Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
A |
T |
10: 100,430,497 (GRCm39) |
R51S |
probably benign |
Het |
1700067P10Rik |
G |
T |
17: 48,400,849 (GRCm39) |
E45* |
probably null |
Het |
Abcb5 |
T |
C |
12: 118,841,566 (GRCm39) |
T960A |
probably benign |
Het |
Abcc3 |
A |
G |
11: 94,242,623 (GRCm39) |
|
probably null |
Het |
Adamtsl3 |
A |
T |
7: 82,077,600 (GRCm39) |
D95V |
possibly damaging |
Het |
Ash1l |
T |
A |
3: 88,891,713 (GRCm39) |
S1197R |
probably damaging |
Het |
BC034090 |
T |
A |
1: 155,097,085 (GRCm39) |
H671L |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 37,102,750 (GRCm39) |
M1443K |
|
Het |
Btnl9 |
T |
C |
11: 49,071,619 (GRCm39) |
E68G |
probably benign |
Het |
C4b |
A |
T |
17: 34,955,541 (GRCm39) |
C714S |
probably damaging |
Het |
Carmil1 |
G |
A |
13: 24,209,863 (GRCm39) |
T1204I |
probably benign |
Het |
Cdk12 |
T |
C |
11: 98,101,915 (GRCm39) |
L591P |
unknown |
Het |
Ces2f |
T |
A |
8: 105,679,758 (GRCm39) |
L417* |
probably null |
Het |
Chl1 |
T |
A |
6: 103,685,390 (GRCm39) |
S810R |
probably benign |
Het |
Ckap2 |
A |
G |
8: 22,658,811 (GRCm39) |
V644A |
possibly damaging |
Het |
Ctdsp2 |
T |
A |
10: 126,829,746 (GRCm39) |
V126E |
probably damaging |
Het |
Dok6 |
G |
T |
18: 89,492,066 (GRCm39) |
H170Q |
probably damaging |
Het |
Dynlrb1 |
T |
C |
2: 155,084,728 (GRCm39) |
|
probably null |
Het |
Eif5b |
T |
C |
1: 38,083,795 (GRCm39) |
L757S |
probably damaging |
Het |
Epas1 |
A |
C |
17: 87,116,896 (GRCm39) |
T189P |
possibly damaging |
Het |
Epha10 |
C |
A |
4: 124,788,777 (GRCm39) |
N283K |
|
Het |
Epha5 |
C |
A |
5: 84,206,975 (GRCm39) |
G853C |
probably damaging |
Het |
Gapvd1 |
A |
T |
2: 34,594,493 (GRCm39) |
H831Q |
probably damaging |
Het |
Gcnt3 |
T |
A |
9: 69,941,996 (GRCm39) |
K191* |
probably null |
Het |
Gm14226 |
T |
A |
2: 154,866,909 (GRCm39) |
S289T |
probably benign |
Het |
Gm4846 |
T |
A |
1: 166,314,674 (GRCm39) |
D323V |
probably damaging |
Het |
Golga3 |
G |
T |
5: 110,356,421 (GRCm39) |
R1036L |
possibly damaging |
Het |
Gopc |
T |
C |
10: 52,229,580 (GRCm39) |
Q213R |
probably damaging |
Het |
Hrh1 |
G |
A |
6: 114,457,564 (GRCm39) |
V282M |
probably benign |
Het |
Ighv5-4 |
T |
C |
12: 113,561,078 (GRCm39) |
Y114C |
probably damaging |
Het |
Igkv10-94 |
A |
T |
6: 68,681,636 (GRCm39) |
I68N |
probably damaging |
Het |
Kcnj3 |
A |
G |
2: 55,336,875 (GRCm39) |
D247G |
possibly damaging |
Het |
Lcn6 |
C |
A |
2: 25,570,718 (GRCm39) |
S102Y |
probably damaging |
Het |
Matk |
C |
A |
10: 81,096,765 (GRCm39) |
H232N |
probably benign |
Het |
Mcm9 |
C |
T |
10: 53,492,068 (GRCm39) |
V366I |
probably benign |
Het |
Nadk |
A |
G |
4: 155,669,844 (GRCm39) |
I176V |
probably benign |
Het |
Nlrp12 |
A |
G |
7: 3,298,111 (GRCm39) |
L20P |
probably damaging |
Het |
Oga |
T |
C |
19: 45,746,511 (GRCm39) |
S763G |
probably benign |
Het |
Or10ag56 |
A |
T |
2: 87,139,583 (GRCm39) |
Q170L |
probably benign |
Het |
Or1e21 |
G |
A |
11: 73,344,309 (GRCm39) |
S243F |
probably damaging |
Het |
Or4a72 |
A |
G |
2: 89,405,329 (GRCm39) |
L247P |
probably damaging |
Het |
Pcdhgb6 |
T |
A |
18: 37,877,237 (GRCm39) |
D648E |
probably damaging |
Het |
Pkd1l3 |
A |
T |
8: 110,362,012 (GRCm39) |
N1018I |
probably damaging |
Het |
Plch2 |
T |
C |
4: 155,083,391 (GRCm39) |
K516E |
probably damaging |
Het |
Pmpca |
G |
C |
2: 26,285,046 (GRCm39) |
E424Q |
possibly damaging |
Het |
Pnma2 |
C |
T |
14: 67,153,972 (GRCm39) |
A132V |
probably benign |
Het |
Prkn |
T |
C |
17: 11,456,472 (GRCm39) |
S99P |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,099,602 (GRCm39) |
E1702G |
probably damaging |
Het |
Qars1 |
T |
A |
9: 108,392,422 (GRCm39) |
H756Q |
probably benign |
Het |
Rab5a |
A |
G |
17: 53,790,877 (GRCm39) |
|
probably benign |
Het |
Rars2 |
A |
G |
4: 34,657,199 (GRCm39) |
D515G |
probably damaging |
Het |
Rpe65 |
T |
A |
3: 159,320,429 (GRCm39) |
