Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700025G04Rik |
A |
G |
1: 151,856,163 (GRCm39) |
|
probably benign |
Het |
Akap9 |
G |
A |
5: 4,105,671 (GRCm39) |
S2914N |
probably benign |
Het |
Alk |
T |
C |
17: 72,207,729 (GRCm39) |
D1002G |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,568,674 (GRCm39) |
|
probably benign |
Het |
Asb15 |
T |
C |
6: 24,562,486 (GRCm39) |
|
probably benign |
Het |
Asxl3 |
C |
A |
18: 22,657,564 (GRCm39) |
P1858Q |
probably benign |
Het |
Bltp1 |
T |
C |
3: 37,098,780 (GRCm39) |
S1136P |
probably damaging |
Het |
Bud31 |
T |
A |
5: 145,079,388 (GRCm39) |
|
probably benign |
Het |
C1qtnf1 |
G |
T |
11: 118,339,095 (GRCm39) |
R255L |
probably damaging |
Het |
Cacna2d4 |
C |
T |
6: 119,284,247 (GRCm39) |
R745W |
probably damaging |
Het |
Cage1 |
C |
T |
13: 38,206,856 (GRCm39) |
E330K |
probably damaging |
Het |
Catsperz |
T |
A |
19: 6,902,317 (GRCm39) |
N59I |
probably benign |
Het |
Ccdc110 |
G |
T |
8: 46,394,922 (GRCm39) |
S271I |
probably benign |
Het |
Ccdc88b |
T |
A |
19: 6,830,581 (GRCm39) |
E787V |
probably damaging |
Het |
Ccna2 |
A |
T |
3: 36,623,119 (GRCm39) |
|
probably benign |
Het |
Cd36 |
T |
A |
5: 18,018,086 (GRCm39) |
D209V |
probably damaging |
Het |
Cers4 |
T |
A |
8: 4,569,475 (GRCm39) |
W161R |
probably damaging |
Het |
Ces2f |
T |
A |
8: 105,680,178 (GRCm39) |
H442Q |
probably damaging |
Het |
Chchd6 |
A |
C |
6: 89,361,669 (GRCm39) |
C245G |
probably damaging |
Het |
Cndp1 |
T |
G |
18: 84,629,750 (GRCm39) |
Q481P |
probably benign |
Het |
Col3a1 |
A |
G |
1: 45,366,761 (GRCm39) |
R234G |
unknown |
Het |
Col3a1 |
A |
T |
1: 45,386,884 (GRCm39) |
N232I |
probably damaging |
Het |
Colgalt2 |
A |
T |
1: 152,378,768 (GRCm39) |
D398V |
probably damaging |
Het |
Cxcl10 |
TACTCAC |
TACTCACTCAC |
5: 92,495,941 (GRCm39) |
|
probably null |
Het |
Dcdc2a |
C |
A |
13: 25,240,290 (GRCm39) |
Q13K |
probably benign |
Het |
Dzip3 |
A |
T |
16: 48,781,571 (GRCm39) |
I240N |
probably damaging |
Het |
Epb41l3 |
T |
A |
17: 69,566,175 (GRCm39) |
L452* |
probably null |
Het |
Fam193b |
C |
T |
13: 55,689,518 (GRCm39) |
A753T |
probably damaging |
Het |
Fam47e |
G |
C |
5: 92,713,781 (GRCm39) |
|
probably benign |
Het |
Fastkd1 |
A |
G |
2: 69,538,993 (GRCm39) |
|
probably benign |
Het |
Fmnl1 |
G |
A |
11: 103,088,196 (GRCm39) |
G69D |
probably benign |
Het |
Foxn2 |
A |
G |
17: 88,781,094 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,821,844 (GRCm39) |
E5859G |
possibly damaging |
Het |
Gm9894 |
T |
A |
13: 67,912,820 (GRCm39) |
|
noncoding transcript |
Het |
H2-T13 |
T |
C |
17: 36,391,983 (GRCm39) |
N44S |
possibly damaging |
Het |
Helz2 |
T |
C |
2: 180,871,608 (GRCm39) |
Y2668C |
probably damaging |
Het |
Hhipl1 |
T |
A |
12: 108,277,952 (GRCm39) |
C93* |
probably null |
Het |
Lig1 |
C |
T |
7: 13,026,079 (GRCm39) |
A278V |
probably benign |
Het |
Lipn |
T |
A |
19: 34,049,158 (GRCm39) |
I108K |
probably benign |
Het |
Lsamp |
A |
G |
16: 41,971,592 (GRCm39) |
|
probably benign |
Het |
Map3k14 |
A |
G |
11: 103,129,743 (GRCm39) |
|
probably benign |
Het |
Mdm4 |
A |
T |
1: 132,919,558 (GRCm39) |
C436S |
probably damaging |
Het |
Mdm4 |
A |
G |
1: 132,940,430 (GRCm39) |
L33P |
probably damaging |
Het |
Meiob |
T |
C |
