Incidental Mutation 'R4732:Dync1h1'
ID |
470521 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dync1h1
|
Ensembl Gene |
ENSMUSG00000018707 |
Gene Name |
dynein cytoplasmic 1 heavy chain 1 |
Synonyms |
MAP1C, Loa, Dnec1, Dnchc1, dynein heavy chain, retrograde transport, 9930018I23Rik, Swl |
MMRRC Submission |
042022-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4732 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
12 |
Chromosomal Location |
110567886-110633379 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
C to T
at 110615941 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Stop codon
at position 3030
(Q3030*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000018851
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000018851]
|
AlphaFold |
no structure available at present |
PDB Structure |
Microtubule binding domain from mouse cytoplasmic dynein as a fusion with seryl-tRNA synthetase [X-RAY DIFFRACTION]
High affinity dynein microtubule binding domain - tubulin complex [ELECTRON MICROSCOPY]
Low affinity dynein microtubule binding domain - tubulin complex [ELECTRON MICROSCOPY]
Structure of the entire stalk region of the dynein motor domain [X-RAY DIFFRACTION]
|
Predicted Effect |
probably null
Transcript: ENSMUST00000018851
AA Change: Q3030*
|
SMART Domains |
Protein: ENSMUSP00000018851 Gene: ENSMUSG00000018707 AA Change: Q3030*
Domain | Start | End | E-Value | Type |
low complexity region
|
46 |
61 |
N/A |
INTRINSIC |
low complexity region
|
83 |
95 |
N/A |
INTRINSIC |
Pfam:DHC_N1
|
237 |
830 |
1.9e-145 |
PFAM |
coiled coil region
|
1171 |
1198 |
N/A |
INTRINSIC |
Pfam:DHC_N2
|
1317 |
1721 |
3.3e-116 |
PFAM |
AAA
|
1899 |
2043 |
5.39e-2 |
SMART |
low complexity region
|
2102 |
2116 |
N/A |
INTRINSIC |
AAA
|
2214 |
2365 |
2.13e0 |
SMART |
low complexity region
|
2394 |
2405 |
N/A |
INTRINSIC |
AAA
|
2585 |
2735 |
8.6e-7 |
SMART |
Blast:AAA
|
2777 |
2811 |
2e-13 |
BLAST |
AAA
|
2927 |
3093 |
4.79e-5 |
SMART |
Pfam:MT
|
3197 |
3534 |
1.1e-44 |
PFAM |
Pfam:AAA_9
|
3554 |
3778 |
8.5e-75 |
PFAM |
Pfam:Dynein_heavy
|
3919 |
4642 |
4.3e-163 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000167395
|
SMART Domains |
Protein: ENSMUSP00000126117 Gene: ENSMUSG00000018707
Domain | Start | End | E-Value | Type |
Pfam:MT
|
1 |
178 |
5.3e-18 |
PFAM |
Pfam:AAA_9
|
154 |
252 |
3.6e-24 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.2%
- 20x: 95.1%
|
Validation Efficiency |
99% (110/111) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Dyneins are a group of microtubule-activated ATPases that function as molecular motors. They are divided into two subgroups of axonemal and cytoplasmic dyneins. The cytoplasmic dyneins function in intracellular motility, including retrograde axonal transport, protein sorting, organelle movement, and spindle dynamics. Molecules of conventional cytoplasmic dynein are comprised of 2 heavy chain polypeptides and a number of intermediate and light chains.This gene encodes a member of the cytoplasmic dynein heavy chain family. [provided by RefSeq, Oct 2008] PHENOTYPE: Mice homozygous for either the Cra1 or Loa ENU mutation exhibit neonatal lethality with reduced anterior horn cell number, abnormal motor neuron innervation, neuronal inclusions, and abnormal axonal transport. Heterozygotes display motor neuron degeneration and muscle spasms. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 192 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
T |
A |
9: 8,222,174 (GRCm39) |
|
noncoding transcript |
Het |
4933409G03Rik |
A |
G |
2: 68,445,065 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
C |
7: 78,748,357 (GRCm39) |
S1043P |
probably damaging |
Het |
Ackr2 |
A |
G |
9: 121,738,249 (GRCm39) |
Y208C |
probably damaging |
Het |
Actg1 |
C |
T |
11: 120,238,305 (GRCm39) |
|
probably benign |
Het |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adam1a |
T |
A |
5: 121,657,497 (GRCm39) |
