Mutagenetix > Incidental Mutation

Incidental Mutation 'R5296:Dnah11'

405434

Institutional Source

Beutler Lab

Gene Symbol

Dnah11

Ensembl Gene

ENSMUSG00000018581

Gene Name

dynein, axonemal, heavy chain 11

Synonyms

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

MMRRC Submission

042879-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.492) question?

Stock #

R5296 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

117877982-118199043 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 117883416 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 4304 (V4304A)

Ref Sequence

ENSEMBL: ENSMUSP00000081867 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021592] [ENSMUST00000084806]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000021592

SMART Domains

Protein: ENSMUSP00000021592
Gene: ENSMUSG00000021175

Domain	Start	End	E-Value	Type
low complexity region	115	125	N/A	INTRINSIC
low complexity region	127	136	N/A	INTRINSIC
low complexity region	233	247	N/A	INTRINSIC
Pfam:zf-4CXXC_R1	333	431	4.3e-40	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000084806
AA Change: V4304A

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000081867
Gene: ENSMUSG00000018581
AA Change: V4304A

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

probably benign
Transcript: ENSMUST00000176756

Meta Mutation Damage Score

0.3257

Coding Region Coverage

1x: 99.5%
3x: 98.9%
10x: 97.9%
20x: 96.6%

Validation Efficiency

100% (65/65)

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: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Apobr	A	C	7: 126,588,024 (GRCm38)	D89A	probably damaging	Het
Bhlhe41	C	T	6: 145,862,968 (GRCm38)		probably benign	Het
Cacna1s	G	A	1: 136,095,785 (GRCm38)	V674M	probably benign	Het
Cavin2	T	C	1: 51,289,870 (GRCm38)		probably null	Het
Cd300lb	T	C	11: 114,924,937 (GRCm38)	S106G	possibly damaging	Het
Ceacam15	A	G	7: 16,673,196 (GRCm38)	V132A	probably benign	Het
Ddi2	G	T	4: 141,684,765 (GRCm38)	Q279K	probably benign	Het
Dnah2	C	T	11: 69,458,920 (GRCm38)	R2399Q	probably benign	Het
Dnase1l1	C	T	X: 74,277,038 (GRCm38)		probably null	Het
Epsti1	T	A	14: 77,904,650 (GRCm38)	H55Q	probably benign	Het
Flad1	T	C	3: 89,411,196 (GRCm38)	T17A	probably damaging	Het
Fzd2	C	T	11: 102,606,155 (GRCm38)	T475M	probably damaging	Het
Gemin5	C	A	11: 58,130,061 (GRCm38)	W1099L	probably damaging	Het
Gm8979	A	T	7: 106,081,848 (GRCm38)		noncoding transcript	Het
Gm9892	T	C	8: 52,196,929 (GRCm38)		noncoding transcript	Het
Gmeb2	A	G	2: 181,255,986 (GRCm38)		probably benign	Het
