Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130023H24Rik |
T |
C |
7: 127,836,191 (GRCm39) |
H134R |
probably damaging |
Het |
Adcy4 |
A |
G |
14: 56,018,362 (GRCm39) |
M195T |
probably benign |
Het |
Aktip |
T |
C |
8: 91,856,285 (GRCm39) |
N64S |
possibly damaging |
Het |
Aldoart1 |
C |
A |
4: 72,770,747 (GRCm39) |
M20I |
probably benign |
Het |
Alms1 |
T |
C |
6: 85,592,333 (GRCm39) |
L395P |
probably damaging |
Het |
Ankrd9 |
C |
A |
12: 110,943,180 (GRCm39) |
V252F |
probably benign |
Het |
Apof |
A |
T |
10: 128,104,885 (GRCm39) |
H13L |
probably benign |
Het |
Bahcc1 |
T |
C |
11: 120,174,172 (GRCm39) |
F1644S |
possibly damaging |
Het |
Baz2a |
A |
G |
10: 127,959,726 (GRCm39) |
D1377G |
possibly damaging |
Het |
Bbox1 |
T |
A |
2: 110,135,794 (GRCm39) |
I62F |
probably damaging |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
TCTGTGGTCACTGGT |
TCTGTGGTCACTGGTGCTGTGGTCACTGGT |
3: 95,795,487 (GRCm39) |
|
probably benign |
Het |
BC028528 |
GTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTG |
GTTCTGTGGTCACTGATTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTG |
3: 95,795,455 (GRCm39) |
|
probably benign |
Het |
Bcas3 |
C |
T |
11: 85,286,213 (GRCm39) |
R124* |
probably null |
Het |
Bpnt1 |
T |
C |
1: 185,078,879 (GRCm39) |
V114A |
probably damaging |
Het |
Ccnd1 |
C |
T |
7: 144,487,793 (GRCm39) |
R228H |
possibly damaging |
Het |
Cd244a |
T |
C |
1: 171,404,853 (GRCm39) |
V235A |
probably benign |
Het |
Cramp1 |
C |
T |
17: 25,201,440 (GRCm39) |
E681K |
probably damaging |
Het |
Crebbp |
C |
T |
16: 3,902,574 (GRCm39) |
A2222T |
probably benign |
Het |
Cyp1a2 |
T |
A |
9: 57,589,620 (GRCm39) |
T65S |
probably benign |
Het |
Cyp26b1 |
T |
G |
6: 84,561,351 (GRCm39) |
K104Q |
probably benign |
Het |
D430041D05Rik |
T |
C |
2: 104,071,581 (GRCm39) |
I556V |
probably benign |
Het |
Dnase1l2 |
A |
G |
17: 24,661,219 (GRCm39) |
L102P |
probably damaging |
Het |
Eef1ece2 |
C |
A |
16: 20,457,417 (GRCm39) |
A483E |
probably damaging |
Het |
Elac1 |
C |
T |
18: 73,871,925 (GRCm39) |
G357S |
probably benign |
Het |
Enam |
C |
A |
5: 88,651,830 (GRCm39) |
T1113N |
possibly damaging |
Het |
Eogt |
A |
T |
6: 97,090,870 (GRCm39) |
I423N |
probably damaging |
Het |
Epc2 |
T |
C |
2: 49,435,831 (GRCm39) |
S612P |
possibly damaging |
Het |
Fam107b |
T |
C |
2: 3,773,959 (GRCm39) |
V24A |
probably damaging |
Het |
Fhip2a |
A |
G |
19: 57,373,750 (GRCm39) |
H670R |
possibly damaging |
Het |
Foxj3 |
C |
T |
4: 119,477,429 (GRCm39) |
P413L |
unknown |
Het |
Frg1 |
T |
C |
8: 41,870,040 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,820,455 (GRCm39) |
V5396D |
possibly damaging |
Het |
Hdlbp |
T |
C |
1: 93,364,821 (GRCm39) |
T149A |
possibly damaging |
Het |
Heatr1 |
A |
T |
13: 12,453,545 (GRCm39) |
Q2140L |
probably damaging |
Het |
Iqcd |
T |
C |
5: 120,744,881 (GRCm39) |
L403P |
probably damaging |
Het |
Kifbp |
A |
G |
10: 62,413,852 (GRCm39) |
I102T |
probably benign |
Het |
Kpna2 |
T |
G |
