Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
C |
5: 8,899,537 (GRCm39) |
F936L |
probably benign |
Het |
Adamts12 |
T |
A |
15: 11,152,143 (GRCm39) |
I211N |
probably benign |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Alas1 |
C |
T |
9: 106,116,845 (GRCm39) |
V293I |
possibly damaging |
Het |
Ap1g1 |
T |
C |
8: 110,580,244 (GRCm39) |
Y569H |
probably damaging |
Het |
Apc2 |
A |
G |
10: 80,148,603 (GRCm39) |
D1190G |
probably damaging |
Het |
Astn2 |
G |
A |
4: 65,664,591 (GRCm39) |
Q679* |
probably null |
Het |
Atp2a1 |
T |
A |
7: 126,062,081 (GRCm39) |
H5L |
probably damaging |
Het |
Baiap3 |
T |
C |
17: 25,468,302 (GRCm39) |
K279E |
probably damaging |
Het |
C2cd2l |
G |
A |
9: 44,227,909 (GRCm39) |
P111S |
probably benign |
Het |
Ccp110 |
C |
T |
7: 118,334,536 (GRCm39) |
T1003I |
probably damaging |
Het |
Cdh22 |
T |
C |
2: 165,012,716 (GRCm39) |
D123G |
probably damaging |
Het |
Cep295 |
C |
T |
9: 15,252,179 (GRCm39) |
E397K |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,768,433 (GRCm39) |
V722A |
probably benign |
Het |
Cpsf4l |
A |
G |
11: 113,592,901 (GRCm39) |
F174S |
probably benign |
Het |
Ctnna3 |
T |
C |
10: 63,688,551 (GRCm39) |
C332R |
probably damaging |
Het |
Cxcl10 |
A |
T |
5: 92,495,714 (GRCm39) |
N76K |
probably damaging |
Het |
Dnaaf9 |
G |
A |
2: 130,551,858 (GRCm39) |
L1010F |
probably damaging |
Het |
Dnaja3 |
G |
A |
16: 4,502,029 (GRCm39) |
R11K |
probably null |
Het |
Efcab10 |
A |
G |
12: 33,445,170 (GRCm39) |
T28A |
possibly damaging |
Het |
Esrrg |
A |
G |
1: 187,775,850 (GRCm39) |
R103G |
probably damaging |
Het |
Exosc2 |
A |
G |
2: 31,560,818 (GRCm39) |
K23E |
probably benign |
Het |
Flot2 |
C |
T |
11: 77,940,373 (GRCm39) |
S40L |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,822,081 (GRCm39) |
V5938A |
probably benign |
Het |
Gclc |
A |
G |
9: 77,683,571 (GRCm39) |
T143A |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,669,623 (GRCm39) |
V407A |
probably benign |
Het |
Gucy2e |
A |
T |
11: 69,122,884 (GRCm39) |
M497K |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,357,960 (GRCm39) |
|
probably null |
Het |
Hnrnpll |
A |
C |
17: 80,341,534 (GRCm39) |
S502A |
probably benign |
Het |
Ipo11 |
G |
T |
13: 106,932,170 (GRCm39) |
T975N |
probably benign |
Het |
Kif17 |
C |
T |
4: 137,990,009 (GRCm39) |
Q66* |
probably null |
Het |
Lrp10 |
T |
C |
14: 54,707,209 (GRCm39) |
V682A |
possibly damaging |
Het |
Lsmem1 |
A |
T |
12: 40,230,677 (GRCm39) |
L75Q |
probably damaging |
Het |
Med16 |
A |
T |
10: 79,735,169 (GRCm39) |
Y430N |
probably benign |
Het |
Med8 |
C |
T |
4: 118,269,931 (GRCm39) |
S72L |
possibly damaging |
Het |
Mex3a |
A |
G |
3: 88,443,682 (GRCm39) |
T253A |
probably damaging |
Het |
Myf6 |
T |
C |
10: 107,329,220 (GRCm39) |
K242E |
probably damaging |
Het |
Ncald |
T |
A |
15: 37,397,587 (GRCm39) |
Y31F |
probably benign |
Het |
Ndufa12 |
T |
A |
10: 94,035,855 (GRCm39) |
Y48N |
probably damaging |
Het |
Or12e10 |
T |
C |
2: 87,641,112 (GRCm39) |
V316A |
probably benign |
Het |
Or51q1c |
T |
A |
7: 103,653,329 (GRCm39) |
Y282* |
probably null |
Het |
Or5as1 |
T |
G |
2: 86,980,123 (GRCm39) |
N294T |
probably damaging |
Het |
