Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts19 |
T |
G |
18: 59,165,001 (GRCm39) |
C1034W |
probably damaging |
Het |
Agbl2 |
G |
T |
2: 90,641,089 (GRCm39) |
K737N |
probably damaging |
Het |
Aqp9 |
T |
A |
9: 71,019,624 (GRCm39) |
I279F |
possibly damaging |
Het |
Aspm |
T |
A |
1: 139,384,855 (GRCm39) |
N166K |
probably benign |
Het |
Atp13a3 |
A |
T |
16: 30,176,084 (GRCm39) |
I186N |
probably benign |
Het |
Btaf1 |
A |
T |
19: 36,972,362 (GRCm39) |
I1366L |
probably benign |
Het |
Camk4 |
A |
C |
18: 33,211,074 (GRCm39) |
K60Q |
possibly damaging |
Het |
Card11 |
G |
T |
5: 140,892,388 (GRCm39) |
Q226K |
possibly damaging |
Het |
Ccdc187 |
T |
C |
2: 26,183,670 (GRCm39) |
D110G |
possibly damaging |
Het |
Col5a2 |
C |
T |
1: 45,446,192 (GRCm39) |
R462Q |
possibly damaging |
Het |
Cp |
A |
T |
3: 20,022,383 (GRCm39) |
|
probably benign |
Het |
Cpz |
A |
T |
5: 35,675,102 (GRCm39) |
V38E |
probably damaging |
Het |
Cxcr6 |
G |
A |
9: 123,639,181 (GRCm39) |
V68I |
probably damaging |
Het |
Cyp2a22 |
C |
A |
7: 26,634,187 (GRCm39) |
E322D |
possibly damaging |
Het |
D130052B06Rik |
C |
T |
11: 33,573,784 (GRCm39) |
T127I |
probably benign |
Het |
Daam2 |
T |
A |
17: 49,797,231 (GRCm39) |
M185L |
possibly damaging |
Het |
Dnaja3 |
G |
A |
16: 4,502,029 (GRCm39) |
R11K |
probably null |
Het |
Dnttip2 |
T |
A |
3: 122,070,397 (GRCm39) |
S537R |
probably benign |
Het |
Dock9 |
G |
T |
14: 121,864,292 (GRCm39) |
H572Q |
probably benign |
Het |
Dpp4 |
T |
A |
2: 62,203,213 (GRCm39) |
|
probably null |
Het |
Enc1 |
T |
G |
13: 97,381,550 (GRCm39) |
I20S |
possibly damaging |
Het |
Ephb6 |
T |
A |
6: 41,596,654 (GRCm39) |
H900Q |
probably benign |
Het |
Ercc3 |
T |
C |
18: 32,400,218 (GRCm39) |
V690A |
possibly damaging |
Het |
Fam90a1a |
C |
T |
8: 22,453,385 (GRCm39) |
Q247* |
probably null |
Het |
Fkbp10 |
G |
A |
11: 100,314,757 (GRCm39) |
R423H |
probably benign |
Het |
Fus |
A |
G |
7: 127,580,717 (GRCm39) |
M265V |
probably benign |
Het |
Gas2l3 |
T |
A |
10: 89,250,127 (GRCm39) |
K330N |
probably damaging |
Het |
Gpam |
T |
G |
19: 55,069,901 (GRCm39) |
L410F |
probably damaging |
Het |
Gpr37l1 |
A |
T |
1: 135,089,273 (GRCm39) |
V264E |
possibly damaging |
Het |
Gsto1 |
G |
T |
19: 47,843,674 (GRCm39) |
V19F |
probably damaging |
Het |
H1f7 |
G |
T |
15: 98,154,016 (GRCm39) |
Q378K |
unknown |
Het |
Hgfac |
G |
A |
5: 35,201,018 (GRCm39) |
C194Y |
probably damaging |
Het |
Hivep1 |
A |
G |
13: 42,311,407 (GRCm39) |
N1216D |
probably damaging |
Het |
Hrg |
C |
T |
16: 22,769,997 (GRCm39) |
A42V |
probably damaging |
Het |
Irx4 |
A |
G |
13: 73,414,824 (GRCm39) |
D136G |
probably benign |
Het |
Kcnn3 |
G |
T |
3: 89,559,397 (GRCm39) |
V556L |
probably benign |
Het |
Klk1b8 |
T |
C |
7: 43,451,545 (GRCm39) |
Y179H |
possibly damaging |
Het |
Klrb1f |
T |
A |
6: 129,031,322 (GRCm39) |
L173* |
probably null |
Het |
Kremen2 |
A |
T |
17: 23,962,373 (GRCm39) |
|
probably null |
Het |
Krt25 |
A |
T |
11: 99,207,378 (GRCm39) |
Y400* |
probably null |
Het |
Lingo4 |
A |
T |
3: 94,310,485 (GRCm39) |
R474S |
probably benign |
