Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700092K14Rik |
A |
C |
11: 114,089,970 (GRCm39) |
|
noncoding transcript |
Het |
Abca17 |
G |
T |
17: 24,518,034 (GRCm39) |
D758E |
possibly damaging |
Het |
Adam28 |
A |
G |
14: 68,885,155 (GRCm39) |
V65A |
possibly damaging |
Het |
Adgra2 |
T |
A |
8: 27,609,272 (GRCm39) |
M616K |
possibly damaging |
Het |
Aldh3b2 |
A |
G |
19: 4,027,636 (GRCm39) |
D59G |
probably benign |
Het |
Ankrd28 |
A |
G |
14: 31,467,182 (GRCm39) |
V260A |
possibly damaging |
Het |
Bbs7 |
A |
G |
3: 36,627,720 (GRCm39) |
V689A |
probably damaging |
Het |
Cacna1e |
A |
G |
1: 154,302,296 (GRCm39) |
F1653S |
probably benign |
Het |
Cd55b |
T |
C |
1: 130,344,596 (GRCm39) |
D213G |
probably damaging |
Het |
Colgalt2 |
G |
A |
1: 152,344,282 (GRCm39) |
V115M |
probably damaging |
Het |
Defa27 |
A |
G |
8: 21,805,632 (GRCm39) |
N24S |
probably benign |
Het |
Defb40 |
A |
G |
8: 19,028,093 (GRCm39) |
S14P |
probably damaging |
Het |
Dnmt3a |
G |
A |
12: 3,951,665 (GRCm39) |
G681R |
probably damaging |
Het |
Dus2 |
C |
T |
8: 106,775,286 (GRCm39) |
A271V |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,245 (GRCm39) |
|
probably null |
Het |
Fancg |
T |
C |
4: 43,003,830 (GRCm39) |
D533G |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,340,770 (GRCm39) |
V1021A |
probably benign |
Het |
Gmip |
T |
A |
8: 70,266,251 (GRCm39) |
|
probably benign |
Het |
Hspb6 |
T |
C |
7: 30,252,889 (GRCm39) |
S44P |
possibly damaging |
Het |
Jsrp1 |
T |
C |
10: 80,646,190 (GRCm39) |
I50V |
probably benign |
Het |
Kansl1 |
T |
C |
11: 104,269,515 (GRCm39) |
N476S |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 180,722,946 (GRCm39) |
D810G |
probably damaging |
Het |
Magea14 |
T |
C |
X: 51,057,867 (GRCm39) |
Y273C |
probably damaging |
Het |
Maml2 |
C |
A |
9: 13,531,406 (GRCm39) |
L207I |
possibly damaging |
Het |
Myo3a |
A |
T |
2: 22,345,089 (GRCm39) |
E508D |
probably benign |
Het |
Nav1 |
T |
A |
1: 135,385,651 (GRCm39) |
|
probably benign |
Het |
Ndrg3 |
A |
T |
2: 156,790,214 (GRCm39) |
C90S |
possibly damaging |
Het |
Orc1 |
A |
G |
4: 108,463,471 (GRCm39) |
S663G |
probably benign |
Het |
Pcdhb14 |
T |
A |
18: 37,583,195 (GRCm39) |
L767H |
probably damaging |
Het |
Pcgf1 |
T |
A |
6: 83,056,714 (GRCm39) |
L90Q |
probably damaging |
Het |
Pnma5 |
T |
C |
X: 72,079,036 (GRCm39) |
M549V |
probably benign |
Het |
Por |
C |
A |
5: 135,744,815 (GRCm39) |
T26K |
possibly damaging |
Het |
Ppp4r3c1 |
A |
T |
X: 88,976,105 (GRCm39) |
W31R |
probably damaging |
Het |
Qsox1 |
T |
A |
1: 155,662,671 (GRCm39) |
|
probably null |
Het |
Rad51ap2 |
T |
A |
12: 11,506,465 (GRCm39) |
V129D |
probably benign |
Het |
Rec8 |
A |
G |
14: 55,856,091 (GRCm39) |
H11R |
probably damaging |
Het |
Rxfp2 |
T |
G |
5: 149,993,735 (GRCm39) |
V585G |
possibly damaging |
Het |
Sftpd |
G |
A |
14: 40,894,537 (GRCm39) |
T294I |
probably benign |
Het |
Sh3gl1 |
A |
G |
17: 56,343,456 (GRCm39) |
S2P |
probably damaging |
Het |
Slc38a10 |
A |
T |
11: 120,020,090 (GRCm39) |
F321I |
probably damaging |
Het |
Slc4a10 |
T |
A |
2: 62,074,687 (GRCm39) |
|
probably null |
Het |
Slco6b1 |
A |
G |
1: 96,925,115 (GRCm39) |
|
noncoding transcript |
Het |
Slit1 |
T |
C |
19: 41,602,856 (GRCm39) |
E985G |
probably benign |
Het |
Smurf1 |
C |
T |
5: 144,819,403 (GRCm39) |
E575K |
probably damaging |
Het |
Sned1 |
A |
T |
1: 93,213,577 (GRCm39) |
R426* |
probably null |
Het |
Tas2r123 |
G |
A |
6: 132,825,008 (GRCm39) |
V302I |
possibly damaging |
Het |
Tmem182 |
T |
C |
1: 40,877,530 (GRCm39) |
I135T |
probably damaging |
Het |
Tmem67 |
T |
C |
4: 12,073,922 (GRCm39) |
Y298C |
probably damaging |
Het |
