Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
C |
11: 110,217,457 (GRCm39) |
D133G |
probably damaging |
Het |
Abcg4 |
G |
T |
9: 44,190,616 (GRCm39) |
H55Q |
probably damaging |
Het |
Acaca |
T |
A |
11: 84,142,116 (GRCm39) |
V641E |
probably benign |
Het |
Adam28 |
T |
C |
14: 68,875,552 (GRCm39) |
I229V |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,837,493 (GRCm39) |
I793N |
probably damaging |
Het |
Akr1d1 |
A |
T |
6: 37,535,336 (GRCm39) |
D240V |
possibly damaging |
Het |
Arhgef25 |
T |
C |
10: 127,018,802 (GRCm39) |
D548G |
probably benign |
Het |
Asl |
A |
G |
5: 130,042,802 (GRCm39) |
|
probably null |
Het |
Atg14 |
C |
T |
14: 47,788,771 (GRCm39) |
R194Q |
probably damaging |
Het |
BC004004 |
T |
A |
17: 29,501,166 (GRCm39) |
F38L |
probably damaging |
Het |
Btg1 |
T |
C |
10: 96,453,259 (GRCm39) |
F25L |
probably benign |
Het |
Btrc |
C |
T |
19: 45,445,026 (GRCm39) |
P35S |
probably benign |
Het |
Calcr |
T |
A |
6: 3,714,705 (GRCm39) |
N142Y |
probably damaging |
Het |
Ccdc138 |
A |
G |
10: 58,397,818 (GRCm39) |
I553V |
probably benign |
Het |
Ccdc198 |
T |
A |
14: 49,482,560 (GRCm39) |
N52I |
probably damaging |
Het |
Cdc42 |
T |
A |
4: 137,056,115 (GRCm39) |
N132I |
probably benign |
Het |
Ces1e |
A |
G |
8: 93,950,716 (GRCm39) |
S22P |
probably benign |
Het |
Clmn |
G |
T |
12: 104,748,307 (GRCm39) |
D413E |
probably benign |
Het |
Cramp1 |
T |
C |
17: 25,201,293 (GRCm39) |
T730A |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,343,784 (GRCm39) |
M2395L |
probably benign |
Het |
Ephx1 |
G |
T |
1: 180,829,488 (GRCm39) |
S20Y |
possibly damaging |
Het |
Exoc5 |
T |
G |
14: 49,289,821 (GRCm39) |
E19A |
probably damaging |
Het |
Fam120b |
T |
C |
17: 15,623,294 (GRCm39) |
L424P |
probably benign |
Het |
Fam89a |
G |
A |
8: 125,467,823 (GRCm39) |
T163I |
possibly damaging |
Het |
Fcrl2 |
G |
A |
3: 87,166,922 (GRCm39) |
L24F |
possibly damaging |
Het |
Fgd6 |
G |
T |
10: 93,975,715 (GRCm39) |
V1377L |
probably benign |
Het |
Glud1 |
T |
A |
14: 34,057,347 (GRCm39) |
I337K |
possibly damaging |
Het |
Gm6370 |
T |
A |
5: 146,430,736 (GRCm39) |
I303N |
probably benign |
Het |
Gm7995 |
T |
C |
14: 42,133,383 (GRCm39) |
Y88H |
probably damaging |
Het |
Gsdma3 |
T |
C |
11: 98,520,393 (GRCm39) |
|
probably null |
Het |
Gsdmc2 |
T |
C |
15: 63,707,614 (GRCm39) |
D60G |
probably damaging |
Het |
Hcn1 |
T |
A |
13: 118,039,431 (GRCm39) |
|
probably null |
Het |
Hectd1 |
A |
T |
12: 51,831,030 (GRCm39) |
C936* |
probably null |
Het |
Herc4 |
T |
A |
10: 63,121,433 (GRCm39) |
S358T |
probably benign |
Het |
Hk3 |
A |
G |
13: 55,158,735 (GRCm39) |
C515R |
probably benign |
Het |
Ighg1 |
A |
G |
12: 113,291,138 (GRCm39) |
|
probably benign |
Het |
Iqgap3 |
T |
A |
3: 88,014,842 (GRCm39) |
C853S |
probably benign |
Het |
Irx4 |
G |
A |
13: 73,415,750 (GRCm39) |
A180T |
probably damaging |
Het |
Kif20b |
A |
G |
19: 34,943,522 (GRCm39) |
T1441A |
probably benign |
Het |
Lifr |
A |
G |
15: 7,215,106 (GRCm39) |
K738E |
possibly damaging |
Het |
Lmntd2 |
A |
T |
7: 140,792,531 (GRCm39) |
S218T |
probably damaging |
