Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
C |
A |
3: 121,862,661 (GRCm39) |
S206R |
probably damaging |
Het |
Abcc6 |
G |
T |
7: 45,663,593 (GRCm39) |
A357E |
probably benign |
Het |
Abhd13 |
T |
A |
8: 10,038,170 (GRCm39) |
C256S |
probably benign |
Het |
Actrt3 |
A |
G |
3: 30,652,716 (GRCm39) |
V126A |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,740,670 (GRCm39) |
|
probably benign |
Het |
Alyref2 |
A |
G |
1: 171,331,838 (GRCm39) |
D205G |
probably damaging |
Het |
Amigo3 |
G |
A |
9: 107,930,835 (GRCm39) |
R86Q |
probably benign |
Het |
Ankrd50 |
G |
C |
3: 38,508,201 (GRCm39) |
P1389A |
probably damaging |
Het |
Aoah |
A |
G |
13: 21,094,264 (GRCm39) |
D183G |
probably damaging |
Het |
Arap3 |
A |
T |
18: 38,129,724 (GRCm39) |
S146T |
probably benign |
Het |
Atp2c2 |
T |
C |
8: 120,476,615 (GRCm39) |
|
probably benign |
Het |
Atp8b2 |
C |
T |
3: 89,853,583 (GRCm39) |
V682M |
probably benign |
Het |
Cacna1i |
T |
C |
15: 80,259,465 (GRCm39) |
I1245T |
probably damaging |
Het |
Card14 |
A |
G |
11: 119,222,085 (GRCm39) |
N460S |
probably benign |
Het |
Ceacam5 |
A |
G |
7: 17,486,309 (GRCm39) |
D602G |
possibly damaging |
Het |
Cyb5d1 |
T |
C |
11: 69,285,566 (GRCm39) |
D115G |
probably benign |
Het |
Dbp |
C |
T |
7: 45,357,744 (GRCm39) |
T67I |
possibly damaging |
Het |
Dennd5b |
C |
T |
6: 148,943,074 (GRCm39) |
V601I |
probably benign |
Het |
Dnah11 |
G |
A |
12: 118,091,291 (GRCm39) |
A947V |
possibly damaging |
Het |
Dpysl3 |
T |
A |
18: 43,571,193 (GRCm39) |
D27V |
probably damaging |
Het |
Drd1 |
A |
T |
13: 54,207,271 (GRCm39) |
D307E |
possibly damaging |
Het |
Dscaml1 |
G |
A |
9: 45,651,778 (GRCm39) |
G277D |
probably damaging |
Het |
Eif4g3 |
C |
T |
4: 137,885,726 (GRCm39) |
R842W |
probably damaging |
Het |
Enam |
C |
T |
5: 88,652,481 (GRCm39) |
T1330I |
possibly damaging |
Het |
Fabp6 |
T |
C |
11: 43,486,994 (GRCm39) |
|
probably null |
Het |
Fcsk |
A |
T |
8: 111,620,010 (GRCm39) |
L289* |
probably null |
Het |
Fhip1a |
T |
C |
3: 85,579,940 (GRCm39) |
D755G |
probably benign |
Het |
Fsip2 |
C |
T |
2: 82,813,772 (GRCm39) |
P3364S |
possibly damaging |
Het |
Gad1 |
C |
T |
2: 70,409,482 (GRCm39) |
S191F |
possibly damaging |
Het |
Gcm1 |
A |
C |
9: 77,972,055 (GRCm39) |
N332T |
probably benign |
Het |
Gin1 |
G |
A |
1: 97,703,172 (GRCm39) |
|
probably benign |
Het |
Gpr25 |
T |
C |
1: 136,188,538 (GRCm39) |
D25G |
probably benign |
Het |
Gstm4 |
T |
C |
3: 107,948,593 (GRCm39) |
T172A |
probably benign |
Het |
Hnrnpll |
A |
G |
17: 80,342,758 (GRCm39) |
|
probably null |
Het |
Il12rb2 |
T |
A |
6: 67,272,270 (GRCm39) |
K339* |
probably null |
Het |
Inpp1 |
A |
G |
1: 52,828,829 (GRCm39) |
*397Q |
probably null |
Het |
Kcp |
G |
T |
6: 29,497,834 (GRCm39) |
|
probably benign |
Het |
Kdm1b |
G |
A |
13: 47,217,596 (GRCm39) |
V352I |
probably benign |
Het |
Klhdc2 |
G |
T |
12: 69,343,734 (GRCm39) |
|
probably benign |
Het |
Krt75 |
T |
A |
15: 101,481,801 (GRCm39) |
T156S |
possibly damaging |
Het |
Lag3 |
T |
A |
6: 124,886,450 (GRCm39) |
I168F |
possibly damaging |
Het |
Lama4 |
T |
G |
10: 38,948,754 (GRCm39) |
V839G |
probably benign |
Het |
Lmtk2 |
G |
T |
5: 144,111,928 (GRCm39) |
V883L |
probably benign |
Het |
Lrrc37a |
C |
A |
11: 103,347,982 (GRCm39) |
K2904N |
unknown |
Het |
Macf1 |
A |
T |
4: 123,266,192 (GRCm39) |
I4775N |
probably damaging |
Het |
Map2k3 |
T |
G |
