Mutagenetix > Incidental Mutation

Incidental Mutation 'R4667:Dnah9'

352065

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

042012-MU

Accession Numbers

Essential gene?

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

Stock #

R4667 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

65722150-66059379 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 66046357 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Tyrosine at position 64 (H64Y)

Ref Sequence

ENSEMBL: ENSMUSP00000104331 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080665] [ENSMUST00000108691]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000080665
AA Change: H262Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: H262Y

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

Predicted Effect

probably benign
Transcript: ENSMUST00000108691
AA Change: H64Y

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000104331
Gene: ENSMUSG00000056752
AA Change: H64Y

Domain	Start	End	E-Value	Type
Pfam:DHC_N1	10	457	2.3e-141	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142836

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.1%
20x: 95.1%

Validation Efficiency

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: 109 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acad8	A	G	9: 26,901,923 (GRCm39)	L147P	probably damaging	Het
Adgra3	T	A	5: 50,136,298 (GRCm39)	Y729F	possibly damaging	Het
Ago2	A	G	15: 73,018,265 (GRCm39)	Y58H	probably damaging	Het
Akap13	A	G	7: 75,378,842 (GRCm39)	T2128A	probably damaging	Het
Ankhd1	C	A	18: 36,781,074 (GRCm39)	P2042Q	possibly damaging	Het
Arhgef15	T	C	11: 68,845,387 (GRCm39)	K155R	probably benign	Het
Atp10b	T	C	11: 43,138,345 (GRCm39)	F1209L	probably damaging	Het
B130006D01Rik	A	T	11: 95,617,335 (GRCm39)		probably benign	Het
Bmpr2	T	C	1: 59,906,875 (GRCm39)	L656S	probably damaging	Het
Bnip5	G	T	17: 29,127,287 (GRCm39)	Q241K	possibly damaging	Het
Btbd17	A	G	11: 114,684,683 (GRCm39)	F119L	possibly damaging	Het
Ccdc191	G	T	16: 43,751,646 (GRCm39)	K267N	probably damaging	Het
Cd200l1	A	G	16: 45,264,526 (GRCm39)	S11P	probably benign	Het
Ceacam20	T	C	7: 19,719,952 (GRCm39)	Y495H	probably damaging	Het
Celf2	T	C	2: 6,726,339 (GRCm39)	I47V	probably benign	Het
Cemip2	G	A	19: 21,774,715 (GRCm39)	R119H	probably benign	Het
Cemip2	C	T	19: 21,822,145 (GRCm39)	A1180V	probably benign	Het
Chd9	T	C	8: 91,760,428 (GRCm39)	S2058P	possibly damaging	Het
Clcn6	T	C	4: 148,108,624 (GRCm39)	E135G	possibly damaging	Het
Cntn1	T	A	15: 92,192,960 (GRCm39)	N687K	probably damaging	Het
Col1a2	A	T	6: 4,512,412 (GRCm39)	M99L	unknown	Het
Cpeb2	T	C	5: 43,391,235 (GRCm39)		probably benign	Het
Csn1s2b	A	G	5: 87,970,170 (GRCm39)	T134A	possibly damaging	Het
Cst13	A	T	2: 148,665,001 (GRCm39)		probably benign	Het
