Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730507C01Rik |
A |
G |
12: 18,583,687 (GRCm39) |
E225G |
possibly damaging |
Het |
Abcb7 |
T |
C |
X: 103,349,005 (GRCm39) |
M153V |
probably benign |
Het |
Abi1 |
A |
T |
2: 22,840,276 (GRCm39) |
V329D |
possibly damaging |
Het |
Ablim3 |
G |
A |
18: 61,982,466 (GRCm39) |
H160Y |
probably benign |
Het |
Acox3 |
A |
T |
5: 35,766,406 (GRCm39) |
D624V |
possibly damaging |
Het |
Adam6b |
A |
G |
12: 113,455,442 (GRCm39) |
D753G |
probably benign |
Het |
Ago1 |
C |
A |
4: 126,333,788 (GRCm39) |
R771L |
probably benign |
Het |
Aktip |
A |
G |
8: 91,852,505 (GRCm39) |
V217A |
possibly damaging |
Het |
Ankk1 |
A |
C |
9: 49,327,150 (GRCm39) |
H676Q |
probably benign |
Het |
Arl1 |
G |
C |
10: 88,569,408 (GRCm39) |
|
probably benign |
Het |
Asxl3 |
T |
A |
18: 22,650,796 (GRCm39) |
D928E |
probably damaging |
Het |
AW209491 |
T |
C |
13: 14,811,318 (GRCm39) |
V57A |
possibly damaging |
Het |
B3galt4 |
G |
T |
17: 34,169,885 (GRCm39) |
Q118K |
probably benign |
Het |
Ccdc187 |
A |
T |
2: 26,166,080 (GRCm39) |
M783K |
probably benign |
Het |
Cdon |
T |
G |
9: 35,394,454 (GRCm39) |
M900R |
probably damaging |
Het |
Ceacam5 |
G |
A |
7: 17,448,835 (GRCm39) |
W67* |
probably null |
Het |
Chd5 |
A |
G |
4: 152,462,727 (GRCm39) |
S1356G |
probably damaging |
Het |
Chil3 |
C |
T |
3: 106,056,117 (GRCm39) |
|
probably null |
Het |
Chmp7 |
C |
T |
14: 69,956,899 (GRCm39) |
M336I |
probably benign |
Het |
Cntn1 |
C |
T |
15: 92,203,021 (GRCm39) |
R768C |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,735,256 (GRCm39) |
I798F |
possibly damaging |
Het |
Cpxcr1 |
T |
A |
X: 115,387,758 (GRCm39) |
L223* |
probably null |
Het |
Cpz |
C |
A |
5: 35,659,902 (GRCm39) |
R581L |
possibly damaging |
Het |
Cxcr2 |
A |
G |
1: 74,198,438 (GRCm39) |
I311V |
probably benign |
Het |
Cym |
T |
A |
3: 107,126,030 (GRCm39) |
I78F |
probably benign |
Het |
Defb8 |
A |
T |
8: 19,495,899 (GRCm39) |
S54T |
probably benign |
Het |
Dennd4a |
A |
G |
9: 64,769,312 (GRCm39) |
T433A |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 113,084,815 (GRCm39) |
T678A |
probably damaging |
Het |
Dspp |
T |
C |
5: 104,321,951 (GRCm39) |
|
probably null |
Het |
Enkur |
G |
T |
2: 21,193,988 (GRCm39) |
A195E |
probably benign |
Het |
Ero1b |
T |
A |
13: 12,619,292 (GRCm39) |
S429T |
possibly damaging |
Het |
Fh1 |
A |
G |
1: 175,435,452 (GRCm39) |
S344P |
probably damaging |
Het |
Flnc |
G |
T |
6: 29,443,478 (GRCm39) |
G553V |
probably damaging |
Het |
Fmo1 |
A |
T |
1: 162,657,554 (GRCm39) |
L529* |
probably null |
Het |
Frem1 |
C |
A |
4: 82,868,737 (GRCm39) |
V1415F |
probably damaging |
Het |
Gatb |
T |
G |
3: 85,526,184 (GRCm39) |
L354R |
probably damaging |
Het |
Gdpgp1 |
A |
T |
7: 79,888,349 (GRCm39) |
N127Y |
probably damaging |
Het |
Gpat2 |
A |
G |
2: 127,276,739 (GRCm39) |
T648A |
possibly damaging |
Het |
Grk6 |
C |
T |
13: 55,599,591 (GRCm39) |
R225* |
probably null |
Het |
Hells |
A |
T |
19: 38,948,120 (GRCm39) |
Q682L |
probably null |
Het |
Hspa5 |
T |
A |
2: 34,664,690 (GRCm39) |
N381K |
possibly damaging |
Het |
Ighmbp2 |
T |
C |
19: 3,312,075 (GRCm39) |
N893S |
probably benign |
