Mutagenetix > Incidental Mutation

Incidental Mutation 'R5682:Dnhd1'

443116

Institutional Source

Beutler Lab

Gene Symbol

Dnhd1

Ensembl Gene

ENSMUSG00000030882

Gene Name

dynein heavy chain domain 1

Synonyms

8030491N06Rik

MMRRC Submission

043318-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.090) question?

Stock #

R5682 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

105300034-105371006 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 105352416 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glutamine at position 2523 (R2523Q)

Ref Sequence

ENSEMBL: ENSMUSP00000121261 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000145988]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000145988
AA Change: R2523Q

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

SMART Domains

Protein: ENSMUSP00000121261
Gene: ENSMUSG00000030882
AA Change: R2523Q

Domain	Start	End	E-Value	Type
low complexity region	5	18	N/A	INTRINSIC
low complexity region	102	115	N/A	INTRINSIC
low complexity region	183	191	N/A	INTRINSIC
low complexity region	253	269	N/A	INTRINSIC
low complexity region	943	962	N/A	INTRINSIC
Pfam:DHC_N2	1018	1472	4.6e-50	PFAM
Pfam:AAA_6	1652	1875	2.7e-14	PFAM
low complexity region	1906	1918	N/A	INTRINSIC
Blast:AAA	1993	2196	1e-34	BLAST
Pfam:AAA_7	2362	2610	3.3e-11	PFAM
low complexity region	2697	2714	N/A	INTRINSIC
low complexity region	2722	2733	N/A	INTRINSIC
low complexity region	2800	2810	N/A	INTRINSIC
low complexity region	3116	3134	N/A	INTRINSIC
Pfam:MT	3178	3470	3.9e-16	PFAM
coiled coil region	3590	3642	N/A	INTRINSIC
coiled coil region	3816	3843	N/A	INTRINSIC
Pfam:Dynein_heavy	3976	4746	7.3e-97	PFAM

Meta Mutation Damage Score

0.5889

Coding Region Coverage

1x: 99.7%
3x: 99.0%
10x: 97.4%
20x: 95.3%

Validation Efficiency

Allele List at MGI

All alleles(1) : Gene trapped(1)

