Mutagenetix > Incidental Mutation

Incidental Mutation 'R8100:Dnah11'

630471

Institutional Source

Beutler Lab

Gene Symbol

Dnah11

Ensembl Gene

ENSMUSG00000018581

Gene Name

dynein, axonemal, heavy chain 11

Synonyms

b2b598Clo, b2b1289Clo, b2b1203Clo, Dnahc11, avc4, b2b1279Clo, b2b1727Clo, lrd

MMRRC Submission

067532-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.603) question?

Stock #

R8100 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

117841717-118162778 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 117930368 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 3326 (S3326P)

Ref Sequence

ENSEMBL: ENSMUSP00000081867 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000084806]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000084806
AA Change: S3326P

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000081867
Gene: ENSMUSG00000018581
AA Change: S3326P

Domain	Start	End	E-Value	Type
low complexity region	18	28	N/A	INTRINSIC
Pfam:DHC_N1	218	794	1.6e-162	PFAM
low complexity region	1266	1282	N/A	INTRINSIC
Pfam:DHC_N2	1297	1705	1e-130	PFAM
low complexity region	1757	1773	N/A	INTRINSIC
AAA	1869	1963	1.51e0	SMART
Pfam:AAA_5	2150	2286	1.6e-12	PFAM
AAA	2474	2619	1.48e-1	SMART
AAA	2819	2931	4.57e-1	SMART
Pfam:MT	3069	3413	3.2e-162	PFAM
Pfam:AAA_9	3434	3656	2.9e-88	PFAM
Pfam:Dynein_heavy	3790	4486	7.1e-235	PFAM

