Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
G |
5: 77,044,308 (GRCm39) |
V194A |
probably damaging |
Het |
Adamts13 |
G |
A |
2: 26,876,691 (GRCm39) |
|
probably null |
Het |
Ahnak |
T |
C |
19: 8,988,508 (GRCm39) |
M3264T |
possibly damaging |
Het |
Birc6 |
T |
A |
17: 74,906,335 (GRCm39) |
C1409S |
probably damaging |
Het |
Camta1 |
C |
A |
4: 151,159,597 (GRCm39) |
R1614L |
probably damaging |
Het |
Dnah2 |
A |
G |
11: 69,338,687 (GRCm39) |
V3161A |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,383,727 (GRCm39) |
Y2983F |
probably damaging |
Het |
Dnah6 |
G |
A |
6: 73,060,107 (GRCm39) |
L2774F |
probably damaging |
Het |
Dst |
A |
T |
1: 34,256,917 (GRCm39) |
T4398S |
probably damaging |
Het |
Efcab5 |
G |
A |
11: 77,031,749 (GRCm39) |
R42W |
probably damaging |
Het |
Efcab5 |
A |
T |
11: 77,063,204 (GRCm39) |
M96K |
probably benign |
Het |
Elavl4 |
A |
G |
4: 110,063,902 (GRCm39) |
|
probably benign |
Het |
Flt4 |
G |
A |
11: 49,535,213 (GRCm39) |
A1214T |
probably benign |
Het |
Fn1 |
G |
T |
1: 71,634,945 (GRCm39) |
T2127N |
probably damaging |
Het |
Foxj1 |
A |
T |
11: 116,222,629 (GRCm39) |
S391R |
possibly damaging |
Het |
Gabrb1 |
A |
T |
5: 72,266,150 (GRCm39) |
Y269F |
probably damaging |
Het |
Ghitm |
A |
G |
14: 36,847,868 (GRCm39) |
S259P |
possibly damaging |
Het |
Gm16332 |
A |
G |
1: 139,851,928 (GRCm39) |
|
noncoding transcript |
Het |
Gm16380 |
T |
A |
9: 53,791,727 (GRCm39) |
|
noncoding transcript |
Het |
Gm9869 |
A |
T |
9: 60,745,344 (GRCm39) |
|
probably benign |
Het |
Gm9936 |
G |
A |
5: 114,995,192 (GRCm39) |
Q142* |
probably null |
Het |
Hmbs |
T |
C |
9: 44,248,305 (GRCm39) |
Y260C |
probably benign |
Het |
Hoxc5 |
T |
A |
15: 102,923,784 (GRCm39) |
C193* |
probably null |
Het |
Idh2 |
C |
T |
7: 79,748,005 (GRCm39) |
A232T |
probably damaging |
Het |
Lce1j |
T |
C |
3: 92,696,695 (GRCm39) |
K28E |
unknown |
Het |
Lpgat1 |
C |
T |
1: 191,451,460 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
C |
13: 13,882,799 (GRCm39) |
|
probably benign |
Het |
Megf11 |
A |
G |
9: 64,547,360 (GRCm39) |
N235D |
probably damaging |
Het |
Mst1r |
T |
A |
9: 107,794,003 (GRCm39) |
|
probably null |
Het |
Nr2c2ap |
A |
G |
8: 70,584,237 (GRCm39) |
D9G |
probably benign |
Het |
Obscn |
T |
C |
11: 59,027,165 (GRCm39) |
T13A |
probably damaging |
Het |
Ofcc1 |
A |
C |
13: 40,367,950 (GRCm39) |
L188* |
probably null |
Het |
Oma1 |
A |
T |
4: 103,182,398 (GRCm39) |
|
probably benign |
Het |
Or10aa3 |
A |
T |
1: 173,877,965 (GRCm39) |
T9S |
probably benign |
Het |
Or5m11 |
A |
G |
2: 85,782,217 (GRCm39) |
E270G |
probably damaging |
Het |
Pglyrp2 |
A |
G |
17: 32,639,836 (GRCm39) |
M1T |
probably null |
Het |
Pnpla5 |
G |
T |
15: 84,004,920 (GRCm39) |
L144M |
probably damaging |
Het |
Prdm10 |
C |
A |
9: 31,227,596 (GRCm39) |
T67K |
probably damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,754,852 (GRCm39) |
H1193Q |
probably benign |
Het |
Sall1 |
A |
G |
8: 89,759,232 (GRCm39) |
S291P |
probably damaging |
Het |
Sdk2 |
T |
C |
11: 113,784,290 (GRCm39) |
T150A |
probably damaging |
Het |
Sel1l2 |
T |
A |
2: 140,117,361 (GRCm39) |
Y170F |
probably benign |
Het |
Sema4a |
C |
T |
3: 88,344,107 (GRCm39) |
V715I |
possibly damaging |
Het |
Smgc |
G |
A |
15: 91,738,841 (GRCm39) |
A500T |
probably benign |
Het |
Spef2 |
A |
G |
15: 9,584,148 (GRCm39) |
V1639A |
probably damaging |
Het |
Srrm4 |
A |
G |
5: 116,620,437 (GRCm39) |
|
probably benign |
Het |
Tbc1d23 |
G |
A |
16: 57,009,636 (GRCm39) |
H418Y |
probably damaging |
Het |
Tbk1 |
A |
G |
10: 121,420,159 (GRCm39) |
L10P |
probably damaging |
Het |
Thumpd3 |
G |
A |
6: 113,042,621 (GRCm39) |
|
probably null |
Het |
Trp53bp1 |
G |
T |
2: 121,035,424 (GRCm39) |
T1609K |
probably damaging |
Het |
Tut1 |
A |
G |
19: 8,932,919 (GRCm39) |
