Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
A |
G |
16: 90,852,822 (GRCm39) |
S105P |
probably damaging |
Het |
Adtrp |
C |
T |
13: 41,981,724 (GRCm39) |
W48* |
probably null |
Het |
Agxt2 |
A |
T |
15: 10,399,151 (GRCm39) |
M413L |
probably benign |
Het |
Aplnr |
T |
A |
2: 84,967,628 (GRCm39) |
C218S |
probably damaging |
Het |
Arhgdib |
T |
A |
6: 136,901,162 (GRCm39) |
E189V |
probably damaging |
Het |
Atp10a |
T |
C |
7: 58,463,596 (GRCm39) |
I1043T |
probably damaging |
Het |
Atp13a5 |
C |
T |
16: 29,133,382 (GRCm39) |
C468Y |
probably damaging |
Het |
Cars2 |
A |
T |
8: 11,564,699 (GRCm39) |
C459S |
probably benign |
Het |
Ccr3 |
T |
A |
9: 123,829,645 (GRCm39) |
Y327N |
probably benign |
Het |
Ceacam1 |
T |
A |
7: 25,171,400 (GRCm39) |
I355F |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,722,932 (GRCm39) |
L2773P |
probably damaging |
Het |
Ces2g |
A |
T |
8: 105,691,521 (GRCm39) |
H192L |
possibly damaging |
Het |
Cfap157 |
A |
G |
2: 32,671,444 (GRCm39) |
F121L |
probably damaging |
Het |
Champ1 |
G |
A |
8: 13,929,234 (GRCm39) |
S464N |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,735,135 (GRCm39) |
L990Q |
probably damaging |
Het |
Col6a3 |
A |
T |
1: 90,706,516 (GRCm39) |
L2806Q |
unknown |
Het |
Cpz |
T |
C |
5: 35,665,536 (GRCm39) |
E435G |
possibly damaging |
Het |
Crbn |
T |
A |
6: 106,761,440 (GRCm39) |
R233* |
probably null |
Het |
Ctc1 |
C |
T |
11: 68,913,352 (GRCm39) |
T116I |
probably benign |
Het |
Cyp4f17 |
T |
C |
17: 32,743,574 (GRCm39) |
S314P |
possibly damaging |
Het |
Dmxl1 |
A |
G |
18: 50,065,030 (GRCm39) |
E2625G |
probably damaging |
Het |
Dock7 |
T |
A |
4: 98,833,796 (GRCm39) |
R1874* |
probably null |
Het |
E130311K13Rik |
A |
T |
3: 63,823,122 (GRCm39) |
L174* |
probably null |
Het |
Etnppl |
A |
G |
3: 130,414,363 (GRCm39) |
D86G |
probably benign |
Het |
Fbxw18 |
C |
A |
9: 109,505,958 (GRCm39) |
E438* |
probably null |
Het |
Gpatch8 |
T |
C |
11: 102,372,668 (GRCm39) |
N290S |
unknown |
Het |
Gpr155 |
A |
C |
2: 73,178,607 (GRCm39) |
L727R |
probably benign |
Het |
Gpr158 |
C |
G |
2: 21,831,682 (GRCm39) |
D927E |
probably benign |
Het |
Igsf10 |
T |
C |
3: 59,225,903 (GRCm39) |
Y2590C |
probably damaging |
Het |
Ints7 |
A |
G |
1: 191,328,348 (GRCm39) |
D207G |
probably damaging |
Het |
Iqsec1 |
A |
G |
6: 90,647,473 (GRCm39) |
L743P |
probably damaging |
Het |
Kansl1l |
A |
T |
1: 66,801,308 (GRCm39) |
S553T |
probably damaging |
Het |
Klhl14 |
G |
T |
18: 21,690,880 (GRCm39) |
Y523* |
probably null |
Het |
Krtap14 |
A |
G |
16: 88,622,515 (GRCm39) |
S155P |
probably damaging |
Het |
Lrrc3b |
A |
G |
14: 15,358,273 (GRCm38) |
V111A |
probably benign |
Het |
Maml2 |
A |
G |
9: 13,531,320 (GRCm39) |
N178S |
|
Het |
Megf8 |
G |
A |
7: 25,041,710 (GRCm39) |
C1208Y |
probably damaging |
Het |
Mocos |
A |
G |
18: 24,819,759 (GRCm39) |
D667G |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,860,158 (GRCm39) |
T1359A |
possibly damaging |
Het |
Nup210 |
T |
C |
6: 91,007,106 (GRCm39) |
E1357G |
probably damaging |
Het |
Or2d2 |
A |
T |
7: 106,727,766 (GRCm39) |
M278K |
probably benign |
Het |
Or4a2 |
A |
T |
2: 89,248,297 (GRCm39) |
H153Q |
probably damaging |
Het |
Or9s15 |
T |