Predicted Effect

Coding Region Coverage

1x: 99.9%
3x: 99.8%
10x: 99.4%
20x: 98.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing Kartagener Syndrome (a combination of situs inversus totalis and Primary Ciliary Dyskinesia (PCD), also called Immotile Cilia Syndrome 1 (ICS1)) and male sterility. [provided by RefSeq, Mar 2013]
PHENOTYPE: Approximately half of live-born homozygous mutants show situs inversus indicating that this gene is no longer properly controlling left-right asymmetry. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adcy4	G	A	14: 56,009,722 (GRCm39)	Q777*	probably null	Het
Art1	T	C	7: 101,756,405 (GRCm39)	S199P	probably damaging	Het
Cadps2	A	T	6: 23,838,808 (GRCm39)	M110K	probably damaging	Het
Cdk13	C	T	13: 17,978,101 (GRCm39)	R379Q	unknown	Het
Cdk7	T	C	13: 100,842,925 (GRCm39)	I272V	probably benign	Het
Cep350	T	C	1: 155,829,148 (GRCm39)	D192G	probably damaging	Het
Chrna6	C	T	8: 27,903,844 (GRCm39)		probably benign	Het
Ciart	G	A	3: 95,788,656 (GRCm39)	P61L	probably damaging	Het
Ckmt1	T	A	2: 121,191,258 (GRCm39)	D223E	probably benign	Het
Col6a5	C	T	9: 105,755,839 (GRCm39)	R2195H	probably damaging	Het
D430041D05Rik	C	T	2: 104,087,287 (GRCm39)	R563H	probably benign	Het
Defa29	A	T	8: 21,816,990 (GRCm39)	M1K	probably null	Het
Dsg3	A	G	18: 20,662,028 (GRCm39)	D431G	probably benign	Het
Ell3	TCTCCTC	TCTC	2: 121,269,937 (GRCm39)		probably benign	Het
Fbln1	T	A	15: 85,169,357 (GRCm39)	F699I	probably damaging	Het
Fndc1	A	G	17: 7,990,685 (GRCm39)	S1004P	unknown	Het
Gpr15	T	A	16: 58,538,076 (GRCm39)	T338S	probably benign	Het
Grin2d	T	C	7: 45,483,171 (GRCm39)	Y1002C	unknown	Het
Hk2	C	T	6: 82,707,859 (GRCm39)	M703I	probably benign	Het
Ifi213	A	C	1: 173,422,748 (GRCm39)	L39R	probably damaging	Het
Kctd17	CAGCTGGAGGAGC	CAGC	15: 78,321,113 (GRCm39)		probably benign	Het
Lama2	C	A	10: 26,917,113 (GRCm39)	A2271S	probably benign	Het
Lmo7	A	T	14: 102,137,899 (GRCm39)	Q867L	probably benign	Het
Loxhd1	T	A	18: 77,492,512 (GRCm39)	S1427T	possibly damaging	Het
Lzts1	A	G	8: 69,593,397 (GRCm39)	V70A	probably damaging	Het
Mocs3	A	G	2: 168,073,257 (GRCm39)	T235A	possibly damaging	Het
Myo15a	G	A	11: 60,408,016 (GRCm39)	R3168H	probably damaging	Het
Ndc1	A	G	4: 107,240,802 (GRCm39)	D260G	possibly damaging	Het
Nfam1	T	C	15: 82,900,730 (GRCm39)	D44G	probably damaging	Het
Or4a47	G	A	2: 89,666,029 (GRCm39)	Q87*	probably null	Het
Osbpl10	G	A	9: 114,996,322 (GRCm39)	R128H	probably benign	Het
Otx1	C	A	11: 21,949,392 (GRCm39)	V29L	probably benign	Het
Pogk	A	T	1: 166,229,511 (GRCm39)	D113E	possibly damaging	Het
Ptgs2	T	C	1: 149,978,472 (GRCm39)	F195L	probably damaging	Het
Ptpn21	T	A	12: 98,648,881 (GRCm39)	E925V	possibly damaging	Het
Ranbp2	T	C	10: 58,326,470 (GRCm39)	F2714L	possibly damaging	Het
Rbm20	T	G	19: 53,839,744 (GRCm39)	I911S	possibly damaging	Het
Rwdd2b	A	G	16: 87,233,509 (GRCm39)	V197A	possibly damaging	Het
Sel1l2	C	G	2: 140,117,329 (GRCm39)	A181P	probably damaging	Het
Sf1	A	G	19: 6,422,368 (GRCm39)	E234G	possibly damaging	Het
Skint2	A	C	4: 112,483,197 (GRCm39)	T201P	probably damaging	Het
Sra1	C	T	18: 36,809,948 (GRCm39)	R199H	probably damaging	Het
Svs5	A	G	2: 164,079,712 (GRCm39)	M65T	probably benign	Het
Tgif1	C	A	17: 71,153,544 (GRCm39)		probably benign	Het
Tmem184c	A	G	8: 78,331,411 (GRCm39)	W113R	possibly damaging	Het
Tmem30a	T	C	9: 79,681,432 (GRCm39)	R282G	probably benign	Het
Top1	T	A	2: 160,540,155 (GRCm39)	Y244*	probably null	Het
Trank1	A	G	9: 111,221,861 (GRCm39)	Y2866C	probably damaging	Het
Trim7	A	C	11: 48,740,346 (GRCm39)	I148L	probably damaging	Het
Triml1	T	A	8: 43,591,717 (GRCm39)	M214L	probably benign	Het
Usp30	T	G	5: 114,249,245 (GRCm39)	V183G	probably damaging	Het
Vmn1r175	G	A	7: 23,508,012 (GRCm39)	S205F	probably damaging	Het
Zbtb32	CTTG	CTTGTTG	7: 30,290,946 (GRCm39)		probably benign	Het
Zfp108	T	A	7: 23,960,602 (GRCm39)	C398S	probably damaging	Het
Zfp592	T	G	7: 80,673,940 (GRCm39)	D301E	probably benign	Het
Zfp764l1	C	T	7: 126,992,496 (GRCm39)	C38Y	probably null	Het

