Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
G |
2: 68,571,810 (GRCm39) |
E562G |
probably benign |
Het |
5730522E02Rik |
A |
G |
11: 25,720,472 (GRCm39) |
|
probably null |
Het |
A930033H14Rik |
A |
T |
10: 69,048,190 (GRCm39) |
|
probably benign |
Het |
Abca17 |
C |
T |
17: 24,536,135 (GRCm39) |
E511K |
probably damaging |
Het |
Abca9 |
C |
T |
11: 110,045,980 (GRCm39) |
|
probably null |
Het |
Abhd5 |
T |
A |
9: 122,192,865 (GRCm39) |
|
probably null |
Het |
Adra2b |
G |
A |
2: 127,206,012 (GRCm39) |
W171* |
probably null |
Het |
Ahcyl |
G |
A |
16: 45,974,555 (GRCm39) |
T274I |
probably damaging |
Het |
Aldh1l1 |
T |
C |
6: 90,573,897 (GRCm39) |
Y799H |
probably benign |
Het |
Arfgef1 |
A |
G |
1: 10,286,772 (GRCm39) |
V46A |
probably benign |
Het |
Arhgap40 |
A |
G |
2: 158,381,639 (GRCm39) |
E374G |
probably damaging |
Het |
Arhgef5 |
G |
A |
6: 43,250,484 (GRCm39) |
V412I |
probably benign |
Het |
Arid3c |
T |
C |
4: 41,730,072 (GRCm39) |
E41G |
possibly damaging |
Het |
Atp8b4 |
T |
A |
2: 126,164,736 (GRCm39) |
K1193N |
probably benign |
Het |
C4a |
C |
T |
17: 35,035,975 (GRCm39) |
|
noncoding transcript |
Het |
Chst2 |
C |
T |
9: 95,287,417 (GRCm39) |
D310N |
probably damaging |
Het |
Crtc3 |
T |
C |
7: 80,327,170 (GRCm39) |
Q52R |
possibly damaging |
Het |
Crybg1 |
T |
C |
10: 43,874,583 (GRCm39) |
I842V |
probably benign |
Het |
Dennd4c |
T |
C |
4: 86,743,511 (GRCm39) |
S1167P |
probably benign |
Het |
Edem3 |
T |
C |
1: 151,668,136 (GRCm39) |
V305A |
possibly damaging |
Het |
Epha10 |
T |
A |
4: 124,780,007 (GRCm39) |
|
probably null |
Het |
Epha6 |
C |
A |
16: 59,474,426 (GRCm39) |
R1117L |
probably damaging |
Het |
Fdx2 |
T |
C |
9: 20,979,160 (GRCm39) |
I144V |
possibly damaging |
Het |
Gm10762 |
C |
T |
2: 128,809,106 (GRCm39) |
W81* |
probably null |
Het |
Hus1 |
A |
G |
11: 8,946,808 (GRCm39) |
|
probably benign |
Het |
Igbp1b |
C |
T |
6: 138,634,803 (GRCm39) |
E214K |
probably benign |
Het |
Inpp5f |
A |
G |
7: 128,286,853 (GRCm39) |
I577M |
probably damaging |
Het |
Kansl2 |
G |
A |
15: 98,424,542 (GRCm39) |
T296I |
possibly damaging |
Het |
Kcna6 |
A |
G |
6: 126,715,387 (GRCm39) |
F501L |
probably benign |
Het |
Kirrel2 |
A |
T |
7: 30,149,293 (GRCm39) |
V579D |
probably benign |
Het |
Larp1b |
T |
C |
3: 40,925,005 (GRCm39) |
Y208H |
probably damaging |
Het |
Lipf |
A |
T |
19: 33,943,088 (GRCm39) |
D132V |
probably benign |
Het |
Lsm12 |
T |
C |
11: 102,057,989 (GRCm39) |
K40E |
probably damaging |
Het |
Mastl |
A |
G |
2: 23,027,038 (GRCm39) |
S275P |
probably benign |
Het |
Mettl25b |
C |
A |
3: 87,832,305 (GRCm39) |
R293L |
probably benign |
Het |
Mrpl44 |
A |
G |
1: 79,758,694 (GRCm39) |
I281V |
probably benign |
Het |
Mtf1 |
T |
A |
4: 124,698,505 (GRCm39) |
M1K |