Pde4dip |
T |
C |
3: 97,610,639 (GRCm39) |
T1858A |
probably benign |
Het |
Pgbd1 |
A |
G |
13: 21,618,651 (GRCm39) |
L2P |
probably damaging |
Het |
Piezo1 |
C |
T |
8: 123,214,241 (GRCm39) |
R1642H |
probably damaging |
Het |
Plxna1 |
A |
T |
6: 89,333,990 (GRCm39) |
M213K |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,965,041 (GRCm39) |
N709S |
probably damaging |
Het |
Pramel1 |
T |
A |
4: 143,124,999 (GRCm39) |
W308R |
probably damaging |
Het |
Prkag2 |
A |
T |
5: 25,076,539 (GRCm39) |
I208N |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,330,864 (GRCm39) |
F156I |
probably damaging |
Het |
Rpusd3 |
A |
G |
6: 113,392,494 (GRCm39) |
*345Q |
probably null |
Het |
Rrp1b |
A |
G |
17: 32,276,178 (GRCm39) |
K575R |
probably benign |
Het |
Shd |
G |
A |
17: 56,281,307 (GRCm39) |
V250I |
probably damaging |
Het |
Slc12a5 |
C |
A |
2: 164,834,296 (GRCm39) |
N749K |
possibly damaging |
Het |
Sorbs2 |
T |
A |
8: 46,254,021 (GRCm39) |
V488D |
probably damaging |
Het |
Sphkap |
G |
A |
1: 83,255,236 (GRCm39) |
R838* |
probably null |
Het |
Srsf4 |
C |
A |
4: 131,627,871 (GRCm39) |
|
probably benign |
Het |
Strn |
T |
C |
17: 78,999,831 (GRCm39) |
Y135C |
probably damaging |
Het |
Synm |
T |
C |
7: 67,409,376 (GRCm39) |
M1V |
probably null |
Het |
Tas1r3 |
T |
G |
4: 155,946,027 (GRCm39) |
Q489P |
probably benign |
Het |
Tas2r103 |
A |
T |
6: 133,013,774 (GRCm39) |
N97K |
probably damaging |
Het |
Tas2r113 |
A |
G |
6: 132,870,755 (GRCm39) |
Y261C |
possibly damaging |
Het |
Tex21 |
T |
C |
12: 76,268,446 (GRCm39) |
E112G |
probably damaging |
Het |
Trappc8 |
T |
C |
18: 20,966,055 (GRCm39) |
S1128G |
probably damaging |
Het |
Ubap1l |
A |
G |
9: 65,279,025 (GRCm39) |
|
probably benign |
Het |
Ubash3a |
A |
G |
17: 31,434,018 (GRCm39) |
D121G |
probably damaging |
Het |
Ubxn4 |
A |
G |
1: 128,180,023 (GRCm39) |
I56V |
possibly damaging |
Het |
Uri1 |
T |
C |
7: 37,662,949 (GRCm39) |
I348M |
probably damaging |
Het |
Usp21 |
C |
A |
1: 171,111,295 (GRCm39) |
L379F |
probably damaging |
Het |
Vmn1r159 |
T |
A |
7: 22,542,390 (GRCm39) |
H214L |
probably damaging |
Het |
Zdbf2 |
A |
G |
1: 63,341,900 (GRCm39) |
E93G |
unknown |
Het |
|
Other mutations in C7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02458:C7
|
APN |
15 |
5,088,871 (GRCm39) |
splice site |
probably benign |
|
IGL02803:C7
|
APN |
15 |
5,079,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:C7
|
UTSW |
15 |
5,076,406 (GRCm39) |
missense |
probably benign |
0.01 |
R0016:C7
|
UTSW |
15 |
5,076,406 (GRCm39) |
missense |
probably benign |
0.01 |
R0271:C7
|
UTSW |
15 |
5,044,862 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0360:C7
|
UTSW |
15 |
5,018,444 (GRCm39) |
missense |
probably benign |
0.00 |
R0433:C7
|
UTSW |
15 |
5,018,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:C7
|
UTSW |
15 |
5,023,624 (GRCm39) |
splice site |
probably benign |
|
R1056:C7
|
UTSW |
15 |
5,075,260 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1443:C7
|
UTSW |
15 |
5,088,901 (GRCm39) |
missense |
probably benign |
0.01 |
R1468:C7
|
UTSW |
15 |
5,041,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:C7
|
UTSW |
15 |
