Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
A |
G |
12: 31,234,914 (GRCm39) |
|
noncoding transcript |
Het |
Adamts8 |
T |
A |
9: 30,862,673 (GRCm39) |
W86R |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,994,508 (GRCm39) |
|
probably null |
Het |
Adipor2 |
A |
T |
6: 119,338,804 (GRCm39) |
W150R |
probably damaging |
Het |
Aff4 |
T |
A |
11: 53,263,351 (GRCm39) |
S124T |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,982,260 (GRCm39) |
K1181N |
probably damaging |
Het |
Alkbh5 |
A |
G |
11: 60,429,873 (GRCm39) |
I209V |
probably benign |
Het |
Ankrd11 |
T |
C |
8: 123,619,463 (GRCm39) |
E1442G |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,297 (GRCm39) |
D162E |
probably benign |
Het |
Asic3 |
G |
A |
5: 24,618,819 (GRCm39) |
G37E |
probably damaging |
Het |
AU040320 |
A |
T |
4: 126,685,824 (GRCm39) |
K133N |
possibly damaging |
Het |
C1qtnf7 |
A |
G |
5: 43,766,481 (GRCm39) |
S34G |
probably benign |
Het |
Ccdc148 |
T |
A |
2: 58,796,374 (GRCm39) |
R463* |
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,824,455 (GRCm39) |
R329G |
probably damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,263 (GRCm39) |
I142T |
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,763,454 (GRCm39) |
P114S |
probably damaging |
Het |
Chst10 |
A |
G |
1: 38,904,772 (GRCm39) |
I311T |
probably damaging |
Het |
Cpne9 |
T |
C |
6: 113,271,698 (GRCm39) |
Y353H |
probably damaging |
Het |
Cubn |
G |
T |
2: 13,330,099 (GRCm39) |
A2594E |
possibly damaging |
Het |
Cyp3a13 |
T |
C |
5: 137,903,827 (GRCm39) |
N277S |
possibly damaging |
Het |
Dctn4 |
A |
G |
18: 60,671,478 (GRCm39) |
T117A |
probably damaging |
Het |
Ddah1 |
A |
T |
3: 145,559,029 (GRCm39) |
K96* |
probably null |
Het |
Ddx5 |
A |
C |
11: 106,675,711 (GRCm39) |
D326E |
probably benign |
Het |
Dlg2 |
T |
C |
7: 91,617,406 (GRCm39) |
S323P |
probably damaging |
Het |
Dnaaf1 |
C |
T |
8: 120,306,049 (GRCm39) |
H109Y |
probably damaging |
Het |
Dnah8 |
C |
A |
17: 30,914,147 (GRCm39) |
R1098S |
possibly damaging |
Het |
Dnajc13 |
T |
C |
9: 104,091,366 (GRCm39) |
T642A |
probably benign |
Het |
Dnajc18 |
A |
G |
18: 35,813,900 (GRCm39) |
S290P |
possibly damaging |
Het |
Dscam |
T |
A |
16: 96,602,453 (GRCm39) |
H663L |
possibly damaging |
Het |
Emc1 |
A |
G |
4: 139,098,248 (GRCm39) |
N740S |
probably damaging |
Het |
Enpp2 |
C |
T |
15: 54,727,208 (GRCm39) |
G541D |
probably damaging |
Het |
Fam234b |
C |
T |
6: 135,205,490 (GRCm39) |
T485I |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,688,989 (GRCm39) |
I773K |
probably benign |
Het |
Fmo4 |
A |
G |
1: 162,621,924 (GRCm39) |
F429S |
possibly damaging |
Het |
Frem1 |
T |
C |
4: 82,930,116 (GRCm39) |
S277G |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,163,810 (GRCm39) |
I221V |
probably benign |
Het |
Helz2 |
T |
C |
2: 180,881,447 (GRCm39) |
E345G |
probably damaging |
Het |
Ifna4 |
G |
T |
4: 88,760,237 (GRCm39) |
R47I |
probably damaging |
Het |
Igsf21 |
C |
A |
4: 139,761,836 (GRCm39) |
A281S |
probably benign |
Het |
Ikzf3 |
T |
A |
11: 98,407,731 (GRCm39) |
I37L |
probably benign |
Het |
Jag1 |
T |
C |
2: 136,957,568 (GRCm39) |
E48G |
probably damaging |
Het |
Jarid2 |
G |
T |
13: 45,001,857 (GRCm39) |
V57F |
probably damaging |
Het |
Kcnj4 |
A |
G |
15: 79,369,605 (GRCm39) |
L125P |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,083,891 (GRCm39) |
K713E |
possibly damaging |
Het |
Layn |
T |
A |
9: 50,968,886 (GRCm39) |
S286C |
probably damaging |
Het |
Lepr |
T |
A |
4: 101,592,878 (GRCm39) |
D164E |
probably benign |
Het |
Macroh2a1 |
A |
T |
13: 56,230,949 (GRCm39) |
S310T |
probably damaging |
Het |
Map3k1 |
T |
C |
13: 111,892,405 (GRCm39) |
H950R |
possibly damaging |
Het |
Map4k5 |
C |
A |
12: 69,852,124 (GRCm39) |
V801L |
possibly damaging |
Het |
Naca |
