Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,057,789 (GRCm39) |
|
probably benign |
Het |
Adam12 |
T |
A |
7: 133,614,077 (GRCm39) |
I60F |
probably benign |
Het |
Adamts10 |
A |
G |
17: 33,747,454 (GRCm39) |
|
probably benign |
Het |
Adamts12 |
C |
T |
15: 11,215,710 (GRCm39) |
R244C |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,061,474 (GRCm39) |
E360G |
probably damaging |
Het |
Atn1 |
A |
T |
6: 124,720,197 (GRCm39) |
|
probably benign |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
Baz2b |
G |
T |
2: 59,743,963 (GRCm39) |
|
probably null |
Het |
Bloc1s6 |
G |
C |
2: 122,587,963 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
C1qa |
T |
A |
4: 136,625,142 (GRCm39) |
T3S |
probably benign |
Het |
Cacna1e |
A |
T |
1: 154,319,647 (GRCm39) |
F1351Y |
probably damaging |
Het |
Car9 |
C |
T |
4: 43,512,206 (GRCm39) |
A356V |
probably benign |
Het |
Ccdc116 |
T |
A |
16: 16,960,598 (GRCm39) |
D73V |
probably damaging |
Het |
Ces2g |
T |
C |
8: 105,694,932 (GRCm39) |
Y518H |
probably damaging |
Het |
Ciz1 |
A |
G |
2: 32,261,431 (GRCm39) |
|
probably benign |
Het |
Cmc1 |
A |
T |
9: 117,894,388 (GRCm39) |
C29S |
probably damaging |
Het |
Coil |
T |
A |
11: 88,875,833 (GRCm39) |
|
probably benign |
Het |
Col3a1 |
C |
T |
1: 45,380,057 (GRCm39) |
|
probably benign |
Het |
Cox15 |
A |
G |
19: 43,737,229 (GRCm39) |
I135T |
possibly damaging |
Het |
Cyld |
T |
C |
8: 89,468,920 (GRCm39) |
S564P |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,378,509 (GRCm39) |
N2948K |
probably damaging |
Het |
Dnah7a |
G |
A |
1: 53,436,301 (GRCm39) |
R4014W |
probably damaging |
Het |
Dnmt3b |
T |
C |
2: 153,518,618 (GRCm39) |
Y594H |
probably damaging |
Het |
Dntt |
A |
G |
19: 41,041,477 (GRCm39) |
K387R |
possibly damaging |
Het |
Efcab7 |
G |
A |
4: 99,749,560 (GRCm39) |
|
probably benign |
Het |
Flvcr1 |
G |
T |
1: 190,753,423 (GRCm39) |
P250T |
possibly damaging |
Het |
Gga2 |
C |
A |
7: 121,590,797 (GRCm39) |
V504L |
probably damaging |
Het |
Gm12239 |
T |
A |
11: 55,906,738 (GRCm39) |
|
noncoding transcript |
Het |
Gm6327 |
T |
C |
16: 12,578,890 (GRCm39) |
|
noncoding transcript |
Het |
Krt26 |
G |
T |
11: 99,224,545 (GRCm39) |
Y324* |
probably null |
Het |
Lamb2 |
A |
T |
9: 108,363,713 (GRCm39) |
H939L |
probably benign |
Het |
Lipo3 |
C |
T |
19: 33,600,086 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
G |
A |
9: 7,386,689 (GRCm39) |
T145M |
probably damaging |
Het |
Mrps27 |
G |
T |
13: 99,501,736 (GRCm39) |
V76L |
probably benign |
Het |
Mup6 |
T |
A |
4: 60,003,995 (GRCm39) |
Y29* |
probably null |
Het |
Nlrc3 |
T |
C |
16: 3,776,822 (GRCm39) |
K756E |
probably damaging |
Het |
Nnt |
T |
C |
13: 119,505,133 (GRCm39) |
H527R |
probably damaging |
Het |
Nudt8 |
T |
C |
19: 4,051,306 (GRCm39) |
V59A |
probably benign |
Het |
Ofcc1 |
A |
T |
13: 40,434,032 (GRCm39) |
|
probably null |
Het |
Or10d1 |
A |
T |
9: 39,484,020 (GRCm39) |
D178E |
probably damaging |
Het |
Or2a25 |
T |
C |
6: 42,888,889 (GRCm39) |
V144A |
probably benign |
Het |
Or51q1c |
T |
C |
7: 103,652,565 (GRCm39) |
W28R |
probably damaging |
Het |
Pdgfd |
T |
C |
9: 6,293,851 (GRCm39) |
S142P |
probably damaging |
Het |
Pias4 |
G |
T |
10: 80,992,921 (GRCm39) |
Q22K |
probably damaging |
Het |
Pin1 |
T |
C |
9: 20,573,600 (GRCm39) |
I95T |
probably benign |
Het |
Pramel23 |
A |
T |
4: 143,424,974 (GRCm39) |
D156E |
probably benign |
Het |
Prickle2 |
G |
A |
6: 92,388,326 (GRCm39) |
Q359* |
probably null |
Het |
Qrich2 |
G |
T |
11: 116,337,639 (GRCm39) |
Q1950K |
possibly damaging |
Het |
Rab10 |
C |
A |
12: 3,359,357 (GRCm39) |
G21V |
probably damaging |
Het |
Rbm27 |
T |
A |
18: 42,447,033 (GRCm39) |
|
probably benign |
Het |
Samd4 |
C |
A |
14: 47,254,017 (GRCm39) |
S160R |
probably benign |
Het |
Scube3 |
A |
C |
17: 28,385,502 (GRCm39) |
|
probably benign |
Het |
Serpinf2 |
A |
G |
11: 75,327,372 (GRCm39) |
L185P |
probably damaging |
Het |
Slc16a12 |
A |
G |
19: 34,652,264 (GRCm39) |
I294T |
probably benign |
Het |
Slc45a3 |
T |
A |
1: 131,905,478 (GRCm39) |
