Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930546C10Rik |
A |
T |
18: 69,083,208 (GRCm39) |
M2K |
unknown |
Het |
Ablim3 |
T |
C |
18: 61,955,065 (GRCm39) |
D308G |
probably damaging |
Het |
Adamts17 |
A |
T |
7: 66,618,597 (GRCm39) |
K370N |
probably benign |
Het |
Adcy4 |
T |
C |
14: 56,015,784 (GRCm39) |
Y435C |
probably damaging |
Het |
Adgb |
A |
T |
10: 10,253,693 (GRCm39) |
F1216I |
possibly damaging |
Het |
Akr1a1 |
G |
A |
4: 116,498,251 (GRCm39) |
T98I |
probably damaging |
Het |
Alyref2 |
G |
T |
1: 171,331,101 (GRCm39) |
|
probably benign |
Het |
Ank3 |
T |
A |
10: 69,658,079 (GRCm39) |
H168Q |
unknown |
Het |
Bnc1 |
A |
C |
7: 81,624,240 (GRCm39) |
L329R |
possibly damaging |
Het |
Btaf1 |
G |
A |
19: 36,935,782 (GRCm39) |
A191T |
probably benign |
Het |
Carmil3 |
T |
G |
14: 55,735,204 (GRCm39) |
|
probably null |
Het |
Cd200r1 |
C |
A |
16: 44,610,211 (GRCm39) |
D143E |
probably benign |
Het |
Cep112 |
A |
G |
11: 108,699,507 (GRCm39) |
H98R |
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,205,831 (GRCm39) |
Q3346L |
probably damaging |
Het |
Cpne4 |
T |
A |
9: 104,749,939 (GRCm39) |
V81E |
possibly damaging |
Het |
Ctnnd2 |
T |
A |
15: 30,966,914 (GRCm39) |
M955K |
probably damaging |
Het |
Ctsj |
A |
T |
13: 61,148,373 (GRCm39) |
M307K |
possibly damaging |
Het |
Ddhd2 |
G |
T |
8: 26,244,318 (GRCm39) |
R103S |
possibly damaging |
Het |
Depdc5 |
A |
G |
5: 33,085,280 (GRCm39) |
T700A |
probably benign |
Het |
Dmbt1 |
G |
A |
7: 130,713,965 (GRCm39) |
G1678S |
unknown |
Het |
Dnajb1 |
A |
G |
8: 84,336,932 (GRCm39) |
D234G |
probably benign |
Het |
Dsc2 |
C |
T |
18: 20,174,983 (GRCm39) |
V431M |
possibly damaging |
Het |
Evi5 |
C |
A |
5: 107,957,689 (GRCm39) |
|
probably null |
Het |
Exoc2 |
T |
C |
13: 31,090,646 (GRCm39) |
|
probably null |
Het |
Foxo3 |
T |
C |
10: 42,073,356 (GRCm39) |
D387G |
probably benign |
Het |
Gda |
A |
G |
19: 21,387,250 (GRCm39) |
I325T |
probably benign |
Het |
Iqgap1 |
A |
G |
7: 80,375,790 (GRCm39) |
S1362P |
probably damaging |
Het |
Klf10 |
G |
T |
15: 38,297,193 (GRCm39) |
N282K |
possibly damaging |
Het |
Mettl13 |
A |
G |
1: 162,375,723 (GRCm39) |
Y35H |
probably damaging |
Het |
Mill2 |
A |
G |
7: 18,592,215 (GRCm39) |
T279A |
probably benign |
Het |
Ncaph2 |
G |
A |
15: 89,254,459 (GRCm39) |
W386* |
probably null |
Het |
Nploc4 |
A |
T |
11: 120,299,707 (GRCm39) |
S338T |
probably benign |
Het |
Nrip1 |
T |
C |
16: 76,090,775 (GRCm39) |
S261G |
probably damaging |
Het |
Or2y16 |
T |
C |
11: 49,335,227 (GRCm39) |
F183S |
possibly damaging |
Het |
Or5al1 |
A |
G |
2: 85,989,874 (GRCm39) |
V280A |
possibly damaging |
Het |
Or7a38 |
T |
A |
10: 78,752,677 (GRCm39) |
M1K |
probably null |
Het |
Palld |
A |
G |
8: 61,985,086 (GRCm39) |
F1060L |
unknown |
Het |
Pfas |
C |
G |
11: 68,894,600 (GRCm39) |
V22L |
probably benign |
Het |
Pygo2 |
T |
G |
3: 89,340,128 (GRCm39) |
F175L |
probably benign |
Het |
Rnf2 |
T |
C |
1: 151,347,131 (GRCm39) |
E316G |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,657,772 (GRCm39) |
M642K |
probably damaging |
Het |
Saa3 |
A |
G |
7: 46,364,347 (GRCm39) |
C60R |
unknown |
Het |
Saxo5 |
A |
G |
8: 3,537,079 (GRCm39) |
K475R |
probably benign |
Het |
Scap |
A |
G |
9: 110,202,237 (GRCm39) |
T202A |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,370,894 (GRCm39) |
D562V |
probably damaging |
Het |
Slc6a19 |
A |
T |
13: 73,838,010 (GRCm39) |
V163E |
possibly damaging |
Het |
Smc5 |
G |
A |
19: 23,192,539 (GRCm39) |
H850Y |
possibly damaging |
Het |
Spef1l |
A |
T |
7: 139,555,965 (GRCm39) |
C225* |
probably null |
Het |
Sqle |
G |
A |
15: 59,202,603 (GRCm39) |
R519Q |
probably benign |
Het |
Sulf1 |
T |
C |
1: 12,908,585 (GRCm39) |
Y533H |
probably benign |
Het |
Thbs2 |
A |
G |
17: 14,893,412 (GRCm39) |
S923P |
possibly damaging |
Het |
Themis |
A |
G |
10: 28,665,743 (GRCm39) |
D602G |
probably benign |
Het |
Tmem132c |
A |
G |
5: 127,640,990 (GRCm39) |
K1054E |
probably benign |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tnrc6c |
T |
A |
11: 117,612,780 (GRCm39) |
C313S |
probably benign |
Het |
Top6bl |
G |
A |
19: 4,713,586 (GRCm39) |
R285* |
probably null |
Het |
