Mutagenetix > Incidental Mutation

Incidental Mutation 'R4825:Dhx8'

371439

Institutional Source

Beutler Lab

Gene Symbol

Dhx8

Ensembl Gene

ENSMUSG00000034931

Gene Name

DEAH-box helicase 8

Synonyms

RNA helicase, Ddx8, mDEAH6

MMRRC Submission

042441-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.968) question?

Stock #

R4825 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

101623782-101658184 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 101628996 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 129 (R129*)

Ref Sequence

ENSEMBL: ENSMUSP00000119430 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039152] [ENSMUST00000129741]

AlphaFold

A2A4P0

Predicted Effect

probably null
Transcript: ENSMUST00000039152
AA Change: R182*

SMART Domains

Protein: ENSMUSP00000037251
Gene: ENSMUSG00000034931
AA Change: R182*

Domain	Start	End	E-Value	Type
low complexity region	2	8	N/A	INTRINSIC
low complexity region	168	240	N/A	INTRINSIC
low complexity region	244	254	N/A	INTRINSIC
S1	287	360	3.52e-18	SMART
low complexity region	453	469	N/A	INTRINSIC
coiled coil region	496	525	N/A	INTRINSIC
DEXDc	587	771	7.26e-33	SMART
HELICc	815	919	7.45e-21	SMART
HA2	980	1070	1.34e-38	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125409

Predicted Effect

probably null
Transcript: ENSMUST00000129741
AA Change: R129*

SMART Domains

Protein: ENSMUSP00000119430
Gene: ENSMUSG00000034931
AA Change: R129*

Domain	Start	End	E-Value	Type
low complexity region	2	8	N/A	INTRINSIC
low complexity region	115	187	N/A	INTRINSIC
low complexity region	191	201	N/A	INTRINSIC
S1	234	307	3.52e-18	SMART
low complexity region	400	416	N/A	INTRINSIC
coiled coil region	443	472	N/A	INTRINSIC
DEXDc	534	718	7.26e-33	SMART
HELICc	762	866	7.45e-21	SMART
HA2	927	1017	1.34e-38	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156842

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.8%
20x: 93.8%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the DEAH box polypeptide family. The encoded protein contains the DEAH (Asp-Glu-Ala-His) motif which is characteristic of all DEAH box proteins, and is thought to function as an ATP-dependent RNA helicase that regulates the release of spliced mRNAs from spliceosomes prior to their export from the nucleus. This protein may be required for the replication of human immunodeficiency virus type 1 (HIV-1). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]

