Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
G |
17: 24,484,507 (GRCm39) |
H1585P |
probably damaging |
Het |
Acaca |
A |
T |
11: 84,167,414 (GRCm39) |
T1063S |
probably benign |
Het |
Actc1 |
T |
A |
2: 113,880,967 (GRCm39) |
K86M |
probably damaging |
Het |
Amz1 |
A |
G |
5: 140,727,190 (GRCm39) |
N51S |
probably benign |
Het |
Arhgap33 |
G |
A |
7: 30,222,648 (GRCm39) |
P1095S |
probably benign |
Het |
Bicra |
T |
C |
7: 15,722,447 (GRCm39) |
T357A |
probably benign |
Het |
C130032M10Rik |
A |
G |
9: 114,345,123 (GRCm39) |
R120G |
unknown |
Het |
Cadps |
A |
G |
14: 12,705,544 (GRCm38) |
F284L |
possibly damaging |
Het |
Ccdc83 |
G |
A |
7: 89,893,290 (GRCm39) |
Q156* |
probably null |
Het |
Cdh20 |
T |
A |
1: 104,861,898 (GRCm39) |
M26K |
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,143,668 (GRCm39) |
L2979P |
probably damaging |
Het |
Cdhr17 |
A |
G |
5: 17,032,012 (GRCm39) |
N556D |
probably benign |
Het |
Crocc2 |
T |
C |
1: 93,141,363 (GRCm39) |
L1172P |
probably damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,288,628 (GRCm39) |
|
probably null |
Het |
Cyp2j9 |
T |
A |
4: 96,479,621 (GRCm39) |
|
probably benign |
Het |
Dgcr2 |
A |
G |
16: 17,677,266 (GRCm39) |
|
probably null |
Het |
Dio3 |
A |
G |
12: 110,246,473 (GRCm39) |
M270V |
|
Het |
Dll1 |
C |
A |
17: 15,588,690 (GRCm39) |
D662Y |
probably damaging |
Het |
Drd1 |
G |
T |
13: 54,207,834 (GRCm39) |
P127T |
probably damaging |
Het |
Evc2 |
T |
C |
5: 37,544,206 (GRCm39) |
S652P |
probably damaging |
Het |
Fam149a |
C |
A |
8: 45,794,280 (GRCm39) |
M708I |
probably benign |
Het |
Fam89a |
T |
C |
8: 125,467,895 (GRCm39) |
E139G |
probably damaging |
Het |
Gpr141 |
T |
C |
13: 19,936,729 (GRCm39) |
I15M |
probably benign |
Het |
Hcn4 |
G |
A |
9: 58,731,218 (GRCm39) |
E142K |
unknown |
Het |
Hivep3 |
T |
A |
4: 119,954,962 (GRCm39) |
S1093T |
possibly damaging |
Het |
Inpp5f |
C |
A |
7: 128,269,433 (GRCm39) |
T261K |
probably benign |
Het |
Ints3 |
A |
T |
3: 90,340,132 (GRCm39) |
D42E |
probably benign |
Het |
Krt90 |
A |
T |
15: 101,466,838 (GRCm39) |
|
probably null |
Het |
Kti12 |
A |
C |
4: 108,705,443 (GRCm39) |
E119A |
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,444 (GRCm39) |
E119D |
probably benign |
Het |
Lrig1 |
C |
A |
6: 94,607,082 (GRCm39) |
|
probably null |
Het |
Mapk14 |
A |
G |
17: 28,947,928 (GRCm39) |
T221A |
probably benign |
Het |
Megf10 |
A |
T |
18: 57,373,807 (GRCm39) |
T202S |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,838,264 (GRCm39) |
F507I |
probably benign |
Het |
Or7a35 |
A |
G |
10: 78,853,264 (GRCm39) |
Y36C |
probably damaging |
Het |
Or8b48 |
A |
T |
9: 38,492,969 (GRCm39) |
Y132F |
probably damaging |
Het |
Or8k37 |
T |
A |
2: 86,469,110 (GRCm39) |
*314L |
probably null |
Het |
Peg10 |
T |
TCCA |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,811,630 (GRCm39) |
Y3724* |
probably null |
Het |
Plxnd1 |
T |
C |
6: 115,943,879 (GRCm39) |
D1140G |
probably benign |
Het |
Pramel22 |
T |
C |
4: 143,382,315 (GRCm39) |
K127R |
possibly damaging |
Het |
Prex1 |
A |
G |
2: 166,463,112 (GRCm39) |
S250P |
probably damaging |
Het |
Prom1 |
A |
T |
5: 44,162,277 (GRCm39) |
M777K |
possibly damaging |
Het |
Prrc2c |
A |
C |
1: 162,519,977 (GRCm39) |
S2125A |
probably benign |
Het |
Ptpn12 |
A |
G |
5: 21,214,449 (GRCm39) |
I229T |
probably damaging |
Het |
Ranbp6 |
A |
G |
19: 29,790,073 (GRCm39) |
V93A |
probably benign |
Het |
Sis |
A |
C |
3: 72,828,471 (GRCm39) |
H1201Q |
probably damaging |
Het |
Slc20a1 |
G |
A |
2: 129,049,757 (GRCm39) |
D340N |
probably benign |
Het |
Slc3a2 |
G |
A |
19: 8,685,182 (GRCm39) |
R535W |
probably damaging |
Het |
Slc5a2 |
T |
A |
7: 127,864,966 (GRCm39) |
L33Q |
probably damaging |
Het |
Sltm |
G |
T |
9: 70,494,431 (GRCm39) |
R927L |
probably damaging |
Het |
Spaca7b |
T |
C |
8: 11,728,645 (GRCm39) |
T9A |
possibly damaging |
Het |
Stat1 |
A |
G |
1: 52,190,440 (GRCm39) |
D565G |
probably benign |
Het |
Terb1 |
T |
C |
8: 105,173,848 (GRCm39) |
K745R |
possibly damaging |
Het |
Tescl |
T |
C |
7: 24,033,113 (GRCm39) |
I71V |
probably damaging |
Het |
Tgm1 |
T |
C |
14: 55,937,883 (GRCm39) |
D742G |
probably damaging |
Het |
Tmem128 |
T |
A |
5: 38,423,875 (GRCm39) |
W30R |
probably benign |
Het |
Tox |
T |
A |
4: 6,822,949 (GRCm39) |
M123L |
probably benign |
Het |
Tsnaxip1 |
