Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9230112D13Rik |
T |
C |
14: 34,236,383 (GRCm39) |
H44R |
unknown |
Het |
Acp6 |
C |
T |
3: 97,078,961 (GRCm39) |
H254Y |
probably damaging |
Het |
Acvrl1 |
A |
G |
15: 101,033,404 (GRCm39) |
N97S |
possibly damaging |
Het |
Afm |
T |
A |
5: 90,696,675 (GRCm39) |
V455E |
probably damaging |
Het |
Ankrd44 |
G |
T |
1: 54,692,952 (GRCm39) |
D927E |
probably benign |
Het |
Ap2a2 |
T |
C |
7: 141,191,258 (GRCm39) |
V275A |
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,701,221 (GRCm39) |
Q673L |
probably damaging |
Het |
Atp6v0a2 |
T |
C |
5: 124,797,061 (GRCm39) |
F814L |
probably damaging |
Het |
Axdnd1 |
G |
A |
1: 156,219,516 (GRCm39) |
A193V |
|
Het |
Bicra |
T |
A |
7: 15,721,481 (GRCm39) |
I679L |
probably benign |
Het |
Ccm2l |
G |
A |
2: 152,909,756 (GRCm39) |
R36H |
probably damaging |
Het |
Cd160 |
T |
A |
3: 96,713,102 (GRCm39) |
D54V |
probably damaging |
Het |
Cela3a |
C |
T |
4: 137,133,222 (GRCm39) |
G50D |
probably benign |
Het |
Cep152 |
T |
A |
2: 125,421,770 (GRCm39) |
R987* |
probably null |
Het |
Cnnm2 |
T |
C |
19: 46,845,362 (GRCm39) |
V618A |
probably benign |
Het |
Crim1 |
G |
A |
17: 78,653,409 (GRCm39) |
R593Q |
possibly damaging |
Het |
Ctsc |
A |
G |
7: 87,959,024 (GRCm39) |
S435G |
probably benign |
Het |
Dcbld1 |
G |
T |
10: 52,195,958 (GRCm39) |
A460S |
probably benign |
Het |
Dcbld2 |
A |
G |
16: 58,276,715 (GRCm39) |
E502G |
probably benign |
Het |
Dhx30 |
A |
T |
9: 109,913,513 (GRCm39) |
L1207* |
probably null |
Het |
Dlx2 |
A |
T |
2: 71,376,716 (GRCm39) |
S7R |
possibly damaging |
Het |
Dmwd |
T |
A |
7: 18,814,973 (GRCm39) |
I541N |
probably damaging |
Het |
Dmxl1 |
T |
G |
18: 49,997,575 (GRCm39) |
L588V |
possibly damaging |
Het |
Dmxl1 |
C |
T |
18: 50,026,741 (GRCm39) |
P1950S |
probably damaging |
Het |
Dnhd1 |
T |
A |
7: 105,358,528 (GRCm39) |
L3339* |
probably null |
Het |
Elovl1 |
C |
A |
4: 118,288,709 (GRCm39) |
P160Q |
probably damaging |
Het |
Epg5 |
T |
A |
18: 78,022,434 (GRCm39) |
L1059Q |
probably damaging |
Het |
Fam149b |
C |
T |
14: 20,402,777 (GRCm39) |
S53F |
probably benign |
Het |
Fat1 |
T |
A |
8: 45,495,331 (GRCm39) |
C4140S |
probably damaging |
Het |
Gria2 |
C |
T |
3: 80,615,200 (GRCm39) |
V427I |
probably damaging |
Het |
H2al2a |
C |
A |
2: 18,001,537 (GRCm39) |
A50S |
probably damaging |
Het |
Igsf9 |
C |
T |
1: 172,312,033 (GRCm39) |
|
probably benign |
Het |
Jup |
C |
T |
11: 100,270,391 (GRCm39) |
C372Y |
probably damaging |
Het |
Katnb1 |
G |
A |
8: 95,822,987 (GRCm39) |
R394Q |
probably damaging |
Het |
Kif1b |
A |
T |
4: 149,332,273 (GRCm39) |
D553E |
probably damaging |
Het |
Kif3a |
T |
A |
11: 53,474,189 (GRCm39) |
L251Q |
probably damaging |
Het |
Klb |
T |
A |
5: 65,533,026 (GRCm39) |
I445K |
probably damaging |
Het |
Klhl29 |
T |
A |
12: 5,190,710 (GRCm39) |