Other mutations in Dnah11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00341:Dnah11	APN	12	118,162,480 (GRCm39)	missense	probably benign	0.28
IGL00422:Dnah11	APN	12	118,031,831 (GRCm39)	missense	probably damaging	1.00
IGL00436:Dnah11	APN	12	118,000,194 (GRCm39)	missense	possibly damaging	0.56
IGL00540:Dnah11	APN	12	118,150,657 (GRCm39)	missense	probably benign	0.01
IGL00687:Dnah11	APN	12	117,885,739 (GRCm39)	splice site	probably benign
IGL00833:Dnah11	APN	12	118,143,315 (GRCm39)	missense	probably damaging	1.00
IGL00906:Dnah11	APN	12	117,874,937 (GRCm39)	missense	probably damaging	1.00
IGL00952:Dnah11	APN	12	118,160,386 (GRCm39)	missense	possibly damaging	0.56
IGL01111:Dnah11	APN	12	118,106,669 (GRCm39)	splice site	probably benign
IGL01121:Dnah11	APN	12	118,014,430 (GRCm39)	missense	probably benign	0.02
IGL01143:Dnah11	APN	12	117,976,475 (GRCm39)	missense	probably damaging	1.00
IGL01359:Dnah11	APN	12	117,946,734 (GRCm39)	missense	probably damaging	0.99
IGL01372:Dnah11	APN	12	118,156,134 (GRCm39)	missense	probably damaging	1.00
IGL01410:Dnah11	APN	12	118,010,991 (GRCm39)	nonsense	probably null
IGL01418:Dnah11	APN	12	117,951,217 (GRCm39)	nonsense	probably null
IGL01444:Dnah11	APN	12	117,983,967 (GRCm39)	missense	possibly damaging	0.91
IGL01606:Dnah11	APN	12	117,946,767 (GRCm39)	missense	probably benign	0.15
IGL01645:Dnah11	APN	12	118,150,733 (GRCm39)	missense	possibly damaging	0.90
IGL01932:Dnah11	APN	12	118,156,005 (GRCm39)	splice site	probably benign
IGL02104:Dnah11	APN	12	118,156,125 (GRCm39)	missense	probably benign
IGL02151:Dnah11	APN	12	118,023,623 (GRCm39)	splice site	probably benign
IGL02189:Dnah11	APN	12	118,046,314 (GRCm39)	missense	probably benign	0.00
IGL02417:Dnah11	APN	12	118,020,915 (GRCm39)	missense	probably damaging	1.00
IGL02421:Dnah11	APN	12	118,150,637 (GRCm39)	missense	probably damaging	1.00
IGL02444:Dnah11	APN	12	117,939,608 (GRCm39)	splice site	probably benign
IGL02474:Dnah11	APN	12	117,991,180 (GRCm39)	splice site	probably null
IGL02526:Dnah11	APN	12	118,143,353 (GRCm39)	missense	possibly damaging	0.70
IGL02887:Dnah11	APN	12	117,874,775 (GRCm39)	missense	probably damaging	1.00
IGL03011:Dnah11	APN	12	117,976,112 (GRCm39)	missense	probably benign	0.08
IGL03061:Dnah11	APN	12	117,866,856 (GRCm39)	missense	probably damaging	1.00
IGL03182:Dnah11	APN	12	117,994,026 (GRCm39)	missense	probably damaging	0.99
IGL03220:Dnah11	APN	12	118,069,720 (GRCm39)	missense	probably benign
IGL03238:Dnah11	APN	12	118,073,633 (GRCm39)	missense	probably damaging	1.00
IGL03493:Dnah11	APN	12	117,976,533 (GRCm39)	missense	probably benign	0.00
P0045:Dnah11	UTSW	12	117,994,062 (GRCm39)	missense	probably benign
R0009:Dnah11	UTSW	12	118,009,257 (GRCm39)	missense	possibly damaging	0.90
R0066:Dnah11	UTSW	12	118,090,621 (GRCm39)	missense	probably benign	0.05
R0172:Dnah11	UTSW	12	117,951,188 (GRCm39)	missense	probably damaging	1.00
R0206:Dnah11	UTSW	12	118,007,509 (GRCm39)	missense	probably damaging	0.98
R0206:Dnah11	UTSW	12	118,007,509 (GRCm39)	missense	probably damaging	0.98
R0208:Dnah11	UTSW	12	118,007,509 (GRCm39)	missense	probably damaging	0.98
R0230:Dnah11	UTSW	12	117,946,791 (GRCm39)	nonsense	probably null
