Mutagenetix > Incidental Mutation

Incidental Mutation 'R2104:Dnah9'

230804

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

040108-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.400) question?

Stock #

R2104 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

65722150-66059379 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 65951950 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 1850 (C1850S)

Ref Sequence

ENSEMBL: ENSMUSP00000079494 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080665]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000080665
AA Change: C1850S

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

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: C1850S

Domain	Start	End	E-Value	Type
Pfam:DHC_N1	209	787	3.6e-164	PFAM
coiled coil region	788	820	N/A	INTRINSIC
low complexity region	1228	1240	N/A	INTRINSIC
Pfam:DHC_N2	1290	1699	1.4e-134	PFAM
AAA	1863	1999	4.9e-1	SMART
AAA	2141	2341	1.99e0	SMART
AAA	2468	2614	6.75e-1	SMART
Pfam:AAA_8	2786	3053	1.1e-165	PFAM
Pfam:MT	3065	3408	7.2e-208	PFAM
Pfam:AAA_9	3430	3652	3.2e-87	PFAM
Pfam:Dynein_heavy	3786	4482	1e-241	PFAM

Meta Mutation Damage Score

0.6493

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.3%

Validation Efficiency

100% (80/80)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the heavy chain subunit of axonemal dynein, a large multi-subunit molecular motor. Axonemal dynein attaches to microtubules and hydrolyzes ATP to mediate the movement of cilia and flagella. The gene expresses at least two transcript variants; additional variants have been described, but their full length nature has not been determined. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsm3	G	A	7: 119,383,527 (GRCm39)	V563I	probably benign	Het
Amer3	T	C	1: 34,627,759 (GRCm39)	V666A	probably benign	Het
Ankrd16	A	G	2: 11,784,711 (GRCm39)		probably benign	Het
Ankub1	G	T	3: 57,580,296 (GRCm39)	C120*	probably null	Het
Arhgap31	T	C	16: 38,445,941 (GRCm39)	I135V	probably benign	Het
Atp2c2	G	A	8: 120,476,584 (GRCm39)	G633D	probably benign	Het
Camta1	T	A	4: 151,537,751 (GRCm39)	Q143L	probably damaging	Het
Casp8ap2	T	C	4: 32,644,727 (GRCm39)	S1267P	probably benign	Het
Ccn4	A	G	15: 66,791,176 (GRCm39)	E326G	probably benign	Het
Cdh1	T	A	8: 107,380,391 (GRCm39)		probably benign	Het
Cdhr4	C	A	9: 107,873,460 (GRCm39)	D397E	probably damaging	Het
Cdk6	T	G	5: 3,394,387 (GRCm39)	S7R	probably benign	Het
Cert1	T	A	13: 96,771,394 (GRCm39)	N550K	probably damaging	Het
Cilp2	C	A	8: 70,335,442 (GRCm39)	E519*	probably null	Het
Clybl	A	G	14: 122,548,718 (GRCm39)	Y40C	probably damaging	Het
Ctnnal1	T	C	4: 56,812,329 (GRCm39)	*732W	probably null	Het
Ctns	A	T	11: 73,083,907 (GRCm39)	S38R	probably benign	Het
Cwh43	A	T	5: 73,578,873 (GRCm39)	K293N	possibly damaging	Het
Dcaf5	G	T	12: 80,385,635 (GRCm39)	D830E	probably benign	Het
Dmxl2	A	G	9: 54,322,848 (GRCm39)	V1512A	probably damaging	Het
Dpp8	C	T	9: 64,981,849 (GRCm39)		probably null	Het
Enam	A	T	5: 88,649,646 (GRCm39)	Q385L	probably damaging	Het
Etv3	A	G	3: 87,443,369 (GRCm39)	T318A	possibly damaging	Het
Exd2	T	G	12: 80,543,575 (GRCm39)	I586S	probably benign	Het
Fat3	A	G	9: 15,909,813 (GRCm39)	V2063A	possibly damaging	Het
Fezf1	A	G	6: 23,247,331 (GRCm39)	F248S	possibly damaging	Het