M167K |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,450,910 (GRCm39) |
L2673Q |
possibly damaging |
Het |
Supt3 |
A |
G |
17: 45,314,028 (GRCm39) |
D139G |
probably damaging |
Het |
Tas1r3 |
T |
C |
4: 155,945,290 (GRCm39) |
M644V |
probably benign |
Het |
Tgfbi |
A |
G |
13: 56,775,781 (GRCm39) |
T276A |
probably damaging |
Het |
Tmem177 |
T |
C |
1: 119,838,308 (GRCm39) |
I124V |
probably benign |
Het |
Tmprss11f |
G |
T |
5: 86,681,484 (GRCm39) |
|
probably benign |
Het |
Tmprss3 |
G |
A |
17: 31,412,876 (GRCm39) |
|
probably benign |
Het |
Twf1 |
A |
G |
15: 94,484,430 (GRCm39) |
|
probably benign |
Het |
Uba52 |
T |
A |
8: 70,961,951 (GRCm39) |
Q166L |
probably damaging |
Het |
Ubr3 |
G |
T |
2: 69,809,756 (GRCm39) |
G1242V |
probably damaging |
Het |
Unc13d |
C |
T |
11: 115,956,308 (GRCm39) |
S835N |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,680,652 (GRCm39) |
K4877E |
possibly damaging |
Het |
Vmn2r98 |
A |
G |
17: 19,286,662 (GRCm39) |
I387V |
probably benign |
Het |
Vps11 |
A |
T |
9: 44,265,809 (GRCm39) |
I490N |
probably damaging |
Het |
Vstm4 |
T |
A |
14: 32,585,768 (GRCm39) |
|
probably null |
Het |
Zfp212 |
C |
T |
6: 47,907,957 (GRCm39) |
P312L |
possibly damaging |
Het |
Zfp329 |
A |
T |
7: 12,544,914 (GRCm39) |
H203Q |
probably damaging |
Het |
Zscan12 |
G |
A |
13: 21,553,139 (GRCm39) |
G321E |
probably damaging |
Het |
|
Other mutations in Zfp110 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00705:Zfp110
|
APN |
7 |
12,583,086 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01094:Zfp110
|
APN |
7 |
12,583,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01576:Zfp110
|
APN |
7 |
12,583,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01859:Zfp110
|
APN |
7 |
12,583,467 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02003:Zfp110
|
APN |
7 |
12,583,832 (GRCm39) |
nonsense |
probably null |
|
R0357:Zfp110
|
UTSW |
7 |
12,570,302 (GRCm39) |
missense |
probably damaging |
0.98 |
R0383:Zfp110
|
UTSW |
7 |
12,583,187 (GRCm39) |
missense |
probably benign |
0.00 |
R0725:Zfp110
|
UTSW |
7 |
12,570,290 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0926:Zfp110
|
UTSW |
7 |
12,583,808 (GRCm39) |
nonsense |
probably null |
|
R1146:Zfp110
|
UTSW |
7 |
12,580,721 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1146:Zfp110
|
UTSW |
7 |
12,580,721 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1472:Zfp110
|
UTSW |
7 |
12,582,468 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1663:Zfp110
|
UTSW |
7 |
12,582,569 (GRCm39) |
missense |
probably benign |
0.08 |
R1975:Zfp110
|
UTSW |
7 |
12,582,429 (GRCm39) |
missense |
probably benign |
0.00 |
R2046:Zfp110
|
UTSW |
7 |
12,583,349 (GRCm39) |
missense |
probably benign |
0.00 |
R2296:Zfp110
|
UTSW |
7 |
12,583,467 (GRCm39) |
missense |
probably damaging |
0.97 |
R2341:Zfp110
|
UTSW |
7 |
12,583,113 (GRCm39) |
missense |
probably benign |
0.04 |
R4332:Zfp110
|
UTSW |
7 |
12,578,498 (GRCm39) |
nonsense |
probably null |
|
R5892:Zfp110
|
UTSW |
7 |
12,582,405 (GRCm39) |
missense |
probably benign |
0.00 |
R5955:Zfp110
|
UTSW |
7 |
12,582,672 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6083:Zfp110
|
UTSW |
7 |
12,578,602 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6115:Zfp110
|
UTSW |
7 |
12,583,701 (GRCm39) |
missense |
probably damaging |
0.98 |
R7187:Zfp110
|
UTSW |
7 |
12,583,753 (GRCm39) |
nonsense |
probably null |
|
R7455:Zfp110
|
UTSW |
7 |
12,581,984 (GRCm39) |
missense |
probably benign |
|
R7570:Zfp110
|
UTSW |
7 |
12,583,267 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7727:Zfp110
|
UTSW |
7 |
12,582,922 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7895:Zfp110
|
UTSW |
7 |
12,571,020 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8179:Zfp110
|
UTSW |
7 |
12,578,498 (GRCm39) |
nonsense |
probably null |
|
R8703:Zfp110
|
UTSW |
7 |
12,582,888 (GRCm39) |
missense |
probably benign |
|
R9207:Zfp110
|
UTSW |
7 |
12,582,485 (GRCm39) |
missense |
probably benign |
0.33 |
R9794:Zfp110
|
UTSW |
7 |
12,578,521 (GRCm39) |
missense |
probably benign |
0.07 |
|