Mutagenetix > Incidental Mutation

Incidental Mutation 'R6931:Dnah9'

540042

Institutional Source

Beutler Lab

Gene Symbol

Dnah9

Ensembl Gene

ENSMUSG00000056752

Gene Name

dynein, axonemal, heavy chain 9

Synonyms

D11Ertd686e, Dnahc9

MMRRC Submission

045326-MU

Accession Numbers

Essential gene?

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

Stock #

R6931 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

65831282-66168551 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 66117626 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Lysine at position 791 (I791K)

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: I791K

PolyPhen 2 Score 0.633 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000079494
Gene: ENSMUSG00000056752
AA Change: I791K

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

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.0%

Validation Efficiency

99% (77/78)

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: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700123L14Rik	T	C	6: 96,165,548 (GRCm38)	T172A	possibly damaging	Het
2310003L06Rik	T	A	5: 87,970,702 (GRCm38)	I15N	probably damaging	Het
2900092C05Rik	T	A	7: 12,512,596 (GRCm38)	S6R	unknown	Het
Abca6	T	A	11: 110,244,328 (GRCm38)	L210F	probably benign	Het
Abcc4	T	C	14: 118,527,988 (GRCm38)	Q919R	probably damaging	Het
Adcy1	A	G	11: 7,150,884 (GRCm38)	D811G	possibly damaging	Het
Akna	A	G	4: 63,387,102 (GRCm38)	S476P	probably benign	Het
Ankrd49	T	C	9: 14,782,826 (GRCm38)	N15S	probably benign	Het
Apcdd1	A	G	18: 62,933,908 (GRCm38)	D31G	probably damaging	Het
Aplp1	G	T	7: 30,443,200 (GRCm38)	R106S	probably damaging	Het
Arhgap40	T	C	2: 158,531,218 (GRCm38)	L132S	probably benign	Het
Atp8b5	G	T	4: 43,364,108 (GRCm38)		probably null	Het
Axl	T	C	7: 25,761,433 (GRCm38)	D717G	probably damaging	Het
Bub1	T	A	2: 127,801,382 (GRCm38)	D1014V	probably damaging	Het
Cacna2d4	T	A	6: 119,282,234 (GRCm38)	V603E	possibly damaging	Het
Cnot11	G	C	1: 39,539,921 (GRCm38)	C289S	probably damaging	Het
Coasy	A	G	11: 101,083,581 (GRCm38)	H191R	probably benign	Het
Cyp11a1	A	T	9: 58,025,120 (GRCm38)	N341Y	possibly damaging	Het
Cyp1a2	T	C	9: 57,682,156 (GRCm38)	N125S	probably benign	Het
Cyp2j8	A	T	4: 96,444,781 (GRCm38)		probably null	Het
Ecm2	A	T	13: 49,529,011 (GRCm38)	Q505H	probably benign	Het
Fam135a	T	A	1: 24,085,487 (GRCm38)	M1L	probably damaging	Het
Fam171a2	A	G	11: 102,438,434 (GRCm38)	S500P	possibly damaging	Het
Fat3	A	G	9: 15,959,942 (GRCm38)	S3718P	possibly damaging	Het
Frem1	G	A	4: 82,970,677 (GRCm38)	P1085S	probably damaging	Het
Gcfc2	A	G	6: 81,942,985 (GRCm38)	I390V	probably benign	Het
Gemin4	A	G	11: 76,210,956 (GRCm38)	L993P	probably damaging	Het
Ggnbp2	T	A	11: 84,833,167 (GRCm38)	D647V	probably damaging	Het
Gm7534	A	T	4: 134,193,153 (GRCm38)	M567K	probably benign	Het
Gpr84	A	C	15: 103,309,014 (GRCm38)	L212R	probably damaging	Het
Hnrnpu	T	C	1: 178,331,432 (GRCm38)		probably benign	Het
Hspg2	G	T	4: 137,540,720 (GRCm38)	C2116F	probably damaging	Het
Icam4	T	A	9: 21,030,451 (GRCm38)	V249E	probably damaging	Het
Itga1	T	C	13: 115,001,563 (GRCm38)	N429D	probably benign	Het
