Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
A |
C |
15: 102,246,826 (GRCm39) |
S511A |
probably benign |
Het |
Abca3 |
C |
T |
17: 24,615,444 (GRCm39) |
T845I |
probably benign |
Het |
Acaa2 |
G |
A |
18: 74,938,945 (GRCm39) |
A377T |
possibly damaging |
Het |
Adcy4 |
C |
A |
14: 56,009,824 (GRCm39) |
E743* |
probably null |
Het |
Ahnak |
T |
A |
19: 8,990,458 (GRCm39) |
L3914* |
probably null |
Het |
Akap1 |
G |
T |
11: 88,736,343 (GRCm39) |
N106K |
possibly damaging |
Het |
Arid2 |
C |
T |
15: 96,270,387 (GRCm39) |
T1500I |
probably benign |
Het |
Atp6v0a2 |
T |
A |
5: 124,783,909 (GRCm39) |
Y252* |
probably null |
Het |
C4bp |
A |
G |
1: 130,581,090 (GRCm39) |
S140P |
probably damaging |
Het |
Cald1 |
A |
G |
6: 34,739,047 (GRCm39) |
I384M |
probably damaging |
Het |
Cdk12 |
A |
G |
11: 98,101,809 (GRCm39) |
I556V |
unknown |
Het |
Chmp2a |
T |
C |
7: 12,766,237 (GRCm39) |
S174G |
probably benign |
Het |
Clybl |
T |
A |
14: 122,548,755 (GRCm39) |
N52K |
probably damaging |
Het |
Cyp4a29 |
C |
A |
4: 115,108,088 (GRCm39) |
S303R |
probably benign |
Het |
Dab2 |
T |
A |
15: 6,447,796 (GRCm39) |
D59E |
probably damaging |
Het |
Dag1 |
C |
A |
9: 108,086,214 (GRCm39) |
R309L |
probably damaging |
Het |
Dync1i2 |
T |
A |
2: 71,088,483 (GRCm39) |
M505K |
probably benign |
Het |
Eif2b1 |
A |
T |
5: 124,717,075 (GRCm39) |
M1K |
probably null |
Het |
Epc1 |
A |
G |
18: 6,448,917 (GRCm39) |
S577P |
probably benign |
Het |
Eps8l1 |
T |
A |
7: 4,463,945 (GRCm39) |
I23N |
possibly damaging |
Het |
Etl4 |
A |
G |
2: 20,535,037 (GRCm39) |
E164G |
probably damaging |
Het |
Firrm |
C |
A |
1: 163,789,613 (GRCm39) |
G641* |
probably null |
Het |
Gadl1 |
A |
T |
9: 115,766,230 (GRCm39) |
M1L |
probably benign |
Het |
Gda |
T |
C |
19: 21,374,908 (GRCm39) |
D336G |
probably damaging |
Het |
Grm2 |
A |
T |
9: 106,527,645 (GRCm39) |
V413D |
probably damaging |
Het |
Hnrnpll |
G |
T |
17: 80,346,051 (GRCm39) |
N403K |
probably damaging |
Het |
Ifit1 |
T |
A |
19: 34,625,238 (GRCm39) |
F125I |
probably damaging |
Het |
Igkv5-43 |
C |
T |
6: 69,800,892 (GRCm39) |
V2I |
probably benign |
Het |
Kat5 |
A |
C |
19: 5,659,507 (GRCm39) |
Y44* |
probably null |
Het |
Klc2 |
A |
G |
19: 5,162,884 (GRCm39) |
V205A |
probably damaging |
Het |
Klrb1c |
T |
A |
6: 128,761,706 (GRCm39) |
T133S |
possibly damaging |
Het |
Krt20 |
A |
G |
11: 99,326,283 (GRCm39) |
L157P |
probably damaging |
Het |
Krt26 |
G |
T |
11: 99,228,597 (GRCm39) |
T45N |
possibly damaging |
Het |
Lama2 |
C |
T |
10: 26,866,876 (GRCm39) |
D2873N |
probably damaging |
Het |
Lig1 |
T |
A |
7: 13,020,532 (GRCm39) |
C114S |
possibly damaging |
Het |
Lonp1 |
G |
C |
17: 56,927,263 (GRCm39) |
