Mutagenetix > Incidental Mutation

Incidental Mutation 'R4655:Dnah9'

352372

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

041915-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.403) question?

Stock #

R4655 (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 65846558 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 2918 (N2918S)

Ref Sequence

ENSEMBL: ENSMUSP00000079494 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000080665
AA Change: N2918S

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: N2918S

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: ENSMUST00000152386
AA Change: N467S

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

SMART Domains

Protein: ENSMUSP00000116499
Gene: ENSMUSG00000056752
AA Change: N467S

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

0.0612

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.7%

Validation Efficiency

96% (79/82)

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: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921509C19Rik	A	G	2: 151,314,778 (GRCm39)	V300A	probably benign	Het
Aadacl4fm2	A	T	4: 144,281,645 (GRCm39)	F382L	probably benign	Het
Abca4	A	G	3: 121,941,147 (GRCm39)	N405S	possibly damaging	Het
Acsl3	A	G	1: 78,668,063 (GRCm39)	T212A	probably damaging	Het
Ahnak	A	G	19: 8,986,065 (GRCm39)	K2450E	probably damaging	Het
Akap9	G	A	5: 4,096,403 (GRCm39)	R2426H	probably benign	Het
Akr1c6	T	C	13: 4,499,428 (GRCm39)	V266A	probably damaging	Het
Ccs	A	G	19: 4,889,232 (GRCm39)	V11A	probably benign	Het
Cdc14a	T	A	3: 116,122,136 (GRCm39)	H228L	probably damaging	Het
Cgn	G	A	3: 94,686,559 (GRCm39)	Q248*	probably null	Het
Cux2	G	A	5: 122,023,997 (GRCm39)	T92M	possibly damaging	Het
Cyb5r4	A	G	9: 86,941,482 (GRCm39)	K68E	probably benign	Het
Dcaf10	G	A	4: 45,372,769 (GRCm39)	R394Q	possibly damaging	Het
Dyrk1b	T	C	7: 27,885,176 (GRCm39)	V438A	probably damaging	Het
Eml1	G	A	12: 108,500,972 (GRCm39)	D625N	probably damaging	Het
Eno2	T	C	6: 124,740,889 (GRCm39)		probably null	Het
Ephb3	G	A	16: 21,040,958 (GRCm39)	G672D	probably damaging	Het
Evx1	A	T	6: 52,291,182 (GRCm39)	D118V	probably damaging	Het
Fbxl13	A	G	5: 21,787,037 (GRCm39)	L300S	probably damaging	Het
Fbxo30	T	C	10: 11,166,837 (GRCm39)	F520L	probably damaging	Het
Flt3	G	A	5: 147,286,403 (GRCm39)	P728S	possibly damaging	Het
Gas2l2	T	C	11: 83,314,001 (GRCm39)	E437G	possibly damaging	Het
Gldc	A	T	19: 30,138,102 (GRCm39)		probably benign	Het
Gm18856	T	C	13: 14,140,232 (GRCm39)		probably benign	Het
Gm7358	A	T	17: 14,279,410 (GRCm39)		noncoding transcript	Het
Grifin	A	G	5: 140,550,300 (GRCm39)	V47A	possibly damaging	Het
H3c7	T	C	13: 23,728,923 (GRCm39)	V90A	probably benign	Het
Hddc2	G	T	10: 31,204,016 (GRCm39)		probably benign	Het
Hkdc1	T	A	10: 62,236,242 (GRCm39)	R433S	probably benign	Het
Htt	A	G	5: 35,063,476 (GRCm39)	D2918G	probably benign	Het
Itga2	A	C	13: 115,009,805 (GRCm39)	D383E	probably benign	Het