T599S |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Adgrf2 |
A |
C |
17: 43,021,645 (GRCm39) |
I393S |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,984,665 (GRCm39) |
G1983V |
probably damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Ak8 |
A |
G |
2: 28,650,083 (GRCm39) |
Y370C |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,063,901 (GRCm39) |
D1750G |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,718,204 (GRCm39) |
V315E |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Ap3b2 |
C |
T |
7: 81,121,680 (GRCm39) |
A519T |
probably damaging |
Het |
Apool |
C |
T |
X: 111,281,897 (GRCm39) |
T166I |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,539,247 (GRCm39) |
K65* |
probably null |
Het |
Arhgef38 |
G |
T |
3: 132,838,030 (GRCm39) |
Y633* |
probably null |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,059,750 (GRCm39) |
D430G |
possibly damaging |
Het |
Atp8a1 |
G |
A |
5: 67,970,463 (GRCm39) |
S92L |
probably benign |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
C130073F10Rik |
C |
A |
4: 101,747,907 (GRCm39) |
S89I |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,334,041 (GRCm39) |
T867A |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,435,906 (GRCm39) |
N1276K |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,306,268 (GRCm39) |
D2012V |
probably damaging |
Het |
Cenpt |
A |
G |
8: 106,573,768 (GRCm39) |
V254A |
probably benign |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cers5 |
C |
T |
15: 99,639,518 (GRCm39) |
R123Q |
probably benign |
Het |
Ces2h |
A |
G |
8: 105,741,236 (GRCm39) |
E76G |
probably damaging |
Het |
Cfap77 |
T |
A |
2: 28,874,400 (GRCm39) |
E143D |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,969,745 (GRCm39) |
R65L |
probably damaging |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec2g |
C |
A |
6: 128,958,842 (GRCm39) |
Y142* |
probably null |
Het |
Coch |
A |
T |
12: 51,651,802 (GRCm39) |
E549V |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,464,779 (GRCm39) |
V348A |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,496,197 (GRCm39) |
H1606R |
probably benign |
Het |
Cpd |
T |
C |
11: 76,702,620 (GRCm39) |
N583D |
probably damaging |
Het |
Cyp2d11 |
T |
A |
15: 82,273,428 (GRCm39) |
Y481F |
probably benign |
Het |
D130043K22Rik |
T |
C |
13: 25,083,648 (GRCm39) |
S1038P |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,503,741 (GRCm39) |
T1653I |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnajc11 |
A |
G |
4: 152,055,424 (GRCm39) |
|
probably benign |
Het |
Dnajc13 |
CT |
C |
9: 104,064,004 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,352,222 (GRCm39) |
|
probably null |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Eif2d |
T |
C |
1: 131,092,464 (GRCm39) |
V374A |
probably damaging |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
F5 |
C |
T |
1: 164,009,226 (GRCm39) |
T332M |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,169,439 (GRCm39) |
T156A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,641,671 (GRCm39) |
|
probably null |
Het |
Fnip2 |
A |
T |
3: 79,388,959 (GRCm39) |
S561T |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,909,998 (GRCm39) |
T455S |
probably benign |
Het |
Fry |
G |
A |
5: 150,309,472 (GRCm39) |
E639K |
|
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galnt2l |
A |
G |
8: 122,997,013 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,032 (GRCm39) |
D844E |
probably benign |
Het |
Gle1 |
T |
C |
2: 29,830,244 (GRCm39) |
S267P |
probably damaging |
Het |
Glg1 |
G |
A |
8: 111,914,387 (GRCm39) |
R466W |
probably damaging |
Het |
Gm10277 |
T |
C |
11: 77,676,923 (GRCm39) |
|
probably benign |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gm9970 |
A |
G |
5: 31,398,410 (GRCm39) |
|
probably benign |
Het |
Gpr35 |
T |
G |
1: 92,911,107 (GRCm39) |
I57S |
probably damaging |
Het |
Gprin1 |
C |
T |
13: 54,887,770 (GRCm39) |
G168E |
possibly damaging |
Het |
Gtdc1 |
A |
G |
2: 44,679,067 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
