Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
A |
G |
4: 144,400,361 (GRCm39) |
V139A |
probably benign |
Het |
Aass |
A |
T |
6: 23,097,195 (GRCm39) |
Y41* |
probably null |
Het |
AI429214 |
G |
A |
8: 37,461,268 (GRCm39) |
V139I |
probably benign |
Het |
Cacna1a |
G |
A |
8: 85,365,426 (GRCm39) |
A2190T |
probably benign |
Het |
Cstpp1 |
A |
G |
2: 91,107,343 (GRCm39) |
Y320H |
probably benign |
Het |
Cutc |
T |
C |
19: 43,744,113 (GRCm39) |
V38A |
probably benign |
Het |
Cxcl10 |
G |
T |
5: 92,495,230 (GRCm39) |
P98H |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,396,003 (GRCm39) |
S822P |
possibly damaging |
Het |
Dusp19 |
T |
C |
2: 80,454,631 (GRCm39) |
L117P |
probably damaging |
Het |
Emc3 |
A |
G |
6: 113,492,868 (GRCm39) |
F261S |
probably damaging |
Het |
Ephx2 |
T |
C |
14: 66,344,725 (GRCm39) |
T200A |
probably benign |
Het |
Eri1 |
A |
C |
8: 35,945,792 (GRCm39) |
D164E |
probably damaging |
Het |
Ethe1 |
T |
C |
7: 24,305,727 (GRCm39) |
I158T |
probably damaging |
Het |
Fancm |
C |
T |
12: 65,167,331 (GRCm39) |
R1547C |
probably damaging |
Het |
Fer1l4 |
T |
A |
2: 155,890,143 (GRCm39) |
T261S |
probably damaging |
Het |
Fyb2 |
A |
G |
4: 104,802,652 (GRCm39) |
R185G |
probably benign |
Het |
Gabrp |
A |
T |
11: 33,504,464 (GRCm39) |
S284T |
possibly damaging |
Het |
Gga2 |
G |
A |
7: 121,590,845 (GRCm39) |
R488* |
probably null |
Het |
Gm9758 |
A |
G |
5: 14,962,230 (GRCm39) |
L126S |
probably damaging |
Het |
Gse1 |
T |
C |
8: 121,294,542 (GRCm39) |
F290L |
probably damaging |
Het |
Hdgfl1 |
A |
G |
13: 26,954,068 (GRCm39) |
S2P |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Huwe1 |
A |
G |
X: 150,669,993 (GRCm39) |
K1482R |
probably benign |
Het |
Lama2 |
A |
T |
10: 27,063,869 (GRCm39) |
W1307R |
probably damaging |
Het |
Mbl1 |
T |
A |
14: 40,875,555 (GRCm39) |
L3Q |
unknown |
Het |
Mepe |
G |
T |
5: 104,485,151 (GRCm39) |
R97L |
probably benign |
Het |
Minpp1 |
T |
A |
19: 32,463,747 (GRCm39) |
M136K |
possibly damaging |
Het |
Mrgprb1 |
T |
A |
7: 48,097,070 (GRCm39) |
I281F |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,349,207 (GRCm39) |
I1374V |
probably benign |
Het |
Or14j8 |
A |
G |
17: 38,263,273 (GRCm39) |
I214T |
probably damaging |
Het |
Or4c12 |
A |
G |
2: 89,773,790 (GRCm39) |
L223S |
probably damaging |
Het |
Or52e19b |
A |
T |
7: 103,032,825 (GRCm39) |
I128N |
probably damaging |
Het |
Or8g34 |
C |
T |
9: 39,373,387 (GRCm39) |
S217F |
probably damaging |
Het |
Or8g37 |
G |
T |
9: 39,730,939 (GRCm39) |
M1I |
probably null |
Het |
Pamr1 |
T |
G |
2: 102,464,766 (GRCm39) |
V305G |
probably benign |
Het |
Pcbp3 |
T |
C |
10: 76,625,670 (GRCm39) |
T125A |
probably benign |
Het |
Peli2 |
G |
A |
14: 48,490,130 (GRCm39) |
E201K |
possibly damaging |
Het |
Pitpnm3 |
T |
C |
11: 71,941,894 (GRCm39) |
E971G |
possibly damaging |
Het |
Pkdrej |
A |
G |
15: 85,702,774 (GRCm39) |
V1054A |
probably damaging |
Het |
Plcb1 |
G |
A |
2: 135,175,429 (GRCm39) |
|
probably benign |
Het |
Prpf40a |
T |
C |
2: 53,042,971 (GRCm39) |
K480E |
probably damaging |
Het |
Psd3 |
A |
G |
8: 68,413,135 (GRCm39) |
I465T |
possibly damaging |
Het |
Pskh1 |
C |
T |
8: 106,656,352 (GRCm39) |
R343W |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,007,371 (GRCm39) |
T1645S |
probably damaging |
Het |
Rasal1 |
T |
C |
5: 120,808,416 (GRCm39) |
F483L |
probably damaging |
Het |
Rbm28 |
T |
C |
6: 29,155,023 (GRCm39) |
|
probably benign |
Het |
Recql |
G |
A |
6: 142,304,612 (GRCm39) |
|
probably benign |
Het |
Rnf40 |
T |
C |
7: 127,196,332 (GRCm39) |
V760A |
probably damaging |
Het |
