Mutagenetix > Incidental Mutation

Incidental Mutation 'R1718:Dnah9'

191218

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

039751-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.294) question?

Stock #

R1718 (G1)

Quality Score

138

Status

Validated

Chromosome

Chromosomal Location

65831282-66168551 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 66168079 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 130 (H130L)

Ref Sequence

ENSEMBL: ENSMUSP00000079494 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000080665
AA Change: H130L

PolyPhen 2 Score 0.816 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: H130L

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

SMART Domains

Protein: ENSMUSP00000104331
Gene: ENSMUSG00000056752

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142836

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144922

Meta Mutation Damage Score

0.1552

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.6%
20x: 93.5%

Validation Efficiency

100% (69/69)

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: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210408I21Rik	G	T	13: 77,245,370 (GRCm38)		probably benign	Het
Acot3	T	G	12: 84,053,943 (GRCm38)		probably null	Het
Acox1	A	T	11: 116,174,682 (GRCm38)	C523*	probably null	Het
Adamts19	G	A	18: 58,972,825 (GRCm38)	C764Y	probably damaging	Het
Agrn	GCTCT	GCTCTCT	4: 156,166,519 (GRCm38)		probably null	Het
Apob	A	G	12: 8,016,087 (GRCm38)	K4319R	probably benign	Het
AU016765	A	C	17: 64,555,438 (GRCm38)		noncoding transcript	Het
Bpifb1	T	A	2: 154,213,983 (GRCm38)		probably null	Het
Btn2a2	A	G	13: 23,481,936 (GRCm38)	V242A	probably benign	Het
Camta1	A	G	4: 151,084,024 (GRCm38)	S1281P	probably benign	Het
Ccdc116	T	C	16: 17,141,908 (GRCm38)	K306E	probably benign	Het
Cemip	A	G	7: 83,935,658 (GRCm38)	V1350A	probably benign	Het
Clip2	A	T	5: 134,502,929 (GRCm38)	L674*	probably null	Het
Cyp2d12	T	A	15: 82,558,050 (GRCm38)	D244E	probably benign	Het
Cyp4x1	A	G	4: 115,111,670 (GRCm38)	V379A	possibly damaging	Het
Enpp7	A	G	11: 118,990,983 (GRCm38)	Y318C	probably damaging	Het
Fras1	A	T	5: 96,554,889 (GRCm38)		probably null	Het
Glra3	G	T	8: 55,940,907 (GRCm38)	A18S	probably benign	Het
Gm28042	T	A	2: 120,036,391 (GRCm38)	S172T	possibly damaging	Het
Gm7808	T	A	9: 19,928,003 (GRCm38)		probably benign	Het
Gm8909	A	G	17: 36,161,784 (GRCm38)		probably benign	Het
Gpr61	C	T	3: 108,150,380 (GRCm38)	V322M	possibly damaging	Het
Hapln3	A	G	7: 79,123,450 (GRCm38)	V15A	unknown	Het
Ip6k1	G	A	9: 108,040,996 (GRCm38)	E77K	possibly damaging	Het
Klk1b4	A	G	7: 44,209,672 (GRCm38)	Y38C	probably damaging	Het
Lrrfip1	A	G	1: 91,115,555 (GRCm38)	K561E	probably damaging	Het
Map3k1	A	G	13: 111,755,419 (GRCm38)	C1101R	probably benign	Het
Mcoln2	A	G	3: 146,190,474 (GRCm38)		probably benign	Het
Mfsd2b	G	A	12: 4,869,037 (GRCm38)	T73I	probably damaging	Het
Mfsd4b5	C	T	10: 39,975,203 (GRCm38)	V19I	probably benign	Het
Mgme1	T	A	2: 144,272,318 (GRCm38)	D113E	probably benign	Het
Mki67	A	G	7: 135,695,494 (GRCm38)	S2604P	probably damaging	Het
Mob3c	A	G	4: 115,831,644 (GRCm38)	I125V	probably benign	Het
Mrps9	G	A	1: 42,903,399 (GRCm38)	R339H	probably damaging	Het
Ndst1	T	C	18: 60,707,803 (GRCm38)	D269G	probably damaging	Het
Nedd9	T	C	13: 41,338,926 (GRCm38)	N30S	probably damaging	Het
Notch4	G	A	17: 34,576,763 (GRCm38)		probably benign	Het
Olfr1095	A	T	2: 86,851,187 (GRCm38)	N170K	probably benign	Het
Olfr250	A	G	9: 38,367,594 (GRCm38)	D6G	probably benign	Het
Olfr877	G	A	9: 37,855,453 (GRCm38)	V212I	probably benign	Het
Olfr995	T	C	2: 85,438,805 (GRCm38)	M118V	probably benign	Het
Papss1	C	A	3: 131,619,185 (GRCm38)	R447S	probably damaging	Het
Pla2g4a	C	T	1: 149,871,523 (GRCm38)		probably benign	Het
Rab11fip2	A	G	19: 59,935,649 (GRCm38)	F266L	probably damaging	Het
Ralgapb	T	A	2: 158,443,280 (GRCm38)	Y554*	probably null	Het
Rem2	T	C	14: 54,479,150 (GRCm38)	V240A	probably damaging	Het
Retsat	T	C	6: 72,602,671 (GRCm38)	V143A	probably benign	Het
Rnf141	G	T	7: 110,821,273 (GRCm38)	Q175K	probably damaging	Het
Rtcb	C	A	10: 85,942,017 (GRCm38)	G431V	probably damaging	Het
Slc7a6os	A	G	8: 106,204,339 (GRCm38)	W222R	probably damaging	Het
Smarcc2	T	C	10: 128,468,998 (GRCm38)		probably benign	Het
Smchd1	A	T	17: 71,448,833 (GRCm38)	Y218N	possibly damaging	Het
Sp110	G	A	1: 85,594,385 (GRCm38)	H66Y	probably benign	Het
Speg	A	G	1: 75,421,744 (GRCm38)	Q1945R	possibly damaging	Het
Speg	G	A	1: 75,417,863 (GRCm38)	E1739K	probably benign	Het
Sprtn	T	C	8: 124,898,357 (GRCm38)	V67A	probably damaging	Het
Tktl2	G	A	8: 66,512,347 (GRCm38)	V186M	probably damaging	Het
Tnks1bp1	G	T	2: 85,071,738 (GRCm38)	E997D	probably benign	Het
Tti1	A	T	2: 158,008,224 (GRCm38)	V365E	probably benign	Het
Tulp4	A	G	17: 6,222,440 (GRCm38)	I590V	probably benign	Het
Vmn2r61	A	G	7: 42,300,697 (GRCm38)	D847G	probably benign	Het
Zfp184	A	G	13: 21,959,272 (GRCm38)	T383A	possibly damaging	Het
Zik1	C	A	7: 10,492,342 (GRCm38)	E33*	probably null	Het
Zik1	T	A	7: 10,492,341 (GRCm38)	E33V	probably damaging	Het

