Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts14 |
T |
C |
10: 61,038,619 (GRCm39) |
T964A |
possibly damaging |
Het |
Adamts7 |
G |
A |
9: 90,075,610 (GRCm39) |
W1156* |
probably null |
Het |
Adcy9 |
T |
C |
16: 4,105,992 (GRCm39) |
I1041V |
possibly damaging |
Het |
Armh4 |
T |
C |
14: 50,010,693 (GRCm39) |
D338G |
probably damaging |
Het |
Art4 |
C |
A |
6: 136,831,349 (GRCm39) |
|
probably null |
Het |
Bcl9 |
A |
G |
3: 97,116,334 (GRCm39) |
S787P |
probably benign |
Het |
Bptf |
T |
C |
11: 106,952,590 (GRCm39) |
T2088A |
probably damaging |
Het |
Cdc45 |
T |
C |
16: 18,627,597 (GRCm39) |
N76S |
probably damaging |
Het |
Cdon |
A |
G |
9: 35,389,950 (GRCm39) |
D868G |
probably damaging |
Het |
Cldn10 |
T |
G |
14: 119,092,439 (GRCm39) |
V13G |
probably benign |
Het |
Cnot6 |
G |
T |
11: 49,575,941 (GRCm39) |
Q178K |
probably benign |
Het |
Csgalnact1 |
T |
A |
8: 68,854,105 (GRCm39) |
H232L |
possibly damaging |
Het |
Cuzd1 |
T |
C |
7: 130,910,626 (GRCm39) |
I556M |
possibly damaging |
Het |
Cyp2c54 |
G |
A |
19: 40,026,857 (GRCm39) |
R433W |
probably damaging |
Het |
Cyp2j11 |
A |
G |
4: 96,207,539 (GRCm39) |
F259L |
probably benign |
Het |
Dhx9 |
C |
T |
1: 153,348,922 (GRCm39) |
G264R |
probably damaging |
Het |
Dnah5 |
G |
A |
15: 28,299,245 (GRCm39) |
V1536M |
probably benign |
Het |
Erlin1 |
T |
A |
19: 44,058,041 (GRCm39) |
|
probably benign |
Het |
Foxb2 |
C |
A |
19: 16,850,347 (GRCm39) |
V220L |
possibly damaging |
Het |
Gigyf2 |
A |
T |
1: 87,338,431 (GRCm39) |
T388S |
probably benign |
Het |
Gimap5 |
T |
C |
6: 48,730,068 (GRCm39) |
C213R |
probably benign |
Het |
Gkap1 |
T |
G |
13: 58,386,506 (GRCm39) |
K57N |
probably damaging |
Het |
H60b |
T |
G |
10: 22,159,421 (GRCm39) |
|
probably benign |
Het |
Hectd4 |
C |
T |
5: 121,442,489 (GRCm39) |
R670* |
probably null |
Het |
Hoxc9 |
A |
G |
15: 102,892,341 (GRCm39) |
N185D |
probably damaging |
Het |
Igkv1-117 |
A |
G |
6: 68,098,766 (GRCm39) |
E105G |
possibly damaging |
Het |
Klk10 |
T |
A |
7: 43,432,239 (GRCm39) |
Y57* |
probably null |
Het |
Lrrc63 |
A |
T |
14: 75,363,312 (GRCm39) |
I273K |
possibly damaging |
Het |
M6pr |
T |
C |
6: 122,292,025 (GRCm39) |
I119T |
probably damaging |
Het |
Mael |
T |
C |
1: 166,063,127 (GRCm39) |
|
probably null |
Het |
Magi1 |
A |
G |
6: 93,681,330 (GRCm39) |
S574P |
possibly damaging |
Het |
Man2c1 |
A |
G |
9: 57,044,061 (GRCm39) |
D291G |
probably benign |
Het |
Mapk1ip1l |
A |
T |
14: 47,547,920 (GRCm39) |
|
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,238,132 (GRCm39) |
T1135A |
possibly damaging |
Het |
Mrpl39 |
A |
G |
16: 84,527,736 (GRCm39) |
V164A |
probably benign |
Het |
Mynn |
C |
A |
3: 30,661,290 (GRCm39) |
P124H |
probably damaging |
Het |
Or11l3 |
T |
G |
11: 58,516,800 (GRCm39) |
Q23P |
probably damaging |
Het |
Or14n1-ps1 |
A |
T |
7: 86,093,062 (GRCm39) |
N291I |
probably damaging |
Het |
Or2k2 |
A |
G |
4: 58,785,203 (GRCm39) |
I173T |
probably damaging |
Het |
Or2t48 |
A |
G |
11: 58,420,329 (GRCm39) |
F161S |
possibly damaging |
Het |
Or6k2 |
A |
G |
1: 173,986,614 (GRCm39) |
I92V |