Itpr1	G	A	6: 108,458,254 (GRCm39)	C2007Y	probably damaging	Het
Krt42	C	A	11: 100,160,671 (GRCm39)	Q9H	probably damaging	Het
Lyrm7	T	C	11: 54,739,434 (GRCm39)	Q72R	probably damaging	Het
Mmp9	A	G	2: 164,793,122 (GRCm39)	S424G	probably benign	Het
Mtr	A	G	13: 12,242,679 (GRCm39)	V457A	probably damaging	Het
Myo15b	T	C	11: 115,781,523 (GRCm39)	L1359P	probably damaging	Het
Neb	A	G	2: 52,117,311 (GRCm39)	L4087P	probably damaging	Het
Npl	T	C	1: 153,391,152 (GRCm39)	D201G	probably damaging	Het
Or1af1	A	G	2: 37,109,885 (GRCm39)	N128S	probably benign	Het
Or8b1c	C	A	9: 38,384,120 (GRCm39)	P26T	probably damaging	Het
Or8k3	A	G	2: 86,059,037 (GRCm39)	S93P	probably benign	Het
Pclo	T	C	5: 14,732,397 (GRCm39)		probably benign	Het
Pdp2	A	G	8: 105,321,168 (GRCm39)	D339G	probably benign	Het
Pfdn6	A	T	17: 34,159,014 (GRCm39)	Y16*	probably null	Het
Pilra	C	T	5: 137,833,588 (GRCm39)		probably null	Het
Prrc2a	A	T	17: 35,374,590 (GRCm39)	N1353K	probably benign	Het
Prss3l	T	A	6: 41,422,984 (GRCm39)	I6F	probably benign	Het
Ptger4	C	A	15: 5,272,545 (GRCm39)	A50S	probably benign	Het
Pus10	T	C	11: 23,622,707 (GRCm39)	V109A	probably benign	Het
Pus3	A	C	9: 35,476,228 (GRCm39)	D39A	probably benign	Het
Rab44	A	G	17: 29,358,168 (GRCm39)	N119D	probably benign	Het
Rasgrp2	T	C	19: 6,454,876 (GRCm39)		probably benign	Het
Rhobtb2	T	A	14: 70,033,438 (GRCm39)	I511F	probably damaging	Het
Sfxn1	C	A	13: 54,246,457 (GRCm39)	A167D	probably benign	Het
Slc12a6	A	G	2: 112,188,111 (GRCm39)		probably null	Het
Smyd4	C	T	11: 75,281,558 (GRCm39)	L344F	probably damaging	Het
Srsf11	A	G	3: 157,728,972 (GRCm39)	V93A	probably benign	Het
Tle1	A	G	4: 72,063,581 (GRCm39)	I224T	possibly damaging	Het
Tmc6	A	T	11: 117,663,868 (GRCm39)	S479R	possibly damaging	Het
Tmprss4	T	C	9: 45,087,702 (GRCm39)	M296V	probably benign	Het
Togaram1	A	G	12: 65,013,894 (GRCm39)	N382D	possibly damaging	Het
Tpcn1	A	G	5: 120,677,322 (GRCm39)	S662P	probably damaging	Het
Tppp	G	T	13: 74,178,983 (GRCm39)	R141S	probably benign	Het
Ttc21a	A	G	9: 119,790,828 (GRCm39)	D858G	possibly damaging	Het
Tuba3a	A	G	6: 125,258,130 (GRCm39)	S287P	possibly damaging	Het
Unc80	T	G	1: 66,710,821 (GRCm39)	S2697A	probably benign	Het
Vmn1r69	A	G	7: 10,314,026 (GRCm39)	V235A	probably benign	Het
Vmn2r26	T	A	6: 124,038,375 (GRCm39)	I650N	probably damaging	Het
Vmn2r53	G	A	7: 12,315,932 (GRCm39)	T629I	possibly damaging	Het
Vmn2r74	T	C	7: 85,610,555 (GRCm39)	T46A	probably benign	Het
Vmn2r84	A	T	10: 130,229,973 (GRCm39)	C46*	probably null	Het
Vps13b	T	C	15: 35,770,835 (GRCm39)	S2093P	probably benign	Het
Wdfy4	T	C	14: 32,711,893 (GRCm39)	R2375G	probably damaging	Het
Wnk2	T	G	13: 49,210,359 (GRCm39)	E1820A	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
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'- ATGCTGTCAGTGCTGCTCAG -3'
(R):5'- CAGTACATGAGGTTGAACATGGTG -3'

Sequencing Primer
(F):5'- TCATCTTGACACAGTCCAGAGGAG -3'
(R):5'- GTGGAAAACCAAGCGACCTATATC -3'

Posted On

2015-10-08