N84S |
probably benign |
Het |
Urb1 |
C |
T |
16: 90,593,287 (GRCm39) |
G282R |
probably damaging |
Het |
Usp19 |
A |
T |
9: 108,376,910 (GRCm39) |
D1160V |
probably damaging |
Het |
Usp9y |
A |
G |
Y: 1,316,933 (GRCm39) |
V1872A |
probably damaging |
Het |
Zfp276 |
C |
A |
8: 123,986,242 (GRCm39) |
Y386* |
probably null |
Het |
|
Other mutations in Pcm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00773:Pcm1
|
APN |
8 |
41,727,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00852:Pcm1
|
APN |
8 |
41,740,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00896:Pcm1
|
APN |
8 |
41,729,160 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00927:Pcm1
|
APN |
8 |
41,740,918 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01085:Pcm1
|
APN |
8 |
41,762,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01684:Pcm1
|
APN |
8 |
41,710,960 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01888:Pcm1
|
APN |
8 |
41,710,993 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02349:Pcm1
|
APN |
8 |
41,741,192 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02562:Pcm1
|
APN |
8 |
41,778,405 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02807:Pcm1
|
APN |
8 |
41,783,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03081:Pcm1
|
APN |
8 |
41,728,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090_Pcm1_148
|
UTSW |
8 |
41,709,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R1534_pcm1_826
|
UTSW |
8 |
41,740,738 (GRCm39) |
missense |
probably benign |
|
R8169_pcm1_970
|
UTSW |
8 |
41,763,153 (GRCm39) |
missense |
possibly damaging |
0.58 |
shaved
|
UTSW |
8 |
41,741,193 (GRCm39) |
critical splice donor site |
probably null |
|
D3080:Pcm1
|
UTSW |
8 |
41,728,976 (GRCm39) |
missense |
probably damaging |
1.00 |
P0045:Pcm1
|
UTSW |
8 |
41,741,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R0090:Pcm1
|
UTSW |
8 |
41,709,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R0109:Pcm1
|
UTSW |
8 |
41,710,974 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0373:Pcm1
|
UTSW |
8 |
41,729,148 (GRCm39) |
nonsense |
probably null |
|
R0452:Pcm1
|
UTSW |
8 |
41,778,942 (GRCm39) |
missense |
probably benign |
0.25 |
R0498:Pcm1
|
UTSW |
8 |
41,746,806 (GRCm39) |
missense |
probably benign |
0.01 |
R0528:Pcm1
|
UTSW |
8 |
41,768,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0587:Pcm1
|
UTSW |
8 |
41,739,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R0635:Pcm1
|
UTSW |
8 |
41,720,216 (GRCm39) |
splice site |
probably benign |
|
R0725:Pcm1
|
UTSW |
8 |
41,740,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R0762:Pcm1
|
UTSW |
8 |
41,714,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R0848:Pcm1
|
UTSW |
8 |
41,735,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R1027:Pcm1
|
UTSW |
8 |
41,746,482 (GRCm39) |
splice site |
probably benign |
|
R1056:Pcm1
|
UTSW |
8 |
41,774,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Pcm1
|
UTSW |
8 |
41,740,738 (GRCm39) |
missense |
probably benign |
|
R1566:Pcm1
|
UTSW |
8 |
41,743,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Pcm1
|
UTSW |
8 |
41,762,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:Pcm1
|
UTSW |
8 |
41,766,396 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1816:Pcm1
|
UTSW |
8 |
41,762,574 (GRCm39) |
missense |
probably damaging |
0.99 |
R2177:Pcm1
|
UTSW |
8 |
41,729,002 (GRCm39) |
missense |
probably benign |
|
R2495:Pcm1
|
UTSW |
8 |
41,746,616 (GRCm39) |
missense |
probably benign |
|
R3737:Pcm1
|
UTSW |
8 |
41,714,080 (GRCm39) |
nonsense |
probably null |
|
R3747:Pcm1
|
UTSW |
8 |
41,785,041 (GRCm39) |
missense |
probably benign |
0.44 |
R3763:Pcm1
|
UTSW |
8 |
41,733,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R3764:Pcm1
|
UTSW |
8 |
