Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre4 |
G |
A |
17: 56,098,952 (GRCm39) |
V153I |
probably benign |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Aldh16a1 |
A |
G |
7: 44,795,331 (GRCm39) |
Y443H |
probably benign |
Het |
Apbb1 |
A |
G |
7: 105,215,339 (GRCm39) |
V434A |
probably benign |
Het |
Atrip |
A |
G |
9: 108,898,422 (GRCm39) |
M199T |
probably damaging |
Het |
Atxn2 |
T |
C |
5: 121,940,330 (GRCm39) |
|
probably null |
Het |
AU040320 |
A |
G |
4: 126,708,103 (GRCm39) |
T240A |
probably benign |
Het |
Btf3l4 |
A |
T |
4: 108,675,589 (GRCm39) |
|
probably null |
Het |
Ccdc106 |
A |
G |
7: 5,063,325 (GRCm39) |
T277A |
probably damaging |
Het |
Cdk15 |
G |
T |
1: 59,328,938 (GRCm39) |
W282L |
probably null |
Het |
Cflar |
T |
A |
1: 58,765,597 (GRCm39) |
M1K |
probably null |
Het |
Champ1 |
C |
A |
8: 13,928,579 (GRCm39) |
P246T |
possibly damaging |
Het |
Crat |
A |
C |
2: 30,299,994 (GRCm39) |
F129V |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,492,640 (GRCm39) |
N2256S |
|
Het |
Cwh43 |
C |
A |
5: 73,569,311 (GRCm39) |
Q118K |
probably damaging |
Het |
Daam1 |
A |
T |
12: 72,032,580 (GRCm39) |
K949* |
probably null |
Het |
Ddn |
C |
G |
15: 98,703,247 (GRCm39) |
E682Q |
possibly damaging |
Het |
Des |
T |
A |
1: 75,339,605 (GRCm39) |
M321K |
possibly damaging |
Het |
Dnm2 |
T |
C |
9: 21,392,672 (GRCm39) |
V460A |
probably damaging |
Het |
Dst |
G |
A |
1: 34,230,236 (GRCm39) |
E2610K |
probably benign |
Het |
Efr3a |
C |
T |
15: 65,729,360 (GRCm39) |
T660I |
possibly damaging |
Het |
Eogt |
T |
C |
6: 97,119,794 (GRCm39) |
E138G |
probably benign |
Het |
Epha8 |
G |
A |
4: 136,658,399 (GRCm39) |
A992V |
possibly damaging |
Het |
Exoc2 |
A |
T |
13: 31,109,716 (GRCm39) |
D217E |
probably damaging |
Het |
Fam222b |
T |
C |
11: 78,045,173 (GRCm39) |
S245P |
probably damaging |
Het |
Fbxo45 |
T |
C |
16: 32,057,339 (GRCm39) |
Y185C |
probably damaging |
Het |
Fbxo47 |
T |
C |
11: 97,755,993 (GRCm39) |
T170A |
probably benign |
Het |
Fbxw26 |
A |
T |
9: 109,561,765 (GRCm39) |
V143E |
probably benign |
Het |
Foxb2 |
T |
C |
19: 16,851,004 (GRCm39) |
M1V |
probably null |
Het |
Gm11596 |
C |
A |
11: 99,683,962 (GRCm39) |
V53L |
unknown |
Het |
Gm47791 |
A |
G |
1: 82,748,547 (GRCm39) |
*140Q |
probably null |
Het |
Gpr179 |
C |
T |
11: 97,226,115 (GRCm39) |
M2013I |
probably benign |
Het |
Hck |
T |
A |
2: 152,971,850 (GRCm39) |
L137* |
probably null |
Het |
Hectd4 |
T |
A |
5: 121,462,024 (GRCm39) |
C964S |
possibly damaging |
Het |
Hexa |
T |
C |
9: 59,464,683 (GRCm39) |
|
probably null |
Het |
Ifna12 |
C |
A |
4: 88,521,502 (GRCm39) |
S15I |
possibly damaging |
Het |
Kif18b |
C |
A |
11: 102,807,234 (GRCm39) |
V34L |
probably damaging |
Het |
Kif18b |
A |
T |
11: 102,803,174 (GRCm39) |
|
probably null |
Het |
Kifap3 |
A |
T |
1: 163,643,402 (GRCm39) |
H209L |
probably benign |
Het |
Klhl1 |
A |
T |
14: 96,360,713 (GRCm39) |
D712E |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,513,530 (GRCm39) |
D3088G |
probably damaging |
Het |
Mageb3 |
A |
G |
2: 121,784,953 (GRCm39) |
Y250H |
probably damaging |
Het |
Manba |
G |
T |
3: 135,250,562 (GRCm39) |
E396D |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,155,448 (GRCm39) |
H41R |
probably benign |
Het |
Mis18a |
T |
G |
16: 90,516,866 (GRCm39) |
M179L |
probably benign |
Het |
Mmp25 |
C |
G |
17: 23,863,756 (GRCm39) |
G25R |
possibly damaging |
Het |
Mmp3 |
A |
G |
9: 7,447,621 (GRCm39) |
