Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
T |
7: 119,854,520 (GRCm39) |
I895F |
probably benign |
Het |
Abca16 |
A |
G |
7: 120,126,974 (GRCm39) |
N1222D |
possibly damaging |
Het |
Abcc4 |
A |
T |
14: 118,852,593 (GRCm39) |
Y499N |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,550,605 (GRCm39) |
C702W |
probably damaging |
Het |
Adk |
C |
A |
14: 21,376,682 (GRCm39) |
P27H |
|
Het |
Ankrd13a |
T |
C |
5: 114,913,293 (GRCm39) |
S2P |
probably damaging |
Het |
Ano1 |
T |
C |
7: 144,209,393 (GRCm39) |
H269R |
probably benign |
Het |
Aox3 |
T |
A |
1: 58,197,688 (GRCm39) |
|
probably null |
Het |
Asl |
G |
A |
5: 130,053,290 (GRCm39) |
|
probably benign |
Het |
Asxl2 |
A |
T |
12: 3,507,066 (GRCm39) |
D86V |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,083,508 (GRCm39) |
|
probably null |
Het |
Bach2 |
A |
G |
4: 32,562,670 (GRCm39) |
D379G |
probably damaging |
Het |
Bdkrb1 |
T |
A |
12: 105,571,142 (GRCm39) |
L236Q |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 29,443,654 (GRCm39) |
Y24C |
unknown |
Het |
Cage1 |
G |
T |
13: 38,207,025 (GRCm39) |
N273K |
probably benign |
Het |
Ccdc51 |
T |
A |
9: 108,920,848 (GRCm39) |
I245N |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,456,325 (GRCm39) |
I229V |
probably benign |
Het |
Chst4 |
T |
A |
8: 110,757,363 (GRCm39) |
S167C |
probably damaging |
Het |
Cntnap4 |
A |
T |
8: 113,537,268 (GRCm39) |
Y713F |
probably damaging |
Het |
Cntnap5b |
G |
A |
1: 99,978,519 (GRCm39) |
|
probably null |
Het |
Cog8 |
G |
T |
8: 107,779,005 (GRCm39) |
T424K |
possibly damaging |
Het |
Cop1 |
T |
G |
1: 159,071,922 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
A |
G |
4: 96,434,019 (GRCm39) |
I97T |
probably damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,088,698 (GRCm39) |
T131A |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,972,936 (GRCm39) |
D1999G |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,863,591 (GRCm39) |
D250G |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,988,618 (GRCm39) |
V3196A |
possibly damaging |
Het |
Dscam |
A |
T |
16: 96,631,117 (GRCm39) |
Y299* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,858,578 (GRCm39) |
N3879S |
unknown |
Het |
Efcab3 |
A |
C |
11: 104,913,764 (GRCm39) |
D4594A |
probably benign |
Het |
Ephb1 |
A |
G |
9: 101,841,157 (GRCm39) |
S774P |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,403,962 (GRCm39) |
V238I |
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,776,785 (GRCm39) |
M234I |
probably benign |
Het |
Fmnl2 |
C |
T |
2: 52,958,552 (GRCm39) |
S212L |
|
Het |
Frem1 |
T |
C |
4: 82,840,532 (GRCm39) |
N1798S |
possibly damaging |
Het |
Gabrd |
T |
A |
4: 155,469,863 (GRCm39) |
M449L |
probably benign |
Het |
Gad1 |
T |
C |
2: 70,417,706 (GRCm39) |
F302L |
probably benign |
Het |
Gm10800 |
A |
AC |
2: 98,497,378 (GRCm39) |
|
probably null |
Het |
Gm21886 |
GGGCCTGCAGACAGTAGGTGCTCACTAGGGCCTGTAAATAGTAGGTGCTCACTGAGGCCTGTAGACAGTAGGTGCTCA |
