Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,236,348 (GRCm39) |
V1233A |
possibly damaging |
Het |
Abcc9 |
G |
A |
6: 142,617,408 (GRCm39) |
T552I |
probably damaging |
Het |
Adgrf4 |
T |
C |
17: 42,978,003 (GRCm39) |
I447V |
possibly damaging |
Het |
Akirin2 |
T |
A |
4: 34,565,944 (GRCm39) |
D178E |
probably damaging |
Het |
Arhgap12 |
T |
C |
18: 6,065,709 (GRCm39) |
E359G |
possibly damaging |
Het |
Arhgef5 |
A |
C |
6: 43,257,216 (GRCm39) |
T1256P |
probably damaging |
Het |
Avpr1a |
A |
C |
10: 122,285,283 (GRCm39) |
I192L |
possibly damaging |
Het |
B4galnt4 |
A |
G |
7: 140,651,197 (GRCm39) |
H926R |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Ccdc68 |
C |
T |
18: 70,089,123 (GRCm39) |
A222V |
probably benign |
Het |
Cdc23 |
T |
C |
18: 34,774,394 (GRCm39) |
Y295C |
probably benign |
Het |
Ceacam10 |
T |
C |
7: 24,480,432 (GRCm39) |
Y188H |
unknown |
Het |
Cfap57 |
T |
A |
4: 118,456,162 (GRCm39) |
T511S |
probably benign |
Het |
Cftr |
T |
C |
6: 18,221,623 (GRCm39) |
V245A |
probably benign |
Het |
Cit |
A |
G |
5: 116,064,633 (GRCm39) |
D505G |
probably damaging |
Het |
Cmah |
T |
G |
13: 24,652,539 (GRCm39) |
N556K |
probably benign |
Het |
Cspg4b |
T |
C |
13: 113,478,964 (GRCm39) |
S1503P |
|
Het |
D430041D05Rik |
C |
A |
2: 104,044,482 (GRCm39) |
D839Y |
probably damaging |
Het |
Dek |
T |
C |
13: 47,259,065 (GRCm39) |
D47G |
unknown |
Het |
Des |
C |
T |
1: 75,337,596 (GRCm39) |
R179C |
probably damaging |
Het |
Desi2 |
A |
G |
1: 178,015,509 (GRCm39) |
N10D |
probably benign |
Het |
Dlg5 |
T |
C |
14: 24,214,615 (GRCm39) |
N679S |
probably damaging |
Het |
Dnajc24 |
T |
C |
2: 105,832,293 (GRCm39) |
Y30C |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,687,065 (GRCm39) |
H34L |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,003,337 (GRCm39) |
V1586A |
probably benign |
Het |
Dpy19l4 |
A |
G |
4: 11,273,125 (GRCm39) |
V576A |
probably benign |
Het |
Dync1h1 |
T |
C |
12: 110,591,036 (GRCm39) |
Y1035H |
probably benign |
Het |
Dysf |
G |
A |
6: 84,172,306 (GRCm39) |
|
probably null |
Het |
En1 |
A |
G |
1: 120,534,817 (GRCm39) |
K369E |
unknown |
Het |
F2r |
A |
G |
13: 95,741,194 (GRCm39) |
Y114H |
probably damaging |
Het |
Fam184a |
T |
C |
10: 53,575,318 (GRCm39) |
Y97C |
probably damaging |
Het |
Fggy |
T |
C |
4: 95,657,717 (GRCm39) |
V286A |
probably benign |
Het |
Flot2 |
T |
C |
11: 77,949,383 (GRCm39) |
I322T |
probably benign |
Het |
Fndc1 |
A |
T |
17: 8,032,318 (GRCm39) |
|
probably null |
Het |
Frs3 |
A |
G |
17: 48,010,450 (GRCm39) |
D28G |
probably damaging |
Het |
Gimap3 |
C |
T |
6: 48,742,280 (GRCm39) |
D217N |
probably benign |
Het |
Gm128 |
A |
G |
3: 95,147,934 (GRCm39) |
V120A |
probably benign |
Het |
Gm17190 |
T |
C |
13: 96,218,970 (GRCm39) |
V102A |
probably damaging |
Het |
Gm17268 |
A |
G |
11: 81,919,057 (GRCm39) |
V20A |