Het |
Lnpep |
T |
C |
17: 17,773,575 (GRCm39) |
K599E |
probably benign |
Het |
Mapk8ip3 |
A |
T |
17: 25,155,824 (GRCm39) |
M2K |
possibly damaging |
Het |
Mat2b |
A |
T |
11: 40,570,904 (GRCm39) |
S307T |
probably benign |
Het |
Mcph1 |
C |
A |
8: 18,681,979 (GRCm39) |
A372D |
probably benign |
Het |
Mfsd6 |
T |
A |
1: 52,748,524 (GRCm39) |
I114F |
probably damaging |
Het |
Mlkl |
A |
G |
8: 112,049,380 (GRCm39) |
S248P |
probably damaging |
Het |
Mmrn1 |
A |
T |
6: 60,954,085 (GRCm39) |
T789S |
probably benign |
Het |
Mphosph8 |
A |
G |
14: 56,930,916 (GRCm39) |
Y735C |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,261,910 (GRCm39) |
Y300N |
probably damaging |
Het |
Mrps11 |
A |
G |
7: 78,442,460 (GRCm39) |
H180R |
probably damaging |
Het |
Msh4 |
T |
C |
3: 153,573,404 (GRCm39) |
D556G |
probably damaging |
Het |
Myh10 |
C |
A |
11: 68,693,122 (GRCm39) |
D1472E |
probably benign |
Het |
Myo16 |
T |
C |
8: 10,492,283 (GRCm39) |
S742P |
probably damaging |
Het |
Nlrp5-ps |
C |
T |
7: 14,316,978 (GRCm39) |
|
noncoding transcript |
Het |
Nrp1 |
C |
T |
8: 129,194,974 (GRCm39) |
P477S |
probably benign |
Het |
Oplah |
G |
T |
15: 76,186,683 (GRCm39) |
C665* |
probably null |
Het |
Or4f14b |
T |
A |
2: 111,775,625 (GRCm39) |
M59L |
probably benign |
Het |
Or4f54 |
T |
C |
2: 111,123,210 (GRCm39) |
V199A |
probably damaging |
Het |
Or51b17 |
T |
C |
7: 103,542,118 (GRCm39) |
S275G |
probably benign |
Het |
Or8g22 |
G |
T |
9: 38,958,678 (GRCm39) |
H57N |
unknown |
Het |
Otogl |
T |
C |
10: 107,619,573 (GRCm39) |
T1696A |
possibly damaging |
Het |
Pdzrn4 |
A |
G |
15: 92,299,855 (GRCm39) |
I242V |
probably benign |
Het |
Phgdh |
G |
A |
3: 98,235,451 (GRCm39) |
T141I |
probably benign |
Het |
Pigv |
T |
C |
4: 133,392,237 (GRCm39) |
Y311C |
probably damaging |
Het |
Pik3c2a |
T |
G |
7: 116,017,755 (GRCm39) |
M1L |
possibly damaging |
Het |
Pitpnm1 |
A |
T |
19: 4,159,960 (GRCm39) |
K760* |
probably null |
Het |
Pnrc1 |
G |
A |
4: 33,246,438 (GRCm39) |
H174Y |
probably damaging |
Het |
Ptgis |
A |
G |
2: 167,033,888 (GRCm39) |
|
probably benign |
Het |
Ptpn4 |
T |
C |
1: 119,643,773 (GRCm39) |
|
probably null |
Het |
Rin3 |
T |
A |
12: 102,335,589 (GRCm39) |
L420* |
probably null |
Het |
Sacs |
T |
G |
14: 61,442,903 (GRCm39) |
F1650V |
probably damaging |
Het |
Sbno2 |
T |
A |
10: 79,894,342 (GRCm39) |
N1081Y |
possibly damaging |
Het |
Sema5b |
C |
T |
16: 35,466,737 (GRCm39) |
P213L |
probably damaging |
Het |
Sharpin |
T |
C |
15: 76,232,136 (GRCm39) |
K240R |
probably benign |
Het |
Skint6 |
T |
A |
4: 113,034,234 (GRCm39) |
|
probably benign |
Het |
Slc4a2 |
A |
G |
5: 24,634,565 (GRCm39) |
E68G |
probably damaging |
Het |
Srcin1 |
C |
T |
11: 97,424,327 (GRCm39) |
V634I |
probably benign |
Het |
Srsf10 |
T |
A |
4: 135,590,476 (GRCm39) |
F134I |
possibly damaging |
Het |
Stab1 |
C |
A |
14: 30,867,260 (GRCm39) |
G1700V |
probably damaging |
Het |
Sun1 |
T |
G |
5: 139,216,544 (GRCm39) |
C290W |
possibly damaging |
Het |
Svs6 |
T |
A |
2: 164,159,577 (GRCm39) |
|
probably benign |
Het |
Tmem8b |
G |
A |