Other mutations in Dnah9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00696:Dnah9	APN	11	65,841,238 (GRCm38)	splice site	probably benign
IGL00805:Dnah9	APN	11	65,881,695 (GRCm38)	missense	probably benign	0.00
IGL00826:Dnah9	APN	11	65,989,942 (GRCm38)	missense	probably damaging	1.00
IGL01108:Dnah9	APN	11	65,849,980 (GRCm38)	missense	possibly damaging	0.93
IGL01152:Dnah9	APN	11	66,072,056 (GRCm38)	missense	probably damaging	1.00
IGL01353:Dnah9	APN	11	66,080,571 (GRCm38)	missense	probably damaging	1.00
IGL01364:Dnah9	APN	11	66,155,459 (GRCm38)	missense	probably damaging	1.00
IGL01479:Dnah9	APN	11	65,955,717 (GRCm38)	missense	probably benign	0.14
IGL01537:Dnah9	APN	11	65,947,680 (GRCm38)	missense	probably benign
IGL01565:Dnah9	APN	11	66,033,829 (GRCm38)	missense	possibly damaging	0.95
IGL01597:Dnah9	APN	11	66,118,830 (GRCm38)	missense	probably damaging	1.00
IGL01619:Dnah9	APN	11	65,831,615 (GRCm38)	nonsense	probably null
IGL01625:Dnah9	APN	11	66,044,645 (GRCm38)	missense	probably damaging	1.00
IGL01803:Dnah9	APN	11	66,118,829 (GRCm38)	missense	probably damaging	1.00
IGL01819:Dnah9	APN	11	66,108,126 (GRCm38)	missense	probably benign	0.33
IGL01896:Dnah9	APN	11	66,130,666 (GRCm38)	missense	possibly damaging	0.89
IGL01922:Dnah9	APN	11	66,075,034 (GRCm38)	splice site	probably benign
IGL01923:Dnah9	APN	11	66,125,235 (GRCm38)	splice site	probably benign
IGL02059:Dnah9	APN	11	66,072,958 (GRCm38)	missense	probably damaging	1.00
IGL02068:Dnah9	APN	11	66,061,045 (GRCm38)	missense	probably damaging	1.00
IGL02135:Dnah9	APN	11	66,117,492 (GRCm38)	missense	possibly damaging	0.63
IGL02146:Dnah9	APN	11	65,927,700 (GRCm38)	missense	probably damaging	1.00
IGL02264:Dnah9	APN	11	66,080,488 (GRCm38)	splice site	probably benign
IGL02325:Dnah9	APN	11	65,834,217 (GRCm38)	missense	probably damaging	1.00
IGL02426:Dnah9	APN	11	66,125,153 (GRCm38)	missense	probably benign
IGL02440:Dnah9	APN	11	65,955,246 (GRCm38)	missense	probably damaging	1.00
IGL02471:Dnah9	APN	11	65,947,618 (GRCm38)	nonsense	probably null
IGL02496:Dnah9	APN	11	66,029,363 (GRCm38)	missense	probably damaging	1.00
IGL02672:Dnah9	APN	11	65,927,601 (GRCm38)	missense	probably benign	0.02
IGL02718:Dnah9	APN	11	65,886,640 (GRCm38)	missense	probably damaging	0.99
IGL02832:Dnah9	APN	11	66,040,346 (GRCm38)	missense	probably damaging	1.00
IGL02851:Dnah9	APN	11	66,037,744 (GRCm38)	splice site	probably benign
IGL02859:Dnah9	APN	11	65,881,619 (GRCm38)	splice site	probably benign
IGL02864:Dnah9	APN	11	66,061,003 (GRCm38)	missense	probably damaging	1.00
IGL02954:Dnah9	APN	11	66,118,967 (GRCm38)	missense	probably damaging	1.00
IGL02987:Dnah9	APN	11	65,841,273 (GRCm38)	missense	probably benign	0.23
IGL02987:Dnah9	APN	11	65,855,272 (GRCm38)	missense	probably damaging	0.98
IGL03160:Dnah9	APN	11	66,108,054 (GRCm38)	missense	probably damaging	0.98
IGL03171:Dnah9	APN	11	65,981,241 (GRCm38)	missense	probably benign	0.13
IGL03180:Dnah9	APN	11	65,886,639 (GRCm38)	missense	probably damaging	0.99
IGL03388:Dnah9	APN	11	65,947,542 (GRCm38)	missense	probably damaging	1.00
anarchy	UTSW	11	65,955,248 (GRCm38)	missense	probably damaging	0.99
