Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
G |
6: 86,933,318 (GRCm39) |
S430A |
unknown |
Het |
Abhd16a |
T |
A |
17: 35,319,991 (GRCm39) |
F337L |
probably benign |
Het |
Acsl1 |
C |
A |
8: 46,984,023 (GRCm39) |
A514E |
probably benign |
Het |
Adam29 |
T |
C |
8: 56,326,124 (GRCm39) |
Y110C |
probably damaging |
Het |
Adamts12 |
C |
A |
15: 11,270,685 (GRCm39) |
Q647K |
probably benign |
Het |
Adamts20 |
T |
A |
15: 94,301,891 (GRCm39) |
H27L |
probably benign |
Het |
Adamtsl1 |
A |
G |
4: 86,260,648 (GRCm39) |
E961G |
possibly damaging |
Het |
AW011738 |
T |
C |
4: 156,287,997 (GRCm39) |
|
probably benign |
Het |
Bcl9 |
T |
C |
3: 97,112,460 (GRCm39) |
M1332V |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,872,977 (GRCm39) |
I412T |
probably damaging |
Het |
Cav1 |
A |
T |
6: 17,339,331 (GRCm39) |
I139F |
probably damaging |
Het |
Col4a4 |
A |
C |
1: 82,444,321 (GRCm39) |
|
probably null |
Het |
Coro2a |
A |
T |
4: 46,539,138 (GRCm39) |
*544R |
probably null |
Het |
Cox15 |
C |
T |
19: 43,735,224 (GRCm39) |
R181H |
probably benign |
Het |
Ddx23 |
G |
A |
15: 98,548,599 (GRCm39) |
R370W |
possibly damaging |
Het |
Dennd2c |
A |
G |
3: 103,040,568 (GRCm39) |
N278D |
probably benign |
Het |
Dgkh |
T |
C |
14: 78,853,945 (GRCm39) |
I265V |
probably damaging |
Het |
Dpp3 |
A |
T |
19: 4,967,888 (GRCm39) |
|
probably benign |
Het |
Drc7 |
G |
A |
8: 95,797,881 (GRCm39) |
R433H |
possibly damaging |
Het |
Ece1 |
A |
G |
4: 137,666,074 (GRCm39) |
K306R |
probably benign |
Het |
Eif4b |
T |
C |
15: 101,997,411 (GRCm39) |
S309P |
unknown |
Het |
Eml3 |
G |
A |
19: 8,914,507 (GRCm39) |
V507M |
probably benign |
Het |
Ezhip |
T |
C |
X: 5,994,817 (GRCm39) |
E66G |
probably benign |
Het |
Fat1 |
C |
T |
8: 45,497,265 (GRCm39) |
T4250M |
possibly damaging |
Het |
Fezf1 |
T |
G |
6: 23,246,906 (GRCm39) |
I309L |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,817,077 (GRCm39) |
L4270H |
probably damaging |
Het |
Gabra4 |
T |
C |
5: 71,795,580 (GRCm39) |
K206E |
probably damaging |
Het |
Gfm1 |
A |
G |
3: 67,363,918 (GRCm39) |
K465E |
probably benign |
Het |
Gpld1 |
A |
T |
13: 25,127,693 (GRCm39) |
I32L |
possibly damaging |
Het |
H4c12 |
A |
T |
13: 21,934,682 (GRCm39) |
|
probably null |
Het |
Hoxd12 |
A |
G |
2: 74,505,857 (GRCm39) |
T143A |
probably benign |
Het |
Hoxd12 |
A |
G |
2: 74,505,875 (GRCm39) |
T149A |
probably benign |
Het |
Hspg2 |
T |
A |
4: 137,267,541 (GRCm39) |
S2050T |
probably damaging |
Het |
Il31ra |
T |
A |
13: 112,677,756 (GRCm39) |
N287I |
probably damaging |
Het |
Itga4 |
G |
A |
2: 79,144,188 (GRCm39) |
|
probably null |
Het |
Itpr2 |
A |
G |
6: 146,141,852 (GRCm39) |
V1730A |
probably benign |
Het |
Klkb1 |
T |
A |
8: 45,728,514 (GRCm39) |
Q415L |
probably benign |
Het |
Lcn10 |
A |
G |
2: 25,574,347 (GRCm39) |
Y118C |
probably damaging |
Het |
Lgi3 |
T |
C |
14: 70,773,708 (GRCm39) |
V294A |
probably damaging |
Het |
Lrp5 |
C |
T |
19: 3,660,131 (GRCm39) |
V978I |
probably benign |
Het |
Naaa |
A |
G |
5: 92,425,894 (GRCm39) |
