Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700011L22Rik |
T |
C |
8: 79,955,996 (GRCm39) |
Y87C |
probably benign |
Het |
5530401A14Rik |
A |
G |
11: 81,784,694 (GRCm39) |
|
probably benign |
Het |
Adamts5 |
T |
C |
16: 85,696,188 (GRCm39) |
D323G |
probably damaging |
Het |
Albfm1 |
A |
T |
5: 90,732,848 (GRCm39) |
Q553L |
possibly damaging |
Het |
Bicc1 |
G |
A |
10: 70,792,911 (GRCm39) |
R248* |
probably null |
Het |
Bivm |
T |
G |
1: 44,158,233 (GRCm39) |
|
probably benign |
Het |
Btnl12 |
G |
T |
16: 37,676,384 (GRCm39) |
Q128K |
probably benign |
Het |
Ccdc8 |
A |
C |
7: 16,729,956 (GRCm39) |
T482P |
unknown |
Het |
Ccnb2 |
T |
C |
9: 70,326,375 (GRCm39) |
I21V |
probably benign |
Het |
Cfap73 |
A |
T |
5: 120,769,777 (GRCm39) |
I82N |
probably damaging |
Het |
Chd3 |
A |
C |
11: 69,242,944 (GRCm39) |
F1426V |
possibly damaging |
Het |
Clcn2 |
A |
T |
16: 20,530,438 (GRCm39) |
|
probably null |
Het |
Col6a5 |
T |
C |
9: 105,803,117 (GRCm39) |
N1283D |
unknown |
Het |
Cyp39a1 |
G |
T |
17: 44,042,882 (GRCm39) |
G411W |
probably damaging |
Het |
D130052B06Rik |
A |
T |
11: 33,574,008 (GRCm39) |
I202L |
unknown |
Het |
Defa38 |
A |
T |
8: 21,585,248 (GRCm39) |
C65S |
possibly damaging |
Het |
Dlgap1 |
T |
C |
17: 71,125,093 (GRCm39) |
L948P |
probably damaging |
Het |
Dnah3 |
C |
T |
7: 119,566,745 (GRCm39) |
V2494M |
probably damaging |
Het |
Dysf |
T |
A |
6: 84,091,054 (GRCm39) |
V1076D |
probably damaging |
Het |
Eif2ak4 |
C |
A |
2: 118,219,296 (GRCm39) |
S36* |
probably null |
Het |
Elmod3 |
C |
T |
6: 72,545,851 (GRCm39) |
R297H |
probably benign |
Het |
Epas1 |
C |
A |
17: 87,116,827 (GRCm39) |
R166S |
probably damaging |
Het |
Erv3 |
A |
G |
2: 131,697,942 (GRCm39) |
L139P |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,275,894 (GRCm39) |
V90A |
probably damaging |
Het |
Fxr2 |
A |
G |
11: 69,541,877 (GRCm39) |
R439G |
possibly damaging |
Het |
Gabrd |
A |
T |
4: 155,470,931 (GRCm39) |
V259D |
possibly damaging |
Het |
Galnt10 |
A |
G |
11: 57,674,619 (GRCm39) |
Y536C |
probably damaging |
Het |
Gbp10 |
A |
T |
5: 105,366,269 (GRCm39) |
L545Q |
probably damaging |
Het |
Gfpt1 |
A |
T |
6: 87,062,239 (GRCm39) |
I517F |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,267,010 (GRCm39) |
Y225H |
probably damaging |
Het |
Gm1110 |
C |
T |
9: 26,794,505 (GRCm39) |
|
probably null |
Het |
Gmps |
C |
T |
3: 63,887,558 (GRCm39) |
P10L |
probably benign |
Het |
Greb1l |
T |
A |
18: 10,547,068 (GRCm39) |
V1465D |
probably damaging |
Het |
Helz2 |
A |
G |
2: 180,882,106 (GRCm39) |
V229A |
probably benign |
Het |
Ifngr1 |
T |
G |
10: 19,484,909 (GRCm39) |
L303V |
possibly damaging |
Het |
Kif22 |
T |
C |
7: 126,630,250 (GRCm39) |
N429D |
probably benign |
Het |
Ktn1 |
T |
C |
14: 47,914,253 (GRCm39) |
Y401H |
probably damaging |
Het |
Lars2 |
T |
G |
9: 123,201,053 (GRCm39) |
I39S |
probably damaging |
Het |
Lipf |
C |
T |
19: 33,944,244 (GRCm39) |
A151V |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,402,469 (GRCm39) |
M2234K |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 40,591,825 (GRCm39) |
V56A |
unknown |
Het |
Lyar |
T |
A |
5: 38,391,352 (GRCm39) |
H350Q |
probably benign |
Het |
Mill2 |
A |
T |
7: 18,590,489 (GRCm39) |
M190L |
probably benign |
Het |
Morc3 |
A |
G |
16: 93,671,733 (GRCm39) |
D921G |
probably damaging |
Het |
Mpp2 |
G |
T |
11: 101,950,180 (GRCm39) |
T558K |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,135,550 (GRCm39) |
D379G |
probably benign |
Het |
Neb |
A |
C |
2: 52,084,437 (GRCm39) |
|
probably null |
Het |
Nedd1 |
G |
A |