probably damaging |
Het |
Pcif1 |
A |
G |
2: 164,726,303 (GRCm39) |
N68S |
probably damaging |
Het |
Pcm1 |
T |
A |
8: 41,728,976 (GRCm39) |
N649K |
probably damaging |
Het |
Pira1 |
T |
C |
7: 3,740,432 (GRCm39) |
Q263R |
probably benign |
Het |
Plxna2 |
T |
A |
1: 194,476,266 (GRCm39) |
I1162N |
probably damaging |
Het |
Pnp2 |
T |
A |
14: 51,201,842 (GRCm39) |
L276Q |
probably damaging |
Het |
Sirpb1c |
T |
A |
3: 15,902,526 (GRCm39) |
I18F |
possibly damaging |
Het |
Slc2a12 |
A |
T |
10: 22,540,678 (GRCm39) |
M178L |
probably damaging |
Het |
Slc35c1 |
G |
T |
2: 92,285,052 (GRCm39) |
F187L |
probably benign |
Het |
Smg1 |
T |
C |
7: 117,770,982 (GRCm39) |
|
probably benign |
Het |
Spmip6 |
A |
G |
4: 41,505,071 (GRCm39) |
S214P |
possibly damaging |
Het |
Spopfm2 |
T |
C |
3: 94,083,497 (GRCm39) |
M105V |
probably benign |
Het |
Stn1 |
T |
C |
19: 47,490,111 (GRCm39) |
H342R |
probably benign |
Het |
Sult1c2 |
A |
T |
17: 54,276,709 (GRCm39) |
H117Q |
probably damaging |
Het |
Thap1 |
G |
A |
8: 26,650,925 (GRCm39) |
R42K |
probably damaging |
Het |
Tpp2 |
A |
T |
1: 44,016,365 (GRCm39) |
|
probably null |
Het |
Trib2 |
G |
T |
12: 15,865,347 (GRCm39) |
P76Q |
probably damaging |
Het |
Ttc24 |
G |
T |
3: 87,980,369 (GRCm39) |
Q111K |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,143,958 (GRCm39) |
S1401P |
probably damaging |
Het |
Uggt1 |
A |
C |
1: 36,215,724 (GRCm39) |
|
probably null |
Het |
Ugt2b1 |
A |
G |
5: 87,074,326 (GRCm39) |
L11S |
probably damaging |
Het |
Uso1 |
T |
G |
5: 92,343,222 (GRCm39) |
S769A |
probably benign |
Het |
Vmn2r117 |
T |
C |
17: 23,698,442 (GRCm39) |
T44A |
probably benign |
Het |
Vmn2r28 |
T |
A |
7: 5,489,347 (GRCm39) |
L497F |
probably benign |
Het |
Vsig10l |
G |
A |
7: 43,114,326 (GRCm39) |
S318N |
probably benign |
Het |
Wbp4 |
A |
G |
14: 79,714,263 (GRCm39) |
L83P |
probably damaging |
Het |
Wnk1 |
G |
A |
6: 119,927,044 (GRCm39) |
R1510W |
probably damaging |
Het |
Zc3hav1l |
C |
T |
6: 38,272,176 (GRCm39) |
V198M |
probably damaging |
Het |
Zfp1004 |
A |
G |
2: 150,034,700 (GRCm39) |
I340M |
probably benign |
Het |
|
Other mutations in Crot |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00756:Crot
|
APN |
5 |
9,026,072 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01013:Crot
|
APN |
5 |
9,043,575 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01085:Crot
|
APN |
5 |
9,023,955 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02017:Crot
|
APN |
5 |
9,020,046 (GRCm39) |
splice site |
probably benign |
|
IGL02306:Crot
|
APN |
5 |
9,018,701 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02612:Crot
|
APN |
5 |
9,019,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Crot
|
APN |
5 |
9,028,197 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03091:Crot
|
APN |
5 |
9,016,897 (GRCm39) |
missense |
probably benign |
|
IGL03356:Crot
|
APN |
5 |
9,038,295 (GRCm39) |
splice site |
probably benign |
|
ouray
|
UTSW |
5 |
9,043,504 (GRCm39) |
critical splice donor site |
probably null |
|
R0383:Crot
|
UTSW |
5 |
9,018,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Crot