G |
T |
5: 31,317,401 (GRCm39) |
P586T |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Gucy2c |
A |
G |
6: 136,744,150 (GRCm39) |
S150P |
probably damaging |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,721 (GRCm39) |
I245M |
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Il2ra |
T |
A |
2: 11,681,731 (GRCm39) |
M112K |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Kcnn2 |
T |
A |
18: 45,693,416 (GRCm39) |
S331T |
possibly damaging |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Klra3 |
T |
A |
6: 130,304,095 (GRCm39) |
Y199F |
possibly damaging |
Het |
Lhx2 |
A |
G |
2: 38,250,003 (GRCm39) |
K274R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,363,899 (GRCm39) |
I313V |
probably benign |
Het |
Lrrfip1 |
A |
T |
1: 91,043,369 (GRCm39) |
E591D |
probably benign |
Het |
Lrrk2 |
G |
A |
15: 91,649,950 (GRCm39) |
E1696K |
probably damaging |
Het |
Lrrk2 |
A |
C |
15: 91,573,052 (GRCm39) |
E200A |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,909,080 (GRCm39) |
M465K |
probably damaging |
Het |
Moxd2 |
T |
G |
6: 40,855,793 (GRCm39) |
I599L |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,048,831 (GRCm39) |
S866P |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,231,772 (GRCm39) |
T79A |
possibly damaging |
Het |
Ncoa6 |
C |
A |
2: 155,263,221 (GRCm39) |
Q404H |
probably damaging |
Het |
Neb |
A |
G |
2: 52,169,091 (GRCm39) |
Y1815H |
probably damaging |
Het |
Nell1 |
A |
G |
7: 50,505,965 (GRCm39) |
D724G |
probably damaging |
Het |
Nkx3-2 |
A |
G |
5: 41,919,487 (GRCm39) |
V167A |
probably benign |
Het |
Nsun3 |
C |
A |
16: 62,555,482 (GRCm39) |
C348F |
possibly damaging |
Het |
Obox6 |
A |
T |
7: 15,568,697 (GRCm39) |
S60T |
possibly damaging |
Het |
Oog2 |
T |
A |
4: 143,920,511 (GRCm39) |
|
probably benign |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or1e16 |
T |
C |
11: 73,286,521 (GRCm39) |
D109G |
probably benign |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or9s18 |
T |
C |
13: 65,300,467 (GRCm39) |
V143A |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pank4 |
A |
T |
4: 155,055,847 (GRCm39) |
M291L |
probably benign |
Het |
Pcf11 |
T |
C |
7: 92,308,041 (GRCm39) |
D709G |
probably benign |
Het |
Pcgf1 |
T |
A |
6: 83,056,938 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
A |
G |
12: 82,042,525 (GRCm39) |
I2256V |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Piezo2 |
C |
T |
18: 63,163,472 (GRCm39) |
A2149T |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,881,711 (GRCm39) |
E781G |
probably benign |
Het |
Pik3r4 |
G |
A |
9: 105,555,375 (GRCm39) |
V1111I |
possibly damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,722,581 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Pnkp |
T |
A |
7: 44,509,878 (GRCm39) |
|
probably benign |
Het |
Polr3c |
A |
T |
3: 96,630,977 (GRCm39) |
F148I |
probably damaging |
Het |
Ppard |
A |
T |
17: 28,505,417 (GRCm39) |
T35S |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Qki |
T |
C |
17: 10,435,217 (GRCm39) |
H269R |
probably damaging |
Het |
Qrsl1 |
T |
C |
10: 43,752,659 (GRCm39) |
Y388C |
probably damaging |
Het |
Rapgef1 |
T |
G |
2: 29,579,172 (GRCm39) |
I182S |
probably damaging |
Het |
Ret |
T |
C |
6: 118,140,154 (GRCm39) |
S1013G |
possibly damaging |
Het |
Rimbp3 |
A |
G |
16: 17,028,465 (GRCm39) |
R630G |
possibly damaging |
Het |
Rnmt |
A |
T |
18: 68,451,031 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Sec31b |
A |
T |
19: 44,521,116 (GRCm39) |
S110T |
probably damaging |
Het |
Serpina3k |
G |
A |
12: 104,307,119 (GRCm39) |
G117D |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,221,902 (GRCm39) |
Y410C |
probably damaging |
Het |
Slc24a1 |
G |
A |
9: 64,856,836 (GRCm39) |
R24C |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slco1a7 |
A |
T |
6: 141,668,905 (GRCm39) |
M509K |
probably benign |
Het |
Slco4a1 |
A |
G |
2: 180,115,408 (GRCm39) |
N662D |
probably damaging |
Het |
