Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,632,056 (GRCm39) |
H4992R |
probably damaging |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Akr1c20 |
T |
C |
13: 4,560,222 (GRCm39) |
E152G |
probably damaging |
Het |
Ano4 |
T |
A |
10: 88,788,189 (GRCm39) |
D877V |
probably damaging |
Het |
Asb18 |
A |
C |
1: 89,942,260 (GRCm39) |
S14A |
probably damaging |
Het |
Atrnl1 |
T |
A |
19: 57,618,724 (GRCm39) |
Y147* |
probably null |
Het |
Cbfa2t2 |
A |
G |
2: 154,342,375 (GRCm39) |
I30M |
possibly damaging |
Het |
Cpd |
A |
T |
11: 76,675,242 (GRCm39) |
L1293* |
probably null |
Het |
Cst9 |
G |
A |
2: 148,680,393 (GRCm39) |
V120I |
possibly damaging |
Het |
Ddah2 |
A |
G |
17: 35,279,664 (GRCm39) |
D128G |
probably damaging |
Het |
Defb11 |
T |
C |
8: 22,395,510 (GRCm39) |
I56V |
probably benign |
Het |
Dnah17 |
A |
T |
11: 117,925,193 (GRCm39) |
L3880Q |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Dop1a |
A |
G |
9: 86,389,623 (GRCm39) |
T508A |
possibly damaging |
Het |
Ephb2 |
T |
A |
4: 136,388,048 (GRCm39) |
H685L |
probably damaging |
Het |
Glrb |
T |
C |
3: 80,752,449 (GRCm39) |
Y387C |
probably damaging |
Het |
Gucy2e |
A |
G |
11: 69,126,859 (GRCm39) |
S205P |
possibly damaging |
Het |
Has2 |
T |
A |
15: 56,531,498 (GRCm39) |
I406F |
probably damaging |
Het |
Hcrtr2 |
A |
C |
9: 76,230,569 (GRCm39) |
V73G |
probably benign |
Het |
Hsd17b4 |
A |
T |
18: 50,316,239 (GRCm39) |
Q622L |
probably benign |
Het |
Nlrp1b |
A |
T |
11: 71,072,022 (GRCm39) |
M607K |
probably benign |
Het |
Nol6 |
T |
A |
4: 41,122,158 (GRCm39) |
D184V |
probably benign |
Het |
Noxa1 |
T |
A |
2: 24,976,253 (GRCm39) |
Q345L |
probably damaging |
Het |
Nudt6 |
T |
C |
3: 37,473,617 (GRCm39) |
T35A |
probably benign |
Het |
Phf8-ps |
C |
A |
17: 33,284,288 (GRCm39) |
R838I |
possibly damaging |
Het |
Plcg2 |
T |
C |
8: 118,337,583 (GRCm39) |
V985A |
probably benign |
Het |
Plxnc1 |
C |
T |
10: 94,635,335 (GRCm39) |
|
probably null |
Het |
Prkdc |
G |
A |
16: 15,551,962 (GRCm39) |
R2056H |
probably benign |
Het |
Ptpn4 |
A |
T |
1: 119,612,246 (GRCm39) |
I49N |
probably benign |
Het |
Ralgapa1 |
T |
G |
12: 55,723,898 (GRCm39) |
S1543R |
probably damaging |
Het |
Rnf135 |
A |
T |
11: 80,089,912 (GRCm39) |
N416I |
probably damaging |
Het |
Scn5a |
A |
G |
9: 119,350,399 (GRCm39) |
L825P |
probably damaging |
Het |
Septin11 |
A |
T |
5: 93,287,309 (GRCm39) |
N8I |
possibly damaging |
Het |
Slc13a3 |
T |
C |
2: 165,250,876 (GRCm39) |
I456V |
probably benign |
Het |
Slc16a3 |
A |
G |
11: 120,847,756 (GRCm39) |
T315A |
probably benign |
Het |
Sun1 |
T |
G |
5: 139,231,171 (GRCm39) |
F657C |
probably damaging |
Het |
Tmco3 |
T |
C |
8: 13,360,314 (GRCm39) |
S34P |
probably damaging |
Het |
Tnrc18 |
G |
A |
5: 142,759,502 (GRCm39) |
P778L |
unknown |
Het |
Ubxn4 |
A |
C |
1: 128,194,058 (GRCm39) |
K284T |
possibly damaging |
Het |
Usp37 |
A |
T |
1: 74,509,785 (GRCm39) |
N461K |
probably damaging |
Het |
Vmn2r106 |
A |
T |
17: 20,499,133 (GRCm39) |
F259L |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,524,956 (GRCm39) |