Tpm1 |
T |
C |
9: 66,935,449 (GRCm39) |
I284M |
probably benign |
Het |
Trpm4 |
A |
T |
7: 44,964,064 (GRCm39) |
L722H |
possibly damaging |
Het |
Trub2 |
T |
G |
2: 29,676,607 (GRCm39) |
Q41P |
probably benign |
Het |
Usp17le |
A |
C |
7: 104,417,514 (GRCm39) |
|
probably null |
Het |
Zfp398 |
G |
A |
6: 47,835,884 (GRCm39) |
V148I |
probably benign |
Het |
Zfp40 |
T |
C |
17: 23,395,981 (GRCm39) |
E202G |
probably damaging |
Het |
Zfp618 |
T |
A |
4: 63,013,622 (GRCm39) |
|
probably null |
Het |
Zfp667 |
T |
A |
7: 6,308,949 (GRCm39) |
I539N |
possibly damaging |
Het |
Zfp738 |
A |
T |
13: 67,818,369 (GRCm39) |
C541S |
probably damaging |
Het |
|
Other mutations in Dhx57 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00642:Dhx57
|
APN |
17 |
80,582,405 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00811:Dhx57
|
APN |
17 |
80,560,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01389:Dhx57
|
APN |
17 |
80,588,652 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01468:Dhx57
|
APN |
17 |
80,563,039 (GRCm39) |
nonsense |
probably null |
|
IGL01908:Dhx57
|
APN |
17 |
80,558,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01965:Dhx57
|
APN |
17 |
80,576,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02147:Dhx57
|
APN |
17 |
80,567,752 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02275:Dhx57
|
APN |
17 |
80,582,268 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02349:Dhx57
|
APN |
17 |
80,563,000 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02405:Dhx57
|
APN |
17 |
80,562,979 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02588:Dhx57
|
APN |
17 |
80,576,300 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02673:Dhx57
|
APN |
17 |
80,574,974 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02836:Dhx57
|
APN |
17 |
80,574,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02889:Dhx57
|
APN |
17 |
80,554,581 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03085:Dhx57
|
APN |
17 |
80,565,526 (GRCm39) |
missense |
possibly damaging |
0.48 |
P0014:Dhx57
|
UTSW |
17 |
80,582,620 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4377001:Dhx57
|
UTSW |
17 |
80,571,404 (GRCm39) |
missense |
probably damaging |
0.96 |
R0100:Dhx57
|
UTSW |
17 |
80,582,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0100:Dhx57
|
UTSW |
17 |
80,582,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0129:Dhx57
|
UTSW |
17 |
80,546,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Dhx57
|
UTSW |
17 |
80,558,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Dhx57
|
UTSW |
17 |
80,582,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Dhx57
|
UTSW |
17 |
80,565,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Dhx57
|
UTSW |
17 |
80,582,226 (GRCm39) |
missense |
probably benign |
0.34 |
R0520:Dhx57
|
UTSW |
17 |
80,565,604 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0554:Dhx57
|
UTSW |
17 |
80,567,665 (GRCm39) |
nonsense |
probably null |
|
R0661:Dhx57
|
UTSW |
17 |
80,576,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Dhx57
|
UTSW |
17 |
80,577,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R0900:Dhx57
|
UTSW |
17 |
80,583,011 (GRCm39) |
missense |
probably benign |
|
R0963:Dhx57
|
UTSW |
17 |
80,582,956 (GRCm39) |
missense |
probably benign |
0.01 |
R1469:Dhx57
|
UTSW |
17 |
80,561,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Dhx57
|
UTSW |
17 |
80,561,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1660:Dhx57
|
UTSW |
17 |
80,553,157 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1707:Dhx57
|
UTSW |
17 |
80,582,655 (GRCm39) |
missense |
probably damaging |
0.96 |
R1822:Dhx57
|
UTSW |
17 |
80,560,514 (GRCm39) |
critical splice donor site |
probably null |
|
R1853:Dhx57
|
UTSW |
17 |
80,582,308 (GRCm39) |
nonsense |
probably null |
|
R1942:Dhx57
|
UTSW |
17 |
80,572,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2043:Dhx57
|
UTSW |
17 |
80,560,509 (GRCm39) |
splice site |
probably benign |
|
R2106:Dhx57
|
UTSW |
17 |
80,582,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Dhx57
|
UTSW |
17 |
80,580,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R2183:Dhx57
|
UTSW |
17 |
