Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
T |
A |
10: 29,100,819 (GRCm39) |
D397E |
probably benign |
Het |
Abcc10 |
A |
G |
17: 46,618,136 (GRCm39) |
F1005L |
probably damaging |
Het |
Ackr4 |
T |
C |
9: 103,975,930 (GRCm39) |
E339G |
probably benign |
Het |
Adam39 |
G |
T |
8: 41,279,328 (GRCm39) |
C573F |
probably damaging |
Het |
Anks1b |
A |
G |
10: 90,346,652 (GRCm39) |
T651A |
probably benign |
Het |
Aoc1 |
C |
A |
6: 48,884,740 (GRCm39) |
H594Q |
probably damaging |
Het |
Arid1a |
A |
C |
4: 133,423,010 (GRCm39) |
|
probably benign |
Het |
Atp4a |
G |
T |
7: 30,423,678 (GRCm39) |
E928* |
probably null |
Het |
Atp5pf |
T |
C |
16: 84,624,862 (GRCm39) |
D104G |
probably benign |
Het |
Atp8b5 |
A |
G |
4: 43,320,629 (GRCm39) |
T206A |
probably damaging |
Het |
Atrn |
G |
A |
2: 130,777,497 (GRCm39) |
W182* |
probably null |
Het |
Bltp2 |
T |
C |
11: 78,168,154 (GRCm39) |
S1530P |
possibly damaging |
Het |
Cacna1e |
G |
A |
1: 154,437,579 (GRCm39) |
T257I |
probably damaging |
Het |
Caskin1 |
G |
A |
17: 24,725,602 (GRCm39) |
S1296N |
probably benign |
Het |
Crebrf |
A |
G |
17: 26,961,938 (GRCm39) |
Y345C |
probably benign |
Het |
Cyp26b1 |
G |
A |
6: 84,551,473 (GRCm39) |
R248W |
probably damaging |
Het |
Dclk3 |
C |
A |
9: 111,297,060 (GRCm39) |
H201Q |
probably benign |
Het |
Ddx17 |
A |
T |
15: 79,422,793 (GRCm39) |
V315E |
probably damaging |
Het |
Dhrs11 |
T |
C |
11: 84,716,342 (GRCm39) |
*51W |
probably null |
Het |
Fgfr4 |
C |
A |
13: 55,309,328 (GRCm39) |
P455Q |
possibly damaging |
Het |
Gabbr1 |
A |
G |
17: 37,380,103 (GRCm39) |
K697E |
probably damaging |
Het |
Gcnt1 |
G |
A |
19: 17,307,641 (GRCm39) |
T28I |
probably benign |
Het |
Gga2 |
G |
A |
7: 121,620,301 (GRCm39) |
T4M |
unknown |
Het |
Gm12185 |
T |
A |
11: 48,799,305 (GRCm39) |
H396L |
possibly damaging |
Het |
Gm21976 |
A |
G |
13: 98,441,839 (GRCm39) |
R123G |
probably benign |
Het |
Hecw1 |
A |
C |
13: 14,531,776 (GRCm39) |
V166G |
probably damaging |
Het |
Hpx |
A |
G |
7: 105,241,295 (GRCm39) |
V372A |
possibly damaging |
Het |
Igkv2-109 |
A |
G |
6: 68,279,962 (GRCm39) |
Y61C |
probably damaging |
Het |
Igsf1 |
A |
G |
X: 48,875,050 (GRCm39) |
F789S |
probably damaging |
Het |
Il4ra |
A |
G |
7: 125,175,280 (GRCm39) |
D496G |
possibly damaging |
Het |
Ilf3 |
A |
G |
9: 21,310,511 (GRCm39) |
T547A |
possibly damaging |
Het |
Insrr |
C |
A |
3: 87,715,978 (GRCm39) |
P558T |
possibly damaging |
Het |
Ints9 |
A |
G |
14: 65,266,381 (GRCm39) |
D411G |
possibly damaging |
Het |
Irak3 |
T |
A |
10: 119,981,813 (GRCm39) |
H393L |
probably damaging |
Het |
Isx |
G |
A |
8: 75,600,298 (GRCm39) |
M10I |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,668,870 (GRCm39) |
D709G |
probably damaging |
Het |
Kcng2 |
G |
T |
18: 80,338,930 (GRCm39) |
R453S |
probably benign |
Het |
Kif5b |
A |
G |
18: 6,214,011 (GRCm39) |
V664A |
probably benign |
Het |
Lalba |
A |
G |
15: 98,380,422 (GRCm39) |
L44P |
probably benign |
Het |
Ldlrad1 |
T |
G |
4: 107,066,715 (GRCm39) |
F17V |
probably benign |
Het |
Lnx1 |
C |
T |
5: 74,780,853 (GRCm39) |
