C	9: 15,472,618 (GRCm39)	R471G	possibly damaging	Het
Dgcr2	T	A	16: 17,675,173 (GRCm39)	I188F	possibly damaging	Het
Dgkg	G	A	16: 22,376,788 (GRCm39)	R524*	probably null	Het
Dnaaf9	G	A	2: 130,656,109 (GRCm39)	T2M	probably damaging	Het
Dnah5	A	T	15: 28,453,425 (GRCm39)	R4399W	probably damaging	Het
Egflam	G	A	15: 7,273,338 (GRCm39)	T579I	possibly damaging	Het
Eif2b2	C	T	12: 85,269,561 (GRCm39)	T211I	probably damaging	Het
Ep400	A	G	5: 110,883,386 (GRCm39)		probably benign	Het
Ermp1	C	G	19: 29,593,129 (GRCm39)	A788P	probably benign	Het
Ern1	A	G	11: 106,317,699 (GRCm39)	S142P	possibly damaging	Het
Fbxo15	T	A	18: 84,999,250 (GRCm39)	C351S	probably damaging	Het
Fndc3a	A	T	14: 72,806,307 (GRCm39)	S444T	probably benign	Het
Gabra6	G	A	11: 42,198,268 (GRCm39)	T384M	probably benign	Het
Gpbp1l1	T	C	4: 116,447,457 (GRCm39)	V379A	probably benign	Het
Hook2	G	T	8: 85,722,375 (GRCm39)	E305*	probably null	Het
Hoxa3	G	A	6: 52,149,568 (GRCm39)	A21V	probably damaging	Het
Hs1bp3	C	A	12: 8,391,915 (GRCm39)	P339Q	probably benign	Het
Igha	T	A	12: 113,223,710 (GRCm39)	T49S	probably benign	Het
Klra4	C	T	6: 130,030,016 (GRCm39)	V190M	possibly damaging	Het
Lats2	A	G	14: 57,933,588 (GRCm39)	L843P	probably damaging	Het
Lcmt1	A	G	7: 123,020,839 (GRCm39)	T255A	probably benign	Het
Lpar6	A	G	14: 73,476,368 (GRCm39)	I110V	probably damaging	Het
Lrrtm4	A	G	6: 79,998,722 (GRCm39)	I44V	probably damaging	Het
Mcm3ap	T	C	10: 76,307,000 (GRCm39)	V371A	probably benign	Het
Muc20	A	T	16: 32,614,944 (GRCm39)	D144E	possibly damaging	Het
Nphp3	T	A	9: 103,897,945 (GRCm39)	D417E	probably damaging	Het
Or7g33	A	T	9: 19,448,629 (GRCm39)	I199K	probably benign	Het
Or8b40	A	G	9: 38,027,670 (GRCm39)	I193V	probably benign	Het
Paqr7	A	C	4: 134,235,031 (GRCm39)	Y296S	probably damaging	Het
Pcdha4	A	T	18: 37,087,808 (GRCm39)	T664S	probably damaging	Het
Pelo	T	A	13: 115,225,379 (GRCm39)	Y282F	probably benign	Het
Plxna2	A	T	1: 194,493,178 (GRCm39)	I1818F	probably damaging	Het
Pnkd	A	G	1: 74,389,833 (GRCm39)	D319G	probably benign	Het
Pnma8a	C	A	7: 16,694,809 (GRCm39)	N221K	probably benign	Het
Ppp1cb	T	A	5: 32,640,810 (GRCm39)		probably null	Het
Prkca	T	G	11: 107,905,136 (GRCm39)	I201L	probably benign	Het
Prp2rt	A	G	13: 97,235,705 (GRCm39)	L14S	probably benign	Het
Rfx2	G	A	17: 57,087,778 (GRCm39)	R538C	probably damaging	Het
Rph3a	T	C	5: 121,101,936 (GRCm39)	Q100R	probably damaging	Het
Rtel1	C	T	2: 180,972,608 (GRCm39)	R29*	probably null	Het
Scel	T	A	14: 103,843,060 (GRCm39)	Y547*	probably null	Het
Sp100	C	T	1: 85,606,804 (GRCm39)	P303L	probably damaging	Het
Stk31	A	G	6: 49,446,236 (GRCm39)	S958G	probably benign	Het
Syne2	T	A	12: 76,055,639 (GRCm39)	V4168E	probably benign	Het
Tenm3	A	T	8: 49,099,533 (GRCm39)	S91T	probably benign	Het
Tmcc2	TTGCTGCTGCTGCTGCTGC	TTGCTGCTGCTGCTGC	1: 132,285,493 (GRCm39)		probably benign	Het
Tmem248	T	A	5: 130,258,349 (GRCm39)	I14N	probably damaging	Het
Tor3a	T	C	1: 156,484,057 (GRCm39)	I298V	probably benign	Het
Trim69	A	T	2: 122,009,075 (GRCm39)	K378N	probably damaging	Het
Ttc28	C	T	5: 111,232,975 (GRCm39)	P151S	possibly damaging	Het
Uaca	T	C	9: 60,779,294 (GRCm39)	V1225A	probably damaging	Het
Vps4b	T	C	1: 106,705,065 (GRCm39)	I343V	probably benign	Het
Wnk4	A	G	11: 101,152,047 (GRCm39)	T184A	probably damaging	Het
Ythdc2	T	A	18: 45,006,023 (GRCm39)	I1172K	possibly damaging	Het