D64G |
possibly damaging |
Het |
|
Other mutations in Csmd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Csmd2
|
APN |
4 |
128,377,266 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01098:Csmd2
|
APN |
4 |
127,952,845 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01114:Csmd2
|
APN |
4 |
128,262,923 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01364:Csmd2
|
APN |
4 |
128,308,081 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01530:Csmd2
|
APN |
4 |
128,308,094 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01582:Csmd2
|
APN |
4 |
128,457,098 (GRCm39) |
nonsense |
probably null |
|
IGL01670:Csmd2
|
APN |
4 |
128,407,164 (GRCm39) |
splice site |
probably benign |
|
IGL01707:Csmd2
|
APN |
4 |
128,276,798 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01810:Csmd2
|
APN |
4 |
128,374,638 (GRCm39) |
splice site |
probably benign |
|
IGL01837:Csmd2
|
APN |
4 |
128,313,363 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01924:Csmd2
|
APN |
4 |
128,453,740 (GRCm39) |
missense |
unknown |
|
IGL02013:Csmd2
|
APN |
4 |
128,215,116 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02020:Csmd2
|
APN |
4 |
128,453,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Csmd2
|
APN |
4 |
128,371,263 (GRCm39) |
splice site |
probably benign |
|
IGL02303:Csmd2
|
APN |
4 |
128,262,801 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02317:Csmd2
|
APN |
4 |
128,357,520 (GRCm39) |
splice site |
probably benign |
|
IGL02322:Csmd2
|
APN |
4 |
128,357,520 (GRCm39) |
splice site |
probably benign |
|
IGL02338:Csmd2
|
APN |
4 |
128,288,859 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02412:Csmd2
|
APN |
4 |
128,407,165 (GRCm39) |
splice site |
probably benign |
|
IGL02428:Csmd2
|
APN |
4 |
128,368,609 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02491:Csmd2
|
APN |
4 |
128,428,050 (GRCm39) |
missense |
probably benign |
|
IGL02701:Csmd2
|
APN |
4 |
128,389,934 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02801:Csmd2
|
APN |
4 |
128,445,868 (GRCm39) |
splice site |
probably null |
|
IGL02818:Csmd2
|
APN |
4 |
128,103,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Csmd2
|
APN |
4 |
128,415,677 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02876:Csmd2
|
APN |
4 |
128,215,128 (GRCm39) |
nonsense |
probably null |
|
IGL02977:Csmd2
|
APN |
4 |
128,387,069 (GRCm39) |
nonsense |
probably null |
|
IGL03006:Csmd2
|
APN |
4 |
128,374,558 (GRCm39) |
splice site |
probably benign |
|
IGL03032:Csmd2
|
APN |
4 |
128,412,834 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03148:Csmd2
|
APN |
4 |
128,278,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Csmd2
|
APN |
4 |
128,308,092 (GRCm39) |
nonsense |
probably null |
|
IGL03245:Csmd2
|
APN |
4 |
128,402,915 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03376:Csmd2
|
APN |
4 |
128,411,464 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03014:Csmd2
|
UTSW |
4 |
128,190,222 (GRCm39) |
missense |
probably benign |
0.01 |
R0109:Csmd2
|
UTSW |