GGGCCTGTAGACAGTAGGTGCTCA |
18: 80,132,697 (GRCm39) |
|
probably benign |
Het |
Gnb3 |
C |
T |
6: 124,813,887 (GRCm39) |
|
probably null |
Het |
Gtf3c1 |
A |
T |
7: 125,271,993 (GRCm39) |
M642K |
possibly damaging |
Het |
Hps3 |
A |
T |
3: 20,063,050 (GRCm39) |
W838R |
probably damaging |
Het |
Ide |
A |
T |
19: 37,273,343 (GRCm39) |
W527R |
|
Het |
Ighe |
A |
T |
12: 113,235,975 (GRCm39) |
I117N |
|
Het |
Ighv1-50 |
T |
C |
12: 115,083,396 (GRCm39) |
E108G |
probably benign |
Het |
Ivl |
G |
A |
3: 92,479,538 (GRCm39) |
P176S |
probably damaging |
Het |
Lamb2 |
T |
A |
9: 108,361,283 (GRCm39) |
L605Q |
possibly damaging |
Het |
Lgi3 |
G |
A |
14: 70,770,832 (GRCm39) |
R157H |
probably damaging |
Het |
Lrp1b |
G |
T |
2: 41,266,006 (GRCm39) |
C1053* |
probably null |
Het |
Mcpt9 |
A |
T |
14: 56,264,445 (GRCm39) |
S217T |
probably damaging |
Het |
Mgat4c |
T |
G |
10: 102,224,357 (GRCm39) |
N190K |
probably damaging |
Het |
Mknk1 |
T |
A |
4: 115,721,789 (GRCm39) |
V111D |
probably damaging |
Het |
Mmp11 |
T |
C |
10: 75,764,280 (GRCm39) |
T62A |
probably benign |
Het |
Mmp1b |
C |
A |
9: 7,385,014 (GRCm39) |
V212F |
probably damaging |
Het |
Mmp7 |
A |
G |
9: 7,697,587 (GRCm39) |
|
probably null |
Het |
Muc5b |
C |
T |
7: 141,417,704 (GRCm39) |
T3550M |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nphp3 |
A |
T |
9: 103,882,036 (GRCm39) |
K169* |
probably null |
Het |
Npy6r |
G |
T |
18: 44,408,788 (GRCm39) |
V70F |
probably benign |
Het |
Nsun2 |
T |
A |
13: 69,774,672 (GRCm39) |
|
probably null |
Het |
Oplah |
T |
A |
15: 76,186,860 (GRCm39) |
I652F |
probably benign |
Het |
Pcdh18 |
T |
C |
3: 49,710,271 (GRCm39) |
N348S |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,409 (GRCm39) |
V263D |
probably damaging |
Het |
Pcdhga1 |
C |
A |
18: 37,795,164 (GRCm39) |
T56N |
probably benign |
Het |
Pdk4 |
A |
G |
6: 5,491,068 (GRCm39) |
|
probably null |
Het |
Pfkp |
C |
A |
13: 6,652,817 (GRCm39) |
V434F |
probably benign |
Het |
Phospho1 |
G |
A |
11: 95,721,732 (GRCm39) |
R134H |
probably damaging |
Het |
Polg2 |
G |
T |
11: 106,663,572 (GRCm39) |
Q374K |
probably benign |
Het |
Ptpra |
T |
C |
2: 130,379,571 (GRCm39) |
|
probably null |
Het |
Rassf3 |
C |
T |
10: 121,252,052 (GRCm39) |
E120K |
probably benign |
Het |
Reln |
A |
T |
5: 22,311,095 (GRCm39) |
S273T |
probably damaging |
Het |
Scarb1 |
C |
T |
5: 125,361,089 (GRCm39) |
A133T |
probably benign |
Het |
Scn3a |
T |
A |
2: 65,313,486 (GRCm39) |
K1142N |
probably damaging |
Het |
Sema3c |
G |
A |
5: 17,899,701 (GRCm39) |
V398I |
probably benign |
Het |
Serpine1 |
C |
A |
5: 137,099,918 (GRCm39) |
Q80H |
probably damaging |
Het |
Sh3gl1 |
G |
A |
17: 56,324,646 (GRCm39) |
T334M |
probably damaging |
Het |
Smg7 |
T |
C |
1: 152,737,576 (GRCm39) |
N122D |
probably benign |
Het |
Speer4b |
T |
C |
5: 27,703,708 (GRCm39) |
I144V |
probably benign |
Het |
Spire2 |
T |
A |
8: 124,095,989 (GRCm39) |
D671E |
probably benign |
Het |