A |
1: 92,524,876 (GRCm39) |
F212I |
probably benign |
Het |
Pign |
A |
G |
1: 105,525,487 (GRCm39) |
V447A |
possibly damaging |
Het |
Pomp |
T |
C |
5: 147,806,229 (GRCm39) |
L57P |
probably benign |
Het |
Pou2af2 |
C |
T |
9: 51,202,992 (GRCm39) |
G54D |
possibly damaging |
Het |
Rbms3 |
T |
A |
9: 116,885,861 (GRCm39) |
Y128F |
probably damaging |
Het |
Slc12a4 |
A |
G |
8: 106,678,228 (GRCm39) |
F322L |
probably benign |
Het |
Slc16a9 |
T |
A |
10: 70,119,762 (GRCm39) |
C468* |
probably null |
Het |
Slc22a18 |
A |
G |
7: 143,046,668 (GRCm39) |
I271V |
probably benign |
Het |
Slc25a41 |
A |
G |
17: 57,346,933 (GRCm39) |
V20A |
possibly damaging |
Het |
Smim7 |
A |
T |
8: 73,324,857 (GRCm39) |
L6Q |
probably damaging |
Het |
Snx29 |
T |
C |
16: 11,218,845 (GRCm39) |
V227A |
probably damaging |
Het |
Sowaha |
A |
T |
11: 53,369,290 (GRCm39) |
L482Q |
probably damaging |
Het |
Srp19 |
A |
G |
18: 34,467,523 (GRCm39) |
Y68C |
probably damaging |
Het |
Tecr |
A |
G |
8: 84,298,884 (GRCm39) |
S298P |
probably damaging |
Het |
Terb2 |
T |
A |
2: 122,035,379 (GRCm39) |
I200N |
probably damaging |
Het |
Togaram1 |
G |
A |
12: 65,030,286 (GRCm39) |
S1030N |
probably damaging |
Het |
Trav7n-4 |
A |
G |
14: 53,329,193 (GRCm39) |
M68V |
probably benign |
Het |
Tshz1 |
A |
C |
18: 84,031,375 (GRCm39) |
L1011R |
possibly damaging |
Het |
Tubb3 |
A |
G |
8: 124,148,396 (GRCm39) |
E443G |
possibly damaging |
Het |
Uba5 |
A |
T |
9: 103,932,396 (GRCm39) |
I189K |
probably damaging |
Het |
Vasn |
A |
G |
16: 4,467,909 (GRCm39) |
T619A |
probably benign |
Het |
Wbp1l |
A |
G |
19: 46,642,761 (GRCm39) |
D254G |
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,741,571 (GRCm39) |
F738L |
probably damaging |
Het |
|
Other mutations in Ahnak2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02257:Ahnak2
|
APN |
12 |
112,748,905 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02994:Ahnak2
|
APN |
12 |
112,749,827 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4480001:Ahnak2
|
UTSW |
12 |
112,740,358 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0025:Ahnak2
|
UTSW |
12 |
112,749,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R0025:Ahnak2
|
UTSW |
12 |
112,749,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R0038:Ahnak2
|
UTSW |
12 |
112,740,896 (GRCm39) |
missense |
probably benign |
0.00 |
R0125:Ahnak2
|
UTSW |
12 |
112,748,776 (GRCm39) |
missense |
probably benign |
0.41 |
R1173:Ahnak2
|
UTSW |
12 |
112,749,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Ahnak2
|
UTSW |
12 |
112,751,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1712:Ahnak2
|
UTSW |
12 |
112,748,998 (GRCm39) |
missense |
probably benign |
0.05 |
R1888:Ahnak2
|
UTSW |
12 |
112,740,325 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1888:Ahnak2
|
UTSW |
12 |
112,740,325 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2042:Ahnak2
|
UTSW |
12 |
112,749,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R2056:Ahnak2
|
UTSW |
12 |
112,748,626 (GRCm39) |
missense |
probably benign |
0.00 |
R2417:Ahnak2
|
UTSW |
12 |
112,741,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R2762:Ahnak2
|
UTSW |
12 |
112,748,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R3618:Ahnak2