Slfn4 |
T |
A |
11: 83,080,108 (GRCm39) |
|
probably benign |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Smim29 |
A |
G |
17: 27,784,244 (GRCm39) |
|
probably benign |
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Spib |
A |
G |
7: 44,178,309 (GRCm39) |
S154P |
probably damaging |
Het |
Spty2d1 |
T |
C |
7: 46,645,858 (GRCm39) |
D595G |
probably damaging |
Het |
St7 |
T |
A |
6: 17,906,515 (GRCm39) |
|
probably null |
Het |
Susd1 |
T |
C |
4: 59,428,029 (GRCm39) |
T52A |
possibly damaging |
Het |
Svs5 |
T |
A |
2: 164,079,043 (GRCm39) |
D288V |
possibly damaging |
Het |
Syt7 |
T |
A |
19: 10,420,288 (GRCm39) |
I355N |
probably damaging |
Het |
Tarm1 |
G |
A |
7: 3,545,416 (GRCm39) |
Q145* |
probably null |
Het |
Teddm2 |
T |
A |
1: 153,726,487 (GRCm39) |
E76V |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,540,923 (GRCm39) |
S343P |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,103,317 (GRCm39) |
|
probably null |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Triobp |
G |
A |
15: 78,851,313 (GRCm39) |
R489K |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,753,380 (GRCm39) |
V1883I |
probably damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,730,171 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Tyrp1 |
A |
T |
4: 80,763,172 (GRCm39) |
D353V |
possibly damaging |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Unc13d |
A |
G |
11: 115,964,408 (GRCm39) |
V312A |
possibly damaging |
Het |
Urb2 |
G |
T |
8: 124,755,636 (GRCm39) |
A448S |
probably damaging |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,803 (GRCm39) |
R250S |
probably benign |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,450,195 (GRCm39) |
T147I |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Vxn |
T |
C |
1: 9,677,201 (GRCm39) |
S24P |
probably benign |
Het |
Washc4 |
A |
T |
10: 83,410,343 (GRCm39) |
M644L |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,569,737 (GRCm39) |
V449E |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,279,867 (GRCm39) |
|
probably benign |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp512b |
A |
G |
2: 181,230,532 (GRCm39) |
S453P |
probably benign |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably damaging |
Het |
|
Other mutations in Dync1h1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01291:Dync1h1
|
APN |
12 |
110,615,538 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01299:Dync1h1
|
APN |
12 |
110,580,541 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01321:Dync1h1
|
APN |
12 |
110,592,041 (GRCm39) |
splice site |
probably benign |
|
IGL01324:Dync1h1
|
APN |
12 |
110,593,299 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01327:Dync1h1
|
APN |
12 |
110,583,126 (GRCm39) |
splice site |
probably benign |
|
IGL01371:Dync1h1
|
APN |
12 |
110,605,285 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01598:Dync1h1
|
APN |
12 |
110,624,562 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01782:Dync1h1
|
APN |
12 |
110,581,374 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01791:Dync1h1
|
APN |
12 |
110,625,364 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01797:Dync1h1
|
APN |
12 |
110,618,630 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02040:Dync1h1
|
APN |
12 |
110,603,558 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02096:Dync1h1
|
APN |
12 |
110,599,254 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02164:Dync1h1
|
APN |
12 |
110,628,993 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02216:Dync1h1
|
APN |
12 |
110,629,436 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02298:Dync1h1
|
APN |
12 |
110,607,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02422:Dync1h1
|
APN |
12 |
110,606,644 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02610:Dync1h1
|
APN |
12 |
110,625,666 (GRCm39) |
nonsense |
probably null |
|
IGL02643:Dync1h1
|
APN |
12 |
110,625,706 (GRCm39) |
unclassified |
probably benign |
|