Sspo |
A |
T |
6: 48,478,029 (GRCm39) |
H5144L |
probably benign |
Het |
Sstr2 |
A |
T |
11: 113,516,179 (GRCm39) |
Q366L |
probably damaging |
Het |
Ssu72 |
T |
C |
4: 155,815,850 (GRCm39) |
F98S |
probably damaging |
Het |
Syde2 |
C |
T |
3: 145,712,870 (GRCm39) |
Q1003* |
probably null |
Het |
Tapbp |
G |
A |
17: 34,144,461 (GRCm39) |
A186T |
possibly damaging |
Het |
Tcf12 |
T |
A |
9: 71,790,385 (GRCm39) |
|
probably null |
Het |
Tnfrsf22 |
A |
T |
7: 143,194,556 (GRCm39) |
C124S |
probably damaging |
Het |
Txlnb |
A |
T |
10: 17,703,546 (GRCm39) |
T235S |
possibly damaging |
Het |
Uaca |
T |
C |
9: 60,777,695 (GRCm39) |
L694P |
probably damaging |
Het |
Unc13a |
T |
A |
8: 72,083,197 (GRCm39) |
N1620Y |
probably damaging |
Het |
Vmn2r10 |
C |
T |
5: 109,151,200 (GRCm39) |
C138Y |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,484,495 (GRCm39) |
E568D |
probably benign |
Het |
Vmn2r57 |
A |
T |
7: 41,097,895 (GRCm39) |
H57Q |
possibly damaging |
Het |
Vwa5b1 |
A |
G |
4: 138,308,923 (GRCm39) |
S756P |
probably benign |
Het |
Washc5 |
C |
A |
15: 59,224,350 (GRCm39) |
E470* |
probably null |
Het |
Xpot |
A |
T |
10: 121,442,678 (GRCm39) |
V508D |
probably damaging |
Het |
Zfp616 |
A |
T |
11: 73,976,087 (GRCm39) |
K785N |
possibly damaging |
Het |
Zfp653 |
T |
C |
9: 21,977,195 (GRCm39) |
N119D |
probably damaging |
Het |
Zfp82 |
T |
A |
7: 29,755,592 (GRCm39) |
T497S |
probably benign |
Het |
Znrf4 |
T |
G |
17: 56,819,305 (GRCm39) |
M1L |
probably benign |
Het |
|
Other mutations in Zfp729b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02083:Zfp729b
|
APN |
13 |
67,743,349 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02852:Zfp729b
|
APN |
13 |
67,740,942 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4449001:Zfp729b
|
UTSW |
13 |
67,739,542 (GRCm39) |
missense |
probably benign |
0.01 |
R0238:Zfp729b
|
UTSW |
13 |
67,740,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R0238:Zfp729b
|
UTSW |
13 |
67,740,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R0450:Zfp729b
|
UTSW |
13 |
67,739,253 (GRCm39) |
missense |
probably benign |
|
R0510:Zfp729b
|
UTSW |
13 |
67,739,253 (GRCm39) |
missense |
probably benign |
|
R1122:Zfp729b
|
UTSW |
13 |
67,743,403 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1400:Zfp729b
|
UTSW |
13 |
67,740,913 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1915:Zfp729b
|
UTSW |
13 |
67,741,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Zfp729b
|
UTSW |
13 |
67,740,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Zfp729b
|
UTSW |
13 |
67,743,384 (GRCm39) |
missense |
probably damaging |
0.99 |
R2270:Zfp729b
|
UTSW |
13 |
67,740,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2271:Zfp729b
|
UTSW |
13 |
67,740,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2344:Zfp729b
|
UTSW |
13 |
67,740,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R2377:Zfp729b
|
UTSW |
13 |