Rp1l1 |
A |
T |
14: 64,268,085 (GRCm39) |
R1224W |
probably benign |
Het |
Rpgrip1 |
T |
C |
14: 52,378,056 (GRCm39) |
V468A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,750,509 (GRCm39) |
I1921F |
possibly damaging |
Het |
Sirpa |
G |
A |
2: 129,435,558 (GRCm39) |
G9D |
unknown |
Het |
Slc28a2b |
A |
T |
2: 122,348,988 (GRCm39) |
T305S |
possibly damaging |
Het |
Slc40a1 |
A |
C |
1: 45,948,699 (GRCm39) |
V527G |
probably damaging |
Het |
Smarca4 |
T |
A |
9: 21,547,497 (GRCm39) |
M260K |
probably benign |
Het |
Smarca5 |
A |
T |
8: 81,460,379 (GRCm39) |
M119K |
probably benign |
Het |
Smg1 |
A |
G |
7: 117,758,887 (GRCm39) |
V2206A |
unknown |
Het |
Sp4 |
A |
T |
12: 118,225,624 (GRCm39) |
V580D |
possibly damaging |
Het |
Spata31d1c |
G |
A |
13: 65,182,376 (GRCm39) |
C75Y |
probably damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Srcap |
T |
C |
7: 127,152,395 (GRCm39) |
S2220P |
probably benign |
Het |
Stra6 |
G |
T |
9: 58,059,265 (GRCm39) |
V543F |
possibly damaging |
Het |
Tenm4 |
T |
A |
7: 96,523,335 (GRCm39) |
F1626I |
probably benign |
Het |
Tjp1 |
T |
C |
7: 64,952,810 (GRCm39) |
N1508S |
probably benign |
Het |
Trrap |
T |
A |
5: 144,782,348 (GRCm39) |
L3298Q |
probably damaging |
Het |
Tsn |
A |
G |
1: 118,232,470 (GRCm39) |
L135P |
probably damaging |
Het |
Ttl |
A |
T |
2: 128,910,778 (GRCm39) |
H54L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,660,251 (GRCm39) |
T12110S |
unknown |
Het |
Uba6 |
T |
C |
5: 86,296,772 (GRCm39) |
I306V |
probably null |
Het |
Ubap2 |
A |
G |
4: 41,223,425 (GRCm39) |
S204P |
possibly damaging |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Ush2a |
A |
T |
1: 187,995,231 (GRCm39) |
M1L |
probably benign |
Het |
Vmn1r159 |
C |
A |
7: 22,542,559 (GRCm39) |
V158F |
probably benign |
Het |
Wif1 |
A |
G |
10: 120,932,621 (GRCm39) |
H333R |
possibly damaging |
Het |
Zfp282 |
T |
A |
6: 47,881,760 (GRCm39) |
N482K |
probably benign |
Het |
|
Other mutations in Map3k6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00922:Map3k6
|
APN |
4 |
132,970,355 (GRCm39) |
splice site |
probably benign |
|
IGL01060:Map3k6
|
APN |
4 |
132,974,613 (GRCm39) |
splice site |
probably null |
|
IGL01116:Map3k6
|
APN |
4 |
132,974,439 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01341:Map3k6
|
APN |
4 |
132,975,371 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02383:Map3k6
|
APN |
4 |
132,973,932 (GRCm39) |
splice site |
probably null |
|
IGL03090:Map3k6
|
APN |
4 |
132,970,677 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03096:Map3k6
|
APN |
4 |
132,978,656 (GRCm39) |
nonsense |
probably null |
|
IGL03149:Map3k6
|
APN |
4 |
132,976,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Map3k6
|
UTSW |
4 |
132,971,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Map3k6
|
UTSW |
4 |
132,978,257 (GRCm39) |
missense |
probably benign |
|
R0189:Map3k6
|
UTSW |
4 |
132,974,252 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0368:Map3k6
|
UTSW |
4 |
132,979,970 (GRCm39) |
missense |
probably benign |
0.23 |
R0417:Map3k6
|
UTSW |
4 |
132,975,393 (GRCm39) |
nonsense |
probably null |
|
R0595:Map3k6
|
UTSW |
4 |
132,968,574 (GRCm39) |
missense |
probably damaging |
0.98 |
R0597:Map3k6
|
UTSW |
4 |
132,972,863 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0699:Map3k6
|
UTSW |
4 |
132,975,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1099:Map3k6
|
UTSW |
4 |
132,974,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R1113:Map3k6
|
UTSW |
4 |
132,973,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1308:Map3k6
|
UTSW |
4 |
