Other mutations in this stock |
Total: 164 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
A |
G |
10: 28,859,922 (GRCm39) |
|
probably null |
Het |
Aadacl3 |
A |
G |
4: 144,182,802 (GRCm39) |
I222T |
probably damaging |
Het |
Abca13 |
G |
T |
11: 9,472,341 (GRCm39) |
G4249V |
possibly damaging |
Het |
Abcc2 |
A |
T |
19: 43,807,800 (GRCm39) |
I814F |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,458,787 (GRCm39) |
D335E |
probably damaging |
Het |
Ankrd44 |
T |
C |
1: 54,801,475 (GRCm39) |
H284R |
probably damaging |
Het |
Arfgef3 |
G |
T |
10: 18,467,654 (GRCm39) |
Q1849K |
probably benign |
Het |
Atp2c2 |
T |
C |
8: 120,474,426 (GRCm39) |
M490T |
probably damaging |
Het |
Bach1 |
T |
A |
16: 87,519,340 (GRCm39) |
D543E |
probably damaging |
Het |
Bahcc1 |
G |
A |
11: 120,173,051 (GRCm39) |
V1558I |
probably benign |
Het |
Bbs5 |
T |
A |
2: 69,485,958 (GRCm39) |
W168R |
probably damaging |
Het |
Bcar3 |
A |
T |
3: 122,323,243 (GRCm39) |
D766V |
probably benign |
Het |
C1ra |
A |
G |
6: 124,490,727 (GRCm39) |
D40G |
probably benign |
Het |
Ccdc138 |
G |
A |
10: 58,409,465 (GRCm39) |
C598Y |
probably damaging |
Het |
Cd200r3 |
T |
A |
16: 44,778,188 (GRCm39) |
N197K |
possibly damaging |
Het |
Cenpf |
T |
A |
1: 189,383,417 (GRCm39) |
E2634D |
probably damaging |
Het |
Cisd2 |
T |
C |
3: 135,116,902 (GRCm39) |
K63R |
probably damaging |
Het |
Clca3a2 |
A |
T |
3: 144,513,112 (GRCm39) |
S478T |
possibly damaging |
Het |
Clptm1l |
T |
C |
13: 73,755,981 (GRCm39) |
M199T |
possibly damaging |
Het |
Cntnap4 |
T |
A |
8: 113,500,222 (GRCm39) |
S505T |
possibly damaging |
Het |
Cr2 |
C |
T |
1: 194,845,619 (GRCm39) |
G112D |
probably damaging |
Het |
Crb2 |
T |
A |
2: 37,683,768 (GRCm39) |
I1090N |
probably benign |
Het |
Csmd3 |
G |
T |
15: 47,484,688 (GRCm39) |
P3057Q |
probably damaging |
Het |
Ctso |
G |
A |
3: 81,861,547 (GRCm39) |
V307I |
probably damaging |
Het |
Cyp3a41b |
T |
A |
5: 145,510,461 (GRCm39) |
T138S |
probably benign |
Het |
Dctn3 |
G |
T |
4: 41,719,904 (GRCm39) |
Y67* |
probably null |
Het |
Dennd4c |
C |
A |
4: 86,738,121 (GRCm39) |
Y918* |
probably null |
Het |
Dlg5 |
C |
T |
14: 24,204,757 (GRCm39) |
G1262D |
probably damaging |
Het |
Dnaaf1 |
G |
A |
8: 120,304,100 (GRCm39) |
G46D |
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,066,681 (GRCm39) |
V2563A |
probably damaging |
Het |
Dnajc13 |
A |
G |
9: 104,052,926 (GRCm39) |
Y1679H |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,864,877 (GRCm39) |
Y578H |
probably benign |
Het |
Endod1 |
C |
T |
9: 14,268,319 (GRCm39) |
V389M |
probably benign |
Het |
Ephb4 |
T |
C |
5: 137,363,768 (GRCm39) |
L582P |
probably damaging |
Het |
Eps15 |
T |
C |
4: 109,181,414 (GRCm39) |
L316S |
possibly damaging |
Het |
Erbb4 |
G |
T |
1: 68,369,405 (GRCm39) |
T412K |
probably damaging |
Het |
Fam117a |
T |
A |
11: 95,254,896 (GRCm39) |
F90I |
probably damaging |
Het |
Fam187b |
T |
G |
7: 30,676,515 (GRCm39) |
V8G |
possibly damaging |
Het |
Far1 |
T |
A |
7: 113,138,660 (GRCm39) |
I59N |
