Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
A |
G |
6: 91,905,707 (GRCm39) |
T493A |
probably damaging |
Het |
Aars1 |
A |
G |
8: 111,776,493 (GRCm39) |
K650E |
probably benign |
Het |
Abcb1b |
C |
T |
5: 8,882,258 (GRCm39) |
S793F |
probably benign |
Het |
Adamts18 |
T |
A |
8: 114,501,908 (GRCm39) |
I318F |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,571,322 (GRCm39) |
I1137T |
probably damaging |
Het |
Ambra1 |
T |
A |
2: 91,603,838 (GRCm39) |
F607L |
probably benign |
Het |
Ankrd46 |
A |
T |
15: 36,479,566 (GRCm39) |
V175D |
possibly damaging |
Het |
Arhgap28 |
C |
A |
17: 68,208,277 (GRCm39) |
E114* |
probably null |
Het |
Arrdc1 |
C |
T |
2: 24,816,158 (GRCm39) |
G282S |
probably damaging |
Het |
Atp1a3 |
A |
T |
7: 24,681,216 (GRCm39) |
L790Q |
probably damaging |
Het |
Bend5 |
T |
A |
4: 111,272,406 (GRCm39) |
V12D |
probably damaging |
Het |
Bod1l |
C |
T |
5: 41,976,608 (GRCm39) |
E1569K |
probably damaging |
Het |
Cdc123 |
T |
A |
2: 5,808,775 (GRCm39) |
I234L |
probably benign |
Het |
Cep126 |
T |
G |
9: 8,120,749 (GRCm39) |
E91D |
probably damaging |
Het |
Cep89 |
T |
A |
7: 35,113,570 (GRCm39) |
D199E |
possibly damaging |
Het |
Ces1d |
T |
C |
8: 93,897,765 (GRCm39) |
T442A |
probably benign |
Het |
Chsy3 |
C |
T |
18: 59,542,299 (GRCm39) |
A479V |
probably benign |
Het |
Clcn4 |
C |
A |
7: 7,296,060 (GRCm39) |
G261C |
probably damaging |
Het |
Clhc1 |
A |
T |
11: 29,507,651 (GRCm39) |
|
probably null |
Het |
Cnot3 |
T |
A |
7: 3,658,565 (GRCm39) |
|
probably null |
Het |
Col9a1 |
C |
A |
1: 24,276,261 (GRCm39) |
P723H |
probably damaging |
Het |
Crybg3 |
A |
T |
16: 59,375,605 (GRCm39) |
M169K |
probably benign |
Het |
Cxxc4 |
A |
G |
3: 133,963,814 (GRCm39) |
R353G |
probably benign |
Het |
Dennd3 |
A |
T |
15: 73,412,657 (GRCm39) |
I440F |
probably damaging |
Het |
Dnai3 |
A |
G |
3: 145,772,675 (GRCm39) |
L457P |
probably damaging |
Het |
Elmo3 |
G |
T |
8: 106,035,649 (GRCm39) |
S553I |
probably damaging |
Het |
Elovl2 |
A |
G |
13: 41,340,943 (GRCm39) |
Y198H |
probably benign |
Het |
Epm2aip1 |
A |
G |
9: 111,101,105 (GRCm39) |
Y26C |
probably damaging |
Het |
Ext1 |
A |
C |
15: 52,953,335 (GRCm39) |
C510G |
possibly damaging |
Het |
Extl3 |
A |
T |
14: 65,314,938 (GRCm39) |
D81E |
probably benign |
Het |
Fbxl5 |
T |
A |
5: 43,916,018 (GRCm39) |
T465S |
probably benign |
Het |
Fbxo31 |
G |
A |
8: 122,291,384 (GRCm39) |
|
probably null |
Het |
Gabrr2 |
A |
T |
4: 33,081,470 (GRCm39) |
K169* |
probably null |
Het |
Haus4 |
A |
G |
14: 54,779,602 (GRCm39) |
Y341H |
probably damaging |
Het |
Itgae |
A |
T |
11: 73,011,099 (GRCm39) |
|
probably null |
Het |
Jmjd7 |
C |
T |
2: 119,860,996 (GRCm39) |
H149Y |
possibly damaging |
Het |
Kcnh2 |
C |
T |
5: 24,529,561 (GRCm39) |
C725Y |
probably damaging |
Het |
Ms4a14 |
A |
G |
19: 11,280,308 (GRCm39) |
F750S |
probably benign |
Het |
Naf1 |
T |
A |
8: 67,313,165 (GRCm39) |
D49E |