17: 25,055,458 (GRCm39) |
W422R |
probably damaging |
Het |
Mppe1 |
T |
C |
18: 67,360,777 (GRCm39) |
Y254C |
probably damaging |
Het |
Mterf1a |
A |
T |
5: 3,940,964 (GRCm39) |
N301K |
probably benign |
Het |
Muc6 |
C |
T |
7: 141,230,500 (GRCm39) |
S1210N |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,437,588 (GRCm39) |
Y2091* |
probably null |
Het |
Mylk |
G |
A |
16: 34,694,409 (GRCm39) |
R156H |
probably benign |
Het |
Myo15a |
G |
T |
11: 60,370,233 (GRCm39) |
D998Y |
probably benign |
Het |
Neb |
A |
T |
2: 52,086,369 (GRCm39) |
Y5235N |
probably damaging |
Het |
Nop58 |
A |
G |
1: 59,743,370 (GRCm39) |
|
probably benign |
Het |
Nr4a3 |
A |
G |
4: 48,051,564 (GRCm39) |
H135R |
probably damaging |
Het |
Nr4a3 |
A |
G |
4: 48,083,324 (GRCm39) |
K619R |
probably benign |
Het |
Nrg1 |
T |
C |
8: 32,327,695 (GRCm39) |
|
probably benign |
Het |
Odr4 |
T |
A |
1: 150,262,142 (GRCm39) |
E99D |
probably benign |
Het |
Or4f59 |
A |
T |
2: 111,872,560 (GRCm39) |
D272E |
probably benign |
Het |
Or5b122 |
T |
C |
19: 13,563,577 (GRCm39) |
V260A |
probably benign |
Het |
Or5m8 |
A |
T |
2: 85,823,040 (GRCm39) |
N293I |
probably damaging |
Het |
Or8g24 |
T |
A |
9: 38,989,525 (GRCm39) |
D172V |
possibly damaging |
Het |
Parp3 |
T |
C |
9: 106,353,204 (GRCm39) |
|
probably benign |
Het |
Pde2a |
A |
G |
7: 101,133,750 (GRCm39) |
E103G |
probably benign |
Het |
Pds5a |
A |
T |
5: 65,792,645 (GRCm39) |
|
probably benign |
Het |
Pip4k2c |
A |
G |
10: 127,047,262 (GRCm39) |
V40A |
unknown |
Het |
Pitrm1 |
T |
C |
13: 6,602,780 (GRCm39) |
|
probably benign |
Het |
Plk4 |
A |
G |
3: 40,756,282 (GRCm39) |
I64M |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Ppp2r1a |
T |
C |
17: 21,171,593 (GRCm39) |
|
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,159,426 (GRCm39) |
N172K |
probably damaging |
Het |
Prkcg |
G |
A |
7: 3,368,177 (GRCm39) |
R357Q |
probably damaging |
Het |
Prmt3 |
T |
C |
7: 49,498,295 (GRCm39) |
|
probably null |
Het |
Prx |
T |
A |
7: 27,217,432 (GRCm39) |
C644* |
probably null |
Het |
Ptpru |
A |
G |
4: 131,535,838 (GRCm39) |
|
probably benign |
Het |
Rbm5 |
A |
T |
9: 107,619,696 (GRCm39) |
D738E |
probably damaging |
Het |
Recql5 |
A |
T |
11: 115,788,060 (GRCm39) |
Y420N |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,663,088 (GRCm39) |
I152T |
probably benign |
Het |
Rnpepl1 |
A |
G |
1: 92,846,917 (GRCm39) |
S580G |
possibly damaging |
Het |
Ryr3 |
C |
T |
2: 112,777,332 (GRCm39) |
G275D |
probably damaging |
Het |
Serpinb9e |
T |
A |
13: 33,441,735 (GRCm39) |
Y222* |
probably null |
Het |
Shld2 |
A |
T |
14: 33,990,448 (GRCm39) |
S153T |
possibly damaging |
Het |
Slc10a1 |
T |
A |
12: 81,002,802 (GRCm39) |
I279F |
probably damaging |
Het |
Slc12a8 |
G |
T |
16: 33,483,347 (GRCm39) |
G584V |
probably damaging |
Het |
Slc35b3 |
T |
A |
13: 39,121,307 (GRCm39) |
Y311F |
probably benign |
Het |
Slc44a5 |
A |
G |
3: 153,963,357 (GRCm39) |
|
probably null |
Het |
Slc6a9 |
A |
G |
4: 117,722,003 (GRCm39) |
E422G |
possibly damaging |
Het |
Smpd2 |
A |
G |
10: 41,364,728 (GRCm39) |
|
probably null |
Het |
Spast |
A |
G |
17: 74,688,963 (GRCm39) |
|
probably null |
Het |
Spink5 |
A |
T |
18: 44,116,630 (GRCm39) |
E208V |
probably benign |
Het |
Stag1 |
