Mutagenetix > Incidental Mutation

Incidental Mutation 'R4097:Dnah9'

317181

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

040984-MU

Accession Numbers

Essential gene?

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

Stock #

R4097 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

65722150-66059379 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 65881285 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Glycine at position 146 (S146G)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000080665
AA Change: S2597G

PolyPhen 2 Score 0.258 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: S2597G

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 damaging
Transcript: ENSMUST00000152386
AA Change: S146G

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

SMART Domains

Protein: ENSMUSP00000116499
Gene: ENSMUSG00000056752
AA Change: S146G

Domain	Start	End	E-Value	Type
Pfam:AAA_7	1	258	3e-155	PFAM
Pfam:AAA_8	336	603	3.9e-166	PFAM
Pfam:MT	615	958	2.3e-208	PFAM
Pfam:AAA_9	980	1202	1.1e-87	PFAM
Pfam:Dynein_heavy	1336	1514	2.4e-52	PFAM
Pfam:Dynein_heavy	1508	1956	8.6e-155	PFAM

Meta Mutation Damage Score

0.1279

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 96.1%

Validation Efficiency

100% (48/48)

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: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aldh1l2	A	G	10: 83,348,228 (GRCm39)	F292L	probably damaging	Het
Ankrd36	A	G	11: 5,578,703 (GRCm39)	D664G	possibly damaging	Het
Bbs1	T	A	19: 4,947,345 (GRCm39)	Y358F	probably damaging	Het
Becn1	C	T	11: 101,185,092 (GRCm39)		probably benign	Het
Cenpp	A	T	13: 49,647,265 (GRCm39)	N47I	possibly damaging	Het
Clec4n	A	T	6: 123,207,700 (GRCm39)	H55L	possibly damaging	Het
Cntnap4	A	G	8: 113,478,939 (GRCm39)	I222V	probably benign	Het
Cttnbp2	T	C	6: 18,420,871 (GRCm39)	E370G	probably benign	Het
Cyp4a10	T	A	4: 115,386,480 (GRCm39)	V413E	probably damaging	Het
Dctn2	C	T	10: 127,113,362 (GRCm39)	L249F	probably damaging	Het
Dzip3	A	T	16: 48,778,852 (GRCm39)	L315*	probably null	Het
Evpl	T	C	11: 116,114,003 (GRCm39)	E1229G	possibly damaging	Het
Ice2	T	C	9: 69,328,953 (GRCm39)	V775A	possibly damaging	Het
Jmjd1c	A	G	10: 67,054,787 (GRCm39)	E69G	probably benign	Het
Lrrc66	T	A	5: 73,765,047 (GRCm39)	R665S	possibly damaging	Het
Mpdz	T	A	4: 81,253,937 (GRCm39)	H1065L	probably damaging	Het
Nrf1	C	T	6: 30,151,671 (GRCm39)	Q503*	probably null	Het
Nt5dc3	G	A	10: 86,669,820 (GRCm39)	A472T	probably benign	Het
Oprk1	T	A	1: 5,673,034 (GRCm39)		probably benign	Het
Or7g17	T	C	9: 18,767,933 (GRCm39)	I4T	probably benign	Het
Or9g3	T	C	2: 85,590,040 (GRCm39)	I227V	possibly damaging	Het
Pramel6	T	G	2: 87,339,697 (GRCm39)	F154V	probably benign	Het
Ralb	T	C	1: 119,411,228 (GRCm39)	D37G	probably benign	Het
Ranbp9	A	T	13: 43,574,733 (GRCm39)	Y412N	probably damaging	Het
Scg2	T	A	1: 79,413,538 (GRCm39)	D395V	probably damaging	Het
Secisbp2l	C	T	2: 125,582,657 (GRCm39)	G933D	possibly damaging	Het
Serpine3	T	A	14: 62,908,395 (GRCm39)	L141Q	probably damaging	Het
Sgpl1	C	T	10: 60,939,017 (GRCm39)	G394D	probably damaging	Het
Sh3pxd2a	T	C	19: 47,412,951 (GRCm39)	Y44C	probably damaging	Het
Slc6a20b	A	G	9: 123,441,822 (GRCm39)		probably benign	Het
Snapc5	T	C	9: 64,087,809 (GRCm39)	I40T	probably damaging	Het
Spopl	T	C	2: 23,401,413 (GRCm39)	H365R	probably benign	Het
Stil	T	A	4: 114,880,797 (GRCm39)	I447N	probably benign	Het
Taf3	C	A	2: 9,957,178 (GRCm39)	V330F	possibly damaging	Het
Tgoln1	T	C	6: 72,592,784 (GRCm39)	E232G	probably damaging	Het
Thrap3	A	G	4: 126,065,595 (GRCm39)	L729P	probably damaging	Het
Tmem269	A	T	4: 119,062,977 (GRCm39)	F220Y	probably damaging	Het
Tnrc18	ATCTTCC	A	5: 142,759,561 (GRCm39)		probably benign	Het
Ubxn6	T	C	17: 56,376,712 (GRCm39)	T227A	probably benign	Het
Wdr17	C	A	8: 55,088,504 (GRCm39)	R1182I	probably damaging	Het
Wdr26	T	C	1: 181,010,352 (GRCm39)	I550V	probably benign	Het
Wdr43	A	G	17: 71,964,532 (GRCm39)	N637S	probably benign	Het
Zfp516	A	G	18: 83,005,381 (GRCm39)	T762A	possibly 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
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'- CTTATCTGAGAGATGCAAGTTGG -3'
(R):5'- AAGTGCTACTTGCCTTTGCC -3'

Sequencing Primer
(F):5'- GTTTGCTACTTTAGTAGGCTAGCAG -3'
(R):5'- GTTTAGAGACAATGCCACTCTGTAGC -3'

Posted On

2015-05-15