IGL03076:Dync1h1
|
APN |
12 |
110,624,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03292:Dync1h1
|
APN |
12 |
110,632,989 (GRCm39) |
splice site |
probably null |
|
IGL03293:Dync1h1
|
APN |
12 |
110,595,168 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03299:Dync1h1
|
APN |
12 |
110,585,644 (GRCm39) |
missense |
possibly damaging |
0.49 |
chinashop
|
UTSW |
12 |
110,624,568 (GRCm39) |
missense |
probably damaging |
1.00 |
Gesund
|
UTSW |
12 |
110,582,838 (GRCm39) |
missense |
probably benign |
0.35 |
gymnast
|
UTSW |
12 |
110,584,802 (GRCm39) |
missense |
probably damaging |
1.00 |
Lightfoot
|
UTSW |
12 |
110,584,354 (GRCm39) |
missense |
probably damaging |
1.00 |
Lissom
|
UTSW |
12 |
110,599,254 (GRCm39) |
missense |
possibly damaging |
0.68 |
Strong
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
waters
|
UTSW |
12 |
110,596,113 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU05:Dync1h1
|
UTSW |
12 |
110,615,538 (GRCm39) |
missense |
probably benign |
0.31 |
H8562:Dync1h1
|
UTSW |
12 |
110,583,241 (GRCm39) |
missense |
probably benign |
0.01 |
R0082:Dync1h1
|
UTSW |
12 |
110,602,880 (GRCm39) |
missense |
probably benign |
|
R0110:Dync1h1
|
UTSW |
12 |
110,606,378 (GRCm39) |
missense |
probably benign |
0.42 |
R0130:Dync1h1
|
UTSW |
12 |
110,585,108 (GRCm39) |
missense |
probably benign |
0.16 |
R0233:Dync1h1
|
UTSW |
12 |
110,607,414 (GRCm39) |
missense |
probably benign |
0.45 |
R0233:Dync1h1
|
UTSW |
12 |
110,607,414 (GRCm39) |
missense |
probably benign |
0.45 |
R0242:Dync1h1
|
UTSW |
12 |
110,616,285 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0242:Dync1h1
|
UTSW |
12 |
110,616,285 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0408:Dync1h1
|
UTSW |
12 |
110,598,126 (GRCm39) |
missense |
probably benign |
|
R0450:Dync1h1
|
UTSW |
12 |
110,606,378 (GRCm39) |
missense |
probably benign |
0.42 |
R0611:Dync1h1
|
UTSW |
12 |
110,599,222 (GRCm39) |
missense |
probably damaging |
0.97 |
R0612:Dync1h1
|
UTSW |
12 |
110,582,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Dync1h1
|
UTSW |
12 |
110,618,181 (GRCm39) |
unclassified |
probably benign |
|
R0685:Dync1h1
|
UTSW |
12 |
110,623,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:Dync1h1
|
UTSW |
12 |
110,595,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R0747:Dync1h1
|
UTSW |
12 |
110,578,845 (GRCm39) |
missense |
probably benign |
|
R0843:Dync1h1
|
UTSW |
12 |
110,631,647 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0970:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1161:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1211:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1214:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1215:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1227:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1230:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1232:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1237:Dync1h1
|
UTSW |
12 |
110,632,393 (GRCm39) |
missense |
probably benign |
0.00 |
R1274:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1275:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1289:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1290:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1331:Dync1h1
|
UTSW |
12 |
110,615,698 (GRCm39) |
missense |
probably damaging |
0.98 |
R1340:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1383:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1394:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1396:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1397:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1413:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1432:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1500:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1661:Dync1h1
|
UTSW |
12 |
110,622,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Dync1h1
|
UTSW |
12 |
110,632,096 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1698:Dync1h1