D382N |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,429,717 (GRCm39) |
Y451C |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,310,406 (GRCm39) |
N2722K |
possibly damaging |
Het |
Mctp1 |
G |
A |
13: 76,973,391 (GRCm39) |
V431I |
probably benign |
Het |
Mmrn2 |
T |
C |
14: 34,125,016 (GRCm39) |
F866L |
possibly damaging |
Het |
Mylk2 |
A |
G |
2: 152,759,330 (GRCm39) |
E367G |
probably damaging |
Het |
Nfatc1 |
A |
G |
18: 80,678,794 (GRCm39) |
S865P |
probably damaging |
Het |
Nol6 |
G |
C |
4: 41,123,526 (GRCm39) |
T74R |
probably damaging |
Het |
Notch2 |
T |
C |
3: 98,053,637 (GRCm39) |
M2100T |
probably benign |
Het |
Parp1 |
A |
G |
1: 180,418,841 (GRCm39) |
K667R |
possibly damaging |
Het |
Phlda3 |
A |
G |
1: 135,694,400 (GRCm39) |
T72A |
probably damaging |
Het |
Polg |
T |
C |
7: 79,105,270 (GRCm39) |
Q758R |
probably benign |
Het |
Polq |
G |
A |
16: 36,868,925 (GRCm39) |
R765H |
probably damaging |
Het |
Pramel19 |
A |
T |
4: 101,798,757 (GRCm39) |
M243L |
probably benign |
Het |
Prkd1 |
T |
C |
12: 50,439,762 (GRCm39) |
D355G |
possibly damaging |
Het |
Prpf8 |
T |
C |
11: 75,382,652 (GRCm39) |
Y398H |
probably damaging |
Het |
Ripk1 |
T |
C |
13: 34,210,731 (GRCm39) |
Y309H |
probably damaging |
Het |
Rngtt |
A |
T |
4: 33,339,032 (GRCm39) |
Q279L |
possibly damaging |
Het |
Rusf1 |
A |
T |
7: 127,875,312 (GRCm39) |
F319Y |
probably damaging |
Het |
Samd4 |
T |
A |
14: 47,315,042 (GRCm39) |
V114D |
probably benign |
Het |
Sec23ip |
G |
A |
7: 128,380,900 (GRCm39) |
E956K |
probably damaging |
Het |
Slc4a1ap |
A |
T |
5: 31,684,747 (GRCm39) |
T128S |
probably benign |
Het |
Slc5a11 |
A |
T |
7: 122,834,858 (GRCm39) |
I6F |
probably benign |
Het |
Slc6a19 |
A |
C |
13: 73,832,094 (GRCm39) |
L494R |
probably damaging |
Het |
Slc6a21 |
A |
G |
7: 44,936,713 (GRCm39) |
D189G |
probably damaging |
Het |
Slc7a1 |
G |
T |
5: 148,277,372 (GRCm39) |
A381D |
probably damaging |
Het |
Smc4 |
T |
A |
3: 68,923,980 (GRCm39) |
|
probably null |
Het |
Stk19 |
T |
C |
17: 35,051,504 (GRCm39) |
E17G |
probably damaging |
Het |
Tekt5 |
A |
C |
16: 10,175,877 (GRCm39) |
V556G |
probably benign |
Het |
Tenm4 |
T |
C |
7: 96,544,070 (GRCm39) |
F2029L |
probably benign |
Het |
Thnsl1 |
T |
C |
2: 21,217,236 (GRCm39) |
V330A |
probably damaging |
Het |
Tnfrsf21 |
A |
G |
17: 43,375,910 (GRCm39) |
D432G |
probably damaging |
Het |
Tnip1 |
T |
A |
11: 54,817,616 (GRCm39) |
S244C |
probably benign |
Het |
Tnrc6c |
A |
T |
11: 117,633,784 (GRCm39) |
N1294I |
possibly damaging |
Het |
Trpm3 |
A |
G |
19: 22,965,381 (GRCm39) |
I1625M |
probably benign |
Het |
Ttn |
A |
T |
2: 76,575,773 (GRCm39) |
V25040E |
probably damaging |
Het |
Vwa5a |
A |
G |
9: 38,633,853 (GRCm39) |
N19D |
possibly damaging |
Het |
Washc2 |
A |
T |
6: 116,197,517 (GRCm39) |
D250V |
probably damaging |
Het |
Xpo1 |
A |
G |
11: 23,237,401 (GRCm39) |
T755A |
possibly damaging |
Het |
Zfp937 |
A |
C |
2: 150,080,431 (GRCm39) |
T154P |
probably damaging |
Het |
Zzef1 |
A |
G |
11: 72,778,996 (GRCm39) |
D1819G |
probably benign |
Het |
|