unknown |
Het |
Grsf1 |
A |
T |
5: 88,813,423 (GRCm39) |
|
probably null |
Het |
Hmcn2 |
A |
T |
2: 31,278,395 (GRCm39) |
Y1699F |
probably benign |
Het |
Hnmt |
T |
A |
2: 23,938,731 (GRCm39) |
M36L |
probably benign |
Het |
Hoxd1 |
C |
A |
2: 74,594,447 (GRCm39) |
T234K |
probably damaging |
Het |
Hydin |
C |
G |
8: 111,232,733 (GRCm39) |
S1679R |
probably damaging |
Het |
Jag1 |
T |
C |
2: 136,926,226 (GRCm39) |
R1059G |
probably benign |
Het |
Kbtbd11 |
T |
C |
8: 15,078,858 (GRCm39) |
W486R |
probably damaging |
Het |
Kcnh6 |
A |
G |
11: 105,909,789 (GRCm39) |
D438G |
possibly damaging |
Het |
Lgals4 |
T |
G |
7: 28,540,724 (GRCm39) |
F276V |
probably benign |
Het |
Lrp6 |
G |
T |
6: 134,427,923 (GRCm39) |
Y1556* |
probably null |
Het |
Mpdz |
G |
A |
4: 81,274,632 (GRCm39) |
L855F |
probably benign |
Het |
Muc16 |
A |
T |
9: 18,554,316 (GRCm39) |
D3992E |
unknown |
Het |
Npc1 |
T |
C |
18: 12,328,237 (GRCm39) |
N1024S |
probably benign |
Het |
Nsfl1c |
A |
G |
2: 151,336,279 (GRCm39) |
T18A |
probably benign |
Het |
Or12e8 |
T |
A |
2: 87,188,555 (GRCm39) |
L256I |
possibly damaging |
Het |
Or12k5 |
A |
T |
2: 36,895,449 (GRCm39) |
M59K |
probably damaging |
Het |
Or2g7 |
G |
A |
17: 38,378,506 (GRCm39) |
W148* |
probably null |
Het |
Or8g31-ps1 |
T |
C |
9: 39,276,775 (GRCm39) |
*307R |
probably null |
Het |
Pcdh15 |
A |
T |
10: 74,420,048 (GRCm39) |
K1235N |
probably damaging |
Het |
Pcif1 |
A |
G |
2: 164,726,251 (GRCm39) |
K51E |
probably damaging |
Het |
Pde1b |
G |
A |
15: 103,429,752 (GRCm39) |
D82N |
probably damaging |
Het |
Phf23 |
T |
A |
11: 69,889,467 (GRCm39) |
V167E |
possibly damaging |
Het |
Pik3c2g |
T |
C |
6: 139,913,620 (GRCm39) |
V1006A |
unknown |
Het |
Pira12 |
T |
A |
7: 3,901,103 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
G |
T |
15: 44,452,882 (GRCm39) |
V3936F |
probably damaging |
Het |
Pnpla1 |
T |
C |
17: 29,100,159 (GRCm39) |
V342A |
probably benign |
Het |
Ppip5k1 |
T |
C |
2: 121,171,329 (GRCm39) |
D620G |
possibly damaging |
Het |
Ppl |
A |
G |
16: 4,907,205 (GRCm39) |
L1030P |
possibly damaging |
Het |
Prelid1 |
A |
T |
13: 55,469,088 (GRCm39) |
|
probably benign |
Het |
Racgap1 |
C |
T |
15: 99,529,081 (GRCm39) |
S264N |
probably benign |
Het |
Rdh13 |
T |
C |
7: 4,430,696 (GRCm39) |
D289G |
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,815,364 (GRCm39) |
I334V |
probably benign |
Het |
Setd2 |
A |
T |
9: 110,392,012 (GRCm39) |
D200V |
|
Het |
Simc1 |
A |
G |
13: 54,651,731 (GRCm39) |
S15G |
unknown |
Het |
Sirpb1c |
A |
T |
3: 15,887,389 (GRCm39) |
M150K |
probably benign |
Het |
Smoc1 |
T |
A |
12: 81,197,475 (GRCm39) |
D202E |
probably damaging |
Het |
Spata31d1b |
A |
G |
13: 59,860,304 (GRCm39) |
Y59C |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,528,761 (GRCm39) |
T1673A |
probably damaging |
Het |
Tbc1d31 |
T |
A |
