Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,773,031 (GRCm39) |
E740G |
probably damaging |
Het |
4930474N05Rik |
G |
T |
14: 35,817,414 (GRCm39) |
V105F |
possibly damaging |
Het |
Actr10 |
A |
G |
12: 70,989,104 (GRCm39) |
I74M |
probably benign |
Het |
Aen |
T |
C |
7: 78,555,660 (GRCm39) |
Y108H |
probably damaging |
Het |
Afm |
A |
T |
5: 90,672,779 (GRCm39) |
K205* |
probably null |
Het |
Ankrd27 |
T |
A |
7: 35,332,410 (GRCm39) |
S846T |
probably benign |
Het |
Ano3 |
A |
G |
2: 110,715,352 (GRCm39) |
S29P |
probably benign |
Het |
Apaf1 |
C |
T |
10: 90,913,476 (GRCm39) |
W138* |
probably null |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Arhgef4 |
A |
G |
1: 34,850,221 (GRCm39) |
Q1798R |
probably damaging |
Het |
Astn1 |
G |
A |
1: 158,337,541 (GRCm39) |
V416I |
probably damaging |
Het |
Atxn2l |
G |
A |
7: 126,092,340 (GRCm39) |
T70I |
probably damaging |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,061,132 (GRCm39) |
|
probably null |
Het |
Bspry |
T |
A |
4: 62,413,034 (GRCm39) |
C256S |
probably damaging |
Het |
C3 |
C |
A |
17: 57,527,135 (GRCm39) |
W771C |
probably damaging |
Het |
Camkv |
A |
G |
9: 107,824,287 (GRCm39) |
D233G |
possibly damaging |
Het |
Catsperd |
T |
A |
17: 56,942,548 (GRCm39) |
V109E |
probably damaging |
Het |
Cd101 |
A |
G |
3: 100,926,233 (GRCm39) |
L162P |
probably damaging |
Het |
Cdr2l |
A |
G |
11: 115,283,603 (GRCm39) |
T154A |
probably damaging |
Het |
Clca3a2 |
G |
C |
3: 144,516,457 (GRCm39) |
Q380E |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,750,081 (GRCm39) |
N251S |
possibly damaging |
Het |
Cttnbp2nl |
A |
G |
3: 104,918,594 (GRCm39) |
V82A |
possibly damaging |
Het |
Cux1 |
G |
A |
5: 136,392,173 (GRCm39) |
Q194* |
probably null |
Het |
Daam2 |
T |
C |
17: 49,792,485 (GRCm39) |
E361G |
probably benign |
Het |
Dcaf17 |
A |
T |
2: 70,908,516 (GRCm39) |
|
probably null |
Het |
Dnai1 |
T |
C |
4: 41,570,020 (GRCm39) |
|
probably null |
Het |
Eml5 |
T |
C |
12: 98,765,098 (GRCm39) |
Y1617C |
probably damaging |
Het |
Epb41l4b |
T |
C |
4: 57,040,993 (GRCm39) |
E490G |
probably damaging |
Het |
Epha7 |
T |
C |
4: 28,963,969 (GRCm39) |
M988T |
possibly damaging |
Het |
Fancm |
T |
C |
12: 65,152,294 (GRCm39) |
C917R |
possibly damaging |
Het |
Fnip1 |
C |
T |
11: 54,371,510 (GRCm39) |
T177I |
probably damaging |
Het |
Gm3604 |
G |
T |
13: 62,517,756 (GRCm39) |
H201N |
probably benign |
Het |
Gnpda1 |
T |
C |
18: 38,466,243 (GRCm39) |
|
probably null |
Het |
Gpatch8 |
A |
G |
11: 102,398,968 (GRCm39) |
|
probably null |
Het |
H2-M3 |
T |
C |
17: 37,582,080 (GRCm39) |
Y179H |
possibly damaging |
Het |
H2-Q10 |
C |
A |
17: 35,781,385 (GRCm39) |
S62R |
probably damaging |
Het |
Hipk2 |
G |
A |
6: 38,795,919 (GRCm39) |
R117* |
probably null |
Het |
Hrg |
A |
T |
16: 22,773,207 (GRCm39) |
Q113H |
probably damaging |
Het |
Kcnj16 |
T |
C |
11: 110,915,779 (GRCm39) |
V147A |
possibly damaging |