Flnc	T	C	6: 29,450,734 (GRCm39)		probably null	Het
Foxc2	A	G	8: 121,844,819 (GRCm39)	Y489C	probably damaging	Het
Gfm2	A	G	13: 97,308,028 (GRCm39)	E540G	probably damaging	Het
Hrg	T	C	16: 22,774,949 (GRCm39)	I193T	probably benign	Het
Ifih1	G	A	2: 62,440,889 (GRCm39)	Q426*	probably null	Het
Ifit1bl2	T	A	19: 34,596,920 (GRCm39)	D232V	probably benign	Het
Igf2bp1	A	G	11: 95,866,122 (GRCm39)	V122A	probably damaging	Het
Inpp1	T	G	1: 52,838,577 (GRCm39)	Q24P	probably damaging	Het
Kifc2	A	G	15: 76,545,454 (GRCm39)	D67G	probably damaging	Het
Lrrc43	G	A	5: 123,639,177 (GRCm39)	G402D	probably benign	Het
Lrrc8c	C	T	5: 105,755,224 (GRCm39)	T333M	possibly damaging	Het
Mab21l3	G	T	3: 101,730,744 (GRCm39)	A165D	probably benign	Het
Mcub	T	A	3: 129,712,337 (GRCm39)	R179S	probably benign	Het
Mdfi	G	C	17: 48,135,562 (GRCm39)	A56G	possibly damaging	Het
Mdn1	A	T	4: 32,743,843 (GRCm39)		probably null	Het
Meox2	A	G	12: 37,217,476 (GRCm39)	T226A	probably damaging	Het
Mipol1	A	G	12: 57,352,842 (GRCm39)		probably null	Het
Mms22l	T	G	4: 24,591,084 (GRCm39)	N1018K	probably benign	Het
Mn1	T	C	5: 111,602,617 (GRCm39)	I1285T	possibly damaging	Het
Muc20	T	G	16: 32,614,547 (GRCm39)	S277R	probably damaging	Het
Muc6	C	A	7: 141,213,991 (GRCm39)	V2845L	probably benign	Het
Mup5	C	A	4: 61,751,962 (GRCm39)	G96C	probably damaging	Het
Neb	T	A	2: 52,146,826 (GRCm39)	M2813L	probably benign	Het
Neb	C	A	2: 52,161,570 (GRCm39)	R2074L	probably damaging	Het
Oasl2	A	T	5: 115,049,063 (GRCm39)	K168*	probably null	Het
Or6c5	T	C	10: 129,074,368 (GRCm39)	S117P	probably damaging	Het
P2rx2	C	T	5: 110,489,007 (GRCm39)	D203N	probably damaging	Het
Ptprg	T	C	14: 11,952,897 (GRCm38)		probably null	Het
Rims4	C	T	2: 163,706,785 (GRCm39)		probably null	Het
Rtn4ip1	T	A	10: 43,808,402 (GRCm39)	W60R	probably benign	Het
Sccpdh	T	C	1: 179,498,162 (GRCm39)	S69P	probably benign	Het
Serpina3b	T	A	12: 104,105,069 (GRCm39)	I415N	probably benign	Het
Slc22a4	T	C	11: 53,874,436 (GRCm39)		probably benign	Het
Slc4a5	G	A	6: 83,274,360 (GRCm39)	A1076T	probably benign	Het
Slit1	T	C	19: 41,590,686 (GRCm39)	K1329E	possibly damaging	Het
Synj2bp	A	C	12: 81,548,826 (GRCm39)	F138V	probably benign	Het
Taar7a	T	C	10: 23,868,959 (GRCm39)	I141V	probably damaging	Het
Tas1r3	T	C	4: 155,946,588 (GRCm39)	E339G	probably benign	Het
Tep1	A	G	14: 51,088,037 (GRCm39)		probably benign	Het
Tgds	A	T	14: 118,359,149 (GRCm39)	Y146*	probably null	Het
Tgm3	G	A	2: 129,879,403 (GRCm39)	V332I	probably benign	Het
Tnnt2	A	G	1: 135,771,547 (GRCm39)		probably benign	Het
Top1	T	A	2: 160,546,739 (GRCm39)	Y340N	probably damaging	Het
Topbp1	T	C	9: 103,195,181 (GRCm39)		probably benign	Het
Tpst1	A	G	5: 130,131,202 (GRCm39)	N224S	probably benign	Het
Traf4	A	G	11: 78,050,840 (GRCm39)	F439L	probably damaging	Het
Trim58	A	G	11: 58,533,964 (GRCm39)		probably benign	Het
Tspan31	T	C	10: 126,904,004 (GRCm39)	N205S	probably damaging	Het
Ube3a	T	A	7: 58,926,225 (GRCm39)	N334K	possibly damaging	Het
Ugt2a3	A	T	5: 87,477,541 (GRCm39)		probably null	Het
Vwf	G	A	6: 125,623,293 (GRCm39)	V1797I	probably benign	Het
Wdr81	G	T	11: 75,343,809 (GRCm39)	P486Q	probably damaging	Het
Whamm	C	T	7: 81,241,519 (GRCm39)	R277*	probably null	Het
Yipf7	T	A	5: 69,678,462 (GRCm39)	N56I	possibly damaging	Het
Zfp523	A	T	17: 28,414,190 (GRCm39)	T75S	probably benign	Het