Het |
Lnx1 |
A |
T |
5: 74,768,530 (GRCm39) |
W353R |
probably benign |
Het |
Lrfn3 |
G |
T |
7: 30,055,238 (GRCm39) |
P569Q |
possibly damaging |
Het |
Mamstr |
A |
G |
7: 45,293,838 (GRCm39) |
I11V |
probably benign |
Het |
Med31 |
T |
C |
11: 72,104,975 (GRCm39) |
N32S |
possibly damaging |
Het |
Mob3c |
A |
T |
4: 115,690,928 (GRCm39) |
I173F |
probably benign |
Het |
Morc3 |
A |
G |
16: 93,667,250 (GRCm39) |
|
probably null |
Het |
Mphosph9 |
T |
C |
5: 124,437,108 (GRCm39) |
K412R |
probably damaging |
Het |
Mtcl3 |
A |
T |
10: 29,072,537 (GRCm39) |
N610Y |
probably damaging |
Het |
Mthfd1l |
C |
T |
10: 3,957,775 (GRCm39) |
P271S |
probably benign |
Het |
Ncam1 |
C |
T |
9: 49,453,183 (GRCm39) |
|
probably null |
Het |
Ncbp3 |
T |
A |
11: 72,960,578 (GRCm39) |
Y279N |
probably damaging |
Het |
Ncoa6 |
G |
A |
2: 155,248,687 (GRCm39) |
T1539I |
probably benign |
Het |
Nedd4 |
G |
A |
9: 72,647,515 (GRCm39) |
|
probably null |
Het |
Neil1 |
A |
G |
9: 57,054,206 (GRCm39) |
V38A |
probably damaging |
Het |
Ngf |
T |
A |
3: 102,427,961 (GRCm39) |
F237I |
probably damaging |
Het |
Nol3 |
A |
G |
8: 106,005,888 (GRCm39) |
Q94R |
possibly damaging |
Het |
Obox1 |
A |
G |
7: 15,290,263 (GRCm39) |
N202S |
probably damaging |
Het |
Odc1 |
T |
A |
12: 17,597,386 (GRCm39) |
N29K |
possibly damaging |
Het |
Or2b7 |
C |
T |
13: 21,739,658 (GRCm39) |
R178H |
probably benign |
Het |
Or2h15 |
T |
C |
17: 38,441,508 (GRCm39) |
T192A |
probably damaging |
Het |
Or4a69 |
C |
T |
2: 89,312,652 (GRCm39) |
V276I |
probably benign |
Het |
Or52a20 |
A |
C |
7: 103,365,914 (GRCm39) |
I38L |
probably benign |
Het |
P2rx7 |
T |
A |
5: 122,819,129 (GRCm39) |
V517E |
probably damaging |
Het |
Parm1 |
A |
G |
5: 91,741,775 (GRCm39) |
T48A |
possibly damaging |
Het |
Pcdh9 |
T |
A |
14: 94,126,164 (GRCm39) |
D2V |
possibly damaging |
Het |
Pgm3 |
G |
T |
9: 86,451,378 (GRCm39) |
T92N |
probably damaging |
Het |
Plcg2 |
G |
T |
8: 118,333,872 (GRCm39) |
G882* |
probably null |
Het |
Ptpn14 |
C |
T |
1: 189,582,997 (GRCm39) |
P615S |
probably damaging |
Het |
Ptprk |
A |
T |
10: 28,464,928 (GRCm39) |
Y1244F |
probably damaging |
Het |
Rfx2 |
T |
C |
17: 57,090,747 (GRCm39) |
E391G |
probably damaging |
Het |
Sema4c |
A |
G |
1: 36,591,097 (GRCm39) |
V414A |
probably damaging |
Het |
Serpinb10 |
A |
T |
1: 107,468,681 (GRCm39) |
N185I |
probably damaging |
Het |
Shroom3 |
T |
G |
5: 93,098,993 (GRCm39) |
M1410R |
probably benign |
Het |
Slc13a1 |
A |
T |
6: 24,134,356 (GRCm39) |
S176T |
probably benign |
Het |
Sntb1 |
A |
T |
15: 55,506,198 (GRCm39) |
Y458* |
probably null |
Het |
Sorcs1 |
C |
T |
19: 50,220,741 (GRCm39) |
V570I |
probably benign |
Het |
Sp8 |
T |
A |
12: 118,812,805 (GRCm39) |
V220E |
probably damaging |
Het |
Spry1 |
C |
T |
3: 37,696,868 (GRCm39) |
T37M |
possibly damaging |
Het |
Sspo |
A |
T |
6: 48,437,756 (GRCm39) |
H1305L |
probably benign |
Het |
Tbc1d22a |
A |
G |
15: 86,381,117 (GRCm39) |
D509G |
possibly damaging |
Het |
Tmem108 |
A |
T |
9: 103,376,276 (GRCm39) |
V391D |
possibly damaging |
Het |
Tmem132d |
T |
A |
5: 128,346,366 (GRCm39) |