Grip1	A	G	10: 119,929,928 (GRCm38)	E55G	probably damaging	Het
Hltf	T	C	3: 20,108,112 (GRCm38)	S825P	probably damaging	Het
Kcnh3	A	T	15: 99,241,939 (GRCm38)	Q902L	probably null	Het
Kcnt2	C	T	1: 140,609,615 (GRCm38)	P1037L	probably damaging	Het
Klhl18	G	C	9: 110,436,127 (GRCm38)	N335K	possibly damaging	Het
Lama5	A	C	2: 180,193,801 (GRCm38)	L1253R	probably damaging	Het
Lancl2	T	G	6: 57,724,582 (GRCm38)	S230A	probably benign	Het
Lmcd1	A	G	6: 112,315,588 (GRCm38)	M134V	probably damaging	Het
Lrrc23	C	A	6: 124,774,482 (GRCm38)	A205S	probably damaging	Het
Mfsd13b	T	A	7: 120,991,738 (GRCm38)	I234N	probably damaging	Het
Mroh3	A	G	1: 136,196,323 (GRCm38)	S386P	probably damaging	Het
Mylk3	A	C	8: 85,355,431 (GRCm38)	F313V	possibly damaging	Het
Myo9b	A	T	8: 71,333,388 (GRCm38)	Q643L	possibly damaging	Het
Nacad	T	C	11: 6,605,745 (GRCm38)	S2G	unknown	Het
Olfr1269	A	T	2: 90,118,699 (GRCm38)	W300R	probably damaging	Het
Olfr136	C	T	17: 38,335,456 (GRCm38)	Q100*	probably null	Het
Olfr419	G	T	1: 174,250,756 (GRCm38)	T57K	possibly damaging	Het
Olfr908	T	C	9: 38,516,116 (GRCm38)	F28S	probably damaging	Het
Pkd1	T	C	17: 24,576,074 (GRCm38)	V2245A	probably damaging	Het
Pkdrej	G	A	15: 85,817,118 (GRCm38)	T1539I	possibly damaging	Het
Plch2	G	T	4: 154,989,999 (GRCm38)		probably null	Het
Pygm	G	A	19: 6,384,579 (GRCm38)	R34H	probably damaging	Het
Rgs12	T	C	5: 35,021,104 (GRCm38)		probably benign	Het
Ruvbl1	T	C	6: 88,485,908 (GRCm38)	I338T	probably damaging	Het
Sapcd1	T	A	17: 35,026,731 (GRCm38)	Q104L	probably damaging	Het
Satb2	T	C	1: 56,796,907 (GRCm38)	E575G	probably damaging	Het
Sema6b	T	A	17: 56,127,091 (GRCm38)		probably null	Het
Slc25a11	T	C	11: 70,646,185 (GRCm38)	N15D	probably damaging	Het
Slc26a6	C	T	9: 108,860,646 (GRCm38)	T526M	probably damaging	Het
Tcaf3	G	T	6: 42,587,510 (GRCm38)	T906K	possibly damaging	Het
Thbd	A	T	2: 148,406,983 (GRCm38)	C322S	probably damaging	Het
Traf2	A	G	2: 25,520,440 (GRCm38)	L399P	probably damaging	Het
Troap	T	A	15: 99,078,817 (GRCm38)	V274D	probably damaging	Het
Utrn	G	A	10: 12,401,355 (GRCm38)	T3406M	probably damaging	Het
Uts2	G	T	4: 150,999,051 (GRCm38)	A40S	possibly damaging	Het
Vmn2r109	T	A	17: 20,554,341 (GRCm38)	I251F	possibly damaging	Het
Vmn2r67	A	G	7: 85,137,022 (GRCm38)	S592P	probably damaging	Het
Vps13b	T	G	15: 35,876,413 (GRCm38)	W2797G	probably damaging	Het
Ythdf1	A	T	2: 180,912,188 (GRCm38)	M51K	probably damaging	Het
Zfp60	T	A	7: 27,738,530 (GRCm38)		probably benign	Het
Zfp882	T	A	8: 71,914,360 (GRCm38)	F344I	probably damaging	Het