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc3	A	T	11: 94,283,723 (GRCm39)	S7T	probably benign	Het
Acot4	G	A	12: 84,085,576 (GRCm39)	V98M	probably damaging	Het
Acsm2	A	T	7: 119,162,774 (GRCm39)	N41I	probably benign	Het
Adamtsl3	A	T	7: 82,255,758 (GRCm39)	N1590I	probably damaging	Het
Ank3	G	A	10: 69,729,347 (GRCm39)	G714R	probably damaging	Het
Armh4	T	C	14: 49,989,043 (GRCm39)	D642G	probably damaging	Het
Ash1l	G	A	3: 88,914,914 (GRCm39)	R1848Q	probably damaging	Het
Atp1a4	A	T	1: 172,081,730 (GRCm39)	Y141N	probably damaging	Het
Atxn3	A	T	12: 101,924,406 (GRCm39)	I1N	probably damaging	Het
Avil	A	C	10: 126,849,973 (GRCm39)	Q608P	probably damaging	Het
Axin1	T	C	17: 26,406,775 (GRCm39)	V456A	probably benign	Het
Cacna1g	A	G	11: 94,349,940 (GRCm39)	L635P	probably damaging	Het
Card11	G	A	5: 140,888,666 (GRCm39)	Q231*	probably null	Het
Ccdc162	G	A	10: 41,432,799 (GRCm39)	R500*	probably null	Het
Cdh24	T	C	14: 54,874,805 (GRCm39)	D400G	probably damaging	Het
Cep112	T	C	11: 108,361,138 (GRCm39)	L164P	probably damaging	Het
Corin	A	G	5: 72,579,497 (GRCm39)	S224P	possibly damaging	Het
Csgalnact2	T	C	6: 118,097,953 (GRCm39)	Y371C	probably damaging	Het
Cspg4	A	T	9: 56,793,480 (GRCm39)	E405V	probably benign	Het
Ctnna3	T	A	10: 64,709,085 (GRCm39)	M708K	probably damaging	Het
Cyp7a1	T	A	4: 6,268,429 (GRCm39)	Y432F	probably benign	Het
Dcaf11	T	A	14: 55,800,883 (GRCm39)	V113E	probably damaging	Het
Dhx29	T	C	13: 113,067,383 (GRCm39)	I88T	probably damaging	Het
Elmo2	A	G	2: 165,139,330 (GRCm39)	F406L	probably damaging	Het
Eps15l1	G	A	8: 73,125,592 (GRCm39)	Q648*	probably null	Het
Fam171a1	G	A	2: 3,227,126 (GRCm39)	R753Q	probably damaging	Het
Figla	T	A	6: 85,995,604 (GRCm39)	V86E	probably damaging	Het
Galnt7	C	A	8: 58,036,967 (GRCm39)	E141*	probably null	Het
Garnl3	A	G	2: 32,944,185 (GRCm39)	Y125H	probably damaging	Het
Gnb5	A	G	9: 75,234,523 (GRCm39)	D74G	probably damaging	Het
Grk1	A	T	8: 13,464,351 (GRCm39)	I408F	possibly damaging	Het
Has1	A	T	17: 18,064,425 (GRCm39)	W405R	possibly damaging	Het
Hdac5	A	G	11: 102,104,749 (GRCm39)		probably benign	Het
Helq	T	A	5: 100,933,170 (GRCm39)	M555L	probably benign	Het
Hipk2	T	C	6: 38,714,408 (GRCm39)	N556S	possibly damaging	Het
Htr7	C	A	19: 35,947,271 (GRCm39)	A248S	probably damaging	Het
Ing3	T	C	6: 21,968,949 (GRCm39)	S144P	probably damaging	Het
Itgb1	G	A	8: 129,453,549 (GRCm39)		probably null	Het
Kcnh4	A	T	11: 100,640,628 (GRCm39)	M466K	possibly damaging	Het
Krit1	T	A	5: 3,880,737 (GRCm39)	N565K	probably damaging	Het