Other mutations in Dnah9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00696:Dnah9	APN	11	65,732,064 (GRCm39)	splice site	probably benign
IGL00805:Dnah9	APN	11	65,772,521 (GRCm39)	missense	probably benign	0.00
IGL00826:Dnah9	APN	11	65,880,768 (GRCm39)	missense	probably damaging	1.00
IGL01108:Dnah9	APN	11	65,740,806 (GRCm39)	missense	possibly damaging	0.93
IGL01152:Dnah9	APN	11	65,962,882 (GRCm39)	missense	probably damaging	1.00
IGL01353:Dnah9	APN	11	65,971,397 (GRCm39)	missense	probably damaging	1.00
IGL01364:Dnah9	APN	11	66,046,285 (GRCm39)	missense	probably damaging	1.00
IGL01479:Dnah9	APN	11	65,846,543 (GRCm39)	missense	probably benign	0.14
IGL01537:Dnah9	APN	11	65,838,506 (GRCm39)	missense	probably benign
IGL01565:Dnah9	APN	11	65,924,655 (GRCm39)	missense	possibly damaging	0.95
IGL01597:Dnah9	APN	11	66,009,656 (GRCm39)	missense	probably damaging	1.00
IGL01619:Dnah9	APN	11	65,722,441 (GRCm39)	nonsense	probably null
IGL01625:Dnah9	APN	11	65,935,471 (GRCm39)	missense	probably damaging	1.00
IGL01803:Dnah9	APN	11	66,009,655 (GRCm39)	missense	probably damaging	1.00
IGL01819:Dnah9	APN	11	65,998,952 (GRCm39)	missense	probably benign	0.33
IGL01896:Dnah9	APN	11	66,021,492 (GRCm39)	missense	possibly damaging	0.89
IGL01922:Dnah9	APN	11	65,965,860 (GRCm39)	splice site	probably benign
IGL01923:Dnah9	APN	11	66,016,061 (GRCm39)	splice site	probably benign
IGL02059:Dnah9	APN	11	65,963,784 (GRCm39)	missense	probably damaging	1.00
IGL02068:Dnah9	APN	11	65,951,871 (GRCm39)	missense	probably damaging	1.00
IGL02135:Dnah9	APN	11	66,008,318 (GRCm39)	missense	possibly damaging	0.63
IGL02146:Dnah9	APN	11	65,818,526 (GRCm39)	missense	probably damaging	1.00
IGL02264:Dnah9	APN	11	65,971,314 (GRCm39)	splice site	probably benign
IGL02325:Dnah9	APN	11	65,725,043 (GRCm39)	missense	probably damaging	1.00
IGL02426:Dnah9	APN	11	66,015,979 (GRCm39)	missense	probably benign
IGL02440:Dnah9	APN	11	65,846,072 (GRCm39)	missense	probably damaging	1.00
IGL02471:Dnah9	APN	11	65,838,444 (GRCm39)	nonsense	probably null
IGL02496:Dnah9	APN	11	65,920,189 (GRCm39)	missense	probably damaging	1.00
IGL02672:Dnah9	APN	11	65,818,427 (GRCm39)	missense	probably benign	0.02
IGL02718:Dnah9	APN	11	65,777,466 (GRCm39)	missense	probably damaging	0.99
IGL02832:Dnah9	APN	11	65,931,172 (GRCm39)	missense	probably damaging	1.00
IGL02851:Dnah9	APN	11	65,928,570 (GRCm39)	splice site	probably benign
IGL02859:Dnah9	APN	11	65,772,445 (GRCm39)	splice site	probably benign
IGL02864:Dnah9	APN	11	65,951,829 (GRCm39)	missense	probably damaging	1.00
IGL02954:Dnah9	APN	11	66,009,793 (GRCm39)	missense	probably damaging	1.00
IGL02987:Dnah9	APN	11	65,732,099 (GRCm39)	missense	probably benign	0.23
IGL02987:Dnah9	APN	11	65,746,098 (GRCm39)	missense	probably damaging	0.98
IGL03160:Dnah9	APN	11	65,998,880 (GRCm39)	missense	probably damaging	0.98
IGL03171:Dnah9	APN	11	65,872,067 (GRCm39)	missense	probably benign	0.13
IGL03180:Dnah9	APN	11	65,777,465 (GRCm39)	missense	probably damaging	0.99
IGL03388:Dnah9	APN	11	65,838,368 (GRCm39)	missense	probably damaging	1.00
anarchy	UTSW	11	65,846,074 (GRCm39)	missense	probably damaging	0.99
sacco	UTSW	11	66,058,905 (GRCm39)	missense	possibly damaging	0.82
Tweed	UTSW	11	65,962,898 (GRCm39)	missense	probably damaging	0.99
vanzetti	UTSW	11	65,746,198 (GRCm39)	nonsense	probably null
IGL02837:Dnah9	UTSW	11	65,765,022 (GRCm39)	missense	probably damaging	1.00
PIT4280001:Dnah9	UTSW	11	65,895,839 (GRCm39)	missense	probably benign	0.44
R0021:Dnah9	UTSW	11	65,860,805 (GRCm39)	missense	probably benign	0.36
R0021:Dnah9	UTSW	11	65,860,805 (GRCm39)	missense	probably benign	0.36
R0025:Dnah9	UTSW	11	65,860,781 (GRCm39)	splice site	probably benign