R0270:Dnah11	UTSW	12	118,004,748 (GRCm39)	missense	probably damaging	1.00
R0311:Dnah11	UTSW	12	118,090,868 (GRCm39)	missense	probably benign	0.03
R0325:Dnah11	UTSW	12	117,976,074 (GRCm39)	missense	probably benign
R0370:Dnah11	UTSW	12	117,958,962 (GRCm39)	missense	probably benign
R0416:Dnah11	UTSW	12	117,874,793 (GRCm39)	missense	probably damaging	1.00
R0505:Dnah11	UTSW	12	118,070,245 (GRCm39)	missense	probably damaging	1.00
R0540:Dnah11	UTSW	12	118,046,246 (GRCm39)	missense	probably damaging	1.00
R0554:Dnah11	UTSW	12	117,894,913 (GRCm39)	missense	probably benign	0.01
R0607:Dnah11	UTSW	12	118,046,246 (GRCm39)	missense	probably damaging	1.00
R0620:Dnah11	UTSW	12	117,951,204 (GRCm39)	missense	probably damaging	1.00
R0635:Dnah11	UTSW	12	117,971,731 (GRCm39)	missense	probably damaging	1.00
R0755:Dnah11	UTSW	12	118,162,360 (GRCm39)	missense	probably benign	0.17
R0755:Dnah11	UTSW	12	117,918,564 (GRCm39)	missense	possibly damaging	0.95
R0789:Dnah11	UTSW	12	117,874,967 (GRCm39)	missense	probably damaging	1.00
R0833:Dnah11	UTSW	12	118,160,397 (GRCm39)	missense	probably benign	0.01
R0835:Dnah11	UTSW	12	117,880,523 (GRCm39)	missense	probably damaging	1.00
R0836:Dnah11	UTSW	12	118,160,397 (GRCm39)	missense	probably benign	0.01
R0846:Dnah11	UTSW	12	117,897,585 (GRCm39)	missense	probably damaging	0.97
R0865:Dnah11	UTSW	12	118,154,579 (GRCm39)	nonsense	probably null
R0928:Dnah11	UTSW	12	118,009,297 (GRCm39)	missense	probably damaging	1.00
R0939:Dnah11	UTSW	12	118,024,142 (GRCm39)	missense	probably damaging	1.00
R1203:Dnah11	UTSW	12	117,897,547 (GRCm39)	missense	possibly damaging	0.81
R1394:Dnah11	UTSW	12	117,936,099 (GRCm39)	missense	possibly damaging	0.75
R1398:Dnah11	UTSW	12	118,020,841 (GRCm39)	nonsense	probably null
R1465:Dnah11	UTSW	12	118,002,430 (GRCm39)	missense	probably damaging	1.00
R1465:Dnah11	UTSW	12	118,002,430 (GRCm39)	missense	probably damaging	1.00
R1500:Dnah11	UTSW	12	117,976,564 (GRCm39)	splice site	probably null
R1535:Dnah11	UTSW	12	117,982,465 (GRCm39)	missense	probably damaging	1.00
R1539:Dnah11	UTSW	12	117,894,991 (GRCm39)	missense	probably benign	0.01
R1554:Dnah11	UTSW	12	118,046,234 (GRCm39)	missense	possibly damaging	0.92
R1574:Dnah11	UTSW	12	118,024,052 (GRCm39)	missense	probably damaging	1.00
R1574:Dnah11	UTSW	12	118,024,052 (GRCm39)	missense	probably damaging	1.00
R1615:Dnah11	UTSW	12	118,014,457 (GRCm39)	missense	probably damaging	1.00
R1618:Dnah11	UTSW	12	117,979,200 (GRCm39)	missense	probably damaging	0.98
R1638:Dnah11	UTSW	12	117,979,154 (GRCm39)	missense	possibly damaging	0.81
R1659:Dnah11	UTSW	12	118,084,459 (GRCm39)	missense	possibly damaging	0.94
R1671:Dnah11	UTSW	12	117,880,523 (GRCm39)	missense	probably damaging	1.00
R1678:Dnah11	UTSW	12	117,897,580 (GRCm39)	missense	possibly damaging	0.50
R1699:Dnah11	UTSW	12	118,154,603 (GRCm39)	missense	probably damaging	1.00
R1712:Dnah11	UTSW	12	118,160,379 (GRCm39)	missense	probably benign	0.32
R1728:Dnah11	UTSW	12	117,880,666 (GRCm39)	missense	probably damaging	1.00
R1729:Dnah11	UTSW	12	117,880,666 (GRCm39)	missense	probably damaging	1.00
R1764:Dnah11	UTSW	12	118,154,560 (GRCm39)	missense	probably benign	0.31
R1780:Dnah11	UTSW	12	117,991,293 (GRCm39)	missense	probably damaging	1.00