Limk1	A	C	5: 134,694,059 (GRCm39)		probably null	Het
Lrif1	T	C	3: 106,639,884 (GRCm39)	I323T	possibly damaging	Het
Macf1	T	C	4: 123,328,552 (GRCm39)	E1811G	probably damaging	Het
Mctp2	A	C	7: 71,895,207 (GRCm39)		probably null	Het
Mmp21	A	G	7: 133,276,358 (GRCm39)	I495T	probably benign	Het
Mpz	A	T	1: 170,986,463 (GRCm39)	T126S	possibly damaging	Het
Napsa	A	G	7: 44,234,768 (GRCm39)	Y301C	possibly damaging	Het
Ncbp1	T	A	4: 46,170,474 (GRCm39)		probably benign	Het
Nup160	A	G	2: 90,510,155 (GRCm39)	E47G	probably benign	Het
Or8b56	A	G	9: 38,739,424 (GRCm39)	I146V	probably benign	Het
Pcdha11	A	G	18: 37,144,502 (GRCm39)	K198E	probably damaging	Het
Pcdha3	A	G	18: 37,081,040 (GRCm39)	D594G	probably damaging	Het
Pdcd5	G	A	7: 35,346,613 (GRCm39)		probably benign	Het
Pdhx	A	T	2: 102,865,685 (GRCm39)	S166T	probably benign	Het
Pigc	A	G	1: 161,798,516 (GRCm39)	Y166C	probably damaging	Het
Prkch	C	T	12: 73,744,724 (GRCm39)	H246Y	probably damaging	Het
Ptk2	A	T	15: 73,134,413 (GRCm39)	L562*	probably null	Het
Rab3ip	C	T	10: 116,743,008 (GRCm39)	W439*	probably null	Het
Rasef	T	A	4: 73,659,208 (GRCm39)	R435*	probably null	Het
Rnf103	C	T	6: 71,485,708 (GRCm39)		probably benign	Het
Rtel1	T	C	2: 180,991,765 (GRCm39)	F388L	probably benign	Het
Sds	A	C	5: 120,621,784 (GRCm39)	S309R	possibly damaging	Het
Sgip1	T	A	4: 102,824,847 (GRCm39)	D736E	possibly damaging	Het
Sgms2	A	G	3: 131,118,611 (GRCm39)	Y291H	probably damaging	Het
Sgsm3	A	G	15: 80,895,661 (GRCm39)		probably null	Het
Siglec1	T	A	2: 130,925,930 (GRCm39)	I259F	probably damaging	Het
Sik2	G	A	9: 50,828,382 (GRCm39)	P220L	probably damaging	Het
Slc29a3	A	G	10: 60,551,991 (GRCm39)	V351A	probably benign	Het
Slc36a3	A	G	11: 55,016,489 (GRCm39)	S369P	probably benign	Het
Srgap1	A	T	10: 121,640,919 (GRCm39)	M649K	probably damaging	Het
Thnsl1	A	G	2: 21,216,879 (GRCm39)	E211G	possibly damaging	Het
Tmprss9	A	G	10: 80,733,207 (GRCm39)		probably null	Het
Tpgs1	G	A	10: 79,511,421 (GRCm39)	V188M	probably damaging	Het
Vmn1r201	G	T	13: 22,659,355 (GRCm39)	V190F	probably damaging	Het
Vmn1r64	A	T	7: 5,886,622 (GRCm39)	L307Q	possibly damaging	Het
Wbp11	T	C	6: 136,791,252 (GRCm39)		probably benign	Het
Wdr35	A	G	12: 9,031,125 (GRCm39)	Y134C	probably damaging	Het
Zan	G	T	5: 137,412,521 (GRCm39)	C3263*	probably null	Het
Zc3h12c	G	T	9: 52,037,876 (GRCm39)	D301E	probably damaging	Het
Zfp365	A	C	10: 67,745,637 (GRCm39)	L47R	probably damaging	Het
Zmym6	C	T	4: 126,998,200 (GRCm39)	P412L	probably damaging	Het