unknown |
Het |
Notch3 |
T |
C |
17: 32,341,747 (GRCm39) |
T2002A |
possibly damaging |
Het |
Or10q12 |
T |
A |
19: 13,745,716 (GRCm39) |
D3E |
probably benign |
Het |
Or14c44 |
A |
G |
7: 86,057,119 (GRCm39) |
|
probably benign |
Het |
Or1e33 |
A |
T |
11: 73,738,333 (GRCm39) |
I206N |
probably benign |
Het |
Or2d3c |
A |
T |
7: 106,525,777 (GRCm39) |
D296E |
probably benign |
Het |
Or2l13b |
A |
T |
16: 19,349,167 (GRCm39) |
C168S |
probably damaging |
Het |
Or7e175 |
A |
T |
9: 20,048,871 (GRCm39) |
N153I |
probably benign |
Het |
Or9s23 |
G |
A |
1: 92,501,810 (GRCm39) |
D306N |
probably benign |
Het |
Pck1 |
A |
G |
2: 172,997,743 (GRCm39) |
T271A |
possibly damaging |
Het |
Penk |
A |
G |
4: 4,133,976 (GRCm39) |
W224R |
possibly damaging |
Het |
Per2 |
C |
A |
1: 91,372,481 (GRCm39) |
V198F |
probably damaging |
Het |
Phf11d |
A |
G |
14: 59,599,280 (GRCm39) |
M23T |
probably damaging |
Het |
Pla2g4d |
A |
G |
2: 120,097,211 (GRCm39) |
V796A |
probably benign |
Het |
Pramel51 |
A |
T |
12: 88,143,122 (GRCm39) |
N360K |
possibly damaging |
Het |
Prdx6 |
A |
T |
1: 161,069,428 (GRCm39) |
|
probably null |
Het |
Prep |
A |
T |
10: 44,967,108 (GRCm39) |
N47I |
probably damaging |
Het |
Prodh2 |
A |
T |
7: 30,212,064 (GRCm39) |
|
probably null |
Het |
Prss38 |
G |
T |
11: 59,265,996 (GRCm39) |
H96N |
probably damaging |
Het |
Rab11a |
C |
A |
9: 64,635,613 (GRCm39) |
E47* |
probably null |
Het |
Rad18 |
C |
T |
6: 112,626,798 (GRCm39) |
G369D |
probably benign |
Het |
Rragc |
T |
C |
4: 123,823,717 (GRCm39) |
V330A |
probably damaging |
Het |
Serpina9 |
A |
T |
12: 103,967,680 (GRCm39) |
H238Q |
probably benign |
Het |
Serpinb3b |
T |
A |
1: 107,085,467 (GRCm39) |
K91N |
probably damaging |
Het |
Slc16a12 |
T |
G |
19: 34,652,730 (GRCm39) |
S139R |
probably benign |
Het |
Slc22a27 |
T |
A |
19: 7,887,472 (GRCm39) |
|
probably null |
Het |
Slc25a11 |
A |
G |
11: 70,536,005 (GRCm39) |
V243A |
probably benign |
Het |
Slc38a9 |
A |
T |
13: 112,868,148 (GRCm39) |
I545F |
probably benign |
Het |
Slc39a8 |
A |
T |
3: 135,590,157 (GRCm39) |
H349L |
probably damaging |
Het |
Slk |
C |
T |
19: 47,630,510 (GRCm39) |
T1227I |
possibly damaging |
Het |
Spdye4b |
A |
G |
5: 143,180,609 (GRCm39) |
E25G |
possibly damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
St3gal1 |
A |
G |
15: 66,983,114 (GRCm39) |
V214A |
probably benign |
Het |
St7l |
T |
A |
3: 104,833,893 (GRCm39) |
M550K |
probably benign |
Het |
Tbk1 |
A |
C |
10: 121,388,151 (GRCm39) |
F638C |
possibly damaging |
Het |
Tex101 |
A |
T |
7: 24,369,190 (GRCm39) |
C114S |
probably damaging |
Het |
Ttll13 |
A |
G |
7: 79,905,135 (GRCm39) |
M384V |
probably benign |
Het |
Ugt2b37 |
A |
T |
5: 87,402,189 (GRCm39) |
D147E |
probably damaging |
Het |
Vmn1r10 |
A |
T |
6: 57,090,686 (GRCm39) |
T93S |
probably benign |
Het |
Wasl |
G |
A |
6: 24,619,396 (GRCm39) |
P375S |
unknown |
Het |
Zfp236 |
C |
A |
