Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
T |
C |
11: 72,049,768 (GRCm39) |
D871G |
probably benign |
Het |
A4galt |
G |
T |
15: 83,112,020 (GRCm39) |
H254Q |
probably damaging |
Het |
AA986860 |
C |
A |
1: 130,670,780 (GRCm39) |
T334K |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,353,874 (GRCm39) |
I3732T |
probably benign |
Het |
Abcf1 |
C |
T |
17: 36,271,956 (GRCm39) |
D353N |
probably damaging |
Het |
Adss1 |
A |
G |
12: 112,594,790 (GRCm39) |
H83R |
probably damaging |
Het |
Amer2 |
C |
A |
14: 60,616,321 (GRCm39) |
A172E |
probably damaging |
Het |
Ankhd1 |
A |
G |
18: 36,787,199 (GRCm39) |
T2300A |
probably benign |
Het |
Ano5 |
G |
A |
7: 51,215,879 (GRCm39) |
|
probably null |
Het |
Apob |
G |
A |
12: 8,051,801 (GRCm39) |
G1109D |
probably damaging |
Het |
Arhgef26 |
A |
T |
3: 62,288,381 (GRCm39) |
N484Y |
probably damaging |
Het |
C6 |
A |
G |
15: 4,793,023 (GRCm39) |
D376G |
probably damaging |
Het |
Caml |
T |
C |
13: 55,772,986 (GRCm39) |
|
probably null |
Het |
Capn12 |
T |
C |
7: 28,588,077 (GRCm39) |
L473S |
probably benign |
Het |
Cdk6 |
G |
A |
5: 3,394,553 (GRCm39) |
|
probably null |
Het |
Cers5 |
A |
T |
15: 99,643,805 (GRCm39) |
C153S |
probably benign |
Het |
Cfap206 |
T |
C |
4: 34,692,530 (GRCm39) |
M499V |
probably benign |
Het |
Chd6 |
A |
G |
2: 160,791,968 (GRCm39) |
M2463T |
probably damaging |
Het |
Chn1 |
T |
C |
2: 73,537,350 (GRCm39) |
E58G |
possibly damaging |
Het |
Clec4a1 |
T |
C |
6: 122,905,001 (GRCm39) |
V100A |
probably benign |
Het |
Col7a1 |
G |
C |
9: 108,810,130 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,246,249 (GRCm39) |
V1050A |
possibly damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dennd5a |
A |
T |
7: 109,497,889 (GRCm39) |
C1044S |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,265,048 (GRCm39) |
T2181A |
probably benign |
Het |
Dnai1 |
T |
C |
4: 41,605,775 (GRCm39) |
V255A |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,135,078 (GRCm39) |
C1518R |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,043,981 (GRCm39) |
V273A |
probably damaging |
Het |
Eif1 |
C |
T |
11: 100,211,223 (GRCm39) |
|
probably benign |
Het |
Eml3 |
T |
C |
19: 8,908,313 (GRCm39) |
I58T |
probably benign |
Het |
Fam171b |
T |
A |
2: 83,709,552 (GRCm39) |
I408N |
probably damaging |
Het |
Fchsd2 |
A |
G |
7: 100,902,747 (GRCm39) |
E351G |
probably benign |
Het |
Focad |
G |
A |
4: 88,325,377 (GRCm39) |
A81T |
possibly damaging |
Het |
Fpr-rs4 |
G |
A |
17: 18,242,748 (GRCm39) |
V252I |
probably benign |
Het |
Fryl |
A |
G |
5: 73,222,824 (GRCm39) |
L1919P |
probably damaging |
Het |
Gm12185 |
C |
T |
11: 48,806,735 (GRCm39) |
R152H |
probably damaging |
Het |
Gm14410 |
C |
T |
2: 176,885,517 (GRCm39) |
G249E |
probably damaging |
Het |
Gm6685 |
A |
T |
11: 28,289,706 (GRCm39) |
S37T |
possibly damaging |
Het |
Greb1 |
G |
A |
12: 16,766,676 (GRCm39) |
P374L |
probably damaging |
Het |
Hdac4 |
A |
T |
1: 91,940,560 (GRCm39) |
|
probably null |
Het |
Hecw1 |
A |
T |
13: 14,409,010 (GRCm39) |
L1099* |
probably null |
Het |
Hivep1 |
T |
C |
13: 42,310,966 (GRCm39) |