10: 92,530,962 (GRCm39) |
R376* |
probably null |
Het |
Nlrc4 |
T |
G |
17: 74,753,954 (GRCm39) |
D143A |
probably damaging |
Het |
Nol10 |
G |
T |
12: 17,398,479 (GRCm39) |
|
probably benign |
Het |
Opn1sw |
A |
G |
6: 29,379,869 (GRCm39) |
S122P |
probably damaging |
Het |
Or10j3b |
C |
T |
1: 173,044,067 (GRCm39) |
T283I |
possibly damaging |
Het |
Or4f14d |
T |
G |
2: 111,960,881 (GRCm39) |
I92L |
possibly damaging |
Het |
Or52h7 |
C |
T |
7: 104,213,974 (GRCm39) |
T182I |
probably benign |
Het |
Or5an9 |
C |
A |
19: 12,187,659 (GRCm39) |
A243D |
probably damaging |
Het |
Or5h27 |
T |
A |
16: 59,006,454 (GRCm39) |
T131S |
probably benign |
Het |
Orm1 |
T |
A |
4: 63,262,929 (GRCm39) |
I32N |
possibly damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,628 (GRCm39) |
V336E |
probably damaging |
Het |
Poli |
C |
T |
18: 70,650,540 (GRCm39) |
R363K |
possibly damaging |
Het |
Rabgap1l |
T |
C |
1: 160,472,893 (GRCm39) |
E515G |
probably benign |
Het |
Rem2 |
C |
A |
14: 54,715,225 (GRCm39) |
T134N |
probably damaging |
Het |
Rfc1 |
A |
G |
5: 65,436,892 (GRCm39) |
I596T |
probably damaging |
Het |
Ruvbl2 |
A |
T |
7: 45,074,433 (GRCm39) |
I202N |
probably damaging |
Het |
S100a6 |
T |
A |
3: 90,521,186 (GRCm39) |
I38N |
probably damaging |
Het |
Scel |
T |
C |
14: 103,829,649 (GRCm39) |
C435R |
probably benign |
Het |
Slc6a13 |
T |
A |
6: 121,298,587 (GRCm39) |
W146R |
probably damaging |
Het |
Sorcs1 |
T |
A |
19: 50,178,555 (GRCm39) |
K856* |
probably null |
Het |
Speer4e1 |
T |
G |
5: 14,987,195 (GRCm39) |
K70T |
possibly damaging |
Het |
Sucla2 |
T |
A |
14: 73,806,404 (GRCm39) |
C158* |
probably null |
Het |
Tie1 |
G |
A |
4: 118,341,888 (GRCm39) |
S187L |
probably benign |
Het |
Tmem200a |
T |
C |
10: 25,868,905 (GRCm39) |
T455A |
probably damaging |
Het |
Tra2a |
A |
G |
6: 49,229,398 (GRCm39) |
|
probably benign |
Het |
Tsnaxip1 |
A |
C |
8: 106,570,819 (GRCm39) |
E615A |
probably benign |
Het |
Tuba3b |
T |
A |
6: 145,566,900 (GRCm39) |
N380K |
probably damaging |
Het |
Umod |
C |
T |
7: 119,076,046 (GRCm39) |
S240N |
probably benign |
Het |
Vmn2r92 |
G |
A |
17: 18,388,305 (GRCm39) |
|
probably null |
Het |
Vps13b |
A |
G |
15: 35,671,462 (GRCm39) |
E1655G |
probably damaging |
Het |
Vwde |
A |
T |
6: 13,219,935 (GRCm39) |
I72N |
probably damaging |
Het |
Wbp11 |
G |
A |
6: 136,798,533 (GRCm39) |
A172V |
probably damaging |
Het |
Zbtb41 |
T |
A |
1: 139,351,770 (GRCm39) |
N294K |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,462,019 (GRCm39) |
H1206Q |
probably damaging |
Het |
|
Other mutations in Hipk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00792:Hipk1
|
APN |
3 |
103,685,476 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01024:Hipk1
|
APN |
3 |
103,667,952 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01069:Hipk1
|
APN |
3 |
103,685,015 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01798:Hipk1
|
APN |
3 |
103,668,875 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01937:Hipk1
|
APN |
3 |
103,651,320 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01945:Hipk1
|
APN |
3 |
103,651,320 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02184:Hipk1
|
APN |
3 |
103,666,066 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02430:Hipk1
|
APN |
3 |
103,667,971 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02603:Hipk1
|
APN |
3 |
103,657,588 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02632:Hipk1
|
APN |
3 |
103,667,861 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02686:Hipk1
|
APN |
3 |
