Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ache |
T |
G |
5: 137,289,104 (GRCm39) |
V270G |
probably damaging |
Het |
Acss1 |
A |
T |
2: 150,470,459 (GRCm39) |
W394R |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,330,791 (GRCm39) |
V6088A |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,580,691 (GRCm39) |
|
probably benign |
Het |
Anxa1 |
A |
T |
19: 20,361,141 (GRCm39) |
Y84N |
probably damaging |
Het |
Arnt2 |
G |
A |
7: 83,996,738 (GRCm39) |
R63C |
probably damaging |
Het |
Avpr1b |
A |
G |
1: 131,527,524 (GRCm39) |
T16A |
probably benign |
Het |
Bpifb1 |
G |
A |
2: 154,048,460 (GRCm39) |
R165H |
possibly damaging |
Het |
Cables1 |
A |
G |
18: 12,056,470 (GRCm39) |
E316G |
possibly damaging |
Het |
Cadm1 |
A |
T |
9: 47,761,629 (GRCm39) |
I427L |
probably damaging |
Het |
Ccdc97 |
T |
C |
7: 25,415,405 (GRCm39) |
D86G |
probably benign |
Het |
Cgnl1 |
C |
A |
9: 71,548,679 (GRCm39) |
D1081Y |
probably damaging |
Het |
Cgnl1 |
T |
A |
9: 71,632,122 (GRCm39) |
R410W |
probably damaging |
Het |
Cntnap4 |
G |
A |
8: 113,512,416 (GRCm39) |
E593K |
probably damaging |
Het |
Dazap1 |
T |
C |
10: 80,097,415 (GRCm39) |
|
probably benign |
Het |
Dip2b |
A |
G |
15: 100,113,121 (GRCm39) |
E1512G |
probably benign |
Het |
Dock1 |
G |
A |
7: 134,710,490 (GRCm39) |
V1171M |
possibly damaging |
Het |
Dock5 |
A |
T |
14: 68,018,485 (GRCm39) |
F1230Y |
probably benign |
Het |
Dym |
G |
A |
18: 75,176,243 (GRCm39) |
E15K |
possibly damaging |
Het |
Ednra |
C |
A |
8: 78,393,951 (GRCm39) |
|
probably null |
Het |
Faf1 |
A |
G |
4: 109,593,821 (GRCm39) |
Q133R |
probably benign |
Het |
Fbxw28 |
A |
G |
9: 109,157,279 (GRCm39) |
I323T |
probably benign |
Het |
Fcer2a |
T |
C |
8: 3,738,111 (GRCm39) |
|
probably benign |
Het |
Fmo2 |
A |
T |
1: 162,713,893 (GRCm39) |
S204R |
probably benign |
Het |
Frmd4b |
A |
G |
6: 97,400,460 (GRCm39) |
V63A |
probably damaging |
Het |
Fzd8 |
G |
A |
18: 9,213,985 (GRCm39) |
A356T |
possibly damaging |
Het |
Ghitm |
A |
G |
14: 36,853,549 (GRCm39) |
L97P |
probably damaging |
Het |
Gins4 |
A |
G |
8: 23,719,526 (GRCm39) |
|
probably benign |
Het |
Golga3 |
T |
A |
5: 110,350,643 (GRCm39) |
F766Y |
possibly damaging |
Het |
Helz |
A |
T |
11: 107,563,384 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,820,231 (GRCm39) |
V2851A |
possibly damaging |
Het |
Igkv8-18 |
G |
A |
6: 70,333,105 (GRCm39) |
|
probably benign |
Het |
Igll1 |
A |
T |
16: 16,681,740 (GRCm39) |
V5E |
probably benign |
Het |
Irx3 |
T |
C |
8: 92,527,168 (GRCm39) |
T179A |
possibly damaging |
Het |
Kif16b |
A |
G |
2: 142,699,225 (GRCm39) |
|
probably null |
Het |
Limk1 |
A |
T |
5: 134,688,725 (GRCm39) |
W507R |
probably damaging |
Het |
Marf1 |
C |
T |
16: 13,960,398 (GRCm39) |
A549T |
probably damaging |
Het |
Mtif3 |
C |
A |
5: 146,893,731 (GRCm39) |
V159F |
probably benign |
Het |
Myh6 |
C |
T |
14: 55,200,861 (GRCm39) |
R169Q |
probably damaging |
Het |
Ncoa7 |
T |
A |
10: 30,523,537 (GRCm39) |
D887V |
probably damaging |
Het |
Obox7 |
C |
T |
7: 14,398,313 (GRCm39) |
P76S |
probably benign |
Het |
Or10ak12 |
A |
G |
4: 118,666,677 (GRCm39) |
M128T |
probably benign |
Het |
Or11l3 |
A |
T |
11: 58,516,494 (GRCm39) |
I126N |
probably damaging |
Het |
Pitpnm2 |
G |
A |
5: 124,262,093 (GRCm39) |
A862V |
probably damaging |
Het |
Pkd1 |
G |
C |
17: 24,783,677 (GRCm39) |
A162P |
probably benign |
Het |
Plce1 |
A |
G |
19: 38,513,628 (GRCm39) |
D309G |
possibly damaging |
Het |
Plk4 |
T |
C |
3: 40,760,307 (GRCm39) |
V401A |
probably benign |
Het |
Prdx3 |
T |
C |
19: 60,862,950 (GRCm39) |
|
probably benign |
Het |
Prrc2c |
C |
T |
1: 162,526,453 (GRCm39) |
V253I |
unknown |
Het |
Ranbp2 |
T |
A |
10: 58,316,353 (GRCm39) |