V33A |
probably benign |
Het |
Nckap5l |
A |
G |
15: 99,325,142 (GRCm39) |
F454L |
probably damaging |
Het |
Nol10 |
A |
G |
12: 17,398,555 (GRCm39) |
M1V |
probably null |
Het |
Olfm1 |
G |
A |
2: 28,112,674 (GRCm39) |
|
probably null |
Het |
Or2at4 |
G |
T |
7: 99,385,067 (GRCm39) |
R239L |
possibly damaging |
Het |
Or6c208 |
T |
A |
10: 129,223,745 (GRCm39) |
M81K |
probably benign |
Het |
Or7g30 |
T |
C |
9: 19,352,647 (GRCm39) |
L146P |
possibly damaging |
Het |
Osbp2 |
T |
C |
11: 3,676,333 (GRCm39) |
|
probably null |
Het |
Osbpl1a |
T |
A |
18: 13,038,251 (GRCm39) |
Q269L |
probably benign |
Het |
Papss2 |
T |
A |
19: 32,616,368 (GRCm39) |
C191* |
probably null |
Het |
Pbxip1 |
A |
T |
3: 89,354,984 (GRCm39) |
|
probably null |
Het |
Pdp1 |
A |
G |
4: 11,962,074 (GRCm39) |
I79T |
probably benign |
Het |
Peg10 |
A |
G |
6: 4,755,778 (GRCm39) |
Y118C |
probably damaging |
Het |
Polr2a |
A |
T |
11: 69,626,201 (GRCm39) |
Y1612N |
unknown |
Het |
Polr3c |
A |
T |
3: 96,626,614 (GRCm39) |
L270H |
probably damaging |
Het |
Prr11 |
A |
T |
11: 86,996,868 (GRCm39) |
L32* |
probably null |
Het |
Ptgfr |
T |
A |
3: 151,540,831 (GRCm39) |
T226S |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,007,354 (GRCm39) |
V1639E |
probably damaging |
Het |
Pttg1ip2 |
C |
A |
5: 5,502,019 (GRCm39) |
W144C |
probably benign |
Het |
Rps6kb1 |
A |
G |
11: 86,423,647 (GRCm39) |
V111A |
possibly damaging |
Het |
Sfxn1 |
A |
T |
13: 54,247,952 (GRCm39) |
I226F |
probably damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,255,947 (GRCm39) |
S924P |
probably benign |
Het |
Slc16a5 |
A |
T |
11: 115,360,194 (GRCm39) |
I126F |
probably damaging |
Het |
Slc8a3 |
G |
T |
12: 81,361,220 (GRCm39) |
T533N |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Spata3 |
A |
C |
1: 85,949,783 (GRCm39) |
|
probably benign |
Het |
St8sia6 |
A |
G |
2: 13,797,623 (GRCm39) |
S48P |
probably benign |
Het |
Stra6l |
A |
T |
4: 45,882,698 (GRCm39) |
R470* |
probably null |
Het |
Stradb |
A |
C |
1: 59,030,264 (GRCm39) |
N173H |
probably benign |
Het |
Sugp1 |
T |
A |
8: 70,524,190 (GRCm39) |
D598E |
probably benign |
Het |
Tekt2 |
T |
C |
4: 126,216,610 (GRCm39) |
|
probably null |
Het |
Tiam2 |
C |
T |
17: 3,565,000 (GRCm39) |
R1413C |
possibly damaging |
Het |
Tmprss2 |
T |
C |
16: 97,370,262 (GRCm39) |
S301G |
probably benign |
Het |
Tnrc18 |
A |
T |
5: 142,762,079 (GRCm39) |
N515K |
unknown |
Het |
Togaram1 |
A |
G |
12: 65,013,709 (GRCm39) |
Y320C |
probably damaging |
Het |
Trim41 |
A |
G |
11: 48,698,319 (GRCm39) |
V549A |
probably damaging |
Het |
Ugt2b1 |
T |
A |
5: 87,065,700 (GRCm39) |
L446F |
probably damaging |
Het |
Unc5b |
T |
C |
10: 60,608,348 (GRCm39) |
T621A |
probably benign |
Het |
Utp25 |
T |
A |
1: 192,800,617 (GRCm39) |
K401I |
probably damaging |
Het |
Vmn1r214 |
C |
A |
13: 23,219,494 (GRCm39) |
H329Q |
possibly damaging |
Het |
Vmn2r109 |
T |
A |
17: 20,774,072 (GRCm39) |
K428* |
probably null |
Het |
Vmn2r81 |
A |
C |
10: 79,129,328 (GRCm39) |
