Other mutations in this stock |
Total: 126 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,606,496 (GRCm39) |
V246A |
probably benign |
Het |
Abcc10 |
T |
C |
17: 46,615,361 (GRCm39) |
S1343G |
possibly damaging |
Het |
Abcd3 |
C |
A |
3: 121,555,059 (GRCm39) |
|
probably null |
Het |
Actl6a |
T |
A |
3: 32,774,642 (GRCm39) |
M335K |
probably damaging |
Het |
Adamts9 |
A |
C |
6: 92,774,999 (GRCm39) |
C1090W |
probably damaging |
Het |
Ajuba |
T |
C |
14: 54,807,855 (GRCm39) |
Y459C |
probably damaging |
Het |
Aldh7a1 |
T |
A |
18: 56,667,325 (GRCm39) |
N316Y |
possibly damaging |
Het |
Ankhd1 |
A |
G |
18: 36,724,548 (GRCm39) |
E402G |
probably damaging |
Het |
Ankrd36 |
A |
G |
11: 5,639,340 (GRCm39) |
|
probably benign |
Het |
Apeh |
A |
T |
9: 107,963,662 (GRCm39) |
L551H |
probably damaging |
Het |
Avpr1a |
T |
A |
10: 122,285,274 (GRCm39) |
F189I |
probably damaging |
Het |
BC034090 |
T |
A |
1: 155,117,773 (GRCm39) |
H115L |
possibly damaging |
Het |
C4b |
A |
T |
17: 34,956,635 (GRCm39) |
D654E |
possibly damaging |
Het |
Carns1 |
T |
A |
19: 4,221,900 (GRCm39) |
|
probably null |
Het |
Ccdc146 |
T |
A |
5: 21,513,711 (GRCm39) |
E469V |
probably benign |
Het |
Cdc27 |
A |
G |
11: 104,397,966 (GRCm39) |
I804T |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,173,541 (GRCm39) |
T1651I |
probably damaging |
Het |
Cenpo |
G |
A |
12: 4,266,646 (GRCm39) |
P154L |
probably damaging |
Het |
Cenpu |
G |
A |
8: 47,015,534 (GRCm39) |
G150R |
probably benign |
Het |
Chrna10 |
C |
A |
7: 101,763,560 (GRCm39) |
L78F |
probably damaging |
Het |
Chrne |
A |
T |
11: 70,505,913 (GRCm39) |
N457K |
possibly damaging |
Het |
Cidea |
A |
T |
18: 67,493,236 (GRCm39) |
D85V |
probably damaging |
Het |
Cldn18 |
T |
C |
9: 99,591,911 (GRCm39) |
S31G |
possibly damaging |
Het |
Clpb |
T |
A |
7: 101,428,548 (GRCm39) |
I436N |
probably damaging |
Het |
Col11a2 |
T |
C |
17: 34,278,148 (GRCm39) |
|
probably null |
Het |
Cul7 |
T |
C |
17: 46,965,403 (GRCm39) |
V527A |
probably benign |
Het |
Dchs1 |
A |
C |
7: 105,407,236 (GRCm39) |
V2119G |
probably damaging |
Het |
Dchs1 |
T |
A |
7: 105,421,262 (GRCm39) |
D386V |
probably damaging |
Het |
Dcstamp |
A |
C |
15: 39,622,715 (GRCm39) |
Q345H |
probably damaging |
Het |
Dlgap3 |
A |
G |
4: 127,130,123 (GRCm39) |
I955V |
probably damaging |
Het |
Dvl1 |
A |
G |
4: 155,938,143 (GRCm39) |
D97G |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,016,791 (GRCm39) |
D3573G |
probably damaging |
Het |
Efr3b |
G |
T |
12: 4,033,419 (GRCm39) |
F129L |
probably benign |
Het |
Etaa1 |
G |
A |
11: 17,897,539 (GRCm39) |
L193F |
probably damaging |
Het |
Fam13c |
G |
A |
10: 70,388,899 (GRCm39) |
S474N |
probably benign |
Het |
Fam171a2 |
C |
A |
11: 102,328,693 (GRCm39) |
V689L |
possibly damaging |
Het |
Fastkd3 |
T |
C |
13: 68,732,704 (GRCm39) |
F342L |
probably benign |
Het |
Fat4 |
T |
C |
3: 39,050,095 (GRCm39) |
S3986P |
possibly damaging |
Het |
Fbxo38 |
A |
G |
18: 62,674,042 (GRCm39) |
M13T |
probably benign |
Het |
Fbxo48 |
G |
T |
11: 16,904,329 (GRCm39) |
L160F |
possibly damaging |
Het |
Fgr |
G |
A |
4: 132,713,664 (GRCm39) |
|
probably null |
Het |
Gbx2 |
T |
C |