Other mutations in Dnhd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00321:Dnhd1	APN	7	105,327,202 (GRCm39)	missense	probably damaging	1.00
IGL00516:Dnhd1	APN	7	105,306,418 (GRCm39)	missense	possibly damaging	0.52
IGL00576:Dnhd1	APN	7	105,341,882 (GRCm39)	missense	probably damaging	1.00
IGL00990:Dnhd1	APN	7	105,370,895 (GRCm39)	missense	possibly damaging	0.85
IGL01346:Dnhd1	APN	7	105,363,116 (GRCm39)	missense	probably benign
IGL01714:Dnhd1	APN	7	105,370,149 (GRCm39)	missense	probably damaging	1.00
IGL01735:Dnhd1	APN	7	105,362,961 (GRCm39)	missense	probably benign	0.37
IGL01814:Dnhd1	APN	7	105,301,237 (GRCm39)	missense	probably benign
IGL01999:Dnhd1	APN	7	105,370,422 (GRCm39)	missense	possibly damaging	0.50
IGL02022:Dnhd1	APN	7	105,327,516 (GRCm39)	missense	probably damaging	1.00
IGL02131:Dnhd1	APN	7	105,370,009 (GRCm39)	missense	probably damaging	1.00
IGL02156:Dnhd1	APN	7	105,370,951 (GRCm39)	missense	probably damaging	1.00
IGL02674:Dnhd1	APN	7	105,370,688 (GRCm39)	missense	probably benign	0.00
IGL02966:Dnhd1	APN	7	105,369,948 (GRCm39)	missense	probably benign	0.00
IGL03066:Dnhd1	APN	7	105,369,089 (GRCm39)	missense	probably damaging	0.99
IGL03298:Dnhd1	APN	7	105,363,682 (GRCm39)	missense	probably damaging	0.98
IGL03378:Dnhd1	APN	7	105,362,940 (GRCm39)	missense	possibly damaging	0.87
IGL02802:Dnhd1	UTSW	7	105,304,930 (GRCm39)	missense	possibly damaging	0.83
R0060:Dnhd1	UTSW	7	105,317,721 (GRCm39)	missense	probably damaging	0.99
R0129:Dnhd1	UTSW	7	105,370,131 (GRCm39)	missense	probably benign	0.19
R0238:Dnhd1	UTSW	7	105,370,738 (GRCm39)	missense	probably benign	0.06
R0238:Dnhd1	UTSW	7	105,370,738 (GRCm39)	missense	probably benign	0.06
R0239:Dnhd1	UTSW	7	105,370,738 (GRCm39)	missense	probably benign	0.06
R0239:Dnhd1	UTSW	7	105,370,738 (GRCm39)	missense	probably benign	0.06
R0384:Dnhd1	UTSW	7	105,369,321 (GRCm39)	missense	possibly damaging	0.56
R0453:Dnhd1	UTSW	7	105,323,651 (GRCm39)	missense	probably benign	0.00
R0540:Dnhd1	UTSW	7	105,369,995 (GRCm39)	missense	probably benign	0.04
R0554:Dnhd1	UTSW	7	105,343,602 (GRCm39)	missense	probably benign	0.10
R0576:Dnhd1	UTSW	7	105,363,252 (GRCm39)	missense	probably damaging	1.00
R0607:Dnhd1	UTSW	7	105,369,995 (GRCm39)	missense	probably benign	0.04
R0631:Dnhd1	UTSW	7	105,300,831 (GRCm39)	missense	probably benign	0.17
R0639:Dnhd1	UTSW	7	105,345,671 (GRCm39)	missense	possibly damaging	0.95
R0668:Dnhd1	UTSW	7	105,344,958 (GRCm39)	missense	probably benign
R0669:Dnhd1	UTSW	7	105,342,911 (GRCm39)	missense	probably benign	0.01
R0670:Dnhd1	UTSW	7	105,345,671 (GRCm39)	missense	possibly damaging	0.95
R0699:Dnhd1	UTSW	7	105,301,113 (GRCm39)	missense	probably damaging	0.98
R1019:Dnhd1	UTSW	7	105,358,378 (GRCm39)	missense	probably damaging	1.00
R1144:Dnhd1	UTSW	7	105,362,238 (GRCm39)	missense	probably damaging	1.00
R1226:Dnhd1	UTSW	7	105,346,106 (GRCm39)	missense	probably damaging	1.00
R1257:Dnhd1	UTSW	7	105,343,360 (GRCm39)	missense	probably damaging	1.00
R1391:Dnhd1	UTSW	7	105,369,331 (GRCm39)	missense	probably damaging	1.00
R1453:Dnhd1	UTSW	7	105,370,480 (GRCm39)	critical splice donor site	probably null
R1501:Dnhd1	UTSW	7	105,317,670 (GRCm39)	missense	probably benign	0.00
R1503:Dnhd1	UTSW	7	105,342,867 (GRCm39)	missense	possibly damaging	0.67
R1515:Dnhd1	UTSW	7	105,353,355 (GRCm39)	missense	probably benign	0.11