Kcns1	T	C	2: 164,164,838 (GRCm38)	T402A	probably damaging	Het
Ky	T	A	9: 102,537,627 (GRCm38)	V246E	probably damaging	Het
March1	A	G	8: 66,468,492 (GRCm38)	T529A	probably benign	Het
Med18	C	G	4: 132,459,883 (GRCm38)	V102L	probably damaging	Het
Mlst8	T	C	17: 24,477,275 (GRCm38)	D160G	probably damaging	Het
Mthfd1	T	C	12: 76,303,698 (GRCm38)	I470T	probably benign	Het
Muc1	C	T	3: 89,229,159 (GRCm38)		probably benign	Het
Mup8	G	A	4: 60,220,322 (GRCm38)	L137F	probably damaging	Het
Mybpc1	A	T	10: 88,542,330 (GRCm38)	L341*	probably null	Het
Nacad	A	G	11: 6,601,877 (GRCm38)	F438S	probably benign	Het
Necap2	C	A	4: 141,078,212 (GRCm38)		probably null	Het
Nifk	T	C	1: 118,332,348 (GRCm38)	L163S	possibly damaging	Het
Npsr1	A	G	9: 24,289,997 (GRCm38)	I73V	probably benign	Het
Olfr1179	G	A	2: 88,402,064 (GRCm38)	T290I	probably benign	Het
Olfr1186	T	A	2: 88,526,194 (GRCm38)	C204S	possibly damaging	Het
Olfr142	A	T	2: 90,252,777 (GRCm38)	C70*	probably null	Het
Olfr715	A	G	7: 107,128,901 (GRCm38)	L164P	probably damaging	Het
Oog3	C	T	4: 144,159,353 (GRCm38)	C225Y	probably benign	Het
Plagl2	C	A	2: 153,235,943 (GRCm38)	K39N	probably benign	Het
Plcg2	T	A	8: 117,557,319 (GRCm38)	D118E	probably benign	Het
Ppp4r3b	A	T	11: 29,211,786 (GRCm38)	K720I	possibly damaging	Het
Prmt3	A	T	7: 49,829,016 (GRCm38)	T442S	probably benign	Het
Prr14l	G	A	5: 32,830,691 (GRCm38)	H487Y	probably damaging	Het
Psmb3	G	A	11: 97,703,971 (GRCm38)	V63I	probably benign	Het
Psmc6	T	A	14: 45,343,725 (GRCm38)	I326K	possibly damaging	Het
Ptcd1	T	C	5: 145,155,075 (GRCm38)	T405A	probably benign	Het
Rbm33	G	A	5: 28,410,745 (GRCm38)	V29M	probably damaging	Het
Rsrc1	C	T	3: 66,994,649 (GRCm38)	P44L	unknown	Het
Scarb1	T	A	5: 125,284,719 (GRCm38)	I107F	probably damaging	Het
Slc39a12	A	G	2: 14,389,375 (GRCm38)	S19G	probably benign	Het
Slc44a5	T	C	3: 154,258,506 (GRCm38)	V503A	probably benign	Het
Slc9a9	T	C	9: 94,670,086 (GRCm38)	S9P	possibly damaging	Het
Snrnp35	A	C	5: 124,490,701 (GRCm38)	R192S	possibly damaging	Het
Tbx15	T	C	3: 99,352,151 (GRCm38)	L446P	probably damaging	Het
Tlnrd1	A	G	7: 83,882,597 (GRCm38)	F209L	probably benign	Het
Tmprss12	C	T	15: 100,285,268 (GRCm38)	R164C	probably damaging	Het
Tnfsf4	T	A	1: 161,417,073 (GRCm38)	F111Y	possibly damaging	Het
Trib2	A	T	12: 15,793,639 (GRCm38)	M198K	probably benign	Het
Ttll8	A	G	15: 88,914,304 (GRCm38)	S743P	possibly damaging	Het
Ush2a	A	T	1: 188,728,383 (GRCm38)	N2614Y	probably benign	Het
Usp6nl	G	A	2: 6,430,458 (GRCm38)	V343I	possibly damaging	Het
Vrtn	C	A	12: 84,650,242 (GRCm38)	Q589K	probably benign	Het
Zbed5	T	A	5: 129,903,329 (GRCm38)	Y706*	probably null	Het
Zc3h10	A	G	10: 128,544,684 (GRCm38)	V268A	probably damaging	Het
Zfp442	C	T	2: 150,410,940 (GRCm38)		probably null	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
R1718:Dnah9	UTSW	11	66,168,079 (GRCm38)	missense	possibly damaging	0.82
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
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'- AGCGTGAATCTTAAGGCCAG -3'
(R):5'- TCCATAGGAGCTAAGTATTTCCTGG -3'

Sequencing Primer
(F):5'- CAGATTCCTGGATGAGACTGTAG -3'
(R):5'- GCTGACTTTTTAATATGCTGGGAAAG -3'

Posted On

2018-11-06