|
probably null |
Het |
Lipf |
A |
G |
19: 33,942,273 (GRCm39) |
K68E |
probably benign |
Het |
Lnx2 |
T |
A |
5: 146,970,236 (GRCm39) |
I169L |
probably benign |
Het |
Lrba |
A |
C |
3: 86,522,388 (GRCm39) |
I2223L |
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,391,896 (GRCm39) |
D2890N |
possibly damaging |
Het |
Lrp1b |
T |
C |
2: 41,325,640 (GRCm39) |
T926A |
|
Het |
Lrrc37a |
T |
A |
11: 103,391,490 (GRCm39) |
I1312F |
probably benign |
Het |
Lrrc71 |
T |
C |
3: 87,647,153 (GRCm39) |
H477R |
possibly damaging |
Het |
Lrrc8e |
T |
C |
8: 4,284,141 (GRCm39) |
V122A |
probably damaging |
Het |
Lsm14b |
T |
C |
2: 179,667,107 (GRCm39) |
|
probably null |
Het |
Magel2 |
A |
C |
7: 62,029,999 (GRCm39) |
I968L |
unknown |
Het |
Mapkbp1 |
T |
C |
2: 119,850,050 (GRCm39) |
V771A |
probably benign |
Het |
Mtmr4 |
T |
C |
11: 87,493,626 (GRCm39) |
S295P |
probably benign |
Het |
Nanos3 |
T |
A |
8: 84,902,815 (GRCm39) |
T116S |
probably benign |
Het |
Nectin3 |
T |
C |
16: 46,269,265 (GRCm39) |
D379G |
probably benign |
Het |
Nelfa |
T |
C |
5: 34,093,539 (GRCm39) |
H14R |
possibly damaging |
Het |
Nnt |
A |
G |
13: 119,502,967 (GRCm39) |
W593R |
unknown |
Het |
Nudt2 |
A |
T |
4: 41,477,575 (GRCm39) |
M19L |
probably benign |
Het |
Or4c115 |
T |
A |
2: 88,927,891 (GRCm39) |
K127* |
probably null |
Het |
Or52p1 |
A |
T |
7: 104,267,467 (GRCm39) |
T194S |
probably damaging |
Het |
Or5m13b |
T |
C |
2: 85,754,328 (GRCm39) |
S239P |
probably damaging |
Het |
Or5w22 |
T |
A |
2: 87,362,580 (GRCm39) |
C68S |
probably benign |
Het |
Or6f1 |
T |
A |
7: 85,970,369 (GRCm39) |
I264F |
possibly damaging |
Het |
Palld |
A |
T |
8: 61,969,735 (GRCm39) |
D1196E |
unknown |
Het |
Parl |
A |
G |
16: 20,116,909 (GRCm39) |
L96P |
probably damaging |
Het |
Pip4k2a |
T |
C |
2: 18,852,367 (GRCm39) |
D305G |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,392,915 (GRCm39) |
V1750A |
possibly damaging |
Het |
Prkdc |
A |
G |
16: 15,493,229 (GRCm39) |
E712G |
probably null |
Het |
Rasgrf2 |
T |
C |
13: 92,158,225 (GRCm39) |
E532G |
possibly damaging |
Het |
Rbp3 |
T |
A |
14: 33,677,792 (GRCm39) |
L580Q |
probably damaging |
Het |
Ribc2 |
G |
T |
15: 85,016,337 (GRCm39) |
|
probably benign |
Het |
Rmnd5b |
T |
C |
11: 51,515,322 (GRCm39) |
S315G |
probably benign |
Het |
Rp1l1 |
T |
A |
14: 64,259,445 (GRCm39) |
V29E |
probably damaging |
Het |
Sclt1 |
T |
C |
3: 41,681,541 (GRCm39) |
T93A |
probably benign |
Het |
Shroom1 |
T |
A |
11: 53,355,994 (GRCm39) |
L348H |
probably damaging |
Het |
Slc13a1 |
T |
C |
6: 24,090,785 (GRCm39) |
K545E |
probably benign |
Het |
Slc20a2 |
C |
T |
8: 23,030,396 (GRCm39) |
P151S |
probably damaging |
Het |
Slc22a4 |
T |
C |
11: 53,879,718 (GRCm39) |
Y447C |
probably damaging |
Het |
Slu7 |
C |
A |
11: 43,333,480 (GRCm39) |
Q367K |
probably benign |
Het |
Spen |
T |
