Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actrt3 |
T |
A |
3: 30,652,781 (GRCm39) |
E104D |
probably damaging |
Het |
Arih2 |
A |
T |
9: 108,493,890 (GRCm39) |
D174E |
probably damaging |
Het |
Asprv1 |
T |
C |
6: 86,606,077 (GRCm39) |
F308L |
probably damaging |
Het |
Baiap2l2 |
A |
G |
15: 79,168,205 (GRCm39) |
|
probably null |
Het |
Btla |
T |
C |
16: 45,064,656 (GRCm39) |
F203L |
possibly damaging |
Het |
C1rb |
A |
T |
6: 124,551,947 (GRCm39) |
D283V |
probably damaging |
Het |
C87436 |
C |
G |
6: 86,442,813 (GRCm39) |
Q462E |
probably benign |
Het |
Ccdc149 |
T |
C |
5: 52,563,352 (GRCm39) |
D147G |
possibly damaging |
Het |
Chd6 |
A |
T |
2: 160,871,793 (GRCm39) |
L214* |
probably null |
Het |
Chrna4 |
C |
A |
2: 180,670,643 (GRCm39) |
R371L |
possibly damaging |
Het |
Cit |
C |
A |
5: 115,984,161 (GRCm39) |
|
probably benign |
Het |
Cpne5 |
A |
G |
17: 29,444,163 (GRCm39) |
|
probably null |
Het |
Cr1l |
T |
C |
1: 194,789,204 (GRCm39) |
E400G |
possibly damaging |
Het |
Creb3l2 |
T |
C |
6: 37,332,583 (GRCm39) |
N304D |
probably damaging |
Het |
Cyp17a1 |
T |
C |
19: 46,656,030 (GRCm39) |
T420A |
probably benign |
Het |
Cyp24a1 |
A |
G |
2: 170,327,853 (GRCm39) |
I463T |
probably damaging |
Het |
Cyp3a41b |
A |
T |
5: 145,514,973 (GRCm39) |
I84N |
probably damaging |
Het |
Dnajc6 |
G |
A |
4: 101,496,559 (GRCm39) |
V909M |
possibly damaging |
Het |
Dtl |
A |
G |
1: 191,288,923 (GRCm39) |
Y264H |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,077,216 (GRCm39) |
R660* |
probably null |
Het |
Egf |
A |
G |
3: 129,529,449 (GRCm39) |
|
probably null |
Het |
Eva1c |
T |
C |
16: 90,701,231 (GRCm39) |
S402P |
probably benign |
Het |
Fcho2 |
A |
T |
13: 98,925,869 (GRCm39) |
|
probably null |
Het |
Fhdc1 |
G |
A |
3: 84,352,290 (GRCm39) |
R197C |
unknown |
Het |
Foxa2 |
T |
A |
2: 147,886,426 (GRCm39) |
M136L |
probably benign |
Het |
Gm10226 |
T |
C |
17: 21,910,866 (GRCm39) |
C34R |
possibly damaging |
Het |
Gm29735 |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
ACAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCAACAGCAGGATTCGCAGCAGCAGGGCTTGCAGCAGCTGGACTGGCAGCAGCAAGGCTTGCAGCAGCTGGACTGGCAGCAGCAGGGCTTGCA |
7: 141,710,266 (GRCm39) |
|
probably benign |
Het |
Gm8947 |
T |
C |
1: 151,068,853 (GRCm39) |
S229P |
probably benign |
Het |
Ighv9-2 |
A |
T |
12: 114,072,896 (GRCm39) |
S26T |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kat6a |
T |
G |
8: 23,420,190 (GRCm39) |
I745M |
probably damaging |
Het |
Klhdc1 |
T |
C |
12: 69,309,968 (GRCm39) |
L290P |
probably damaging |
Het |
Lcp2 |
C |
T |
11: 34,039,688 (GRCm39) |
T496I |
|
Het |
Map4k4 |
T |
C |
1: 40,042,923 (GRCm39) |
W593R |
probably benign |
Het |
Mefv |
T |
G |
16: 3,535,841 (GRCm39) |
Q29P |
probably damaging |
Het |
Mgat5b |
T |
C |
11: 116,859,269 (GRCm39) |
Y34H |
|
Het |
Mlip |
C |
T |
9: 77,137,080 (GRCm39) |
R609Q |
probably benign |
Het |
Muc2 |
A |
G |
7: 141,290,816 (GRCm39) |
D34G |
|
Het |
Nbeal1 |
C |
T |
1: 60,307,548 (GRCm39) |
P1687S |
possibly damaging |
Het |
Notch1 |
T |
A |
2: 26,369,895 (GRCm39) |
I477L |
probably damaging |
Het |
Odad2 |
T |
A |
18: 7,217,846 (GRCm39) |
K623* |
probably null |
Het |
Or1l4b |
G |
A |
2: 37,037,047 (GRCm39) |
M274I |
probably benign |
Het |
Or1s2 |
T |
C |
19: 13,758,333 (GRCm39) |
V117A |
probably benign |
Het |
Or4a2 |
A |
T |
2: 89,248,712 (GRCm39) |
L15Q |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,320,124 (GRCm39) |
N38I |
probably damaging |
Het |
Or6c214 |
A |
G |
10: 129,591,148 (GRCm39) |
M57T |
probably damaging |
Het |
Pak5 |
A |
T |
2: 135,958,688 (GRCm39) |
S133R |
probably damaging |
Het |
Pcyt1a |
C |
A |
16: 32,285,332 (GRCm39) |
D187E |
probably benign |
Het |
Pdlim7 |
G |
T |
13: 55,655,354 (GRCm39) |
T161K |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,547,108 (GRCm39) |