|
UTSW |
5 |
9,019,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R0502:Crot
|
UTSW |
5 |
9,026,075 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0503:Crot
|
UTSW |
5 |
9,026,075 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0676:Crot
|
UTSW |
5 |
9,043,622 (GRCm39) |
utr 5 prime |
probably benign |
|
R1079:Crot
|
UTSW |
5 |
9,043,504 (GRCm39) |
critical splice donor site |
probably null |
|
R1472:Crot
|
UTSW |
5 |
9,016,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Crot
|
UTSW |
5 |
9,024,186 (GRCm39) |
missense |
probably benign |
0.00 |
R1757:Crot
|
UTSW |
5 |
9,037,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R1828:Crot
|
UTSW |
5 |
9,019,080 (GRCm39) |
missense |
probably benign |
0.01 |
R1846:Crot
|
UTSW |
5 |
9,038,248 (GRCm39) |
missense |
probably benign |
0.36 |
R2142:Crot
|
UTSW |
5 |
9,037,780 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3973:Crot
|
UTSW |
5 |
9,027,541 (GRCm39) |
missense |
probably benign |
|
R3974:Crot
|
UTSW |
5 |
9,027,541 (GRCm39) |
missense |
probably benign |
|
R3975:Crot
|
UTSW |
5 |
9,027,541 (GRCm39) |
missense |
probably benign |
|
R4445:Crot
|
UTSW |
5 |
9,023,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R4446:Crot
|
UTSW |
5 |
9,023,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Crot
|
UTSW |
5 |
9,024,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R5084:Crot
|
UTSW |
5 |
9,019,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R5464:Crot
|
UTSW |
5 |
9,033,690 (GRCm39) |
splice site |
probably null |
|
R5673:Crot
|
UTSW |
5 |
9,038,131 (GRCm39) |
missense |
probably benign |
0.00 |
R5814:Crot
|
UTSW |
5 |
9,023,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R5935:Crot
|
UTSW |
5 |
9,024,192 (GRCm39) |
missense |
probably benign |
|
R5951:Crot
|
UTSW |
5 |
9,019,120 (GRCm39) |
nonsense |
probably null |
|
R6862:Crot
|
UTSW |
5 |
9,039,641 (GRCm39) |
missense |
probably damaging |
0.99 |
R6885:Crot
|
UTSW |
5 |
9,023,635 (GRCm39) |
missense |
probably benign |
0.00 |
R6983:Crot
|
UTSW |
5 |
9,028,280 (GRCm39) |
missense |
probably benign |
0.06 |
R7150:Crot
|
UTSW |
5 |
9,037,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R7228:Crot
|
UTSW |
5 |
9,026,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Crot
|
UTSW |
5 |
9,027,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7662:Crot
|
UTSW |
5 |
9,019,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R7747:Crot
|
UTSW |
5 |
9,018,869 (GRCm39) |
critical splice donor site |
probably null |
|
R8002:Crot
|
UTSW |
5 |
9,043,599 (GRCm39) |
missense |
probably benign |
0.36 |
R8105:Crot
|
UTSW |
5 |
9,027,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R8233:Crot
|
UTSW |
5 |
9,026,027 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8474:Crot
|
UTSW |
5 |
9,043,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R8734:Crot
|
UTSW |
5 |
9,028,208 (GRCm39) |
missense |
probably benign |
0.02 |
R9528:Crot
|
UTSW |
5 |
9,043,575 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9649:Crot
|
UTSW |
5 |
9,024,170 (GRCm39) |
missense |
probably benign |
0.03 |
|