Mutagenetix > Incidental Mutation

Incidental Mutation 'R3276:Dhx58'

475834

Institutional Source

Beutler Lab

Gene Symbol

Dhx58

Ensembl Gene

ENSMUSG00000017830

Gene Name

DEXH (Asp-Glu-X-His) box polypeptide 58

Synonyms

D11Lgp2e, B430001I08Rik, LPG2

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.159) question?

Stock #

R3276 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

100694884-100704271 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 100696979 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 584 (F584S)

Ref Sequence

ENSEMBL: ENSMUSP00000017974 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000017974] [ENSMUST00000153494]

AlphaFold

Q99J87

Predicted Effect

probably damaging
Transcript: ENSMUST00000017974
AA Change: F584S

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

SMART Domains

Protein: ENSMUSP00000017974
Gene: ENSMUSG00000017830
AA Change: F584S

Domain	Start	End	E-Value	Type
DEXDc	2	207	2.86e-22	SMART
HELICc	387	475	3.85e-14	SMART
Blast:HELICc	497	543	4e-12	BLAST
Pfam:RIG-I_C-RD	552	667	1.5e-37	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126167

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000137154

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140543

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149869

Predicted Effect

probably benign
Transcript: ENSMUST00000153494

SMART Domains

Protein: ENSMUSP00000115268
Gene: ENSMUSG00000014198

Domain	Start	End	E-Value	Type
Pfam:zf-met	42	67	6.4e-8	PFAM
low complexity region	79	102	N/A	INTRINSIC

Meta Mutation Damage Score

0.8758

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.9%
20x: 93.7%

Validation Efficiency

96% (47/49)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to EMCV infection and decreased susceptibility to VSV infection. Mice homozygous for a different knock-out allele exhibit increased susceptibility to WNV infection. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc12	C	T	8: 86,506,866	R1269H	probably damaging	Het
Ace	A	G	11: 105,976,702	E164G	probably null	Het
Als2	A	T	1: 59,170,008	V1464E	possibly damaging	Het
Atox1	A	G	11: 55,450,553	L52P	possibly damaging	Het
Btnl10	A	G	11: 58,922,390	K282E	probably benign	Het
Cdkn3	T	C	14: 46,771,477		probably benign	Het
Col16a1	A	G	4: 130,057,999	K72E	probably damaging	Het
Col6a5	G	A	9: 105,911,107	R1565*	probably null	Het
Col6a6	T	C	9: 105,786,230	H36R	probably benign	Het
Cyp4b1	T	C	4: 115,625,850	N415D	possibly damaging	Het
Dennd4a	G	T	9: 64,888,993	R767L	probably damaging	Het
Dhcr24	T	C	4: 106,561,239	F25L	probably benign	Het
Dhrs3	A	G	4: 144,923,940	T219A	probably benign	Het
Dmbt1	A	G	7: 131,088,071	T715A	probably benign	Het
Eogt	T	A	6: 97,131,394	I229F	probably benign	Het
Ern2	T	C	7: 122,180,964	T164A	possibly damaging	Het
Fam133b	A	T	5: 3,558,522	N84I	probably damaging	Het
Fbxl21	T	A	13: 56,537,122	Y346*	probably null	Het
Fcgbp	C	A	7: 28,091,661	H782Q	probably damaging	Het
Gm11492	T	C	11: 87,567,244	V148A	possibly damaging	Het
Gm5592	A	G	7: 41,288,380	E362G	probably benign	Het
Golga3	T	C	5: 110,201,998		probably benign	Het
Gpatch2l	A	G	12: 86,244,315	T91A	possibly damaging	Het
Hsp90aa1	T	A	12: 110,695,680	M1L	possibly damaging	Het
Hsp90aa1	C	A	12: 110,695,681		probably null	Het
Itgad	C	A	7: 128,190,981	H651N	possibly damaging	Het
Itgav	A	G	2: 83,776,542	D409G	probably damaging	Het
Kcnt2	A	G	1: 140,609,639	N1119S	probably benign	Het
Klhl32	T	C	4: 24,682,063	I207V	probably benign	Het
Klk14	G	A	7: 43,692,077	C51Y	probably damaging	Het
Lhfpl5	T	C	17: 28,579,946	I143T	possibly damaging	Het
Lrrk1	T	C	7: 66,305,521	K431E	possibly damaging	Het
Mag	C	T	7: 30,901,648		probably null	Het
Maml3	A	T	3: 51,856,930	N204K	possibly damaging	Het
Mrpl19	T	C	6: 81,964,066	S115G	probably damaging	Het
Mthfd1l	G	C	10: 4,148,025	G954A	probably damaging	Het
Mut	A	G	17: 40,958,872		probably null	Het
Myo19	A	G	11: 84,892,175	I172V	probably benign	Het
Naca	T	C	10: 128,040,661		probably benign	Het
Nfatc2	T	C	2: 168,506,994	N638D	possibly damaging	Het
Nsun6	A	G	2: 15,009,404		probably benign	Het
Olfr1412	A	G	1: 92,588,813	N161S	probably benign	Het
Olfr584	C	A	7: 103,085,750	D72E	probably damaging	Het
Olfr913	T	A	9: 38,594,643	C141S	probably damaging	Het
Padi6	A	G	4: 140,735,389	L307P	probably damaging	Het
Pafah1b1	G	A	11: 74,690,232	S57F	probably damaging	Het
Prcd	A	G	11: 116,659,811	E103G	possibly damaging	Het
Prkx	A	T	X: 77,771,275	F260I	probably damaging	Het
Rad54l2	A	G	9: 106,753,943		probably null	Het
Ranbp1	T	C	16: 18,247,429		probably benign	Het
Rb1cc1	T	A	1: 6,249,366	M1003K	probably benign	Het
Scap	A	T	9: 110,374,025	M256L	probably benign	Het
Sema4c	C	T	1: 36,549,879	R722H	possibly damaging	Het
Sgk1	C	T	10: 21,996,601	R171W	probably damaging	Het
Spata7	A	G	12: 98,637,598	N75D	possibly damaging	Het
Tmem120b	T	A	5: 123,114,104	I146N	probably damaging	Het
Ttc23l	A	G	15: 10,547,232	F99L	possibly damaging	Het
Ube3a	T	A	7: 59,276,519	C348*	probably null	Het
Ubr4	T	A	4: 139,421,855	D1777E	probably benign	Het
Unc79	C	A	12: 103,113,217	D1880E	probably damaging	Het
Usp36	C	T	11: 118,276,759		probably null	Het
Zswim9	T	C	7: 13,277,270	T51A	possibly damaging	Het