18: 82,692,481 (GRCm39) |
E165* |
probably null |
Het |
Zfp839 |
A |
T |
12: 110,822,060 (GRCm39) |
R291S |
probably damaging |
Het |
|
Other mutations in Mroh1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01574:Mroh1
|
APN |
15 |
76,316,488 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02141:Mroh1
|
APN |
15 |
76,330,799 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02146:Mroh1
|
APN |
15 |
76,318,879 (GRCm39) |
splice site |
probably benign |
|
IGL02205:Mroh1
|
APN |
15 |
76,321,439 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02261:Mroh1
|
APN |
15 |
76,313,360 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02818:Mroh1
|
APN |
15 |
76,316,601 (GRCm39) |
splice site |
probably null |
|
IGL02949:Mroh1
|
APN |
15 |
76,293,168 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02951:Mroh1
|
APN |
15 |
76,311,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Mroh1
|
APN |
15 |
76,337,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Mroh1
|
UTSW |
15 |
76,276,661 (GRCm39) |
critical splice donor site |
probably null |
|
R0068:Mroh1
|
UTSW |
15 |
76,330,892 (GRCm39) |
splice site |
probably benign |
|
R0068:Mroh1
|
UTSW |
15 |
76,330,892 (GRCm39) |
splice site |
probably benign |
|
R0076:Mroh1
|
UTSW |
15 |
76,335,340 (GRCm39) |
missense |
probably benign |
0.00 |
R0180:Mroh1
|
UTSW |
15 |
76,312,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R0315:Mroh1
|
UTSW |
15 |
76,311,800 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0350:Mroh1
|
UTSW |
15 |
76,316,449 (GRCm39) |
missense |
probably damaging |
0.98 |
R0399:Mroh1
|
UTSW |
15 |
76,336,299 (GRCm39) |
missense |
probably benign |
0.44 |
R0835:Mroh1
|
UTSW |
15 |
76,336,083 (GRCm39) |
missense |
probably damaging |
0.96 |
R0893:Mroh1
|
UTSW |
15 |
76,293,138 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1109:Mroh1
|
UTSW |
15 |
76,330,709 (GRCm39) |
splice site |
probably benign |
|
R1527:Mroh1
|
UTSW |
15 |
76,336,463 (GRCm39) |
missense |
probably benign |
0.03 |
R1595:Mroh1
|
UTSW |
15 |
76,317,730 (GRCm39) |
splice site |
probably benign |
|
R1900:Mroh1
|
UTSW |
15 |
76,317,585 (GRCm39) |
missense |
probably benign |
0.00 |
R1901:Mroh1
|
UTSW |
15 |
76,320,249 (GRCm39) |
missense |
probably benign |
|
R2223:Mroh1
|
UTSW |
15 |
76,292,245 (GRCm39) |
critical splice donor site |
probably null |
|
R2415:Mroh1
|
UTSW |
15 |
76,305,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R3113:Mroh1
|
UTSW |
15 |
76,292,736 (GRCm39) |
splice site |
probably benign |
|
R3437:Mroh1
|
UTSW |
15 |
76,317,808 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3618:Mroh1
|
UTSW |
15 |
76,336,546 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3833:Mroh1
|
UTSW |
15 |
76,285,819 (GRCm39) |
missense |
probably benign |
0.08 |
R4073:Mroh1
|
UTSW |
15 |
76,292,185 (GRCm39) |
missense |
probably benign |
0.13 |
R4156:Mroh1
|
UTSW |
15 |
76,286,326 (GRCm39) |