C |
4: 141,201,889 (GRCm39) |
N2246S |
possibly damaging |
Het |
Tac4 |
T |
G |
11: 95,156,045 (GRCm39) |
I42S |
possibly damaging |
Het |
Tmem87a |
A |
G |
2: 120,190,541 (GRCm39) |
V530A |
|
Het |
Tnrc6c |
T |
C |
11: 117,640,089 (GRCm39) |
I1208T |
possibly damaging |
Het |
Vmn1r230 |
C |
T |
17: 21,067,321 (GRCm39) |
T170I |
possibly damaging |
Het |
Vps29 |
A |
G |
5: 122,498,212 (GRCm39) |
D51G |
probably benign |
Het |
Washc2 |
T |
C |
6: 116,231,399 (GRCm39) |
L874P |
probably damaging |
Het |
Wdr5b |
T |
C |
16: 35,861,926 (GRCm39) |
L15P |
probably benign |
Het |
Zscan20 |
T |
A |
4: 128,479,847 (GRCm39) |
Q881H |
probably damaging |
Het |
Zscan20 |
T |
G |
4: 128,479,848 (GRCm39) |
Q881P |
probably damaging |
Het |
|
Other mutations in Hspbp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00921:Hspbp1
|
APN |
7 |
4,667,750 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02072:Hspbp1
|
APN |
7 |
4,680,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02548:Hspbp1
|
APN |
7 |
4,684,840 (GRCm39) |
splice site |
probably benign |
|
IGL02573:Hspbp1
|
APN |
7 |
4,680,852 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03177:Hspbp1
|
APN |
7 |
4,667,700 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03181:Hspbp1
|
APN |
7 |
4,687,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0568:Hspbp1
|
UTSW |
7 |
4,687,431 (GRCm39) |
nonsense |
probably null |
|
R0670:Hspbp1
|
UTSW |
7 |
4,680,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R3013:Hspbp1
|
UTSW |
7 |
4,666,483 (GRCm39) |
missense |
probably benign |
0.18 |
R3729:Hspbp1
|
UTSW |
7 |
4,680,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R3934:Hspbp1
|
UTSW |
7 |
4,667,594 (GRCm39) |
missense |
probably benign |
0.41 |
R6031:Hspbp1
|
UTSW |
7 |
4,666,465 (GRCm39) |
missense |
probably benign |
0.28 |
R6031:Hspbp1
|
UTSW |
7 |
4,666,465 (GRCm39) |
missense |
probably benign |
0.28 |
R6034:Hspbp1
|
UTSW |
7 |
4,680,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Hspbp1
|
UTSW |
7 |
4,680,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R6728:Hspbp1
|
UTSW |
7 |
4,663,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6797:Hspbp1
|
UTSW |
7 |
4,663,781 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6930:Hspbp1
|
UTSW |
7 |
4,687,606 (GRCm39) |
missense |
probably benign |
|
R6992:Hspbp1
|
UTSW |
7 |
4,667,714 (GRCm39) |
missense |
probably benign |
0.23 |
R7459:Hspbp1
|
UTSW |
7 |
4,687,577 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Hspbp1
|
UTSW |
7 |
4,666,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R7608:Hspbp1
|
UTSW |
7 |
4,663,821 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7962:Hspbp1
|
UTSW |
7 |
4,684,841 (GRCm39) |
critical splice donor site |
probably null |
|
R8812:Hspbp1
|
UTSW |
7 |
4,667,783 (GRCm39) |
missense |
probably benign |
0.01 |
|