Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
A |
C |
15: 94,229,339 (GRCm39) |
C927G |
probably damaging |
Het |
Afdn |
T |
A |
17: 14,116,436 (GRCm39) |
D190E |
probably benign |
Het |
Ankrd28 |
T |
C |
14: 31,430,719 (GRCm39) |
D850G |
probably damaging |
Het |
Arhgap45 |
T |
C |
10: 79,852,813 (GRCm39) |
M1T |
probably null |
Het |
Atp6v0a4 |
T |
G |
6: 38,065,581 (GRCm39) |
K128N |
possibly damaging |
Het |
Bcat1 |
T |
A |
6: 144,955,834 (GRCm39) |
D349V |
probably damaging |
Het |
Cacna1i |
T |
C |
15: 80,240,388 (GRCm39) |
F370S |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,634,348 (GRCm39) |
I82V |
probably benign |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cyfip2 |
T |
C |
11: 46,152,333 (GRCm39) |
D485G |
probably benign |
Het |
Cyp27b1 |
G |
T |
10: 126,886,929 (GRCm39) |
V382L |
probably damaging |
Het |
Dnaaf5 |
T |
C |
5: 139,167,320 (GRCm39) |
V447A |
possibly damaging |
Het |
Dpp9 |
A |
T |
17: 56,506,113 (GRCm39) |
F429I |
possibly damaging |
Het |
Eng |
C |
T |
2: 32,569,059 (GRCm39) |
R528C |
probably damaging |
Het |
Gcn1 |
A |
T |
5: 115,730,191 (GRCm39) |
Q835L |
probably benign |
Het |
Gprc6a |
CAAA |
CA |
10: 51,491,776 (GRCm39) |
|
probably null |
Het |
Hlx |
T |
A |
1: 184,462,889 (GRCm39) |
|
probably null |
Het |
Htt |
T |
A |
5: 34,979,062 (GRCm39) |
V815D |
probably benign |
Het |
Il36rn |
G |
T |
2: 24,169,692 (GRCm39) |
L17F |
probably damaging |
Het |
Itga1 |
C |
T |
13: 115,167,446 (GRCm39) |
V157I |
probably benign |
Het |
Krtap19-3 |
T |
G |
16: 88,674,607 (GRCm39) |
*88C |
probably null |
Het |
Lzic |
G |
C |
4: 149,573,185 (GRCm39) |
E112D |
probably null |
Het |
Mark2 |
G |
C |
19: 7,260,112 (GRCm39) |
S111C |
probably damaging |
Het |
Mep1b |
C |
T |
18: 21,219,296 (GRCm39) |
T150I |
possibly damaging |
Het |
Mroh7 |
G |
C |
4: 106,557,378 (GRCm39) |
S777R |
probably damaging |
Het |
Nrxn1 |
G |
A |
17: 90,469,859 (GRCm39) |
R35C |
probably damaging |
Het |
Or12e10 |
T |
A |
2: 87,640,704 (GRCm39) |
I180K |
probably damaging |
Het |
Or5p69 |
C |
A |
7: 107,966,769 (GRCm39) |
P24Q |
probably benign |
Het |
Pacs2 |
A |
G |
12: 113,014,567 (GRCm39) |
T243A |
probably benign |
Het |
Pan2 |
A |
G |
10: 128,140,091 (GRCm39) |
E4G |
possibly damaging |
Het |
Pdp1 |
A |
G |
4: 11,961,123 (GRCm39) |
V396A |
probably damaging |
Het |
Pdzd7 |
A |
G |
19: 45,024,494 (GRCm39) |
|
probably null |
Het |
Peg10 |
T |
A |
6: 4,755,914 (GRCm39) |
|
probably benign |
Het |
Pgc |
C |
A |
17: 48,040,236 (GRCm39) |
F93L |
probably null |
Het |
Piezo2 |
A |
G |
18: 63,214,733 (GRCm39) |
|
probably null |
Het |
Pja2 |
T |
C |
17: 64,616,397 (GRCm39) |
D166G |
probably benign |
Het |
Ppp1r9b |
T |
C |
11: 94,888,877 (GRCm39) |
L97P |
probably damaging |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
S100a10 |
T |
C |
3: 93,471,680 (GRCm39) |
V88A |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,364,573 (GRCm39) |
Y789F |
probably damaging |
Het |
Slit3 |
A |
T |
11: 35,579,509 (GRCm39) |
S1229C |
probably null |
Het |
Spata31g1 |
A |
G |
4: 42,972,238 (GRCm39) |
T524A |
possibly damaging |
Het |
Sptan1 |
T |
C |
2: 29,908,588 (GRCm39) |
|
probably benign |
Het |
Srrd |
G |
T |
5: 112,490,810 (GRCm39) |
|
probably benign |
Het |
Tdrd3 |
A |
G |
14: 87,718,221 (GRCm39) |
T201A |
probably damaging |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Ttll4 |
A |
G |
1: 74,725,550 (GRCm39) |
K653E |
probably damaging |
Het |
Usp43 |
A |
G |
11: 67,770,795 (GRCm39) |
L613P |
probably damaging |
Het |
Vmn1r167 |
T |
C |
7: 23,204,224 (GRCm39) |
D264G |
possibly damaging |
Het |
Whamm |
A |
G |
7: 81,221,089 (GRCm39) |
D7G |
probably damaging |
Het |
Zcchc17 |
T |
C |
4: 130,232,317 (GRCm39) |
D62G |
probably benign |
Het |
Zfp280d |
T |
A |
9: 72,206,104 (GRCm39) |
I62K |
probably damaging |
Het |
Zfp445 |
T |
G |
9: 122,681,541 (GRCm39) |
E800A |
probably damaging |
Het |
Zfp516 |
A |
G |
18: 83,005,063 (GRCm39) |
R656G |
possibly damaging |
Het |
|
Other mutations in Or51v8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02419:