T |
A |
10: 127,884,157 (GRCm39) |
M2157K |
probably damaging |
Het |
Nav2 |
T |
C |
7: 49,011,952 (GRCm39) |
I61T |
probably damaging |
Het |
Nkx2-5 |
C |
A |
17: 27,058,253 (GRCm39) |
A234S |
probably benign |
Het |
Nol8 |
G |
A |
13: 49,830,264 (GRCm39) |
S1116N |
probably benign |
Het |
Nppa |
T |
C |
4: 148,085,304 (GRCm39) |
S5P |
probably benign |
Het |
Nup210 |
A |
G |
6: 91,030,551 (GRCm39) |
V123A |
possibly damaging |
Het |
Or13a21 |
G |
T |
7: 139,999,286 (GRCm39) |
N133K |
probably benign |
Het |
Osbpl11 |
A |
G |
16: 33,049,455 (GRCm39) |
K604R |
probably damaging |
Het |
Osbpl1a |
C |
T |
18: 13,047,615 (GRCm39) |
S113N |
probably benign |
Het |
P2rx4 |
C |
A |
5: 122,852,602 (GRCm39) |
P92Q |
probably damaging |
Het |
Pde9a |
A |
T |
17: 31,692,136 (GRCm39) |
Q148L |
probably benign |
Het |
Phf21b |
T |
A |
15: 84,689,160 (GRCm39) |
H122L |
probably damaging |
Het |
Pik3ca |
T |
A |
3: 32,515,990 (GRCm39) |
F977I |
probably damaging |
Het |
Potefam1 |
A |
G |
2: 111,055,748 (GRCm39) |
|
probably null |
Het |
Pp2d1 |
T |
G |
17: 53,823,015 (GRCm39) |
K17T |
possibly damaging |
Het |
Ppp4r2 |
A |
G |
6: 100,843,527 (GRCm39) |
E415G |
probably damaging |
Het |
Pramel19 |
T |
A |
4: 101,798,503 (GRCm39) |
L158Q |
probably damaging |
Het |
Prkg1 |
A |
G |
19: 30,556,270 (GRCm39) |
S559P |
probably damaging |
Het |
Prss45 |
A |
T |
9: 110,670,019 (GRCm39) |
Y276F |
possibly damaging |
Het |
Ptk7 |
G |
T |
17: 46,883,517 (GRCm39) |
N849K |
probably damaging |
Het |
Rnf121 |
A |
G |
7: 101,680,782 (GRCm39) |
I125T |
possibly damaging |
Het |
Rnf17 |
A |
G |
14: 56,699,368 (GRCm39) |
N502S |
probably damaging |
Het |
Sap25 |
T |
A |
5: 137,640,622 (GRCm39) |
Y167* |
probably null |
Het |
Sdk2 |
G |
A |
11: 113,720,906 (GRCm39) |
T1341I |
possibly damaging |
Het |
Sgcb |
A |
G |
5: 73,792,896 (GRCm39) |
V302A |
probably benign |
Het |
Skor1 |
T |
A |
9: 63,047,393 (GRCm39) |
M865L |
possibly damaging |
Het |
Slc35g1 |
C |
A |
19: 38,391,665 (GRCm39) |
L316I |
probably benign |
Het |
Slco1a8 |
C |
T |
6: 141,938,243 (GRCm39) |
W225* |
probably null |
Het |
Spint4 |
T |
A |
2: 164,540,568 (GRCm39) |
L33H |
probably damaging |
Het |
Sptlc3 |
A |
T |
2: 139,389,154 (GRCm39) |
D178V |
probably benign |
Het |
Tbc1d2 |
T |
A |
4: 46,606,491 (GRCm39) |
Y818F |
possibly damaging |
Het |
Tbc1d24 |
A |
T |
17: 24,400,197 (GRCm39) |
|
probably null |
Het |
Teddm2 |
C |
T |
1: 153,726,277 (GRCm39) |
W146* |
probably null |
Het |
Ttn |
T |
A |
2: 76,589,338 (GRCm39) |
D12948V |
probably damaging |
Het |
Txndc8 |
T |
C |
4: 58,000,274 (GRCm39) |
T102A |
probably damaging |
Het |
Uxs1 |
G |
A |
1: 43,804,076 (GRCm39) |
Q280* |
probably null |
Het |
Vmn1r167 |
T |
C |
7: 23,204,681 (GRCm39) |
T112A |
possibly damaging |
Het |
Vmn1r195 |
A |
T |
13: 22,463,348 (GRCm39) |
I273L |
probably benign |
Het |
Vmn1r28 |
T |
A |
6: 58,242,217 (GRCm39) |
M20K |
probably benign |
Het |
Vmn1r53 |
G |
A |
6: 90,200,914 (GRCm39) |
L137F |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,709,630 (GRCm39) |
A1859V |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,415,019 (GRCm39) |
H347R |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,235,451 (GRCm39) |
P655S |
probably damaging |
Het |
Zan |
T |
G |
5: 137,418,191 (GRCm39) |
D2969A |
unknown |
Het |
Zbtb24 |
A |
G |
10: 41,331,075 (GRCm39) |
H334R |
probably damaging |
Het |
Zfp108 |
A |
G |
7: 23,959,973 (GRCm39) |
D188G |
probably benign |
Het |
Zfp784 |
A |
T |
7: 5,038,800 (GRCm39) |
C253S |
possibly damaging |
Het |
Zfr |
T |
G |
15: 12,146,458 (GRCm39) |
C336W |
probably 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 |
|
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 |
R7467:Mapkbp1
|
UTSW |
2 |
119,852,669 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|