K962R |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,759,433 (GRCm39) |
K1516E |
probably damaging |
Het |
Plk5 |
C |
G |
10: 80,193,830 (GRCm39) |
R40G |
probably damaging |
Het |
Ptchd3 |
A |
T |
11: 121,733,180 (GRCm39) |
Y690F |
probably benign |
Het |
Ptpn13 |
A |
T |
5: 103,649,735 (GRCm39) |
R379S |
possibly damaging |
Het |
Rbm27 |
C |
T |
18: 42,438,829 (GRCm39) |
A410V |
probably benign |
Het |
Rnase4 |
A |
G |
14: 51,342,662 (GRCm39) |
T129A |
probably benign |
Het |
Serpinb11 |
C |
T |
1: 107,304,533 (GRCm39) |
T166I |
probably benign |
Het |
Shank2 |
A |
G |
7: 143,963,705 (GRCm39) |
T438A |
possibly damaging |
Het |
Slc13a2 |
T |
C |
11: 78,295,258 (GRCm39) |
N172D |
probably damaging |
Het |
Slc2a8 |
A |
G |
2: 32,864,864 (GRCm39) |
F428L |
probably damaging |
Het |
Slc38a6 |
T |
C |
12: 73,398,544 (GRCm39) |
M358T |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,213,155 (GRCm39) |
H107R |
probably benign |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Spint3 |
G |
A |
2: 164,415,154 (GRCm39) |
A21V |
probably benign |
Het |
Susd1 |
A |
T |
4: 59,412,226 (GRCm39) |
V162E |
probably benign |
Het |
Syne2 |
T |
G |
12: 75,977,834 (GRCm39) |
N1426K |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,067,875 (GRCm39) |
V638A |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,538,589 (GRCm39) |
L1473Q |
probably damaging |
Het |
Trim36 |
G |
A |
18: 46,300,580 (GRCm39) |
S697L |
possibly damaging |
Het |
Ttbk1 |
A |
T |
17: 46,781,517 (GRCm39) |
I412N |
possibly damaging |
Het |
Tubb2a |
T |
C |
13: 34,258,578 (GRCm39) |
D404G |
probably damaging |
Het |
Tyk2 |
T |
A |
9: 21,035,841 (GRCm39) |
N114Y |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,185,678 (GRCm39) |
D139G |
probably damaging |
Het |
Vmn2r101 |
T |
A |
17: 19,810,244 (GRCm39) |
N343K |
probably benign |
Het |
Vnn1 |
A |
G |
10: 23,780,464 (GRCm39) |
D484G |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,770,919 (GRCm39) |
T2121A |
probably benign |
Het |
Wdr81 |
T |
C |
11: 75,345,216 (GRCm39) |
E17G |
probably benign |
Het |
Wnk2 |
T |
G |
13: 49,224,505 (GRCm39) |
K1117Q |
probably benign |
Het |
Zbtb46 |
C |
T |
2: 181,066,138 (GRCm39) |
R4Q |
probably benign |
Het |
Zfp608 |
T |
A |
18: 55,032,190 (GRCm39) |
K583N |
probably damaging |
Het |
Zfp729b |
A |
T |
13: 67,740,480 (GRCm39) |
L595H |
probably damaging |
Het |
|
Other mutations in Phf8-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00470:Phf8-ps
|
APN |
17 |
33,284,837 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00790:Phf8-ps
|
APN |
17 |
33,286,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01146:Phf8-ps
|
APN |
17 |
33,284,357 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01755:Phf8-ps
|
APN |
17 |
33,285,951 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01880:Phf8-ps
|
APN |
17 |
33,285,690 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01981:Phf8-ps
|
APN |
17 |
33,286,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Phf8-ps
|
APN |
17 |
33,285,289 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02047:Phf8-ps
|
APN |
17 |
33,286,275 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02070:Phf8-ps
|
APN |
17 |
33,285,104 (GRCm39) |
missense |
probably damaging |
0.98 |
R0055:Phf8-ps
|
UTSW |
17 |
33,285,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Phf8-ps
|
UTSW |
17 |
33,285,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R0893:Phf8-ps
|
UTSW |
17 |
33,284,263 (GRCm39) |
missense |
probably benign |
0.34 |
R1528:Phf8-ps
|
UTSW |
17 |
33,286,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R1558:Phf8-ps
|
UTSW |
17 |
33,284,679 (GRCm39) |
missense |
probably benign |
0.20 |
R1664:Phf8-ps
|
UTSW |
17 |
33,285,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Phf8-ps
|
UTSW |
17 |