A |
G |
8: 106,569,413 (GRCm39) |
S547G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,567,539 (GRCm39) |
K27785* |
probably null |
Het |
Tut7 |
T |
C |
13: 59,932,628 (GRCm39) |
I1345V |
probably benign |
Het |
Usp38 |
A |
C |
8: 81,727,712 (GRCm39) |
S340R |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,340,956 (GRCm39) |
H2840Q |
probably damaging |
Het |
Vars2 |
T |
C |
17: 35,975,731 (GRCm39) |
I229V |
probably damaging |
Het |
Vmn1r16 |
A |
T |
6: 57,300,380 (GRCm39) |
Y81N |
probably damaging |
Het |
Vmn2r98 |
A |
T |
17: 19,287,493 (GRCm39) |
D442V |
probably benign |
Het |
Vps13d |
T |
C |
4: 144,813,389 (GRCm39) |
I3296V |
|
Het |
Wwtr1 |
A |
G |
3: 57,483,020 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rtn3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00791:Rtn3
|
APN |
19 |
7,412,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01025:Rtn3
|
APN |
19 |
7,460,406 (GRCm39) |
missense |
unknown |
|
IGL01347:Rtn3
|
APN |
19 |
7,434,645 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01845:Rtn3
|
APN |
19 |
7,435,241 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02217:Rtn3
|
APN |
19 |
7,412,449 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03024:Rtn3
|
APN |
19 |
7,460,455 (GRCm39) |
utr 5 prime |
probably benign |
|
R0399:Rtn3
|
UTSW |
19 |
7,435,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0633:Rtn3
|
UTSW |
19 |
7,434,958 (GRCm39) |
missense |
probably benign |
0.03 |
R0826:Rtn3
|
UTSW |
19 |
7,445,245 (GRCm39) |
intron |
probably benign |
|
R1327:Rtn3
|
UTSW |
19 |
7,408,376 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1735:Rtn3
|
UTSW |
19 |
7,435,276 (GRCm39) |
missense |
probably damaging |
0.96 |
R2093:Rtn3
|
UTSW |
19 |
7,434,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Rtn3
|
UTSW |
19 |
7,409,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R3894:Rtn3
|
UTSW |
19 |
7,412,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R3961:Rtn3
|
UTSW |
19 |
7,435,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R3962:Rtn3
|
UTSW |
19 |
7,435,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R3963:Rtn3
|
UTSW |
19 |
7,435,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R4161:Rtn3
|
UTSW |
19 |
7,460,444 (GRCm39) |
missense |
probably benign |
0.38 |
R4960:Rtn3
|
UTSW |
19 |
7,433,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Rtn3
|
UTSW |
19 |
7,435,560 (GRCm39) |
missense |
probably benign |
0.12 |
R5735:Rtn3
|
UTSW |
19 |
7,434,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R5796:Rtn3
|
UTSW |
19 |
7,434,832 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5807:Rtn3
|
UTSW |
19 |
7,434,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Rtn3
|
UTSW |
19 |
7,412,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R6322:Rtn3
|
UTSW |
19 |
7,435,503 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6703:Rtn3
|
UTSW |
19 |
7,412,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R6885:Rtn3
|
UTSW |
19 |
7,435,696 (GRCm39) |
missense |
probably benign |
0.31 |
R6888:Rtn3
|
UTSW |
19 |
7,434,614 (GRCm39) |
missense |
probably benign |
0.00 |
R6989:Rtn3
|
UTSW |
19 |
7,433,856 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6992:Rtn3
|
UTSW |
19 |
7,412,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7506:Rtn3
|
UTSW |
19 |
7,407,118 (GRCm39) |
missense |
probably benign |
0.08 |
R7610:Rtn3
|
UTSW |
19 |
7,435,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R7639:Rtn3
|
UTSW |
19 |
7,435,356 (GRCm39) |
missense |
probably benign |
0.01 |
R7909:Rtn3
|
UTSW |
19 |
7,433,827 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8088:Rtn3
|
UTSW |
19 |
7,412,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R8549:Rtn3
|
UTSW |
19 |
7,434,624 (GRCm39) |
missense |
probably benign |
0.03 |
R8725:Rtn3
|
UTSW |
19 |
7,434,726 (GRCm39) |
missense |
probably benign |
|
R8727:Rtn3
|
UTSW |
19 |
7,434,726 (GRCm39) |
missense |
probably benign |
|
R8917:Rtn3
|
UTSW |
19 |
7,434,105 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9225:Rtn3
|
UTSW |
19 |
7,434,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Rtn3
|
UTSW |
19 |
7,460,328 (GRCm39) |
missense |
unknown |
|
X0060:Rtn3
|
UTSW |
19 |
7,409,936 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1192:Rtn3
|
UTSW |
19 |
7,460,342 (GRCm39) |
missense |
unknown |
|
|