R0025:Dnah9	UTSW	11	65,860,781 (GRCm39)	splice site	probably benign
R0070:Dnah9	UTSW	11	66,050,866 (GRCm39)	missense	probably benign	0.10
R0164:Dnah9	UTSW	11	65,809,630 (GRCm39)	nonsense	probably null
R0164:Dnah9	UTSW	11	65,809,630 (GRCm39)	nonsense	probably null
R0180:Dnah9	UTSW	11	66,038,116 (GRCm39)	missense	probably damaging	1.00
R0195:Dnah9	UTSW	11	65,786,731 (GRCm39)	missense	probably benign	0.30
R0230:Dnah9	UTSW	11	65,746,141 (GRCm39)	missense	probably damaging	1.00
R0243:Dnah9	UTSW	11	65,802,678 (GRCm39)	missense	possibly damaging	0.91
R0279:Dnah9	UTSW	11	65,802,615 (GRCm39)	critical splice donor site	probably null
R0288:Dnah9	UTSW	11	65,915,960 (GRCm39)	critical splice donor site	probably null
R0309:Dnah9	UTSW	11	65,917,798 (GRCm39)	splice site	probably benign
R0356:Dnah9	UTSW	11	66,021,388 (GRCm39)	critical splice donor site	probably null
R0403:Dnah9	UTSW	11	65,975,615 (GRCm39)	missense	possibly damaging	0.90
R0413:Dnah9	UTSW	11	65,998,961 (GRCm39)	missense	probably damaging	1.00
R0448:Dnah9	UTSW	11	65,809,539 (GRCm39)	splice site	probably benign
R0496:Dnah9	UTSW	11	65,965,961 (GRCm39)	missense	probably null	1.00
R0557:Dnah9	UTSW	11	65,975,492 (GRCm39)	missense	probably damaging	1.00
R0584:Dnah9	UTSW	11	65,881,315 (GRCm39)	missense	probably damaging	1.00
R0598:Dnah9	UTSW	11	66,009,703 (GRCm39)	missense	probably benign	0.02
R0599:Dnah9	UTSW	11	65,856,515 (GRCm39)	missense	probably damaging	1.00
R0606:Dnah9	UTSW	11	65,732,159 (GRCm39)	missense	probably damaging	1.00
R0666:Dnah9	UTSW	11	65,976,284 (GRCm39)	missense	probably benign	0.01
R0715:Dnah9	UTSW	11	65,972,074 (GRCm39)	splice site	probably benign
R0726:Dnah9	UTSW	11	65,856,507 (GRCm39)	missense	probably damaging	1.00
R0737:Dnah9	UTSW	11	65,998,724 (GRCm39)	missense	probably damaging	1.00
R0763:Dnah9	UTSW	11	66,046,356 (GRCm39)	missense	probably benign	0.30
R0792:Dnah9	UTSW	11	65,786,827 (GRCm39)	missense	possibly damaging	0.84
R0829:Dnah9	UTSW	11	65,896,002 (GRCm39)	missense	probably benign	0.00
R0973:Dnah9	UTSW	11	65,896,663 (GRCm39)	splice site	probably null
R0974:Dnah9	UTSW	11	65,896,663 (GRCm39)	splice site	probably null
R1055:Dnah9	UTSW	11	66,050,837 (GRCm39)	missense	probably damaging	1.00
R1081:Dnah9	UTSW	11	65,975,703 (GRCm39)	missense	probably damaging	0.99
R1184:Dnah9	UTSW	11	65,975,438 (GRCm39)	critical splice donor site	probably null
R1225:Dnah9	UTSW	11	65,761,886 (GRCm39)	missense	possibly damaging	0.94
R1304:Dnah9	UTSW	11	65,818,414 (GRCm39)	missense	probably damaging	0.98
R1417:Dnah9	UTSW	11	65,846,573 (GRCm39)	missense	probably damaging	0.96
R1439:Dnah9	UTSW	11	65,764,958 (GRCm39)	missense	probably benign	0.22
R1447:Dnah9	UTSW	11	65,999,308 (GRCm39)	missense	possibly damaging	0.65
R1450:Dnah9	UTSW	11	65,818,612 (GRCm39)	missense	probably damaging	1.00
R1470:Dnah9	UTSW	11	65,818,648 (GRCm39)	missense	probably benign	0.11
R1470:Dnah9	UTSW	11	65,818,648 (GRCm39)	missense	probably benign	0.11
R1486:Dnah9	UTSW	11	65,725,098 (GRCm39)	missense	probably damaging	1.00
R1519:Dnah9	UTSW	11	65,772,587 (GRCm39)	missense	probably damaging	0.96
R1570:Dnah9	UTSW	11	66,003,156 (GRCm39)	missense	probably benign
R1617:Dnah9	UTSW	11	65,786,747 (GRCm39)	missense	probably damaging	1.00
R1623:Dnah9	UTSW	11	65,928,463 (GRCm39)	missense	probably damaging	1.00
R1626:Dnah9	UTSW	11	65,976,093 (GRCm39)	missense	probably benign	0.05
R1671:Dnah9	UTSW	11	65,818,789 (GRCm39)	missense	probably damaging	0.99
R1694:Dnah9	UTSW	11	65,845,650 (GRCm39)	nonsense	probably null
R1701:Dnah9	UTSW	11	65,802,750 (GRCm39)	missense	probably damaging	1.00
R1702:Dnah9	UTSW	11	65,976,021 (GRCm39)	missense	possibly damaging	0.72