Other mutations in Dnah11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00341:Dnah11	APN	12	118,198,745 (GRCm38)	missense	probably benign	0.28
IGL00422:Dnah11	APN	12	118,068,096 (GRCm38)	missense	probably damaging	1.00
IGL00436:Dnah11	APN	12	118,036,459 (GRCm38)	missense	possibly damaging	0.56
IGL00540:Dnah11	APN	12	118,186,922 (GRCm38)	missense	probably benign	0.01
IGL00687:Dnah11	APN	12	117,922,004 (GRCm38)	splice site	probably benign
IGL00833:Dnah11	APN	12	118,179,580 (GRCm38)	missense	probably damaging	1.00
IGL00906:Dnah11	APN	12	117,911,202 (GRCm38)	missense	probably damaging	1.00
IGL00952:Dnah11	APN	12	118,196,651 (GRCm38)	missense	possibly damaging	0.56
IGL01111:Dnah11	APN	12	118,142,934 (GRCm38)	splice site	probably benign
IGL01121:Dnah11	APN	12	118,050,695 (GRCm38)	missense	probably benign	0.02
IGL01143:Dnah11	APN	12	118,012,740 (GRCm38)	missense	probably damaging	1.00
IGL01359:Dnah11	APN	12	117,982,999 (GRCm38)	missense	probably damaging	0.99
IGL01372:Dnah11	APN	12	118,192,399 (GRCm38)	missense	probably damaging	1.00
IGL01410:Dnah11	APN	12	118,047,256 (GRCm38)	nonsense	probably null
IGL01418:Dnah11	APN	12	117,987,482 (GRCm38)	nonsense	probably null
IGL01444:Dnah11	APN	12	118,020,232 (GRCm38)	missense	possibly damaging	0.91
IGL01606:Dnah11	APN	12	117,983,032 (GRCm38)	missense	probably benign	0.15
IGL01645:Dnah11	APN	12	118,186,998 (GRCm38)	missense	possibly damaging	0.90
IGL01932:Dnah11	APN	12	118,192,270 (GRCm38)	splice site	probably benign
IGL02104:Dnah11	APN	12	118,192,390 (GRCm38)	missense	probably benign
IGL02151:Dnah11	APN	12	118,059,888 (GRCm38)	splice site	probably benign
IGL02189:Dnah11	APN	12	118,082,579 (GRCm38)	missense	probably benign	0.00
IGL02417:Dnah11	APN	12	118,057,180 (GRCm38)	missense	probably damaging	1.00
IGL02421:Dnah11	APN	12	118,186,902 (GRCm38)	missense	probably damaging	1.00
IGL02444:Dnah11	APN	12	117,975,873 (GRCm38)	splice site	probably benign
IGL02474:Dnah11	APN	12	118,027,445 (GRCm38)	splice site	probably null
IGL02526:Dnah11	APN	12	118,179,618 (GRCm38)	missense	possibly damaging	0.70
IGL02887:Dnah11	APN	12	117,911,040 (GRCm38)	missense	probably damaging	1.00
IGL03011:Dnah11	APN	12	118,012,377 (GRCm38)	missense	probably benign	0.08
IGL03061:Dnah11	APN	12	117,903,121 (GRCm38)	missense	probably damaging	1.00
IGL03182:Dnah11	APN	12	118,030,291 (GRCm38)	missense	probably damaging	0.99
IGL03220:Dnah11	APN	12	118,105,985 (GRCm38)	missense	probably benign
IGL03238:Dnah11	APN	12	118,109,898 (GRCm38)	missense	probably damaging	1.00
IGL03493:Dnah11	APN	12	118,012,798 (GRCm38)	missense	probably benign	0.00
P0045:Dnah11	UTSW	12	118,030,327 (GRCm38)	missense	probably benign
R0009:Dnah11	UTSW	12	118,045,522 (GRCm38)	missense	possibly damaging	0.90
R0066:Dnah11	UTSW	12	118,126,886 (GRCm38)	missense	probably benign	0.05
R0172:Dnah11	UTSW	12	117,987,453 (GRCm38)	missense	probably damaging	1.00
R0206:Dnah11	UTSW	12	118,043,774 (GRCm38)	missense	probably damaging	0.98
R0206:Dnah11	UTSW	12	118,043,774 (GRCm38)	missense	probably damaging	0.98
R0208:Dnah11	UTSW	12	118,043,774 (GRCm38)	missense	probably damaging	0.98
R0230:Dnah11	UTSW	12	117,983,056 (GRCm38)	nonsense	probably null