132,973,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1607:Map3k6
|
UTSW |
4 |
132,979,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R2217:Map3k6
|
UTSW |
4 |
132,973,983 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3734:Map3k6
|
UTSW |
4 |
132,975,707 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3735:Map3k6
|
UTSW |
4 |
132,973,683 (GRCm39) |
missense |
probably benign |
0.21 |
R3743:Map3k6
|
UTSW |
4 |
132,972,384 (GRCm39) |
missense |
probably benign |
0.26 |
R4244:Map3k6
|
UTSW |
4 |
132,979,258 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4245:Map3k6
|
UTSW |
4 |
132,979,258 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4465:Map3k6
|
UTSW |
4 |
132,973,644 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4482:Map3k6
|
UTSW |
4 |
132,970,710 (GRCm39) |
missense |
probably benign |
0.00 |
R4827:Map3k6
|
UTSW |
4 |
132,976,160 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5092:Map3k6
|
UTSW |
4 |
132,979,054 (GRCm39) |
missense |
probably benign |
0.00 |
R5110:Map3k6
|
UTSW |
4 |
132,974,859 (GRCm39) |
intron |
probably benign |
|
R5258:Map3k6
|
UTSW |
4 |
132,974,953 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5369:Map3k6
|
UTSW |
4 |
132,974,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Map3k6
|
UTSW |
4 |
132,972,855 (GRCm39) |
missense |
probably damaging |
0.99 |
R5648:Map3k6
|
UTSW |
4 |
132,970,646 (GRCm39) |
missense |
probably benign |
0.25 |
R6102:Map3k6
|
UTSW |
4 |
132,974,442 (GRCm39) |
critical splice donor site |
probably null |
|
R6144:Map3k6
|
UTSW |
4 |
132,972,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Map3k6
|
UTSW |
4 |
132,977,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R6511:Map3k6
|
UTSW |
4 |
132,975,389 (GRCm39) |
missense |
probably damaging |
0.98 |
R6522:Map3k6
|
UTSW |
4 |
132,977,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6706:Map3k6
|
UTSW |
4 |
132,978,250 (GRCm39) |
nonsense |
probably null |
|
R6874:Map3k6
|
UTSW |
4 |
132,977,967 (GRCm39) |
missense |
probably benign |
0.02 |
R7069:Map3k6
|
UTSW |
4 |
132,979,023 (GRCm39) |
missense |
probably benign |
0.01 |
R7216:Map3k6
|
UTSW |
4 |
132,974,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R7417:Map3k6
|
UTSW |
4 |
132,975,707 (GRCm39) |
missense |
probably benign |
0.43 |
R7538:Map3k6
|
UTSW |
4 |
132,979,238 (GRCm39) |
missense |
probably benign |
|
R7569:Map3k6
|
UTSW |
4 |
132,977,388 (GRCm39) |
missense |
probably benign |
0.04 |
R8003:Map3k6
|
UTSW |
4 |
132,976,193 (GRCm39) |
missense |
probably benign |
0.05 |
R8407:Map3k6
|
UTSW |
4 |
132,974,904 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8939:Map3k6
|
UTSW |
4 |
132,979,954 (GRCm39) |
unclassified |
probably benign |
|
R9285:Map3k6
|
UTSW |
4 |
132,972,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R9308:Map3k6
|
UTSW |
4 |
132,970,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:Map3k6
|
UTSW |
4 |
132,968,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Map3k6
|
UTSW |
4 |
132,968,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R9573:Map3k6
|
UTSW |
4 |
132,979,774 (GRCm39) |
missense |
probably damaging |
0.99 |
R9677:Map3k6
|
UTSW |
4 |
132,968,427 (GRCm39) |
missense |
probably benign |
0.04 |
R9682:Map3k6
|
UTSW |
4 |
132,975,419 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9745:Map3k6
|
UTSW |
4 |
132,979,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R9751:Map3k6
|
UTSW |
4 |
132,979,168 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1088:Map3k6
|
UTSW |
4 |
132,972,377 (GRCm39) |
missense |
probably damaging |
0.99 |
|