T |
C |
9: 100,770,506 (GRCm39) |
|
probably benign |
Het |
Stambp |
A |
G |
6: 83,540,803 (GRCm39) |
|
probably null |
Het |
Sult3a2 |
A |
T |
10: 33,653,188 (GRCm39) |
M184K |
possibly damaging |
Het |
Tcp11 |
T |
C |
17: 28,290,636 (GRCm39) |
D162G |
probably damaging |
Het |
Themis |
A |
C |
10: 28,544,744 (GRCm39) |
E30A |
possibly damaging |
Het |
Tmc7 |
G |
A |
7: 118,150,483 (GRCm39) |
S350L |
probably benign |
Het |
Tmem131 |
A |
T |
1: 36,873,979 (GRCm39) |
Y271* |
probably null |
Het |
Trim35 |
T |
A |
14: 66,546,248 (GRCm39) |
S338R |
probably benign |
Het |
Trim42 |
C |
A |
9: 97,245,673 (GRCm39) |
V376F |
probably benign |
Het |
Tshr |
A |
T |
12: 91,504,871 (GRCm39) |
K11M |
probably damaging |
Het |
Vps8 |
A |
G |
16: 21,278,570 (GRCm39) |
|
probably benign |
Het |
Wdr11 |
T |
C |
7: 129,208,831 (GRCm39) |
|
probably benign |
Het |
Wdr26 |
A |
T |
1: 181,008,859 (GRCm39) |
|
probably benign |
Het |
Wdtc1 |
A |
G |
4: 133,024,857 (GRCm39) |
Y447H |
probably damaging |
Het |
Zfp687 |
C |
T |
3: 94,915,784 (GRCm39) |
C996Y |
probably damaging |
Het |
Zranb2 |
T |
C |
3: 157,247,502 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zfp984 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00428:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00469:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00550:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4791001:Zfp984
|
UTSW |
4 |
147,840,603 (GRCm39) |
missense |
probably benign |
0.15 |
R0281:Zfp984
|
UTSW |
4 |
147,839,722 (GRCm39) |
missense |
probably benign |
|
R0731:Zfp984
|
UTSW |
4 |
147,840,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1293:Zfp984
|
UTSW |
4 |
147,840,398 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1518:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
R2041:Zfp984
|
UTSW |
4 |
147,839,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R2360:Zfp984
|
UTSW |
4 |
147,839,234 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5038:Zfp984
|
UTSW |
4 |
147,839,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Zfp984
|
UTSW |
4 |
147,840,362 (GRCm39) |
missense |
probably benign |
0.00 |
R6254:Zfp984
|
UTSW |
4 |
147,840,643 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6418:Zfp984
|
UTSW |
4 |
147,845,703 (GRCm39) |
missense |
probably benign |
0.00 |
R6527:Zfp984
|
UTSW |
4 |
147,840,381 (GRCm39) |
missense |
probably benign |
0.45 |
R6974:Zfp984
|
UTSW |
4 |
147,845,707 (GRCm39) |
start codon destroyed |
possibly damaging |
0.94 |
R7058:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
R7495:Zfp984
|
UTSW |
4 |
147,839,287 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7843:Zfp984
|
UTSW |
4 |
147,842,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8462:Zfp984
|
UTSW |
4 |
147,839,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8520:Zfp984
|
UTSW |
4 |
147,840,668 (GRCm39) |
missense |
probably benign |
0.01 |
R8918:Zfp984
|
UTSW |
4 |
147,840,623 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9387:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
Z1176:Zfp984
|
UTSW |
4 |
147,839,921 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfp984
|
UTSW |
4 |
147,840,577 (GRCm39) |
missense |
probably benign |
0.04 |
|