Trappc9 |
A |
G |
15: 72,462,641 (GRCm39) |
C1026R |
probably damaging |
Het |
Troap |
A |
G |
15: 98,976,713 (GRCm39) |
D279G |
probably benign |
Het |
Ttn |
T |
A |
2: 76,585,168 (GRCm39) |
I22042F |
probably damaging |
Het |
Vmn1r23 |
T |
C |
6: 57,903,452 (GRCm39) |
T109A |
probably benign |
Het |
Vmn2r25 |
A |
T |
6: 123,800,606 (GRCm39) |
C579S |
probably damaging |
Het |
Zbtb18 |
A |
G |
1: 177,275,045 (GRCm39) |
D126G |
probably damaging |
Het |
|
Other mutations in Ddx60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Ddx60
|
APN |
8 |
62,411,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00915:Ddx60
|
APN |
8 |
62,440,465 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00931:Ddx60
|
APN |
8 |
62,422,617 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01023:Ddx60
|
APN |
8 |
62,395,548 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01313:Ddx60
|
APN |
8 |
62,435,560 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01615:Ddx60
|
APN |
8 |
62,416,774 (GRCm39) |
missense |
probably null |
0.81 |
IGL01733:Ddx60
|
APN |
8 |
62,436,899 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01779:Ddx60
|
APN |
8 |
62,470,857 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01900:Ddx60
|
APN |
8 |
62,453,743 (GRCm39) |
splice site |
probably benign |
|
IGL02110:Ddx60
|
APN |
8 |
62,470,281 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02302:Ddx60
|
APN |
8 |
62,428,866 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02468:Ddx60
|
APN |
8 |
62,411,676 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02569:Ddx60
|
APN |
8 |
62,477,985 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02622:Ddx60
|
APN |
8 |
62,395,470 (GRCm39) |
splice site |
probably null |
|
IGL02657:Ddx60
|
APN |
8 |
62,437,149 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02677:Ddx60
|
APN |
8 |
62,441,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02701:Ddx60
|
APN |
8 |
62,432,375 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02806:Ddx60
|
APN |
8 |
62,409,156 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03137:Ddx60
|
APN |
8 |
62,441,117 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03295:Ddx60
|
APN |
8 |
62,409,155 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03387:Ddx60
|
APN |
8 |
62,465,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03411:Ddx60
|
APN |
8 |
62,430,916 (GRCm39) |
critical splice acceptor site |
probably null |
|
Scatter
|
UTSW |
8 |
62,474,348 (GRCm39) |
missense |
possibly damaging |
0.80 |
shotgun
|
UTSW |
8 |
62,490,101 (GRCm39) |
missense |
probably benign |
0.28 |
splay
|
UTSW |
8 |
62,474,343 (GRCm39) |
missense |
possibly damaging |
0.80 |
G1Funyon:Ddx60
|
UTSW |
8 |
62,453,631 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4504001:Ddx60
|
UTSW |
8 |
62,411,147 (GRCm39) |
missense |
probably benign |
|
PIT4677001:Ddx60
|
UTSW |
8 |
62,425,288 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0090:Ddx60
|
UTSW |
8 |
62,395,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0266:Ddx60
|
UTSW |
8 |
62,486,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0325:Ddx60
|
UTSW |
8 |
62,436,889 (GRCm39) |
missense |
probably benign |
0.00 |
R0367:Ddx60
|
UTSW |
8 |
62,470,783 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0403:Ddx60
|
UTSW |
8 |
62,447,575 (GRCm39) |
splice site |
probably benign |
|
R0479:Ddx60
|
UTSW |
8 |
62,422,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Ddx60
|
UTSW |
8 |
62,470,828 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0844:Ddx60
|
UTSW |
8 |
62,440,395 (GRCm39) |
missense |
probably benign |
0.27 |
R1119:Ddx60
|
UTSW |