Other mutations in Zfp462 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00162:Zfp462
|
APN |
4 |
55,011,483 (GRCm39) |
splice site |
probably null |
|
IGL00421:Zfp462
|
APN |
4 |
55,023,576 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00899:Zfp462
|
APN |
4 |
55,007,732 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Zfp462
|
APN |
4 |
55,013,181 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01627:Zfp462
|
APN |
4 |
55,008,912 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01715:Zfp462
|
APN |
4 |
55,008,586 (GRCm39) |
missense |
probably benign |
0.20 |
IGL01862:Zfp462
|
APN |
4 |
55,023,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01878:Zfp462
|
APN |
4 |
55,010,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01913:Zfp462
|
APN |
4 |
55,012,138 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02029:Zfp462
|
APN |
4 |
55,079,395 (GRCm39) |
splice site |
probably benign |
|
IGL02338:Zfp462
|
APN |
4 |
55,010,292 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02552:Zfp462
|
APN |
4 |
55,010,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Zfp462
|
APN |
4 |
55,012,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02750:Zfp462
|
APN |
4 |
55,060,236 (GRCm39) |
missense |
probably null |
1.00 |
IGL02815:Zfp462
|
APN |
4 |
55,051,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03204:Zfp462
|
APN |
4 |
55,080,785 (GRCm39) |
missense |
possibly damaging |
0.80 |
FR4304:Zfp462
|
UTSW |
4 |
55,009,758 (GRCm39) |
unclassified |
probably benign |
|
FR4304:Zfp462
|
UTSW |
4 |
55,009,757 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Zfp462
|
UTSW |
4 |
55,009,760 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Zfp462
|
UTSW |
4 |
55,009,758 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Zfp462
|
UTSW |
4 |
55,009,761 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Zfp462
|
UTSW |
4 |
55,009,760 (GRCm39) |
unclassified |
probably benign |
|
P0035:Zfp462
|
UTSW |
4 |
55,009,086 (GRCm39) |
missense |
probably benign |
|
R0052:Zfp462
|
UTSW |
4 |
55,011,762 (GRCm39) |
missense |
probably benign |
0.03 |
R0143:Zfp462
|
UTSW |
4 |
55,023,402 (GRCm39) |
splice site |
probably benign |
|
R0145:Zfp462
|
UTSW |
4 |
55,010,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R0315:Zfp462
|
UTSW |
4 |
55,079,314 (GRCm39) |
missense |
probably damaging |
0.99 |
R0349:Zfp462
|
UTSW |
4 |
55,008,768 (GRCm39) |
missense |
probably benign |
|
R0359:Zfp462
|
UTSW |
4 |
55,013,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Zfp462
|
UTSW |
4 |
55,010,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R0554:Zfp462
|
UTSW |
4 |
55,013,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Zfp462
|
UTSW |
4 |
55,011,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Zfp462
|
UTSW |
4 |
55,007,563 (GRCm39) |
start codon destroyed |
possibly damaging |
0.60 |
R1086:Zfp462
|
UTSW |
4 |
55,013,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Zfp462
|
UTSW |
4 |
55,060,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Zfp462
|
UTSW |
4 |
55,007,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Zfp462
|