1: 89,856,635 (GRCm39) |
T252A |
probably damaging |
Het |
Gm20671 |
A |
G |
5: 32,977,286 (GRCm39) |
S1823P |
probably damaging |
Het |
Gpatch8 |
A |
T |
11: 102,399,053 (GRCm39) |
|
probably null |
Het |
Gsdma |
A |
T |
11: 98,557,275 (GRCm39) |
|
probably null |
Het |
Gucy2g |
G |
A |
19: 55,203,548 (GRCm39) |
A750V |
probably damaging |
Het |
Hdac9 |
A |
G |
12: 34,479,557 (GRCm39) |
Y223H |
probably damaging |
Het |
Igsf5 |
C |
A |
16: 96,192,226 (GRCm39) |
T275N |
probably benign |
Het |
Il23r |
G |
A |
6: 67,463,275 (GRCm39) |
H73Y |
probably benign |
Het |
Ipo4 |
G |
T |
14: 55,863,653 (GRCm39) |
R1026S |
probably benign |
Het |
Jade1 |
T |
A |
3: 41,546,137 (GRCm39) |
I54N |
probably damaging |
Het |
Khdrbs1 |
G |
T |
4: 129,635,729 (GRCm39) |
D75E |
possibly damaging |
Het |
Lrwd1 |
A |
T |
5: 136,152,728 (GRCm39) |
D511E |
possibly damaging |
Het |
Ly75 |
A |
T |
2: 60,164,831 (GRCm39) |
C782* |
probably null |
Het |
Mmp3 |
C |
T |
9: 7,451,759 (GRCm39) |
R366* |
probably null |
Het |
Mrgpra6 |
A |
G |
7: 46,838,629 (GRCm39) |
C190R |
probably damaging |
Het |
Mtcl3 |
A |
G |
10: 29,072,766 (GRCm39) |
D686G |
probably benign |
Het |
Myh10 |
T |
A |
11: 68,692,434 (GRCm39) |
L1369Q |
probably damaging |
Het |
Myof |
C |
T |
19: 37,941,435 (GRCm39) |
A792T |
probably damaging |
Het |
Ncf1 |
A |
G |
5: 134,250,659 (GRCm39) |
L373P |
probably damaging |
Het |
Ncoa7 |
C |
A |
10: 30,598,813 (GRCm39) |
A37S |
probably benign |
Het |
Nfkb1 |
A |
G |
3: 135,318,303 (GRCm39) |
V310A |
possibly damaging |
Het |
Nmur2 |
T |
A |
11: 55,931,040 (GRCm39) |
I224F |
probably damaging |
Het |
Nr1d2 |
A |
T |
14: 18,211,922 (GRCm38) |
S394T |
probably benign |
Het |
Nudt12 |
A |
G |
17: 59,310,434 (GRCm39) |
W390R |
probably damaging |
Het |
Or11g24 |
T |
A |
14: 50,662,846 (GRCm39) |
V290E |
possibly damaging |
Het |
Or2m13 |
A |
G |
16: 19,226,547 (GRCm39) |
L73P |
probably damaging |
Het |
Or4a79 |
T |
A |
2: 89,551,649 (GRCm39) |
I269F |
possibly damaging |
Het |
Or4e1 |
T |
A |
14: 52,700,714 (GRCm39) |
T251S |
probably benign |
Het |
Or52a20 |
T |
C |
7: 103,366,562 (GRCm39) |
F254L |
probably benign |
Het |
Pate2 |
A |
G |
9: 35,581,837 (GRCm39) |
M44V |
probably damaging |
Het |
Pikfyve |
T |
C |
1: 65,283,568 (GRCm39) |
L735S |
probably damaging |
Het |
Plce1 |
C |
A |
19: 38,748,535 (GRCm39) |
N1755K |
probably damaging |
Het |
Pld1 |
C |
A |
3: 28,079,469 (GRCm39) |
R90S |
probably damaging |
Het |
Pnpla7 |
C |
A |
2: 24,931,031 (GRCm39) |
P882Q |
probably damaging |
Het |
Pold2 |
A |
G |
11: 5,826,760 (GRCm39) |
L58P |
probably damaging |
Het |
Ppm1d |
A |
G |
11: 85,202,609 (GRCm39) |
E104G |
probably damaging |
Het |
Ppm1e |
A |
T |
11: 87,249,377 (GRCm39) |
L118Q |
possibly damaging |
Het |
Ppp1r42 |
A |
G |
1: 10,069,660 (GRCm39) |
L134P |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,386,625 (GRCm39) |
D1038G |
probably damaging |
Het |
Prss36 |
C |
A |
7: 127,535,871 (GRCm39) |
R288L |
probably damaging |
Het |
Prss51 |
T |
A |
14: 64,334,543 (GRCm39) |
V108E |
probably damaging |
Het |
Psma3 |
G |
T |
12: 71,021,539 (GRCm39) |
G7W |
probably damaging |
Het |
Psmc3ip |
A |
T |
11: 100,983,430 (GRCm39) |