R1708:Dnah9	UTSW	11	65,805,980 (GRCm39)	missense	probably benign	0.11
R1718:Dnah9	UTSW	11	66,058,905 (GRCm39)	missense	possibly damaging	0.82
R1729:Dnah9	UTSW	11	65,975,846 (GRCm39)	missense	possibly damaging	0.51
R1760:Dnah9	UTSW	11	65,872,048 (GRCm39)	missense	probably benign	0.31
R1784:Dnah9	UTSW	11	65,975,846 (GRCm39)	missense	possibly damaging	0.51
R1793:Dnah9	UTSW	11	66,010,420 (GRCm39)	critical splice donor site	probably null
R1801:Dnah9	UTSW	11	65,846,123 (GRCm39)	missense	probably damaging	0.99
R1827:Dnah9	UTSW	11	65,740,887 (GRCm39)	missense	probably damaging	0.97
R1836:Dnah9	UTSW	11	66,009,667 (GRCm39)	missense	probably benign	0.10
R1840:Dnah9	UTSW	11	65,725,024 (GRCm39)	nonsense	probably null
R1847:Dnah9	UTSW	11	65,725,212 (GRCm39)	missense	probably damaging	1.00
R1872:Dnah9	UTSW	11	65,928,316 (GRCm39)	missense	probably benign	0.16
R1929:Dnah9	UTSW	11	65,867,224 (GRCm39)	missense	probably benign	0.05
R1969:Dnah9	UTSW	11	65,739,197 (GRCm39)	missense	probably damaging	1.00
R1971:Dnah9	UTSW	11	65,739,197 (GRCm39)	missense	probably damaging	1.00
R2027:Dnah9	UTSW	11	65,846,164 (GRCm39)	missense	probably benign	0.11
R2049:Dnah9	UTSW	11	65,935,509 (GRCm39)	missense	probably damaging	1.00
R2064:Dnah9	UTSW	11	66,036,261 (GRCm39)	missense	probably benign	0.31
R2109:Dnah9	UTSW	11	65,928,411 (GRCm39)	missense	probably damaging	1.00
R2160:Dnah9	UTSW	11	66,008,309 (GRCm39)	missense	probably damaging	1.00
R2172:Dnah9	UTSW	11	65,963,605 (GRCm39)	missense	probably damaging	1.00
R2198:Dnah9	UTSW	11	65,750,325 (GRCm39)	missense	possibly damaging	0.50
R2271:Dnah9	UTSW	11	66,003,188 (GRCm39)	missense	probably benign	0.37
R2272:Dnah9	UTSW	11	66,003,188 (GRCm39)	missense	probably benign	0.37
R2396:Dnah9	UTSW	11	65,975,984 (GRCm39)	missense	probably benign	0.01
R2398:Dnah9	UTSW	11	65,806,029 (GRCm39)	missense	probably damaging	1.00
R2418:Dnah9	UTSW	11	65,986,241 (GRCm39)	nonsense	probably null
R2419:Dnah9	UTSW	11	65,986,241 (GRCm39)	nonsense	probably null
R2510:Dnah9	UTSW	11	65,895,995 (GRCm39)	missense	probably damaging	1.00
R2680:Dnah9	UTSW	11	65,924,751 (GRCm39)	missense	probably benign	0.00
R2875:Dnah9	UTSW	11	66,059,287 (GRCm39)	missense	possibly damaging	0.89
R2979:Dnah9	UTSW	11	66,008,414 (GRCm39)	missense	possibly damaging	0.89
R3236:Dnah9	UTSW	11	65,845,815 (GRCm39)	missense	probably benign	0.11
R3237:Dnah9	UTSW	11	65,845,815 (GRCm39)	missense	probably benign	0.11
R3433:Dnah9	UTSW	11	65,965,938 (GRCm39)	missense	possibly damaging	0.85
R3737:Dnah9	UTSW	11	66,047,734 (GRCm39)	nonsense	probably null
R3820:Dnah9	UTSW	11	65,741,829 (GRCm39)	critical splice donor site	probably null
R3821:Dnah9	UTSW	11	65,741,829 (GRCm39)	critical splice donor site	probably null
R3822:Dnah9	UTSW	11	65,741,829 (GRCm39)	critical splice donor site	probably null
R3861:Dnah9	UTSW	11	65,943,820 (GRCm39)	splice site	probably benign
R3918:Dnah9	UTSW	11	65,761,800 (GRCm39)	missense	possibly damaging	0.54
R4011:Dnah9	UTSW	11	65,725,290 (GRCm39)	missense	probably damaging	0.98
R4044:Dnah9	UTSW	11	66,024,461 (GRCm39)	missense	probably benign	0.03
R4072:Dnah9	UTSW	11	65,975,730 (GRCm39)	missense	probably benign	0.00
R4076:Dnah9	UTSW	11	65,975,730 (GRCm39)	missense	probably benign	0.00
R4097:Dnah9	UTSW	11	65,881,285 (GRCm39)	missense	probably damaging	1.00
R4409:Dnah9	UTSW	11	65,976,303 (GRCm39)	missense	possibly damaging	0.51
R4410:Dnah9	UTSW	11	65,976,303 (GRCm39)	missense	possibly damaging	0.51
R4417:Dnah9	UTSW	11	65,872,040 (GRCm39)	missense	possibly damaging	0.75
R4420:Dnah9	UTSW	11	66,009,575 (GRCm39)	missense	probably benign	0.00
R4434:Dnah9	UTSW	11	65,998,901 (GRCm39)	missense	possibly damaging	0.67