R1615:Dnhd1	UTSW	7	105,362,913 (GRCm39)	missense	possibly damaging	0.74
R1615:Dnhd1	UTSW	7	105,352,413 (GRCm39)	missense	probably benign	0.00
R1656:Dnhd1	UTSW	7	105,363,488 (GRCm39)	missense	probably damaging	1.00
R1720:Dnhd1	UTSW	7	105,343,035 (GRCm39)	missense	probably benign
R1723:Dnhd1	UTSW	7	105,364,127 (GRCm39)	missense	possibly damaging	0.60
R1766:Dnhd1	UTSW	7	105,343,179 (GRCm39)	missense	possibly damaging	0.50
R1799:Dnhd1	UTSW	7	105,304,974 (GRCm39)	missense	probably benign	0.31
R1860:Dnhd1	UTSW	7	105,353,412 (GRCm39)	missense	probably benign
R1920:Dnhd1	UTSW	7	105,362,614 (GRCm39)	missense	probably benign	0.00
R1925:Dnhd1	UTSW	7	105,323,061 (GRCm39)	missense	probably damaging	0.96
R1925:Dnhd1	UTSW	7	105,301,459 (GRCm39)	missense	probably damaging	1.00
R1934:Dnhd1	UTSW	7	105,357,789 (GRCm39)	missense	probably benign	0.05
R1935:Dnhd1	UTSW	7	105,323,183 (GRCm39)	missense	probably benign	0.09
R1936:Dnhd1	UTSW	7	105,323,183 (GRCm39)	missense	probably benign	0.09
R2035:Dnhd1	UTSW	7	105,354,128 (GRCm39)	missense	probably damaging	0.99
R2125:Dnhd1	UTSW	7	105,327,178 (GRCm39)	missense	probably benign	0.35
R2127:Dnhd1	UTSW	7	105,342,928 (GRCm39)	missense	possibly damaging	0.56
R2254:Dnhd1	UTSW	7	105,352,979 (GRCm39)	missense	probably damaging	1.00
R2301:Dnhd1	UTSW	7	105,354,606 (GRCm39)	missense	probably damaging	1.00
R2316:Dnhd1	UTSW	7	105,323,628 (GRCm39)	missense	probably damaging	1.00
R2324:Dnhd1	UTSW	7	105,359,297 (GRCm39)	missense	probably damaging	1.00
R2337:Dnhd1	UTSW	7	105,352,674 (GRCm39)	missense	probably benign	0.07
R2381:Dnhd1	UTSW	7	105,342,871 (GRCm39)	missense	probably benign	0.42
R2394:Dnhd1	UTSW	7	105,369,438 (GRCm39)	missense	probably benign	0.19
R2862:Dnhd1	UTSW	7	105,361,766 (GRCm39)	missense	probably benign	0.01
R3038:Dnhd1	UTSW	7	105,369,436 (GRCm39)	missense	probably damaging	0.99
R3114:Dnhd1	UTSW	7	105,345,772 (GRCm39)	critical splice donor site	probably null
R3404:Dnhd1	UTSW	7	105,343,968 (GRCm39)	nonsense	probably null
R3405:Dnhd1	UTSW	7	105,343,968 (GRCm39)	nonsense	probably null
R3439:Dnhd1	UTSW	7	105,343,992 (GRCm39)	missense	probably damaging	1.00
R3959:Dnhd1	UTSW	7	105,362,329 (GRCm39)	missense	probably benign	0.21
R4014:Dnhd1	UTSW	7	105,364,045 (GRCm39)	missense	probably damaging	0.99
R4084:Dnhd1	UTSW	7	105,358,795 (GRCm39)	missense	probably damaging	1.00
R4181:Dnhd1	UTSW	7	105,343,161 (GRCm39)	missense	probably damaging	1.00
R4255:Dnhd1	UTSW	7	105,362,205 (GRCm39)	missense	probably damaging	1.00
R4302:Dnhd1	UTSW	7	105,343,161 (GRCm39)	missense	probably damaging	1.00
R4440:Dnhd1	UTSW	7	105,345,935 (GRCm39)	nonsense	probably null
R4565:Dnhd1	UTSW	7	105,301,163 (GRCm39)	missense	possibly damaging	0.92
R4569:Dnhd1	UTSW	7	105,306,373 (GRCm39)	splice site	probably null
R4584:Dnhd1	UTSW	7	105,327,256 (GRCm39)	missense	probably damaging	1.00
R4586:Dnhd1	UTSW	7	105,327,256 (GRCm39)	missense	probably damaging	1.00
R4590:Dnhd1	UTSW	7	105,363,237 (GRCm39)	missense	probably damaging	1.00
R4593:Dnhd1	UTSW	7	105,364,653 (GRCm39)	missense	probably benign	0.02
R4600:Dnhd1	UTSW	7	105,352,851 (GRCm39)	missense	probably damaging	1.00
R4705:Dnhd1	UTSW	7	105,304,948 (GRCm39)	missense	probably damaging	1.00
R4731:Dnhd1	UTSW	7	105,323,056 (GRCm39)	missense	probably benign	0.00
R4732:Dnhd1	UTSW	7	105,323,056 (GRCm39)	missense	probably benign	0.00