|
probably null |
Het |
Qser1 |
T |
C |
2: 104,616,987 (GRCm39) |
E1275G |
probably damaging |
Het |
Rai2 |
A |
G |
X: 160,561,636 (GRCm39) |
N363S |
probably benign |
Het |
Ranbp17 |
A |
T |
11: 33,169,241 (GRCm39) |
V991D |
possibly damaging |
Het |
Rcc2 |
A |
T |
4: 140,447,877 (GRCm39) |
K468* |
probably null |
Het |
S1pr2 |
T |
C |
9: 20,878,890 (GRCm39) |
T313A |
probably benign |
Het |
Sec1 |
C |
A |
7: 45,328,264 (GRCm39) |
R261L |
probably benign |
Het |
Sfi1 |
ACA |
ACATCTTCCCAAAGCCAGTCA |
11: 3,103,382 (GRCm39) |
|
probably benign |
Homo |
Sgip1 |
G |
A |
4: 102,791,763 (GRCm39) |
V362I |
possibly damaging |
Het |
Shroom4 |
T |
A |
X: 6,497,523 (GRCm39) |
C894* |
probably null |
Het |
Slc12a9 |
A |
T |
5: 137,329,276 (GRCm39) |
L126Q |
probably damaging |
Het |
Slx4 |
A |
G |
16: 3,808,669 (GRCm39) |
S424P |
probably damaging |
Het |
Smg5 |
T |
C |
3: 88,258,600 (GRCm39) |
S524P |
probably damaging |
Het |
Sncaip |
A |
G |
18: 53,018,113 (GRCm39) |
D418G |
probably damaging |
Het |
Spink6 |
A |
G |
18: 44,215,347 (GRCm39) |
T66A |
probably damaging |
Het |
Sppl2c |
T |
A |
11: 104,078,127 (GRCm39) |
I309K |
possibly damaging |
Het |
Stk39 |
T |
A |
2: 68,240,383 (GRCm39) |
D116V |
probably damaging |
Het |
Supv3l1 |
A |
T |
10: 62,266,375 (GRCm39) |
N600K |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,104,545 (GRCm39) |
K1226R |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 4,991,494 (GRCm39) |
V557I |
probably benign |
Het |
Tas2r117 |
G |
T |
6: 132,780,117 (GRCm39) |
S85I |
probably benign |
Het |
Tcf20 |
T |
A |
15: 82,740,400 (GRCm39) |
Q350H |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,105,774 (GRCm39) |
L82Q |
probably damaging |
Het |
Tfb2m |
A |
C |
1: 179,373,437 (GRCm39) |
|
probably null |
Het |
Tm9sf1 |
C |
T |
14: 55,880,301 (GRCm39) |
G32D |
possibly damaging |
Het |
Tpd52 |
A |
T |
3: 8,996,255 (GRCm39) |
|
probably null |
Het |
Trappc8 |
A |
T |
18: 20,966,119 (GRCm39) |
|
probably null |
Het |
Trbv30 |
A |
G |
6: 41,258,854 (GRCm39) |
T88A |
probably benign |
Het |
Trim40 |
T |
A |
17: 37,199,757 (GRCm39) |
N107I |
probably damaging |
Het |
Trim80 |
A |
T |
11: 115,338,843 (GRCm39) |
T558S |
probably benign |
Het |
Ttn |
A |
G |
2: 76,708,692 (GRCm39) |
|
probably benign |
Het |
Vav3 |
A |
G |
3: 109,434,791 (GRCm39) |
M441V |
possibly damaging |
Het |
Vmn1r42 |
T |
A |
6: 89,822,366 (GRCm39) |
I68F |
probably damaging |
Het |
Vmn2r118 |
C |
T |
17: 55,918,565 (GRCm39) |
G109D |
probably benign |
Het |
Vmn2r5 |
T |
A |
3: 64,416,931 (GRCm39) |
M76L |
probably benign |
Het |
Vwa7 |
G |
T |
17: 35,243,902 (GRCm39) |
|
probably null |
Het |
Xndc1 |
T |
C |
7: 101,731,395 (GRCm39) |
V378A |
probably benign |
Het |
Zc3h12d |
A |
T |
10: 7,729,014 (GRCm39) |
D126V |
probably damaging |
Het |
Zc3h13 |
A |
G |
14: 75,581,059 (GRCm39) |
N1682S |
probably benign |
Het |
Zc3h15 |
T |
C |
2: 83,490,574 (GRCm39) |
I236T |
possibly damaging |
Het |
Zfp13 |
A |
T |
17: 23,800,156 (GRCm39) |
I34N |
probably damaging |
Het |
Zfp169 |
A |
T |
13: 48,643,751 (GRCm39) |
C459S |
possibly damaging |
Het |
Zfyve28 |
A |
G |
5: 34,374,311 (GRCm39) |
C568R |
probably damaging |