R4451:Dnah9	UTSW	11	65,772,467 (GRCm39)	missense	probably benign	0.07
R4452:Dnah9	UTSW	11	65,917,908 (GRCm39)	missense	probably damaging	0.96
R4454:Dnah9	UTSW	11	66,038,215 (GRCm39)	missense	probably damaging	0.96
R4551:Dnah9	UTSW	11	65,732,192 (GRCm39)	missense	probably damaging	1.00
R4552:Dnah9	UTSW	11	65,732,192 (GRCm39)	missense	probably damaging	1.00
R4590:Dnah9	UTSW	11	65,931,218 (GRCm39)	missense	probably damaging	1.00
R4595:Dnah9	UTSW	11	66,058,978 (GRCm39)	missense	probably benign
R4655:Dnah9	UTSW	11	65,846,558 (GRCm39)	missense	probably benign	0.00
R4667:Dnah9	UTSW	11	66,046,357 (GRCm39)	missense	probably benign
R4718:Dnah9	UTSW	11	65,976,299 (GRCm39)	missense	probably benign
R4720:Dnah9	UTSW	11	65,967,184 (GRCm39)	missense	probably damaging	1.00
R4734:Dnah9	UTSW	11	65,724,941 (GRCm39)	missense	probably damaging	1.00
R4749:Dnah9	UTSW	11	65,724,941 (GRCm39)	missense	probably damaging	1.00
R4765:Dnah9	UTSW	11	65,818,552 (GRCm39)	missense	probably damaging	1.00
R4905:Dnah9	UTSW	11	65,764,950 (GRCm39)	nonsense	probably null
R4963:Dnah9	UTSW	11	65,975,437 (GRCm39)	splice site	probably null
R5074:Dnah9	UTSW	11	65,740,866 (GRCm39)	missense	probably damaging	1.00
R5230:Dnah9	UTSW	11	65,975,492 (GRCm39)	missense	probably damaging	0.99
R5262:Dnah9	UTSW	11	66,003,159 (GRCm39)	missense	probably benign	0.34
R5364:Dnah9	UTSW	11	65,772,522 (GRCm39)	missense	possibly damaging	0.93
R5370:Dnah9	UTSW	11	65,920,180 (GRCm39)	missense	probably damaging	1.00
R5386:Dnah9	UTSW	11	65,920,182 (GRCm39)	missense	probably damaging	1.00
R5389:Dnah9	UTSW	11	65,986,140 (GRCm39)	nonsense	probably null
R5541:Dnah9	UTSW	11	66,036,162 (GRCm39)	missense	probably damaging	1.00
R5560:Dnah9	UTSW	11	65,772,566 (GRCm39)	missense	probably benign	0.00
R5576:Dnah9	UTSW	11	65,724,922 (GRCm39)	splice site	probably null
R5648:Dnah9	UTSW	11	65,818,581 (GRCm39)	missense	probably benign	0.00
R5653:Dnah9	UTSW	11	65,740,806 (GRCm39)	missense	probably damaging	0.99
R5713:Dnah9	UTSW	11	65,916,049 (GRCm39)	missense	possibly damaging	0.92
R5763:Dnah9	UTSW	11	65,846,065 (GRCm39)	missense	probably damaging	1.00
R5825:Dnah9	UTSW	11	66,017,427 (GRCm39)	missense	probably benign	0.01
R5831:Dnah9	UTSW	11	65,998,947 (GRCm39)	missense	probably benign	0.00
R5847:Dnah9	UTSW	11	65,986,066 (GRCm39)	frame shift	probably null
R5870:Dnah9	UTSW	11	65,976,036 (GRCm39)	missense	probably benign	0.01
R5902:Dnah9	UTSW	11	65,916,013 (GRCm39)	missense	probably benign	0.08
R5918:Dnah9	UTSW	11	65,725,025 (GRCm39)	missense	probably damaging	1.00
R5979:Dnah9	UTSW	11	65,725,307 (GRCm39)	missense	probably damaging	1.00
R6065:Dnah9	UTSW	11	66,036,223 (GRCm39)	missense	possibly damaging	0.65
R6065:Dnah9	UTSW	11	65,746,164 (GRCm39)	missense	probably benign	0.05
R6086:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
R6086:Dnah9	UTSW	11	65,880,741 (GRCm39)	missense	probably damaging	0.99
R6102:Dnah9	UTSW	11	65,881,342 (GRCm39)	missense	probably damaging	0.97
R6120:Dnah9	UTSW	11	66,038,225 (GRCm39)	missense	probably benign
R6154:Dnah9	UTSW	11	65,746,164 (GRCm39)	missense	probably benign	0.00
R6262:Dnah9	UTSW	11	65,772,631 (GRCm39)	splice site	probably null
R6265:Dnah9	UTSW	11	66,058,920 (GRCm39)	missense	probably benign	0.04
R6290:Dnah9	UTSW	11	65,732,201 (GRCm39)	missense	probably damaging	1.00
R6345:Dnah9	UTSW	11	65,928,519 (GRCm39)	missense	probably damaging	0.97
R6357:Dnah9	UTSW	11	65,765,022 (GRCm39)	missense	probably damaging	1.00
R6534:Dnah9	UTSW	11	65,846,074 (GRCm39)	missense	probably damaging	0.99
R6574:Dnah9	UTSW	11	66,059,107 (GRCm39)	missense	probably benign	0.37