H52L |
possibly damaging |
Het |
Tmem132d |
T |
A |
5: 128,346,364 (GRCm39) |
I53F |
probably damaging |
Het |
Tnnt2 |
A |
T |
1: 135,775,496 (GRCm39) |
R87* |
probably null |
Het |
Ube3a |
A |
T |
7: 58,893,198 (GRCm39) |
M1L |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,060,592 (GRCm39) |
T1119A |
probably damaging |
Het |
Usf3 |
A |
T |
16: 44,039,942 (GRCm39) |
H1474L |
probably damaging |
Het |
Vcpip1 |
G |
A |
1: 9,817,423 (GRCm39) |
T320I |
probably damaging |
Het |
Vmn1r56 |
A |
G |
7: 5,199,443 (GRCm39) |
L58P |
probably damaging |
Het |
Wdr53 |
A |
T |
16: 32,075,796 (GRCm39) |
K334* |
probably null |
Het |
Zbtb40 |
T |
A |
4: 136,728,241 (GRCm39) |
R459W |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,246,547 (GRCm39) |
L878Q |
probably damaging |
Het |
Zfp286 |
T |
C |
11: 62,671,455 (GRCm39) |
D206G |
probably benign |
Het |
Zfp46 |
T |
A |
4: 136,017,792 (GRCm39) |
C209S |
probably damaging |
Het |
Zup1 |
G |
T |
10: 33,825,038 (GRCm39) |
T148K |
probably damaging |
Het |
|
Other mutations in Rere |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00821:Rere
|
APN |
4 |
150,703,920 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01465:Rere
|
APN |
4 |
150,594,451 (GRCm39) |
missense |
unknown |
|
IGL01523:Rere
|
APN |
4 |
150,700,012 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01688:Rere
|
APN |
4 |
150,702,893 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02057:Rere
|
APN |
4 |
150,699,289 (GRCm39) |
unclassified |
probably benign |
|
IGL02621:Rere
|
APN |
4 |
150,698,269 (GRCm39) |
unclassified |
probably benign |
|
IGL02672:Rere
|
APN |
4 |
150,594,483 (GRCm39) |
missense |
unknown |
|
R0116:Rere
|
UTSW |
4 |
150,701,433 (GRCm39) |
missense |
probably benign |
0.18 |
R0119:Rere
|
UTSW |
4 |
150,699,779 (GRCm39) |
unclassified |
probably benign |
|
R0344:Rere
|
UTSW |
4 |
150,695,438 (GRCm39) |
unclassified |
probably benign |
|
R0504:Rere
|
UTSW |
4 |
150,699,779 (GRCm39) |
unclassified |
probably benign |
|
R0630:Rere
|
UTSW |
4 |
150,703,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R0961:Rere
|
UTSW |
4 |
150,699,829 (GRCm39) |
unclassified |
probably benign |
|
R1164:Rere
|
UTSW |
4 |
150,619,341 (GRCm39) |
missense |
unknown |
|
R1424:Rere
|
UTSW |
4 |
150,701,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Rere
|
UTSW |
4 |
150,700,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Rere
|
UTSW |
4 |
150,696,522 (GRCm39) |
unclassified |
probably benign |
|
R1953:Rere
|
UTSW |
4 |
150,701,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Rere
|
UTSW |
4 |
150,553,247 (GRCm39) |
missense |
probably benign |
0.23 |
R1966:Rere
|
UTSW |
4 |
150,701,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R1975:Rere
|
UTSW |
4 |
150,700,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R2070:Rere
|
UTSW |
4 |
150,699,047 (GRCm39) |
unclassified |
probably benign |
|
R2115:Rere
|
UTSW |
4 |
150,697,018 (GRCm39) |
unclassified |
probably benign |
|
R2144:Rere
|
UTSW |
4 |
150,701,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R2270:Rere
|
UTSW |
4 |