R1789:Dnah11	UTSW	12	118,002,515 (GRCm39)	missense	probably damaging	0.99
R1800:Dnah11	UTSW	12	117,880,523 (GRCm39)	missense	probably damaging	1.00
R1863:Dnah11	UTSW	12	118,027,587 (GRCm39)	missense	possibly damaging	0.92
R1892:Dnah11	UTSW	12	118,070,209 (GRCm39)	missense	possibly damaging	0.53
R1907:Dnah11	UTSW	12	118,091,291 (GRCm39)	missense	possibly damaging	0.66
R1964:Dnah11	UTSW	12	118,106,027 (GRCm39)	missense	possibly damaging	0.56
R1967:Dnah11	UTSW	12	117,880,523 (GRCm39)	missense	probably damaging	1.00
R1997:Dnah11	UTSW	12	118,046,203 (GRCm39)	missense	possibly damaging	0.64
R2086:Dnah11	UTSW	12	118,077,606 (GRCm39)	missense	possibly damaging	0.82
R2092:Dnah11	UTSW	12	117,976,451 (GRCm39)	missense	possibly damaging	0.50
R2108:Dnah11	UTSW	12	117,984,088 (GRCm39)	missense	probably damaging	1.00
R2140:Dnah11	UTSW	12	117,972,545 (GRCm39)	missense	probably benign	0.01
R2261:Dnah11	UTSW	12	117,930,374 (GRCm39)	missense	probably damaging	0.99
R2261:Dnah11	UTSW	12	117,843,760 (GRCm39)	missense	probably benign	0.06
R2262:Dnah11	UTSW	12	117,930,374 (GRCm39)	missense	probably damaging	0.99
R2262:Dnah11	UTSW	12	117,843,760 (GRCm39)	missense	probably benign	0.06
R2263:Dnah11	UTSW	12	117,843,760 (GRCm39)	missense	probably benign	0.06
R2263:Dnah11	UTSW	12	117,930,374 (GRCm39)	missense	probably damaging	0.99
R2328:Dnah11	UTSW	12	117,850,421 (GRCm39)	missense	probably damaging	0.98
R2352:Dnah11	UTSW	12	117,892,065 (GRCm39)	missense	probably damaging	1.00
R2410:Dnah11	UTSW	12	117,991,262 (GRCm39)	missense	probably damaging	1.00
R2885:Dnah11	UTSW	12	117,951,162 (GRCm39)	nonsense	probably null
R3499:Dnah11	UTSW	12	117,874,758 (GRCm39)	missense	probably damaging	1.00
R3741:Dnah11	UTSW	12	118,095,076 (GRCm39)	missense	probably benign	0.05
R3742:Dnah11	UTSW	12	118,095,076 (GRCm39)	missense	probably benign	0.05
R3779:Dnah11	UTSW	12	118,094,448 (GRCm39)	splice site	probably benign
R3785:Dnah11	UTSW	12	117,981,337 (GRCm39)	missense	probably damaging	1.00
R3883:Dnah11	UTSW	12	117,942,188 (GRCm39)	splice site	probably benign
R4014:Dnah11	UTSW	12	117,938,649 (GRCm39)	missense	probably benign	0.16
R4043:Dnah11	UTSW	12	117,843,678 (GRCm39)	missense	probably damaging	1.00
R4072:Dnah11	UTSW	12	118,070,227 (GRCm39)	missense	probably damaging	1.00
R4073:Dnah11	UTSW	12	118,009,413 (GRCm39)	missense	probably benign	0.01
R4074:Dnah11	UTSW	12	118,009,413 (GRCm39)	missense	probably benign	0.01
R4076:Dnah11	UTSW	12	118,009,413 (GRCm39)	missense	probably benign	0.01
R4201:Dnah11	UTSW	12	117,930,394 (GRCm39)	missense	possibly damaging	0.63
R4224:Dnah11	UTSW	12	118,094,627 (GRCm39)	missense	probably benign	0.06
R4233:Dnah11	UTSW	12	117,880,526 (GRCm39)	missense	probably damaging	1.00
R4358:Dnah11	UTSW	12	118,089,578 (GRCm39)	nonsense	probably null
R4430:Dnah11	UTSW	12	117,946,746 (GRCm39)	missense	probably benign	0.26
R4465:Dnah11	UTSW	12	117,951,186 (GRCm39)	missense	probably benign	0.09
R4489:Dnah11	UTSW	12	117,880,631 (GRCm39)	missense	probably benign	0.31
R4572:Dnah11	UTSW	12	117,973,860 (GRCm39)	missense	probably benign	0.00
R4574:Dnah11	UTSW	12	117,975,990 (GRCm39)	critical splice donor site	probably null
