Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010L04Rik |
T |
A |
7: 82,503,150 (GRCm39) |
|
noncoding transcript |
Het |
6030469F06Rik |
A |
G |
12: 31,234,862 (GRCm39) |
|
noncoding transcript |
Het |
A830031A19Rik |
T |
A |
11: 24,008,776 (GRCm39) |
I13F |
unknown |
Het |
Adam32 |
A |
T |
8: 25,412,328 (GRCm39) |
M76K |
probably damaging |
Het |
Adamts14 |
C |
A |
10: 61,066,222 (GRCm39) |
R297L |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,051,247 (GRCm39) |
|
probably null |
Het |
Asb14 |
A |
G |
14: 26,622,408 (GRCm39) |
K80E |
possibly damaging |
Het |
Baiap2l1 |
T |
C |
5: 144,217,759 (GRCm39) |
T276A |
probably benign |
Het |
Cacna1d |
G |
A |
14: 29,764,086 (GRCm39) |
P2127S |
probably benign |
Het |
Ces2g |
A |
G |
8: 105,693,527 (GRCm39) |
T403A |
probably benign |
Het |
Cgn |
A |
C |
3: 94,687,299 (GRCm39) |
M1R |
probably null |
Het |
Chd5 |
T |
G |
4: 152,461,087 (GRCm39) |
S1226A |
probably benign |
Het |
Col18a1 |
A |
G |
10: 76,894,558 (GRCm39) |
V1497A |
probably damaging |
Het |
Cpd |
A |
T |
11: 76,688,727 (GRCm39) |
Y848* |
probably null |
Het |
Cyp2a12 |
T |
C |
7: 26,730,656 (GRCm39) |
V207A |
probably benign |
Het |
Cyth1 |
G |
A |
11: 118,073,593 (GRCm39) |
R247W |
probably benign |
Het |
Derl3 |
T |
C |
10: 75,730,324 (GRCm39) |
V129A |
possibly damaging |
Het |
Ehmt2 |
C |
T |
17: 35,118,067 (GRCm39) |
R40* |
probably null |
Het |
Eml1 |
A |
T |
12: 108,487,635 (GRCm39) |
I518L |
probably damaging |
Het |
Eri1 |
A |
G |
8: 35,945,763 (GRCm39) |
V174A |
probably benign |
Het |
Fgd3 |
T |
A |
13: 49,431,053 (GRCm39) |
I435F |
probably damaging |
Het |
Foxd1 |
T |
G |
13: 98,492,412 (GRCm39) |
S429A |
unknown |
Het |
Ftcd |
T |
A |
10: 76,425,165 (GRCm39) |
|
probably benign |
Het |
Gm5478 |
G |
T |
15: 101,553,102 (GRCm39) |
N323K |
probably benign |
Het |
Gnpda1 |
G |
T |
18: 38,468,161 (GRCm39) |
P45Q |
probably damaging |
Het |
Kif20a |
G |
T |
18: 34,763,678 (GRCm39) |
|
probably null |
Het |
Klrb1 |
T |
C |
6: 128,689,296 (GRCm39) |
|
probably null |
Het |
Lcorl |
C |
A |
5: 45,932,864 (GRCm39) |
|
probably null |
Het |
Lcorl |
T |
A |
5: 45,932,865 (GRCm39) |
|
probably null |
Het |
Lrp1b |
T |
A |
2: 41,000,900 (GRCm39) |
K2108M |
probably damaging |
Het |
Lyst |
C |
T |
13: 13,921,364 (GRCm39) |
P3437S |
probably benign |
Het |
Macrod2 |
A |
T |
2: 142,159,863 (GRCm39) |
M349L |
possibly damaging |
Het |
Marchf7 |
T |
C |
2: 60,075,647 (GRCm39) |
|
probably benign |
Het |
Mcm9 |
A |
T |
10: 53,424,786 (GRCm39) |
C601* |
probably null |
Het |
Muc19 |
G |
T |
15: 91,778,587 (GRCm39) |
|
noncoding transcript |
Het |
Mycbp2 |
T |
C |
14: 103,532,673 (GRCm39) |
D427G |
probably damaging |
Het |
Nap1l5 |
C |
A |
6: 58,883,763 (GRCm39) |
V64L |
possibly damaging |
Het |
Ncam2 |
C |
T |
16: 81,231,766 (GRCm39) |
R77* |
probably null |
Het |
Npas3 |
T |
C |
12: 54,115,721 (GRCm39) |
V863A |
possibly damaging |
Het |
Nr2c2 |
T |
A |
6: 92,116,746 (GRCm39) |
|
probably null |
Het |
Oosp3 |
T |
C |
19: 11,682,794 (GRCm39) |
F56S |
possibly damaging |
Het |
Or1a1b |
A |
T |
11: 74,097,409 (GRCm39) |
L211Q |
probably damaging |
Het |
Or5k17 |
C |
T |
16: 58,746,172 (GRCm39) |
C254Y |
probably benign |
Het |
Or8g20 |
C |
T |
9: 39,396,283 (GRCm39) |
V89M |
probably damaging |
Het |
Plgrkt |
G |
A |
19: 29,327,850 (GRCm39) |
P78S |
probably damaging |
Het |
Prss36 |
G |
A |
7: 127,533,637 (GRCm39) |
Q56* |
probably null |
Het |
Ptprz1 |
A |
G |
6: 22,986,317 (GRCm39) |
|
probably null |
Het |
Qsox2 |
A |
T |
2: 26,107,699 (GRCm39) |
F265I |
probably damaging |
Het |
R3hcc1l |
G |