5,041,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:C7
|
UTSW |
15 |
5,041,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1801:C7
|
UTSW |
15 |
5,041,503 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1809:C7
|
UTSW |
15 |
5,063,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R1986:C7
|
UTSW |
15 |
5,041,494 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2037:C7
|
UTSW |
15 |
5,063,720 (GRCm39) |
nonsense |
probably null |
|
R2047:C7
|
UTSW |
15 |
5,075,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R2073:C7
|
UTSW |
15 |
5,019,910 (GRCm39) |
missense |
probably benign |
0.09 |
R3972:C7
|
UTSW |
15 |
5,037,133 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4080:C7
|
UTSW |
15 |
5,019,946 (GRCm39) |
missense |
probably benign |
0.09 |
R4200:C7
|
UTSW |
15 |
5,019,791 (GRCm39) |
critical splice donor site |
probably null |
|
R4576:C7
|
UTSW |
15 |
5,032,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:C7
|
UTSW |
15 |
5,088,887 (GRCm39) |
missense |
probably benign |
0.16 |
R4995:C7
|
UTSW |
15 |
5,079,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5300:C7
|
UTSW |
15 |
5,061,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R5562:C7
|
UTSW |
15 |
5,061,397 (GRCm39) |
nonsense |
probably null |
|
R5708:C7
|
UTSW |
15 |
5,044,883 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5740:C7
|
UTSW |
15 |
5,086,522 (GRCm39) |
missense |
probably benign |
0.00 |
R5873:C7
|
UTSW |
15 |
5,034,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6222:C7
|
UTSW |
15 |
5,041,423 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6516:C7
|
UTSW |
15 |
5,086,563 (GRCm39) |
missense |
probably damaging |
0.98 |
R6810:C7
|
UTSW |
15 |
5,037,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R7019:C7
|
UTSW |
15 |
5,075,164 (GRCm39) |
missense |
probably benign |
0.04 |
R7199:C7
|
UTSW |
15 |
5,023,725 (GRCm39) |
missense |
probably benign |
0.09 |
R7276:C7
|
UTSW |
15 |
5,041,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:C7
|
UTSW |
15 |
5,041,538 (GRCm39) |
missense |
probably benign |
0.13 |
R7652:C7
|
UTSW |
15 |
5,041,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:C7
|
UTSW |
15 |
5,037,192 (GRCm39) |
missense |
probably benign |
0.08 |
R8266:C7
|
UTSW |
15 |
5,037,141 (GRCm39) |
missense |
probably damaging |
0.99 |
R8295:C7
|
UTSW |
15 |
5,018,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:C7
|
UTSW |
15 |
5,088,911 (GRCm39) |
missense |
probably damaging |
0.96 |
R8951:C7
|
UTSW |
15 |
5,032,231 (GRCm39) |
missense |
probably benign |
0.00 |
R9008:C7
|
UTSW |
15 |
5,040,409 (GRCm39) |
missense |
|
|
R9256:C7
|
UTSW |
15 |
5,023,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:C7
|
UTSW |
15 |
5,044,884 (GRCm39) |
missense |
probably benign |
0.05 |
R9562:C7
|
UTSW |
15 |
5,086,579 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9565:C7
|
UTSW |
15 |
5,086,579 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9655:C7
|
UTSW |
15 |
5,041,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R9757:C7
|
UTSW |
15 |
5,075,134 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:C7
|
UTSW |
15 |
5,044,857 (GRCm39) |
missense |
probably benign |
0.05 |
|