R0270:Dnah11	UTSW	12	118,041,013 (GRCm38)	missense	probably damaging	1.00
R0311:Dnah11	UTSW	12	118,127,133 (GRCm38)	missense	probably benign	0.03
R0325:Dnah11	UTSW	12	118,012,339 (GRCm38)	missense	probably benign
R0370:Dnah11	UTSW	12	117,995,227 (GRCm38)	missense	probably benign
R0416:Dnah11	UTSW	12	117,911,058 (GRCm38)	missense	probably damaging	1.00
R0505:Dnah11	UTSW	12	118,106,510 (GRCm38)	missense	probably damaging	1.00
R0540:Dnah11	UTSW	12	118,082,511 (GRCm38)	missense	probably damaging	1.00
R0554:Dnah11	UTSW	12	117,931,178 (GRCm38)	missense	probably benign	0.01
R0607:Dnah11	UTSW	12	118,082,511 (GRCm38)	missense	probably damaging	1.00
R0620:Dnah11	UTSW	12	117,987,469 (GRCm38)	missense	probably damaging	1.00
R0635:Dnah11	UTSW	12	118,007,996 (GRCm38)	missense	probably damaging	1.00
R0755:Dnah11	UTSW	12	118,198,625 (GRCm38)	missense	probably benign	0.17
R0755:Dnah11	UTSW	12	117,954,829 (GRCm38)	missense	possibly damaging	0.95
R0789:Dnah11	UTSW	12	117,911,232 (GRCm38)	missense	probably damaging	1.00
R0833:Dnah11	UTSW	12	118,196,662 (GRCm38)	missense	probably benign	0.01
R0835:Dnah11	UTSW	12	117,916,788 (GRCm38)	missense	probably damaging	1.00
R0836:Dnah11	UTSW	12	118,196,662 (GRCm38)	missense	probably benign	0.01
R0846:Dnah11	UTSW	12	117,933,850 (GRCm38)	missense	probably damaging	0.97
R0865:Dnah11	UTSW	12	118,190,844 (GRCm38)	nonsense	probably null
R0928:Dnah11	UTSW	12	118,045,562 (GRCm38)	missense	probably damaging	1.00
R0939:Dnah11	UTSW	12	118,060,407 (GRCm38)	missense	probably damaging	1.00
R1203:Dnah11	UTSW	12	117,933,812 (GRCm38)	missense	possibly damaging	0.81
R1394:Dnah11	UTSW	12	117,972,364 (GRCm38)	missense	possibly damaging	0.75
R1398:Dnah11	UTSW	12	118,057,106 (GRCm38)	nonsense	probably null
R1465:Dnah11	UTSW	12	118,038,695 (GRCm38)	missense	probably damaging	1.00
R1465:Dnah11	UTSW	12	118,038,695 (GRCm38)	missense	probably damaging	1.00
R1500:Dnah11	UTSW	12	118,012,829 (GRCm38)	splice site	probably null
R1535:Dnah11	UTSW	12	118,018,730 (GRCm38)	missense	probably damaging	1.00
R1539:Dnah11	UTSW	12	117,931,256 (GRCm38)	missense	probably benign	0.01
R1554:Dnah11	UTSW	12	118,082,499 (GRCm38)	missense	possibly damaging	0.92
R1574:Dnah11	UTSW	12	118,060,317 (GRCm38)	missense	probably damaging	1.00
R1574:Dnah11	UTSW	12	118,060,317 (GRCm38)	missense	probably damaging	1.00
R1615:Dnah11	UTSW	12	118,050,722 (GRCm38)	missense	probably damaging	1.00
R1618:Dnah11	UTSW	12	118,015,465 (GRCm38)	missense	probably damaging	0.98
R1638:Dnah11	UTSW	12	118,015,419 (GRCm38)	missense	possibly damaging	0.81
R1659:Dnah11	UTSW	12	118,120,724 (GRCm38)	missense	possibly damaging	0.94
R1671:Dnah11	UTSW	12	117,916,788 (GRCm38)	missense	probably damaging	1.00
R1678:Dnah11	UTSW	12	117,933,845 (GRCm38)	missense	possibly damaging	0.50
R1699:Dnah11	UTSW	12	118,190,868 (GRCm38)	missense	probably damaging	1.00
R1712:Dnah11	UTSW	12	118,196,644 (GRCm38)	missense	probably benign	0.32
R1728:Dnah11	UTSW	12	117,916,931 (GRCm38)	missense	probably damaging	1.00
R1729:Dnah11	UTSW	12	117,916,931 (GRCm38)	missense	probably damaging	1.00
R1764:Dnah11	UTSW	12	118,190,825 (GRCm38)	missense	probably benign	0.31
R1780:Dnah11	UTSW	12	118,027,558 (GRCm38)	missense	probably damaging	1.00