S1069P |
probably benign |
Het |
Itgad |
T |
C |
7: 127,784,959 (GRCm39) |
I288T |
possibly damaging |
Het |
Kif9 |
A |
G |
9: 110,317,612 (GRCm39) |
M96V |
possibly damaging |
Het |
Kncn |
T |
A |
4: 115,741,987 (GRCm39) |
V18E |
probably damaging |
Het |
Lrrc74a |
G |
A |
12: 86,805,330 (GRCm39) |
G384D |
probably damaging |
Het |
Ltb4r2 |
T |
C |
14: 56,000,108 (GRCm39) |
V243A |
probably damaging |
Het |
Mtnr1b |
T |
A |
9: 15,774,082 (GRCm39) |
I326L |
probably benign |
Het |
Mylip |
C |
T |
13: 45,561,957 (GRCm39) |
T253I |
probably damaging |
Het |
Necap1 |
T |
A |
6: 122,857,611 (GRCm39) |
|
probably null |
Het |
Nedd4 |
C |
T |
9: 72,633,720 (GRCm39) |
P409S |
probably damaging |
Het |
Npat |
A |
T |
9: 53,456,538 (GRCm39) |
E36D |
probably damaging |
Het |
Ovch2 |
C |
T |
7: 107,384,648 (GRCm39) |
V490M |
probably damaging |
Het |
Pax9 |
T |
C |
12: 56,756,480 (GRCm39) |
S273P |
probably benign |
Het |
Plce1 |
A |
G |
19: 38,734,289 (GRCm39) |
E1563G |
probably damaging |
Het |
Podxl2 |
C |
A |
6: 88,826,299 (GRCm39) |
G336* |
probably null |
Het |
Prdm1 |
A |
G |
10: 44,322,782 (GRCm39) |
|
probably null |
Het |
Psme4 |
T |
C |
11: 30,803,245 (GRCm39) |
I29T |
possibly damaging |
Het |
Ptprd |
A |
T |
4: 75,984,528 (GRCm39) |
D780E |
probably benign |
Het |
Retsat |
T |
C |
6: 72,581,918 (GRCm39) |
M294T |
probably benign |
Het |
Robo2 |
A |
T |
16: 73,764,672 (GRCm39) |
V652D |
probably damaging |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Serpinb3d |
G |
T |
1: 107,010,490 (GRCm39) |
T66K |
probably benign |
Het |
Setd1b |
A |
T |
5: 123,296,461 (GRCm39) |
|
probably benign |
Het |
Slc7a10 |
G |
T |
7: 34,886,012 (GRCm39) |
A36S |
possibly damaging |
Het |
Sstr3 |
T |
A |
15: 78,423,788 (GRCm39) |
I320F |
probably damaging |
Het |
Syne1 |
G |
T |
10: 5,299,071 (GRCm39) |
A1005E |
probably damaging |
Het |
Syngap1 |
C |
A |
17: 27,181,931 (GRCm39) |
S975* |
probably null |
Het |
Tinagl1 |
C |
T |
4: 130,066,725 (GRCm39) |
C124Y |
probably null |
Het |
Tm9sf1 |
C |
T |
14: 55,873,827 (GRCm39) |
R557H |
probably damaging |
Het |
Tmed2 |
T |
A |
5: 124,685,055 (GRCm39) |
I68K |
possibly damaging |
Het |
Tmem104 |
A |
G |
11: 115,134,819 (GRCm39) |
T451A |
probably benign |
Het |
Tmem141 |
T |
C |
2: 25,511,693 (GRCm39) |
|
probably null |
Het |
Tmem184a |
C |
A |
5: 139,798,827 (GRCm39) |
V41L |
probably benign |
Het |
Tmem39b |
C |
T |
4: 129,580,584 (GRCm39) |
V303I |
possibly damaging |
Het |
Tsn |
T |
C |
1: 118,232,939 (GRCm39) |
I122V |
probably benign |
Het |
Ttc41 |
G |
T |
10: 86,612,527 (GRCm39) |
V1267L |
probably benign |
Het |
Uggt1 |
A |
T |
1: 36,202,309 (GRCm39) |
L1096Q |
probably damaging |
Het |
Usp50 |
A |
T |
2: 126,617,713 (GRCm39) |
I244N |
probably benign |
Het |
Vil1 |
A |
G |
1: 74,471,498 (GRCm39) |
S760G |
probably benign |
Het |
Wasf1 |
T |
A |
10: 40,813,741 (GRCm39) |
V541E |
unknown |
Het |
Zfp180 |
G |
T |
7: 23,804,530 (GRCm39) |
K316N |
probably damaging |
Het |
Zfp582 |
T |
C |
7: 6,356,945 (GRCm39) |
C253R |
probably damaging |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp759 |