Allele List at MGI

Other mutations in this stock

Total: 130 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700012B07Rik	C	A	11: 109,682,498 (GRCm39)	L229F	probably benign	Het
A930002H24Rik	A	C	17: 64,170,603 (GRCm39)	S62A	unknown	Het
Abca12	T	A	1: 71,341,844 (GRCm39)	Q1039L	possibly damaging	Het
Adgrg5	T	A	8: 95,668,362 (GRCm39)	F476I	possibly damaging	Het
Alms1	A	G	6: 85,655,227 (GRCm39)	K2789E	probably damaging	Het
Arrdc2	G	A	8: 71,291,921 (GRCm39)		probably null	Het
Atp2b1	T	A	10: 98,845,426 (GRCm39)	I743K	probably damaging	Het
Atp6v1c2	C	T	12: 17,339,061 (GRCm39)	G230D	probably benign	Het
AU040320	G	A	4: 126,685,586 (GRCm39)	C54Y	probably damaging	Het
BC024139	C	T	15: 76,004,517 (GRCm39)	V680I	possibly damaging	Het
Bckdhb	A	G	9: 83,870,958 (GRCm39)	D156G	probably damaging	Het
Bltp3a	G	A	17: 28,096,368 (GRCm39)	A107T	probably damaging	Het
Canx	T	A	11: 50,199,636 (GRCm39)	D143V	probably benign	Het
Ccdc180	T	A	4: 45,912,794 (GRCm39)	V591E	possibly damaging	Het
Ccno	T	C	13: 113,124,633 (GRCm39)	S68P	probably benign	Het
Cdc45	C	T	16: 18,603,613 (GRCm39)	E527K	probably damaging	Het
Cep290	T	A	10: 100,324,210 (GRCm39)	D14E	probably damaging	Het
Cgnl1	A	G	9: 71,537,806 (GRCm39)	V1238A	probably benign	Het
Ciz1	C	T	2: 32,261,753 (GRCm39)	A455V	probably damaging	Het
Coro2b	T	A	9: 62,361,905 (GRCm39)	Y86F	probably benign	Het
Csf2ra	C	T	19: 61,214,990 (GRCm39)	R158Q	probably benign	Het
Cubn	A	T	2: 13,330,036 (GRCm39)	I2615N	probably damaging	Het
Disc1	T	A	8: 125,862,041 (GRCm39)	M471K	possibly damaging	Het
Dmxl2	G	T	9: 54,311,325 (GRCm39)	L1799I	probably benign	Het
Dnah2	A	G	11: 69,314,031 (GRCm39)	S4108P	probably damaging	Het
Ecpas	G	A	4: 58,850,911 (GRCm39)	L421F	probably damaging	Het
Ehmt2	C	G	17: 35,125,940 (GRCm39)	P211R	probably benign	Het
Eif4g3	A	G	4: 137,921,392 (GRCm39)	D1557G	probably benign	Het
Epha5	T	C	5: 84,381,699 (GRCm39)	D384G	probably damaging	Het
Etl4	A	G	2: 20,811,738 (GRCm39)	I1274V	probably damaging	Het
Fhip1a	G	A	3: 85,580,739 (GRCm39)	P489S	possibly damaging	Het
Fip1l1	G	A	5: 74,748,866 (GRCm39)		probably null	Het
Fubp1	T	C	3: 151,923,527 (GRCm39)		probably null	Het
Glul	T	C	1: 153,778,790 (GRCm39)	V33A	probably benign	Het
Gm4846	A	G	1: 166,319,237 (GRCm39)	F167S	probably damaging	Het
Heatr6	T	A	11: 83,649,148 (GRCm39)	L168M	probably damaging	Het
Hif1a	T	A	12: 73,979,175 (GRCm39)	I233N	probably damaging	Het
Hivep2	T	A	10: 14,007,063 (GRCm39)	H1220Q	possibly damaging	Het
Igkv8-21	T	C	6: 70,292,410 (GRCm39)	I9M	probably benign	Het
Izumo1	T	A	7: 45,274,411 (GRCm39)	C62*	probably null	Het
Jakmip3	G	A	7: 138,628,495 (GRCm39)	E424K	probably damaging	Het
Klhl2	A	G	8: 65,205,847 (GRCm39)	V358A	probably damaging	Het
