Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
T |
C |
5: 138,561,198 (GRCm39) |
S155G |
probably benign |
Het |
Abcc4 |
T |
C |
14: 118,865,066 (GRCm39) |
N320S |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,439,010 (GRCm39) |
D451G |
possibly damaging |
Het |
Ano8 |
T |
A |
8: 71,937,754 (GRCm39) |
D36V |
probably damaging |
Het |
Aqp3 |
A |
G |
4: 41,098,003 (GRCm39) |
V36A |
probably benign |
Het |
Atf7ip |
A |
G |
6: 136,537,708 (GRCm39) |
T314A |
probably benign |
Het |
Atp2c1 |
A |
T |
9: 105,300,198 (GRCm39) |
D700E |
probably damaging |
Het |
Axin2 |
G |
A |
11: 108,830,202 (GRCm39) |
V341M |
possibly damaging |
Het |
Bin3 |
A |
G |
14: 70,371,976 (GRCm39) |
Q139R |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,455,802 (GRCm39) |
D181G |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,325,295 (GRCm39) |
E466G |
probably damaging |
Het |
Ccdc14 |
T |
A |
16: 34,543,989 (GRCm39) |
Y830* |
probably null |
Het |
Cdk12 |
T |
C |
11: 98,111,910 (GRCm39) |
F723L |
unknown |
Het |
Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
Cip2a |
T |
A |
16: 48,822,016 (GRCm39) |
S215T |
probably benign |
Het |
Clca3a2 |
T |
A |
3: 144,804,545 (GRCm39) |
I61F |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,628,529 (GRCm39) |
T393A |
not run |
Het |
Cldn5 |
G |
A |
16: 18,595,845 (GRCm39) |
A34T |
probably damaging |
Het |
Cobll1 |
A |
T |
2: 64,928,717 (GRCm39) |
S870T |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,613,642 (GRCm39) |
K68E |
probably damaging |
Het |
Crnn |
A |
T |
3: 93,055,841 (GRCm39) |
Q209L |
probably damaging |
Het |
Cwf19l1 |
A |
T |
19: 44,120,579 (GRCm39) |
F45I |
probably damaging |
Het |
Cyfip2 |
T |
A |
11: 46,098,267 (GRCm39) |
K1052* |
probably null |
Het |
D930020B18Rik |
G |
A |
10: 121,503,716 (GRCm39) |
|
probably null |
Het |
Dcc |
G |
A |
18: 71,959,194 (GRCm39) |
P193S |
probably damaging |
Het |
Dda1 |
T |
A |
8: 71,927,137 (GRCm39) |
C48S |
probably benign |
Het |
Disc1 |
A |
G |
8: 125,881,780 (GRCm39) |
R572G |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,536,297 (GRCm39) |
M2582K |
probably benign |
Het |
Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
Dynlrb2 |
T |
C |
8: 117,241,696 (GRCm39) |
V80A |
probably benign |
Het |
Eif3a |
A |
T |
19: 60,755,082 (GRCm39) |
D1033E |
unknown |
Het |
Enam |
C |
A |
5: 88,649,347 (GRCm39) |
H285Q |
possibly damaging |
Het |
Ep400 |
T |
C |
5: 110,867,480 (GRCm39) |
D980G |
unknown |
Het |
Epha7 |
C |
T |
4: 28,871,937 (GRCm39) |
S422L |
probably benign |
Het |
Erc2 |
A |
C |
14: 27,762,346 (GRCm39) |
D703A |
probably damaging |
Het |
Ezh2 |
G |
T |
6: 47,510,692 (GRCm39) |
S639* |
probably null |
Het |
Fbn1 |
G |
A |
2: 125,193,969 (GRCm39) |
H1333Y |
probably damaging |
Het |
Flad1 |
A |
G |
3: 89,315,972 (GRCm39) |
S197P |
possibly damaging |
Het |
Foxl3 |
A |
G |
5: 138,806,736 (GRCm39) |
H82R |
probably damaging |
Het |
Gfm2 |
G |
T |
13: 97,279,529 (GRCm39) |
C26F |
probably benign |
Het |
Golga2 |
C |
T |
2: 32,193,013 (GRCm39) |
Q444* |
probably null |
Het |
Gp5 |
A |
T |
