Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
T |
A |
17: 84,978,575 (GRCm39) |
E294D |
probably benign |
Het |
Adnp2 |
A |
G |
18: 80,172,385 (GRCm39) |
F675L |
probably benign |
Het |
Akna |
G |
A |
4: 63,295,137 (GRCm39) |
T1024I |
probably benign |
Het |
Ambn |
T |
A |
5: 88,608,617 (GRCm39) |
|
probably benign |
Het |
Aox3 |
T |
C |
1: 58,191,708 (GRCm39) |
|
probably benign |
Het |
Arhgef10 |
A |
G |
8: 14,984,820 (GRCm39) |
D200G |
probably damaging |
Het |
Arhgef26 |
A |
T |
3: 62,247,704 (GRCm39) |
N263Y |
probably damaging |
Het |
Arpp21 |
A |
G |
9: 111,965,738 (GRCm39) |
S375P |
probably damaging |
Het |
Bscl2 |
G |
T |
19: 8,817,146 (GRCm39) |
E25* |
probably null |
Het |
Ccl12 |
T |
A |
11: 81,992,776 (GRCm39) |
S17R |
probably damaging |
Het |
Cdh1 |
A |
G |
8: 107,390,842 (GRCm39) |
I653V |
probably benign |
Het |
Ceacam9 |
T |
A |
7: 16,455,928 (GRCm39) |
F12I |
probably benign |
Het |
Cfap47 |
T |
C |
X: 78,553,927 (GRCm39) |
I267V |
probably benign |
Het |
Cldn23 |
A |
G |
8: 36,293,389 (GRCm39) |
V33A |
probably benign |
Het |
Cog1 |
T |
C |
11: 113,540,424 (GRCm39) |
L13P |
probably damaging |
Het |
Col20a1 |
G |
C |
2: 180,638,249 (GRCm39) |
A346P |
probably damaging |
Het |
Col6a3 |
T |
C |
1: 90,738,087 (GRCm39) |
D537G |
probably damaging |
Het |
Ctnnd2 |
G |
A |
15: 30,669,660 (GRCm39) |
R423H |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,736,071 (GRCm39) |
*493W |
probably null |
Het |
Dcdc2a |
T |
G |
13: 25,303,268 (GRCm39) |
S266R |
possibly damaging |
Het |
Diaph1 |
A |
T |
18: 38,029,442 (GRCm39) |
M330K |
unknown |
Het |
Dnah5 |
C |
T |
15: 28,297,151 (GRCm39) |
|
probably benign |
Het |
F13a1 |
T |
A |
13: 37,209,653 (GRCm39) |
Y104F |
probably benign |
Het |
Fam78b |
G |
A |
1: 166,906,278 (GRCm39) |
V146M |
probably damaging |
Het |
Fancl |
G |
T |
11: 26,409,841 (GRCm39) |
|
probably benign |
Het |
Gm10477 |
A |
G |
X: 55,570,192 (GRCm39) |
K31E |
probably damaging |
Het |
Gstm7 |
T |
C |
3: 107,834,230 (GRCm39) |
M175V |
probably benign |
Het |
Hcn4 |
T |
C |
9: 58,731,341 (GRCm39) |
S183P |
unknown |
Het |
Heatr1 |
T |
C |
13: 12,418,145 (GRCm39) |
V359A |
probably benign |
Het |
Ikbkb |
T |
C |
8: 23,157,233 (GRCm39) |
|
probably benign |
Het |
Ints6l |
T |
A |
X: 55,550,228 (GRCm39) |
S718T |
probably benign |
Het |
Kctd5 |
T |
C |
17: 24,274,940 (GRCm39) |
T212A |
probably benign |
Het |
Kdm3b |
T |
C |
18: 34,929,833 (GRCm39) |
|
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,617,154 (GRCm39) |
V1031E |
possibly damaging |
Het |
Lyst |
A |
G |
13: 13,835,556 (GRCm39) |
Y1746C |
probably damaging |
Het |
Mageb5 |
A |
G |
X: 90,823,701 (GRCm39) |
I226T |
probably damaging |
Het |
Mdc1 |
C |
T |
17: 36,158,835 (GRCm39) |
A405V |
probably benign |
Het |
Mlc1 |
A |
G |
15: 88,847,634 (GRCm39) |
Y305H |
probably benign |
Het |
Mtcl2 |
T |
C |
2: 156,875,245 (GRCm39) |
E835G |
probably damaging |
Het |
Muc4 |
A |
G |
16: 32,580,612 (GRCm39) |
Y2474C |
unknown |
Het |
Mybphl |
A |
C |
3: 108,282,492 (GRCm39) |
N175T |
probably damaging |
Het |
Neb |
A |
G |
2: 52,154,076 (GRCm39) |
F2345S |
probably damaging |
Het |
Nlrp6 |
T |
C |
7: 140,506,357 (GRCm39) |
V766A |
probably benign |
Het |
Odad4 |
T |
A |
11: 100,457,837 (GRCm39) |
|
probably null |
Het |
Or7e173 |
T |
G |
9: 19,938,797 (GRCm39) |
I146L |
probably benign |
Het |
Or8j3 |
T |
A |
2: 86,028,340 (GRCm39) |
Y252F |
possibly damaging |
Het |
Palb2 |
T |
C |
7: 121,727,004 (GRCm39) |
T289A |
possibly damaging |
Het |
Pde10a |
A |
T |
17: 9,196,047 (GRCm39) |
Q657L |
probably damaging |
Het |
Ppp2r2a |
A |
T |
14: 67,260,577 (GRCm39) |
F234I |
probably damaging |
Het |
Prl3c1 |
T |
A |
13: 27,383,325 (GRCm39) |
|
probably null |
Het |
Psg20 |