Klk10	C	G	7: 43,433,022 (GRCm39)	D139E	probably damaging	Het
Klk14	T	C	7: 43,341,500 (GRCm39)	C51R	probably damaging	Het
Klk1b5	T	G	7: 43,494,814 (GRCm39)	I99S	probably damaging	Het
L3hypdh	T	C	12: 72,124,167 (GRCm39)	T258A	probably benign	Het
Lrp5	A	G	19: 3,664,292 (GRCm39)	Y812H	probably damaging	Het
Lrrc40	T	A	3: 157,766,967 (GRCm39)	L474*	probably null	Het
Mkks	A	T	2: 136,722,575 (GRCm39)	M194K	probably benign	Het
Mmp20	A	G	9: 7,654,121 (GRCm39)	D347G	probably damaging	Het
Mmp27	A	G	9: 7,581,195 (GRCm39)	E460G	probably damaging	Het
Mms22l	T	C	4: 24,536,226 (GRCm39)	F605S	probably damaging	Het
Mpzl3	A	G	9: 44,979,627 (GRCm39)	S193G	probably benign	Het
Muc4	A	T	16: 32,570,565 (GRCm39)	T542S	probably benign	Het
Muc5b	T	C	7: 141,422,202 (GRCm39)	L4446P	possibly damaging	Het
Mxi1	C	A	19: 53,358,769 (GRCm39)	S131*	probably null	Het
Nanog	G	T	6: 122,690,299 (GRCm39)	A210S	probably benign	Het
Nrcam	C	T	12: 44,622,769 (GRCm39)	Q988*	probably null	Het
Nsg1	C	A	5: 38,316,391 (GRCm39)		probably benign	Het
Ogfod3	G	A	11: 121,086,027 (GRCm39)	A189V	probably benign	Het
Or10g9b	A	T	9: 39,918,038 (GRCm39)	M69K	possibly damaging	Het
Or12e9	T	A	2: 87,202,432 (GRCm39)	C185*	probably null	Het
Or4a68	A	G	2: 89,270,209 (GRCm39)	V138A	probably benign	Het
Or4c122	T	C	2: 89,079,034 (GRCm39)		probably null	Het
Or4c35	G	A	2: 89,808,497 (GRCm39)	C125Y	probably damaging	Het
Or51ai2	T	C	7: 103,586,710 (GRCm39)	V41A	probably benign	Het
Or52b4i	T	A	7: 102,191,587 (GRCm39)	V148E	possibly damaging	Het
Or5b111	A	T	19: 13,291,684 (GRCm39)		probably null	Het
Or7e165	T	G	9: 19,694,872 (GRCm39)	S148A	possibly damaging	Het
Or8b53	A	T	9: 38,667,703 (GRCm39)	T240S	probably damaging	Het
Orc3	A	T	4: 34,571,774 (GRCm39)	M665K	possibly damaging	Het
Pabpc1	A	G	15: 36,597,255 (GRCm39)	S591P	probably damaging	Het
Pacc1	A	T	1: 191,073,040 (GRCm39)	I154F	probably damaging	Het
Parp6	T	A	9: 59,531,645 (GRCm39)		probably null	Het
Pcdh1	T	C	18: 38,322,912 (GRCm39)	M974V	possibly damaging	Het
Pcdhb22	T	A	18: 37,653,713 (GRCm39)	V727E	possibly damaging	Het
Pex5l	T	C	3: 33,047,134 (GRCm39)	E272G	probably damaging	Het
Pglyrp2	G	T	17: 32,637,235 (GRCm39)	N264K	probably benign	Het
Phxr4	T	A	9: 13,342,882 (GRCm39)		probably benign	Het
Piezo2	A	G	18: 63,278,025 (GRCm39)	F293S	probably damaging	Het
Pkhd1	T	C	1: 20,607,625 (GRCm39)	D1077G	probably damaging	Het
Plekhs1	A	G	19: 56,461,700 (GRCm39)		probably null	Het
Prex1	G	T	2: 166,427,777 (GRCm39)	C788*	probably null	Het
Prrt3	A	T	6: 113,475,099 (GRCm39)	M41K	probably benign	Het
Ptgir	T	C	7: 16,642,768 (GRCm39)	V326A	probably damaging	Het
Ptprg	T	A	14: 12,220,654 (GRCm38)	D455E	probably damaging	Het