Het |
Ipo11 |
A |
T |
13: 106,948,765 (GRCm39) |
V914E |
possibly damaging |
Het |
Lars1 |
T |
C |
18: 42,345,673 (GRCm39) |
N1001S |
probably benign |
Het |
Lats2 |
A |
G |
14: 57,934,912 (GRCm39) |
L606P |
probably damaging |
Het |
Map4k1 |
T |
C |
7: 28,699,209 (GRCm39) |
Y521H |
probably benign |
Het |
Marchf11 |
T |
A |
15: 26,387,916 (GRCm39) |
V257E |
probably damaging |
Het |
Med23 |
G |
A |
10: 24,786,768 (GRCm39) |
|
probably null |
Het |
Meltf |
A |
G |
16: 31,715,395 (GRCm39) |
D696G |
probably benign |
Het |
Ms4a7 |
T |
A |
19: 11,301,788 (GRCm39) |
M212L |
probably benign |
Het |
Mx1 |
A |
T |
16: 97,249,403 (GRCm39) |
L608Q |
probably damaging |
Het |
Myh1 |
T |
C |
11: 67,095,224 (GRCm39) |
Y195H |
probably damaging |
Het |
Napb |
G |
T |
2: 148,548,909 (GRCm39) |
H110Q |
probably benign |
Het |
Ngly1 |
C |
T |
14: 16,260,585 (GRCm38) |
P90S |
probably damaging |
Het |
Nlrp1b |
T |
A |
11: 71,073,442 (GRCm39) |
I134L |
possibly damaging |
Het |
Nup210 |
A |
G |
6: 90,993,036 (GRCm39) |
L1017P |
probably damaging |
Het |
Nup85 |
T |
A |
11: 115,472,643 (GRCm39) |
I233N |
probably damaging |
Het |
Obsl1 |
A |
G |
1: 75,469,537 (GRCm39) |
V965A |
probably damaging |
Het |
Or4c12 |
A |
C |
2: 89,774,158 (GRCm39) |
Y100* |
probably null |
Het |
Or4f6 |
T |
C |
2: 111,839,036 (GRCm39) |
D165G |
probably benign |
Het |
Or6c5c |
T |
C |
10: 129,299,370 (GRCm39) |
L275P |
probably damaging |
Het |
Pak1ip1 |
A |
G |
13: 41,164,708 (GRCm39) |
T264A |
possibly damaging |
Het |
Pard6g |
C |
T |
18: 80,160,357 (GRCm39) |
R157C |
probably damaging |
Het |
Pcdhb7 |
A |
T |
18: 37,475,631 (GRCm39) |
T256S |
possibly damaging |
Het |
Pigw |
A |
T |
11: 84,768,874 (GRCm39) |
F152I |
probably damaging |
Het |
Pip4k2c |
A |
G |
10: 127,036,744 (GRCm39) |
S222P |
probably damaging |
Het |
Pjvk |
A |
G |
2: 76,487,775 (GRCm39) |
|
probably null |
Het |
Plxnd1 |
C |
T |
6: 115,940,875 (GRCm39) |
V1355M |
probably damaging |
Het |
Pramel26 |
T |
C |
4: 143,539,396 (GRCm39) |
I32M |
probably benign |
Het |
Prss22 |
G |
A |
17: 24,215,288 (GRCm39) |
P163S |
probably damaging |
Het |
Prune2 |
A |
G |
19: 17,176,503 (GRCm39) |
I154V |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,533,637 (GRCm39) |
D362E |
probably benign |
Het |
Retreg2 |
A |
G |
1: 75,123,319 (GRCm39) |
K416E |
probably benign |
Het |
Scn7a |
T |
C |
2: 66,510,635 (GRCm39) |
I1256V |
probably benign |
Het |
Sema4d |
A |
G |
13: 51,865,258 (GRCm39) |
V362A |
possibly damaging |
Het |
Septin4 |
T |
A |
11: 87,459,741 (GRCm39) |
D496E |
probably damaging |
Het |
Slc25a34 |
G |
A |
4: 141,349,579 (GRCm39) |
T192I |
probably benign |
Het |
Tacc3 |
G |
T |
5: 33,825,544 (GRCm39) |
V425L |
probably benign |
Het |
Tfdp2 |
A |
T |
9: 96,179,762 (GRCm39) |
K125I |
probably damaging |
Het |
Tjp2 |
C |
T |
19: 24,076,899 (GRCm39) |
R952Q |
possibly damaging |
Het |
Tk2 |
G |
T |
8: 104,975,077 (GRCm39) |
S30* |
probably null |
Het |
Tmem74 |
A |
T |
15: 43,730,559 (GRCm39) |
D161E |
probably benign |
Het |
Tmprss9 |
G |
A |
10: 80,728,119 (GRCm39) |
V570M |
probably damaging |
Het |
Tnk2 |
C |
A |
16: 32,498,280 (GRCm39) |
P26Q |
probably damaging |