Het |
Kif1a |
T |
C |
1: 92,946,753 (GRCm39) |
I1650V |
possibly damaging |
Het |
Kmt2a |
C |
T |
9: 44,731,642 (GRCm39) |
|
probably benign |
Het |
Krt90 |
A |
T |
15: 101,465,665 (GRCm39) |
Y319N |
probably damaging |
Het |
Lipo4 |
T |
C |
19: 33,476,671 (GRCm39) |
N359S |
possibly damaging |
Het |
Lrp1b |
G |
T |
2: 41,618,741 (GRCm39) |
T225K |
probably benign |
Het |
Map1a |
C |
T |
2: 121,137,493 (GRCm39) |
P2532S |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,119,600 (GRCm39) |
D193G |
probably benign |
Het |
Mpped2 |
T |
A |
2: 106,697,377 (GRCm39) |
I284N |
probably damaging |
Het |
Msh6 |
A |
G |
17: 88,292,553 (GRCm39) |
H436R |
probably benign |
Het |
Mterf3 |
A |
T |
13: 67,078,126 (GRCm39) |
S48T |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,399,768 (GRCm39) |
F414L |
unknown |
Het |
Mylk4 |
A |
T |
13: 32,908,836 (GRCm39) |
D90E |
probably benign |
Het |
Nherf4 |
T |
C |
9: 44,161,600 (GRCm39) |
D93G |
possibly damaging |
Het |
Nploc4 |
A |
G |
11: 120,295,055 (GRCm39) |
Y420H |
probably damaging |
Het |
Npr2 |
T |
A |
4: 43,640,578 (GRCm39) |
Y344N |
probably damaging |
Het |
Nsun5 |
A |
G |
5: 135,404,452 (GRCm39) |
T397A |
probably benign |
Het |
Ntsr2 |
A |
T |
12: 16,704,111 (GRCm39) |
Q204L |
probably damaging |
Het |
Nwd2 |
T |
A |
5: 63,963,523 (GRCm39) |
Y1036N |
probably damaging |
Het |
Oacyl |
T |
C |
18: 65,843,618 (GRCm39) |
V105A |
possibly damaging |
Het |
Or6c2 |
T |
A |
10: 129,362,918 (GRCm39) |
V274D |
probably damaging |
Het |
Parp3 |
T |
A |
9: 106,352,316 (GRCm39) |
Q70L |
possibly damaging |
Het |
Parp4 |
T |
C |
14: 56,861,474 (GRCm39) |
S936P |
probably damaging |
Het |
Phkb |
A |
G |
8: 86,648,790 (GRCm39) |
E202G |
probably benign |
Het |
Pink1 |
T |
C |
4: 138,041,331 (GRCm39) |
N530S |
probably benign |
Het |
Pou3f2 |
T |
C |
4: 22,487,119 (GRCm39) |
D338G |
probably damaging |
Het |
Prss8 |
G |
T |
7: 127,529,030 (GRCm39) |
L9I |
probably benign |
Het |
Ptpn22 |
G |
A |
3: 103,784,054 (GRCm39) |
|
probably null |
Het |
Rasef |
A |
G |
4: 73,662,351 (GRCm39) |
S200P |
possibly damaging |
Het |
Rb1 |
T |
A |
14: 73,450,430 (GRCm39) |
K645* |
probably null |
Het |
Robo2 |
C |
T |
16: 73,696,042 (GRCm39) |
G1367D |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,422,894 (GRCm39) |
V52A |
probably damaging |
Het |
Samd13 |
T |
C |
3: 146,368,467 (GRCm39) |
T23A |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,530,317 (GRCm39) |
H676R |
probably damaging |
Het |
Serpinb6b |
A |
G |
13: 33,162,223 (GRCm39) |
I222V |
probably benign |
Het |
Slc2a8 |
T |
C |
2: 32,870,091 (GRCm39) |
Y150C |
probably damaging |
Het |
Slc7a6os |
C |
A |
8: 106,937,196 (GRCm39) |
R88L |
probably damaging |
Het |
Slc8a2 |
A |
G |
7: 15,886,845 (GRCm39) |
I657V |
probably benign |
Het |
Slit2 |
C |
A |
5: 48,348,358 (GRCm39) |
|
probably benign |
Het |
Spire2 |
A |
G |
8: 124,089,810 (GRCm39) |
D447G |
probably benign |