possibly damaging |
Het |
Fbxo34 |
T |
A |
14: 47,768,326 (GRCm39) |
L562Q |
probably damaging |
Het |
Frem1 |
T |
A |
4: 82,834,865 (GRCm39) |
|
probably benign |
Het |
Gfra3 |
G |
T |
18: 34,853,245 (GRCm39) |
P10Q |
probably damaging |
Het |
Gm19965 |
T |
A |
1: 116,749,626 (GRCm39) |
Y436N |
probably benign |
Het |
Gm5799 |
A |
T |
14: 43,782,005 (GRCm39) |
H59L |
probably damaging |
Het |
Gmppb |
T |
A |
9: 107,927,416 (GRCm39) |
V121E |
probably benign |
Het |
Ighv7-4 |
G |
C |
12: 114,186,899 (GRCm39) |
|
probably benign |
Het |
Ipo4 |
A |
G |
14: 55,868,671 (GRCm39) |
S446P |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,272,829 (GRCm39) |
T855A |
probably damaging |
Het |
Jaml |
T |
C |
9: 45,012,362 (GRCm39) |
I283T |
possibly damaging |
Het |
Kcnn2 |
T |
C |
18: 45,818,334 (GRCm39) |
|
probably benign |
Het |
Klhl32 |
T |
C |
4: 24,649,698 (GRCm39) |
Y399C |
possibly damaging |
Het |
Litafd |
A |
G |
16: 8,501,209 (GRCm39) |
T22A |
unknown |
Het |
Lratd2 |
C |
A |
15: 60,695,793 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
G |
A |
10: 103,057,179 (GRCm39) |
T207I |
probably benign |
Het |
Lrriq3 |
A |
T |
3: 154,893,607 (GRCm39) |
H436L |
probably benign |
Het |
Mad2l1bp |
T |
C |
17: 46,459,189 (GRCm39) |
K114E |
possibly damaging |
Het |
Mamstr |
T |
C |
7: 45,291,842 (GRCm39) |
V64A |
possibly damaging |
Het |
Map4 |
T |
A |
9: 109,864,325 (GRCm39) |
S517T |
probably benign |
Het |
Matn1 |
A |
T |
4: 130,677,336 (GRCm39) |
I182F |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,880,380 (GRCm39) |
I484T |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,169,599 (GRCm39) |
I1922F |
probably damaging |
Het |
Metap2 |
A |
G |
10: 93,704,757 (GRCm39) |
V137A |
probably damaging |
Het |
Mex3d |
A |
G |
10: 80,222,788 (GRCm39) |
V156A |
possibly damaging |
Het |
Mfsd6 |
G |
A |
1: 52,748,755 (GRCm39) |
P37S |
probably benign |
Het |
Mmut |
A |
G |
17: 41,248,242 (GRCm39) |
T90A |
probably benign |
Het |
Mrgprx1 |
A |
C |
7: 47,670,959 (GRCm39) |
S263A |
possibly damaging |
Het |
Mrtfa |
T |
C |
15: 80,989,000 (GRCm39) |
E7G |
probably benign |
Het |
Msantd5f6 |
C |
T |
4: 73,319,504 (GRCm39) |
W80* |
probably null |
Het |
Msl1 |
C |
T |
11: 98,694,795 (GRCm39) |
R505* |
probably null |
Het |
Mta2 |
T |
C |
19: 8,923,215 (GRCm39) |
S96P |
probably damaging |
Het |
Mtr |
A |
T |
13: 12,210,137 (GRCm39) |
N986K |
probably benign |
Het |
Mutyh |
C |
T |
4: 116,674,226 (GRCm39) |
T259I |
probably benign |
Het |
Myof |
T |
C |
19: 37,934,186 (GRCm39) |
T908A |
probably benign |
Het |
Nav2 |
A |
T |
7: 49,195,600 (GRCm39) |
D992V |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,090,715 (GRCm39) |
T1352A |
possibly damaging |
Het |
Nfix |
CAAAAA |
CAAAA |
8: 85,442,876 (GRCm39) |
|
probably null |
Het |
Nudt6 |
G |
A |
3: 37,459,503 (GRCm39) |
R161C |
probably benign |
Het |
Olr1 |
A |
G |
6: 129,465,053 (GRCm39) |
F141S |
possibly damaging |
Het |
Oprl1 |
G |
T |
2: 181,361,046 (GRCm39) |
M340I |
probably benign |
Het |
Or10ag57 |
T |
A |
2: 87,218,553 (GRCm39) |