Other mutations in 4930590J08Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01090:4930590J08Rik	APN	6	91,896,099 (GRCm39)	missense	possibly damaging	0.74
IGL01478:4930590J08Rik	APN	6	91,911,590 (GRCm39)	missense	probably benign	0.01
IGL01481:4930590J08Rik	APN	6	91,910,079 (GRCm39)	missense	probably damaging	1.00
IGL01485:4930590J08Rik	APN	6	91,927,003 (GRCm39)	missense	probably damaging	0.96
IGL01794:4930590J08Rik	APN	6	91,895,093 (GRCm39)	nonsense	probably null
IGL01795:4930590J08Rik	APN	6	91,895,093 (GRCm39)	nonsense	probably null
IGL02040:4930590J08Rik	APN	6	91,895,091 (GRCm39)	missense	probably benign
IGL02171:4930590J08Rik	APN	6	91,921,237 (GRCm39)	missense	probably benign	0.01
IGL02968:4930590J08Rik	APN	6	91,900,454 (GRCm39)	missense	probably damaging	1.00
IGL03358:4930590J08Rik	APN	6	91,905,716 (GRCm39)	missense	probably damaging	1.00
PIT4519001:4930590J08Rik	UTSW	6	91,894,038 (GRCm39)	missense	probably damaging	1.00
R0531:4930590J08Rik	UTSW	6	91,892,127 (GRCm39)	missense	probably benign
R0569:4930590J08Rik	UTSW	6	91,919,559 (GRCm39)	nonsense	probably null
R1536:4930590J08Rik	UTSW	6	91,894,016 (GRCm39)	missense	probably benign	0.20
R1730:4930590J08Rik	UTSW	6	91,896,259 (GRCm39)	missense	possibly damaging	0.60
R1758:4930590J08Rik	UTSW	6	91,892,203 (GRCm39)	missense	possibly damaging	0.79
R1783:4930590J08Rik	UTSW	6	91,896,259 (GRCm39)	missense	possibly damaging	0.60
R1911:4930590J08Rik	UTSW	6	91,927,050 (GRCm39)	splice site	probably benign
R1930:4930590J08Rik	UTSW	6	91,892,002 (GRCm39)	missense	probably benign	0.01
R1936:4930590J08Rik	UTSW	6	91,894,061 (GRCm39)	missense	possibly damaging	0.90
R2157:4930590J08Rik	UTSW	6	91,919,468 (GRCm39)	missense	possibly damaging	0.48
R2157:4930590J08Rik	UTSW	6	91,894,679 (GRCm39)	splice site	probably null
R4072:4930590J08Rik	UTSW	6	91,922,342 (GRCm39)	splice site	probably null
R4662:4930590J08Rik	UTSW	6	91,891,939 (GRCm39)	missense	probably benign
R4900:4930590J08Rik	UTSW	6	91,895,091 (GRCm39)	missense	probably benign
R4936:4930590J08Rik	UTSW	6	91,921,245 (GRCm39)	missense	probably damaging	1.00
R5394:4930590J08Rik	UTSW	6	91,896,174 (GRCm39)	missense	probably benign	0.00
R5887:4930590J08Rik	UTSW	6	91,892,124 (GRCm39)	nonsense	probably null
R6174:4930590J08Rik	UTSW	6	91,919,517 (GRCm39)	missense	probably damaging	0.99
R6179:4930590J08Rik	UTSW	6	91,919,311 (GRCm39)	missense	probably damaging	0.96
R6380:4930590J08Rik	UTSW	6	91,900,118 (GRCm39)	missense	probably damaging	1.00
R6531:4930590J08Rik	UTSW	6	91,926,980 (GRCm39)	missense	possibly damaging	0.88
R7570:4930590J08Rik	UTSW	6	91,911,591 (GRCm39)	missense	probably benign	0.03
R7860:4930590J08Rik	UTSW	6	91,905,707 (GRCm39)	missense	probably damaging	1.00
R7936:4930590J08Rik	UTSW	6	91,900,445 (GRCm39)	nonsense	probably null
R7958:4930590J08Rik	UTSW	6	91,911,464 (GRCm39)	missense	probably benign	0.02
R7968:4930590J08Rik	UTSW	6	91,922,441 (GRCm39)	missense
R8111:4930590J08Rik	UTSW	6	91,894,691 (GRCm39)	missense	probably benign
R8953:4930590J08Rik	UTSW	6	91,892,002 (GRCm39)	missense	probably benign	0.01
R9084:4930590J08Rik	UTSW	6	91,892,016 (GRCm39)	missense	probably damaging	0.97
R9154:4930590J08Rik	UTSW	6	91,926,926 (GRCm39)	missense	probably benign	0.09
R9319:4930590J08Rik	UTSW	6	91,922,446 (GRCm39)	missense	probably damaging	0.97

Predicted Primers

PCR Primer
(F):5'- TAATCTTCCCAGGGCACTGC -3'
(R):5'- ATGCAGCTTGATGGGCTTC -3'

Sequencing Primer
(F):5'- ACTACCTTAGCATATGAGGAAGAAC -3'
(R):5'- CAGCTTGATGGGCTTCTTGGG -3'

Posted On

2017-02-28