Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,773,313 (GRCm39) |
T834M |
possibly damaging |
Het |
Ak1 |
T |
C |
2: 32,520,313 (GRCm39) |
L32P |
probably damaging |
Het |
Ankrd24 |
A |
G |
10: 81,470,754 (GRCm39) |
D61G |
probably damaging |
Het |
Atp13a2 |
T |
C |
4: 140,721,113 (GRCm39) |
S99P |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Bmp10 |
A |
G |
6: 87,410,779 (GRCm39) |
I191V |
probably benign |
Het |
C2cd6 |
A |
T |
1: 59,106,944 (GRCm39) |
S294T |
possibly damaging |
Het |
C4b |
T |
A |
17: 34,962,743 (GRCm39) |
K20* |
probably null |
Het |
Caps2 |
C |
T |
10: 112,015,377 (GRCm39) |
T139I |
probably benign |
Het |
Cdc25a |
T |
C |
9: 109,705,157 (GRCm39) |
S34P |
probably benign |
Het |
Cenpv |
T |
C |
11: 62,427,121 (GRCm39) |
I146V |
probably benign |
Het |
Cep57 |
A |
T |
9: 13,732,850 (GRCm39) |
F32I |
probably benign |
Het |
Cep85 |
A |
G |
4: 133,894,711 (GRCm39) |
W32R |
probably damaging |
Het |
Cntrl |
T |
C |
2: 35,059,329 (GRCm39) |
|
probably null |
Het |
Cpd |
A |
G |
11: 76,675,224 (GRCm39) |
V1299A |
probably damaging |
Het |
Cpne6 |
T |
C |
14: 55,752,092 (GRCm39) |
V283A |
probably benign |
Het |
Crot |
A |
G |
5: 9,016,941 (GRCm39) |
C584R |
probably damaging |
Het |
Ctsc |
A |
C |
7: 87,930,670 (GRCm39) |
H83P |
possibly damaging |
Het |
Dido1 |
T |
C |
2: 180,302,513 (GRCm39) |
N1797S |
probably benign |
Het |
Dlgap4 |
C |
T |
2: 156,602,821 (GRCm39) |
Q148* |
probably null |
Het |
Dnah3 |
T |
C |
7: 119,670,181 (GRCm39) |
D688G |
probably benign |
Het |
Dnmt1 |
T |
C |
9: 20,843,472 (GRCm39) |
E138G |
probably benign |
Het |
Edc4 |
T |
A |
8: 106,619,460 (GRCm39) |
M1396K |
probably damaging |
Het |
Haao |
T |
A |
17: 84,146,267 (GRCm39) |
Q69L |
probably benign |
Het |
Hsd3b6 |
A |
T |
3: 98,715,255 (GRCm39) |
|
probably null |
Het |
Itpr3 |
T |
A |
17: 27,333,199 (GRCm39) |
I1937N |
probably benign |
Het |
Kcnk15 |
C |
A |
2: 163,700,127 (GRCm39) |
T103K |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,864,541 (GRCm39) |
|
probably null |
Het |
Lama3 |
T |
A |
18: 12,615,102 (GRCm39) |
F1342Y |
probably benign |
Het |
Lilra6 |
A |
T |
7: 3,915,718 (GRCm39) |
M98K |
probably damaging |
Het |
Map3k21 |
T |
C |
8: 126,668,417 (GRCm39) |
S668P |
probably benign |
Het |
Mcpt8 |
T |
C |
14: 56,319,791 (GRCm39) |
T220A |
probably benign |
Het |
Mettl13 |
C |
T |
1: 162,364,736 (GRCm39) |
V548I |
possibly damaging |
Het |
Mfsd4b4 |
A |
G |
10: 39,767,860 (GRCm39) |
M411T |
probably benign |
Het |
Mrfap1 |
A |
G |
5: 36,953,817 (GRCm39) |
S41P |
possibly damaging |
Het |
Mroh2b |
A |
G |
15: 4,978,137 (GRCm39) |
I1302V |
probably benign |
Het |
Mrpl45 |
C |
T |
11: 97,214,681 (GRCm39) |
R123* |
probably null |
Het |
Mstn |
T |
A |
1: 53,101,157 (GRCm39) |
I78K |
probably damaging |
Het |
Mtdh |
T |
C |
15: 34,114,191 (GRCm39) |
S168P |
possibly damaging |
Het |
Muc15 |
G |
T |
2: 110,561,905 (GRCm39) |
V114F |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,238,144 (GRCm39) |
E112G |
probably benign |
Het |
Myocd |
G |
T |
11: 65,078,330 (GRCm39) |
H360Q |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,563,802 (GRCm39) |
E1627G |
probably damaging |
Het |
Nlrp14 |
T |
C |
7: 106,781,910 (GRCm39) |
L369P |
probably benign |
Het |
Nlrp6 |
A |
G |
7: 140,503,408 (GRCm39) |
T505A |