|
UTSW |
12 |
110,593,426 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1767:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1776:Dync1h1
|
UTSW |
12 |
110,599,362 (GRCm39) |
splice site |
probably benign |
|
R1812:Dync1h1
|
UTSW |
12 |
110,629,334 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1831:Dync1h1
|
UTSW |
12 |
110,580,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Dync1h1
|
UTSW |
12 |
110,580,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1857:Dync1h1
|
UTSW |
12 |
110,629,059 (GRCm39) |
missense |
probably damaging |
0.96 |
R1879:Dync1h1
|
UTSW |
12 |
110,591,070 (GRCm39) |
missense |
probably benign |
0.04 |
R1892:Dync1h1
|
UTSW |
12 |
110,612,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Dync1h1
|
UTSW |
12 |
110,629,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Dync1h1
|
UTSW |
12 |
110,602,943 (GRCm39) |
missense |
probably benign |
0.04 |
R1974:Dync1h1
|
UTSW |
12 |
110,592,166 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1999:Dync1h1
|
UTSW |
12 |
110,632,857 (GRCm39) |
critical splice donor site |
probably null |
|
R2073:Dync1h1
|
UTSW |
12 |
110,581,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Dync1h1
|
UTSW |
12 |
110,616,022 (GRCm39) |
missense |
probably benign |
0.07 |
R2113:Dync1h1
|
UTSW |
12 |
110,596,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Dync1h1
|
UTSW |
12 |
110,607,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R2134:Dync1h1
|
UTSW |
12 |
110,623,065 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2496:Dync1h1
|
UTSW |
12 |
110,607,654 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2680:Dync1h1
|
UTSW |
12 |
110,609,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R2890:Dync1h1
|
UTSW |
12 |
110,583,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R2964:Dync1h1
|
UTSW |
12 |
110,607,460 (GRCm39) |
critical splice donor site |
probably null |
|
R3705:Dync1h1
|
UTSW |
12 |
110,607,020 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3708:Dync1h1
|
UTSW |
12 |
110,609,563 (GRCm39) |
missense |
probably damaging |
0.96 |
R3735:Dync1h1
|
UTSW |
12 |
110,598,109 (GRCm39) |
missense |
probably benign |
|
R3736:Dync1h1
|
UTSW |
12 |
110,598,109 (GRCm39) |
missense |
probably benign |
|
R3882:Dync1h1
|
UTSW |
12 |
110,595,492 (GRCm39) |
missense |
probably benign |
0.41 |
R3971:Dync1h1
|
UTSW |
12 |
110,632,399 (GRCm39) |
missense |
probably benign |
0.00 |
R4017:Dync1h1
|
UTSW |
12 |
110,609,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R4032:Dync1h1
|
UTSW |
12 |
110,584,483 (GRCm39) |
nonsense |
probably null |
|
R4355:Dync1h1
|
UTSW |
12 |
110,599,333 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4514:Dync1h1
|
UTSW |
12 |
110,623,573 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4586:Dync1h1
|
UTSW |
12 |
110,615,917 (GRCm39) |
missense |
probably benign |
0.30 |
R4619:Dync1h1
|
UTSW |
12 |
110,605,278 (GRCm39) |
missense |
probably benign |
0.09 |
R4659:Dync1h1
|
UTSW |
12 |
110,595,201 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4676:Dync1h1
|
UTSW |
12 |
110,628,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R4688:Dync1h1
|
UTSW |
12 |
110,621,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R4733:Dync1h1
|
UTSW |
12 |
110,615,941 (GRCm39) |
nonsense |
probably null |
|
R4780:Dync1h1
|
UTSW |
12 |
110,627,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R4846:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4861:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4861:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Dync1h1
|
UTSW |
12 |
110,606,235 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4872:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4874:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4927:Dync1h1
|
UTSW |
12 |