150,561,837 (GRCm39) |
missense |
unknown |
|
R2969:Rere
|
UTSW |
4 |
150,654,673 (GRCm39) |
missense |
unknown |
|
R3699:Rere
|
UTSW |
4 |
150,561,819 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3723:Rere
|
UTSW |
4 |
150,553,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Rere
|
UTSW |
4 |
150,554,785 (GRCm39) |
missense |
probably benign |
0.42 |
R4234:Rere
|
UTSW |
4 |
150,701,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Rere
|
UTSW |
4 |
150,561,909 (GRCm39) |
missense |
unknown |
|
R4798:Rere
|
UTSW |
4 |
150,699,624 (GRCm39) |
unclassified |
probably benign |
|
R4914:Rere
|
UTSW |
4 |
150,703,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Rere
|
UTSW |
4 |
150,703,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Rere
|
UTSW |
4 |
150,703,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4918:Rere
|
UTSW |
4 |
150,703,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4966:Rere
|
UTSW |
4 |
150,698,273 (GRCm39) |
unclassified |
probably benign |
|
R5172:Rere
|
UTSW |
4 |
150,654,726 (GRCm39) |
missense |
unknown |
|
R5643:Rere
|
UTSW |
4 |
150,701,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6058:Rere
|
UTSW |
4 |
150,553,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R7112:Rere
|
UTSW |
4 |
150,491,061 (GRCm39) |
missense |
probably benign |
|
R7173:Rere
|
UTSW |
4 |
150,553,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Rere
|
UTSW |
4 |
150,695,410 (GRCm39) |
missense |
unknown |
|
R7699:Rere
|
UTSW |
4 |
150,701,555 (GRCm39) |
missense |
|
|
R7990:Rere
|
UTSW |
4 |
150,699,327 (GRCm39) |
missense |
unknown |
|
R8070:Rere
|
UTSW |
4 |
150,701,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R8101:Rere
|
UTSW |
4 |
150,701,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Rere
|
UTSW |
4 |
150,701,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8215:Rere
|
UTSW |
4 |
150,701,424 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8254:Rere
|
UTSW |
4 |
150,697,129 (GRCm39) |
missense |
unknown |
|
R8348:Rere
|
UTSW |
4 |
150,703,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8448:Rere
|
UTSW |
4 |
150,703,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Rere
|
UTSW |
4 |
150,701,792 (GRCm39) |
nonsense |
probably null |
|
R8790:Rere
|
UTSW |
4 |
150,593,332 (GRCm39) |
missense |
unknown |
|
R8921:Rere
|
UTSW |
4 |
150,696,471 (GRCm39) |
missense |
unknown |
|
R8937:Rere
|
UTSW |
4 |
150,699,331 (GRCm39) |
unclassified |
probably benign |
|
R9345:Rere
|
UTSW |
4 |
150,554,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R9377:Rere
|
UTSW |
4 |
150,593,342 (GRCm39) |
missense |
unknown |
|
R9490:Rere
|
UTSW |
4 |
150,516,040 (GRCm39) |
missense |
probably benign |
0.16 |
R9523:Rere
|
UTSW |
4 |
150,703,636 (GRCm39) |
missense |
probably damaging |
0.98 |
R9653:Rere
|
UTSW |
4 |
150,516,010 (GRCm39) |
missense |
probably benign |
0.28 |
R9657:Rere
|
UTSW |
4 |
150,699,390 (GRCm39) |
missense |
unknown |
|
Z1176:Rere
|
UTSW |
4 |
150,553,240 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rere
|
UTSW |
4 |
150,700,268 (GRCm39) |
missense |
|
|
|