probably damaging |
Het |
Npbwr1 |
T |
C |
1: 5,986,900 (GRCm39) |
S205G |
probably damaging |
Het |
Nsmaf |
G |
A |
4: 6,423,448 (GRCm39) |
R307* |
probably null |
Het |
Or5h19 |
A |
T |
16: 58,856,920 (GRCm39) |
L60Q |
probably damaging |
Het |
Or9i1b |
T |
C |
19: 13,897,208 (GRCm39) |
S275P |
probably damaging |
Het |
Parp9 |
T |
G |
16: 35,774,050 (GRCm39) |
S341A |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,289,533 (GRCm39) |
N346S |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,263,360 (GRCm39) |
F503Y |
probably damaging |
Het |
Polr1e |
G |
T |
4: 45,028,026 (GRCm39) |
A290S |
probably damaging |
Het |
Ppp1r21 |
A |
T |
17: 88,866,033 (GRCm39) |
H305L |
probably damaging |
Het |
Prss47 |
A |
G |
13: 65,197,103 (GRCm39) |
L117P |
probably damaging |
Het |
Psmb2 |
A |
G |
4: 126,580,825 (GRCm39) |
Y73C |
probably damaging |
Het |
Rcn2 |
C |
T |
9: 55,963,537 (GRCm39) |
P222L |
probably benign |
Het |
Rnf144b |
T |
C |
13: 47,396,361 (GRCm39) |
Y233H |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,665,436 (GRCm39) |
L196P |
probably damaging |
Het |
Sik2 |
A |
G |
9: 50,920,111 (GRCm39) |
I22T |
probably damaging |
Het |
Sis |
A |
G |
3: 72,796,360 (GRCm39) |
V1807A |
probably benign |
Het |
Slc1a2 |
T |
A |
2: 102,568,254 (GRCm39) |
I88N |
probably damaging |
Het |
Slc22a22 |
A |
G |
15: 57,110,916 (GRCm39) |
F437S |
probably benign |
Het |
Slc39a13 |
A |
T |
2: 90,899,050 (GRCm39) |
C20* |
probably null |
Het |
Sos2 |
C |
T |
12: 69,632,090 (GRCm39) |
|
probably null |
Het |
Sst |
A |
G |
16: 23,709,448 (GRCm39) |
V16A |
probably benign |
Het |
Stab1 |
C |
T |
14: 30,863,543 (GRCm39) |
G2073D |
probably benign |
Het |
Stxbp1 |
A |
T |
2: 32,684,648 (GRCm39) |
S594T |
probably benign |
Het |
Sugct |
A |
T |
13: 17,627,131 (GRCm39) |
C241S |
probably benign |
Het |
Svil |
T |
A |
18: 5,048,950 (GRCm39) |
C76S |
probably benign |
Het |
Tcaf1 |
A |
G |
6: 42,663,382 (GRCm39) |
V166A |
possibly damaging |
Het |
Tmem131 |
A |
T |
1: 36,855,322 (GRCm39) |
N801K |
possibly damaging |
Het |
Tox3 |
T |
C |
8: 90,980,973 (GRCm39) |
N277S |
probably damaging |
Het |
Tril |
G |
T |
6: 53,795,012 (GRCm39) |
R737S |
probably damaging |
Het |
Trpm2 |
C |
A |
10: 77,801,841 (GRCm39) |
V75L |
probably damaging |
Het |
Tshz1 |
A |
C |
18: 84,031,930 (GRCm39) |
L826R |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,597,196 (GRCm39) |
V19906I |
probably damaging |
Het |
Wnt5a |
C |
T |
14: 28,240,461 (GRCm39) |
R184* |
probably null |
Het |
Wnt5b |
G |
A |
6: 119,410,442 (GRCm39) |
R333C |
probably damaging |
Het |
Zbtb6 |
T |
C |
2: 37,319,356 (GRCm39) |
T191A |
probably benign |
Het |
Zc3h7a |
C |
T |
16: 10,978,890 (GRCm39) |
R95H |
probably damaging |
Het |
Zfp110 |
T |
C |
7: 12,582,468 (GRCm39) |
V372A |
possibly damaging |
Het |
Zmym2 |
C |
T |
14: 57,148,640 (GRCm39) |
S318L |
probably benign |
Het |
|
Other mutations in Zc3h4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Zc3h4
|
APN |
7 |
16,156,159 (GRCm39) |
missense |
unknown |
|
IGL00923:Zc3h4
|
APN |
7 |
16,163,617 (GRCm39) |
missense |
unknown |
|
IGL01541:Zc3h4
|
APN |
7 |
16,168,257 (GRCm39) |
missense |
unknown |
|
IGL02115:Zc3h4
|
APN |
7 |
16,159,708 (GRCm39) |
missense |
unknown |
|
IGL02303:Zc3h4
|
APN |
7 |
16,168,002 (GRCm39) |
missense |