8 |
62,395,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R1428:Ddx60
|
UTSW |
8 |
62,411,193 (GRCm39) |
splice site |
probably benign |
|
R1778:Ddx60
|
UTSW |
8 |
62,427,210 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1840:Ddx60
|
UTSW |
8 |
62,422,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R1964:Ddx60
|
UTSW |
8 |
62,401,903 (GRCm39) |
missense |
probably benign |
0.10 |
R1970:Ddx60
|
UTSW |
8 |
62,425,240 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2101:Ddx60
|
UTSW |
8 |
62,393,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Ddx60
|
UTSW |
8 |
62,470,234 (GRCm39) |
missense |
probably benign |
0.01 |
R2174:Ddx60
|
UTSW |
8 |
62,409,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Ddx60
|
UTSW |
8 |
62,411,097 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2332:Ddx60
|
UTSW |
8 |
62,490,125 (GRCm39) |
missense |
probably benign |
0.08 |
R2338:Ddx60
|
UTSW |
8 |
62,465,470 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2379:Ddx60
|
UTSW |
8 |
62,490,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R4010:Ddx60
|
UTSW |
8 |
62,409,178 (GRCm39) |
missense |
probably benign |
0.25 |
R4010:Ddx60
|
UTSW |
8 |
62,407,569 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4133:Ddx60
|
UTSW |
8 |
62,425,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R4382:Ddx60
|
UTSW |
8 |
62,402,012 (GRCm39) |
splice site |
probably null |
|
R4561:Ddx60
|
UTSW |
8 |
62,395,495 (GRCm39) |
missense |
probably damaging |
0.96 |
R4572:Ddx60
|
UTSW |
8 |
62,440,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R4581:Ddx60
|
UTSW |
8 |
62,476,295 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4635:Ddx60
|
UTSW |
8 |
62,490,101 (GRCm39) |
missense |
probably benign |
0.28 |
R4698:Ddx60
|
UTSW |
8 |
62,465,458 (GRCm39) |
missense |
probably benign |
0.01 |
R4807:Ddx60
|
UTSW |
8 |
62,432,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Ddx60
|
UTSW |
8 |
62,474,348 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4964:Ddx60
|
UTSW |
8 |
62,432,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R5120:Ddx60
|
UTSW |
8 |
62,398,940 (GRCm39) |
missense |
probably benign |
0.01 |
R5187:Ddx60
|
UTSW |
8 |
62,427,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Ddx60
|
UTSW |
8 |
62,437,192 (GRCm39) |
missense |
probably damaging |
0.99 |
R5400:Ddx60
|
UTSW |
8 |
62,463,036 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5500:Ddx60
|
UTSW |
8 |
62,403,485 (GRCm39) |
missense |
probably benign |
0.28 |
R5514:Ddx60
|
UTSW |
8 |
62,411,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R5668:Ddx60
|
UTSW |
8 |
62,453,612 (GRCm39) |
missense |
probably benign |
0.38 |
R5742:Ddx60
|
UTSW |
8 |
62,401,955 (GRCm39) |
missense |
probably benign |
|
R5772:Ddx60
|
UTSW |
8 |
62,401,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Ddx60
|
UTSW |
8 |
62,465,422 (GRCm39) |
nonsense |
probably null |
|
R5815:Ddx60
|
UTSW |
8 |
62,416,756 (GRCm39) |
missense |
probably damaging |
0.98 |
R5820:Ddx60
|
UTSW |
8 |
62,409,155 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5866:Ddx60
|
UTSW |
8 |
62,393,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R5881:Ddx60
|
UTSW |
8 |
62,490,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Ddx60
|
UTSW |
8 |
62,474,444 (GRCm39) |
critical splice donor site |
probably null |
|
R6048:Ddx60
|
UTSW |
8 |
62,453,616 (GRCm39) |
missense |
probably benign |
0.01 |
R6061:Ddx60
|
UTSW |
8 |
62,476,275 (GRCm39) |
missense |
probably null |
0.01 |
R6153:Ddx60
|
UTSW |
8 |
62,398,974 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6287:Ddx60
|
UTSW |
8 |
