Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930426L09Rik |
T |
C |
2: 19,003,653 (GRCm39) |
|
probably benign |
Het |
4930590J08Rik |
T |
C |
6: 91,919,311 (GRCm39) |
S657P |
probably damaging |
Het |
Abca9 |
T |
C |
11: 110,025,080 (GRCm39) |
I988V |
probably benign |
Het |
Acte1 |
A |
G |
7: 143,425,524 (GRCm39) |
T58A |
probably benign |
Het |
Aox4 |
T |
A |
1: 58,270,662 (GRCm39) |
D280E |
probably benign |
Het |
Apob |
T |
A |
12: 8,055,060 (GRCm39) |
L1353* |
probably null |
Het |
Atp2b1 |
C |
T |
10: 98,858,691 (GRCm39) |
R222C |
probably damaging |
Het |
AW209491 |
T |
G |
13: 14,811,668 (GRCm39) |
S174A |
possibly damaging |
Het |
B930094E09Rik |
G |
C |
18: 31,742,911 (GRCm39) |
|
probably benign |
Het |
Cbln3 |
G |
T |
14: 56,121,517 (GRCm39) |
P43Q |
possibly damaging |
Het |
Ccdc181 |
A |
T |
1: 164,107,487 (GRCm39) |
T57S |
probably benign |
Het |
Ccr2 |
A |
C |
9: 123,906,008 (GRCm39) |
N96T |
probably damaging |
Het |
Cep131 |
T |
C |
11: 119,956,837 (GRCm39) |
I868V |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,094,071 (GRCm39) |
I1535T |
probably damaging |
Het |
Chl1 |
A |
T |
6: 103,660,204 (GRCm39) |
T377S |
probably benign |
Het |
Cpeb3 |
A |
G |
19: 37,065,853 (GRCm39) |
F439L |
probably damaging |
Het |
Crb2 |
T |
C |
2: 37,680,269 (GRCm39) |
V399A |
probably damaging |
Het |
Cry2 |
C |
T |
2: 92,244,187 (GRCm39) |
G329R |
probably damaging |
Het |
Dock4 |
A |
G |
12: 40,781,868 (GRCm39) |
E691G |
probably benign |
Het |
Edil3 |
A |
T |
13: 88,970,108 (GRCm39) |
H3L |
probably benign |
Het |
Endod1 |
T |
C |
9: 14,268,757 (GRCm39) |
I243V |
probably benign |
Het |
Fpr3 |
G |
A |
17: 18,190,919 (GRCm39) |
W63* |
probably null |
Het |
Gtse1 |
T |
G |
15: 85,753,158 (GRCm39) |
N424K |
possibly damaging |
Het |
Kcnt1 |
G |
A |
2: 25,783,192 (GRCm39) |
V252M |
probably damaging |
Het |
Kifbp |
G |
A |
10: 62,399,029 (GRCm39) |
Q130* |
probably null |
Het |
Lmbrd2 |
T |
G |
15: 9,149,262 (GRCm39) |
I48M |
probably damaging |
Het |
Lrrc7 |
T |
G |
3: 158,059,069 (GRCm39) |
I13L |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,822,386 (GRCm39) |
S408P |
probably benign |
Het |
Mphosph10 |
A |
G |
7: 64,028,529 (GRCm39) |
V542A |
possibly damaging |
Het |
Msto1 |
C |
A |
3: 88,818,254 (GRCm39) |
R331L |
probably damaging |
Het |
Myh10 |
G |
A |
11: 68,692,979 (GRCm39) |
E1425K |
probably damaging |
Het |
Nup43 |
T |
C |
10: 7,554,437 (GRCm39) |
I340T |
probably benign |
Het |
Or1j4 |
T |
C |
2: 36,740,846 (GRCm39) |
S263P |
possibly damaging |
Het |
Phf20 |
T |
A |
2: 156,140,573 (GRCm39) |
L749H |
probably damaging |
Het |
Pigp |
T |
C |
16: 94,171,226 (GRCm39) |
R22G |
probably null |
Het |
Polr2b |
T |
C |
5: 77,468,824 (GRCm39) |
M200T |
probably damaging |
Het |
Ppig |
T |
A |
2: 69,580,471 (GRCm39) |
D668E |
unknown |
Het |
Prss3 |
G |
A |
6: 41,352,060 (GRCm39) |
R68C |
probably benign |
Het |
Retreg3 |
G |
A |
11: 100,994,721 (GRCm39) |
|
probably benign |
Het |
Shank1 |
T |
C |
7: 44,006,630 (GRCm39) |
F2116L |
possibly damaging |
Het |
Spg21 |
T |
C |
9: 65,376,090 (GRCm39) |
S33P |
possibly damaging |
Het |
Spns3 |
A |
G |
11: 72,390,349 (GRCm39) |
S432P |
probably damaging |
Het |
Stra6 |
A |
G |
9: 58,042,452 (GRCm39) |
E27G |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,673,320 (GRCm39) |
Q1468R |
probably benign |
Het |
Tbce |
T |
G |
13: 14,194,362 (GRCm39) |
E99A |
probably benign |
Het |
Tmem106b |
T |
C |
6: 13,084,252 (GRCm39) |
V252A |
probably damaging |
Het |
Trim10 |
A |
G |
17: 37,187,923 (GRCm39) |
T380A |
probably damaging |
Het |
Trim31 |
T |
A |
17: 37,220,501 (GRCm39) |
D472E |
probably damaging |
Het |
Vmn2r28 |
G |
A |
7: 5,491,003 (GRCm39) |
Q415* |
probably null |
Het |
Vwf |
G |
A |
6: 125,626,252 (GRCm39) |
C7Y |
unknown |
Het |
Yeats2 |
C |
T |
16: 20,033,225 (GRCm39) |
P1088L |
probably benign |
Het |
Zfp40 |
C |
A |
17: 23,397,354 (GRCm39) |
V48L |
possibly damaging |
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 |
|
R0386:Pcm1
|
UTSW |
8 |
41,769,060 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|