R4733:Dnhd1	UTSW	7	105,323,056 (GRCm39)	missense	probably benign	0.00
R4786:Dnhd1	UTSW	7	105,323,651 (GRCm39)	missense	probably benign	0.00
R4791:Dnhd1	UTSW	7	105,370,324 (GRCm39)	missense	probably damaging	1.00
R4811:Dnhd1	UTSW	7	105,363,488 (GRCm39)	missense	probably damaging	0.99
R4822:Dnhd1	UTSW	7	105,353,171 (GRCm39)	missense	probably benign	0.00
R4886:Dnhd1	UTSW	7	105,364,015 (GRCm39)	missense	probably benign	0.00
R4890:Dnhd1	UTSW	7	105,306,164 (GRCm39)	missense	possibly damaging	0.47
R4973:Dnhd1	UTSW	7	105,362,840 (GRCm39)	missense	probably benign	0.24
R5007:Dnhd1	UTSW	7	105,362,283 (GRCm39)	missense	probably damaging	1.00
R5048:Dnhd1	UTSW	7	105,342,904 (GRCm39)	missense	probably benign	0.01
R5151:Dnhd1	UTSW	7	105,362,647 (GRCm39)	missense	probably benign	0.22
R5179:Dnhd1	UTSW	7	105,363,759 (GRCm39)	missense	probably damaging	1.00
R5182:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5183:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5185:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5209:Dnhd1	UTSW	7	105,345,667 (GRCm39)	missense	probably benign	0.00
R5225:Dnhd1	UTSW	7	105,353,130 (GRCm39)	missense	possibly damaging	0.73
R5250:Dnhd1	UTSW	7	105,334,968 (GRCm39)	missense	probably damaging	1.00
R5257:Dnhd1	UTSW	7	105,323,244 (GRCm39)	missense	probably benign
R5258:Dnhd1	UTSW	7	105,323,244 (GRCm39)	missense	probably benign
R5273:Dnhd1	UTSW	7	105,363,689 (GRCm39)	missense	probably damaging	0.99
R5288:Dnhd1	UTSW	7	105,363,644 (GRCm39)	missense	possibly damaging	0.94
R5396:Dnhd1	UTSW	7	105,362,891 (GRCm39)	missense	probably benign	0.00
R5453:Dnhd1	UTSW	7	105,359,330 (GRCm39)	missense	probably damaging	1.00
R5511:Dnhd1	UTSW	7	105,363,363 (GRCm39)	missense	probably damaging	1.00
R5518:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5523:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5528:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5529:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5561:Dnhd1	UTSW	7	105,364,028 (GRCm39)	missense	probably damaging	0.99
R5681:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5683:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5684:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5686:Dnhd1	UTSW	7	105,352,416 (GRCm39)	missense	probably damaging	1.00
R5697:Dnhd1	UTSW	7	105,323,395 (GRCm39)	missense	probably damaging	1.00
R5789:Dnhd1	UTSW	7	105,354,217 (GRCm39)	missense	possibly damaging	0.50
R5790:Dnhd1	UTSW	7	105,304,981 (GRCm39)	missense	probably damaging	1.00
R5814:Dnhd1	UTSW	7	105,369,102 (GRCm39)	missense	possibly damaging	0.69
R5828:Dnhd1	UTSW	7	105,369,388 (GRCm39)	missense	probably benign	0.00
R5852:Dnhd1	UTSW	7	105,344,955 (GRCm39)	missense	probably damaging	1.00
R5883:Dnhd1	UTSW	7	105,369,711 (GRCm39)	missense	probably damaging	0.98
R6115:Dnhd1	UTSW	7	105,363,194 (GRCm39)	missense	probably benign	0.00
R6119:Dnhd1	UTSW	7	105,358,647 (GRCm39)	missense	probably benign	0.18
R6212:Dnhd1	UTSW	7	105,353,255 (GRCm39)	missense	probably damaging	1.00
R6243:Dnhd1	UTSW	7	105,301,216 (GRCm39)	missense	probably damaging	1.00
R6265:Dnhd1	UTSW	7	105,342,577 (GRCm39)	missense	probably benign	0.07
R6332:Dnhd1	UTSW	7	105,343,273 (GRCm39)	missense	probably benign	0.02
R6344:Dnhd1	UTSW	7	105,343,817 (GRCm39)	missense	probably benign	0.38