41,783,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R3798:Pcm1
|
UTSW |
8 |
41,711,051 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3968:Pcm1
|
UTSW |
8 |
41,778,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Pcm1
|
UTSW |
8 |
41,740,775 (GRCm39) |
missense |
probably damaging |
0.99 |
R4798:Pcm1
|
UTSW |
8 |
41,746,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Pcm1
|
UTSW |
8 |
41,712,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R5221:Pcm1
|
UTSW |
8 |
41,741,193 (GRCm39) |
critical splice donor site |
probably null |
|
R5250:Pcm1
|
UTSW |
8 |
41,765,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R5466:Pcm1
|
UTSW |
8 |
41,725,499 (GRCm39) |
critical splice donor site |
probably null |
|
R5470:Pcm1
|
UTSW |
8 |
41,740,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Pcm1
|
UTSW |
8 |
41,782,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Pcm1
|
UTSW |
8 |
41,781,815 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6179:Pcm1
|
UTSW |
8 |
41,736,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R6186:Pcm1
|
UTSW |
8 |
41,746,830 (GRCm39) |
missense |
probably benign |
0.23 |
R6227:Pcm1
|
UTSW |
8 |
41,783,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R6368:Pcm1
|
UTSW |
8 |
41,746,581 (GRCm39) |
missense |
probably benign |
0.09 |
R6438:Pcm1
|
UTSW |
8 |
41,778,418 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6459:Pcm1
|
UTSW |
8 |
41,714,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Pcm1
|
UTSW |
8 |
41,746,547 (GRCm39) |
missense |
probably benign |
0.11 |
R7401:Pcm1
|
UTSW |
8 |
41,762,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R7478:Pcm1
|
UTSW |
8 |
41,714,410 (GRCm39) |
missense |
probably benign |
0.17 |
R7570:Pcm1
|
UTSW |
8 |
41,720,381 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7648:Pcm1
|
UTSW |
8 |
41,728,736 (GRCm39) |
missense |
probably damaging |
0.99 |
R7773:Pcm1
|
UTSW |
8 |
41,762,610 (GRCm39) |
nonsense |
probably null |
|
R7779:Pcm1
|
UTSW |
8 |
41,782,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Pcm1
|
UTSW |
8 |
41,780,621 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7863:Pcm1
|
UTSW |
8 |
41,714,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R8169:Pcm1
|
UTSW |
8 |
41,763,153 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8210:Pcm1
|
UTSW |
8 |
41,766,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R8303:Pcm1
|
UTSW |
8 |
41,736,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R8397:Pcm1
|
UTSW |
8 |
41,736,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R8489:Pcm1
|
UTSW |
8 |
41,766,437 (GRCm39) |
missense |
probably benign |
0.19 |
R8519:Pcm1
|
UTSW |
8 |
41,728,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Pcm1
|
UTSW |
8 |
41,732,825 (GRCm39) |
missense |
probably benign |
0.19 |
R9245:Pcm1
|
UTSW |
8 |
41,732,877 (GRCm39) |
missense |
probably damaging |
0.99 |
R9263:Pcm1
|
UTSW |
8 |
41,732,790 (GRCm39) |
missense |
probably benign |
0.00 |
R9406:Pcm1
|
UTSW |
8 |
41,728,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R9412:Pcm1
|
UTSW |
8 |
41,740,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R9541:Pcm1
|
UTSW |
8 |
41,780,616 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:Pcm1
|
UTSW |
8 |
41,723,541 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9716:Pcm1
|
UTSW |
8 |
41,728,168 (GRCm39) |
missense |
probably damaging |
0.98 |
R9747:Pcm1
|
UTSW |
8 |
41,757,135 (GRCm39) |
missense |
probably benign |
0.00 |
R9781:Pcm1
|
UTSW |
8 |
41,720,398 (GRCm39) |
missense |
probably damaging |
0.99 |
X0025:Pcm1
|
UTSW |
8 |
41,783,679 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Pcm1
|
UTSW |
8 |
41,740,781 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Pcm1
|
UTSW |
8 |
41,727,208 (GRCm39) |
missense |
possibly damaging |
0.94 |
|