110,629,289 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4949:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4954:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4956:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4958:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Dync1h1
|
UTSW |
12 |
110,624,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5029:Dync1h1
|
UTSW |
12 |
110,584,444 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5032:Dync1h1
|
UTSW |
12 |
110,593,326 (GRCm39) |
nonsense |
probably null |
|
R5036:Dync1h1
|
UTSW |
12 |
110,596,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5037:Dync1h1
|
UTSW |
12 |
110,607,341 (GRCm39) |
missense |
probably benign |
0.09 |
R5105:Dync1h1
|
UTSW |
12 |
110,584,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R5122:Dync1h1
|
UTSW |
12 |
110,596,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Dync1h1
|
UTSW |
12 |
110,595,264 (GRCm39) |
missense |
probably benign |
0.00 |
R5290:Dync1h1
|
UTSW |
12 |
110,581,502 (GRCm39) |
missense |
probably benign |
0.03 |
R5453:Dync1h1
|
UTSW |
12 |
110,599,099 (GRCm39) |
missense |
probably benign |
0.12 |
R5540:Dync1h1
|
UTSW |
12 |
110,627,384 (GRCm39) |
missense |
probably benign |
0.00 |
R5613:Dync1h1
|
UTSW |
12 |
110,599,254 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5626:Dync1h1
|
UTSW |
12 |
110,607,575 (GRCm39) |
missense |
probably benign |
0.01 |
R5652:Dync1h1
|
UTSW |
12 |
110,632,422 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5655:Dync1h1
|
UTSW |
12 |
110,595,496 (GRCm39) |
missense |
probably benign |
0.03 |
R5686:Dync1h1
|
UTSW |
12 |
110,582,838 (GRCm39) |
missense |
probably benign |
0.35 |
R5772:Dync1h1
|
UTSW |
12 |
110,612,707 (GRCm39) |
nonsense |
probably null |
|
R5806:Dync1h1
|
UTSW |
12 |
110,618,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R5891:Dync1h1
|
UTSW |
12 |
110,580,654 (GRCm39) |
critical splice donor site |
probably null |
|
R5921:Dync1h1
|
UTSW |
12 |
110,584,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Dync1h1
|
UTSW |
12 |
110,599,212 (GRCm39) |
missense |
probably benign |
|
R6113:Dync1h1
|
UTSW |
12 |
110,586,848 (GRCm39) |
missense |
probably benign |
|
R6119:Dync1h1
|
UTSW |
12 |
110,594,440 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6154:Dync1h1
|
UTSW |
12 |
110,584,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Dync1h1
|
UTSW |
12 |
110,612,639 (GRCm39) |
missense |
probably damaging |
0.97 |
R6522:Dync1h1
|
UTSW |
12 |
110,583,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R6531:Dync1h1
|
UTSW |
12 |
110,584,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Dync1h1
|
UTSW |
12 |
110,616,282 (GRCm39) |
missense |
probably benign |
0.06 |
R6672:Dync1h1
|
UTSW |
12 |
110,624,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R6746:Dync1h1
|
UTSW |
12 |
110,618,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Dync1h1
|
UTSW |
12 |
110,596,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Dync1h1
|
UTSW |
12 |
110,624,981 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6863:Dync1h1
|
UTSW |
12 |
110,618,614 (GRCm39) |
missense |
probably benign |
0.07 |
R6881:Dync1h1
|
UTSW |
12 |
110,590,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R6892:Dync1h1
|
UTSW |
12 |
110,605,335 (GRCm39) |
missense |
probably benign |
0.00 |
R7015:Dync1h1
|
UTSW |
12 |
110,632,521 (GRCm39) |
nonsense |
probably null |
|
R7096:Dync1h1
|
UTSW |
12 |
110,623,512 (GRCm39) |
missense |
probably damaging |
0.99 |
R7173:Dync1h1
|
UTSW |
12 |
110,568,173 (GRCm39) |
missense |
probably benign |
|
R7224:Dync1h1
|
UTSW |
12 |
110,584,196 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7295:Dync1h1
|
UTSW |
12 |
110,631,183 (GRCm39) |
critical splice donor site |
probably null |
|
R7308:Dync1h1
|
UTSW |
12 |
110,631,596 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7346:Dync1h1
|
UTSW |
12 |
110,602,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:Dync1h1
|
UTSW |
12 |
110,591,036 (GRCm39) |
missense |
probably benign |
0.00 |
R7405:Dync1h1
|
UTSW |
12 |