4 |
128,438,536 (GRCm39) |
missense |
probably benign |
0.03 |
R0112:Csmd2
|
UTSW |
4 |
128,389,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0157:Csmd2
|
UTSW |
4 |
128,415,704 (GRCm39) |
missense |
probably benign |
0.02 |
R0390:Csmd2
|
UTSW |
4 |
128,027,466 (GRCm39) |
intron |
probably benign |
|
R0441:Csmd2
|
UTSW |
4 |
128,414,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Csmd2
|
UTSW |
4 |
128,380,798 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0743:Csmd2
|
UTSW |
4 |
128,007,469 (GRCm39) |
missense |
probably benign |
0.00 |
R0746:Csmd2
|
UTSW |
4 |
128,308,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Csmd2
|
UTSW |
4 |
128,389,981 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1019:Csmd2
|
UTSW |
4 |
128,415,807 (GRCm39) |
missense |
probably benign |
0.00 |
R1476:Csmd2
|
UTSW |
4 |
128,380,794 (GRCm39) |
missense |
probably benign |
0.08 |
R1641:Csmd2
|
UTSW |
4 |
128,377,188 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1709:Csmd2
|
UTSW |
4 |
128,389,988 (GRCm39) |
missense |
probably damaging |
0.96 |
R2866:Csmd2
|
UTSW |
4 |
128,308,185 (GRCm39) |
critical splice donor site |
probably null |
|
R2870:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2870:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2873:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2893:Csmd2
|
UTSW |
4 |
128,432,786 (GRCm39) |
splice site |
probably null |
|
R3796:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3797:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3798:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3914:Csmd2
|
UTSW |
4 |
128,215,117 (GRCm39) |
missense |
probably benign |
0.07 |
R4198:Csmd2
|
UTSW |
4 |
128,404,717 (GRCm39) |
missense |
probably benign |
0.07 |
R4489:Csmd2
|
UTSW |
4 |
128,275,738 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4571:Csmd2
|
UTSW |
4 |
128,373,888 (GRCm39) |
splice site |
probably null |
|
R4581:Csmd2
|
UTSW |
4 |
128,262,881 (GRCm39) |
missense |
probably benign |
0.02 |
R4599:Csmd2
|
UTSW |
4 |
127,881,921 (GRCm39) |
missense |
probably benign |
0.35 |
R4649:Csmd2
|
UTSW |
4 |
128,439,866 (GRCm39) |
missense |
probably benign |
|
R4706:Csmd2
|
UTSW |
4 |
128,438,544 (GRCm39) |
missense |
probably benign |
|
R4776:Csmd2
|
UTSW |
4 |
128,336,685 (GRCm39) |
missense |
probably benign |
0.09 |
R4838:Csmd2
|
UTSW |
4 |
128,411,542 (GRCm39) |
missense |
probably benign |
|
R4900:Csmd2
|
UTSW |
4 |
128,346,318 (GRCm39) |
missense |
probably benign |
0.03 |
R4999:Csmd2
|
UTSW |
4 |
128,415,723 (GRCm39) |
missense |
probably benign |
0.00 |
R5024:Csmd2
|
UTSW |
4 |
128,215,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5034:Csmd2
|
UTSW |
4 |
127,952,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R5152:Csmd2
|
UTSW |
4 |
128,445,828 (GRCm39) |
missense |
probably benign |
0.27 |
R5172:Csmd2
|
UTSW |
4 |
128,371,190 (GRCm39) |
missense |
probably benign |
0.10 |
R5231:Csmd2
|
UTSW |
4 |
128,439,842 (GRCm39) |
missense |
probably benign |
0.00 |
R5279:Csmd2
|
UTSW |