16: 30,127,426 (GRCm39) |
V416D |
probably damaging |
Het |
Gpat2 |
A |
G |
2: 127,268,901 (GRCm39) |
|
probably null |
Het |
Gpr137c |
A |
G |
14: 45,516,471 (GRCm39) |
D353G |
probably damaging |
Het |
Hoxa13 |
A |
C |
6: 52,236,862 (GRCm39) |
W133G |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,284,294 (GRCm39) |
I3189F |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,327,905 (GRCm39) |
K4804M |
probably damaging |
Het |
Ice2 |
T |
C |
9: 69,307,794 (GRCm39) |
F26S |
probably damaging |
Het |
Ints11 |
T |
C |
4: 155,956,687 (GRCm39) |
|
probably null |
Het |
Ipo5 |
A |
G |
14: 121,157,497 (GRCm39) |
I112V |
probably benign |
Het |
Itgax |
T |
A |
7: 127,734,481 (GRCm39) |
S346R |
probably damaging |
Het |
Kcnj13 |
T |
A |
1: 87,316,739 (GRCm39) |
M125L |
probably damaging |
Het |
Lmbrd1 |
T |
A |
1: 24,783,948 (GRCm39) |
V359E |
possibly damaging |
Het |
Lrrc7 |
T |
G |
3: 157,903,798 (GRCm39) |
K287N |
probably damaging |
Het |
Mau2 |
C |
T |
8: 70,481,884 (GRCm39) |
A191T |
possibly damaging |
Het |
Mkx |
C |
A |
18: 7,000,747 (GRCm39) |
R65L |
possibly damaging |
Het |
Mroh4 |
T |
A |
15: 74,482,220 (GRCm39) |
K746* |
probably null |
Het |
Myh4 |
A |
G |
11: 67,133,674 (GRCm39) |
T238A |
probably damaging |
Het |
Nlrp9c |
T |
A |
7: 26,070,822 (GRCm39) |
N920Y |
possibly damaging |
Het |
Nr4a3 |
T |
G |
4: 48,051,290 (GRCm39) |
S15A |
possibly damaging |
Het |
Ntn4 |
T |
C |
10: 93,480,666 (GRCm39) |
L130P |
probably damaging |
Het |
Or2ag13 |
A |
G |
7: 106,313,171 (GRCm39) |
V239A |
probably benign |
Het |
Or4a68 |
A |
G |
2: 89,270,542 (GRCm39) |
V27A |
probably benign |
Het |
Or4f59 |
A |
T |
2: 111,873,359 (GRCm39) |
V6E |
possibly damaging |
Het |
Or56a42-ps1 |
T |
A |
7: 104,777,552 (GRCm39) |
I21F |
probably benign |
Het |
Or8d23 |
A |
T |
9: 38,842,072 (GRCm39) |
I202F |
probably damaging |
Het |
Otog |
T |
C |
7: 45,947,732 (GRCm39) |
L110P |
probably damaging |
Het |
Platr25 |
G |
A |
13: 62,848,719 (GRCm39) |
H48Y |
probably benign |
Het |
Plcxd2 |
T |
C |
16: 45,800,789 (GRCm39) |
E145G |
probably damaging |
Het |
Pltp |
A |
T |
2: 164,696,242 (GRCm39) |
N143K |
probably damaging |
Het |
Pnpt1 |
T |
C |
11: 29,111,334 (GRCm39) |
Y735H |
probably damaging |
Het |
Prom1 |
A |
G |
5: 44,178,173 (GRCm39) |
Y520H |
probably damaging |
Het |
Rag2 |
A |
G |
2: 101,461,118 (GRCm39) |
Y476C |
probably damaging |
Het |
Rdh16f2 |
A |
G |
10: 127,712,893 (GRCm39) |
Y297C |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,785,180 (GRCm39) |
E1844G |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,655,161 (GRCm39) |
C3679R |
probably damaging |
Het |
Sirt1 |
A |
G |
10: 63,157,782 (GRCm39) |
I544T |
probably benign |
Het |
Slc26a10 |
A |
T |
10: 127,012,716 (GRCm39) |
I382N |
possibly damaging |
Het |
Sox2 |
C |
A |
3: 34,705,121 (GRCm39) |
P186Q |
possibly damaging |
Het |
Spata31e5 |
A |
T |
1: 28,819,233 (GRCm39) |
M16K |
probably benign |
Het |
Tnpo3 |
A |
G |
6: 29,556,995 (GRCm39) |
L752P |
probably damaging |
Het |
Top2b |
T |
A |
14: 16,416,649 (GRCm38) |
N1136K |
probably benign |