C329S |
probably damaging |
Het |
Rps6ka2 |
G |
A |
17: 7,523,316 (GRCm39) |
V231M |
possibly damaging |
Het |
Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Scrt1 |
G |
T |
15: 76,403,843 (GRCm39) |
S49* |
probably null |
Het |
Sec23b |
C |
G |
2: 144,428,308 (GRCm39) |
D640E |
possibly damaging |
Het |
Setdb1 |
C |
T |
3: 95,261,979 (GRCm39) |
V96M |
possibly damaging |
Het |
Sik3 |
C |
A |
9: 46,066,746 (GRCm39) |
A175E |
probably damaging |
Het |
Smarcad1 |
A |
G |
6: 65,060,908 (GRCm39) |
K463E |
probably benign |
Het |
Sobp |
A |
C |
10: 43,003,888 (GRCm39) |
C154G |
probably damaging |
Het |
Sox6 |
A |
G |
7: 115,141,033 (GRCm39) |
S482P |
probably benign |
Het |
Spen |
C |
T |
4: 141,197,681 (GRCm39) |
A3396T |
probably benign |
Het |
Spink11 |
T |
A |
18: 44,324,748 (GRCm39) |
R75* |
probably null |
Het |
Sptb |
T |
C |
12: 76,659,561 (GRCm39) |
H1113R |
probably benign |
Het |
Sypl2 |
A |
T |
3: 108,125,004 (GRCm39) |
V119E |
probably damaging |
Het |
Tbc1d24 |
T |
C |
17: 24,427,903 (GRCm39) |
S20G |
unknown |
Het |
Tektl1 |
T |
C |
10: 78,583,035 (GRCm39) |
K450E |
probably damaging |
Het |
Top2a |
A |
T |
11: 98,912,549 (GRCm39) |
V106D |
probably damaging |
Het |
Tspyl4 |
G |
C |
10: 34,174,261 (GRCm39) |
R251P |
probably damaging |
Het |
Ttc21a |
T |
A |
9: 119,787,835 (GRCm39) |
L801Q |
probably damaging |
Het |
Vgll3 |
A |
G |
16: 65,624,844 (GRCm39) |
E64G |
probably damaging |
Het |
Vmn2r30 |
A |
G |
7: 7,315,655 (GRCm39) |
I726T |
possibly damaging |
Het |
Vmn2r81 |
T |
C |
10: 79,106,467 (GRCm39) |
S482P |
possibly damaging |
Het |
Wasf1 |
T |
G |
10: 40,806,648 (GRCm39) |
M97R |
possibly damaging |
Het |
Wdr33 |
T |
A |
18: 31,962,947 (GRCm39) |
M98K |
probably benign |
Het |
Wdr73 |
G |
A |
7: 80,548,254 (GRCm39) |
T95I |
probably damaging |
Het |
|
Other mutations in C1qtnf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01805:C1qtnf1
|
APN |
11 |
118,338,993 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02376:C1qtnf1
|
APN |
11 |
118,338,894 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02609:C1qtnf1
|
APN |
11 |
118,338,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:C1qtnf1
|
UTSW |
11 |
118,337,454 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1170:C1qtnf1
|
UTSW |
11 |
118,339,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:C1qtnf1
|
UTSW |
11 |
118,339,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:C1qtnf1
|
UTSW |
11 |
118,334,616 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1540:C1qtnf1
|
UTSW |
11 |
118,338,749 (GRCm39) |
missense |
probably benign |
0.28 |
R1896:C1qtnf1
|
UTSW |
11 |
118,334,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:C1qtnf1
|
UTSW |
11 |
118,339,110 (GRCm39) |
missense |
probably benign |
0.04 |
R2012:C1qtnf1
|
UTSW |
11 |
118,339,110 (GRCm39) |
missense |
probably benign |
0.04 |
R2901:C1qtnf1
|
UTSW |
11 |
118,338,930 (GRCm39) |
splice site |
probably null |
|
R2902:C1qtnf1
|
UTSW |
11 |
118,338,930 (GRCm39) |
splice site |
probably null |
|
R4011:C1qtnf1
|
UTSW |
11 |
118,337,365 (GRCm39) |
missense |
probably benign |
|
R4897:C1qtnf1
|
UTSW |
11 |
118,338,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:C1qtnf1
|
UTSW |
11 |
118,338,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:C1qtnf1
|
UTSW |
11 |
118,339,176 (GRCm39) |
makesense |
probably null |
|
R8322:C1qtnf1
|
UTSW |
11 |
118,338,683 (GRCm39) |
missense |
probably benign |
0.00 |
R8679:C1qtnf1
|
UTSW |
11 |
118,337,340 (GRCm39) |
nonsense |
probably null |
|
R8920:C1qtnf1
|
UTSW |
11 |
118,339,068 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9289:C1qtnf1
|
UTSW |
11 |
118,334,672 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:C1qtnf1
|
UTSW |
11 |
118,334,606 (GRCm39) |
nonsense |
probably null |
|
Z1177:C1qtnf1
|
UTSW |
11 |
118,334,580 (GRCm39) |
missense |
probably benign |
0.00 |
|