11: 60,823,055 (GRCm39) |
S3A |
possibly damaging |
Het |
Mast1 |
G |
A |
8: 85,642,895 (GRCm39) |
R967C |
probably damaging |
Het |
Mettl2 |
T |
G |
11: 105,017,666 (GRCm39) |
S59A |
probably benign |
Het |
Mtr |
G |
A |
13: 12,240,418 (GRCm39) |
T530I |
probably damaging |
Het |
Myo7b |
A |
T |
18: 32,110,052 (GRCm39) |
C1137S |
possibly damaging |
Het |
Nacad |
T |
A |
11: 6,552,540 (GRCm39) |
H217L |
probably benign |
Het |
Ncstn |
A |
T |
1: 171,899,710 (GRCm39) |
V324E |
probably damaging |
Het |
Ndufaf7 |
C |
A |
17: 79,249,546 (GRCm39) |
H148N |
possibly damaging |
Het |
Or10a49 |
T |
A |
7: 108,467,705 (GRCm39) |
I219F |
possibly damaging |
Het |
Or52a24 |
T |
A |
7: 103,381,190 (GRCm39) |
I19N |
probably damaging |
Het |
Or52n2b |
G |
A |
7: 104,566,272 (GRCm39) |
T77I |
probably damaging |
Het |
Or7g12 |
T |
C |
9: 18,899,737 (GRCm39) |
I151T |
possibly damaging |
Het |
Or8b12 |
T |
G |
9: 37,657,729 (GRCm39) |
L100V |
probably benign |
Het |
Or8k17 |
T |
C |
2: 86,066,454 (GRCm39) |
K242E |
possibly damaging |
Het |
Pcdh20 |
T |
C |
14: 88,706,140 (GRCm39) |
I387V |
probably benign |
Het |
Pclo |
A |
G |
5: 14,728,525 (GRCm39) |
|
probably benign |
Het |
Pcp2 |
G |
A |
8: 3,674,904 (GRCm39) |
|
probably benign |
Het |
Pde1a |
T |
A |
2: 79,698,651 (GRCm39) |
D393V |
probably damaging |
Het |
Pias4 |
T |
C |
10: 80,990,197 (GRCm39) |
D421G |
possibly damaging |
Het |
Pign |
T |
C |
1: 105,565,940 (GRCm39) |
T362A |
possibly damaging |
Het |
Pik3c2g |
A |
C |
6: 139,789,768 (GRCm39) |
K304Q |
probably damaging |
Het |
Pkd2 |
T |
A |
5: 104,634,672 (GRCm39) |
W568R |
probably damaging |
Het |
Pld2 |
T |
A |
11: 70,435,010 (GRCm39) |
I306N |
probably damaging |
Het |
Plppr3 |
T |
C |
10: 79,709,903 (GRCm39) |
K9R |
probably damaging |
Het |
Pramel11 |
T |
A |
4: 143,622,061 (GRCm39) |
R431S |
possibly damaging |
Het |
Psme4 |
T |
C |
11: 30,760,922 (GRCm39) |
V397A |
probably damaging |
Het |
Ptbp2 |
A |
T |
3: 119,555,398 (GRCm39) |
S23R |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,728,575 (GRCm39) |
D2074G |
probably null |
Het |
Rab34 |
T |
A |
11: 78,082,081 (GRCm39) |
L166H |
probably damaging |
Het |
Rabgap1l |
T |
A |
1: 160,472,880 (GRCm39) |
R519S |
probably benign |
Het |
Rasa1 |
A |
T |
13: 85,374,691 (GRCm39) |
L218* |
probably null |
Het |
Reln |
A |
G |
5: 22,249,960 (GRCm39) |
|
probably null |
Het |
Rer1 |
T |
C |
4: 155,162,956 (GRCm39) |
D94G |
possibly damaging |
Het |
Rhpn1 |
T |
C |
15: 75,583,673 (GRCm39) |
V386A |
probably benign |
Het |
Samd3 |
T |
A |
10: 26,147,754 (GRCm39) |
C476* |
probably null |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sipa1l3 |
A |
G |
7: 29,038,592 (GRCm39) |
S352P |
possibly damaging |
Het |
Slc27a2 |
A |
G |
2: 126,428,262 (GRCm39) |
Y549C |
probably benign |
Het |
Slc7a9 |
A |
G |
7: 35,149,279 (GRCm39) |
T7A |
probably benign |
Het |
Slco4c1 |
C |
T |
1: 96,770,224 (GRCm39) |
G280D |
probably damaging |
Het |
Snx19 |
T |
A |
9: 30,344,872 (GRCm39) |
V657E |
probably damaging |
Het |
Spata31d1c |
A |
G |
13: 65,183,690 (GRCm39) |
M411V |
probably benign |
Het |
Spice1 |
T |
A |
16: 44,178,193 (GRCm39) |
L72* |
probably null |
Het |
Stard9 |
G |
T |
2: 120,544,293 (GRCm39) |
V4471L |
probably damaging |
Het |
Syt14 |
A |
G |
1: 192,584,143 (GRCm39) |
L707P |
probably damaging |
Het |
Tab1 |
T |
C |
15: 80,037,869 (GRCm39) |
I234T |
probably damaging |
Het |