103,685,333 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03293:Hipk1
|
APN |
3 |
103,684,575 (GRCm39) |
missense |
possibly damaging |
0.83 |
effluvient
|
UTSW |
3 |
103,661,641 (GRCm39) |
splice site |
probably null |
|
R0012:Hipk1
|
UTSW |
3 |
103,670,996 (GRCm39) |
missense |
probably damaging |
0.98 |
R0012:Hipk1
|
UTSW |
3 |
103,670,996 (GRCm39) |
missense |
probably damaging |
0.98 |
R0512:Hipk1
|
UTSW |
3 |
103,667,890 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0741:Hipk1
|
UTSW |
3 |
103,654,128 (GRCm39) |
missense |
probably benign |
0.17 |
R0785:Hipk1
|
UTSW |
3 |
103,661,641 (GRCm39) |
splice site |
probably null |
|
R0786:Hipk1
|
UTSW |
3 |
103,651,620 (GRCm39) |
missense |
probably benign |
|
R0833:Hipk1
|
UTSW |
3 |
103,661,612 (GRCm39) |
missense |
probably damaging |
0.98 |
R0836:Hipk1
|
UTSW |
3 |
103,661,612 (GRCm39) |
missense |
probably damaging |
0.98 |
R1165:Hipk1
|
UTSW |
3 |
103,668,840 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1322:Hipk1
|
UTSW |
3 |
103,651,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Hipk1
|
UTSW |
3 |
103,666,090 (GRCm39) |
splice site |
probably benign |
|
R1521:Hipk1
|
UTSW |
3 |
103,685,098 (GRCm39) |
missense |
probably benign |
0.16 |
R1543:Hipk1
|
UTSW |
3 |
103,685,480 (GRCm39) |
missense |
probably benign |
0.00 |
R2085:Hipk1
|
UTSW |
3 |
103,657,670 (GRCm39) |
missense |
probably benign |
0.00 |
R2158:Hipk1
|
UTSW |
3 |
103,667,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R2291:Hipk1
|
UTSW |
3 |
103,668,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Hipk1
|
UTSW |
3 |
103,651,430 (GRCm39) |
missense |
probably damaging |
0.96 |
R4516:Hipk1
|
UTSW |
3 |
103,657,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R4518:Hipk1
|
UTSW |
3 |
103,657,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Hipk1
|
UTSW |
3 |
103,651,338 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5023:Hipk1
|
UTSW |
3 |
103,684,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R6641:Hipk1
|
UTSW |
3 |
103,660,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R6904:Hipk1
|
UTSW |
3 |
103,684,828 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6925:Hipk1
|
UTSW |
3 |
103,685,561 (GRCm39) |
missense |
unknown |
|
R7169:Hipk1
|
UTSW |
3 |
103,651,533 (GRCm39) |
missense |
probably benign |
|
R7212:Hipk1
|
UTSW |
3 |
103,684,926 (GRCm39) |
nonsense |
probably null |
|
R7313:Hipk1
|
UTSW |
3 |
103,685,574 (GRCm39) |
missense |
unknown |
|
R7678:Hipk1
|
UTSW |
3 |
103,667,866 (GRCm39) |
missense |
probably damaging |
0.98 |
R8133:Hipk1
|
UTSW |
3 |
103,660,710 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8154:Hipk1
|
UTSW |
3 |
103,656,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R8166:Hipk1
|
UTSW |
3 |
103,685,489 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8941:Hipk1
|
UTSW |
3 |
103,660,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R8989:Hipk1
|
UTSW |
3 |
103,668,960 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9236:Hipk1
|
UTSW |
3 |
103,671,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Hipk1
|
UTSW |
3 |
103,685,099 (GRCm39) |
missense |
probably benign |
0.01 |
R9383:Hipk1
|
UTSW |
3 |
103,684,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R9401:Hipk1
|
UTSW |
3 |
103,685,295 (GRCm39) |
missense |
probably benign |
|
R9729:Hipk1
|
UTSW |
3 |
103,668,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9798:Hipk1
|
UTSW |
3 |
103,651,431 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1088:Hipk1
|
UTSW |
3 |
103,671,860 (GRCm39) |
missense |
possibly damaging |
0.95 |
|