sacco	UTSW	11	66,168,079 (GRCm38)	missense	possibly damaging	0.82
Tweed	UTSW	11	66,072,072 (GRCm38)	missense	probably damaging	0.99
vanzetti	UTSW	11	65,855,372 (GRCm38)	nonsense	probably null
IGL02837:Dnah9	UTSW	11	65,874,196 (GRCm38)	missense	probably damaging	1.00
PIT4280001:Dnah9	UTSW	11	66,005,013 (GRCm38)	missense	probably benign	0.44
R0021:Dnah9	UTSW	11	65,969,979 (GRCm38)	missense	probably benign	0.36
R0021:Dnah9	UTSW	11	65,969,979 (GRCm38)	missense	probably benign	0.36
R0025:Dnah9	UTSW	11	65,969,955 (GRCm38)	splice site	probably benign
R0025:Dnah9	UTSW	11	65,969,955 (GRCm38)	splice site	probably benign
R0070:Dnah9	UTSW	11	66,160,040 (GRCm38)	missense	probably benign	0.10
R0164:Dnah9	UTSW	11	65,918,804 (GRCm38)	nonsense	probably null
R0164:Dnah9	UTSW	11	65,918,804 (GRCm38)	nonsense	probably null
R0180:Dnah9	UTSW	11	66,147,290 (GRCm38)	missense	probably damaging	1.00
R0195:Dnah9	UTSW	11	65,895,905 (GRCm38)	missense	probably benign	0.30
R0230:Dnah9	UTSW	11	65,855,315 (GRCm38)	missense	probably damaging	1.00
R0243:Dnah9	UTSW	11	65,911,852 (GRCm38)	missense	possibly damaging	0.91
R0279:Dnah9	UTSW	11	65,911,789 (GRCm38)	critical splice donor site	probably null
R0288:Dnah9	UTSW	11	66,025,134 (GRCm38)	critical splice donor site	probably null
R0309:Dnah9	UTSW	11	66,026,972 (GRCm38)	splice site	probably benign
R0356:Dnah9	UTSW	11	66,130,562 (GRCm38)	critical splice donor site	probably null
R0403:Dnah9	UTSW	11	66,084,789 (GRCm38)	missense	possibly damaging	0.90
R0413:Dnah9	UTSW	11	66,108,135 (GRCm38)	missense	probably damaging	1.00
R0448:Dnah9	UTSW	11	65,918,713 (GRCm38)	splice site	probably benign
R0496:Dnah9	UTSW	11	66,075,135 (GRCm38)	missense	probably null	1.00
R0557:Dnah9	UTSW	11	66,084,666 (GRCm38)	missense	probably damaging	1.00
R0584:Dnah9	UTSW	11	65,990,489 (GRCm38)	missense	probably damaging	1.00
R0598:Dnah9	UTSW	11	66,118,877 (GRCm38)	missense	probably benign	0.02
R0599:Dnah9	UTSW	11	65,965,689 (GRCm38)	missense	probably damaging	1.00
R0606:Dnah9	UTSW	11	65,841,333 (GRCm38)	missense	probably damaging	1.00
R0666:Dnah9	UTSW	11	66,085,458 (GRCm38)	missense	probably benign	0.01
R0715:Dnah9	UTSW	11	66,081,248 (GRCm38)	splice site	probably benign
R0726:Dnah9	UTSW	11	65,965,681 (GRCm38)	missense	probably damaging	1.00
R0737:Dnah9	UTSW	11	66,107,898 (GRCm38)	missense	probably damaging	1.00
R0763:Dnah9	UTSW	11	66,155,530 (GRCm38)	missense	probably benign	0.30
R0792:Dnah9	UTSW	11	65,896,001 (GRCm38)	missense	possibly damaging	0.84
R0829:Dnah9	UTSW	11	66,005,176 (GRCm38)	missense	probably benign	0.00
R0973:Dnah9	UTSW	11	66,005,837 (GRCm38)	splice site	probably null
R0974:Dnah9	UTSW	11	66,005,837 (GRCm38)	splice site	probably null
R1055:Dnah9	UTSW	11	66,160,011 (GRCm38)	missense	probably damaging	1.00
R1081:Dnah9	UTSW	11	66,084,877 (GRCm38)	missense	probably damaging	0.99
R1184:Dnah9	UTSW	11	66,084,612 (GRCm38)	critical splice donor site	probably null
R1225:Dnah9	UTSW	11	65,871,060 (GRCm38)	missense	possibly damaging	0.94
R1304:Dnah9	UTSW	11	65,927,588 (GRCm38)	missense	probably damaging	0.98
R1417:Dnah9	UTSW	11	65,955,747 (GRCm38)	missense	probably damaging	0.96