D202G |
possibly damaging |
Het |
Mmp3 |
C |
T |
9: 7,450,125 (GRCm39) |
P286S |
probably benign |
Het |
Mrgpra2b |
G |
A |
7: 47,114,277 (GRCm39) |
H152Y |
possibly damaging |
Het |
Mslnl |
A |
T |
17: 25,955,895 (GRCm39) |
M1L |
probably benign |
Het |
Myo1d |
G |
A |
11: 80,477,743 (GRCm39) |
T880I |
probably damaging |
Het |
Ncaph |
T |
A |
2: 126,975,795 (GRCm39) |
|
probably benign |
Het |
Nln |
T |
C |
13: 104,161,530 (GRCm39) |
D680G |
possibly damaging |
Het |
Noct |
C |
T |
3: 51,132,622 (GRCm39) |
A33V |
probably benign |
Het |
Nolc1 |
A |
G |
19: 46,070,773 (GRCm39) |
T325A |
unknown |
Het |
Nr2e3 |
A |
G |
9: 59,856,434 (GRCm39) |
|
probably null |
Het |
Nrg2 |
T |
A |
18: 36,155,459 (GRCm39) |
H450L |
probably benign |
Het |
Or13a21 |
T |
C |
7: 139,999,287 (GRCm39) |
N133S |
probably benign |
Het |
Or2t43 |
A |
C |
11: 58,457,288 (GRCm39) |
N294K |
possibly damaging |
Het |
Or5ak24 |
T |
G |
2: 85,261,171 (GRCm39) |
M1L |
possibly damaging |
Het |
Or5an1 |
T |
A |
19: 12,260,839 (GRCm39) |
C142* |
probably null |
Het |
Or6b3 |
T |
A |
1: 92,439,570 (GRCm39) |
Y60F |
possibly damaging |
Het |
Pank2 |
T |
A |
2: 131,115,967 (GRCm39) |
N128K |
possibly damaging |
Het |
Pcdha3 |
T |
C |
18: 37,080,584 (GRCm39) |
V442A |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,659,792 (GRCm39) |
S252T |
probably damaging |
Het |
Pfpl |
T |
C |
19: 12,405,878 (GRCm39) |
L43S |
probably damaging |
Het |
Pigu |
T |
A |
2: 155,141,009 (GRCm39) |
I295F |
probably damaging |
Het |
Piwil4 |
T |
C |
9: 14,616,337 (GRCm39) |
Y673C |
probably damaging |
Het |
Pls1 |
A |
G |
9: 95,651,166 (GRCm39) |
Y414H |
possibly damaging |
Het |
Ppp1r13l |
A |
T |
7: 19,105,305 (GRCm39) |
Q359L |
probably damaging |
Het |
Ppp2r5c |
A |
G |
12: 110,519,317 (GRCm39) |
Y263C |
probably damaging |
Het |
Prrc2c |
A |
T |
1: 162,504,932 (GRCm39) |
S2638R |
possibly damaging |
Het |
Prss39 |
T |
A |
1: 34,538,473 (GRCm39) |
|
probably null |
Het |
Psmd1 |
G |
A |
1: 86,044,355 (GRCm39) |
V648M |
probably damaging |
Het |
Rad50 |
T |
C |
11: 53,545,735 (GRCm39) |
D1196G |
probably damaging |
Het |
Rfx1 |
T |
C |
8: 84,800,542 (GRCm39) |
Y48H |
possibly damaging |
Het |
Rgs20 |
A |
G |
1: 4,982,553 (GRCm39) |
I305T |
probably benign |
Het |
Rpl9 |
T |
C |
5: 65,548,310 (GRCm39) |
T9A |
probably benign |
Het |
Samd4 |
A |
G |
14: 47,325,313 (GRCm39) |
N598D |
probably benign |
Het |
Sema7a |
T |
C |
9: 57,868,705 (GRCm39) |
Y606H |
probably damaging |
Het |
Sf3b3 |
A |
G |
8: 111,538,088 (GRCm39) |
S1150P |
possibly damaging |
Het |
Sirt1 |
T |
C |
10: 63,157,929 (GRCm39) |
N495S |
probably benign |
Het |
Slc17a3 |
T |
C |
13: 24,030,950 (GRCm39) |
|
probably null |
Het |
Slc25a22 |
T |
C |
7: 141,013,889 (GRCm39) |
T24A |
probably benign |
Het |
Slc30a9 |
T |
C |
5: 67,502,987 (GRCm39) |
I363T |
probably benign |
Het |
Srbd1 |
A |
G |
17: 86,406,702 (GRCm39) |
V561A |
probably damaging |
Het |
Srgap1 |
C |
A |
10: 121,691,344 (GRCm39) |
E297* |
probably null |
Het |
Srgap2 |
T |
C |
1: 131,220,405 (GRCm39) |
S896G |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,463,237 (GRCm39) |
C3730R |
probably damaging |
Het |
Stat2 |
T |
A |
10: 128,113,772 (GRCm39) |
|
probably null |
Het |
Tcof1 |
T |
C |
18: 60,964,977 (GRCm39) |
K581E |
unknown |
Het |
Tdpoz6 |
T |
A |
3: 93,600,265 (GRCm39) |
T35S |
probably benign |
Het |
Thbs1 |
T |
C |
2: 117,948,681 (GRCm39) |
S446P |
probably damaging |
Het |