R1789:Dnah11	UTSW	12	118,038,780 (GRCm38)	missense	probably damaging	0.99
R1800:Dnah11	UTSW	12	117,916,788 (GRCm38)	missense	probably damaging	1.00
R1863:Dnah11	UTSW	12	118,063,852 (GRCm38)	missense	possibly damaging	0.92
R1892:Dnah11	UTSW	12	118,106,474 (GRCm38)	missense	possibly damaging	0.53
R1907:Dnah11	UTSW	12	118,127,556 (GRCm38)	missense	possibly damaging	0.66
R1964:Dnah11	UTSW	12	118,142,292 (GRCm38)	missense	possibly damaging	0.56
R1967:Dnah11	UTSW	12	117,916,788 (GRCm38)	missense	probably damaging	1.00
R1997:Dnah11	UTSW	12	118,082,468 (GRCm38)	missense	possibly damaging	0.64
R2086:Dnah11	UTSW	12	118,113,871 (GRCm38)	missense	possibly damaging	0.82
R2092:Dnah11	UTSW	12	118,012,716 (GRCm38)	missense	possibly damaging	0.50
R2108:Dnah11	UTSW	12	118,020,353 (GRCm38)	missense	probably damaging	1.00
R2140:Dnah11	UTSW	12	118,008,810 (GRCm38)	missense	probably benign	0.01
R2261:Dnah11	UTSW	12	117,966,639 (GRCm38)	missense	probably damaging	0.99
R2261:Dnah11	UTSW	12	117,880,025 (GRCm38)	missense	probably benign	0.06
R2262:Dnah11	UTSW	12	117,966,639 (GRCm38)	missense	probably damaging	0.99
R2262:Dnah11	UTSW	12	117,880,025 (GRCm38)	missense	probably benign	0.06
R2263:Dnah11	UTSW	12	117,880,025 (GRCm38)	missense	probably benign	0.06
R2263:Dnah11	UTSW	12	117,966,639 (GRCm38)	missense	probably damaging	0.99
R2328:Dnah11	UTSW	12	117,886,686 (GRCm38)	missense	probably damaging	0.98
R2352:Dnah11	UTSW	12	117,928,330 (GRCm38)	missense	probably damaging	1.00
R2410:Dnah11	UTSW	12	118,027,527 (GRCm38)	missense	probably damaging	1.00
R2885:Dnah11	UTSW	12	117,987,427 (GRCm38)	nonsense	probably null
R3499:Dnah11	UTSW	12	117,911,023 (GRCm38)	missense	probably damaging	1.00
R3741:Dnah11	UTSW	12	118,131,341 (GRCm38)	missense	probably benign	0.05
R3742:Dnah11	UTSW	12	118,131,341 (GRCm38)	missense	probably benign	0.05
R3779:Dnah11	UTSW	12	118,130,713 (GRCm38)	splice site	probably benign
R3785:Dnah11	UTSW	12	118,017,602 (GRCm38)	missense	probably damaging	1.00
R3883:Dnah11	UTSW	12	117,978,453 (GRCm38)	splice site	probably benign
R4014:Dnah11	UTSW	12	117,974,914 (GRCm38)	missense	probably benign	0.16
R4043:Dnah11	UTSW	12	117,879,943 (GRCm38)	missense	probably damaging	1.00
R4072:Dnah11	UTSW	12	118,106,492 (GRCm38)	missense	probably damaging	1.00
R4073:Dnah11	UTSW	12	118,045,678 (GRCm38)	missense	probably benign	0.01
R4074:Dnah11	UTSW	12	118,045,678 (GRCm38)	missense	probably benign	0.01
R4076:Dnah11	UTSW	12	118,045,678 (GRCm38)	missense	probably benign	0.01
R4201:Dnah11	UTSW	12	117,966,659 (GRCm38)	missense	possibly damaging	0.63
R4224:Dnah11	UTSW	12	118,130,892 (GRCm38)	missense	probably benign	0.06
R4233:Dnah11	UTSW	12	117,916,791 (GRCm38)	missense	probably damaging	1.00
R4358:Dnah11	UTSW	12	118,125,843 (GRCm38)	nonsense	probably null
R4430:Dnah11	UTSW	12	117,983,011 (GRCm38)	missense	probably benign	0.26
R4465:Dnah11	UTSW	12	117,987,451 (GRCm38)	missense	probably benign	0.09
R4489:Dnah11	UTSW	12	117,916,896 (GRCm38)	missense	probably benign	0.31
R4572:Dnah11	UTSW	12	118,010,125 (GRCm38)	missense	probably benign	0.00
R4574:Dnah11	UTSW	12	118,012,255 (GRCm38)	critical splice donor site	probably null