R4657:Dnah11	UTSW	12	118,156,162 (GRCm39)	missense	probably benign	0.02
R4709:Dnah11	UTSW	12	117,982,495 (GRCm39)	missense	probably benign	0.26
R4740:Dnah11	UTSW	12	118,084,279 (GRCm39)	missense	probably benign	0.28
R4803:Dnah11	UTSW	12	118,091,343 (GRCm39)	missense	possibly damaging	0.50
R4896:Dnah11	UTSW	12	117,958,935 (GRCm39)	missense	probably damaging	1.00
R4908:Dnah11	UTSW	12	118,090,618 (GRCm39)	missense	probably benign	0.37
R5018:Dnah11	UTSW	12	118,094,463 (GRCm39)	missense	probably benign	0.00
R5071:Dnah11	UTSW	12	118,046,188 (GRCm39)	nonsense	probably null
R5074:Dnah11	UTSW	12	118,046,188 (GRCm39)	nonsense	probably null
R5080:Dnah11	UTSW	12	118,162,565 (GRCm39)	start codon destroyed	probably null	0.01
R5097:Dnah11	UTSW	12	117,981,435 (GRCm39)	missense	probably damaging	1.00
R5131:Dnah11	UTSW	12	117,918,486 (GRCm39)	missense	probably damaging	1.00
R5215:Dnah11	UTSW	12	118,121,096 (GRCm39)	missense	probably benign	0.09
R5252:Dnah11	UTSW	12	118,089,676 (GRCm39)	missense	probably damaging	1.00
R5296:Dnah11	UTSW	12	117,847,151 (GRCm39)	missense	probably damaging	1.00
R5308:Dnah11	UTSW	12	118,049,415 (GRCm39)	missense	possibly damaging	0.60
R5368:Dnah11	UTSW	12	117,918,628 (GRCm39)	missense	probably damaging	1.00
R5383:Dnah11	UTSW	12	118,049,432 (GRCm39)	missense	probably damaging	0.99
R5499:Dnah11	UTSW	12	118,070,209 (GRCm39)	missense	possibly damaging	0.53
R5503:Dnah11	UTSW	12	117,844,186 (GRCm39)	critical splice donor site	probably null
R5546:Dnah11	UTSW	12	117,939,583 (GRCm39)	missense	possibly damaging	0.83
R5578:Dnah11	UTSW	12	117,982,537 (GRCm39)	missense	probably damaging	0.99
R5657:Dnah11	UTSW	12	117,847,352 (GRCm39)	missense	probably damaging	1.00
R5702:Dnah11	UTSW	12	118,077,642 (GRCm39)	missense	probably benign	0.04
R5706:Dnah11	UTSW	12	117,987,670 (GRCm39)	missense	probably damaging	1.00
R5727:Dnah11	UTSW	12	118,090,841 (GRCm39)	missense	probably damaging	1.00
R5737:Dnah11	UTSW	12	118,156,125 (GRCm39)	missense	probably benign
R5884:Dnah11	UTSW	12	118,141,269 (GRCm39)	missense	probably benign	0.00
R5900:Dnah11	UTSW	12	118,046,166 (GRCm39)	splice site	probably null
R5905:Dnah11	UTSW	12	117,918,659 (GRCm39)	missense	probably damaging	1.00
R5928:Dnah11	UTSW	12	117,878,371 (GRCm39)	splice site	probably null
R5973:Dnah11	UTSW	12	118,074,687 (GRCm39)	missense	probably benign	0.02
R6024:Dnah11	UTSW	12	117,994,007 (GRCm39)	missense	probably benign	0.34
R6056:Dnah11	UTSW	12	117,892,191 (GRCm39)	missense	probably benign	0.03
R6075:Dnah11	UTSW	12	118,068,586 (GRCm39)	missense	probably damaging	1.00
R6092:Dnah11	UTSW	12	117,892,191 (GRCm39)	missense	probably benign
R6191:Dnah11	UTSW	12	118,154,632 (GRCm39)	missense	probably benign
R6197:Dnah11	UTSW	12	118,143,482 (GRCm39)	missense	probably benign	0.03
R6262:Dnah11	UTSW	12	117,894,913 (GRCm39)	missense	probably damaging	0.98
R6321:Dnah11	UTSW	12	118,106,027 (GRCm39)	missense	possibly damaging	0.56
R6454:Dnah11	UTSW	12	117,880,590 (GRCm39)	missense	probably benign	0.01
R6614:Dnah11	UTSW	12	117,850,411 (GRCm39)	missense	possibly damaging	0.72
R6694:Dnah11	UTSW	12	118,150,617 (GRCm39)	splice site	probably null
R6712:Dnah11	UTSW	12	118,014,457 (GRCm39)	missense	probably damaging	1.00