110,600,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Dync1h1
|
UTSW |
12 |
110,602,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Dync1h1
|
UTSW |
12 |
110,602,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R7472:Dync1h1
|
UTSW |
12 |
110,632,109 (GRCm39) |
missense |
probably damaging |
0.99 |
R7532:Dync1h1
|
UTSW |
12 |
110,618,011 (GRCm39) |
missense |
probably benign |
0.00 |
R7543:Dync1h1
|
UTSW |
12 |
110,580,541 (GRCm39) |
missense |
probably benign |
0.04 |
R7555:Dync1h1
|
UTSW |
12 |
110,597,059 (GRCm39) |
missense |
probably benign |
0.03 |
R7632:Dync1h1
|
UTSW |
12 |
110,627,327 (GRCm39) |
missense |
probably benign |
0.10 |
R7701:Dync1h1
|
UTSW |
12 |
110,585,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R7704:Dync1h1
|
UTSW |
12 |
110,632,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Dync1h1
|
UTSW |
12 |
110,621,893 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7891:Dync1h1
|
UTSW |
12 |
110,609,590 (GRCm39) |
missense |
probably benign |
0.02 |
R7895:Dync1h1
|
UTSW |
12 |
110,582,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:Dync1h1
|
UTSW |
12 |
110,595,168 (GRCm39) |
missense |
probably benign |
0.12 |
R8164:Dync1h1
|
UTSW |
12 |
110,582,794 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8257:Dync1h1
|
UTSW |
12 |
110,602,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Dync1h1
|
UTSW |
12 |
110,632,226 (GRCm39) |
missense |
probably benign |
0.21 |
R8432:Dync1h1
|
UTSW |
12 |
110,584,576 (GRCm39) |
missense |
probably benign |
0.00 |
R8510:Dync1h1
|
UTSW |
12 |
110,583,177 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8731:Dync1h1
|
UTSW |
12 |
110,607,018 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8739:Dync1h1
|
UTSW |
12 |
110,581,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R8756:Dync1h1
|
UTSW |
12 |
110,583,261 (GRCm39) |
missense |
probably benign |
0.06 |
R8855:Dync1h1
|
UTSW |
12 |
110,602,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R8866:Dync1h1
|
UTSW |
12 |
110,602,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Dync1h1
|
UTSW |
12 |
110,583,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8893:Dync1h1
|
UTSW |
12 |
110,608,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Dync1h1
|
UTSW |
12 |
110,624,602 (GRCm39) |
missense |
probably benign |
0.14 |
R8937:Dync1h1
|
UTSW |
12 |
110,584,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R8958:Dync1h1
|
UTSW |
12 |
110,586,805 (GRCm39) |
missense |
probably benign |
0.00 |
R9000:Dync1h1
|
UTSW |
12 |
110,606,397 (GRCm39) |
missense |
probably benign |
|
R9036:Dync1h1
|
UTSW |
12 |
110,606,186 (GRCm39) |
missense |
probably benign |
|
R9090:Dync1h1
|
UTSW |
12 |
110,583,310 (GRCm39) |
missense |
probably benign |
0.06 |
R9108:Dync1h1
|
UTSW |
12 |
110,622,706 (GRCm39) |
intron |
probably benign |
|
R9161:Dync1h1
|
UTSW |
12 |
110,625,023 (GRCm39) |
missense |
probably benign |
0.01 |
R9185:Dync1h1
|
UTSW |
12 |
110,601,937 (GRCm39) |
missense |
probably benign |
0.33 |
R9271:Dync1h1
|
UTSW |
12 |
110,583,310 (GRCm39) |
missense |
probably benign |
0.06 |
R9436:Dync1h1
|
UTSW |
12 |
110,582,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R9478:Dync1h1
|
UTSW |
12 |
110,625,137 (GRCm39) |
missense |
probably benign |
0.02 |
R9547:Dync1h1
|
UTSW |
12 |
110,624,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R9561:Dync1h1
|
UTSW |
12 |
110,615,533 (GRCm39) |
missense |
probably damaging |
0.99 |
R9586:Dync1h1
|
UTSW |
12 |
110,582,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Dync1h1
|
UTSW |
12 |
110,607,362 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Dync1h1
|
UTSW |
12 |
110,596,351 (GRCm39) |
frame shift |
probably null |
|
Z1177:Dync1h1
|
UTSW |
12 |
110,624,951 (GRCm39) |
nonsense |
probably null |
|
Z1177:Dync1h1
|
UTSW |
12 |
110,607,611 (GRCm39) |
frame shift |
probably null |
|
Z1177:Dync1h1
|
UTSW |
12 |
110,603,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
|
Posted On |
2017-03-08 |