11: 106,879,789 (GRCm39) |
N505T |
probably benign |
Het |
Lipo3 |
T |
A |
19: 33,757,785 (GRCm39) |
E228V |
probably benign |
Het |
Map4k3 |
C |
T |
17: 80,922,500 (GRCm39) |
V474I |
possibly damaging |
Het |
Mrpl11 |
T |
C |
19: 5,012,424 (GRCm39) |
S2P |
probably damaging |
Het |
Mug2 |
A |
G |
6: 122,017,678 (GRCm39) |
I472V |
probably benign |
Het |
Myom1 |
G |
A |
17: 71,391,235 (GRCm39) |
V915M |
possibly damaging |
Het |
Nedd9 |
A |
T |
13: 41,492,198 (GRCm39) |
I104N |
possibly damaging |
Het |
Nphp3 |
A |
G |
9: 103,909,159 (GRCm39) |
M790V |
probably benign |
Het |
Nr3c2 |
C |
T |
8: 77,635,838 (GRCm39) |
P313L |
probably damaging |
Het |
Obsl1 |
A |
G |
1: 75,469,365 (GRCm39) |
V1192A |
probably benign |
Het |
Or10j2 |
C |
T |
1: 173,098,440 (GRCm39) |
R233W |
probably benign |
Het |
Or52e7 |
A |
G |
7: 104,684,750 (GRCm39) |
H115R |
probably damaging |
Het |
Or5t16 |
T |
C |
2: 86,818,663 (GRCm39) |
I286V |
possibly damaging |
Het |
Prr5l |
T |
G |
2: 101,565,083 (GRCm39) |
E151A |
probably damaging |
Het |
Psmb8 |
G |
T |
17: 34,417,404 (GRCm39) |
R11L |
probably benign |
Het |
Ptprg |
T |
A |
14: 12,211,668 (GRCm38) |
H983Q |
probably benign |
Het |
Ptprj |
T |
C |
2: 90,290,940 (GRCm39) |
N600D |
possibly damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,118,424 (GRCm39) |
I522V |
probably damaging |
Het |
Rc3h1 |
A |
G |
1: 160,778,454 (GRCm39) |
S460G |
probably damaging |
Het |
Rhot2 |
A |
G |
17: 26,062,079 (GRCm39) |
|
probably null |
Het |
Sall1 |
T |
C |
8: 89,757,927 (GRCm39) |
T726A |
probably damaging |
Het |
Samd9l |
G |
A |
6: 3,373,646 (GRCm39) |
T1205I |
probably benign |
Het |
Sh2b3 |
C |
T |
5: 121,956,822 (GRCm39) |
|
probably null |
Het |
Slc22a18 |
G |
T |
7: 143,044,557 (GRCm39) |
C170F |
probably damaging |
Het |
Slc24a1 |
G |
A |
9: 64,855,209 (GRCm39) |
T566I |
unknown |
Het |
Slc4a5 |
T |
A |
6: 83,237,517 (GRCm39) |
C167S |
probably damaging |
Het |
Slc8b1 |
T |
G |
5: 120,671,100 (GRCm39) |
V579G |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,063,822 (GRCm39) |
V667A |
probably damaging |
Het |
Sp8 |
C |
A |
12: 118,813,070 (GRCm39) |
S308R |
possibly damaging |
Het |
Srsf9 |
T |
A |
5: 115,468,619 (GRCm39) |
V85E |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,168,527 (GRCm39) |
I5285V |
probably benign |
Het |
Tmem245 |
T |
C |
4: 56,947,069 (GRCm39) |
I115V |
probably benign |
Het |
Triqk |
A |
G |
4: 12,980,502 (GRCm39) |
D82G |
probably benign |
Het |
Trmt11 |
A |
T |
10: 30,463,520 (GRCm39) |
S198R |
probably damaging |
Het |
Ube4b |
C |
T |
4: 149,471,661 (GRCm39) |
R75Q |
probably benign |
Het |
Ugt3a1 |
C |
T |
15: 9,310,779 (GRCm39) |
Q354* |
probably null |
Het |
Vmn1r202 |
A |
G |
13: 22,685,850 (GRCm39) |
V189A |
probably benign |
Het |
Wdr6 |
T |
C |
9: 108,450,947 (GRCm39) |
K914R |
probably benign |
Het |
Zfat |
T |
C |
15: 68,130,535 (GRCm39) |
M1V |
probably null |
Het |
Zfp207 |
A |
G |
11: 80,280,116 (GRCm39) |
M171V |
probably benign |
Het |
