Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700037C18Rik |
A |
G |
16: 3,725,511 (GRCm39) |
V5A |
probably damaging |
Het |
Abi3bp |
A |
G |
16: 56,424,375 (GRCm39) |
|
probably null |
Het |
Acot11 |
G |
A |
4: 106,619,224 (GRCm39) |
R184C |
probably damaging |
Het |
Adgre5 |
A |
T |
8: 84,458,627 (GRCm39) |
I133N |
probably damaging |
Het |
Afap1 |
A |
T |
5: 36,108,347 (GRCm39) |
Q231L |
probably damaging |
Het |
Alg12 |
T |
C |
15: 88,695,630 (GRCm39) |
T289A |
probably benign |
Het |
Ank3 |
T |
A |
10: 69,718,374 (GRCm39) |
S542T |
possibly damaging |
Het |
Ankmy2 |
G |
A |
12: 36,232,389 (GRCm39) |
R138Q |
possibly damaging |
Het |
Ascc2 |
C |
T |
11: 4,622,302 (GRCm39) |
A456V |
probably benign |
Het |
Atg4c |
G |
A |
4: 99,112,719 (GRCm39) |
V289I |
probably benign |
Het |
Bbs7 |
A |
T |
3: 36,657,022 (GRCm39) |
Y269N |
probably damaging |
Het |
Bcas3 |
T |
A |
11: 85,386,676 (GRCm39) |
D370E |
probably damaging |
Het |
Bicc1 |
T |
G |
10: 70,761,145 (GRCm39) |
E955A |
probably damaging |
Het |
Bok |
T |
C |
1: 93,616,999 (GRCm39) |
F115S |
probably damaging |
Het |
Caap1 |
A |
T |
4: 94,438,758 (GRCm39) |
|
probably null |
Het |
Cacna2d3 |
T |
A |
14: 29,256,476 (GRCm39) |
M95L |
possibly damaging |
Het |
Calcrl |
T |
A |
2: 84,200,435 (GRCm39) |
D115V |
probably benign |
Het |
Car7 |
A |
T |
8: 105,270,170 (GRCm39) |
M57L |
probably benign |
Het |
Casq1 |
G |
T |
1: 172,037,957 (GRCm39) |
|
probably benign |
Het |
Cep290 |
A |
T |
10: 100,385,206 (GRCm39) |
D1894V |
possibly damaging |
Het |
Clec4a2 |
T |
A |
6: 123,100,588 (GRCm39) |
N14K |
probably damaging |
Het |
Col5a1 |
T |
C |
2: 27,880,109 (GRCm39) |
|
probably benign |
Het |
Col5a2 |
A |
T |
1: 45,417,642 (GRCm39) |
I1311N |
probably damaging |
Het |
Col5a3 |
T |
C |
9: 20,694,004 (GRCm39) |
T1050A |
probably damaging |
Het |
Colgalt2 |
A |
T |
1: 152,360,622 (GRCm39) |
I220F |
probably damaging |
Het |
Cpb1 |
A |
T |
3: 20,329,792 (GRCm39) |
V8E |
unknown |
Het |
Dchs1 |
C |
T |
7: 105,421,934 (GRCm39) |
R162H |
probably benign |
Het |
Dhx37 |
A |
G |
5: 125,499,295 (GRCm39) |
Y638H |
probably benign |
Het |
Dhx40 |
T |
G |
11: 86,662,088 (GRCm39) |
|
probably benign |
Het |
Ehd2 |
T |
A |
7: 15,686,001 (GRCm39) |
Q357L |
probably benign |
Het |
Ewsr1 |
T |
C |
11: 5,020,737 (GRCm39) |
|
probably benign |
Het |
Fcho1 |
C |
T |
8: 72,165,204 (GRCm39) |
A418T |
probably benign |
Het |
Gid8 |
T |
A |
2: 180,355,004 (GRCm39) |
Y3* |
probably null |
Het |
Gm10212 |
A |
C |
19: 11,548,174 (GRCm39) |
|
noncoding transcript |
Het |
Grin3b |
T |
A |
10: 79,809,890 (GRCm39) |
N465K |
possibly damaging |
Het |
H1f3 |
A |
T |
13: 23,739,924 (GRCm39) |
K221* |
probably null |
Het |
Htr4 |
A |
T |
18: 62,561,225 (GRCm39) |
N162I |
probably damaging |
Het |
Irag2 |
T |
C |
6: 145,110,938 (GRCm39) |
C248R |
probably damaging |
Het |
Itga3 |
T |
C |
11: 94,952,796 (GRCm39) |
D325G |
probably benign |
Het |
Itpr3 |
T |
G |
17: 27,330,903 (GRCm39) |
V1737G |
probably damaging |
Het |
Kcnab2 |
C |
T |
4: 152,479,439 (GRCm39) |
V251I |
probably benign |
Het |
Kcnn2 |
A |
T |
18: 45,693,215 (GRCm39) |
I264L |