Ptpru	T	A	4: 131,526,914 (GRCm39)	Q686L	probably benign	Het
Pxdc1	G	T	13: 34,814,343 (GRCm39)	T190K	probably benign	Het
Rap1b	A	T	10: 117,654,487 (GRCm39)	C118S	probably benign	Het
Rapgef2	T	C	3: 78,990,534 (GRCm39)	M915V	probably benign	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Rpe65	C	T	3: 159,330,318 (GRCm39)	A495V	probably benign	Het
Samd15	A	G	12: 87,247,608 (GRCm39)	T98A	possibly damaging	Het
Sdk1	T	G	5: 141,568,049 (GRCm39)	D82E	probably benign	Het
Slc26a7	T	C	4: 14,546,309 (GRCm39)	D340G	probably benign	Het
Slc6a15	T	A	10: 103,253,921 (GRCm39)	M619K	probably benign	Het
Slc7a4	C	A	16: 17,392,385 (GRCm39)	D350Y	probably damaging	Het
Slk	T	G	19: 47,608,395 (GRCm39)	N449K	probably benign	Het
Spta1	A	T	1: 174,071,608 (GRCm39)		probably null	Het
Sptbn5	A	T	2: 119,886,374 (GRCm39)		probably benign	Het
Srd5a2	A	T	17: 74,354,800 (GRCm39)	V8D	probably benign	Het
Srgap3	G	A	6: 112,704,271 (GRCm39)	A906V	probably benign	Het
Stab2	A	T	10: 86,783,011 (GRCm39)	M679K	probably benign	Het
Stk3	T	C	15: 35,000,054 (GRCm39)	I291V	probably benign	Het
Supt6	T	A	11: 78,098,960 (GRCm39)	Q1637L	possibly damaging	Het
Svil	T	C	18: 5,114,564 (GRCm39)	F2047S	probably damaging	Het
Swsap1	A	G	9: 21,867,284 (GRCm39)	E76G	probably benign	Het
Syndig1	G	T	2: 149,741,473 (GRCm39)	G20C	probably damaging	Het
Synj2bp	A	T	12: 81,548,926 (GRCm39)	N104K	probably damaging	Het
Synpo2	T	A	3: 122,908,068 (GRCm39)	D416V	probably damaging	Het
Tacc3	G	T	5: 33,829,357 (GRCm39)	C620F	probably damaging	Het
Tanc1	A	G	2: 59,529,766 (GRCm39)	E19G	probably damaging	Het
Tars3	C	T	7: 65,297,302 (GRCm39)	A139V	probably benign	Het
Tbc1d22a	T	A	15: 86,235,935 (GRCm39)	C365S	probably damaging	Het
Tdpoz2	T	C	3: 93,559,381 (GRCm39)	H197R	possibly damaging	Het
Tha1	A	T	11: 117,760,205 (GRCm39)	N300K	probably damaging	Het
Tm6sf1	T	A	7: 81,515,008 (GRCm39)	F70L	probably damaging	Het
Tmem132b	T	A	5: 125,860,497 (GRCm39)	S581T	probably benign	Het
Tnfsf13	G	T	11: 69,576,075 (GRCm39)	S4*	probably null	Het
Tonsl	G	A	15: 76,517,448 (GRCm39)	S757L	probably benign	Het
Trem2	G	T	17: 48,658,719 (GRCm39)	R161S	possibly damaging	Het
Trpm2	A	T	10: 77,777,007 (GRCm39)	V430E	probably damaging	Het
Ttc14	T	A	3: 33,855,518 (GRCm39)	D154E	possibly damaging	Het
Ugt2b37	T	C	5: 87,398,498 (GRCm39)	M313V	possibly damaging	Het
Vmn2r24	A	G	6: 123,792,739 (GRCm39)	I689V	probably benign	Het
Wdr76	A	G	2: 121,372,975 (GRCm39)	T601A	probably benign	Het
Xirp1	T	C	9: 119,846,069 (GRCm39)	D938G	possibly damaging	Het
Zfp608	A	T	18: 55,031,041 (GRCm39)	D966E	probably benign	Het
Zfp957	A	G	14: 79,451,796 (GRCm39)	M1T	probably null	Het
Zkscan16	A	T	4: 58,957,809 (GRCm39)	H697L	possibly damaging	Het