Zfp568 |
C |
T |
7: 29,697,212 (GRCm39) |
T44I |
probably damaging |
Het |
|
Other mutations in Vmn2r26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01070:Vmn2r26
|
APN |
6 |
124,038,566 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01370:Vmn2r26
|
APN |
6 |
124,038,715 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01603:Vmn2r26
|
APN |
6 |
124,030,833 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01651:Vmn2r26
|
APN |
6 |
124,027,632 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02282:Vmn2r26
|
APN |
6 |
124,038,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Vmn2r26
|
APN |
6 |
124,038,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02551:Vmn2r26
|
APN |
6 |
124,003,100 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02690:Vmn2r26
|
APN |
6 |
124,003,091 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03002:Vmn2r26
|
APN |
6 |
124,016,754 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03270:Vmn2r26
|
APN |
6 |
124,027,778 (GRCm39) |
missense |
probably benign |
0.16 |
R0032:Vmn2r26
|
UTSW |
6 |
124,016,858 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0052:Vmn2r26
|
UTSW |
6 |
124,038,992 (GRCm39) |
makesense |
probably null |
|
R0083:Vmn2r26
|
UTSW |
6 |
124,030,940 (GRCm39) |
splice site |
probably null |
|
R0682:Vmn2r26
|
UTSW |
6 |
124,038,129 (GRCm39) |
missense |
probably damaging |
0.97 |
R1061:Vmn2r26
|
UTSW |
6 |
124,038,603 (GRCm39) |
missense |
probably benign |
0.12 |
R1077:Vmn2r26
|
UTSW |
6 |
124,030,872 (GRCm39) |
missense |
probably benign |
0.00 |
R1263:Vmn2r26
|
UTSW |
6 |
124,027,667 (GRCm39) |
missense |
probably benign |
|
R1579:Vmn2r26
|
UTSW |
6 |
124,016,706 (GRCm39) |
missense |
probably benign |
0.00 |
R1741:Vmn2r26
|
UTSW |
6 |
124,038,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:Vmn2r26
|
UTSW |
6 |
124,038,369 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1838:Vmn2r26
|
UTSW |
6 |
124,001,730 (GRCm39) |
missense |
probably benign |
|
R1956:Vmn2r26
|
UTSW |
6 |
124,030,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1996:Vmn2r26
|
UTSW |
6 |
124,038,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Vmn2r26
|
UTSW |
6 |
124,038,196 (GRCm39) |
missense |
probably benign |
0.01 |
R2327:Vmn2r26
|
UTSW |
6 |
124,016,708 (GRCm39) |
missense |
probably benign |
0.07 |
R2417:Vmn2r26
|
UTSW |
6 |
124,038,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R3930:Vmn2r26
|
UTSW |
6 |
124,002,938 (GRCm39) |
missense |
probably benign |
|
R4490:Vmn2r26
|
UTSW |
6 |
124,027,697 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4629:Vmn2r26
|
UTSW |
6 |
124,038,150 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4655:Vmn2r26
|
UTSW |
6 |
124,038,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Vmn2r26
|
UTSW |
6 |
124,030,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Vmn2r26
|
UTSW |
6 |
124,003,070 (GRCm39) |
missense |
probably benign |
0.00 |
R5297:Vmn2r26
|
UTSW |
6 |