67,739,820 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2930:Zfp729b
|
UTSW |
13 |
67,739,973 (GRCm39) |
missense |
probably benign |
|
R3053:Zfp729b
|
UTSW |
13 |
67,741,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Zfp729b
|
UTSW |
13 |
67,739,283 (GRCm39) |
missense |
probably damaging |
0.98 |
R4118:Zfp729b
|
UTSW |
13 |
67,740,829 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4947:Zfp729b
|
UTSW |
13 |
67,744,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Zfp729b
|
UTSW |
13 |
67,739,563 (GRCm39) |
missense |
probably benign |
0.18 |
R5511:Zfp729b
|
UTSW |
13 |
67,740,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R5542:Zfp729b
|
UTSW |
13 |
67,739,140 (GRCm39) |
missense |
probably benign |
|
R5908:Zfp729b
|
UTSW |
13 |
67,739,374 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Zfp729b
|
UTSW |
13 |
67,739,740 (GRCm39) |
missense |
probably benign |
0.03 |
R5996:Zfp729b
|
UTSW |
13 |
67,741,977 (GRCm39) |
missense |
probably benign |
0.18 |
R7086:Zfp729b
|
UTSW |
13 |
67,741,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R7217:Zfp729b
|
UTSW |
13 |
67,743,367 (GRCm39) |
missense |
probably damaging |
0.96 |
R7332:Zfp729b
|
UTSW |
13 |
67,757,755 (GRCm39) |
splice site |
probably null |
|
R7472:Zfp729b
|
UTSW |
13 |
67,742,002 (GRCm39) |
missense |
probably benign |
0.00 |
R7615:Zfp729b
|
UTSW |
13 |
67,739,617 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7639:Zfp729b
|
UTSW |
13 |
67,739,971 (GRCm39) |
missense |
probably benign |
0.02 |
R7652:Zfp729b
|
UTSW |
13 |
67,739,371 (GRCm39) |
missense |
probably benign |
0.00 |
R7738:Zfp729b
|
UTSW |
13 |
67,740,194 (GRCm39) |
missense |
probably benign |
0.00 |
R8137:Zfp729b
|
UTSW |
13 |
67,740,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8381:Zfp729b
|
UTSW |
13 |
67,739,617 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8402:Zfp729b
|
UTSW |
13 |
67,740,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8941:Zfp729b
|
UTSW |
13 |
67,741,218 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9014:Zfp729b
|
UTSW |
13 |
67,740,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Zfp729b
|
UTSW |
13 |
67,740,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Zfp729b
|
UTSW |
13 |
67,741,942 (GRCm39) |
nonsense |
probably null |
|
R9270:Zfp729b
|
UTSW |
13 |
67,740,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:Zfp729b
|
UTSW |
13 |
67,742,014 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9390:Zfp729b
|
UTSW |
13 |
67,739,182 (GRCm39) |
missense |
probably benign |
0.00 |
R9442:Zfp729b
|
UTSW |
13 |
67,739,337 (GRCm39) |
missense |
probably benign |
0.25 |
R9620:Zfp729b
|
UTSW |
13 |
67,739,787 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Zfp729b
|
UTSW |
13 |
67,740,578 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0028:Zfp729b
|
UTSW |
13 |
67,740,313 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Zfp729b
|
UTSW |
13 |
67,741,189 (GRCm39) |
missense |
possibly damaging |
0.88 |
|