Tas2r107 |
T |
C |
6: 131,636,951 (GRCm39) |
M33V |
probably benign |
Het |
Tbx4 |
T |
A |
11: 85,805,349 (GRCm39) |
S479R |
possibly damaging |
Het |
Tssk5 |
C |
T |
15: 76,257,093 (GRCm39) |
R263Q |
probably benign |
Het |
Ttn |
T |
C |
2: 76,701,200 (GRCm39) |
|
probably benign |
Het |
Ugt2b5 |
T |
A |
5: 87,287,489 (GRCm39) |
Q226L |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,447,261 (GRCm39) |
S2483L |
probably benign |
Het |
Wdr95 |
A |
G |
5: 149,475,891 (GRCm39) |
Y63C |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,346,700 (GRCm39) |
I2980M |
probably damaging |
Het |
Yeats4 |
G |
A |
10: 117,051,636 (GRCm39) |
T207I |
probably benign |
Het |
Ythdc1 |
A |
G |
5: 86,978,489 (GRCm39) |
R561G |
probably damaging |
Het |
Zbtb14 |
G |
A |
17: 69,694,385 (GRCm39) |
E28K |
possibly damaging |
Het |
Zfp931 |
A |
T |
2: 177,711,684 (GRCm39) |
L21Q |
probably damaging |
Het |
Zyg11b |
A |
C |
4: 108,112,423 (GRCm39) |
M415R |
probably damaging |
Het |
|
Other mutations in Cecr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00435:Cecr2
|
APN |
6 |
120,733,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00782:Cecr2
|
APN |
6 |
120,738,582 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01137:Cecr2
|
APN |
6 |
120,738,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01446:Cecr2
|
APN |
6 |
120,735,560 (GRCm39) |
missense |
probably benign |
|
IGL02108:Cecr2
|
APN |
6 |
120,739,519 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02195:Cecr2
|
APN |
6 |
120,708,367 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02689:Cecr2
|
APN |
6 |
120,739,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03189:Cecr2
|
APN |
6 |
120,739,391 (GRCm39) |
missense |
probably benign |
0.13 |
PIT1430001:Cecr2
|
UTSW |
6 |
120,735,440 (GRCm39) |
missense |
probably benign |
0.01 |
R0200:Cecr2
|
UTSW |
6 |
120,738,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Cecr2
|
UTSW |
6 |
120,734,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R0715:Cecr2
|
UTSW |
6 |
120,735,159 (GRCm39) |
missense |
probably benign |
0.21 |
R0784:Cecr2
|
UTSW |
6 |
120,735,110 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1185:Cecr2
|
UTSW |
6 |
120,735,166 (GRCm39) |
nonsense |
probably null |
|
R1185:Cecr2
|
UTSW |
6 |
120,735,166 (GRCm39) |
nonsense |
probably null |
|
R1185:Cecr2
|
UTSW |
6 |
120,735,166 (GRCm39) |
nonsense |
probably null |
|
R1343:Cecr2
|
UTSW |
6 |
120,731,672 (GRCm39) |
missense |
probably damaging |
0.99 |
R1349:Cecr2
|
UTSW |
6 |
120,734,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R1386:Cecr2
|
UTSW |
6 |
120,739,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R1438:Cecr2
|
UTSW |
6 |
120,738,433 (GRCm39) |
nonsense |
probably null |
|
R1602:Cecr2
|
UTSW |
6 |
120,732,548 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1664:Cecr2
|
UTSW |
6 |
120,738,987 (GRCm39) |
missense |
probably damaging |
0.96 |
R1731:Cecr2
|
UTSW |
6 |
120,735,141 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1817:Cecr2
|
UTSW |
6 |
120,708,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Cecr2
|
UTSW |
6 |
120,708,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1819:Cecr2
|
UTSW |
6 |
120,708,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Cecr2
|
UTSW |
6 |
120,734,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Cecr2
|
UTSW |
6 |
120,739,526 (GRCm39) |
unclassified |