UTSW |
4 |
55,009,002 (GRCm39) |
missense |
probably benign |
|
R1541:Zfp462
|
UTSW |
4 |
55,008,928 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1691:Zfp462
|
UTSW |
4 |
55,013,489 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1843:Zfp462
|
UTSW |
4 |
55,010,010 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2086:Zfp462
|
UTSW |
4 |
55,010,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Zfp462
|
UTSW |
4 |
55,008,496 (GRCm39) |
missense |
probably benign |
0.00 |
R2148:Zfp462
|
UTSW |
4 |
55,013,670 (GRCm39) |
missense |
probably benign |
0.01 |
R2179:Zfp462
|
UTSW |
4 |
55,009,524 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2325:Zfp462
|
UTSW |
4 |
55,013,712 (GRCm39) |
missense |
probably benign |
|
R2352:Zfp462
|
UTSW |
4 |
55,008,313 (GRCm39) |
missense |
probably null |
|
R2566:Zfp462
|
UTSW |
4 |
55,008,522 (GRCm39) |
missense |
probably benign |
0.00 |
R3879:Zfp462
|
UTSW |
4 |
55,060,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R3969:Zfp462
|
UTSW |
4 |
55,012,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Zfp462
|
UTSW |
4 |
55,008,411 (GRCm39) |
missense |
probably benign |
0.00 |
R4413:Zfp462
|
UTSW |
4 |
55,012,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R4511:Zfp462
|
UTSW |
4 |
55,008,934 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4609:Zfp462
|
UTSW |
4 |
55,011,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Zfp462
|
UTSW |
4 |
55,012,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Zfp462
|
UTSW |
4 |
55,009,349 (GRCm39) |
missense |
probably benign |
|
R4682:Zfp462
|
UTSW |
4 |
55,011,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R4696:Zfp462
|
UTSW |
4 |
55,008,612 (GRCm39) |
missense |
probably benign |
|
R4744:Zfp462
|
UTSW |
4 |
55,011,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Zfp462
|
UTSW |
4 |
55,013,476 (GRCm39) |
missense |
probably benign |
0.00 |
R4819:Zfp462
|
UTSW |
4 |
55,060,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4827:Zfp462
|
UTSW |
4 |
55,012,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:Zfp462
|
UTSW |
4 |
55,010,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Zfp462
|
UTSW |
4 |
55,009,444 (GRCm39) |
missense |
probably benign |
0.02 |
R4891:Zfp462
|
UTSW |
4 |
55,060,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R4993:Zfp462
|
UTSW |
4 |
55,051,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5118:Zfp462
|
UTSW |
4 |
55,010,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Zfp462
|
UTSW |
4 |
55,016,986 (GRCm39) |
splice site |
probably null |
|
R5173:Zfp462
|
UTSW |
4 |
55,011,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R5221:Zfp462
|
UTSW |
4 |
55,016,887 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5268:Zfp462
|
UTSW |
4 |
55,012,299 (GRCm39) |
missense |
probably benign |
|
R5314:Zfp462
|
UTSW |
4 |
55,013,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5429:Zfp462
|
UTSW |
4 |
55,060,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Zfp462
|
UTSW |
4 |
55,009,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R5525:Zfp462
|
UTSW |