124,038,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5482:Vmn2r26
|
UTSW |
6 |
124,038,285 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5517:Vmn2r26
|
UTSW |
6 |
124,027,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R5737:Vmn2r26
|
UTSW |
6 |
124,016,408 (GRCm39) |
missense |
probably benign |
0.00 |
R5739:Vmn2r26
|
UTSW |
6 |
124,002,925 (GRCm39) |
missense |
probably benign |
0.00 |
R5873:Vmn2r26
|
UTSW |
6 |
124,038,633 (GRCm39) |
missense |
probably benign |
0.01 |
R5907:Vmn2r26
|
UTSW |
6 |
124,016,830 (GRCm39) |
missense |
probably benign |
0.00 |
R6086:Vmn2r26
|
UTSW |
6 |
124,016,519 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6134:Vmn2r26
|
UTSW |
6 |
124,038,444 (GRCm39) |
missense |
probably damaging |
0.97 |
R6391:Vmn2r26
|
UTSW |
6 |
124,038,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R6428:Vmn2r26
|
UTSW |
6 |
124,003,039 (GRCm39) |
missense |
probably benign |
0.17 |
R6637:Vmn2r26
|
UTSW |
6 |
124,038,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R6927:Vmn2r26
|
UTSW |
6 |
124,016,057 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6953:Vmn2r26
|
UTSW |
6 |
124,016,741 (GRCm39) |
missense |
probably benign |
0.00 |
R7173:Vmn2r26
|
UTSW |
6 |
124,038,255 (GRCm39) |
missense |
probably benign |
0.16 |
R7206:Vmn2r26
|
UTSW |
6 |
124,016,727 (GRCm39) |
missense |
probably benign |
0.17 |
R7208:Vmn2r26
|
UTSW |
6 |
124,038,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R7283:Vmn2r26
|
UTSW |
6 |
124,002,914 (GRCm39) |
missense |
probably damaging |
0.97 |
R7506:Vmn2r26
|
UTSW |
6 |
124,016,700 (GRCm39) |
missense |
probably benign |
0.00 |
R7674:Vmn2r26
|
UTSW |
6 |
124,016,321 (GRCm39) |
missense |
probably benign |
|
R7696:Vmn2r26
|
UTSW |
6 |
124,038,494 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7716:Vmn2r26
|
UTSW |
6 |
124,038,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Vmn2r26
|
UTSW |
6 |
124,016,758 (GRCm39) |
nonsense |
probably null |
|
R8063:Vmn2r26
|
UTSW |
6 |
124,001,914 (GRCm39) |
missense |
probably benign |
0.00 |
R8331:Vmn2r26
|
UTSW |
6 |
124,038,887 (GRCm39) |
missense |
probably benign |
0.22 |
R8352:Vmn2r26
|
UTSW |
6 |
124,016,577 (GRCm39) |
missense |
probably benign |
0.09 |
R8445:Vmn2r26
|
UTSW |
6 |
124,002,995 (GRCm39) |
missense |
probably damaging |
0.97 |
R8452:Vmn2r26
|
UTSW |
6 |
124,016,577 (GRCm39) |
missense |
probably benign |
0.09 |
R8681:Vmn2r26
|
UTSW |
6 |
124,001,877 (GRCm39) |
missense |
probably benign |
0.00 |
R8914:Vmn2r26
|
UTSW |
6 |
124,038,983 (GRCm39) |
missense |
probably benign |
|
R9333:Vmn2r26
|
UTSW |
6 |
124,003,009 (GRCm39) |
missense |
probably benign |
0.13 |
R9351:Vmn2r26
|
UTSW |
6 |
124,016,333 (GRCm39) |
missense |
probably benign |
|
R9436:Vmn2r26
|
UTSW |
6 |
124,002,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R9515:Vmn2r26
|
UTSW |
6 |
124,038,137 (GRCm39) |
missense |
probably damaging |
1.00 |
RF010:Vmn2r26
|
UTSW |
6 |
124,016,448 (GRCm39) |
missense |
possibly damaging |
0.90 |
|