80,582,760 (GRCm39) |
missense |
probably benign |
0.07 |
R2249:Dhx57
|
UTSW |
17 |
80,588,663 (GRCm39) |
missense |
probably damaging |
0.98 |
R2400:Dhx57
|
UTSW |
17 |
80,567,845 (GRCm39) |
missense |
probably damaging |
0.99 |
R2404:Dhx57
|
UTSW |
17 |
80,561,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R2513:Dhx57
|
UTSW |
17 |
80,549,378 (GRCm39) |
splice site |
probably null |
|
R2869:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R2869:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R2870:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R2870:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R2871:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R2871:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R2874:Dhx57
|
UTSW |
17 |
80,558,805 (GRCm39) |
missense |
probably benign |
0.22 |
R3819:Dhx57
|
UTSW |
17 |
80,572,503 (GRCm39) |
critical splice donor site |
probably null |
|
R3964:Dhx57
|
UTSW |
17 |
80,572,541 (GRCm39) |
nonsense |
probably null |
|
R4535:Dhx57
|
UTSW |
17 |
80,582,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Dhx57
|
UTSW |
17 |
80,582,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Dhx57
|
UTSW |
17 |
80,582,760 (GRCm39) |
missense |
probably benign |
0.01 |
R4822:Dhx57
|
UTSW |
17 |
80,549,596 (GRCm39) |
splice site |
probably null |
|
R4863:Dhx57
|
UTSW |
17 |
80,560,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4988:Dhx57
|
UTSW |
17 |
80,558,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R5391:Dhx57
|
UTSW |
17 |
80,582,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R5559:Dhx57
|
UTSW |
17 |
80,561,808 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5644:Dhx57
|
UTSW |
17 |
80,546,302 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5997:Dhx57
|
UTSW |
17 |
80,553,235 (GRCm39) |
missense |
probably damaging |
0.96 |
R6090:Dhx57
|
UTSW |
17 |
80,571,375 (GRCm39) |
critical splice donor site |
probably null |
|
R6177:Dhx57
|
UTSW |
17 |
80,580,395 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6283:Dhx57
|
UTSW |
17 |
80,582,234 (GRCm39) |
missense |
probably benign |
0.00 |
R6802:Dhx57
|
UTSW |
17 |
80,582,750 (GRCm39) |
missense |
probably benign |
0.43 |
R6924:Dhx57
|
UTSW |
17 |
80,546,244 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7151:Dhx57
|
UTSW |
17 |
80,580,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Dhx57
|
UTSW |
17 |
80,563,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Dhx57
|
UTSW |
17 |
80,554,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R7602:Dhx57
|
UTSW |
17 |
80,582,290 (GRCm39) |
missense |
probably benign |
0.06 |
R7733:Dhx57
|
UTSW |
17 |
80,572,503 (GRCm39) |
critical splice donor site |
probably null |
|
R7748:Dhx57
|
UTSW |
17 |
80,572,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7749:Dhx57
|
UTSW |
17 |
80,546,287 (GRCm39) |
missense |
probably benign |
0.04 |
R7772:Dhx57
|
UTSW |
17 |
80,580,507 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8213:Dhx57
|
UTSW |
17 |
80,582,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8370:Dhx57
|
UTSW |
17 |
80,553,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R8371:Dhx57
|
UTSW |
17 |
80,582,919 (GRCm39) |
missense |
probably benign |
0.18 |
R8403:Dhx57
|
UTSW |
17 |
80,585,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R8467:Dhx57
|
UTSW |
17 |
80,561,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8690:Dhx57
|
UTSW |
17 |
80,577,794 (GRCm39) |
critical splice donor site |
probably benign |
|
R9210:Dhx57
|
UTSW |
17 |
80,576,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R9212:Dhx57
|
UTSW |
17 |
80,576,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R9447:Dhx57
|
UTSW |
17 |
80,549,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Dhx57
|
UTSW |
17 |
80,561,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R9669:Dhx57
|
UTSW |
17 |
80,553,130 (GRCm39) |
missense |
probably benign |
0.09 |
R9717:Dhx57
|
UTSW |
17 |
80,582,447 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dhx57
|
UTSW |
17 |
80,558,777 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dhx57
|
UTSW |
17 |
80,553,234 (GRCm39) |
missense |
probably damaging |
0.96 |
|