I740L |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,089,358 (GRCm39) |
L612P |
probably damaging |
Het |
Zfp109 |
G |
A |
7: 23,928,161 (GRCm39) |
T424M |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,677 (GRCm39) |
K540N |
possibly damaging |
Het |
|
Other mutations in Pnisr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Pnisr
|
APN |
4 |
21,870,407 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01467:Pnisr
|
APN |
4 |
21,874,650 (GRCm39) |
unclassified |
probably benign |
|
IGL01997:Pnisr
|
APN |
4 |
21,871,537 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02641:Pnisr
|
APN |
4 |
21,860,908 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02756:Pnisr
|
APN |
4 |
21,862,175 (GRCm39) |
missense |
probably benign |
0.07 |
R0106:Pnisr
|
UTSW |
4 |
21,874,617 (GRCm39) |
unclassified |
probably benign |
|
R0106:Pnisr
|
UTSW |
4 |
21,874,617 (GRCm39) |
unclassified |
probably benign |
|
R0620:Pnisr
|
UTSW |
4 |
21,874,092 (GRCm39) |
unclassified |
probably benign |
|
R0636:Pnisr
|
UTSW |
4 |
21,873,800 (GRCm39) |
unclassified |
probably benign |
|
R1179:Pnisr
|
UTSW |
4 |
21,865,937 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1388:Pnisr
|
UTSW |
4 |
21,862,041 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1450:Pnisr
|
UTSW |
4 |
21,874,912 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1609:Pnisr
|
UTSW |
4 |
21,871,440 (GRCm39) |
nonsense |
probably null |
|
R1663:Pnisr
|
UTSW |
4 |
21,873,857 (GRCm39) |
unclassified |
probably benign |
|
R1670:Pnisr
|
UTSW |
4 |
21,865,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Pnisr
|
UTSW |
4 |
21,874,086 (GRCm39) |
unclassified |
probably benign |
|
R1792:Pnisr
|
UTSW |
4 |
21,860,968 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1867:Pnisr
|
UTSW |
4 |
21,874,086 (GRCm39) |
unclassified |
probably benign |
|
R1868:Pnisr
|
UTSW |
4 |
21,874,086 (GRCm39) |
unclassified |
probably benign |
|
R1909:Pnisr
|
UTSW |
4 |
21,869,517 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4843:Pnisr
|
UTSW |
4 |
21,857,400 (GRCm39) |
intron |
probably benign |
|
R4917:Pnisr
|
UTSW |
4 |
21,859,330 (GRCm39) |
intron |
probably benign |
|
R5076:Pnisr
|
UTSW |
4 |
21,874,990 (GRCm39) |
unclassified |
probably benign |
|
R5164:Pnisr
|
UTSW |
4 |
21,859,237 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5227:Pnisr
|
UTSW |
4 |
21,874,587 (GRCm39) |
unclassified |
probably benign |
|
R6722:Pnisr
|
UTSW |
4 |
21,859,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R7878:Pnisr
|
UTSW |
4 |
21,874,370 (GRCm39) |
missense |
unknown |
|
R8512:Pnisr
|
UTSW |
4 |
21,870,372 (GRCm39) |
nonsense |
probably null |
|
R9049:Pnisr
|
UTSW |
4 |
21,854,391 (GRCm39) |
missense |
unknown |
|
R9680:Pnisr
|
UTSW |
4 |
21,873,586 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Pnisr
|
UTSW |
4 |
21,873,684 (GRCm39) |
missense |
probably benign |
|
Z1176:Pnisr
|
UTSW |
4 |
21,873,684 (GRCm39) |
missense |
probably benign |
|
Z1177:Pnisr
|
UTSW |
4 |
21,873,684 (GRCm39) |
missense |
probably benign |
|
|