probably benign |
Het |
Klhl41 |
T |
C |
2: 69,501,600 (GRCm39) |
Y354H |
probably damaging |
Het |
Klra6 |
T |
C |
6: 130,000,601 (GRCm39) |
I68V |
probably benign |
Het |
Letm2 |
G |
T |
8: 26,082,574 (GRCm39) |
P178Q |
probably damaging |
Het |
Lypd11 |
C |
A |
7: 24,422,170 (GRCm39) |
C193F |
possibly damaging |
Het |
Mbtps1 |
A |
T |
8: 120,249,340 (GRCm39) |
|
probably benign |
Het |
Mecom |
C |
T |
3: 30,035,121 (GRCm39) |
|
probably benign |
Het |
Mrps5 |
T |
A |
2: 127,433,745 (GRCm39) |
S45T |
possibly damaging |
Het |
Msra |
T |
A |
14: 64,678,210 (GRCm39) |
I29F |
possibly damaging |
Het |
Mup5 |
T |
C |
4: 61,751,229 (GRCm39) |
|
probably null |
Het |
Myo1a |
T |
C |
10: 127,555,111 (GRCm39) |
|
probably benign |
Het |
Myrip |
C |
A |
9: 120,270,443 (GRCm39) |
N564K |
probably benign |
Het |
Naa20 |
T |
A |
2: 145,757,592 (GRCm39) |
D148E |
probably damaging |
Het |
Naga |
T |
G |
15: 82,220,956 (GRCm39) |
|
probably benign |
Het |
Npc1 |
A |
G |
18: 12,346,503 (GRCm39) |
V231A |
probably benign |
Het |
Nphs1 |
T |
C |
7: 30,166,940 (GRCm39) |
F716L |
probably benign |
Het |
Or8s5 |
T |
C |
15: 98,238,810 (GRCm39) |
H20R |
probably benign |
Het |
Parn |
G |
C |
16: 13,472,299 (GRCm39) |
|
probably benign |
Het |
Polk |
A |
T |
13: 96,620,272 (GRCm39) |
C664S |
probably benign |
Het |
Prkar2b |
A |
G |
12: 32,026,034 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,651,604 (GRCm39) |
E3747G |
probably damaging |
Het |
Prmt5 |
A |
T |
14: 54,748,712 (GRCm39) |
M362K |
probably damaging |
Het |
Prob1 |
T |
C |
18: 35,786,878 (GRCm39) |
T459A |
possibly damaging |
Het |
Rttn |
C |
T |
18: 89,108,543 (GRCm39) |
|
probably benign |
Het |
Scn1a |
T |
C |
2: 66,104,269 (GRCm39) |
M1664V |
probably damaging |
Het |
Sez6 |
T |
A |
11: 77,844,639 (GRCm39) |
L154H |
probably damaging |
Het |
Sh3tc1 |
A |
G |
5: 35,859,356 (GRCm39) |
|
probably benign |
Het |
Shkbp1 |
C |
T |
7: 27,048,006 (GRCm39) |
G334D |
probably damaging |
Het |
Slc8a1 |
A |
T |
17: 81,955,422 (GRCm39) |
F539I |
probably damaging |
Het |
Spata31e5 |
G |
T |
1: 28,817,223 (GRCm39) |
Q270K |
probably damaging |
Het |
Sptan1 |
T |
C |
2: 29,903,860 (GRCm39) |
|
probably benign |
Het |
Ssc5d |
C |
T |
7: 4,940,470 (GRCm39) |
T861M |
probably damaging |
Het |
Tbx5 |
A |
T |
5: 120,021,523 (GRCm39) |
M510L |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,876,101 (GRCm39) |
T351A |
probably benign |
Het |
Tmc8 |
T |
A |
11: 117,682,904 (GRCm39) |
|
probably benign |
Het |
Tmco5 |
T |
A |
2: 116,720,588 (GRCm39) |
D205E |
probably benign |
Het |
Tmprss2 |
T |
C |
16: 97,373,194 (GRCm39) |
|
probably benign |
Het |
Top6bl |
A |
T |
19: 4,708,442 (GRCm39) |
I350N |
probably damaging |
Het |
Tph1 |
T |
A |
7: 46,299,448 (GRCm39) |
K364N |
probably benign |
Het |
Trim24 |
T |
C |
6: 37,934,001 (GRCm39) |
L648P |
probably damaging |
Het |
Trmt6 |
C |
A |
2: 132,650,950 (GRCm39) |
|
probably benign |
Het |
Ube2i |
A |
T |
17: 25,488,259 (GRCm39) |
|
probably benign |
Het |
Vcan |
A |
C |
13: 89,852,779 (GRCm39) |
L727R |
possibly damaging |
Het |
Vmn2r28 |
T |
C |
7: 5,491,689 (GRCm39) |
Y186C |