Cyp2c66	T	A	19: 39,165,100 (GRCm39)	D360E	probably damaging	Het
Dhx8	A	G	11: 101,628,987 (GRCm39)	S179G	unknown	Het
Dip2b	A	G	15: 100,049,241 (GRCm39)	I212V	probably benign	Het
Dnal1	T	C	12: 84,183,474 (GRCm39)		probably benign	Het
Dse	T	G	10: 34,029,008 (GRCm39)	Y694S	probably damaging	Het
Dync2h1	T	C	9: 7,051,411 (GRCm39)	I3175V	probably benign	Het
Elf5	A	G	2: 103,279,405 (GRCm39)	N209D	probably damaging	Het
Elovl1	A	G	4: 118,287,984 (GRCm39)	Y40C	probably damaging	Het
Erp27	T	C	6: 136,885,150 (GRCm39)	E216G	possibly damaging	Het
F5	G	A	1: 164,001,755 (GRCm39)	V153I	probably benign	Het
Fam186a	G	A	15: 99,842,413 (GRCm39)	T1277I	possibly damaging	Het
Fam90a1a	A	T	8: 22,453,362 (GRCm39)	H239L	possibly damaging	Het
Fchsd2	G	T	7: 100,899,656 (GRCm39)	R334L	probably damaging	Het
Fermt3	T	C	19: 6,980,288 (GRCm39)	Y369C	probably damaging	Het
Fhod3	C	T	18: 25,199,395 (GRCm39)	P689S	probably benign	Het
Fnbp1l	G	T	3: 122,350,216 (GRCm39)	Q332K	probably benign	Het
Frem3	T	C	8: 81,390,049 (GRCm39)	S1767P	probably damaging	Het
Ggt5	T	C	10: 75,438,865 (GRCm39)	L121P	probably damaging	Het
Gphn	T	C	12: 78,501,591 (GRCm39)	S119P	probably damaging	Het
Herc2	A	G	7: 55,781,001 (GRCm39)	D1222G	probably damaging	Het
Hmx3	T	C	7: 131,146,111 (GRCm39)	I273T	possibly damaging	Het
Hnrnpu	A	G	1: 178,159,746 (GRCm39)		probably benign	Het
Hspg2	C	T	4: 137,266,956 (GRCm39)	T1987I	possibly damaging	Het
Ighv1-22	T	A	12: 114,710,071 (GRCm39)	Q58L	probably damaging	Het
Ighv14-3	T	A	12: 114,023,875 (GRCm39)	I7F	probably benign	Het
Kcns3	C	A	12: 11,141,784 (GRCm39)	R305L	probably damaging	Het
Kcnu1	C	T	8: 26,400,949 (GRCm39)	A699V	possibly damaging	Het
Kif22	A	C	7: 126,632,500 (GRCm39)	L270W	probably damaging	Het
Lrp2	G	T	2: 69,319,642 (GRCm39)	H1960Q	probably benign	Het
Marchf7	C	T	2: 60,071,394 (GRCm39)	Q94*	probably null	Het
Mcoln3	A	T	3: 145,836,959 (GRCm39)	I264F	probably benign	Het
Mdn1	A	C	4: 32,679,572 (GRCm39)	T706P	probably damaging	Het
Mfsd2b	A	G	12: 4,917,636 (GRCm39)	C137R	probably benign	Het
Mmp25	A	G	17: 23,863,581 (GRCm39)	V83A	probably benign	Het
Mocos	T	C	18: 24,799,491 (GRCm39)	Y242H	probably benign	Het
Msh6	T	C	17: 88,292,234 (GRCm39)	S330P	possibly damaging	Het
Mtus2	T	C	5: 148,235,070 (GRCm39)	S1156P	possibly damaging	Het
Muc5b	G	A	7: 141,396,116 (GRCm39)	R124H	unknown	Het
Mybbp1a	G	A	11: 72,338,797 (GRCm39)	E775K	possibly damaging	Het
Myo10	A	G	15: 25,793,239 (GRCm39)	E1272G	possibly damaging	Het
Nars1	A	G	18: 64,638,302 (GRCm39)	S254P	possibly damaging	Het
Ncapd2	A	G	6: 125,161,481 (GRCm39)	I211T	possibly damaging	Het
Ncoa7	A	T	10: 30,566,786 (GRCm39)	W582R	probably damaging	Het
Npr3	T	A	15: 11,905,553 (GRCm39)	D58V	possibly damaging	Het
Nr3c1	G	T	18: 39,561,780 (GRCm39)	T430K	probably benign	Het
Odf2l	A	G	3: 144,833,801 (GRCm39)	T111A	probably benign	Het