Het |
Sptlc3 |
A |
G |
2: 139,408,595 (GRCm39) |
N237D |
possibly damaging |
Het |
Stk3 |
G |
A |
15: 35,073,363 (GRCm39) |
T119I |
probably damaging |
Het |
Suv39h2 |
G |
A |
2: 3,465,353 (GRCm39) |
T334I |
probably damaging |
Het |
Syt5 |
G |
T |
7: 4,543,278 (GRCm39) |
T327N |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,949,156 (GRCm39) |
D1253G |
possibly damaging |
Het |
Timd5 |
A |
G |
11: 46,419,358 (GRCm39) |
D58G |
possibly damaging |
Het |
Tnks |
A |
T |
8: 35,342,386 (GRCm39) |
V388D |
probably damaging |
Het |
Ugt2b1 |
T |
C |
5: 87,073,859 (GRCm39) |
T167A |
probably benign |
Het |
Usp40 |
G |
A |
1: 87,923,564 (GRCm39) |
R236C |
possibly damaging |
Het |
Utrn |
T |
C |
10: 12,331,224 (GRCm39) |
D2904G |
probably benign |
Het |
Vmn1r226 |
T |
C |
17: 20,907,842 (GRCm39) |
S25P |
probably damaging |
Het |
Vmn2r23 |
T |
C |
6: 123,689,969 (GRCm39) |
S282P |
possibly damaging |
Het |
Vps45 |
T |
C |
3: 95,953,752 (GRCm39) |
E200G |
probably benign |
Het |
Wnt7b |
T |
A |
15: 85,443,281 (GRCm39) |
I41F |
probably damaging |
Het |
Zmym6 |
T |
A |
4: 126,997,207 (GRCm39) |
N275K |
probably damaging |
Het |
|
Other mutations in Rad54b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00770:Rad54b
|
APN |
4 |
11,593,765 (GRCm39) |
missense |
probably benign |
|
IGL00774:Rad54b
|
APN |
4 |
11,593,765 (GRCm39) |
missense |
probably benign |
|
IGL00956:Rad54b
|
APN |
4 |
11,597,833 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00961:Rad54b
|
APN |
4 |
11,599,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01064:Rad54b
|
APN |
4 |
11,604,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02150:Rad54b
|
APN |
4 |
11,610,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02326:Rad54b
|
APN |
4 |
11,612,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Rad54b
|
APN |
4 |
11,615,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03143:Rad54b
|
APN |
4 |
11,599,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Rad54b
|
APN |
4 |
11,569,833 (GRCm39) |
missense |
possibly damaging |
0.83 |
kerplunk
|
UTSW |
4 |
11,612,655 (GRCm39) |
missense |
probably damaging |
1.00 |
Schnipfel
|
UTSW |
4 |
11,583,689 (GRCm39) |
unclassified |
probably benign |
|
P0033:Rad54b
|
UTSW |
4 |
11,609,285 (GRCm39) |
unclassified |
probably benign |
|
R0076:Rad54b
|
UTSW |
4 |
11,609,480 (GRCm39) |
unclassified |
probably benign |
|
R0094:Rad54b
|
UTSW |
4 |
11,599,681 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0391:Rad54b
|
UTSW |
4 |
11,601,702 (GRCm39) |
missense |
probably damaging |
0.98 |
R0441:Rad54b
|
UTSW |
4 |
11,563,394 (GRCm39) |
missense |
probably benign |
0.08 |
R0442:Rad54b
|
UTSW |
4 |
11,610,362 (GRCm39) |
missense |
probably benign |
0.02 |
R0442:Rad54b
|
UTSW |
4 |
11,609,480 (GRCm39) |
unclassified |
probably benign |
|
R0449:Rad54b
|
UTSW |
4 |
11,606,131 (GRCm39) |
missense |
probably benign |
0.43 |
R0519:Rad54b
|
UTSW |