probably damaging |
Het |
Wars1 |
C |
A |
12: 108,841,083 (GRCm39) |
D232Y |
probably damaging |
Het |
Xrcc5 |
T |
C |
1: 72,378,104 (GRCm39) |
|
probably benign |
Het |
Zbtb24 |
T |
A |
10: 41,340,532 (GRCm39) |
S543T |
probably damaging |
Het |
Zfp91 |
A |
G |
19: 12,753,353 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Col16a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Col16a1
|
APN |
4 |
129,988,345 (GRCm39) |
splice site |
probably null |
|
IGL00885:Col16a1
|
APN |
4 |
129,990,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01931:Col16a1
|
APN |
4 |
129,966,634 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02142:Col16a1
|
APN |
4 |
129,945,440 (GRCm39) |
splice site |
probably null |
|
IGL02307:Col16a1
|
APN |
4 |
129,952,802 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02731:Col16a1
|
APN |
4 |
129,947,323 (GRCm39) |
unclassified |
probably benign |
|
IGL02742:Col16a1
|
APN |
4 |
129,955,172 (GRCm39) |
unclassified |
probably benign |
|
PIT4520001:Col16a1
|
UTSW |
4 |
129,945,456 (GRCm39) |
missense |
unknown |
|
R0127:Col16a1
|
UTSW |
4 |
129,946,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Col16a1
|
UTSW |
4 |
129,960,889 (GRCm39) |
missense |
unknown |
|
R0131:Col16a1
|
UTSW |
4 |
129,960,889 (GRCm39) |
missense |
unknown |
|
R0132:Col16a1
|
UTSW |
4 |
129,960,889 (GRCm39) |
missense |
unknown |
|
R0299:Col16a1
|
UTSW |
4 |
129,952,111 (GRCm39) |
frame shift |
probably null |
|
R0355:Col16a1
|
UTSW |
4 |
129,952,206 (GRCm39) |
splice site |
probably benign |
|
R0395:Col16a1
|
UTSW |
4 |
129,966,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Col16a1
|
UTSW |
4 |
129,962,268 (GRCm39) |
splice site |
probably benign |
|
R1274:Col16a1
|
UTSW |
4 |
129,991,594 (GRCm39) |
missense |
probably damaging |
0.98 |
R1619:Col16a1
|
UTSW |
4 |
129,992,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Col16a1
|
UTSW |
4 |
129,978,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Col16a1
|
UTSW |
4 |
129,970,850 (GRCm39) |
splice site |
probably null |
|
R1861:Col16a1
|
UTSW |
4 |
129,955,517 (GRCm39) |
unclassified |
probably benign |
|
R1862:Col16a1
|
UTSW |
4 |
129,986,575 (GRCm39) |
critical splice donor site |
probably null |
|
R1981:Col16a1
|
UTSW |
4 |
129,959,236 (GRCm39) |
missense |
unknown |
|
R2265:Col16a1
|
UTSW |
4 |
129,946,711 (GRCm39) |
missense |
probably benign |
0.02 |
R2269:Col16a1
|
UTSW |
4 |
129,946,711 (GRCm39) |
missense |
probably benign |
0.02 |
R2291:Col16a1
|
UTSW |
4 |
129,960,833 (GRCm39) |
missense |
unknown |
|
R3176:Col16a1
|
UTSW |
4 |
129,951,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R3276:Col16a1
|
UTSW |
4 |
129,951,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R3552:Col16a1
|
UTSW |
4 |
129,970,834 (GRCm39) |
missense |
probably benign |
0.10 |
R4049:Col16a1
|
UTSW |
4 |
129,962,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R4241:Col16a1
|
UTSW |
4 |
129,992,843 (GRCm39) |
missense |
probably damaging |
0.98 |
R4327:Col16a1
|
UTSW |
4 |
129,988,344 (GRCm39) |
critical splice donor site |
probably null |
|
R4591:Col16a1
|
UTSW |
4 |
129,955,592 (GRCm39) |