Other mutations in Dhx8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01922:Dhx8	APN	11	101,630,633 (GRCm39)	missense	probably damaging	0.99
IGL01957:Dhx8	APN	11	101,645,652 (GRCm39)	missense	possibly damaging	0.48
IGL02039:Dhx8	APN	11	101,654,853 (GRCm39)	critical splice donor site	probably null
IGL02115:Dhx8	APN	11	101,643,214 (GRCm39)	missense	probably damaging	1.00
IGL02161:Dhx8	APN	11	101,648,432 (GRCm39)	missense	probably damaging	1.00
IGL02691:Dhx8	APN	11	101,642,830 (GRCm39)	splice site	probably benign
IGL02697:Dhx8	APN	11	101,645,607 (GRCm39)	missense	probably damaging	1.00
FR4304:Dhx8	UTSW	11	101,629,014 (GRCm39)	small insertion	probably benign
FR4342:Dhx8	UTSW	11	101,629,032 (GRCm39)	frame shift	probably null
FR4449:Dhx8	UTSW	11	101,629,020 (GRCm39)	small insertion	probably benign
FR4449:Dhx8	UTSW	11	101,629,032 (GRCm39)	small insertion	probably benign
FR4449:Dhx8	UTSW	11	101,629,033 (GRCm39)	small insertion	probably benign
FR4449:Dhx8	UTSW	11	101,629,010 (GRCm39)	small insertion	probably benign
FR4449:Dhx8	UTSW	11	101,629,016 (GRCm39)	small deletion	probably benign
FR4589:Dhx8	UTSW	11	101,629,014 (GRCm39)	small insertion	probably benign
FR4737:Dhx8	UTSW	11	101,629,015 (GRCm39)	small insertion	probably benign
FR4737:Dhx8	UTSW	11	101,629,005 (GRCm39)	small insertion	probably benign
FR4737:Dhx8	UTSW	11	101,629,008 (GRCm39)	small insertion	probably benign
R0402:Dhx8	UTSW	11	101,643,223 (GRCm39)	missense	probably damaging	1.00
R0525:Dhx8	UTSW	11	101,654,754 (GRCm39)	missense	probably damaging	1.00
R0969:Dhx8	UTSW	11	101,630,526 (GRCm39)	splice site	probably benign
R1497:Dhx8	UTSW	11	101,626,213 (GRCm39)	intron	probably benign
R1576:Dhx8	UTSW	11	101,643,145 (GRCm39)	missense	probably damaging	1.00
R1758:Dhx8	UTSW	11	101,657,564 (GRCm39)	missense	probably damaging	1.00
R1773:Dhx8	UTSW	11	101,643,189 (GRCm39)	missense	possibly damaging	0.87
R1941:Dhx8	UTSW	11	101,643,024 (GRCm39)	critical splice donor site	probably null
R1954:Dhx8	UTSW	11	101,644,105 (GRCm39)	missense	probably damaging	0.98
R2124:Dhx8	UTSW	11	101,653,071 (GRCm39)	missense	probably damaging	0.99
R2128:Dhx8	UTSW	11	101,629,235 (GRCm39)	missense	probably benign	0.06
R2148:Dhx8	UTSW	11	101,629,203 (GRCm39)	nonsense	probably null
R2206:Dhx8	UTSW	11	101,641,797 (GRCm39)	missense	probably benign	0.03
R2207:Dhx8	UTSW	11	101,641,797 (GRCm39)	missense	probably benign	0.03
R4667:Dhx8	UTSW	11	101,628,987 (GRCm39)	missense	unknown
R4678:Dhx8	UTSW	11	101,630,634 (GRCm39)	missense	probably damaging	1.00
R4943:Dhx8	UTSW	11	101,628,526 (GRCm39)	nonsense	probably null
R5341:Dhx8	UTSW	11	101,629,016 (GRCm39)	small deletion	probably benign
R5586:Dhx8	UTSW	11	101,623,862 (GRCm39)	unclassified	probably benign
R5662:Dhx8	UTSW	11	101,657,584 (GRCm39)	missense	possibly damaging	0.89
R5664:Dhx8	UTSW	11	101,631,577 (GRCm39)	missense	probably damaging	1.00
R6082:Dhx8	UTSW	11	101,655,139 (GRCm39)	missense	probably damaging	1.00
R6085:Dhx8	UTSW	11	101,655,139 (GRCm39)	missense	probably damaging	1.00
R6415:Dhx8	UTSW	11	101,628,513 (GRCm39)	missense	unknown
R6658:Dhx8	UTSW	11	101,655,748 (GRCm39)	missense	probably damaging	1.00
R6841:Dhx8	UTSW	11	101,655,618 (GRCm39)	missense	probably damaging	0.98
R6918:Dhx8	UTSW	11	101,629,247 (GRCm39)	nonsense	probably null
R7011:Dhx8	UTSW	11	101,632,346 (GRCm39)	missense	probably damaging	1.00
R7098:Dhx8	UTSW	11	101,628,594 (GRCm39)	critical splice donor site	probably null
R7153:Dhx8	UTSW	11	101,631,001 (GRCm39)	splice site	probably null
R7284:Dhx8	UTSW	11	101,645,648 (GRCm39)	missense	probably damaging	1.00
R7604:Dhx8	UTSW	11	101,655,623 (GRCm39)	missense	probably damaging	1.00
R8135:Dhx8	UTSW	11	101,629,090 (GRCm39)	missense	unknown
R8137:Dhx8	UTSW	11	101,654,808 (GRCm39)	missense	probably damaging	1.00
R8256:Dhx8	UTSW	11	101,631,588 (GRCm39)	missense	possibly damaging	0.93
R8284:Dhx8	UTSW	11	101,648,455 (GRCm39)	missense	probably damaging	1.00
R8289:Dhx8	UTSW	11	101,631,571 (GRCm39)	missense	probably benign	0.01
R8696:Dhx8	UTSW	11	101,623,958 (GRCm39)	missense	unknown
R9061:Dhx8	UTSW	11	101,632,406 (GRCm39)	missense	possibly damaging	0.61
R9076:Dhx8	UTSW	11	101,629,021 (GRCm39)	missense
R9443:Dhx8	UTSW	11	101,655,740 (GRCm39)	missense	probably damaging	1.00
R9492:Dhx8	UTSW	11	101,654,808 (GRCm39)	missense	possibly damaging	0.67
R9554:Dhx8	UTSW	11	101,645,614 (GRCm39)	nonsense	probably null
R9700:Dhx8	UTSW	11	101,624,015 (GRCm39)	critical splice donor site	probably null
R9780:Dhx8	UTSW	11	101,632,403 (GRCm39)	missense	possibly damaging	0.73
Z1177:Dhx8	UTSW	11	101,648,486 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTATGTCATTACTGGCCTGTGG -3'
(R):5'- TTGAAGGGACTCTGACTTCTGC -3'

Sequencing Primer
(F):5'- GGGATTGTGGTCCAGTTAAGAAG -3'
(R):5'- AGGGACTCTGACTTCTGCTCCTAG -3'

Posted On

2016-03-01