T |
A |
7: 18,414,947 (GRCm39) |
Y316F |
probably benign |
Het |
Sap18 |
T |
A |
14: 58,036,011 (GRCm39) |
S66T |
probably damaging |
Het |
Serpina3m |
A |
G |
12: 104,355,941 (GRCm39) |
M203V |
possibly damaging |
Het |
Slc6a21 |
A |
T |
7: 44,937,886 (GRCm39) |
I726F |
probably benign |
Het |
Spmap2l |
A |
T |
5: 77,208,605 (GRCm39) |
I378L |
probably benign |
Het |
Syt10 |
C |
T |
15: 89,674,979 (GRCm39) |
D456N |
probably damaging |
Het |
Tfdp2 |
T |
C |
9: 96,177,067 (GRCm39) |
S75P |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,538,591 (GRCm39) |
E351G |
probably benign |
Het |
Tmed11 |
G |
A |
5: 108,943,198 (GRCm39) |
|
probably benign |
Het |
Tmem81 |
C |
A |
1: 132,435,847 (GRCm39) |
Q218K |
probably benign |
Het |
Tnfsf11 |
G |
A |
14: 78,537,333 (GRCm39) |
T110I |
probably benign |
Het |
Tub |
G |
A |
7: 108,625,944 (GRCm39) |
G232S |
probably damaging |
Het |
Vmn2r121 |
A |
T |
X: 123,043,439 (GRCm39) |
|
probably null |
Het |
Vwa5b1 |
T |
C |
4: 138,315,880 (GRCm39) |
T621A |
probably benign |
Het |
Ythdf3 |
T |
C |
3: 16,259,356 (GRCm39) |
F501S |
possibly damaging |
Het |
|
Other mutations in Ncbp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Ncbp3
|
APN |
11 |
72,964,355 (GRCm39) |
splice site |
probably benign |
|
R0180:Ncbp3
|
UTSW |
11 |
72,955,804 (GRCm39) |
splice site |
probably null |
|
R0464:Ncbp3
|
UTSW |
11 |
72,960,647 (GRCm39) |
splice site |
probably benign |
|
R0620:Ncbp3
|
UTSW |
11 |
72,940,671 (GRCm39) |
splice site |
probably benign |
|
R2024:Ncbp3
|
UTSW |
11 |
72,944,346 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4610:Ncbp3
|
UTSW |
11 |
72,969,844 (GRCm39) |
missense |
probably damaging |
0.98 |
R4693:Ncbp3
|
UTSW |
11 |
72,966,503 (GRCm39) |
missense |
probably benign |
0.00 |
R4883:Ncbp3
|
UTSW |
11 |
72,960,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R4974:Ncbp3
|
UTSW |
11 |
72,944,355 (GRCm39) |
critical splice donor site |
probably null |
|
R5212:Ncbp3
|
UTSW |
11 |
72,944,373 (GRCm39) |
intron |
probably benign |
|
R5740:Ncbp3
|
UTSW |
11 |
72,944,323 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5906:Ncbp3
|
UTSW |
11 |
72,964,327 (GRCm39) |
missense |
probably benign |
0.04 |
R6026:Ncbp3
|
UTSW |
11 |
72,958,548 (GRCm39) |
missense |
probably benign |
0.00 |
R6154:Ncbp3
|
UTSW |
11 |
72,940,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6403:Ncbp3
|
UTSW |
11 |
72,969,802 (GRCm39) |
missense |
probably benign |
0.00 |
R6626:Ncbp3
|
UTSW |
11 |
72,964,210 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6838:Ncbp3
|
UTSW |
11 |
72,964,300 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7155:Ncbp3
|
UTSW |
11 |
72,938,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Ncbp3
|
UTSW |
11 |
72,968,747 (GRCm39) |
missense |
probably benign |
0.00 |
R7587:Ncbp3
|
UTSW |
11 |
72,957,591 (GRCm39) |
splice site |
probably null |
|
R7657:Ncbp3
|
UTSW |
11 |
72,964,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Ncbp3
|
UTSW |
11 |
72,938,808 (GRCm39) |
missense |
probably benign |
|
R8774-TAIL:Ncbp3
|
UTSW |
11 |
72,938,808 (GRCm39) |
missense |
probably benign |
|
R9063:Ncbp3
|
UTSW |
11 |
72,964,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R9478:Ncbp3
|
UTSW |
11 |
72,968,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9513:Ncbp3
|
UTSW |
11 |
72,938,727 (GRCm39) |
start codon destroyed |
probably null |
0.95 |
R9670:Ncbp3
|
UTSW |
11 |
72,944,323 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9762:Ncbp3
|
UTSW |
11 |
72,961,668 (GRCm39) |
missense |
probably benign |
0.35 |
Y5379:Ncbp3
|
UTSW |
11 |
72,964,086 (GRCm39) |
small deletion |
probably benign |
|
Z1177:Ncbp3
|
UTSW |
11 |
72,938,794 (GRCm39) |
frame shift |
probably null |
|
|