S2358T |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,423,494 (GRCm39) |
V2183E |
probably damaging |
Het |
Sgsm1 |
T |
A |
5: 113,432,953 (GRCm39) |
S232C |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,904,012 (GRCm39) |
|
probably benign |
Het |
Slc15a2 |
A |
G |
16: 36,574,909 (GRCm39) |
I531T |
probably benign |
Het |
Slc36a1 |
C |
T |
11: 55,112,820 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
C |
A |
8: 46,249,300 (GRCm39) |
D831E |
probably damaging |
Het |
Sorbs2 |
T |
A |
8: 46,238,291 (GRCm39) |
|
probably null |
Het |
Sptan1 |
T |
C |
2: 29,883,708 (GRCm39) |
|
probably null |
Het |
Stam |
T |
C |
2: 14,142,952 (GRCm39) |
C336R |
probably damaging |
Het |
Stil |
G |
T |
4: 114,898,495 (GRCm39) |
A1042S |
probably damaging |
Het |
Stxbp5l |
T |
A |
16: 36,962,736 (GRCm39) |
D773V |
possibly damaging |
Het |
Sugct |
A |
T |
13: 17,847,166 (GRCm39) |
L39Q |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,071,522 (GRCm39) |
V2041A |
possibly damaging |
Het |
Tex15 |
C |
T |
8: 34,071,530 (GRCm39) |
|
probably benign |
Het |
Tlr9 |
T |
G |
9: 106,102,164 (GRCm39) |
L485R |
possibly damaging |
Het |
Tmem207 |
A |
G |
16: 26,343,579 (GRCm39) |
|
probably benign |
Het |
Triml2 |
T |
C |
8: 43,638,306 (GRCm39) |
|
probably benign |
Het |
Trip6 |
A |
G |
5: 137,309,107 (GRCm39) |
|
probably benign |
Het |
Tspear |
T |
C |
10: 77,705,465 (GRCm39) |
F288L |
probably benign |
Het |
Vmn1r179 |
C |
T |
7: 23,628,592 (GRCm39) |
T261I |
possibly damaging |
Het |
Zfp644 |
A |
T |
5: 106,784,869 (GRCm39) |
S559R |
possibly damaging |
Het |
|
Other mutations in Hapln1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00235:Hapln1
|
APN |
13 |
89,756,261 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00494:Hapln1
|
APN |
13 |
89,753,590 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01865:Hapln1
|
APN |
13 |
89,749,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02706:Hapln1
|
APN |
13 |
89,753,578 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02990:Hapln1
|
APN |
13 |
89,749,725 (GRCm39) |
missense |
probably benign |
0.03 |
R0033:Hapln1
|
UTSW |
13 |
89,749,932 (GRCm39) |
missense |
probably benign |
0.20 |
R0058:Hapln1
|
UTSW |
13 |
89,755,997 (GRCm39) |
missense |
probably benign |
0.17 |
R0127:Hapln1
|
UTSW |
13 |
89,755,988 (GRCm39) |
missense |
probably benign |
0.22 |
R0519:Hapln1
|
UTSW |
13 |
89,732,835 (GRCm39) |
start gained |
probably benign |
|
R3862:Hapln1
|
UTSW |
13 |
89,753,418 (GRCm39) |
nonsense |
probably null |
|
R3982:Hapln1
|
UTSW |
13 |
89,753,560 (GRCm39) |
missense |
probably benign |
|
R4717:Hapln1
|
UTSW |
13 |
89,753,579 (GRCm39) |
missense |
probably benign |
0.11 |
R4861:Hapln1
|
UTSW |
13 |
89,749,571 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4861:Hapln1
|
UTSW |
13 |
89,749,571 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4862:Hapln1
|
UTSW |
13 |
89,749,571 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4899:Hapln1
|
UTSW |
13 |
89,749,769 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5402:Hapln1
|
UTSW |
13 |
89,753,530 (GRCm39) |
missense |
probably benign |
0.07 |
R5629:Hapln1
|
UTSW |
13 |
89,749,634 (GRCm39) |
missense |
probably damaging |
0.98 |
R6019:Hapln1
|
UTSW |
13 |
89,756,219 (GRCm39) |
missense |
probably benign |
0.45 |
R7917:Hapln1
|
UTSW |
13 |
89,755,997 (GRCm39) |
missense |
probably benign |
0.17 |
R7938:Hapln1
|
UTSW |
13 |
89,753,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R8312:Hapln1
|
UTSW |
13 |
89,749,563 (GRCm39) |
missense |
probably benign |
|
R8345:Hapln1
|
UTSW |
13 |
89,732,902 (GRCm39) |
missense |
probably benign |
|
Z1088:Hapln1
|
UTSW |
13 |
89,749,617 (GRCm39) |
missense |
probably benign |
|
|