V168E |
probably benign |
Het |
Or10d1 |
T |
G |
9: 39,484,154 (GRCm39) |
M134L |
probably benign |
Het |
Or11g2 |
A |
G |
14: 50,856,479 (GRCm39) |
T267A |
probably benign |
Het |
Or14j1 |
T |
C |
17: 38,146,240 (GRCm39) |
Y117H |
probably damaging |
Het |
Or1e17 |
T |
A |
11: 73,831,696 (GRCm39) |
I208K |
possibly damaging |
Het |
Or2ak6 |
T |
C |
11: 58,592,617 (GRCm39) |
V30A |
probably benign |
Het |
Or2r2 |
A |
T |
6: 42,463,613 (GRCm39) |
N171K |
probably benign |
Het |
Or4f53 |
T |
A |
2: 111,087,497 (GRCm39) |
F12L |
probably damaging |
Het |
Or5d43 |
T |
A |
2: 88,105,223 (GRCm39) |
M57L |
probably damaging |
Het |
Or5g26 |
T |
A |
2: 85,494,622 (GRCm39) |
D52V |
probably damaging |
Het |
Or9s15 |
T |
A |
1: 92,524,720 (GRCm39) |
C160S |
probably benign |
Het |
Otogl |
A |
C |
10: 107,737,197 (GRCm39) |
C72W |
probably damaging |
Het |
Pcdha11 |
T |
A |
18: 37,138,518 (GRCm39) |
I49N |
probably damaging |
Het |
Pcdha4 |
T |
A |
18: 37,087,008 (GRCm39) |
L397* |
probably null |
Het |
Pcdhb14 |
A |
G |
18: 37,581,331 (GRCm39) |
S146G |
probably benign |
Het |
Pclo |
T |
A |
5: 14,725,829 (GRCm39) |
H1562Q |
unknown |
Het |
Pcsk9 |
T |
C |
4: 106,304,766 (GRCm39) |
E434G |
probably benign |
Het |
Phc2 |
A |
G |
4: 128,645,391 (GRCm39) |
K833E |
probably damaging |
Het |
Pja2 |
A |
T |
17: 64,599,857 (GRCm39) |
S480R |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,797,070 (GRCm39) |
G2493D |
probably damaging |
Het |
Plk5 |
G |
A |
10: 80,195,138 (GRCm39) |
V179M |
possibly damaging |
Het |
Polr1a |
G |
A |
6: 71,953,054 (GRCm39) |
V1541I |
probably benign |
Het |
Ppard |
C |
G |
17: 28,505,348 (GRCm39) |
R12G |
unknown |
Het |
Ppp1r14a |
A |
G |
7: 28,990,951 (GRCm39) |
D73G |
probably damaging |
Het |
Psd3 |
C |
T |
8: 68,573,800 (GRCm39) |
R127H |
probably benign |
Het |
Pten |
G |
T |
19: 32,735,903 (GRCm39) |
G20V |
possibly damaging |
Het |
Ptprg |
T |
C |
14: 11,554,233 (GRCm38) |
|
probably benign |
Het |
Rad54l |
T |
C |
4: 115,980,121 (GRCm39) |
D21G |
probably null |
Het |
Rgs14 |
T |
C |
13: 55,528,770 (GRCm39) |
Y304H |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,131,694 (GRCm39) |
K346R |
probably damaging |
Het |
Rnf169 |
C |
G |
7: 99,575,653 (GRCm39) |
G314A |
probably damaging |
Het |
Rpgrip1l |
T |
A |
8: 91,996,805 (GRCm39) |
T692S |
probably damaging |
Het |
Rtf1 |
T |
C |
2: 119,505,709 (GRCm39) |
V54A |
possibly damaging |
Het |
Rtn4 |
T |
C |
11: 29,658,660 (GRCm39) |
V938A |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,702,818 (GRCm39) |
D2890V |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,723,113 (GRCm39) |
T2509A |
probably damaging |
Het |
Scel |
A |
C |
14: 103,820,536 (GRCm39) |
T348P |
probably benign |
Het |
Scgb1b2 |
G |
T |
7: 30,990,998 (GRCm39) |
L37I |
possibly damaging |
Het |
Sdf4 |
A |
G |
4: 156,085,178 (GRCm39) |
H171R |
possibly damaging |
Het |
Sec31a |
A |
G |
5: 100,541,222 (GRCm39) |
V295A |
probably damaging |
Het |
Semp2l2a |
T |
A |
8: 13,886,970 (GRCm39) |
I374F |
possibly damaging |