R6720:Dnah11	UTSW	12	118,009,381 (GRCm39)	missense	probably damaging	1.00
R6742:Dnah11	UTSW	12	118,077,629 (GRCm39)	missense	possibly damaging	0.82
R6806:Dnah11	UTSW	12	117,951,411 (GRCm39)	splice site	probably null
R6895:Dnah11	UTSW	12	117,958,926 (GRCm39)	missense	probably damaging	0.99
R6939:Dnah11	UTSW	12	118,070,297 (GRCm39)	missense	probably damaging	1.00
R6940:Dnah11	UTSW	12	118,162,503 (GRCm39)	missense	probably benign
R6945:Dnah11	UTSW	12	118,024,045 (GRCm39)	missense	probably damaging	1.00
R6958:Dnah11	UTSW	12	117,897,544 (GRCm39)	missense	probably damaging	1.00
R6970:Dnah11	UTSW	12	118,072,679 (GRCm39)	missense	probably benign	0.00
R6976:Dnah11	UTSW	12	118,162,378 (GRCm39)	missense	probably benign	0.16
R7000:Dnah11	UTSW	12	117,981,396 (GRCm39)	missense	probably damaging	1.00
R7011:Dnah11	UTSW	12	117,885,753 (GRCm39)	frame shift	probably null
R7101:Dnah11	UTSW	12	118,031,880 (GRCm39)	missense	probably benign
R7106:Dnah11	UTSW	12	117,924,884 (GRCm39)	missense	probably benign	0.15
R7203:Dnah11	UTSW	12	118,009,257 (GRCm39)	missense	possibly damaging	0.90
R7219:Dnah11	UTSW	12	118,090,624 (GRCm39)	missense	probably benign	0.00
R7219:Dnah11	UTSW	12	118,004,830 (GRCm39)	missense	possibly damaging	0.95
R7308:Dnah11	UTSW	12	117,959,010 (GRCm39)	missense	probably damaging	1.00
R7361:Dnah11	UTSW	12	117,982,477 (GRCm39)	missense	probably damaging	1.00
R7367:Dnah11	UTSW	12	117,951,177 (GRCm39)	missense	possibly damaging	0.59
R7399:Dnah11	UTSW	12	118,089,520 (GRCm39)	missense	probably damaging	1.00
R7399:Dnah11	UTSW	12	117,991,212 (GRCm39)	missense	probably benign	0.00
R7404:Dnah11	UTSW	12	118,068,543 (GRCm39)	missense	probably benign	0.36
R7473:Dnah11	UTSW	12	117,866,911 (GRCm39)	missense	probably benign	0.19
R7545:Dnah11	UTSW	12	117,894,939 (GRCm39)	missense	probably damaging	1.00
R7608:Dnah11	UTSW	12	118,104,505 (GRCm39)	splice site	probably null
R7625:Dnah11	UTSW	12	118,160,377 (GRCm39)	missense	probably benign
R7761:Dnah11	UTSW	12	117,987,648 (GRCm39)	missense	probably damaging	1.00
R7879:Dnah11	UTSW	12	118,004,744 (GRCm39)	missense	probably damaging	1.00
R7881:Dnah11	UTSW	12	117,951,237 (GRCm39)	missense	probably benign	0.04
R7904:Dnah11	UTSW	12	117,867,003 (GRCm39)	missense	possibly damaging	0.72
R8179:Dnah11	UTSW	12	117,842,284 (GRCm39)	missense	possibly damaging	0.90
R8192:Dnah11	UTSW	12	117,976,181 (GRCm39)	missense	probably benign
R8254:Dnah11	UTSW	12	117,842,259 (GRCm39)	missense	possibly damaging	0.89
R8268:Dnah11	UTSW	12	117,991,243 (GRCm39)	nonsense	probably null
R8272:Dnah11	UTSW	12	118,074,752 (GRCm39)	missense	probably benign	0.01
R8344:Dnah11	UTSW	12	118,049,466 (GRCm39)	missense	probably benign	0.00
R8515:Dnah11	UTSW	12	117,939,533 (GRCm39)	missense	probably damaging	1.00
R8528:Dnah11	UTSW	12	117,972,538 (GRCm39)	missense	probably damaging	0.96
R8557:Dnah11	UTSW	12	117,842,247 (GRCm39)	missense	probably benign
R8676:Dnah11	UTSW	12	118,154,539 (GRCm39)	missense	probably damaging	1.00
R8738:Dnah11	UTSW	12	118,049,384 (GRCm39)	critical splice donor site	probably null
R8773:Dnah11	UTSW	12	117,958,950 (GRCm39)	missense	possibly damaging	0.94
R8818:Dnah11	UTSW	12	117,874,764 (GRCm39)	missense	probably damaging	1.00