4 |
11,599,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0843:Rad54b
|
UTSW |
4 |
11,609,471 (GRCm39) |
critical splice donor site |
probably null |
|
R1118:Rad54b
|
UTSW |
4 |
11,563,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Rad54b
|
UTSW |
4 |
11,606,152 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1763:Rad54b
|
UTSW |
4 |
11,604,989 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1812:Rad54b
|
UTSW |
4 |
11,612,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Rad54b
|
UTSW |
4 |
11,601,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Rad54b
|
UTSW |
4 |
11,601,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Rad54b
|
UTSW |
4 |
11,601,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Rad54b
|
UTSW |
4 |
11,606,088 (GRCm39) |
missense |
probably benign |
0.08 |
R2386:Rad54b
|
UTSW |
4 |
11,597,874 (GRCm39) |
missense |
probably benign |
|
R2437:Rad54b
|
UTSW |
4 |
11,606,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4299:Rad54b
|
UTSW |
4 |
11,597,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R4391:Rad54b
|
UTSW |
4 |
11,615,570 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Rad54b
|
UTSW |
4 |
11,609,449 (GRCm39) |
missense |
probably benign |
0.05 |
R4673:Rad54b
|
UTSW |
4 |
11,609,449 (GRCm39) |
missense |
probably benign |
0.05 |
R4826:Rad54b
|
UTSW |
4 |
11,599,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R4930:Rad54b
|
UTSW |
4 |
11,615,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R5796:Rad54b
|
UTSW |
4 |
11,615,446 (GRCm39) |
missense |
probably benign |
0.01 |
R5901:Rad54b
|
UTSW |
4 |
11,595,919 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6185:Rad54b
|
UTSW |
4 |
11,593,804 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6355:Rad54b
|
UTSW |
4 |
11,604,989 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6576:Rad54b
|
UTSW |
4 |
11,601,577 (GRCm39) |
missense |
probably benign |
|
R6684:Rad54b
|
UTSW |
4 |
11,583,689 (GRCm39) |
unclassified |
probably benign |
|
R6821:Rad54b
|
UTSW |
4 |
11,612,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R6947:Rad54b
|
UTSW |
4 |
11,569,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7177:Rad54b
|
UTSW |
4 |
11,599,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Rad54b
|
UTSW |
4 |
11,599,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Rad54b
|
UTSW |
4 |
11,610,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R7511:Rad54b
|
UTSW |
4 |
11,578,956 (GRCm39) |
splice site |
probably null |
|
R7847:Rad54b
|
UTSW |
4 |
11,612,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Rad54b
|
UTSW |
4 |
11,595,868 (GRCm39) |
missense |
probably null |
0.01 |
R8198:Rad54b
|
UTSW |
4 |
11,612,440 (GRCm39) |
critical splice donor site |
probably null |
|
R9140:Rad54b
|
UTSW |
4 |
11,610,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Rad54b
|
UTSW |
4 |
11,609,321 (GRCm39) |
nonsense |
probably null |
|
|