|
UTSW |
12 |
112,749,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R3706:Ahnak2
|
UTSW |
12 |
112,740,085 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3739:Ahnak2
|
UTSW |
12 |
112,740,992 (GRCm39) |
missense |
probably benign |
0.05 |
R3950:Ahnak2
|
UTSW |
12 |
112,749,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R4485:Ahnak2
|
UTSW |
12 |
112,745,944 (GRCm39) |
unclassified |
probably benign |
|
R4651:Ahnak2
|
UTSW |
12 |
112,741,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4652:Ahnak2
|
UTSW |
12 |
112,741,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4831:Ahnak2
|
UTSW |
12 |
112,742,183 (GRCm39) |
missense |
probably damaging |
0.99 |
R4836:Ahnak2
|
UTSW |
12 |
112,740,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Ahnak2
|
UTSW |
12 |
112,749,359 (GRCm39) |
missense |
probably benign |
0.00 |
R4864:Ahnak2
|
UTSW |
12 |
112,740,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R4908:Ahnak2
|
UTSW |
12 |
112,741,706 (GRCm39) |
missense |
probably benign |
0.00 |
R5067:Ahnak2
|
UTSW |
12 |
112,748,936 (GRCm39) |
missense |
probably benign |
0.01 |
R5146:Ahnak2
|
UTSW |
12 |
112,742,160 (GRCm39) |
missense |
probably benign |
0.00 |
R5228:Ahnak2
|
UTSW |
12 |
112,741,820 (GRCm39) |
missense |
probably benign |
0.03 |
R5255:Ahnak2
|
UTSW |
12 |
112,739,812 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5323:Ahnak2
|
UTSW |
12 |
112,745,989 (GRCm39) |
unclassified |
probably benign |
|
R5523:Ahnak2
|
UTSW |
12 |
112,741,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R5733:Ahnak2
|
UTSW |
12 |
112,742,100 (GRCm39) |
nonsense |
probably null |
|
R5799:Ahnak2
|
UTSW |
12 |
112,745,365 (GRCm39) |
unclassified |
probably benign |
|
R5817:Ahnak2
|
UTSW |
12 |
112,740,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:Ahnak2
|
UTSW |
12 |
112,742,230 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6083:Ahnak2
|
UTSW |
12 |
112,746,589 (GRCm39) |
missense |
probably benign |
0.01 |
R6083:Ahnak2
|
UTSW |
12 |
112,746,715 (GRCm39) |
missense |
probably benign |
0.06 |
R6167:Ahnak2
|
UTSW |
12 |
112,747,750 (GRCm39) |
missense |
probably benign |
0.03 |
R6168:Ahnak2
|
UTSW |
12 |
112,747,750 (GRCm39) |
missense |
probably benign |
0.03 |
R6405:Ahnak2
|
UTSW |
12 |
112,739,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6460:Ahnak2
|
UTSW |
12 |
112,750,610 (GRCm39) |
missense |
probably null |
0.27 |
R6495:Ahnak2
|
UTSW |
12 |
112,740,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6544:Ahnak2
|
UTSW |
12 |
112,746,829 (GRCm39) |
unclassified |
probably benign |
|
R6656:Ahnak2
|
UTSW |
12 |
112,748,991 (GRCm39) |
missense |
probably benign |
0.02 |
R6679:Ahnak2
|
UTSW |
12 |
112,739,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R6723:Ahnak2
|
UTSW |
12 |
112,745,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Ahnak2
|
UTSW |
12 |
112,740,172 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6884:Ahnak2
|
UTSW |
12 |
112,741,863 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6906:Ahnak2
|
UTSW |
12 |
112,748,933 (GRCm39) |
missense |
probably benign |
0.00 |
R6919:Ahnak2
|
UTSW |
12 |
112,741,118 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7036:Ahnak2