Het |
Tnpo2 |
T |
G |
8: 85,778,401 (GRCm39) |
V610G |
probably damaging |
Het |
Trim37 |
T |
C |
11: 87,109,132 (GRCm39) |
F953S |
probably damaging |
Het |
U2surp |
T |
A |
9: 95,364,150 (GRCm39) |
K589* |
probably null |
Het |
Usp2 |
G |
A |
9: 43,987,263 (GRCm39) |
R187H |
probably benign |
Het |
Vmn2r1 |
C |
T |
3: 64,008,926 (GRCm39) |
T535I |
probably benign |
Het |
Wdr20rt |
T |
A |
12: 65,273,925 (GRCm39) |
S463T |
possibly damaging |
Het |
Zbtb25 |
C |
A |
12: 76,396,488 (GRCm39) |
G245W |
probably damaging |
Het |
Zc3h14 |
T |
A |
12: 98,726,613 (GRCm39) |
L27* |
probably null |
Het |
Zfp2 |
T |
C |
11: 50,791,915 (GRCm39) |
K43E |
probably benign |
Het |
Zfp268 |
T |
G |
4: 145,350,820 (GRCm39) |
|
probably benign |
Het |
Zfp654 |
A |
G |
16: 64,605,491 (GRCm39) |
Y904H |
probably benign |
Het |
|
Other mutations in Phrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00551:Phrf1
|
APN |
7 |
140,838,790 (GRCm39) |
unclassified |
probably benign |
|
IGL01391:Phrf1
|
APN |
7 |
140,842,394 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01472:Phrf1
|
APN |
7 |
140,836,403 (GRCm39) |
splice site |
probably benign |
|
IGL01633:Phrf1
|
APN |
7 |
140,840,413 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01808:Phrf1
|
APN |
7 |
140,840,879 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02004:Phrf1
|
APN |
7 |
140,840,246 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02138:Phrf1
|
APN |
7 |
140,839,196 (GRCm39) |
unclassified |
probably benign |
|
IGL02678:Phrf1
|
APN |
7 |
140,840,195 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03077:Phrf1
|
APN |
7 |
140,834,881 (GRCm39) |
nonsense |
probably null |
|
PIT4466001:Phrf1
|
UTSW |
7 |
140,838,725 (GRCm39) |
missense |
unknown |
|
R0036:Phrf1
|
UTSW |
7 |
140,841,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Phrf1
|
UTSW |
7 |
140,841,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Phrf1
|
UTSW |
7 |
140,823,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0358:Phrf1
|
UTSW |
7 |
140,838,217 (GRCm39) |
unclassified |
probably benign |
|
R0445:Phrf1
|
UTSW |
7 |
140,827,244 (GRCm39) |
utr 3 prime |
probably benign |
|
R0535:Phrf1
|
UTSW |
7 |
140,839,978 (GRCm39) |
missense |
probably benign |
0.07 |
R0561:Phrf1
|
UTSW |
7 |
140,834,876 (GRCm39) |
missense |
probably benign |
0.00 |
R0940:Phrf1
|
UTSW |
7 |
140,834,768 (GRCm39) |
splice site |
probably benign |
|
R1499:Phrf1
|
UTSW |
7 |
140,836,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Phrf1
|
UTSW |
7 |
140,839,714 (GRCm39) |
unclassified |
probably benign |
|
R1651:Phrf1
|
UTSW |
7 |
140,817,434 (GRCm39) |
missense |
probably benign |
|
R1691:Phrf1
|
UTSW |
7 |
140,841,787 (GRCm39) |
nonsense |
probably null |
|
R1778:Phrf1
|
UTSW |
7 |
140,812,369 (GRCm39) |
missense |
probably benign |
0.01 |
R2239:Phrf1
|
UTSW |
7 |
140,817,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Phrf1
|
UTSW |
7 |
140,839,593 (GRCm39) |
unclassified |
probably benign |
|
R3796:Phrf1
|
UTSW |
7 |
140,839,831 (GRCm39) |
nonsense |
probably null |
|
R3797:Phrf1
|
UTSW |
7 |
140,839,831 (GRCm39) |
nonsense |
probably null |
|
R3798:Phrf1
|
UTSW |
7 |