Het |
Tpsg1 |
G |
T |
17: 25,592,184 (GRCm39) |
G86V |
probably damaging |
Het |
Ttf2 |
C |
A |
3: 100,870,618 (GRCm39) |
D152Y |
possibly damaging |
Het |
Txndc15 |
T |
C |
13: 55,862,601 (GRCm39) |
L4P |
unknown |
Het |
Unc5a |
T |
C |
13: 55,144,386 (GRCm39) |
V237A |
possibly damaging |
Het |
Urb1 |
CACTTAC |
CAC |
16: 90,569,461 (GRCm39) |
|
probably benign |
Het |
Vav3 |
C |
A |
3: 109,535,415 (GRCm39) |
P616T |
possibly damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,441,105 (GRCm39) |
D251V |
probably benign |
Het |
Vmn2r15 |
A |
G |
5: 109,445,388 (GRCm39) |
L12S |
probably benign |
Het |
Wfs1 |
A |
C |
5: 37,125,076 (GRCm39) |
I605S |
probably benign |
Het |
Wif1 |
G |
A |
10: 120,919,814 (GRCm39) |
R187Q |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,207,738 (GRCm39) |
|
probably null |
Het |
Zdhhc20 |
G |
T |
14: 58,111,377 (GRCm39) |
F74L |
possibly damaging |
Het |
Zfp507 |
T |
C |
7: 35,475,843 (GRCm39) |
T303A |
unknown |
Het |
Zfp763 |
A |
T |
17: 33,252,352 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Akr1c19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00663:Akr1c19
|
APN |
13 |
4,298,128 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01522:Akr1c19
|
APN |
13 |
4,289,098 (GRCm39) |
splice site |
probably benign |
|
IGL01625:Akr1c19
|
APN |
13 |
4,283,816 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Akr1c19
|
APN |
13 |
4,287,112 (GRCm39) |
nonsense |
probably null |
|
IGL03094:Akr1c19
|
APN |
13 |
4,286,184 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03232:Akr1c19
|
APN |
13 |
4,288,462 (GRCm39) |
missense |
probably damaging |
0.96 |
R0504:Akr1c19
|
UTSW |
13 |
4,286,250 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0538:Akr1c19
|
UTSW |
13 |
4,287,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Akr1c19
|
UTSW |
13 |
4,288,459 (GRCm39) |
missense |
probably benign |
0.09 |
R2068:Akr1c19
|
UTSW |
13 |
4,288,391 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3701:Akr1c19
|
UTSW |
13 |
4,293,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R3893:Akr1c19
|
UTSW |
13 |
4,288,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4369:Akr1c19
|
UTSW |
13 |
4,283,779 (GRCm39) |
nonsense |
probably null |
|
R4434:Akr1c19
|
UTSW |
13 |
4,292,615 (GRCm39) |
missense |
probably benign |
0.28 |
R5545:Akr1c19
|
UTSW |
13 |
4,292,594 (GRCm39) |
missense |
probably benign |
0.01 |
R5584:Akr1c19
|
UTSW |
13 |
4,293,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R6988:Akr1c19
|
UTSW |
13 |
4,283,757 (GRCm39) |
start gained |
probably benign |
|
R7286:Akr1c19
|
UTSW |
13 |
4,296,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Akr1c19
|
UTSW |
13 |
4,286,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Akr1c19
|
UTSW |
13 |
4,292,591 (GRCm39) |
missense |
probably benign |
0.01 |
R8868:Akr1c19
|
UTSW |
13 |
4,293,070 (GRCm39) |
missense |
probably benign |
0.00 |
R9248:Akr1c19
|
UTSW |
13 |
4,292,974 (GRCm39) |
missense |
probably benign |
|
R9447:Akr1c19
|
UTSW |
13 |
4,296,838 (GRCm39) |
missense |
probably benign |
|
|