R4657:Dnah11	UTSW	12	118,192,427 (GRCm38)	missense	probably benign	0.02
R4709:Dnah11	UTSW	12	118,018,760 (GRCm38)	missense	probably benign	0.26
R4740:Dnah11	UTSW	12	118,120,544 (GRCm38)	missense	probably benign	0.28
R4803:Dnah11	UTSW	12	118,127,608 (GRCm38)	missense	possibly damaging	0.50
R4896:Dnah11	UTSW	12	117,995,200 (GRCm38)	missense	probably damaging	1.00
R4908:Dnah11	UTSW	12	118,126,883 (GRCm38)	missense	probably benign	0.37
R5018:Dnah11	UTSW	12	118,130,728 (GRCm38)	missense	probably benign	0.00
R5071:Dnah11	UTSW	12	118,082,453 (GRCm38)	nonsense	probably null
R5074:Dnah11	UTSW	12	118,082,453 (GRCm38)	nonsense	probably null
R5080:Dnah11	UTSW	12	118,198,830 (GRCm38)	start codon destroyed	probably null	0.01
R5097:Dnah11	UTSW	12	118,017,700 (GRCm38)	missense	probably damaging	1.00
R5131:Dnah11	UTSW	12	117,954,751 (GRCm38)	missense	probably damaging	1.00
R5215:Dnah11	UTSW	12	118,157,361 (GRCm38)	missense	probably benign	0.09
R5252:Dnah11	UTSW	12	118,125,941 (GRCm38)	missense	probably damaging	1.00
R5308:Dnah11	UTSW	12	118,085,680 (GRCm38)	missense	possibly damaging	0.60
R5368:Dnah11	UTSW	12	117,954,893 (GRCm38)	missense	probably damaging	1.00
R5383:Dnah11	UTSW	12	118,085,697 (GRCm38)	missense	probably damaging	0.99
R5499:Dnah11	UTSW	12	118,106,474 (GRCm38)	missense	possibly damaging	0.53
R5503:Dnah11	UTSW	12	117,880,451 (GRCm38)	critical splice donor site	probably null
R5546:Dnah11	UTSW	12	117,975,848 (GRCm38)	missense	possibly damaging	0.83
R5578:Dnah11	UTSW	12	118,018,802 (GRCm38)	missense	probably damaging	0.99
R5657:Dnah11	UTSW	12	117,883,617 (GRCm38)	missense	probably damaging	1.00
R5702:Dnah11	UTSW	12	118,113,907 (GRCm38)	missense	probably benign	0.04
R5706:Dnah11	UTSW	12	118,023,935 (GRCm38)	missense	probably damaging	1.00
R5727:Dnah11	UTSW	12	118,127,106 (GRCm38)	missense	probably damaging	1.00
R5737:Dnah11	UTSW	12	118,192,390 (GRCm38)	missense	probably benign
R5884:Dnah11	UTSW	12	118,177,534 (GRCm38)	missense	probably benign	0.00
R5900:Dnah11	UTSW	12	118,082,431 (GRCm38)	splice site	probably null
R5905:Dnah11	UTSW	12	117,954,924 (GRCm38)	missense	probably damaging	1.00
R5928:Dnah11	UTSW	12	117,914,636 (GRCm38)	splice site	probably null
R5973:Dnah11	UTSW	12	118,110,952 (GRCm38)	missense	probably benign	0.02
R6024:Dnah11	UTSW	12	118,030,272 (GRCm38)	missense	probably benign	0.34
R6056:Dnah11	UTSW	12	117,928,456 (GRCm38)	missense	probably benign	0.03
R6075:Dnah11	UTSW	12	118,104,851 (GRCm38)	missense	probably damaging	1.00
R6092:Dnah11	UTSW	12	117,928,456 (GRCm38)	missense	probably benign
R6191:Dnah11	UTSW	12	118,190,897 (GRCm38)	missense	probably benign
R6197:Dnah11	UTSW	12	118,179,747 (GRCm38)	missense	probably benign	0.03
R6262:Dnah11	UTSW	12	117,931,178 (GRCm38)	missense	probably damaging	0.98
R6321:Dnah11	UTSW	12	118,142,292 (GRCm38)	missense	possibly damaging	0.56
R6454:Dnah11	UTSW	12	117,916,855 (GRCm38)	missense	probably benign	0.01
R6614:Dnah11	UTSW	12	117,886,676 (GRCm38)	missense	possibly damaging	0.72
R6694:Dnah11	UTSW	12	118,186,882 (GRCm38)	splice site	probably null
R6712:Dnah11	UTSW	12	118,050,722 (GRCm38)	missense	probably damaging	1.00
R6720:Dnah11	UTSW	12	118,045,646 (GRCm38)	missense	probably damaging	1.00