A |
G |
13: 67,288,524 (GRCm39) |
T692A |
probably benign |
Het |
Zfyve26 |
A |
G |
12: 79,329,758 (GRCm39) |
V476A |
probably benign |
Het |
|
Other mutations in Zc3h13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00945:Zc3h13
|
APN |
14 |
75,567,587 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01129:Zc3h13
|
APN |
14 |
75,573,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01599:Zc3h13
|
APN |
14 |
75,547,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01844:Zc3h13
|
APN |
14 |
75,581,209 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02132:Zc3h13
|
APN |
14 |
75,567,787 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03108:Zc3h13
|
APN |
14 |
75,569,206 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03299:Zc3h13
|
APN |
14 |
75,531,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03377:Zc3h13
|
APN |
14 |
75,531,416 (GRCm39) |
missense |
possibly damaging |
0.53 |
B5639:Zc3h13
|
UTSW |
14 |
75,553,479 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Zc3h13
|
UTSW |
14 |
75,561,050 (GRCm39) |
small insertion |
probably benign |
|
FR4304:Zc3h13
|
UTSW |
14 |
75,561,043 (GRCm39) |
small insertion |
probably benign |
|
FR4340:Zc3h13
|
UTSW |
14 |
75,561,032 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Zc3h13
|
UTSW |
14 |
75,561,041 (GRCm39) |
nonsense |
probably null |
|
FR4548:Zc3h13
|
UTSW |
14 |
75,561,039 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Zc3h13
|
UTSW |
14 |
75,561,038 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Zc3h13
|
UTSW |
14 |
75,561,032 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Zc3h13
|
UTSW |
14 |
75,561,037 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zc3h13
|
UTSW |
14 |
75,561,039 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zc3h13
|
UTSW |
14 |
75,561,036 (GRCm39) |
small insertion |
probably benign |
|
PIT4696001:Zc3h13
|
UTSW |
14 |
75,569,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Zc3h13
|
UTSW |
14 |
75,567,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R0103:Zc3h13
|
UTSW |
14 |
75,567,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R0127:Zc3h13
|
UTSW |
14 |
75,560,694 (GRCm39) |
missense |
unknown |
|
R0374:Zc3h13
|
UTSW |
14 |
75,546,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Zc3h13
|
UTSW |
14 |
75,560,922 (GRCm39) |
missense |
unknown |
|
R0408:Zc3h13
|
UTSW |
14 |
75,529,626 (GRCm39) |
nonsense |
probably null |
|
R0967:Zc3h13
|
UTSW |
14 |
75,581,179 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1006:Zc3h13
|
UTSW |
14 |
75,567,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R1142:Zc3h13
|
UTSW |
14 |
75,553,424 (GRCm39) |
missense |
probably benign |
0.14 |
R1605:Zc3h13
|
UTSW |
14 |
75,574,923 (GRCm39) |
nonsense |
probably null |
|
R2021:Zc3h13
|
UTSW |
14 |
75,567,635 (GRCm39) |
missense |
probably damaging |
0.96 |
R2270:Zc3h13
|
UTSW |
14 |
75,569,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3508:Zc3h13
|
UTSW |
14 |
75,546,380 (GRCm39) |
nonsense |
probably null |
|
R3745:Zc3h13
|
UTSW |
14 |
75,568,101 (GRCm39) |
missense |
