Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adap1 |
A |
G |
5: 139,293,489 (GRCm39) |
|
probably benign |
Het |
Bnip3 |
A |
G |
7: 138,500,401 (GRCm39) |
|
probably benign |
Het |
Brwd1 |
A |
C |
16: 95,860,852 (GRCm39) |
S311R |
probably damaging |
Het |
C2cd3 |
G |
A |
7: 100,067,729 (GRCm39) |
V871M |
possibly damaging |
Het |
Chd2 |
G |
T |
7: 73,105,267 (GRCm39) |
T192K |
probably damaging |
Het |
Chrna10 |
T |
C |
7: 101,764,264 (GRCm39) |
N40S |
possibly damaging |
Het |
Copb1 |
T |
A |
7: 113,836,643 (GRCm39) |
K366N |
probably damaging |
Het |
Dpysl4 |
T |
G |
7: 138,677,799 (GRCm39) |
I412S |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,153,697 (GRCm39) |
V3505A |
probably benign |
Het |
Fbxo24 |
A |
G |
5: 137,620,256 (GRCm39) |
F101S |
probably damaging |
Het |
Gcnt3 |
T |
C |
9: 69,941,367 (GRCm39) |
I400M |
probably benign |
Het |
Gm2962 |
T |
A |
1: 170,752,908 (GRCm39) |
|
probably benign |
Het |
Gsap |
T |
A |
5: 21,431,227 (GRCm39) |
|
probably benign |
Het |
Hipk1 |
A |
G |
3: 103,670,996 (GRCm39) |
M467T |
probably damaging |
Het |
Hmgb4 |
T |
A |
4: 128,154,518 (GRCm39) |
I17F |
probably damaging |
Het |
Ints15 |
A |
G |
5: 143,299,937 (GRCm39) |
L137P |
probably damaging |
Het |
Kif17 |
T |
G |
4: 138,021,059 (GRCm39) |
S606A |
probably damaging |
Het |
Lypd4 |
A |
G |
7: 24,564,757 (GRCm39) |
L127P |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,862,279 (GRCm39) |
H2605R |
probably benign |
Het |
Mob1b |
G |
A |
5: 88,903,943 (GRCm39) |
|
probably benign |
Het |
Mthfd2l |
A |
T |
5: 91,109,242 (GRCm39) |
H224L |
probably damaging |
Het |
Nectin2 |
T |
C |
7: 19,464,669 (GRCm39) |
|
probably benign |
Het |
Rae1 |
T |
A |
2: 172,844,466 (GRCm39) |
F4I |
unknown |
Het |
Ralgapa2 |
A |
G |
2: 146,254,672 (GRCm39) |
Y821H |
probably benign |
Het |
Sharpin |
G |
T |
15: 76,232,543 (GRCm39) |
P156T |
possibly damaging |
Het |
Slc38a4 |
C |
T |
15: 96,897,510 (GRCm39) |
R435H |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,070,469 (GRCm39) |
V1061A |
probably benign |
Het |
Suclg1 |
A |
G |
6: 73,247,980 (GRCm39) |
T234A |
possibly damaging |
Het |
Tet2 |
T |
C |
3: 133,182,319 (GRCm39) |
Y1215C |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,979,523 (GRCm39) |
|
probably benign |
Het |
Tnpo3 |
T |
C |
6: 29,589,176 (GRCm39) |
E58G |
probably damaging |
Het |
Trp53bp2 |
T |
A |
1: 182,272,283 (GRCm39) |
M464K |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,918,339 (GRCm39) |
S560G |
possibly damaging |
Het |
Unc80 |
T |
C |
1: 66,546,550 (GRCm39) |
S541P |
probably damaging |
Het |
Ushbp1 |
T |
C |
8: 71,847,684 (GRCm39) |
|
probably benign |
Het |
Zfp644 |
T |
G |
5: 106,782,909 (GRCm39) |
E1155A |
probably benign |
Het |
|
Other mutations in Map3k4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Map3k4
|
APN |
17 |
12,451,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01124:Map3k4
|
APN |
17 |
12,474,087 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01125:Map3k4
|
APN |
17 |
12,490,849 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01585:Map3k4
|
APN |
17 |
12,467,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Map3k4
|
APN |
17 |
12,482,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02194:Map3k4
|
APN |
17 |
12,467,882 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02292:Map3k4
|
APN |
17 |
12,454,045 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02326:Map3k4
|
APN |
17 |
12,467,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02388:Map3k4
|
APN |
17 |
12,490,497 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02621:Map3k4
|
APN |
17 |
12,482,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02668:Map3k4
|
APN |
17 |
12,454,840 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02850:Map3k4
|
APN |
17 |
12,490,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Map3k4
|
APN |
17 |
12,491,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Map3k4
|
APN |
17 |
12,457,045 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03238:Map3k4
|
APN |
17 |
12,490,045 (GRCm39) |
missense |
probably benign |
0.10 |
ANU74:Map3k4
|
UTSW |
17 |
12,451,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Map3k4
|
UTSW |
17 |
12,457,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0128:Map3k4
|
UTSW |
17 |
12,466,950 (GRCm39) |
missense |
probably damaging |
0.99 |
R0183:Map3k4
|
UTSW |
17 |
12,454,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Map3k4
|
UTSW |
17 |
12,489,902 (GRCm39) |
frame shift |
probably null |
|
R0355:Map3k4
|
UTSW |
17 |
12,473,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Map3k4
|
UTSW |
17 |
12,476,928 (GRCm39) |
splice site |
probably benign |
|
R1103:Map3k4
|
UTSW |
17 |
12,455,950 (GRCm39) |
splice site |
probably null |
|
R1446:Map3k4
|
UTSW |
17 |
12,475,681 (GRCm39) |
nonsense |
probably null |
|
R1542:Map3k4
|
UTSW |
17 |
12,454,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R1713:Map3k4
|
UTSW |
17 |
12,468,458 (GRCm39) |
missense |
probably benign |
0.39 |
R1777:Map3k4
|
UTSW |
17 |
12,490,617 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1797:Map3k4
|
UTSW |
17 |
12,482,906 (GRCm39) |
missense |
probably benign |