4 |
128,350,707 (GRCm39) |
missense |
probably benign |
0.30 |
R5287:Csmd2
|
UTSW |
4 |
128,380,677 (GRCm39) |
missense |
probably benign |
0.01 |
R5403:Csmd2
|
UTSW |
4 |
128,380,677 (GRCm39) |
missense |
probably benign |
0.01 |
R5410:Csmd2
|
UTSW |
4 |
128,442,612 (GRCm39) |
missense |
probably benign |
|
R5551:Csmd2
|
UTSW |
4 |
128,404,741 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5566:Csmd2
|
UTSW |
4 |
128,356,682 (GRCm39) |
critical splice donor site |
probably null |
|
R5907:Csmd2
|
UTSW |
4 |
128,091,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R5913:Csmd2
|
UTSW |
4 |
128,445,781 (GRCm39) |
missense |
probably benign |
0.01 |
R5970:Csmd2
|
UTSW |
4 |
128,439,944 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Csmd2
|
UTSW |
4 |
127,952,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Csmd2
|
UTSW |
4 |
128,453,739 (GRCm39) |
missense |
unknown |
|
R6075:Csmd2
|
UTSW |
4 |
128,380,658 (GRCm39) |
missense |
probably benign |
0.15 |
R6129:Csmd2
|
UTSW |
4 |
128,387,127 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6363:Csmd2
|
UTSW |
4 |
128,294,172 (GRCm39) |
missense |
probably benign |
0.00 |
R6366:Csmd2
|
UTSW |
4 |
128,377,245 (GRCm39) |
missense |
probably benign |
0.00 |
R6404:Csmd2
|
UTSW |
4 |
128,415,743 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6437:Csmd2
|
UTSW |
4 |
127,881,893 (GRCm39) |
missense |
probably benign |
0.24 |
R6441:Csmd2
|
UTSW |
4 |
128,288,757 (GRCm39) |
missense |
probably benign |
0.03 |
R6643:Csmd2
|
UTSW |
4 |
128,266,390 (GRCm39) |
missense |
probably benign |
0.14 |
R6724:Csmd2
|
UTSW |
4 |
128,457,164 (GRCm39) |
missense |
probably damaging |
0.97 |
R6734:Csmd2
|
UTSW |
4 |
128,357,606 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Csmd2
|
UTSW |
4 |
128,091,018 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6801:Csmd2
|
UTSW |
4 |
128,277,743 (GRCm39) |
missense |
probably benign |
0.11 |
R6842:Csmd2
|
UTSW |
4 |
128,402,952 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6843:Csmd2
|
UTSW |
4 |
128,357,587 (GRCm39) |
missense |
probably benign |
0.27 |
R6868:Csmd2
|
UTSW |
4 |
128,336,633 (GRCm39) |
missense |
probably benign |
|
R6882:Csmd2
|
UTSW |
4 |
128,343,062 (GRCm39) |
missense |
probably benign |
0.01 |
R7019:Csmd2
|
UTSW |
4 |
128,262,856 (GRCm39) |
missense |
|
|
R7028:Csmd2
|
UTSW |
4 |
128,171,021 (GRCm39) |
missense |
|
|
R7096:Csmd2
|
UTSW |
4 |
128,356,519 (GRCm39) |
missense |
|
|
R7122:Csmd2
|
UTSW |
4 |
128,343,020 (GRCm39) |
missense |
|
|
R7125:Csmd2
|
UTSW |
4 |
128,389,955 (GRCm39) |
missense |
|
|
R7197:Csmd2
|
UTSW |
4 |
128,404,826 (GRCm39) |
missense |
|
|
R7234:Csmd2
|
UTSW |
4 |
128,350,572 (GRCm39) |
missense |
|
|
R7299:Csmd2
|
UTSW |
4 |
128,422,055 (GRCm39) |
missense |
|
|
R7301:Csmd2
|
UTSW |
4 |
128,422,055 (GRCm39) |
missense |
|
|
R7319:Csmd2
|
UTSW |
4 |
128,287,472 (GRCm39) |
missense |
|
|
R7331:Csmd2
|
UTSW |
4 |
128,458,021 (GRCm39) |
splice site |
probably null |
|
R7332:Csmd2
|
UTSW |
4 |
128,313,360 (GRCm39) |
missense |
|
|
R7352:Csmd2