R6477:Dnhd1	UTSW	7	105,327,093 (GRCm39)	missense	probably benign	0.05
R6642:Dnhd1	UTSW	7	105,353,006 (GRCm39)	missense	probably benign
R6663:Dnhd1	UTSW	7	105,334,899 (GRCm39)	splice site	probably null
R6730:Dnhd1	UTSW	7	105,353,082 (GRCm39)	missense	probably benign	0.00
R6748:Dnhd1	UTSW	7	105,369,844 (GRCm39)	missense	probably benign	0.03
R6833:Dnhd1	UTSW	7	105,352,580 (GRCm39)	missense	probably benign	0.01
R6850:Dnhd1	UTSW	7	105,369,137 (GRCm39)	missense	possibly damaging	0.68
R6853:Dnhd1	UTSW	7	105,352,935 (GRCm39)	missense	probably benign
R6860:Dnhd1	UTSW	7	105,327,473 (GRCm39)	missense	probably benign
R6898:Dnhd1	UTSW	7	105,336,584 (GRCm39)	missense	probably damaging	0.99
R6927:Dnhd1	UTSW	7	105,364,770 (GRCm39)	missense	probably damaging	1.00
R6952:Dnhd1	UTSW	7	105,362,895 (GRCm39)	missense	probably damaging	1.00
R6987:Dnhd1	UTSW	7	105,353,792 (GRCm39)	missense	probably damaging	0.98
R6988:Dnhd1	UTSW	7	105,363,417 (GRCm39)	missense	probably damaging	1.00
R7022:Dnhd1	UTSW	7	105,370,005 (GRCm39)	missense	probably benign	0.36
R7053:Dnhd1	UTSW	7	105,344,161 (GRCm39)	missense	probably damaging	1.00
R7085:Dnhd1	UTSW	7	105,364,468 (GRCm39)	missense	probably benign	0.26
R7086:Dnhd1	UTSW	7	105,357,739 (GRCm39)	missense	probably benign	0.03
R7112:Dnhd1	UTSW	7	105,363,192 (GRCm39)	missense	probably damaging	1.00
R7140:Dnhd1	UTSW	7	105,342,973 (GRCm39)	missense	probably benign	0.00
R7151:Dnhd1	UTSW	7	105,359,234 (GRCm39)	missense	probably benign	0.03
R7178:Dnhd1	UTSW	7	105,344,200 (GRCm39)	missense	probably damaging	0.98
R7326:Dnhd1	UTSW	7	105,370,137 (GRCm39)	missense	probably damaging	0.96
R7345:Dnhd1	UTSW	7	105,353,174 (GRCm39)	missense	probably benign	0.17
R7349:Dnhd1	UTSW	7	105,359,330 (GRCm39)	missense	probably damaging	1.00
R7397:Dnhd1	UTSW	7	105,354,504 (GRCm39)	missense	possibly damaging	0.87
R7520:Dnhd1	UTSW	7	105,345,255 (GRCm39)	missense	probably benign	0.07
R7536:Dnhd1	UTSW	7	105,358,768 (GRCm39)	missense	probably damaging	1.00
R7539:Dnhd1	UTSW	7	105,370,119 (GRCm39)	missense	probably damaging	1.00
R7541:Dnhd1	UTSW	7	105,327,516 (GRCm39)	missense	probably damaging	1.00
R7619:Dnhd1	UTSW	7	105,323,475 (GRCm39)	missense	probably benign	0.01
R7676:Dnhd1	UTSW	7	105,333,294 (GRCm39)	missense	probably benign	0.09
R7689:Dnhd1	UTSW	7	105,363,170 (GRCm39)	missense	probably benign	0.07
R7712:Dnhd1	UTSW	7	105,300,831 (GRCm39)	missense	probably benign	0.17
R7729:Dnhd1	UTSW	7	105,354,472 (GRCm39)	missense	probably damaging	1.00
R7767:Dnhd1	UTSW	7	105,343,817 (GRCm39)	missense	probably benign	0.38
R7768:Dnhd1	UTSW	7	105,370,302 (GRCm39)	missense	possibly damaging	0.87
R7779:Dnhd1	UTSW	7	105,327,122 (GRCm39)	missense	probably benign	0.01
R7879:Dnhd1	UTSW	7	105,352,646 (GRCm39)	missense	probably benign	0.09
R7922:Dnhd1	UTSW	7	105,317,721 (GRCm39)	missense	probably damaging	1.00
R7951:Dnhd1	UTSW	7	105,327,211 (GRCm39)	missense	probably damaging	1.00
R8259:Dnhd1	UTSW	7	105,343,995 (GRCm39)	missense	probably benign	0.38
R8350:Dnhd1	UTSW	7	105,327,231 (GRCm39)	missense	probably damaging	0.99
R8380:Dnhd1	UTSW	7	105,327,073 (GRCm39)	missense	probably benign	0.31
R8392:Dnhd1	UTSW	7	105,352,550 (GRCm39)	missense	possibly damaging	0.84
R8478:Dnhd1	UTSW	7	105,332,001 (GRCm39)	missense	probably benign	0.00
R8708:Dnhd1	UTSW	7	105,343,487 (GRCm39)	nonsense	probably null