62,403,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R6415:Ddx60
|
UTSW |
8 |
62,436,939 (GRCm39) |
missense |
probably benign |
0.00 |
R6416:Ddx60
|
UTSW |
8 |
62,451,715 (GRCm39) |
missense |
probably benign |
|
R6416:Ddx60
|
UTSW |
8 |
62,430,984 (GRCm39) |
missense |
probably benign |
0.00 |
R6660:Ddx60
|
UTSW |
8 |
62,409,273 (GRCm39) |
missense |
probably benign |
0.00 |
R6694:Ddx60
|
UTSW |
8 |
62,490,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R6715:Ddx60
|
UTSW |
8 |
62,436,924 (GRCm39) |
missense |
probably benign |
0.03 |
R6720:Ddx60
|
UTSW |
8 |
62,453,723 (GRCm39) |
missense |
probably benign |
0.10 |
R6937:Ddx60
|
UTSW |
8 |
62,490,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7153:Ddx60
|
UTSW |
8 |
62,441,142 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7274:Ddx60
|
UTSW |
8 |
62,393,142 (GRCm39) |
critical splice donor site |
probably null |
|
R7409:Ddx60
|
UTSW |
8 |
62,411,612 (GRCm39) |
missense |
probably benign |
0.24 |
R7464:Ddx60
|
UTSW |
8 |
62,393,708 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7670:Ddx60
|
UTSW |
8 |
62,428,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Ddx60
|
UTSW |
8 |
62,430,924 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7992:Ddx60
|
UTSW |
8 |
62,407,569 (GRCm39) |
missense |
probably benign |
0.03 |
R8124:Ddx60
|
UTSW |
8 |
62,436,945 (GRCm39) |
missense |
probably benign |
|
R8125:Ddx60
|
UTSW |
8 |
62,436,945 (GRCm39) |
missense |
probably benign |
|
R8126:Ddx60
|
UTSW |
8 |
62,436,945 (GRCm39) |
missense |
probably benign |
|
R8155:Ddx60
|
UTSW |
8 |
62,470,205 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8174:Ddx60
|
UTSW |
8 |
62,470,284 (GRCm39) |
splice site |
probably null |
|
R8192:Ddx60
|
UTSW |
8 |
62,431,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Ddx60
|
UTSW |
8 |
62,393,142 (GRCm39) |
critical splice donor site |
probably null |
|
R8301:Ddx60
|
UTSW |
8 |
62,453,631 (GRCm39) |
missense |
probably benign |
0.01 |
R8304:Ddx60
|
UTSW |
8 |
62,451,803 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8319:Ddx60
|
UTSW |
8 |
62,395,669 (GRCm39) |
critical splice donor site |
probably null |
|
R8374:Ddx60
|
UTSW |
8 |
62,427,205 (GRCm39) |
missense |
probably benign |
0.01 |
R8401:Ddx60
|
UTSW |
8 |
62,409,277 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8487:Ddx60
|
UTSW |
8 |
62,427,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Ddx60
|
UTSW |
8 |
62,411,640 (GRCm39) |
missense |
probably benign |
0.27 |
R8826:Ddx60
|
UTSW |
8 |
62,398,990 (GRCm39) |
missense |
probably benign |
0.02 |
R8829:Ddx60
|
UTSW |
8 |
62,393,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Ddx60
|
UTSW |
8 |
62,474,343 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8884:Ddx60
|
UTSW |
8 |
62,447,553 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8990:Ddx60
|
UTSW |
8 |
62,427,168 (GRCm39) |
nonsense |
probably null |
|
R9122:Ddx60
|
UTSW |
8 |
62,442,898 (GRCm39) |
missense |
probably benign |
0.16 |
R9225:Ddx60
|
UTSW |
8 |
62,470,875 (GRCm39) |
missense |
probably benign |
0.36 |
R9278:Ddx60
|
UTSW |
8 |
62,431,012 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9293:Ddx60
|
UTSW |
8 |
62,462,994 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9405:Ddx60
|
UTSW |
8 |
62,425,248 (GRCm39) |
missense |
probably benign |
0.03 |
R9766:Ddx60
|
UTSW |
8 |
62,465,312 (GRCm39) |
missense |
probably damaging |
1.00 |
X0003:Ddx60
|
UTSW |
8 |
62,486,451 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0019:Ddx60
|
UTSW |
8 |
62,416,726 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Ddx60
|
UTSW |
8 |
62,453,622 (GRCm39) |
missense |
possibly damaging |
0.92 |
|