R1439:Dnah9	UTSW	11	65,874,132 (GRCm38)	missense	probably benign	0.22
R1447:Dnah9	UTSW	11	66,108,482 (GRCm38)	missense	possibly damaging	0.65
R1450:Dnah9	UTSW	11	65,927,786 (GRCm38)	missense	probably damaging	1.00
R1470:Dnah9	UTSW	11	65,927,822 (GRCm38)	missense	probably benign	0.11
R1470:Dnah9	UTSW	11	65,927,822 (GRCm38)	missense	probably benign	0.11
R1486:Dnah9	UTSW	11	65,834,272 (GRCm38)	missense	probably damaging	1.00
R1519:Dnah9	UTSW	11	65,881,761 (GRCm38)	missense	probably damaging	0.96
R1570:Dnah9	UTSW	11	66,112,330 (GRCm38)	missense	probably benign
R1617:Dnah9	UTSW	11	65,895,921 (GRCm38)	missense	probably damaging	1.00
R1623:Dnah9	UTSW	11	66,037,637 (GRCm38)	missense	probably damaging	1.00
R1626:Dnah9	UTSW	11	66,085,267 (GRCm38)	missense	probably benign	0.05
R1671:Dnah9	UTSW	11	65,927,963 (GRCm38)	missense	probably damaging	0.99
R1694:Dnah9	UTSW	11	65,954,824 (GRCm38)	nonsense	probably null
R1701:Dnah9	UTSW	11	65,911,924 (GRCm38)	missense	probably damaging	1.00
R1702:Dnah9	UTSW	11	66,085,195 (GRCm38)	missense	possibly damaging	0.72
R1708:Dnah9	UTSW	11	65,915,154 (GRCm38)	missense	probably benign	0.11
R1729:Dnah9	UTSW	11	66,085,020 (GRCm38)	missense	possibly damaging	0.51
R1760:Dnah9	UTSW	11	65,981,222 (GRCm38)	missense	probably benign	0.31
R1784:Dnah9	UTSW	11	66,085,020 (GRCm38)	missense	possibly damaging	0.51
R1793:Dnah9	UTSW	11	66,119,594 (GRCm38)	critical splice donor site	probably null
R1801:Dnah9	UTSW	11	65,955,297 (GRCm38)	missense	probably damaging	0.99
R1827:Dnah9	UTSW	11	65,850,061 (GRCm38)	missense	probably damaging	0.97
R1836:Dnah9	UTSW	11	66,118,841 (GRCm38)	missense	probably benign	0.10
R1840:Dnah9	UTSW	11	65,834,198 (GRCm38)	nonsense	probably null
R1847:Dnah9	UTSW	11	65,834,386 (GRCm38)	missense	probably damaging	1.00
R1872:Dnah9	UTSW	11	66,037,490 (GRCm38)	missense	probably benign	0.16
R1929:Dnah9	UTSW	11	65,976,398 (GRCm38)	missense	probably benign	0.05
R1969:Dnah9	UTSW	11	65,848,371 (GRCm38)	missense	probably damaging	1.00
R1971:Dnah9	UTSW	11	65,848,371 (GRCm38)	missense	probably damaging	1.00
R2027:Dnah9	UTSW	11	65,955,338 (GRCm38)	missense	probably benign	0.11
R2049:Dnah9	UTSW	11	66,044,683 (GRCm38)	missense	probably damaging	1.00
R2064:Dnah9	UTSW	11	66,145,435 (GRCm38)	missense	probably benign	0.31
R2104:Dnah9	UTSW	11	66,061,124 (GRCm38)	missense	probably damaging	1.00
R2109:Dnah9	UTSW	11	66,037,585 (GRCm38)	missense	probably damaging	1.00
R2160:Dnah9	UTSW	11	66,117,483 (GRCm38)	missense	probably damaging	1.00
R2172:Dnah9	UTSW	11	66,072,779 (GRCm38)	missense	probably damaging	1.00
R2198:Dnah9	UTSW	11	65,859,499 (GRCm38)	missense	possibly damaging	0.50
R2271:Dnah9	UTSW	11	66,112,362 (GRCm38)	missense	probably benign	0.37
R2272:Dnah9	UTSW	11	66,112,362 (GRCm38)	missense	probably benign	0.37
R2396:Dnah9	UTSW	11	66,085,158 (GRCm38)	missense	probably benign	0.01
R2398:Dnah9	UTSW	11	65,915,203 (GRCm38)	missense	probably damaging	1.00
R2418:Dnah9	UTSW	11	66,095,415 (GRCm38)	nonsense	probably null
R2419:Dnah9	UTSW	11	66,095,415 (GRCm38)	nonsense	probably null
R2510:Dnah9	UTSW	11	66,005,169 (GRCm38)	missense	probably damaging	1.00