Het |
Setx |
T |
A |
2: 29,036,385 (GRCm39) |
S957T |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Six5 |
A |
G |
7: 18,830,894 (GRCm39) |
N507S |
probably benign |
Het |
Slc12a7 |
T |
C |
13: 73,912,011 (GRCm39) |
|
probably null |
Het |
Slc1a7 |
T |
A |
4: 107,850,237 (GRCm39) |
V116E |
probably damaging |
Het |
Slc22a1 |
A |
G |
17: 12,894,422 (GRCm39) |
L42P |
probably damaging |
Het |
Slc25a31 |
A |
T |
3: 40,675,975 (GRCm39) |
I174F |
probably damaging |
Het |
Slc31a2 |
A |
T |
4: 62,210,869 (GRCm39) |
M3L |
probably damaging |
Het |
Slco1a4 |
T |
A |
6: 141,791,223 (GRCm39) |
|
probably benign |
Het |
Smcr8 |
C |
T |
11: 60,669,436 (GRCm39) |
|
probably null |
Het |
Smg5 |
G |
T |
3: 88,262,999 (GRCm39) |
E801* |
probably null |
Het |
Smgc |
C |
A |
15: 91,738,819 (GRCm39) |
H492Q |
probably benign |
Het |
Smyd4 |
G |
T |
11: 75,294,010 (GRCm39) |
G694V |
probably damaging |
Het |
Sorcs3 |
A |
G |
19: 48,387,183 (GRCm39) |
T223A |
possibly damaging |
Het |
Stab1 |
G |
T |
14: 30,863,328 (GRCm39) |
C2119* |
probably null |
Het |
Taar9 |
A |
G |
10: 23,984,741 (GRCm39) |
I231T |
probably damaging |
Het |
Tacr2 |
A |
G |
10: 62,097,327 (GRCm39) |
Y269C |
probably damaging |
Het |
Taf3 |
T |
G |
2: 9,955,934 (GRCm39) |
K744N |
possibly damaging |
Het |
Tcstv1b |
T |
A |
13: 120,634,758 (GRCm39) |
S13R |
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,555,452 (GRCm39) |
V2682E |
probably damaging |
Het |
Tet1 |
A |
C |
10: 62,658,442 (GRCm39) |
L1468R |
probably damaging |
Het |
Tgds |
T |
C |
14: 118,354,445 (GRCm39) |
|
probably benign |
Het |
Tgfb2 |
A |
T |
1: 186,361,110 (GRCm39) |
Y380* |
probably null |
Het |
Tgm5 |
T |
G |
2: 120,882,953 (GRCm39) |
K435Q |
probably damaging |
Het |
Themis |
A |
G |
10: 28,637,507 (GRCm39) |
T204A |
probably benign |
Het |
Tm4sf1 |
T |
C |
3: 57,202,100 (GRCm39) |
Y37C |
probably damaging |
Het |
Tmed2b |
A |
G |
9: 33,640,068 (GRCm39) |
|
noncoding transcript |
Het |
Tnn |
T |
C |
1: 159,972,603 (GRCm39) |
N333S |
possibly damaging |
Het |
Tppp2 |
A |
G |
14: 52,156,805 (GRCm39) |
N61D |
probably benign |
Het |
Treml2 |
A |
G |
17: 48,616,187 (GRCm39) |
T276A |
probably benign |
Het |
Trit1 |
T |
C |
4: 122,910,431 (GRCm39) |
V10A |
probably benign |
Het |
Uba1y |
T |
G |
Y: 825,890 (GRCm39) |
|
probably null |
Het |
Uqcc1 |
T |
C |
2: 155,700,026 (GRCm39) |
|
probably benign |
Het |
Vcam1 |
C |
G |
3: 115,909,584 (GRCm39) |
G581A |
probably damaging |
Het |
Vmn1r16 |
G |
A |
6: 57,300,175 (GRCm39) |
T149I |
probably benign |
Het |
Vmn1r209 |
T |
C |
13: 22,989,826 (GRCm39) |
D288G |
probably damaging |
Het |
Vmn1r78 |
T |
A |
7: 11,886,891 (GRCm39) |
Y167* |
probably null |
Het |
Vmn2r103 |
T |
A |
17: 20,015,338 (GRCm39) |
S493T |
probably benign |
Het |
Vmn2r105 |
T |
A |
17: 20,447,556 (GRCm39) |
M423L |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,871,564 (GRCm39) |
F3244L |
probably damaging |
Het |
Zfp119b |
A |
T |
17: 56,246,642 (GRCm39) |
D149E |
probably damaging |
Het |
Zfp345 |
T |
C |