Het |
|
Other mutations in Spata31d1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01525:Spata31d1b
|
APN |
13 |
59,860,280 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02317:Spata31d1b
|
APN |
13 |
59,865,854 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02885:Spata31d1b
|
APN |
13 |
59,866,941 (GRCm39) |
utr 3 prime |
probably benign |
|
R0017:Spata31d1b
|
UTSW |
13 |
59,863,883 (GRCm39) |
missense |
probably benign |
|
R0071:Spata31d1b
|
UTSW |
13 |
59,863,163 (GRCm39) |
missense |
probably benign |
0.26 |
R0071:Spata31d1b
|
UTSW |
13 |
59,863,163 (GRCm39) |
missense |
probably benign |
0.26 |
R0595:Spata31d1b
|
UTSW |
13 |
59,864,091 (GRCm39) |
missense |
probably benign |
0.09 |
R0961:Spata31d1b
|
UTSW |
13 |
59,865,618 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1054:Spata31d1b
|
UTSW |
13 |
59,865,332 (GRCm39) |
missense |
probably damaging |
0.96 |
R1124:Spata31d1b
|
UTSW |
13 |
59,864,468 (GRCm39) |
missense |
probably benign |
|
R1338:Spata31d1b
|
UTSW |
13 |
59,865,975 (GRCm39) |
frame shift |
probably null |
|
R1539:Spata31d1b
|
UTSW |
13 |
59,863,733 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1662:Spata31d1b
|
UTSW |
13 |
59,864,442 (GRCm39) |
missense |
probably benign |
0.00 |
R1688:Spata31d1b
|
UTSW |
13 |
59,863,274 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1776:Spata31d1b
|
UTSW |
13 |
59,864,381 (GRCm39) |
missense |
probably benign |
|
R1793:Spata31d1b
|
UTSW |
13 |
59,863,779 (GRCm39) |
missense |
probably benign |
|
R1838:Spata31d1b
|
UTSW |
13 |
59,865,279 (GRCm39) |
missense |
probably benign |
0.00 |
R1838:Spata31d1b
|
UTSW |
13 |
59,863,671 (GRCm39) |
missense |
probably benign |
|
R1861:Spata31d1b
|
UTSW |
13 |
59,865,150 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1903:Spata31d1b
|
UTSW |
13 |
59,865,882 (GRCm39) |
missense |
probably damaging |
0.99 |
R1940:Spata31d1b
|
UTSW |
13 |
59,865,835 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1994:Spata31d1b
|
UTSW |
13 |
59,864,194 (GRCm39) |
missense |
probably benign |
|
R1995:Spata31d1b
|
UTSW |
13 |
59,864,194 (GRCm39) |
missense |
probably benign |
|
R2407:Spata31d1b
|
UTSW |
13 |
59,864,660 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3692:Spata31d1b
|
UTSW |
13 |
59,865,705 (GRCm39) |
missense |
probably benign |
0.03 |
R4576:Spata31d1b
|
UTSW |
13 |
59,864,675 (GRCm39) |
missense |
probably damaging |
0.98 |
R4734:Spata31d1b
|
UTSW |
13 |
59,866,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4742:Spata31d1b
|
UTSW |
13 |
59,864,426 (GRCm39) |
missense |
probably damaging |
0.98 |
R4749:Spata31d1b
|
UTSW |
13 |
59,866,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Spata31d1b
|
UTSW |
13 |
59,863,535 (GRCm39) |
missense |
probably benign |
0.32 |
R4808:Spata31d1b
|
UTSW |
13 |
59,863,535 (GRCm39) |
missense |
probably benign |
0.32 |
R4844:Spata31d1b
|
UTSW |
13 |
59,866,169 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4942:Spata31d1b
|
UTSW |
13 |
59,864,917 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4953:Spata31d1b
|
UTSW |
13 |
59,864,097 (GRCm39) |
missense |
probably damaging |
0.96 |
R5093:Spata31d1b
|
UTSW |
13 |