Ogdh	G	T	11: 6,290,600 (GRCm39)	C406F	probably benign	Het
Olfml2a	T	G	2: 38,839,022 (GRCm39)	S190A	probably damaging	Het
Optn	T	C	2: 5,037,950 (GRCm39)	K415E	probably benign	Het
Or10n1	T	C	9: 39,525,034 (GRCm39)	M57T	probably damaging	Het
Or52a20	A	G	7: 103,365,845 (GRCm39)	T15A	probably benign	Het
Or8b12i	T	C	9: 20,082,394 (GRCm39)	I158V	probably benign	Het
Or8g52	G	T	9: 39,631,005 (GRCm39)	V161F	probably benign	Het
Pakap	A	T	4: 57,855,655 (GRCm39)	D328V	possibly damaging	Het
Perm1	C	A	4: 156,304,663 (GRCm39)	S803*	probably null	Het
Pex14	T	C	4: 149,068,542 (GRCm39)	T84A	probably benign	Het
Pih1d2	T	A	9: 50,532,252 (GRCm39)	Y103*	probably null	Het
Pikfyve	T	A	1: 65,289,432 (GRCm39)	C1235S	probably damaging	Het
Polr1a	A	G	6: 71,894,805 (GRCm39)	N171S	probably benign	Het
Prrx1	A	G	1: 163,081,616 (GRCm39)	S201P	probably benign	Het
Psme2b	A	T	11: 48,836,493 (GRCm39)	N151K	probably benign	Het
Serpinb5	A	T	1: 106,800,025 (GRCm39)	T72S	probably benign	Het
Sgsm1	A	G	5: 113,407,913 (GRCm39)		probably null	Het
Sipa1l2	T	C	8: 126,180,209 (GRCm39)	R1063G	possibly damaging	Het
Slc19a3	T	C	1: 83,000,520 (GRCm39)	T166A	probably benign	Het
Slc5a4b	T	C	10: 75,910,879 (GRCm39)	Y319C	possibly damaging	Het
Stard3nl	T	A	13: 19,560,689 (GRCm39)	N29Y	probably damaging	Het
Sult6b2	G	T	6: 142,747,421 (GRCm39)	C109*	probably null	Het
Tcf25	A	G	8: 124,123,764 (GRCm39)	E467G	possibly damaging	Het
Tmem177	A	T	1: 119,837,950 (GRCm39)	V243D	probably benign	Het
Top2b	T	G	14: 16,409,189 (GRCm38)	I777M	probably damaging	Het
Tspan11	T	A	6: 127,920,678 (GRCm39)	C208*	probably null	Het
Ttc1	A	G	11: 43,636,144 (GRCm39)	V33A	probably benign	Het
Tut4	G	A	4: 108,352,356 (GRCm39)	E357K	probably damaging	Het
Uck1	T	A	2: 32,146,046 (GRCm39)	H283L	probably damaging	Het
Utrn	A	C	10: 12,573,797 (GRCm39)	V1091G	probably benign	Het
Vmn1r11	A	T	6: 57,114,483 (GRCm39)	H49L	probably damaging	Het
Vmn1r160	G	T	7: 22,571,478 (GRCm39)	S277I	probably benign	Het
Vmn1r18	A	T	6: 57,367,069 (GRCm39)	S162T	probably benign	Het
Vps37b	A	G	5: 124,148,795 (GRCm39)	L80P	probably damaging	Het
Wfdc3	T	C	2: 164,585,006 (GRCm39)	M1V	probably null	Het
Wrn	A	T	8: 33,814,366 (GRCm39)	N116K	probably benign	Het
Wscd2	G	T	5: 113,715,333 (GRCm39)	G391V	probably damaging	Het
Zfp286	A	G	11: 62,671,428 (GRCm39)	V215A	probably benign	Het
Zfp568	A	G	7: 29,722,702 (GRCm39)	H549R	probably damaging	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
R2104:Dnah9	UTSW	11	65,951,950 (GRCm39)	missense	probably damaging	1.00
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
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'- GCCACCATGCTGTCTCATAC -3'
(R):5'- TGAAACAGATGTCTGAGTTCGG -3'

Sequencing Primer
(F):5'- GACACGGTGCTAATGACAACTTTG -3'
(R):5'- AAACAGATGTCTGAGTTCGGTTCTTG -3'

Posted On

2015-10-08