R6742:Dnah11	UTSW	12	118,113,894 (GRCm38)	missense	possibly damaging	0.82
R6806:Dnah11	UTSW	12	117,987,676 (GRCm38)	splice site	probably null
R6895:Dnah11	UTSW	12	117,995,191 (GRCm38)	missense	probably damaging	0.99
R6939:Dnah11	UTSW	12	118,106,562 (GRCm38)	missense	probably damaging	1.00
R6940:Dnah11	UTSW	12	118,198,768 (GRCm38)	missense	probably benign
R6945:Dnah11	UTSW	12	118,060,310 (GRCm38)	missense	probably damaging	1.00
R6958:Dnah11	UTSW	12	117,933,809 (GRCm38)	missense	probably damaging	1.00
R6970:Dnah11	UTSW	12	118,108,944 (GRCm38)	missense	probably benign	0.00
R6976:Dnah11	UTSW	12	118,198,643 (GRCm38)	missense	probably benign	0.16
R7000:Dnah11	UTSW	12	118,017,661 (GRCm38)	missense	probably damaging	1.00
R7011:Dnah11	UTSW	12	117,922,018 (GRCm38)	frame shift	probably null
R7101:Dnah11	UTSW	12	118,068,145 (GRCm38)	missense	probably benign
R7106:Dnah11	UTSW	12	117,961,149 (GRCm38)	missense	probably benign	0.15
R7203:Dnah11	UTSW	12	118,045,522 (GRCm38)	missense	possibly damaging	0.90
R7219:Dnah11	UTSW	12	118,126,889 (GRCm38)	missense	probably benign	0.00
R7219:Dnah11	UTSW	12	118,041,095 (GRCm38)	missense	possibly damaging	0.95
R7308:Dnah11	UTSW	12	117,995,275 (GRCm38)	missense	probably damaging	1.00
R7361:Dnah11	UTSW	12	118,018,742 (GRCm38)	missense	probably damaging	1.00
R7367:Dnah11	UTSW	12	117,987,442 (GRCm38)	missense	possibly damaging	0.59
R7399:Dnah11	UTSW	12	118,125,785 (GRCm38)	missense	probably damaging	1.00
R7399:Dnah11	UTSW	12	118,027,477 (GRCm38)	missense	probably benign	0.00
R7404:Dnah11	UTSW	12	118,104,808 (GRCm38)	missense	probably benign	0.36
R7473:Dnah11	UTSW	12	117,903,176 (GRCm38)	missense	probably benign	0.19
R7545:Dnah11	UTSW	12	117,931,204 (GRCm38)	missense	probably damaging	1.00
R7608:Dnah11	UTSW	12	118,140,770 (GRCm38)	splice site	probably null
R7625:Dnah11	UTSW	12	118,196,642 (GRCm38)	missense	probably benign
R7761:Dnah11	UTSW	12	118,023,913 (GRCm38)	missense	probably damaging	1.00
R7879:Dnah11	UTSW	12	118,041,009 (GRCm38)	missense	probably damaging	1.00
R7881:Dnah11	UTSW	12	117,987,502 (GRCm38)	missense	probably benign	0.04
R7904:Dnah11	UTSW	12	117,903,268 (GRCm38)	missense	possibly damaging	0.72
R8100:Dnah11	UTSW	12	117,966,633 (GRCm38)	missense	probably damaging	0.99
R8179:Dnah11	UTSW	12	117,878,549 (GRCm38)	missense	possibly damaging	0.90
R8192:Dnah11	UTSW	12	118,012,446 (GRCm38)	missense	probably benign
R8254:Dnah11	UTSW	12	117,878,524 (GRCm38)	missense	possibly damaging	0.89
R8268:Dnah11	UTSW	12	118,027,508 (GRCm38)	nonsense	probably null
R8272:Dnah11	UTSW	12	118,111,017 (GRCm38)	missense	probably benign	0.01
R8344:Dnah11	UTSW	12	118,085,731 (GRCm38)	missense	probably benign	0.00
R8515:Dnah11	UTSW	12	117,975,798 (GRCm38)	missense	probably damaging	1.00
R8528:Dnah11	UTSW	12	118,008,803 (GRCm38)	missense	probably damaging	0.96
R8557:Dnah11	UTSW	12	117,878,512 (GRCm38)	missense	probably benign
R8676:Dnah11	UTSW	12	118,190,804 (GRCm38)	missense	probably damaging	1.00
R8738:Dnah11	UTSW	12	118,085,649 (GRCm38)	critical splice donor site	probably null
R8773:Dnah11	UTSW	12	117,995,215 (GRCm38)	missense	possibly damaging	0.94
R8818:Dnah11	UTSW	12	117,911,029 (GRCm38)	missense	probably damaging	1.00