0.30 |
R1997:Map3k4
|
UTSW |
17 |
12,473,882 (GRCm39) |
critical splice donor site |
probably null |
|
R2042:Map3k4
|
UTSW |
17 |
12,496,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R2878:Map3k4
|
UTSW |
17 |
12,482,954 (GRCm39) |
missense |
probably benign |
0.00 |
R2939:Map3k4
|
UTSW |
17 |
12,480,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R2940:Map3k4
|
UTSW |
17 |
12,480,157 (GRCm39) |
missense |
probably damaging |
0.98 |
R3405:Map3k4
|
UTSW |
17 |
12,475,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R3930:Map3k4
|
UTSW |
17 |
12,454,880 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4291:Map3k4
|
UTSW |
17 |
12,474,147 (GRCm39) |
missense |
probably benign |
0.08 |
R4410:Map3k4
|
UTSW |
17 |
12,467,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Map3k4
|
UTSW |
17 |
12,451,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Map3k4
|
UTSW |
17 |
12,482,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Map3k4
|
UTSW |
17 |
12,451,851 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4730:Map3k4
|
UTSW |
17 |
12,467,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R4832:Map3k4
|
UTSW |
17 |
12,490,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R4896:Map3k4
|
UTSW |
17 |
12,490,906 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4934:Map3k4
|
UTSW |
17 |
12,490,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Map3k4
|
UTSW |
17 |
12,468,382 (GRCm39) |
critical splice donor site |
probably null |
|
R4980:Map3k4
|
UTSW |
17 |
12,490,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Map3k4
|
UTSW |
17 |
12,451,321 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5337:Map3k4
|
UTSW |
17 |
12,490,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R5356:Map3k4
|
UTSW |
17 |
12,466,195 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5550:Map3k4
|
UTSW |
17 |
12,462,445 (GRCm39) |
nonsense |
probably null |
|
R5824:Map3k4
|
UTSW |
17 |
12,448,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Map3k4
|
UTSW |
17 |
12,490,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Map3k4
|
UTSW |
17 |
12,482,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6380:Map3k4
|
UTSW |
17 |
12,490,954 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6383:Map3k4
|
UTSW |
17 |
12,468,470 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6571:Map3k4
|
UTSW |
17 |
12,461,579 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6584:Map3k4
|
UTSW |
17 |
12,479,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Map3k4
|
UTSW |
17 |
12,490,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Map3k4
|
UTSW |
17 |
12,451,297 (GRCm39) |
critical splice donor site |
probably null |
|
R6909:Map3k4
|
UTSW |
17 |
12,489,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Map3k4
|
UTSW |
17 |
12,479,456 (GRCm39) |
nonsense |
probably null |
|
R6970:Map3k4
|
UTSW |
17 |
12,467,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7120:Map3k4
|
UTSW |
17 |
12,490,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7253:Map3k4
|
UTSW |
17 |
12,490,955 (GRCm39) |
missense |
probably benign |
0.00 |
R7267:Map3k4
|
UTSW |
17 |
12,490,536 (GRCm39) |
nonsense |
probably null |
|
R7322:Map3k4
|
UTSW |
17 |
12,489,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R7522:Map3k4
|
UTSW |
17 |
12,480,219 (GRCm39) |
missense |
probably benign |
0.39 |
R7554:Map3k4
|
UTSW |
17 |
12,451,301 (GRCm39) |
nonsense |
probably null |
|
R7554:Map3k4
|
UTSW |
17 |
12,451,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R7681:Map3k4
|
UTSW |
17 |
12,537,430 (GRCm39) |
missense |
unknown |
|
R7734:Map3k4
|
UTSW |
17 |
12,482,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Map3k4
|
UTSW |
17 |
12,490,030 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8013:Map3k4
|
UTSW |
17 |
12,489,918 (GRCm39) |
nonsense |
probably null |
|
R8014:Map3k4
|
UTSW |
17 |
12,489,918 (GRCm39) |
nonsense |
probably null |
|
R8235:Map3k4
|
UTSW |
17 |
12,458,968 (GRCm39) |
splice site |
probably null |
|
R8294:Map3k4
|
UTSW |
17 |
12,537,500 (GRCm39) |
missense |
unknown |
|
R8528:Map3k4
|
UTSW |
17 |
12,451,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R8858:Map3k4
|
UTSW |
17 |
12,490,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Map3k4
|
UTSW |
17 |
12,490,433 (GRCm39) |
missense |
probably benign |
0.00 |
R9063:Map3k4
|
UTSW |
17 |
12,482,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Map3k4
|
UTSW |
17 |
12,456,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9446:Map3k4
|
UTSW |
17 |
12,451,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Map3k4
|
UTSW |
17 |
12,489,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9488:Map3k4
|
UTSW |
17 |
12,489,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9591:Map3k4
|
UTSW |
17 |
12,454,795 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9617:Map3k4
|
UTSW |
17 |
12,476,871 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9722:Map3k4
|
UTSW |
17 |
12,490,523 (GRCm39) |
missense |
probably benign |
0.01 |
X0067:Map3k4
|
UTSW |
17 |
12,482,981 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Map3k4
|
UTSW |
17 |
12,490,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|