R2680:Dnah9	UTSW	11	66,033,925 (GRCm38)	missense	probably benign	0.00
R2875:Dnah9	UTSW	11	66,168,461 (GRCm38)	missense	possibly damaging	0.89
R2979:Dnah9	UTSW	11	66,117,588 (GRCm38)	missense	possibly damaging	0.89
R3236:Dnah9	UTSW	11	65,954,989 (GRCm38)	missense	probably benign	0.11
R3237:Dnah9	UTSW	11	65,954,989 (GRCm38)	missense	probably benign	0.11
R3433:Dnah9	UTSW	11	66,075,112 (GRCm38)	missense	possibly damaging	0.85
R3737:Dnah9	UTSW	11	66,156,908 (GRCm38)	nonsense	probably null
R3820:Dnah9	UTSW	11	65,851,003 (GRCm38)	critical splice donor site	probably null
R3821:Dnah9	UTSW	11	65,851,003 (GRCm38)	critical splice donor site	probably null
R3822:Dnah9	UTSW	11	65,851,003 (GRCm38)	critical splice donor site	probably null
R3861:Dnah9	UTSW	11	66,052,994 (GRCm38)	splice site	probably benign
R3918:Dnah9	UTSW	11	65,870,974 (GRCm38)	missense	possibly damaging	0.54
R4011:Dnah9	UTSW	11	65,834,464 (GRCm38)	missense	probably damaging	0.98
R4044:Dnah9	UTSW	11	66,133,635 (GRCm38)	missense	probably benign	0.03
R4072:Dnah9	UTSW	11	66,084,904 (GRCm38)	missense	probably benign	0.00
R4076:Dnah9	UTSW	11	66,084,904 (GRCm38)	missense	probably benign	0.00
R4097:Dnah9	UTSW	11	65,990,459 (GRCm38)	missense	probably damaging	1.00
R4409:Dnah9	UTSW	11	66,085,477 (GRCm38)	missense	possibly damaging	0.51
R4410:Dnah9	UTSW	11	66,085,477 (GRCm38)	missense	possibly damaging	0.51
R4417:Dnah9	UTSW	11	65,981,214 (GRCm38)	missense	possibly damaging	0.75
R4420:Dnah9	UTSW	11	66,118,749 (GRCm38)	missense	probably benign	0.00
R4434:Dnah9	UTSW	11	66,108,075 (GRCm38)	missense	possibly damaging	0.67
R4451:Dnah9	UTSW	11	65,881,641 (GRCm38)	missense	probably benign	0.07
R4452:Dnah9	UTSW	11	66,027,082 (GRCm38)	missense	probably damaging	0.96
R4454:Dnah9	UTSW	11	66,147,389 (GRCm38)	missense	probably damaging	0.96
R4551:Dnah9	UTSW	11	65,841,366 (GRCm38)	missense	probably damaging	1.00
R4552:Dnah9	UTSW	11	65,841,366 (GRCm38)	missense	probably damaging	1.00
R4590:Dnah9	UTSW	11	66,040,392 (GRCm38)	missense	probably damaging	1.00
R4595:Dnah9	UTSW	11	66,168,152 (GRCm38)	missense	probably benign
R4655:Dnah9	UTSW	11	65,955,732 (GRCm38)	missense	probably benign	0.00
R4667:Dnah9	UTSW	11	66,155,531 (GRCm38)	missense	probably benign
R4718:Dnah9	UTSW	11	66,085,473 (GRCm38)	missense	probably benign
R4720:Dnah9	UTSW	11	66,076,358 (GRCm38)	missense	probably damaging	1.00
R4734:Dnah9	UTSW	11	65,834,115 (GRCm38)	missense	probably damaging	1.00
R4749:Dnah9	UTSW	11	65,834,115 (GRCm38)	missense	probably damaging	1.00
R4765:Dnah9	UTSW	11	65,927,726 (GRCm38)	missense	probably damaging	1.00
R4905:Dnah9	UTSW	11	65,874,124 (GRCm38)	nonsense	probably null
R4963:Dnah9	UTSW	11	66,084,611 (GRCm38)	splice site	probably null
R5074:Dnah9	UTSW	11	65,850,040 (GRCm38)	missense	probably damaging	1.00
R5230:Dnah9	UTSW	11	66,084,666 (GRCm38)	missense	probably damaging	0.99
R5262:Dnah9	UTSW	11	66,112,333 (GRCm38)	missense	probably benign	0.34
R5364:Dnah9	UTSW	11	65,881,696 (GRCm38)	missense	possibly damaging	0.93
R5370:Dnah9	UTSW	11	66,029,354 (GRCm38)	missense	probably damaging	1.00
R5386:Dnah9	UTSW	11	66,029,356 (GRCm38)	missense	probably damaging	1.00