Thsd7a |
T |
C |
6: 12,331,584 (GRCm39) |
Y1330C |
|
Het |
Tmem121 |
C |
A |
12: 113,152,690 (GRCm39) |
P303T |
probably benign |
Het |
Tmem87b |
T |
A |
2: 128,691,071 (GRCm39) |
|
probably null |
Het |
Tmem98 |
A |
T |
11: 80,711,011 (GRCm39) |
|
probably null |
Het |
Trpm3 |
T |
A |
19: 22,955,698 (GRCm39) |
I1091N |
possibly damaging |
Het |
Urb2 |
A |
G |
8: 124,755,250 (GRCm39) |
E319G |
probably benign |
Het |
Vmn1r170 |
A |
T |
7: 23,306,320 (GRCm39) |
M241L |
not run |
Het |
Vmn1r238 |
T |
C |
18: 3,123,393 (GRCm39) |
N7S |
probably benign |
Het |
Wdr6 |
T |
C |
9: 108,450,201 (GRCm39) |
H1109R |
probably benign |
Het |
Zdhhc13 |
T |
C |
7: 48,454,156 (GRCm39) |
V193A |
probably benign |
Het |
Zfp354c |
T |
C |
11: 50,706,253 (GRCm39) |
Y274C |
probably damaging |
Het |
Zfp738 |
T |
A |
13: 67,821,080 (GRCm39) |
E89V |
probably benign |
Het |
Zswim3 |
T |
A |
2: 164,661,795 (GRCm39) |
F92I |
possibly damaging |
Het |
|
Other mutations in Mapkbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01102:Mapkbp1
|
APN |
2 |
119,852,339 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01309:Mapkbp1
|
APN |
2 |
119,849,423 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01728:Mapkbp1
|
APN |
2 |
119,854,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01808:Mapkbp1
|
APN |
2 |
119,853,650 (GRCm39) |
splice site |
probably null |
|
IGL02185:Mapkbp1
|
APN |
2 |
119,845,144 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02421:Mapkbp1
|
APN |
2 |
119,850,136 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02691:Mapkbp1
|
APN |
2 |
119,803,655 (GRCm39) |
splice site |
probably benign |
|
IGL03146:Mapkbp1
|
APN |
2 |
119,828,955 (GRCm39) |
splice site |
probably benign |
|
IGL03387:Mapkbp1
|
APN |
2 |
119,828,979 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03054:Mapkbp1
|
UTSW |
2 |
119,845,881 (GRCm39) |
missense |
probably damaging |
0.97 |
R0118:Mapkbp1
|
UTSW |
2 |
119,855,696 (GRCm39) |
missense |
probably benign |
0.00 |
R0393:Mapkbp1
|
UTSW |
2 |
119,843,384 (GRCm39) |
splice site |
probably null |
|
R0463:Mapkbp1
|
UTSW |
2 |
119,853,632 (GRCm39) |
missense |
probably benign |
0.01 |
R0788:Mapkbp1
|
UTSW |
2 |
119,854,482 (GRCm39) |
missense |
probably benign |
0.02 |
R0928:Mapkbp1
|
UTSW |
2 |
119,845,849 (GRCm39) |
missense |
probably benign |
0.00 |
R1104:Mapkbp1
|
UTSW |
2 |
119,841,554 (GRCm39) |
splice site |
probably benign |
|
R1162:Mapkbp1
|
UTSW |
2 |
119,855,799 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1219:Mapkbp1
|
UTSW |
2 |
119,849,831 (GRCm39) |
nonsense |
probably null |
|
R1299:Mapkbp1
|
UTSW |
2 |
119,845,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Mapkbp1
|
UTSW |
2 |
119,844,136 (GRCm39) |
missense |
probably benign |
0.25 |
R1342:Mapkbp1
|
UTSW |
2 |
119,829,015 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1456:Mapkbp1
|
UTSW |
2 |
119,803,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Mapkbp1
|
UTSW |
2 |
119,851,742 (GRCm39) |
missense |
probably benign |
|
R1464:Mapkbp1
|
UTSW |
2 |
119,851,742 (GRCm39) |
missense |
probably benign |
|
R1470:Mapkbp1
|
UTSW |
2 |
119,848,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Mapkbp1
|
UTSW |
2 |
119,848,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R1660:Mapkbp1
|
UTSW |
2 |
119,849,029 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2008:Mapkbp1
|
UTSW |
2 |
119,843,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Mapkbp1