R8855:Dnah11	UTSW	12	118,192,372 (GRCm38)	missense	probably benign	0.03
R8866:Dnah11	UTSW	12	118,192,372 (GRCm38)	missense	probably benign	0.03
R8881:Dnah11	UTSW	12	118,126,815 (GRCm38)	missense	probably benign	0.05
R8881:Dnah11	UTSW	12	118,113,912 (GRCm38)	missense	probably benign	0.00
R8920:Dnah11	UTSW	12	118,113,939 (GRCm38)	missense	probably damaging	0.99
R8944:Dnah11	UTSW	12	118,127,646 (GRCm38)	missense	possibly damaging	0.63
R8945:Dnah11	UTSW	12	118,023,983 (GRCm38)	missense	probably benign	0.36
R8962:Dnah11	UTSW	12	117,954,895 (GRCm38)	missense	probably damaging	1.00
R8962:Dnah11	UTSW	12	117,952,538 (GRCm38)	missense	probably damaging	1.00
R9059:Dnah11	UTSW	12	118,130,843 (GRCm38)	missense	probably benign	0.00
R9155:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9162:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9164:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9171:Dnah11	UTSW	12	117,931,183 (GRCm38)	missense	probably damaging	0.99
R9186:Dnah11	UTSW	12	118,190,897 (GRCm38)	missense	probably benign
R9205:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9208:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9234:Dnah11	UTSW	12	117,987,360 (GRCm38)	missense	probably damaging	1.00
R9264:Dnah11	UTSW	12	118,027,527 (GRCm38)	missense	probably damaging	1.00
R9290:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9291:Dnah11	UTSW	12	118,027,516 (GRCm38)	missense	probably damaging	0.99
R9315:Dnah11	UTSW	12	118,179,606 (GRCm38)	missense	probably benign	0.11
R9353:Dnah11	UTSW	12	118,179,699 (GRCm38)	missense	probably benign	0.00
R9375:Dnah11	UTSW	12	117,920,968 (GRCm38)	missense	possibly damaging	0.67
R9392:Dnah11	UTSW	12	118,177,555 (GRCm38)	missense	probably benign	0.00
R9392:Dnah11	UTSW	12	118,047,320 (GRCm38)	nonsense	probably null
R9433:Dnah11	UTSW	12	118,012,272 (GRCm38)	missense	probably damaging	1.00
R9511:Dnah11	UTSW	12	117,914,617 (GRCm38)	missense	probably damaging	1.00
R9526:Dnah11	UTSW	12	118,186,976 (GRCm38)	missense	probably damaging	0.98
R9566:Dnah11	UTSW	12	117,974,993 (GRCm38)	missense	possibly damaging	0.69
R9673:Dnah11	UTSW	12	118,018,778 (GRCm38)	missense	possibly damaging	0.91
R9705:Dnah11	UTSW	12	118,131,035 (GRCm38)	missense	probably damaging	1.00
R9716:Dnah11	UTSW	12	118,060,413 (GRCm38)	missense	probably damaging	0.99
R9746:Dnah11	UTSW	12	117,878,576 (GRCm38)	nonsense	probably null
R9764:Dnah11	UTSW	12	117,920,969 (GRCm38)	missense	probably benign	0.05
RF023:Dnah11	UTSW	12	117,954,850 (GRCm38)	missense	probably damaging	1.00
RF047:Dnah11	UTSW	12	118,010,083 (GRCm38)	missense	probably damaging	1.00
Z1088:Dnah11	UTSW	12	117,895,012 (GRCm38)	missense	probably damaging	1.00
Z1088:Dnah11	UTSW	12	117,982,969 (GRCm38)	missense	probably damaging	1.00
Z1176:Dnah11	UTSW	12	118,130,799 (GRCm38)	missense	probably damaging	0.97
Z1176:Dnah11	UTSW	12	118,127,119 (GRCm38)	missense	probably benign	0.00
Z1176:Dnah11	UTSW	12	117,931,177 (GRCm38)	missense	possibly damaging	0.81

Predicted Primers

PCR Primer
(F):5'- CTACAAGATGATGGTCACGGAG -3'
(R):5'- GTGTGAGAGGATGAACGTTCTC -3'

Sequencing Primer
(F):5'- TCACGGAGCAGGAGTTCTG -3'
(R):5'- GATGAACGTTCTCATCCGGGAAATC -3'

Posted On

2016-07-22