R6582:Dnah9	UTSW	11	65,951,923 (GRCm39)	missense	probably damaging	1.00
R6700:Dnah9	UTSW	11	65,846,192 (GRCm39)	missense	probably damaging	1.00
R6800:Dnah9	UTSW	11	65,963,565 (GRCm39)	critical splice donor site	probably null
R6812:Dnah9	UTSW	11	65,872,155 (GRCm39)	missense	probably damaging	0.99
R6931:Dnah9	UTSW	11	66,008,452 (GRCm39)	missense	possibly damaging	0.63
R6944:Dnah9	UTSW	11	65,975,975 (GRCm39)	missense	possibly damaging	0.91
R6958:Dnah9	UTSW	11	65,967,167 (GRCm39)	missense	probably damaging	1.00
R6977:Dnah9	UTSW	11	65,998,735 (GRCm39)	missense	probably benign	0.37
R7021:Dnah9	UTSW	11	65,872,057 (GRCm39)	missense	probably benign
R7161:Dnah9	UTSW	11	65,746,198 (GRCm39)	nonsense	probably null
R7175:Dnah9	UTSW	11	66,024,463 (GRCm39)	missense	probably benign	0.03
R7199:Dnah9	UTSW	11	66,009,770 (GRCm39)	missense	probably benign	0.04
R7231:Dnah9	UTSW	11	65,856,473 (GRCm39)	missense	probably damaging	1.00
R7284:Dnah9	UTSW	11	65,881,302 (GRCm39)	missense	probably damaging	0.99
R7314:Dnah9	UTSW	11	65,880,677 (GRCm39)	missense	probably benign	0.00
R7350:Dnah9	UTSW	11	65,971,404 (GRCm39)	missense	probably damaging	1.00
R7420:Dnah9	UTSW	11	66,008,233 (GRCm39)	critical splice donor site	probably null
R7427:Dnah9	UTSW	11	65,846,045 (GRCm39)	missense	probably benign
R7477:Dnah9	UTSW	11	65,883,557 (GRCm39)	missense	probably damaging	0.98
R7515:Dnah9	UTSW	11	65,732,240 (GRCm39)	missense	probably benign	0.01
R7521:Dnah9	UTSW	11	65,880,663 (GRCm39)	missense	probably damaging	0.98
R7573:Dnah9	UTSW	11	66,016,041 (GRCm39)	missense	probably benign	0.43
R7659:Dnah9	UTSW	11	65,880,606 (GRCm39)	missense	probably damaging	0.99
R7707:Dnah9	UTSW	11	66,009,784 (GRCm39)	missense	probably damaging	1.00
R7749:Dnah9	UTSW	11	65,802,656 (GRCm39)	missense	probably damaging	1.00
R7792:Dnah9	UTSW	11	65,740,839 (GRCm39)	missense	probably damaging	1.00
R7808:Dnah9	UTSW	11	65,896,631 (GRCm39)	nonsense	probably null
R7814:Dnah9	UTSW	11	65,896,486 (GRCm39)	missense	probably damaging	1.00
R7818:Dnah9	UTSW	11	65,916,037 (GRCm39)	missense	possibly damaging	0.64
R7890:Dnah9	UTSW	11	65,962,898 (GRCm39)	missense	probably damaging	0.99
R7976:Dnah9	UTSW	11	65,732,227 (GRCm39)	missense	possibly damaging	0.91
R8121:Dnah9	UTSW	11	65,908,201 (GRCm39)	missense	probably benign	0.02
R8232:Dnah9	UTSW	11	65,746,149 (GRCm39)	missense	possibly damaging	0.91
R8311:Dnah9	UTSW	11	65,880,644 (GRCm39)	missense	probably benign	0.00
R8326:Dnah9	UTSW	11	66,008,452 (GRCm39)	missense	probably benign	0.01
R8338:Dnah9	UTSW	11	65,732,067 (GRCm39)	critical splice donor site	probably null
R8356:Dnah9	UTSW	11	66,047,764 (GRCm39)	missense	probably damaging	0.99
R8456:Dnah9	UTSW	11	66,047,764 (GRCm39)	missense	probably damaging	0.99
R8468:Dnah9	UTSW	11	65,722,556 (GRCm39)	missense	probably benign	0.00
R8721:Dnah9	UTSW	11	65,986,124 (GRCm39)	missense	probably damaging	1.00
R8747:Dnah9	UTSW	11	65,818,816 (GRCm39)	missense	possibly damaging	0.69
R8798:Dnah9	UTSW	11	65,796,057 (GRCm39)	missense	probably damaging	0.99
R8806:Dnah9	UTSW	11	65,750,309 (GRCm39)	missense	probably damaging	1.00
R8826:Dnah9	UTSW	11	65,740,742 (GRCm39)	missense	probably benign	0.13
R8837:Dnah9	UTSW	11	65,746,060 (GRCm39)	missense	possibly damaging	0.72
R8886:Dnah9	UTSW	11	65,943,840 (GRCm39)	missense	probably damaging	1.00
R8887:Dnah9	UTSW	11	65,746,210 (GRCm39)	missense	probably benign	0.01
R8921:Dnah9	UTSW	11	65,802,747 (GRCm39)	missense	probably benign
R8933:Dnah9	UTSW	11	65,746,078 (GRCm39)	missense	possibly damaging	0.88
R8949:Dnah9	UTSW	11	66,059,226 (GRCm39)	missense	possibly damaging	0.91
R8967:Dnah9	UTSW	11	66,015,938 (GRCm39)	critical splice donor site	probably null