33,286,662 (GRCm39) |
missense |
probably benign |
0.06 |
R1881:Phf8-ps
|
UTSW |
17 |
33,284,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Phf8-ps
|
UTSW |
17 |
33,285,941 (GRCm39) |
missense |
probably benign |
0.15 |
R2029:Phf8-ps
|
UTSW |
17 |
33,286,598 (GRCm39) |
nonsense |
probably null |
|
R2152:Phf8-ps
|
UTSW |
17 |
33,285,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2298:Phf8-ps
|
UTSW |
17 |
33,285,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R2395:Phf8-ps
|
UTSW |
17 |
33,284,936 (GRCm39) |
missense |
probably benign |
0.28 |
R2424:Phf8-ps
|
UTSW |
17 |
33,284,730 (GRCm39) |
missense |
probably benign |
0.00 |
R3973:Phf8-ps
|
UTSW |
17 |
33,285,405 (GRCm39) |
missense |
probably benign |
0.24 |
R3976:Phf8-ps
|
UTSW |
17 |
33,285,405 (GRCm39) |
missense |
probably benign |
0.24 |
R4159:Phf8-ps
|
UTSW |
17 |
33,285,023 (GRCm39) |
missense |
probably benign |
0.01 |
R4160:Phf8-ps
|
UTSW |
17 |
33,285,023 (GRCm39) |
missense |
probably benign |
0.01 |
R4161:Phf8-ps
|
UTSW |
17 |
33,285,023 (GRCm39) |
missense |
probably benign |
0.01 |
R4761:Phf8-ps
|
UTSW |
17 |
33,286,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4855:Phf8-ps
|
UTSW |
17 |
33,285,713 (GRCm39) |
missense |
probably benign |
0.00 |
R5039:Phf8-ps
|
UTSW |
17 |
33,286,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5255:Phf8-ps
|
UTSW |
17 |
33,285,739 (GRCm39) |
nonsense |
probably null |
|
R5383:Phf8-ps
|
UTSW |
17 |
33,284,231 (GRCm39) |
missense |
probably benign |
|
R5520:Phf8-ps
|
UTSW |
17 |
33,284,367 (GRCm39) |
missense |
probably benign |
0.03 |
R5588:Phf8-ps
|
UTSW |
17 |
33,285,249 (GRCm39) |
nonsense |
probably null |
|
R5685:Phf8-ps
|
UTSW |
17 |
33,285,746 (GRCm39) |
missense |
probably benign |
0.04 |
R5826:Phf8-ps
|
UTSW |
17 |
33,284,288 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5907:Phf8-ps
|
UTSW |
17 |
33,285,124 (GRCm39) |
missense |
probably benign |
0.01 |
R6397:Phf8-ps
|
UTSW |
17 |
33,285,219 (GRCm39) |
missense |
probably benign |
0.28 |
R6731:Phf8-ps
|
UTSW |
17 |
33,285,200 (GRCm39) |
missense |
probably benign |
0.02 |
R6750:Phf8-ps
|
UTSW |
17 |
33,285,372 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7043:Phf8-ps
|
UTSW |
17 |
33,284,306 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7242:Phf8-ps
|
UTSW |
17 |
33,286,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R7262:Phf8-ps
|
UTSW |
17 |
33,285,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R7265:Phf8-ps
|
UTSW |
17 |
33,285,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R7286:Phf8-ps
|
UTSW |
17 |
33,284,501 (GRCm39) |
missense |
probably benign |
|
R7797:Phf8-ps
|
UTSW |
17 |
33,286,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R8314:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8315:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8376:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8377:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8378:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8404:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8405:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8406:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8425:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8501:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R8502:Phf8-ps
|
UTSW |
17 |
33,286,038 (GRCm39) |
missense |
probably benign |
0.04 |
R9220:Phf8-ps
|
UTSW |
17 |
33,286,494 (GRCm39) |
missense |
probably benign |
0.26 |
R9270:Phf8-ps
|
UTSW |
17 |
33,286,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Phf8-ps
|
UTSW |
17 |
33,285,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R9766:Phf8-ps
|
UTSW |
17 |
33,285,647 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Phf8-ps
|
UTSW |
17 |
33,284,631 (GRCm39) |
missense |
possibly damaging |
0.95 |
|