Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
C |
11: 9,273,951 |
R443S |
probably damaging |
Het |
Adgrl3 |
A |
G |
5: 81,792,347 |
|
probably benign |
Het |
Anapc1 |
T |
C |
2: 128,680,452 |
|
probably benign |
Het |
Aqr |
T |
A |
2: 114,149,016 |
I313F |
probably damaging |
Het |
Arfgap3 |
A |
T |
15: 83,322,721 |
|
probably benign |
Het |
Asah2 |
G |
T |
19: 32,018,977 |
H374N |
probably benign |
Het |
Ccdc106 |
C |
A |
7: 5,057,545 |
Q35K |
probably benign |
Het |
Ccm2l |
G |
T |
2: 153,067,919 |
E64* |
probably null |
Het |
Cep85l |
A |
T |
10: 53,278,174 |
D776E |
possibly damaging |
Het |
Cfap52 |
T |
A |
11: 67,925,125 |
I611F |
possibly damaging |
Het |
Cldn22 |
C |
T |
8: 47,824,554 |
T9M |
probably benign |
Het |
Coa7 |
T |
C |
4: 108,338,141 |
L89P |
possibly damaging |
Het |
Cox7a2l |
A |
T |
17: 83,514,272 |
Y2N |
probably damaging |
Het |
Cyp27a1 |
A |
C |
1: 74,735,915 |
E301A |
probably benign |
Het |
Dennd4c |
A |
G |
4: 86,812,446 |
Y860C |
probably benign |
Het |
Dhx58 |
T |
C |
11: 100,695,270 |
T642A |
probably damaging |
Het |
Dlg4 |
A |
G |
11: 70,031,193 |
Y87C |
probably damaging |
Het |
Dnah6 |
C |
T |
6: 73,092,172 |
E2511K |
probably damaging |
Het |
Entpd5 |
C |
A |
12: 84,396,943 |
E9* |
probably null |
Het |
Fbln2 |
A |
C |
6: 91,271,550 |
I1066L |
probably benign |
Het |
Fhl2 |
C |
T |
1: 43,153,221 |
R4H |
probably benign |
Het |
Frmpd1 |
T |
A |
4: 45,229,884 |
I17K |
probably damaging |
Het |
Gbp7 |
T |
A |
3: 142,546,538 |
N627K |
probably benign |
Het |
Gm16432 |
A |
G |
1: 178,116,205 |
N703D |
unknown |
Het |
Gnptab |
A |
G |
10: 88,429,519 |
Y331C |
probably damaging |
Het |
Hibadh |
T |
A |
6: 52,557,877 |
M173L |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,016,254 |
I211V |
probably benign |
Het |
Keg1 |
A |
T |
19: 12,718,916 |
I155F |
possibly damaging |
Het |
Ltb |
A |
G |
17: 35,195,040 |
|
probably benign |
Het |
Manea |
A |
T |
4: 26,329,080 |
|
probably null |
Het |
Ms4a4a |
T |
A |
19: 11,392,684 |
M202K |
possibly damaging |
Het |
Myo9b |
C |
T |
8: 71,323,849 |
|
probably benign |
Het |
Nanos3 |
C |
T |
8: 84,176,134 |
R133Q |
probably damaging |
Het |
Ncor1 |
G |
T |
11: 62,343,045 |
Q444K |
possibly damaging |
Het |
Nek7 |
A |
T |
1: 138,544,242 |
C53* |
probably null |
Het |
Obscn |
G |
T |
11: 59,062,696 |
Y4044* |
probably null |
Het |
Pcsk6 |
T |
C |
7: 65,929,097 |
|
probably benign |
Het |
Phax |
T |
A |
18: 56,562,713 |
V7D |
probably benign |
Het |
Phxr4 |
T |
C |
9: 13,431,791 |
|
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,523,359 |
D1510V |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,597,141 |
C4249R |
probably benign |
Het |
Prpf39 |
T |
C |
12: 65,055,283 |
V378A |
possibly damaging |
Het |
Psd2 |
A |
G |
18: 36,004,717 |
N455S |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,443,594 |
V1007D |
probably damaging |
Het |
Rab4b |
A |
G |
7: 27,174,502 |
I117T |
probably benign |
Het |
Rad9b |
A |
T |
5: 122,331,527 |
V348E |
probably damaging |
Het |
Rcor1 |
T |
C |
12: 111,109,778 |
|
probably benign |
Het |
Rhoc |
A |
T |
3: 104,791,991 |
E32V |
possibly damaging |
Het |
Rnf40 |
T |
G |
7: 127,600,571 |
V925G |
probably damaging |
Het |
Slc25a32 |
A |
T |
15: 39,099,897 |
Y176* |
probably null |
Het |
Slc7a1 |
T |
A |
5: 148,352,426 |
K4* |
probably null |
Het |
Taar2 |
G |
A |
10: 23,941,495 |
R311H |
probably benign |
Het |
Taar4 |
A |
T |
10: 23,961,406 |
N305Y |
probably damaging |
Het |
Tcaf1 |
G |
T |
6: 42,686,390 |
D185E |
probably benign |
Het |
Tmem138 |
T |
C |
19: 10,574,952 |
N62S |
possibly damaging |
Het |
Tnfrsf25 |
C |
T |
4: 152,116,948 |
P65S |
possibly damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,236,759 |
S495R |
possibly damaging |
Het |
Trpv3 |
T |
C |
11: 73,293,979 |
F597S |
probably damaging |
Het |
Ugt2a3 |
A |
G |
5: 87,336,718 |
V149A |
possibly damaging |
Het |
Ush2a |
T |
G |
1: 188,319,070 |
I251R |
possibly damaging |
Het |
Vamp4 |
T |
C |
1: 162,589,539 |
C114R |
possibly damaging |
Het |
Zc3h13 |
T |
A |
14: 75,330,468 |
V1067E |
probably damaging |
Het |
Zcwpw1 |
G |
A |
5: 137,810,113 |
W274* |
probably null |
Het |
|