R5389:Dnah9	UTSW	11	66,095,314 (GRCm38)	nonsense	probably null
R5541:Dnah9	UTSW	11	66,145,336 (GRCm38)	missense	probably damaging	1.00
R5560:Dnah9	UTSW	11	65,881,740 (GRCm38)	missense	probably benign	0.00
R5576:Dnah9	UTSW	11	65,834,096 (GRCm38)	splice site	probably null
R5648:Dnah9	UTSW	11	65,927,755 (GRCm38)	missense	probably benign	0.00
R5653:Dnah9	UTSW	11	65,849,980 (GRCm38)	missense	probably damaging	0.99
R5713:Dnah9	UTSW	11	66,025,223 (GRCm38)	missense	possibly damaging	0.92
R5763:Dnah9	UTSW	11	65,955,239 (GRCm38)	missense	probably damaging	1.00
R5825:Dnah9	UTSW	11	66,126,601 (GRCm38)	missense	probably benign	0.01
R5831:Dnah9	UTSW	11	66,108,121 (GRCm38)	missense	probably benign	0.00
R5847:Dnah9	UTSW	11	66,095,240 (GRCm38)	frame shift	probably null
R5870:Dnah9	UTSW	11	66,085,210 (GRCm38)	missense	probably benign	0.01
R5902:Dnah9	UTSW	11	66,025,187 (GRCm38)	missense	probably benign	0.08
R5918:Dnah9	UTSW	11	65,834,199 (GRCm38)	missense	probably damaging	1.00
R5979:Dnah9	UTSW	11	65,834,481 (GRCm38)	missense	probably damaging	1.00
R6065:Dnah9	UTSW	11	66,145,397 (GRCm38)	missense	possibly damaging	0.65
R6065:Dnah9	UTSW	11	65,855,338 (GRCm38)	missense	probably benign	0.05
R6086:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
R6086:Dnah9	UTSW	11	65,989,915 (GRCm38)	missense	probably damaging	0.99
R6102:Dnah9	UTSW	11	65,990,516 (GRCm38)	missense	probably damaging	0.97
R6120:Dnah9	UTSW	11	66,147,399 (GRCm38)	missense	probably benign
R6154:Dnah9	UTSW	11	65,855,338 (GRCm38)	missense	probably benign	0.00
R6262:Dnah9	UTSW	11	65,881,805 (GRCm38)	splice site	probably null
R6265:Dnah9	UTSW	11	66,168,094 (GRCm38)	missense	probably benign	0.04
R6290:Dnah9	UTSW	11	65,841,375 (GRCm38)	missense	probably damaging	1.00
R6345:Dnah9	UTSW	11	66,037,693 (GRCm38)	missense	probably damaging	0.97
R6357:Dnah9	UTSW	11	65,874,196 (GRCm38)	missense	probably damaging	1.00
R6534:Dnah9	UTSW	11	65,955,248 (GRCm38)	missense	probably damaging	0.99
R6574:Dnah9	UTSW	11	66,168,281 (GRCm38)	missense	probably benign	0.37
R6582:Dnah9	UTSW	11	66,061,097 (GRCm38)	missense	probably damaging	1.00
R6700:Dnah9	UTSW	11	65,955,366 (GRCm38)	missense	probably damaging	1.00
R6800:Dnah9	UTSW	11	66,072,739 (GRCm38)	critical splice donor site	probably null
R6812:Dnah9	UTSW	11	65,981,329 (GRCm38)	missense	probably damaging	0.99
R6931:Dnah9	UTSW	11	66,117,626 (GRCm38)	missense	possibly damaging	0.63
R6944:Dnah9	UTSW	11	66,085,149 (GRCm38)	missense	possibly damaging	0.91
R6958:Dnah9	UTSW	11	66,076,341 (GRCm38)	missense	probably damaging	1.00
R6977:Dnah9	UTSW	11	66,107,909 (GRCm38)	missense	probably benign	0.37
R7021:Dnah9	UTSW	11	65,981,231 (GRCm38)	missense	probably benign
R7161:Dnah9	UTSW	11	65,855,372 (GRCm38)	nonsense	probably null
R7175:Dnah9	UTSW	11	66,133,637 (GRCm38)	missense	probably benign	0.03
R7199:Dnah9	UTSW	11	66,118,944 (GRCm38)	missense	probably benign	0.04
R7231:Dnah9	UTSW	11	65,965,647 (GRCm38)	missense	probably damaging	1.00
R7284:Dnah9	UTSW	11	65,990,476 (GRCm38)	missense	probably damaging	0.99
R7314:Dnah9	UTSW	11	65,989,851 (GRCm38)	missense	probably benign	0.00
R7350:Dnah9	UTSW	11	66,080,578 (GRCm38)	missense	probably damaging	1.00