|
UTSW |
2 |
119,845,963 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2371:Mapkbp1
|
UTSW |
2 |
119,841,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Mapkbp1
|
UTSW |
2 |
119,855,071 (GRCm39) |
missense |
probably benign |
0.00 |
R3976:Mapkbp1
|
UTSW |
2 |
119,852,339 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4009:Mapkbp1
|
UTSW |
2 |
119,854,086 (GRCm39) |
missense |
probably benign |
0.00 |
R4183:Mapkbp1
|
UTSW |
2 |
119,848,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R4246:Mapkbp1
|
UTSW |
2 |
119,843,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R4503:Mapkbp1
|
UTSW |
2 |
119,846,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R4513:Mapkbp1
|
UTSW |
2 |
119,854,174 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4517:Mapkbp1
|
UTSW |
2 |
119,855,545 (GRCm39) |
intron |
probably benign |
|
R4742:Mapkbp1
|
UTSW |
2 |
119,847,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Mapkbp1
|
UTSW |
2 |
119,845,982 (GRCm39) |
splice site |
probably benign |
|
R5079:Mapkbp1
|
UTSW |
2 |
119,844,214 (GRCm39) |
missense |
probably damaging |
0.99 |
R5137:Mapkbp1
|
UTSW |
2 |
119,852,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R5255:Mapkbp1
|
UTSW |
2 |
119,847,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R5530:Mapkbp1
|
UTSW |
2 |
119,845,836 (GRCm39) |
missense |
probably benign |
|
R5546:Mapkbp1
|
UTSW |
2 |
119,849,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Mapkbp1
|
UTSW |
2 |
119,803,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Mapkbp1
|
UTSW |
2 |
119,852,201 (GRCm39) |
splice site |
probably null |
|
R5891:Mapkbp1
|
UTSW |
2 |
119,854,413 (GRCm39) |
nonsense |
probably null |
|
R6263:Mapkbp1
|
UTSW |
2 |
119,853,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R6807:Mapkbp1
|
UTSW |
2 |
119,851,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R6890:Mapkbp1
|
UTSW |
2 |
119,846,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R7159:Mapkbp1
|
UTSW |
2 |
119,855,613 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7536:Mapkbp1
|
UTSW |
2 |
119,849,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R7564:Mapkbp1
|
UTSW |
2 |
119,844,232 (GRCm39) |
missense |
probably benign |
0.09 |
R7801:Mapkbp1
|
UTSW |
2 |
119,842,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7886:Mapkbp1
|
UTSW |
2 |
119,843,128 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8095:Mapkbp1
|
UTSW |
2 |
119,848,131 (GRCm39) |
missense |
probably benign |
0.11 |
R8421:Mapkbp1
|
UTSW |
2 |
119,849,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R8548:Mapkbp1
|
UTSW |
2 |
119,854,572 (GRCm39) |
missense |
probably benign |
0.33 |
R8856:Mapkbp1
|
UTSW |
2 |
119,845,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R8971:Mapkbp1
|
UTSW |
2 |
119,850,050 (GRCm39) |
missense |
probably benign |
|
R9007:Mapkbp1
|
UTSW |
2 |
119,850,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R9251:Mapkbp1
|
UTSW |
2 |
119,853,671 (GRCm39) |
missense |
probably benign |
0.00 |
R9255:Mapkbp1
|
UTSW |
2 |
119,843,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R9361:Mapkbp1
|
UTSW |
2 |
119,845,252 (GRCm39) |
missense |
probably benign |
0.02 |
R9587:Mapkbp1
|
UTSW |
2 |
119,847,277 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9685:Mapkbp1
|
UTSW |
2 |
119,851,664 (GRCm39) |
missense |
probably benign |
0.35 |
R9803:Mapkbp1
|
UTSW |
2 |
119,841,256 (GRCm39) |
missense |
probably benign |
0.11 |
|