unknown |
|
IGL02336:Zc3h4
|
APN |
7 |
16,159,702 (GRCm39) |
missense |
unknown |
|
IGL02734:Zc3h4
|
APN |
7 |
16,157,849 (GRCm39) |
missense |
unknown |
|
IGL02736:Zc3h4
|
APN |
7 |
16,151,308 (GRCm39) |
nonsense |
probably null |
|
BB008:Zc3h4
|
UTSW |
7 |
16,166,909 (GRCm39) |
missense |
unknown |
|
BB018:Zc3h4
|
UTSW |
7 |
16,166,909 (GRCm39) |
missense |
unknown |
|
R0032:Zc3h4
|
UTSW |
7 |
16,168,565 (GRCm39) |
missense |
unknown |
|
R0032:Zc3h4
|
UTSW |
7 |
16,168,565 (GRCm39) |
missense |
unknown |
|
R0220:Zc3h4
|
UTSW |
7 |
16,163,198 (GRCm39) |
missense |
unknown |
|
R0336:Zc3h4
|
UTSW |
7 |
16,169,103 (GRCm39) |
missense |
unknown |
|
R0416:Zc3h4
|
UTSW |
7 |
16,154,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0666:Zc3h4
|
UTSW |
7 |
16,168,697 (GRCm39) |
missense |
unknown |
|
R0864:Zc3h4
|
UTSW |
7 |
16,154,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R1068:Zc3h4
|
UTSW |
7 |
16,163,161 (GRCm39) |
missense |
unknown |
|
R1145:Zc3h4
|
UTSW |
7 |
16,150,838 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1145:Zc3h4
|
UTSW |
7 |
16,150,838 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1665:Zc3h4
|
UTSW |
7 |
16,163,505 (GRCm39) |
missense |
unknown |
|
R2087:Zc3h4
|
UTSW |
7 |
16,150,865 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2182:Zc3h4
|
UTSW |
7 |
16,156,441 (GRCm39) |
missense |
unknown |
|
R2508:Zc3h4
|
UTSW |
7 |
16,168,264 (GRCm39) |
missense |
unknown |
|
R3037:Zc3h4
|
UTSW |
7 |
16,155,410 (GRCm39) |
missense |
unknown |
|
R4439:Zc3h4
|
UTSW |
7 |
16,163,036 (GRCm39) |
missense |
unknown |
|
R4576:Zc3h4
|
UTSW |
7 |
16,168,579 (GRCm39) |
missense |
unknown |
|
R5030:Zc3h4
|
UTSW |
7 |
16,156,155 (GRCm39) |
missense |
unknown |
|
R5160:Zc3h4
|
UTSW |
7 |
16,168,573 (GRCm39) |
missense |
unknown |
|
R5270:Zc3h4
|
UTSW |
7 |
16,168,440 (GRCm39) |
missense |
unknown |
|
R5490:Zc3h4
|
UTSW |
7 |
16,162,930 (GRCm39) |
missense |
unknown |
|
R5519:Zc3h4
|
UTSW |
7 |
16,169,157 (GRCm39) |
missense |
unknown |
|
R5770:Zc3h4
|
UTSW |
7 |
16,163,536 (GRCm39) |
missense |
unknown |
|
R7067:Zc3h4
|
UTSW |
7 |
16,162,976 (GRCm39) |
nonsense |
probably null |
|
R7234:Zc3h4
|
UTSW |
7 |
16,162,961 (GRCm39) |
missense |
unknown |
|
R7316:Zc3h4
|
UTSW |
7 |
16,169,260 (GRCm39) |
missense |
unknown |
|
R7771:Zc3h4
|
UTSW |
7 |
16,163,824 (GRCm39) |
missense |
unknown |
|
R7852:Zc3h4
|
UTSW |
7 |
16,156,392 (GRCm39) |
missense |
unknown |
|
R7922:Zc3h4
|
UTSW |
7 |
16,159,647 (GRCm39) |
missense |
unknown |
|
R7931:Zc3h4
|
UTSW |
7 |
16,166,909 (GRCm39) |
missense |
unknown |
|
R7965:Zc3h4
|
UTSW |
7 |
16,163,770 (GRCm39) |
missense |
unknown |
|
R8827:Zc3h4
|
UTSW |
7 |
16,163,123 (GRCm39) |
missense |
unknown |
|
R8859:Zc3h4
|
UTSW |
7 |
16,168,939 (GRCm39) |
missense |
unknown |
|
R9457:Zc3h4
|
UTSW |
7 |
16,168,675 (GRCm39) |
missense |
unknown |
|
R9562:Zc3h4
|
UTSW |
7 |
16,168,891 (GRCm39) |
missense |
unknown |
|
R9609:Zc3h4
|
UTSW |
7 |
16,150,751 (GRCm39) |
missense |
unknown |
|
R9721:Zc3h4
|
UTSW |
7 |
16,168,770 (GRCm39) |
missense |
unknown |
|
RF001:Zc3h4
|
UTSW |
7 |
16,163,612 (GRCm39) |
small insertion |
probably benign |
|
RF039:Zc3h4
|
UTSW |
7 |
16,163,543 (GRCm39) |
small deletion |
probably benign |
|
X0064:Zc3h4
|
UTSW |
7 |
16,156,441 (GRCm39) |
missense |
unknown |
|
|