Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck1 |
A |
G |
12: 88,413,489 (GRCm39) |
R274G |
probably benign |
Het |
Agbl5 |
T |
G |
5: 31,053,158 (GRCm39) |
S83R |
probably damaging |
Het |
Ankib1 |
A |
G |
5: 3,751,907 (GRCm39) |
I711T |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,397,224 (GRCm39) |
|
probably null |
Het |
Atad2 |
C |
G |
15: 57,971,744 (GRCm39) |
V702L |
probably benign |
Het |
B4galnt4 |
A |
G |
7: 140,648,392 (GRCm39) |
E636G |
probably benign |
Het |
Btbd2 |
A |
G |
10: 80,482,223 (GRCm39) |
I244T |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,182,290 (GRCm39) |
N531K |
possibly damaging |
Het |
Ces3b |
T |
A |
8: 105,813,527 (GRCm39) |
M266K |
probably benign |
Het |
Cfap54 |
A |
T |
10: 92,737,937 (GRCm39) |
|
probably benign |
Het |
Coq8a |
A |
G |
1: 179,994,903 (GRCm39) |
V590A |
possibly damaging |
Het |
Drc7 |
A |
G |
8: 95,798,267 (GRCm39) |
Y504C |
probably damaging |
Het |
Elovl4 |
T |
C |
9: 83,688,091 (GRCm39) |
M1V |
probably null |
Het |
Exd1 |
C |
T |
2: 119,350,807 (GRCm39) |
A485T |
probably benign |
Het |
Fads2 |
A |
G |
19: 10,059,958 (GRCm39) |
F239L |
probably benign |
Het |
Gcc2 |
A |
T |
10: 58,121,953 (GRCm39) |
|
probably null |
Het |
Ggact |
C |
T |
14: 123,128,987 (GRCm39) |
R76H |
probably benign |
Het |
Gm17535 |
T |
A |
9: 3,035,786 (GRCm39) |
L218H |
probably benign |
Het |
Gm3739 |
A |
T |
14: 18,506,218 (GRCm39) |
F13I |
probably damaging |
Het |
Gng2 |
T |
C |
14: 19,925,898 (GRCm39) |
K65E |
possibly damaging |
Het |
Gnmt |
A |
G |
17: 47,038,245 (GRCm39) |
Y94H |
possibly damaging |
Het |
Gzme |
C |
A |
14: 56,356,755 (GRCm39) |
R69M |
probably null |
Het |
Hdc |
G |
A |
2: 126,436,233 (GRCm39) |
P546L |
probably benign |
Het |
Ibtk |
C |
A |
9: 85,610,607 (GRCm39) |
V326F |
probably benign |
Het |
Inpp5b |
G |
T |
4: 124,637,643 (GRCm39) |
|
probably benign |
Het |
Kcnh7 |
A |
T |
2: 62,546,564 (GRCm39) |
C1006S |
probably benign |
Het |
Kcnk18 |
A |
T |
19: 59,208,362 (GRCm39) |
N66I |
probably damaging |
Het |
Lpar6 |
T |
A |
14: 73,476,190 (GRCm39) |
N50K |
probably damaging |
Het |
Lrba |
G |
T |
3: 86,267,457 (GRCm39) |
D1716Y |
possibly damaging |
Het |
Ltf |
T |
A |
9: 110,856,445 (GRCm39) |
|
probably benign |
Het |
Map3k6 |
A |
G |
4: 132,976,160 (GRCm39) |
T794A |
possibly damaging |
Het |
Mcm8 |
A |
G |
2: 132,665,174 (GRCm39) |
T217A |
probably damaging |
Het |
Meaf6 |
A |
G |
4: 124,996,713 (GRCm39) |
E141G |
probably damaging |
Het |
Mmp13 |
A |
G |
9: 7,278,880 (GRCm39) |
T324A |
possibly damaging |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Msl2 |
T |
G |
9: 100,979,350 (GRCm39) |