splice site |
probably null |
|
R4276:Mroh1
|
UTSW |
15 |
76,278,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4745:Mroh1
|
UTSW |
15 |
76,292,730 (GRCm39) |
critical splice donor site |
probably null |
|
R5450:Mroh1
|
UTSW |
15 |
76,316,547 (GRCm39) |
intron |
probably benign |
|
R5574:Mroh1
|
UTSW |
15 |
76,318,131 (GRCm39) |
missense |
probably benign |
|
R5673:Mroh1
|
UTSW |
15 |
76,314,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R5970:Mroh1
|
UTSW |
15 |
76,335,691 (GRCm39) |
missense |
probably benign |
0.24 |
R5993:Mroh1
|
UTSW |
15 |
76,330,880 (GRCm39) |
missense |
probably damaging |
0.99 |
R6008:Mroh1
|
UTSW |
15 |
76,335,557 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6082:Mroh1
|
UTSW |
15 |
76,314,423 (GRCm39) |
missense |
probably benign |
0.06 |
R6302:Mroh1
|
UTSW |
15 |
76,320,319 (GRCm39) |
critical splice donor site |
probably null |
|
R7030:Mroh1
|
UTSW |
15 |
76,321,517 (GRCm39) |
missense |
probably benign |
0.01 |
R7098:Mroh1
|
UTSW |
15 |
76,292,657 (GRCm39) |
nonsense |
probably null |
|
R7334:Mroh1
|
UTSW |
15 |
76,311,838 (GRCm39) |
missense |
probably benign |
0.00 |
R7337:Mroh1
|
UTSW |
15 |
76,335,676 (GRCm39) |
missense |
probably benign |
0.00 |
R7352:Mroh1
|
UTSW |
15 |
76,335,674 (GRCm39) |
missense |
probably benign |
0.06 |
R7446:Mroh1
|
UTSW |
15 |
76,336,472 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7453:Mroh1
|
UTSW |
15 |
76,317,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7669:Mroh1
|
UTSW |
15 |
76,336,048 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7753:Mroh1
|
UTSW |
15 |
76,317,475 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7990:Mroh1
|
UTSW |
15 |
76,336,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8140:Mroh1
|
UTSW |
15 |
76,318,073 (GRCm39) |
missense |
probably benign |
0.00 |
R8325:Mroh1
|
UTSW |
15 |
76,316,415 (GRCm39) |
frame shift |
probably null |
|
R8334:Mroh1
|
UTSW |
15 |
76,330,756 (GRCm39) |
missense |
probably benign |
|
R8529:Mroh1
|
UTSW |
15 |
76,311,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8544:Mroh1
|
UTSW |
15 |
76,327,558 (GRCm39) |
nonsense |
probably null |
|
R8688:Mroh1
|
UTSW |
15 |
76,312,550 (GRCm39) |
missense |
probably benign |
0.00 |
R8769:Mroh1
|
UTSW |
15 |
76,297,126 (GRCm39) |
missense |
probably benign |
0.00 |
R8782:Mroh1
|
UTSW |
15 |
76,298,496 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8887:Mroh1
|
UTSW |
15 |
76,331,474 (GRCm39) |
missense |
probably benign |
0.43 |
R8934:Mroh1
|
UTSW |
15 |
76,334,386 (GRCm39) |
missense |
probably benign |
0.03 |
R9254:Mroh1
|
UTSW |
15 |
76,292,215 (GRCm39) |
missense |
probably benign |
0.16 |
R9400:Mroh1
|
UTSW |
15 |
76,336,093 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9443:Mroh1
|
UTSW |
15 |
76,318,964 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mroh1
|
UTSW |
15 |
76,307,961 (GRCm39) |
missense |
probably damaging |
1.00 |
|