probably benign |
0.03 |
R3954:Zc3h13
|
UTSW |
14 |
75,567,178 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4205:Zc3h13
|
UTSW |
14 |
75,565,041 (GRCm39) |
missense |
unknown |
|
R4799:Zc3h13
|
UTSW |
14 |
75,576,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5042:Zc3h13
|
UTSW |
14 |
75,576,836 (GRCm39) |
missense |
probably damaging |
0.98 |
R5133:Zc3h13
|
UTSW |
14 |
75,573,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Zc3h13
|
UTSW |
14 |
75,581,059 (GRCm39) |
missense |
probably benign |
0.14 |
R5432:Zc3h13
|
UTSW |
14 |
75,568,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R5611:Zc3h13
|
UTSW |
14 |
75,568,348 (GRCm39) |
missense |
probably benign |
0.10 |
R5687:Zc3h13
|
UTSW |
14 |
75,569,400 (GRCm39) |
nonsense |
probably null |
|
R5726:Zc3h13
|
UTSW |
14 |
75,568,269 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5817:Zc3h13
|
UTSW |
14 |
75,565,572 (GRCm39) |
missense |
probably damaging |
0.96 |
R6087:Zc3h13
|
UTSW |
14 |
75,568,149 (GRCm39) |
missense |
probably damaging |
0.96 |
R6224:Zc3h13
|
UTSW |
14 |
75,574,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R6278:Zc3h13
|
UTSW |
14 |
75,567,863 (GRCm39) |
missense |
probably benign |
0.01 |
R6315:Zc3h13
|
UTSW |
14 |
75,546,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R6490:Zc3h13
|
UTSW |
14 |
75,560,998 (GRCm39) |
small deletion |
probably benign |
|
R6598:Zc3h13
|
UTSW |
14 |
75,569,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R7051:Zc3h13
|
UTSW |
14 |
75,568,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7054:Zc3h13
|
UTSW |
14 |
75,559,227 (GRCm39) |
missense |
probably benign |
0.19 |
R7135:Zc3h13
|
UTSW |
14 |
75,559,161 (GRCm39) |
missense |
unknown |
|
R7307:Zc3h13
|
UTSW |
14 |
75,567,981 (GRCm39) |
missense |
probably damaging |
0.96 |
R7515:Zc3h13
|
UTSW |
14 |
75,546,349 (GRCm39) |
missense |
unknown |
|
R7680:Zc3h13
|
UTSW |
14 |
75,567,955 (GRCm39) |
missense |
probably damaging |
0.99 |
R8031:Zc3h13
|
UTSW |
14 |
75,568,070 (GRCm39) |
missense |
not run |
|
R8048:Zc3h13
|
UTSW |
14 |
75,561,977 (GRCm39) |
missense |
unknown |
|
R8059:Zc3h13
|
UTSW |
14 |
75,565,250 (GRCm39) |
missense |
unknown |
|
R8362:Zc3h13
|
UTSW |
14 |
75,561,909 (GRCm39) |
missense |
unknown |
|
R8391:Zc3h13
|
UTSW |
14 |
75,568,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R8724:Zc3h13
|
UTSW |
14 |
75,569,512 (GRCm39) |
missense |
probably benign |
0.05 |
R9081:Zc3h13
|
UTSW |
14 |
75,569,381 (GRCm39) |
small deletion |
probably benign |
|
R9082:Zc3h13
|
UTSW |
14 |
75,569,381 (GRCm39) |
small deletion |
probably benign |
|
R9101:Zc3h13
|
UTSW |
14 |
75,561,042 (GRCm39) |
missense |
unknown |
|
R9214:Zc3h13
|
UTSW |
14 |
75,560,991 (GRCm39) |
missense |
unknown |
|
R9308:Zc3h13
|
UTSW |
14 |
75,565,418 (GRCm39) |
missense |
unknown |
|
R9376:Zc3h13
|
UTSW |
14 |
75,561,128 (GRCm39) |
missense |
unknown |
|
R9618:Zc3h13
|
UTSW |
14 |
75,567,542 (GRCm39) |
missense |
|
|
R9665:Zc3h13
|
UTSW |
14 |
75,567,989 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Zc3h13
|
UTSW |
14 |
75,565,505 (GRCm39) |
missense |
unknown |
|
|