4: 43,690,228 (GRCm39) |
|
probably null |
Het |
Usp49 |
A |
G |
17: 47,983,238 (GRCm39) |
D81G |
probably damaging |
Het |
Vmn1r215 |
T |
A |
13: 23,260,848 (GRCm39) |
V296D |
probably benign |
Het |
Vmn1r6 |
T |
A |
6: 56,979,607 (GRCm39) |
S90T |
probably damaging |
Het |
Wbp2 |
A |
G |
11: 115,974,709 (GRCm39) |
F42L |
probably benign |
Het |
Wdr20rt |
C |
T |
12: 65,274,055 (GRCm39) |
T333I |
possibly damaging |
Het |
Zfp341 |
C |
T |
2: 154,483,298 (GRCm39) |
A552V |
probably benign |
Het |
Zfp607b |
A |
T |
7: 27,391,949 (GRCm39) |
H8L |
possibly damaging |
Het |
Zfp758 |
G |
T |
17: 22,594,830 (GRCm39) |
D439Y |
probably damaging |
Het |
Zfp946 |
T |
C |
17: 22,672,538 (GRCm39) |
Y46H |
probably damaging |
Het |
Zic2 |
G |
A |
14: 122,716,359 (GRCm39) |
E432K |
probably damaging |
Het |
|
Other mutations in Grk6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01733:Grk6
|
APN |
13 |
55,599,204 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02054:Grk6
|
APN |
13 |
55,602,210 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02156:Grk6
|
APN |
13 |
55,597,174 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02442:Grk6
|
APN |
13 |
55,606,750 (GRCm39) |
splice site |
probably benign |
|
IGL02750:Grk6
|
APN |
13 |
55,599,356 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03340:Grk6
|
APN |
13 |
55,601,003 (GRCm39) |
missense |
probably damaging |
1.00 |
Damper
|
UTSW |
13 |
55,606,733 (GRCm39) |
missense |
probably damaging |
1.00 |
Piano
|
UTSW |
13 |
55,602,340 (GRCm39) |
critical splice donor site |
probably null |
|
R0080:Grk6
|
UTSW |
13 |
55,606,723 (GRCm39) |
missense |
probably benign |
0.00 |
R1077:Grk6
|
UTSW |
13 |
55,602,340 (GRCm39) |
critical splice donor site |
probably null |
|
R1530:Grk6
|
UTSW |
13 |
55,606,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R1531:Grk6
|
UTSW |
13 |
55,599,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Grk6
|
UTSW |
13 |
55,599,591 (GRCm39) |
nonsense |
probably null |
|
R1874:Grk6
|
UTSW |
13 |
55,598,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Grk6
|
UTSW |
13 |
55,602,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R2875:Grk6
|
UTSW |
13 |
55,600,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R5187:Grk6
|
UTSW |
13 |
55,599,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R7010:Grk6
|
UTSW |
13 |
55,598,113 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7104:Grk6
|
UTSW |
13 |
55,602,219 (GRCm39) |
missense |
probably benign |
0.36 |
R7111:Grk6
|
UTSW |
13 |
55,606,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7769:Grk6
|
UTSW |
13 |
55,598,820 (GRCm39) |
missense |
probably benign |
0.01 |
R7982:Grk6
|
UTSW |
13 |
55,599,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8401:Grk6
|
UTSW |
13 |
55,599,981 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8468:Grk6
|
UTSW |
13 |
55,599,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Grk6
|
UTSW |
13 |
55,606,877 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9731:Grk6
|
UTSW |
13 |
55,607,640 (GRCm39) |
missense |
possibly damaging |
0.71 |
|