R8979:Dnah9	UTSW	11	65,895,978 (GRCm39)	missense	probably benign
R8991:Dnah9	UTSW	11	65,777,506 (GRCm39)	missense	probably damaging	0.96
R9016:Dnah9	UTSW	11	65,998,856 (GRCm39)	missense	probably damaging	0.99
R9025:Dnah9	UTSW	11	65,896,651 (GRCm39)	missense	probably damaging	1.00
R9043:Dnah9	UTSW	11	65,845,680 (GRCm39)	missense
R9047:Dnah9	UTSW	11	65,962,925 (GRCm39)	missense	possibly damaging	0.89
R9076:Dnah9	UTSW	11	66,008,464 (GRCm39)	missense	probably benign	0.21
R9113:Dnah9	UTSW	11	65,880,713 (GRCm39)	missense	probably damaging	1.00
R9152:Dnah9	UTSW	11	66,021,457 (GRCm39)	missense	probably damaging	1.00
R9187:Dnah9	UTSW	11	65,895,972 (GRCm39)	missense	probably benign
R9198:Dnah9	UTSW	11	65,846,570 (GRCm39)	missense	probably benign	0.02
R9203:Dnah9	UTSW	11	65,746,113 (GRCm39)	missense	possibly damaging	0.58
R9234:Dnah9	UTSW	11	65,924,751 (GRCm39)	missense	possibly damaging	0.68
R9245:Dnah9	UTSW	11	65,786,731 (GRCm39)	missense	probably benign	0.30
R9265:Dnah9	UTSW	11	65,732,081 (GRCm39)	missense	probably benign	0.01
R9307:Dnah9	UTSW	11	65,976,300 (GRCm39)	missense	probably benign	0.14
R9336:Dnah9	UTSW	11	65,761,775 (GRCm39)	missense	probably damaging	1.00
R9386:Dnah9	UTSW	11	65,838,368 (GRCm39)	missense	probably damaging	1.00
R9498:Dnah9	UTSW	11	65,739,199 (GRCm39)	missense	probably damaging	0.99
R9508:Dnah9	UTSW	11	65,725,089 (GRCm39)	missense	probably damaging	1.00
R9524:Dnah9	UTSW	11	65,976,309 (GRCm39)	missense	possibly damaging	0.92
R9577:Dnah9	UTSW	11	65,867,347 (GRCm39)	missense	probably benign	0.00
R9583:Dnah9	UTSW	11	65,856,507 (GRCm39)	missense	probably damaging	1.00
R9587:Dnah9	UTSW	11	65,999,217 (GRCm39)	missense	probably null	0.92
R9612:Dnah9	UTSW	11	65,818,475 (GRCm39)	missense	probably benign	0.00
R9748:Dnah9	UTSW	11	65,976,290 (GRCm39)	missense	possibly damaging	0.51
R9749:Dnah9	UTSW	11	65,986,202 (GRCm39)	missense	probably damaging	1.00
R9759:Dnah9	UTSW	11	65,965,944 (GRCm39)	missense	probably null	0.93
R9784:Dnah9	UTSW	11	65,975,960 (GRCm39)	missense	probably damaging	0.99
V3553:Dnah9	UTSW	11	65,860,902 (GRCm39)	missense	probably damaging	1.00
X0027:Dnah9	UTSW	11	65,976,305 (GRCm39)	missense	probably benign	0.07
X0028:Dnah9	UTSW	11	65,881,278 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,860,910 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,818,679 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,786,798 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,963,661 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,928,300 (GRCm39)	missense	probably damaging	1.00
Z1177:Dnah9	UTSW	11	66,017,476 (GRCm39)	missense	probably damaging	1.00
Z1186:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1186:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1187:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1187:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1188:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1188:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1189:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1189:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1190:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1190:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1191:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1191:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign
Z1192:Dnah9	UTSW	11	66,038,207 (GRCm39)	missense	probably benign
Z1192:Dnah9	UTSW	11	65,976,000 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ACCATGCCCCTGATCTGATC -3'
(R):5'- CAGTCGAGATCGGGTTGTTC -3'

Sequencing Primer
(F):5'- GTCCCAGTCTCTCCATAAGATGAG -3'
(R):5'- TTGTTCCCTGGGAAGTTCAG -3'

Posted On

2014-09-18