probably null |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,067,081 (GRCm39) |
G179R |
probably damaging |
Het |
Nfasc |
T |
C |
1: 132,531,568 (GRCm39) |
T739A |
possibly damaging |
Het |
Nfatc3 |
G |
A |
8: 106,835,011 (GRCm39) |
V778I |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,797,690 (GRCm39) |
|
probably benign |
Het |
Obox7 |
T |
A |
7: 14,398,410 (GRCm39) |
L108Q |
probably damaging |
Het |
Or51ah3 |
T |
A |
7: 103,209,968 (GRCm39) |
F95I |
probably benign |
Het |
Pax3 |
A |
G |
1: 78,108,869 (GRCm39) |
V263A |
probably damaging |
Het |
Pdlim1 |
C |
T |
19: 40,211,580 (GRCm39) |
V238I |
probably damaging |
Het |
Pik3ip1 |
G |
A |
11: 3,280,928 (GRCm39) |
|
probably benign |
Het |
Ptprq |
A |
G |
10: 107,546,442 (GRCm39) |
V284A |
possibly damaging |
Het |
Rad9b |
G |
A |
5: 122,477,839 (GRCm39) |
T179I |
probably damaging |
Het |
Sirt4 |
G |
T |
5: 115,617,785 (GRCm39) |
D290E |
possibly damaging |
Het |
Skint6 |
T |
A |
4: 112,812,589 (GRCm39) |
|
probably benign |
Het |
Slc18a1 |
A |
C |
8: 69,492,951 (GRCm39) |
I466S |
probably damaging |
Het |
Slc35e4 |
C |
T |
11: 3,862,889 (GRCm39) |
R100H |
probably benign |
Het |
Sptbn5 |
T |
G |
2: 119,898,449 (GRCm39) |
K470Q |
probably benign |
Het |
Tas1r1 |
C |
G |
4: 152,117,131 (GRCm39) |
V168L |
probably benign |
Het |
Tmem233 |
T |
A |
5: 116,221,222 (GRCm39) |
Q8L |
possibly damaging |
Het |
Ttc17 |
G |
T |
2: 94,163,236 (GRCm39) |
Q862K |
possibly damaging |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfp1004 |
T |
A |
2: 150,033,981 (GRCm39) |
C132S |
probably damaging |
Het |
Zfp229 |
T |
C |
17: 21,962,885 (GRCm39) |
I68T |
probably benign |
Het |
Zfp423 |
A |
G |
8: 88,631,128 (GRCm39) |
V30A |
probably benign |
Het |
|
Other mutations in Npm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02929:Npm2
|
APN |
14 |
70,889,678 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03120:Npm2
|
APN |
14 |
70,890,039 (GRCm39) |
utr 5 prime |
probably benign |
|
R0410:Npm2
|
UTSW |
14 |
70,889,993 (GRCm39) |
missense |
probably benign |
0.15 |
R1172:Npm2
|
UTSW |
14 |
70,889,661 (GRCm39) |
nonsense |
probably null |
|
R2179:Npm2
|
UTSW |
14 |
70,885,749 (GRCm39) |
missense |
probably benign |
0.02 |
R3714:Npm2
|
UTSW |
14 |
70,890,060 (GRCm39) |
splice site |
probably null |
|
R4134:Npm2
|
UTSW |
14 |
70,885,822 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4485:Npm2
|
UTSW |
14 |
70,885,749 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5760:Npm2
|
UTSW |
14 |
70,886,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R7807:Npm2
|
UTSW |
14 |
70,889,947 (GRCm39) |
splice site |
probably null |
|
R8819:Npm2
|
UTSW |
14 |
70,885,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8820:Npm2
|
UTSW |
14 |
70,885,768 (GRCm39) |
missense |
probably damaging |
1.00 |
|