2: 150,315,228 (GRCm39) |
Y103C |
possibly damaging |
Het |
Zmym6 |
C |
T |
4: 127,017,009 (GRCm39) |
T930I |
probably benign |
Het |
|
Other mutations in Abcb10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02219:Abcb10
|
APN |
8 |
124,681,166 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02279:Abcb10
|
APN |
8 |
124,681,100 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02302:Abcb10
|
APN |
8 |
124,685,411 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02342:Abcb10
|
APN |
8 |
124,688,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03062:Abcb10
|
APN |
8 |
124,681,054 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03409:Abcb10
|
APN |
8 |
124,691,762 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0320:Abcb10
|
UTSW |
8 |
124,689,746 (GRCm39) |
missense |
probably benign |
0.00 |
R0436:Abcb10
|
UTSW |
8 |
124,697,740 (GRCm39) |
missense |
probably benign |
0.01 |
R1074:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1224:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1225:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1226:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1251:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1254:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1255:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1256:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1370:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1424:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Abcb10
|
UTSW |
8 |
124,688,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R2096:Abcb10
|
UTSW |
8 |
124,709,195 (GRCm39) |
missense |
probably benign |
0.01 |
R2125:Abcb10
|
UTSW |
8 |
124,691,831 (GRCm39) |
missense |
probably benign |
0.29 |
R2274:Abcb10
|
UTSW |
8 |
124,709,491 (GRCm39) |
missense |
probably benign |
0.23 |
R4802:Abcb10
|
UTSW |
8 |
124,693,266 (GRCm39) |
missense |
probably benign |
0.12 |
R4850:Abcb10
|
UTSW |
8 |
124,709,429 (GRCm39) |
missense |
probably benign |
0.01 |
R5320:Abcb10
|
UTSW |
8 |
124,697,763 (GRCm39) |
missense |
probably benign |
0.11 |
R5947:Abcb10
|
UTSW |
8 |
124,694,737 (GRCm39) |
splice site |
probably null |
|
R6006:Abcb10
|
UTSW |
8 |
124,694,804 (GRCm39) |
missense |
probably benign |
0.00 |
R6328:Abcb10
|
UTSW |
8 |
124,688,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R7168:Abcb10
|
UTSW |
8 |
124,693,350 (GRCm39) |
missense |
|
|
R8130:Abcb10
|
UTSW |
8 |
124,691,757 (GRCm39) |
missense |
|
|
R8131:Abcb10
|
UTSW |
8 |
124,691,757 (GRCm39) |
missense |
|
|
R8132:Abcb10
|
UTSW |
8 |
124,691,757 (GRCm39) |
missense |
|
|
R8431:Abcb10
|
UTSW |
8 |
124,694,873 (GRCm39) |
missense |
|
|
R9111:Abcb10
|
UTSW |
8 |
124,696,646 (GRCm39) |
missense |
|
|
R9258:Abcb10
|
UTSW |
8 |
124,709,347 (GRCm39) |
missense |
probably benign |
|
R9423:Abcb10
|
UTSW |
8 |
124,688,819 (GRCm39) |
missense |
|
|
V7581:Abcb10
|
UTSW |
8 |
124,696,500 (GRCm39) |
intron |
probably benign |
|
Z1176:Abcb10
|
UTSW |
8 |
124,709,402 (GRCm39) |
missense |
possibly damaging |
0.92 |
|