A330G |
probably benign |
Het |
Maml2 |
A |
T |
9: 13,608,616 (GRCm39) |
R21S |
probably damaging |
Het |
Mrpl35 |
C |
T |
6: 71,794,720 (GRCm39) |
V83I |
probably benign |
Het |
Myo3b |
A |
G |
2: 70,069,254 (GRCm39) |
R498G |
probably benign |
Het |
Nup153 |
C |
A |
13: 46,837,482 (GRCm39) |
E1247* |
probably null |
Het |
Or2t48 |
A |
T |
11: 58,420,557 (GRCm39) |
M85K |
probably damaging |
Het |
Pcdhac2 |
A |
G |
18: 37,277,257 (GRCm39) |
N79S |
probably benign |
Het |
Pcgf6 |
C |
T |
19: 47,036,406 (GRCm39) |
G221D |
probably damaging |
Het |
Phf11b |
C |
T |
14: 59,558,953 (GRCm39) |
D260N |
probably benign |
Het |
Pla2g5 |
T |
C |
4: 138,531,921 (GRCm39) |
M28V |
possibly damaging |
Het |
Prpf8 |
T |
C |
11: 75,395,927 (GRCm39) |
S1934P |
possibly damaging |
Het |
Prr5 |
A |
G |
15: 84,640,570 (GRCm39) |
S140G |
probably benign |
Het |
Prrc2c |
T |
C |
1: 162,501,098 (GRCm39) |
D1235G |
probably damaging |
Het |
Rasgrp2 |
T |
C |
19: 6,455,031 (GRCm39) |
S254P |
probably damaging |
Het |
Rassf8 |
C |
T |
6: 145,765,907 (GRCm39) |
|
probably benign |
Het |
Rgs20 |
T |
A |
1: 4,982,666 (GRCm39) |
E167D |
probably damaging |
Het |
Rmnd1 |
G |
T |
10: 4,372,159 (GRCm39) |
A180E |
probably damaging |
Het |
Rnf103 |
A |
G |
6: 71,486,992 (GRCm39) |
D541G |
probably benign |
Het |
Rpl9 |
G |
T |
5: 65,546,468 (GRCm39) |
Q140K |
probably benign |
Het |
Sfmbt1 |
T |
G |
14: 30,506,148 (GRCm39) |
|
probably null |
Het |
Shank1 |
C |
A |
7: 43,962,160 (GRCm39) |
D10E |
unknown |
Het |
Srrm4 |
G |
T |
5: 116,587,672 (GRCm39) |
|
probably benign |
Het |
Sucla2 |
T |
A |
14: 73,832,836 (GRCm39) |
V447E |
probably damaging |
Het |
Tbc1d1 |
A |
G |
5: 64,331,055 (GRCm39) |
D78G |
probably benign |
Het |
Tcp1 |
T |
A |
17: 13,138,224 (GRCm39) |
|
probably null |
Het |
Tctn3 |
C |
A |
19: 40,597,361 (GRCm39) |
E230* |
probably null |
Het |
Thsd7b |
G |
A |
1: 130,090,673 (GRCm39) |
|
probably null |
Het |
Tmem63a |
A |
G |
1: 180,797,811 (GRCm39) |
M621V |
probably benign |
Het |
Tnxb |
A |
T |
17: 34,936,504 (GRCm39) |
K2756* |
probably null |
Het |
Trpm8 |
G |
A |
1: 88,287,373 (GRCm39) |
|
probably null |
Het |
Txndc16 |
C |
A |
14: 45,373,335 (GRCm39) |
V764F |
possibly damaging |
Het |
Ush2a |
A |
T |
1: 188,492,020 (GRCm39) |
D3103V |
possibly damaging |
Het |
Usp22 |
A |
T |
11: 61,049,206 (GRCm39) |
I381N |
probably damaging |
Het |
Zfp64 |
T |
A |
2: 168,741,888 (GRCm39) |
M347L |
possibly damaging |
Het |
Zfp69 |
T |
C |
4: 120,787,719 (GRCm39) |
D532G |
probably 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 |
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 |
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 |
|
|