R8855:Dnah11	UTSW	12	118,156,107 (GRCm39)	missense	probably benign	0.03
R8866:Dnah11	UTSW	12	118,156,107 (GRCm39)	missense	probably benign	0.03
R8881:Dnah11	UTSW	12	118,090,550 (GRCm39)	missense	probably benign	0.05
R8881:Dnah11	UTSW	12	118,077,647 (GRCm39)	missense	probably benign	0.00
R8920:Dnah11	UTSW	12	118,077,674 (GRCm39)	missense	probably damaging	0.99
R8944:Dnah11	UTSW	12	118,091,381 (GRCm39)	missense	possibly damaging	0.63
R8945:Dnah11	UTSW	12	117,987,718 (GRCm39)	missense	probably benign	0.36
R8962:Dnah11	UTSW	12	117,918,630 (GRCm39)	missense	probably damaging	1.00
R8962:Dnah11	UTSW	12	117,916,273 (GRCm39)	missense	probably damaging	1.00
R9059:Dnah11	UTSW	12	118,094,578 (GRCm39)	missense	probably benign	0.00
R9155:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9162:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9164:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9171:Dnah11	UTSW	12	117,894,918 (GRCm39)	missense	probably damaging	0.99
R9186:Dnah11	UTSW	12	118,154,632 (GRCm39)	missense	probably benign
R9205:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9208:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9234:Dnah11	UTSW	12	117,951,095 (GRCm39)	missense	probably damaging	1.00
R9264:Dnah11	UTSW	12	117,991,262 (GRCm39)	missense	probably damaging	1.00
R9290:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9291:Dnah11	UTSW	12	117,991,251 (GRCm39)	missense	probably damaging	0.99
R9315:Dnah11	UTSW	12	118,143,341 (GRCm39)	missense	probably benign	0.11
R9353:Dnah11	UTSW	12	118,143,434 (GRCm39)	missense	probably benign	0.00
R9375:Dnah11	UTSW	12	117,884,703 (GRCm39)	missense	possibly damaging	0.67
R9392:Dnah11	UTSW	12	118,141,290 (GRCm39)	missense	probably benign	0.00
R9392:Dnah11	UTSW	12	118,011,055 (GRCm39)	nonsense	probably null
R9433:Dnah11	UTSW	12	117,976,007 (GRCm39)	missense	probably damaging	1.00
R9511:Dnah11	UTSW	12	117,878,352 (GRCm39)	missense	probably damaging	1.00
R9526:Dnah11	UTSW	12	118,150,711 (GRCm39)	missense	probably damaging	0.98
R9566:Dnah11	UTSW	12	117,938,728 (GRCm39)	missense	possibly damaging	0.69
R9673:Dnah11	UTSW	12	117,982,513 (GRCm39)	missense	possibly damaging	0.91
R9705:Dnah11	UTSW	12	118,094,770 (GRCm39)	missense	probably damaging	1.00
R9716:Dnah11	UTSW	12	118,024,148 (GRCm39)	missense	probably damaging	0.99
R9746:Dnah11	UTSW	12	117,842,311 (GRCm39)	nonsense	probably null
R9764:Dnah11	UTSW	12	117,884,704 (GRCm39)	missense	probably benign	0.05
RF023:Dnah11	UTSW	12	117,918,585 (GRCm39)	missense	probably damaging	1.00
RF047:Dnah11	UTSW	12	117,973,818 (GRCm39)	missense	probably damaging	1.00
Z1088:Dnah11	UTSW	12	117,858,747 (GRCm39)	missense	probably damaging	1.00
Z1088:Dnah11	UTSW	12	117,946,704 (GRCm39)	missense	probably damaging	1.00
Z1176:Dnah11	UTSW	12	118,094,534 (GRCm39)	missense	probably damaging	0.97
Z1176:Dnah11	UTSW	12	118,090,854 (GRCm39)	missense	probably benign	0.00
Z1176:Dnah11	UTSW	12	117,894,912 (GRCm39)	missense	possibly damaging	0.81

Predicted Primers

PCR Primer
(F):5'- TGGTAACTTGTATCCTTAAGTCTGG -3'
(R):5'- GGGTGCCTGTGACATATTATTCATC -3'

Sequencing Primer
(F):5'- ACTTGTATCCTTAAGTCTGGGTAATG -3'
(R):5'- AGCTTCCTTTCTTCCATTAATATGC -3'

Posted On

2020-06-30