15: 57,779,504 (GRCm39) |
H72Q |
probably benign |
Het |
Tgfbrap1 |
C |
A |
1: 43,114,693 (GRCm39) |
V136L |
probably damaging |
Het |
Top2b |
A |
G |
14: 16,407,376 (GRCm38) |
N720S |
probably null |
Het |
Vmn1r11 |
T |
C |
6: 57,115,184 (GRCm39) |
S283P |
probably damaging |
Het |
Vmn1r19 |
A |
G |
6: 57,382,080 (GRCm39) |
H211R |
probably damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,370,538 (GRCm39) |
M836K |
probably benign |
Het |
Vmn2r61 |
A |
C |
7: 41,915,407 (GRCm39) |
H118P |
probably benign |
Het |
Vps33a |
A |
G |
5: 123,696,696 (GRCm39) |
I319T |
probably benign |
Het |
Vwf |
T |
A |
6: 125,543,220 (GRCm39) |
S151T |
|
Het |
Zfp423 |
T |
C |
8: 88,508,871 (GRCm39) |
N491S |
possibly damaging |
Het |
Zfp626 |
T |
C |
7: 27,507,660 (GRCm39) |
F23S |
probably damaging |
Het |
|
Other mutations in Dusp6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02272:Dusp6
|
APN |
10 |
99,101,881 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02687:Dusp6
|
APN |
10 |
99,102,044 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02996:Dusp6
|
APN |
10 |
99,100,628 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL03024:Dusp6
|
APN |
10 |
99,102,156 (GRCm39) |
missense |
probably damaging |
0.97 |
R1134:Dusp6
|
UTSW |
10 |
99,100,816 (GRCm39) |
missense |
probably damaging |
0.98 |
R1695:Dusp6
|
UTSW |
10 |
99,099,555 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R2078:Dusp6
|
UTSW |
10 |
99,099,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:Dusp6
|
UTSW |
10 |
99,099,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Dusp6
|
UTSW |
10 |
99,099,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Dusp6
|
UTSW |
10 |
99,099,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R4413:Dusp6
|
UTSW |
10 |
99,099,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4501:Dusp6
|
UTSW |
10 |
99,100,457 (GRCm39) |
missense |
probably benign |
0.41 |
R5175:Dusp6
|
UTSW |
10 |
99,099,864 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5381:Dusp6
|
UTSW |
10 |
99,102,129 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5560:Dusp6
|
UTSW |
10 |
99,102,103 (GRCm39) |
missense |
probably damaging |
0.97 |
R5820:Dusp6
|
UTSW |
10 |
99,099,864 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7398:Dusp6
|
UTSW |
10 |
99,100,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R8075:Dusp6
|
UTSW |
10 |
99,100,810 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8491:Dusp6
|
UTSW |
10 |
99,102,081 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8826:Dusp6
|
UTSW |
10 |
99,099,469 (GRCm39) |
start gained |
probably benign |
|
R9084:Dusp6
|
UTSW |
10 |
99,099,692 (GRCm39) |
missense |
probably benign |
0.13 |
R9125:Dusp6
|
UTSW |
10 |
99,102,074 (GRCm39) |
nonsense |
probably null |
|
R9389:Dusp6
|
UTSW |
10 |
99,099,839 (GRCm39) |
missense |
possibly damaging |
0.94 |
|