59,863,838 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5169:Spata31d1b
|
UTSW |
13 |
59,864,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Spata31d1b
|
UTSW |
13 |
59,866,866 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5502:Spata31d1b
|
UTSW |
13 |
59,864,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R5751:Spata31d1b
|
UTSW |
13 |
59,866,787 (GRCm39) |
missense |
probably benign |
0.03 |
R6054:Spata31d1b
|
UTSW |
13 |
59,863,464 (GRCm39) |
missense |
probably benign |
|
R6433:Spata31d1b
|
UTSW |
13 |
59,864,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R6571:Spata31d1b
|
UTSW |
13 |
59,865,269 (GRCm39) |
missense |
probably benign |
|
R6980:Spata31d1b
|
UTSW |
13 |
59,863,236 (GRCm39) |
missense |
probably benign |
0.26 |
R7047:Spata31d1b
|
UTSW |
13 |
59,860,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Spata31d1b
|
UTSW |
13 |
59,863,955 (GRCm39) |
missense |
probably benign |
|
R7147:Spata31d1b
|
UTSW |
13 |
59,866,028 (GRCm39) |
missense |
probably benign |
0.28 |
R7273:Spata31d1b
|
UTSW |
13 |
59,865,446 (GRCm39) |
missense |
probably benign |
|
R7359:Spata31d1b
|
UTSW |
13 |
59,860,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R7457:Spata31d1b
|
UTSW |
13 |
59,864,723 (GRCm39) |
missense |
probably damaging |
0.99 |
R7469:Spata31d1b
|
UTSW |
13 |
59,863,278 (GRCm39) |
missense |
probably benign |
0.04 |
R7519:Spata31d1b
|
UTSW |
13 |
59,864,726 (GRCm39) |
missense |
probably benign |
0.43 |
R7548:Spata31d1b
|
UTSW |
13 |
59,864,468 (GRCm39) |
missense |
probably benign |
|
R7586:Spata31d1b
|
UTSW |
13 |
59,866,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7657:Spata31d1b
|
UTSW |
13 |
59,863,577 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7778:Spata31d1b
|
UTSW |
13 |
59,865,047 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7824:Spata31d1b
|
UTSW |
13 |
59,865,047 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7989:Spata31d1b
|
UTSW |
13 |
59,866,182 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8078:Spata31d1b
|
UTSW |
13 |
59,863,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R8176:Spata31d1b
|
UTSW |
13 |
59,865,117 (GRCm39) |
missense |
probably benign |
|
R8530:Spata31d1b
|
UTSW |
13 |
59,864,964 (GRCm39) |
missense |
unknown |
|
R8776:Spata31d1b
|
UTSW |
13 |
59,863,283 (GRCm39) |
missense |
probably benign |
0.00 |
R8776-TAIL:Spata31d1b
|
UTSW |
13 |
59,863,283 (GRCm39) |
missense |
probably benign |
0.00 |
R9385:Spata31d1b
|
UTSW |
13 |
59,863,403 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Spata31d1b
|
UTSW |
13 |
59,863,467 (GRCm39) |
missense |
probably benign |
0.08 |
R9522:Spata31d1b
|
UTSW |
13 |
59,864,780 (GRCm39) |
missense |
probably benign |
0.00 |
R9786:Spata31d1b
|
UTSW |
13 |
59,866,155 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9789:Spata31d1b
|
UTSW |
13 |
59,860,196 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Spata31d1b
|
UTSW |
13 |
59,866,674 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Spata31d1b
|
UTSW |
13 |
59,863,265 (GRCm39) |
missense |
probably benign |
0.44 |
Z1177:Spata31d1b
|
UTSW |
13 |
59,860,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|