4 |
55,050,281 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5620:Zfp462
|
UTSW |
4 |
55,013,464 (GRCm39) |
missense |
probably benign |
0.01 |
R5775:Zfp462
|
UTSW |
4 |
55,010,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R6126:Zfp462
|
UTSW |
4 |
55,023,573 (GRCm39) |
missense |
probably benign |
0.01 |
R6280:Zfp462
|
UTSW |
4 |
55,010,253 (GRCm39) |
missense |
probably benign |
0.00 |
R6325:Zfp462
|
UTSW |
4 |
55,080,680 (GRCm39) |
missense |
probably benign |
0.04 |
R6542:Zfp462
|
UTSW |
4 |
55,023,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6612:Zfp462
|
UTSW |
4 |
55,012,324 (GRCm39) |
splice site |
probably null |
|
R6663:Zfp462
|
UTSW |
4 |
55,008,933 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6872:Zfp462
|
UTSW |
4 |
55,012,326 (GRCm39) |
missense |
probably benign |
0.01 |
R6889:Zfp462
|
UTSW |
4 |
55,007,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Zfp462
|
UTSW |
4 |
55,009,544 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6913:Zfp462
|
UTSW |
4 |
55,007,775 (GRCm39) |
missense |
probably benign |
0.25 |
R6988:Zfp462
|
UTSW |
4 |
55,080,716 (GRCm39) |
missense |
probably benign |
0.00 |
R7131:Zfp462
|
UTSW |
4 |
55,009,380 (GRCm39) |
missense |
probably benign |
|
R7151:Zfp462
|
UTSW |
4 |
55,051,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R7684:Zfp462
|
UTSW |
4 |
55,008,908 (GRCm39) |
missense |
probably benign |
|
R7741:Zfp462
|
UTSW |
4 |
55,008,637 (GRCm39) |
missense |
probably benign |
0.00 |
R7750:Zfp462
|
UTSW |
4 |
55,016,958 (GRCm39) |
missense |
probably benign |
0.06 |
R7812:Zfp462
|
UTSW |
4 |
55,008,509 (GRCm39) |
missense |
probably benign |
0.00 |
R7863:Zfp462
|
UTSW |
4 |
55,007,747 (GRCm39) |
missense |
probably benign |
|
R7898:Zfp462
|
UTSW |
4 |
55,012,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R7993:Zfp462
|
UTSW |
4 |
55,011,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R7995:Zfp462
|
UTSW |
4 |
55,011,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R8023:Zfp462
|
UTSW |
4 |
55,073,106 (GRCm39) |
critical splice donor site |
probably null |
|
R8394:Zfp462
|
UTSW |
4 |
55,011,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Zfp462
|
UTSW |
4 |
55,051,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R8877:Zfp462
|
UTSW |
4 |
55,011,097 (GRCm39) |
missense |
probably damaging |
0.98 |
R8980:Zfp462
|
UTSW |
4 |
55,009,681 (GRCm39) |
unclassified |
probably benign |
|
R9023:Zfp462
|
UTSW |
4 |
55,007,563 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R9243:Zfp462
|
UTSW |
4 |
55,009,595 (GRCm39) |
nonsense |
probably null |
|
R9378:Zfp462
|
UTSW |
4 |
55,011,510 (GRCm39) |
missense |
probably benign |
0.00 |
R9417:Zfp462
|
UTSW |
4 |
55,016,988 (GRCm39) |
missense |
probably benign |
0.26 |
R9476:Zfp462
|
UTSW |
4 |
55,080,735 (GRCm39) |
missense |
probably benign |
|
R9510:Zfp462
|
UTSW |
4 |
55,080,735 (GRCm39) |
missense |
probably benign |
|
R9610:Zfp462
|
UTSW |
4 |
55,009,545 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9628:Zfp462
|
UTSW |
4 |
55,009,423 (GRCm39) |
missense |
probably benign |
|
|