R8767:Dnhd1	UTSW	7	105,301,330 (GRCm39)	missense	probably damaging	1.00
R8825:Dnhd1	UTSW	7	105,343,174 (GRCm39)	missense	possibly damaging	0.95
R8849:Dnhd1	UTSW	7	105,370,723 (GRCm39)	missense	probably benign	0.00
R8903:Dnhd1	UTSW	7	105,362,855 (GRCm39)	nonsense	probably null
R8910:Dnhd1	UTSW	7	105,332,904 (GRCm39)	missense	possibly damaging	0.92
R8940:Dnhd1	UTSW	7	105,363,854 (GRCm39)	intron	probably benign
R8954:Dnhd1	UTSW	7	105,343,986 (GRCm39)	missense	probably benign	0.35
R8956:Dnhd1	UTSW	7	105,341,852 (GRCm39)	missense	probably damaging	0.99
R8971:Dnhd1	UTSW	7	105,358,528 (GRCm39)	nonsense	probably null
R8996:Dnhd1	UTSW	7	105,323,242 (GRCm39)	missense	probably damaging	1.00
R9051:Dnhd1	UTSW	7	105,341,933 (GRCm39)	missense	possibly damaging	0.54
R9058:Dnhd1	UTSW	7	105,333,270 (GRCm39)	missense	probably benign	0.01
R9109:Dnhd1	UTSW	7	105,333,173 (GRCm39)	missense	probably damaging	0.98
R9284:Dnhd1	UTSW	7	105,301,091 (GRCm39)	missense	probably damaging	1.00
R9295:Dnhd1	UTSW	7	105,363,348 (GRCm39)	missense	probably benign
R9298:Dnhd1	UTSW	7	105,333,173 (GRCm39)	missense	probably damaging	0.98
R9299:Dnhd1	UTSW	7	105,369,806 (GRCm39)	missense	probably benign	0.00
R9308:Dnhd1	UTSW	7	105,353,484 (GRCm39)	missense	probably damaging	1.00
R9337:Dnhd1	UTSW	7	105,369,806 (GRCm39)	missense	probably benign	0.00
R9385:Dnhd1	UTSW	7	105,361,972 (GRCm39)	missense	probably damaging	1.00
R9463:Dnhd1	UTSW	7	105,344,223 (GRCm39)	missense	probably benign
R9463:Dnhd1	UTSW	7	105,306,454 (GRCm39)	missense	probably benign	0.00
R9476:Dnhd1	UTSW	7	105,352,889 (GRCm39)	missense	possibly damaging	0.74
R9489:Dnhd1	UTSW	7	105,300,804 (GRCm39)	missense	probably benign
R9500:Dnhd1	UTSW	7	105,353,709 (GRCm39)	missense	probably benign
R9510:Dnhd1	UTSW	7	105,352,889 (GRCm39)	missense	possibly damaging	0.74
R9513:Dnhd1	UTSW	7	105,354,179 (GRCm39)	missense	probably damaging	1.00
R9537:Dnhd1	UTSW	7	105,344,740 (GRCm39)	missense	probably damaging	0.99
R9567:Dnhd1	UTSW	7	105,353,473 (GRCm39)	missense	probably benign	0.03
R9622:Dnhd1	UTSW	7	105,353,342 (GRCm39)	missense	probably benign
R9623:Dnhd1	UTSW	7	105,344,134 (GRCm39)	missense	probably damaging	1.00
R9623:Dnhd1	UTSW	7	105,335,773 (GRCm39)	missense	probably damaging	1.00
R9674:Dnhd1	UTSW	7	105,363,429 (GRCm39)	missense	probably damaging	1.00
R9756:Dnhd1	UTSW	7	105,353,135 (GRCm39)	missense	probably benign	0.19
R9777:Dnhd1	UTSW	7	105,369,456 (GRCm39)	missense	probably benign	0.14
R9778:Dnhd1	UTSW	7	105,353,240 (GRCm39)	missense	probably benign
R9781:Dnhd1	UTSW	7	105,352,917 (GRCm39)	missense	probably benign	0.31
R9796:Dnhd1	UTSW	7	105,342,537 (GRCm39)	missense	probably damaging	1.00
Z1088:Dnhd1	UTSW	7	105,361,934 (GRCm39)	missense	probably benign	0.00
Z1176:Dnhd1	UTSW	7	105,352,243 (GRCm39)	critical splice acceptor site	probably null
Z1176:Dnhd1	UTSW	7	105,327,506 (GRCm39)	missense	probably benign
Z1176:Dnhd1	UTSW	7	105,317,754 (GRCm39)	missense	probably damaging	0.98
Z1176:Dnhd1	UTSW	7	105,352,787 (GRCm39)	frame shift	probably null
Z1177:Dnhd1	UTSW	7	105,332,048 (GRCm39)	missense	possibly damaging	0.90

Predicted Primers

PCR Primer
(F):5'- GATCCAGAGAAGAACTGCCAGC -3'
(R):5'- GCTGCAGGCTTCCCAAAATG -3'

Sequencing Primer
(F):5'- CAGTCAACTTCCTTGCCA -3'
(R):5'- TGAAGGCATGAAACACTTGCAC -3'

Posted On

2016-11-09