splice site |
probably null |
|
R4664:Col16a1
|
UTSW |
4 |
129,955,883 (GRCm39) |
unclassified |
probably benign |
|
R4803:Col16a1
|
UTSW |
4 |
129,948,901 (GRCm39) |
unclassified |
probably benign |
|
R4925:Col16a1
|
UTSW |
4 |
129,947,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4961:Col16a1
|
UTSW |
4 |
129,948,272 (GRCm39) |
splice site |
probably null |
|
R5016:Col16a1
|
UTSW |
4 |
129,972,988 (GRCm39) |
missense |
probably benign |
0.31 |
R5027:Col16a1
|
UTSW |
4 |
129,972,988 (GRCm39) |
missense |
probably benign |
0.31 |
R5085:Col16a1
|
UTSW |
4 |
129,947,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Col16a1
|
UTSW |
4 |
129,972,988 (GRCm39) |
missense |
probably benign |
0.31 |
R5089:Col16a1
|
UTSW |
4 |
129,972,988 (GRCm39) |
missense |
probably benign |
0.31 |
R5408:Col16a1
|
UTSW |
4 |
129,986,898 (GRCm39) |
utr 3 prime |
probably benign |
|
R5472:Col16a1
|
UTSW |
4 |
129,986,564 (GRCm39) |
utr 3 prime |
probably benign |
|
R5564:Col16a1
|
UTSW |
4 |
129,947,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5597:Col16a1
|
UTSW |
4 |
129,952,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5703:Col16a1
|
UTSW |
4 |
129,947,092 (GRCm39) |
missense |
probably damaging |
0.96 |
R6054:Col16a1
|
UTSW |
4 |
129,955,515 (GRCm39) |
unclassified |
probably benign |
|
R6226:Col16a1
|
UTSW |
4 |
129,948,882 (GRCm39) |
unclassified |
probably benign |
|
R6362:Col16a1
|
UTSW |
4 |
129,959,983 (GRCm39) |
missense |
unknown |
|
R6448:Col16a1
|
UTSW |
4 |
129,952,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R6449:Col16a1
|
UTSW |
4 |
129,960,486 (GRCm39) |
missense |
unknown |
|
R6502:Col16a1
|
UTSW |
4 |
129,949,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Col16a1
|
UTSW |
4 |
129,953,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R6969:Col16a1
|
UTSW |
4 |
129,986,880 (GRCm39) |
utr 3 prime |
probably benign |
|
R7086:Col16a1
|
UTSW |
4 |
129,946,773 (GRCm39) |
splice site |
probably null |
|
R7375:Col16a1
|
UTSW |
4 |
129,959,294 (GRCm39) |
missense |
unknown |
|
R7703:Col16a1
|
UTSW |
4 |
129,990,295 (GRCm39) |
missense |
unknown |
|
R7808:Col16a1
|
UTSW |
4 |
129,967,057 (GRCm39) |
missense |
unknown |
|
R7904:Col16a1
|
UTSW |
4 |
129,948,001 (GRCm39) |
nonsense |
probably null |
|
R7936:Col16a1
|
UTSW |
4 |
129,990,664 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7981:Col16a1
|
UTSW |
4 |
129,980,347 (GRCm39) |
critical splice donor site |
probably null |
|
R8161:Col16a1
|
UTSW |
4 |
129,954,262 (GRCm39) |
missense |
unknown |
|
R8178:Col16a1
|
UTSW |
4 |
129,947,270 (GRCm39) |
missense |
unknown |
|
R8266:Col16a1
|
UTSW |
4 |
129,959,224 (GRCm39) |
missense |
unknown |
|
R8312:Col16a1
|
UTSW |
4 |
129,948,244 (GRCm39) |
missense |
unknown |
|
R8714:Col16a1
|
UTSW |
4 |
129,947,961 (GRCm39) |
missense |
unknown |
|
R9011:Col16a1
|
UTSW |
4 |
129,946,652 (GRCm39) |
missense |
unknown |
|
R9088:Col16a1
|
UTSW |
4 |
129,971,016 (GRCm39) |
missense |
unknown |
|
RF014:Col16a1
|
UTSW |
4 |
129,986,860 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1176:Col16a1
|
UTSW |
4 |
129,966,671 (GRCm39) |
missense |
unknown |
|
|