R7420:Dnah9	UTSW	11	66,117,407 (GRCm38)	critical splice donor site	probably null
R7427:Dnah9	UTSW	11	65,955,219 (GRCm38)	missense	probably benign
R7477:Dnah9	UTSW	11	65,992,731 (GRCm38)	missense	probably damaging	0.98
R7515:Dnah9	UTSW	11	65,841,414 (GRCm38)	missense	probably benign	0.01
R7521:Dnah9	UTSW	11	65,989,837 (GRCm38)	missense	probably damaging	0.98
R7573:Dnah9	UTSW	11	66,125,215 (GRCm38)	missense	probably benign	0.43
R7659:Dnah9	UTSW	11	65,989,780 (GRCm38)	missense	probably damaging	0.99
R7707:Dnah9	UTSW	11	66,118,958 (GRCm38)	missense	probably damaging	1.00
R7749:Dnah9	UTSW	11	65,911,830 (GRCm38)	missense	probably damaging	1.00
R7792:Dnah9	UTSW	11	65,850,013 (GRCm38)	missense	probably damaging	1.00
R7808:Dnah9	UTSW	11	66,005,805 (GRCm38)	nonsense	probably null
R7814:Dnah9	UTSW	11	66,005,660 (GRCm38)	missense	probably damaging	1.00
R7818:Dnah9	UTSW	11	66,025,211 (GRCm38)	missense	possibly damaging	0.64
R7890:Dnah9	UTSW	11	66,072,072 (GRCm38)	missense	probably damaging	0.99
R7976:Dnah9	UTSW	11	65,841,401 (GRCm38)	missense	possibly damaging	0.91
R8121:Dnah9	UTSW	11	66,017,375 (GRCm38)	missense	probably benign	0.02
R8232:Dnah9	UTSW	11	65,855,323 (GRCm38)	missense	possibly damaging	0.91
R8311:Dnah9	UTSW	11	65,989,818 (GRCm38)	missense	probably benign	0.00
R8326:Dnah9	UTSW	11	66,117,626 (GRCm38)	missense	probably benign	0.01
R8338:Dnah9	UTSW	11	65,841,241 (GRCm38)	critical splice donor site	probably null
R8356:Dnah9	UTSW	11	66,156,938 (GRCm38)	missense	probably damaging	0.99
R8456:Dnah9	UTSW	11	66,156,938 (GRCm38)	missense	probably damaging	0.99
R8468:Dnah9	UTSW	11	65,831,730 (GRCm38)	missense	probably benign	0.00
R8721:Dnah9	UTSW	11	66,095,298 (GRCm38)	missense	probably damaging	1.00
R8747:Dnah9	UTSW	11	65,927,990 (GRCm38)	missense	possibly damaging	0.69
R8798:Dnah9	UTSW	11	65,905,231 (GRCm38)	missense	probably damaging	0.99
R8806:Dnah9	UTSW	11	65,859,483 (GRCm38)	missense	probably damaging	1.00
R8826:Dnah9	UTSW	11	65,849,916 (GRCm38)	missense	probably benign	0.13
R8837:Dnah9	UTSW	11	65,855,234 (GRCm38)	missense	possibly damaging	0.72
R8886:Dnah9	UTSW	11	66,053,014 (GRCm38)	missense	probably damaging	1.00
R8887:Dnah9	UTSW	11	65,855,384 (GRCm38)	missense	probably benign	0.01
R8921:Dnah9	UTSW	11	65,911,921 (GRCm38)	missense	probably benign
R8933:Dnah9	UTSW	11	65,855,252 (GRCm38)	missense	possibly damaging	0.88
R8949:Dnah9	UTSW	11	66,168,400 (GRCm38)	missense	possibly damaging	0.91
R8967:Dnah9	UTSW	11	66,125,112 (GRCm38)	critical splice donor site	probably null
R8979:Dnah9	UTSW	11	66,005,152 (GRCm38)	missense	probably benign
R8991:Dnah9	UTSW	11	65,886,680 (GRCm38)	missense	probably damaging	0.96
R9016:Dnah9	UTSW	11	66,108,030 (GRCm38)	missense	probably damaging	0.99
R9025:Dnah9	UTSW	11	66,005,825 (GRCm38)	missense	probably damaging	1.00
R9043:Dnah9	UTSW	11	65,954,854 (GRCm38)	missense
R9047:Dnah9	UTSW	11	66,072,099 (GRCm38)	missense	possibly damaging	0.89
R9076:Dnah9	UTSW	11	66,117,638 (GRCm38)	missense	probably benign	0.21
R9113:Dnah9	UTSW	11	65,989,887 (GRCm38)	missense	probably damaging	1.00
R9152:Dnah9	UTSW	11	66,130,631 (GRCm38)	missense	probably damaging	1.00