probably benign |
|
R2135:Cecr2
|
UTSW |
6 |
120,697,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Cecr2
|
UTSW |
6 |
120,733,702 (GRCm39) |
missense |
probably benign |
0.00 |
R2275:Cecr2
|
UTSW |
6 |
120,733,702 (GRCm39) |
missense |
probably benign |
0.00 |
R3713:Cecr2
|
UTSW |
6 |
120,735,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4271:Cecr2
|
UTSW |
6 |
120,739,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4706:Cecr2
|
UTSW |
6 |
120,732,539 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4873:Cecr2
|
UTSW |
6 |
120,727,877 (GRCm39) |
missense |
probably damaging |
0.99 |
R4875:Cecr2
|
UTSW |
6 |
120,727,877 (GRCm39) |
missense |
probably damaging |
0.99 |
R5137:Cecr2
|
UTSW |
6 |
120,732,478 (GRCm39) |
missense |
probably benign |
|
R5153:Cecr2
|
UTSW |
6 |
120,711,521 (GRCm39) |
missense |
probably benign |
0.03 |
R5377:Cecr2
|
UTSW |
6 |
120,733,530 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5598:Cecr2
|
UTSW |
6 |
120,708,407 (GRCm39) |
splice site |
probably null |
|
R5651:Cecr2
|
UTSW |
6 |
120,732,521 (GRCm39) |
missense |
probably damaging |
0.96 |
R5680:Cecr2
|
UTSW |
6 |
120,738,387 (GRCm39) |
missense |
probably benign |
|
R5813:Cecr2
|
UTSW |
6 |
120,739,169 (GRCm39) |
missense |
probably damaging |
0.99 |
R5970:Cecr2
|
UTSW |
6 |
120,697,868 (GRCm39) |
missense |
probably damaging |
0.98 |
R6255:Cecr2
|
UTSW |
6 |
120,735,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R6266:Cecr2
|
UTSW |
6 |
120,738,647 (GRCm39) |
missense |
probably benign |
|
R6630:Cecr2
|
UTSW |
6 |
120,739,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Cecr2
|
UTSW |
6 |
120,714,084 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6754:Cecr2
|
UTSW |
6 |
120,734,539 (GRCm39) |
missense |
probably damaging |
0.98 |
R6807:Cecr2
|
UTSW |
6 |
120,711,503 (GRCm39) |
splice site |
probably null |
|
R7187:Cecr2
|
UTSW |
6 |
120,733,647 (GRCm39) |
missense |
probably benign |
|
R7256:Cecr2
|
UTSW |
6 |
120,739,490 (GRCm39) |
missense |
probably benign |
|
R7282:Cecr2
|
UTSW |
6 |
120,738,582 (GRCm39) |
missense |
|
|
R7548:Cecr2
|
UTSW |
6 |
120,738,675 (GRCm39) |
missense |
|
|
R7596:Cecr2
|
UTSW |
6 |
120,739,167 (GRCm39) |
missense |
probably benign |
|
R7802:Cecr2
|
UTSW |
6 |
120,720,808 (GRCm39) |
missense |
probably benign |
0.45 |
R8112:Cecr2
|
UTSW |
6 |
120,739,175 (GRCm39) |
missense |
probably benign |
0.00 |
R8289:Cecr2
|
UTSW |
6 |
120,735,077 (GRCm39) |
missense |
probably benign |
0.24 |
R8294:Cecr2
|
UTSW |
6 |
120,710,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R8470:Cecr2
|
UTSW |
6 |
120,733,894 (GRCm39) |
missense |
probably benign |
0.21 |
R8697:Cecr2
|
UTSW |
6 |
120,710,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Cecr2
|
UTSW |
6 |
120,715,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Cecr2
|
UTSW |
6 |
120,739,229 (GRCm39) |
missense |
probably benign |
0.01 |
R9416:Cecr2
|
UTSW |
6 |
120,735,538 (GRCm39) |
missense |
|
|
R9477:Cecr2
|
UTSW |
6 |
120,720,743 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9588:Cecr2
|
UTSW |
6 |
120,733,770 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0012:Cecr2
|
UTSW |
6 |
120,710,735 (GRCm39) |
missense |
probably damaging |
0.99 |
X0063:Cecr2
|
UTSW |
6 |
120,739,032 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Cecr2
|
UTSW |
6 |
120,697,923 (GRCm39) |
missense |
probably damaging |
1.00 |
|