T |
19: 42,552,307 (GRCm39) |
E435* |
probably null |
Het |
Shbg |
T |
C |
11: 69,507,588 (GRCm39) |
D163G |
probably benign |
Het |
Skint7 |
T |
A |
4: 111,837,546 (GRCm39) |
L108H |
probably damaging |
Het |
Smtnl1 |
T |
A |
2: 84,649,238 (GRCm39) |
E5D |
probably benign |
Het |
Spock1 |
C |
T |
13: 57,704,608 (GRCm39) |
G120D |
probably damaging |
Het |
Stk11ip |
G |
T |
1: 75,508,971 (GRCm39) |
C700F |
probably damaging |
Het |
Sult4a1 |
C |
T |
15: 83,974,159 (GRCm39) |
|
probably null |
Het |
Syngap1 |
A |
G |
17: 27,176,126 (GRCm39) |
H138R |
probably damaging |
Het |
Tdrd7 |
A |
G |
4: 46,034,301 (GRCm39) |
K1016E |
probably benign |
Het |
Tmem167b |
T |
C |
3: 108,467,569 (GRCm39) |
K26E |
possibly damaging |
Het |
Tnfaip3 |
A |
G |
10: 18,883,943 (GRCm39) |
S146P |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,607,060 (GRCm39) |
V16242I |
possibly damaging |
Het |
Vmn2r-ps3 |
T |
A |
3: 63,960,870 (GRCm39) |
|
noncoding transcript |
Het |
Vps13c |
T |
C |
9: 67,864,838 (GRCm39) |
F3049S |
probably damaging |
Het |
Vstm2l |
T |
C |
2: 157,777,355 (GRCm39) |
W78R |
probably damaging |
Het |
Wbp1l |
C |
A |
19: 46,642,695 (GRCm39) |
A216D |
possibly damaging |
Het |
Zer1 |
C |
G |
2: 29,994,866 (GRCm39) |
V510L |
probably damaging |
Het |
Zfp28 |
A |
T |
7: 6,397,850 (GRCm39) |
|
probably null |
Het |
Zfp352 |
C |
A |
4: 90,113,341 (GRCm39) |
P494T |
possibly damaging |
Het |
Zfp353-ps |
A |
G |
8: 42,535,600 (GRCm39) |
|
noncoding transcript |
Het |
Zfp563 |
A |
T |
17: 33,321,515 (GRCm39) |
|
probably null |
Het |
Zim1 |
T |
C |
7: 6,680,320 (GRCm39) |
N448D |
probably benign |
Het |
|
Other mutations in Acsbg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01474:Acsbg2
|
APN |
17 |
57,168,621 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02119:Acsbg2
|
APN |
17 |
57,175,459 (GRCm39) |
splice site |
probably benign |
|
IGL02418:Acsbg2
|
APN |
17 |
57,156,730 (GRCm39) |
missense |
probably benign |
|
R0023:Acsbg2
|
UTSW |
17 |
57,154,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R0023:Acsbg2
|
UTSW |
17 |
57,154,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R0149:Acsbg2
|
UTSW |
17 |
57,160,924 (GRCm39) |
splice site |
probably benign |
|
R1542:Acsbg2
|
UTSW |
17 |
57,156,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Acsbg2
|
UTSW |
17 |
57,160,855 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4170:Acsbg2
|
UTSW |
17 |
57,160,846 (GRCm39) |
missense |
probably benign |
0.00 |
R4465:Acsbg2
|
UTSW |
17 |
57,168,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4867:Acsbg2
|
UTSW |
17 |
57,169,914 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5169:Acsbg2
|
UTSW |
17 |
57,156,913 (GRCm39) |
missense |
probably benign |
0.07 |
R6521:Acsbg2
|
UTSW |
17 |
57,168,565 (GRCm39) |
missense |
probably benign |
0.00 |
R6531:Acsbg2
|
UTSW |
17 |
57,153,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Acsbg2
|
UTSW |
17 |
57,153,633 (GRCm39) |
missense |
probably damaging |
0.99 |
R7167:Acsbg2
|
UTSW |
17 |
57,164,000 (GRCm39) |
missense |
probably benign |
0.44 |
R7423:Acsbg2
|
UTSW |
17 |
57,175,257 (GRCm39) |
missense |
probably benign |
|
R7970:Acsbg2
|
UTSW |
17 |
57,156,728 (GRCm39) |
missense |
probably benign |
0.43 |
R8023:Acsbg2
|
UTSW |
17 |
57,152,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R8104:Acsbg2
|
UTSW |
17 |
57,152,443 (GRCm39) |
missense |
probably benign |
0.27 |
R8887:Acsbg2
|
UTSW |
17 |
57,175,285 (GRCm39) |
missense |
probably benign |
0.25 |
Z1177:Acsbg2
|
UTSW |
17 |
57,160,898 (GRCm39) |
missense |
probably benign |
0.02 |
|