Other mutations in Dhx58

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01395:Dhx58	APN	11	100703926	missense	probably damaging	0.97
IGL02476:Dhx58	APN	11	100702264	missense	probably benign	0.00
R0103:Dhx58	UTSW	11	100695270	missense	probably damaging	1.00
R0103:Dhx58	UTSW	11	100695270	missense	probably damaging	1.00
R0137:Dhx58	UTSW	11	100696997	missense	probably damaging	0.99
R0164:Dhx58	UTSW	11	100695324	missense	probably benign	0.42
R0164:Dhx58	UTSW	11	100695324	missense	probably benign	0.42
R0369:Dhx58	UTSW	11	100701548	critical splice donor site	probably null
R0390:Dhx58	UTSW	11	100699264	missense	probably damaging	1.00
R0606:Dhx58	UTSW	11	100702251	missense	probably benign	0.00
R1710:Dhx58	UTSW	11	100703574	missense	probably benign	0.20
R1816:Dhx58	UTSW	11	100703152	missense	probably damaging	0.98
R1993:Dhx58	UTSW	11	100703490	splice site	probably null
R2281:Dhx58	UTSW	11	100698154	critical splice donor site	probably null
R3176:Dhx58	UTSW	11	100696979	missense	probably damaging	1.00
R4651:Dhx58	UTSW	11	100701359	missense	probably damaging	1.00
R4652:Dhx58	UTSW	11	100701359	missense	probably damaging	1.00
R4716:Dhx58	UTSW	11	100696971	splice site	probably null
R5030:Dhx58	UTSW	11	100696137	missense	probably damaging	1.00
R5082:Dhx58	UTSW	11	100696976	missense	probably benign	0.29
R5098:Dhx58	UTSW	11	100695173	missense	probably benign
R5394:Dhx58	UTSW	11	100698208	missense	probably benign	0.00
R5397:Dhx58	UTSW	11	100703920	missense	probably damaging	1.00
R5787:Dhx58	UTSW	11	100701319	missense	possibly damaging	0.91
R5975:Dhx58	UTSW	11	100702209	missense	probably damaging	0.98
R6310:Dhx58	UTSW	11	100699367	missense	probably benign	0.01
R6935:Dhx58	UTSW	11	100698406	splice site	probably null
R7311:Dhx58	UTSW	11	100698171	missense	probably benign
R7908:Dhx58	UTSW	11	100695304	missense	probably damaging	0.99
R8317:Dhx58	UTSW	11	100703562	missense	probably damaging	1.00
R8821:Dhx58	UTSW	11	100703980	missense	probably damaging	1.00
R8831:Dhx58	UTSW	11	100703980	missense	probably damaging	1.00
R9717:Dhx58	UTSW	11	100701307	missense	probably benign	0.02

Predicted Primers

Posted On

2017-05-11