R9187:Dnah9	UTSW	11	66,005,146 (GRCm38)	missense	probably benign
R9198:Dnah9	UTSW	11	65,955,744 (GRCm38)	missense	probably benign	0.02
R9203:Dnah9	UTSW	11	65,855,287 (GRCm38)	missense	possibly damaging	0.58
R9234:Dnah9	UTSW	11	66,033,925 (GRCm38)	missense	possibly damaging	0.68
R9245:Dnah9	UTSW	11	65,895,905 (GRCm38)	missense	probably benign	0.30
R9265:Dnah9	UTSW	11	65,841,255 (GRCm38)	missense	probably benign	0.01
R9307:Dnah9	UTSW	11	66,085,474 (GRCm38)	missense	probably benign	0.14
R9336:Dnah9	UTSW	11	65,870,949 (GRCm38)	missense	probably damaging	1.00
R9386:Dnah9	UTSW	11	65,947,542 (GRCm38)	missense	probably damaging	1.00
R9498:Dnah9	UTSW	11	65,848,373 (GRCm38)	missense	probably damaging	0.99
R9508:Dnah9	UTSW	11	65,834,263 (GRCm38)	missense	probably damaging	1.00
R9524:Dnah9	UTSW	11	66,085,483 (GRCm38)	missense	possibly damaging	0.92
R9577:Dnah9	UTSW	11	65,976,521 (GRCm38)	missense	probably benign	0.00
R9583:Dnah9	UTSW	11	65,965,681 (GRCm38)	missense	probably damaging	1.00
R9587:Dnah9	UTSW	11	66,108,391 (GRCm38)	missense	probably null	0.92
R9612:Dnah9	UTSW	11	65,927,649 (GRCm38)	missense	probably benign	0.00
R9748:Dnah9	UTSW	11	66,085,464 (GRCm38)	missense	possibly damaging	0.51
R9749:Dnah9	UTSW	11	66,095,376 (GRCm38)	missense	probably damaging	1.00
R9759:Dnah9	UTSW	11	66,075,118 (GRCm38)	missense	probably null	0.93
R9784:Dnah9	UTSW	11	66,085,134 (GRCm38)	missense	probably damaging	0.99
V3553:Dnah9	UTSW	11	65,970,076 (GRCm38)	missense	probably damaging	1.00
X0027:Dnah9	UTSW	11	66,085,479 (GRCm38)	missense	probably benign	0.07
X0028:Dnah9	UTSW	11	65,990,452 (GRCm38)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,970,084 (GRCm38)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,927,853 (GRCm38)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	65,895,972 (GRCm38)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	66,072,835 (GRCm38)	missense	probably damaging	1.00
Z1176:Dnah9	UTSW	11	66,037,474 (GRCm38)	missense	probably damaging	1.00
Z1177:Dnah9	UTSW	11	66,126,650 (GRCm38)	missense	probably damaging	1.00
Z1186:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
Z1186:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1187:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1187:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
Z1188:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1188:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
Z1189:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1189:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
Z1190:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1190:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
Z1191:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1191:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign
Z1192:Dnah9	UTSW	11	66,147,381 (GRCm38)	missense	probably benign
Z1192:Dnah9	UTSW	11	66,085,174 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GCGTGATGACTTACAAAGCTGCC -3'
(R):5'- TCCTGGATCACAACGCTGCCTC -3'

Sequencing Primer
(F):5'- CTGACCCAAAGCTGGTTCATATTG -3'
(R):5'- GCTGGTGGTTCAGTCCG -3'

Posted On

2014-05-14