|
UTSW |
4 |
128,451,429 (GRCm39) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,215,889 (GRCm39) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,215,888 (GRCm39) |
missense |
|
|
R7474:Csmd2
|
UTSW |
4 |
128,439,920 (GRCm39) |
missense |
|
|
R7555:Csmd2
|
UTSW |
4 |
128,346,251 (GRCm39) |
missense |
|
|
R7592:Csmd2
|
UTSW |
4 |
128,357,591 (GRCm39) |
missense |
|
|
R7700:Csmd2
|
UTSW |
4 |
128,439,549 (GRCm39) |
splice site |
probably null |
|
R7714:Csmd2
|
UTSW |
4 |
128,276,743 (GRCm39) |
nonsense |
probably null |
|
R7734:Csmd2
|
UTSW |
4 |
128,445,850 (GRCm39) |
missense |
|
|
R7735:Csmd2
|
UTSW |
4 |
128,350,723 (GRCm39) |
critical splice donor site |
probably null |
|
R7757:Csmd2
|
UTSW |
4 |
128,377,249 (GRCm39) |
missense |
|
|
R7805:Csmd2
|
UTSW |
4 |
128,313,366 (GRCm39) |
missense |
|
|
R7823:Csmd2
|
UTSW |
4 |
128,103,698 (GRCm39) |
missense |
|
|
R7904:Csmd2
|
UTSW |
4 |
128,313,346 (GRCm39) |
missense |
|
|
R7946:Csmd2
|
UTSW |
4 |
128,414,058 (GRCm39) |
missense |
|
|
R7964:Csmd2
|
UTSW |
4 |
128,417,303 (GRCm39) |
missense |
|
|
R7968:Csmd2
|
UTSW |
4 |
128,091,118 (GRCm39) |
missense |
|
|
R8003:Csmd2
|
UTSW |
4 |
128,432,980 (GRCm39) |
nonsense |
probably null |
|
R8071:Csmd2
|
UTSW |
4 |
128,287,331 (GRCm39) |
missense |
|
|
R8504:Csmd2
|
UTSW |
4 |
128,440,483 (GRCm39) |
missense |
|
|
R8511:Csmd2
|
UTSW |
4 |
128,262,692 (GRCm39) |
missense |
|
|
R8517:Csmd2
|
UTSW |
4 |
128,446,479 (GRCm39) |
missense |
|
|
R8704:Csmd2
|
UTSW |
4 |
128,091,147 (GRCm39) |
missense |
|
|
R8722:Csmd2
|
UTSW |
4 |
128,445,743 (GRCm39) |
unclassified |
probably benign |
|
R8729:Csmd2
|
UTSW |
4 |
128,356,638 (GRCm39) |
missense |
|
|
R8801:Csmd2
|
UTSW |
4 |
128,457,195 (GRCm39) |
missense |
probably damaging |
0.97 |
R8803:Csmd2
|
UTSW |
4 |
128,440,477 (GRCm39) |
missense |
|
|
R8839:Csmd2
|
UTSW |
4 |
128,336,681 (GRCm39) |
missense |
|
|
R8867:Csmd2
|
UTSW |
4 |
128,451,469 (GRCm39) |
missense |
|
|
R8913:Csmd2
|
UTSW |
4 |
128,417,351 (GRCm39) |
missense |
|
|
R8928:Csmd2
|
UTSW |
4 |
128,369,582 (GRCm39) |
missense |
|
|
R8974:Csmd2
|
UTSW |
4 |
128,446,380 (GRCm39) |
missense |
|
|
R9001:Csmd2
|
UTSW |
4 |
128,308,079 (GRCm39) |
missense |
|
|
R9132:Csmd2
|
UTSW |
4 |
128,443,007 (GRCm39) |
missense |
|
|
R9245:Csmd2
|
UTSW |
4 |
128,200,168 (GRCm39) |
missense |
|
|
R9249:Csmd2
|
UTSW |
4 |
128,313,323 (GRCm39) |
nonsense |
probably null |
|
R9254:Csmd2
|
UTSW |
4 |
128,091,112 (GRCm39) |
missense |
|
|
R9265:Csmd2
|
UTSW |
4 |
128,294,163 (GRCm39) |
missense |
|
|
R9407:Csmd2
|
UTSW |
4 |
128,442,613 (GRCm39) |
missense |
|
|
R9432:Csmd2
|
UTSW |
4 |
128,171,004 (GRCm39) |
missense |
|
|
R9559:Csmd2
|
UTSW |
4 |
128,438,561 (GRCm39) |
missense |
|
|
R9673:Csmd2
|
UTSW |
4 |
128,308,062 (GRCm39) |
missense |
|
|
R9735:Csmd2
|
UTSW |
4 |
128,402,901 (GRCm39) |
missense |
|
|
R9749:Csmd2
|
UTSW |
4 |
128,389,921 (GRCm39) |
missense |
|
|
R9803:Csmd2
|
UTSW |
4 |
128,262,986 (GRCm39) |
missense |
|
|
Z1177:Csmd2
|
UTSW |
4 |
128,424,590 (GRCm39) |
missense |
|
|
|