140,839,831 (GRCm39) |
nonsense |
probably null |
|
R3799:Phrf1
|
UTSW |
7 |
140,839,831 (GRCm39) |
nonsense |
probably null |
|
R4080:Phrf1
|
UTSW |
7 |
140,839,633 (GRCm39) |
unclassified |
probably benign |
|
R4081:Phrf1
|
UTSW |
7 |
140,838,970 (GRCm39) |
unclassified |
probably benign |
|
R4557:Phrf1
|
UTSW |
7 |
140,838,842 (GRCm39) |
unclassified |
probably benign |
|
R5217:Phrf1
|
UTSW |
7 |
140,840,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5218:Phrf1
|
UTSW |
7 |
140,841,214 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5276:Phrf1
|
UTSW |
7 |
140,839,196 (GRCm39) |
unclassified |
probably benign |
|
R5442:Phrf1
|
UTSW |
7 |
140,820,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R5501:Phrf1
|
UTSW |
7 |
140,839,834 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5695:Phrf1
|
UTSW |
7 |
140,838,378 (GRCm39) |
unclassified |
probably benign |
|
R5837:Phrf1
|
UTSW |
7 |
140,839,974 (GRCm39) |
missense |
probably benign |
0.34 |
R5907:Phrf1
|
UTSW |
7 |
140,840,453 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5996:Phrf1
|
UTSW |
7 |
140,839,015 (GRCm39) |
unclassified |
probably benign |
|
R6024:Phrf1
|
UTSW |
7 |
140,838,898 (GRCm39) |
unclassified |
probably benign |
|
R6244:Phrf1
|
UTSW |
7 |
140,817,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R6512:Phrf1
|
UTSW |
7 |
140,840,309 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7016:Phrf1
|
UTSW |
7 |
140,817,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R7311:Phrf1
|
UTSW |
7 |
140,820,846 (GRCm39) |
missense |
unknown |
|
R7409:Phrf1
|
UTSW |
7 |
140,839,205 (GRCm39) |
missense |
unknown |
|
R7517:Phrf1
|
UTSW |
7 |
140,836,523 (GRCm39) |
missense |
unknown |
|
R7560:Phrf1
|
UTSW |
7 |
140,811,138 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7699:Phrf1
|
UTSW |
7 |
140,834,842 (GRCm39) |
missense |
unknown |
|
R7700:Phrf1
|
UTSW |
7 |
140,834,842 (GRCm39) |
missense |
unknown |
|
R7867:Phrf1
|
UTSW |
7 |
140,836,524 (GRCm39) |
missense |
unknown |
|
R7895:Phrf1
|
UTSW |
7 |
140,839,288 (GRCm39) |
missense |
unknown |
|
R8179:Phrf1
|
UTSW |
7 |
140,836,493 (GRCm39) |
missense |
unknown |
|
R8705:Phrf1
|
UTSW |
7 |
140,838,651 (GRCm39) |
missense |
unknown |
|
R8708:Phrf1
|
UTSW |
7 |
140,812,446 (GRCm39) |
missense |
unknown |
|
R8748:Phrf1
|
UTSW |
7 |
140,838,148 (GRCm39) |
missense |
unknown |
|
R8768:Phrf1
|
UTSW |
7 |
140,838,651 (GRCm39) |
missense |
unknown |
|
R8789:Phrf1
|
UTSW |
7 |
140,836,581 (GRCm39) |
missense |
unknown |
|
R8859:Phrf1
|
UTSW |
7 |
140,836,516 (GRCm39) |
missense |
unknown |
|
R8991:Phrf1
|
UTSW |
7 |
140,823,671 (GRCm39) |
missense |
unknown |
|
R9086:Phrf1
|
UTSW |
7 |
140,839,412 (GRCm39) |
missense |
unknown |
|
R9158:Phrf1
|
UTSW |
7 |
140,836,466 (GRCm39) |
missense |
unknown |
|
R9287:Phrf1
|
UTSW |
7 |
140,840,055 (GRCm39) |
missense |
probably benign |
0.35 |
R9561:Phrf1
|
UTSW |
7 |
140,834,815 (GRCm39) |
missense |
unknown |
|
X0027:Phrf1
|
UTSW |
7 |
140,836,481 (GRCm39) |
missense |
probably benign |
|
Z1176:Phrf1
|
UTSW |
7 |
140,838,731 (GRCm39) |
missense |
unknown |
|
Z1176:Phrf1
|
UTSW |
7 |
140,823,796 (GRCm39) |
missense |
unknown |
|
|