F575V |
probably benign |
Het |
Ncoa4-ps |
C |
T |
12: 119,225,529 (GRCm39) |
|
noncoding transcript |
Het |
Nlrp2 |
A |
T |
7: 5,331,950 (GRCm39) |
W149R |
possibly damaging |
Het |
Ntng1 |
C |
A |
3: 110,042,727 (GRCm39) |
C33F |
probably damaging |
Het |
Nxn |
A |
G |
11: 76,152,418 (GRCm39) |
Y359H |
probably benign |
Het |
Olfml2a |
A |
C |
2: 38,850,033 (GRCm39) |
D583A |
probably damaging |
Het |
Or12j5 |
A |
C |
7: 140,083,583 (GRCm39) |
L263R |
probably damaging |
Het |
Or1e32 |
A |
T |
11: 73,705,547 (GRCm39) |
Y120* |
probably null |
Het |
Or2t48 |
A |
G |
11: 58,420,422 (GRCm39) |
I130T |
probably damaging |
Het |
Or4b1b |
A |
T |
2: 90,112,547 (GRCm39) |
I124N |
probably damaging |
Het |
Or51ac3 |
A |
T |
7: 103,213,752 (GRCm39) |
S245T |
probably damaging |
Het |
Pcdha4 |
T |
C |
18: 37,086,251 (GRCm39) |
S145P |
probably damaging |
Het |
Pcsk2 |
A |
T |
2: 143,643,099 (GRCm39) |
K459* |
probably null |
Het |
Pirb |
C |
T |
7: 3,720,602 (GRCm39) |
G299S |
probably benign |
Het |
Plch2 |
A |
G |
4: 155,075,570 (GRCm39) |
F653S |
probably damaging |
Het |
Plpp3 |
T |
C |
4: 105,088,167 (GRCm39) |
I296T |
probably benign |
Het |
Polr2b |
A |
G |
5: 77,490,398 (GRCm39) |
E846G |
probably benign |
Het |
Ptpro |
A |
T |
6: 137,419,708 (GRCm39) |
N157Y |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,723,222 (GRCm39) |
L1815P |
probably damaging |
Het |
Sap18 |
A |
G |
14: 58,036,020 (GRCm39) |
N69D |
probably damaging |
Het |
Sncg |
C |
A |
14: 34,095,284 (GRCm39) |
V74F |
probably damaging |
Het |
Spata31e2 |
T |
C |
1: 26,724,923 (GRCm39) |
K86E |
possibly damaging |
Het |
Spmip4 |
A |
C |
6: 50,572,836 (GRCm39) |
S26A |
possibly damaging |
Het |
Tmem186 |
A |
T |
16: 8,453,681 (GRCm39) |
Y193* |
probably null |
Het |
Trrap |
A |
G |
5: 144,737,758 (GRCm39) |
S1045G |
probably benign |
Het |
Tti2 |
T |
G |
8: 31,640,998 (GRCm39) |
S41A |
probably benign |
Het |
Unc13c |
T |
C |
9: 73,838,568 (GRCm39) |
E761G |
probably damaging |
Het |
Vamp2 |
T |
A |
11: 68,980,637 (GRCm39) |
D68E |
probably benign |
Het |
Vmn1r200 |
A |
T |
13: 22,579,265 (GRCm39) |
M14L |
probably benign |
Het |
Vps35 |
T |
A |
8: 86,000,186 (GRCm39) |
D480V |
possibly damaging |
Het |
Zfp512 |
G |
A |
5: 31,630,158 (GRCm39) |
M274I |
probably benign |
Het |
Znfx1 |
C |
G |
2: 166,886,151 (GRCm39) |
G803A |
possibly damaging |
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 |
R4510:Zfp462
|
UTSW |
4 |
55,008,934 (GRCm39) |
missense |
possibly damaging |
0.86 |
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 |
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 |
|
|