|
UTSW |
12 |
112,745,216 (GRCm39) |
unclassified |
probably benign |
|
R7037:Ahnak2
|
UTSW |
12 |
112,740,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R7064:Ahnak2
|
UTSW |
12 |
112,746,919 (GRCm39) |
unclassified |
probably benign |
|
R7072:Ahnak2
|
UTSW |
12 |
112,751,786 (GRCm39) |
missense |
|
|
R7112:Ahnak2
|
UTSW |
12 |
112,747,747 (GRCm39) |
missense |
|
|
R7268:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
R7269:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
R7270:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
R7271:Ahnak2
|
UTSW |
12 |
112,780,802 (GRCm38) |
missense |
|
|
R7444:Ahnak2
|
UTSW |
12 |
112,745,831 (GRCm39) |
missense |
|
|
R7448:Ahnak2
|
UTSW |
12 |
112,746,605 (GRCm39) |
missense |
|
|
R7488:Ahnak2
|
UTSW |
12 |
112,748,641 (GRCm39) |
missense |
|
|
R7508:Ahnak2
|
UTSW |
12 |
112,740,839 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7560:Ahnak2
|
UTSW |
12 |
112,745,851 (GRCm39) |
missense |
|
|
R7611:Ahnak2
|
UTSW |
12 |
112,751,749 (GRCm39) |
missense |
|
|
R7743:Ahnak2
|
UTSW |
12 |
112,748,383 (GRCm39) |
missense |
not run |
|
R7762:Ahnak2
|
UTSW |
12 |
112,742,114 (GRCm39) |
missense |
probably benign |
0.27 |
R7780:Ahnak2
|
UTSW |
12 |
112,746,716 (GRCm39) |
missense |
|
|
R7930:Ahnak2
|
UTSW |
12 |
112,745,560 (GRCm39) |
missense |
|
|
R7985:Ahnak2
|
UTSW |
12 |
112,745,398 (GRCm39) |
missense |
|
|
R8114:Ahnak2
|
UTSW |
12 |
112,741,163 (GRCm39) |
missense |
probably benign |
0.05 |
R8122:Ahnak2
|
UTSW |
12 |
112,742,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8240:Ahnak2
|
UTSW |
12 |
112,741,082 (GRCm39) |
missense |
probably benign |
0.03 |
R8289:Ahnak2
|
UTSW |
12 |
112,742,242 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8315:Ahnak2
|
UTSW |
12 |
112,745,756 (GRCm39) |
missense |
|
|
R8430:Ahnak2
|
UTSW |
12 |
112,741,121 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8476:Ahnak2
|
UTSW |
12 |
112,747,100 (GRCm39) |
unclassified |
probably benign |
|
R8712:Ahnak2
|
UTSW |
12 |
112,750,709 (GRCm39) |
missense |
|
|
R8712:Ahnak2
|
UTSW |
12 |
112,749,872 (GRCm39) |
missense |
|
|
R8778:Ahnak2
|
UTSW |
12 |
112,783,158 (GRCm38) |
missense |
|
|
R8830:Ahnak2
|
UTSW |
12 |
112,750,656 (GRCm39) |
missense |
|
|
R9014:Ahnak2
|
UTSW |
12 |
112,740,170 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9055:Ahnak2
|
UTSW |
12 |
112,741,019 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9327:Ahnak2
|
UTSW |
12 |
112,748,446 (GRCm39) |
missense |
|
|
R9386:Ahnak2
|
UTSW |
12 |
112,745,428 (GRCm39) |
missense |
|
|
R9445:Ahnak2
|
UTSW |
12 |
112,745,978 (GRCm39) |
missense |
|
|
R9462:Ahnak2
|
UTSW |
12 |
112,750,655 (GRCm39) |
missense |
|
|
R9559:Ahnak2
|
UTSW |
12 |
112,749,782 (GRCm39) |
critical splice donor site |
probably null |
|
R9571:Ahnak2
|
UTSW |
12 |
112,742,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9589:Ahnak2
|
UTSW |
12 |
112,746,831 (GRCm39) |
missense |
|
|
R9664:Ahnak2
|
UTSW |
12 |
112,741,363 (GRCm39) |
missense |
probably damaging |
0.97 |
R9711:Ahnak2
|
UTSW |
12 |
112,739,468 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Ahnak2
|
UTSW |
12 |
112,745,822 (GRCm39) |
missense |
|
|
|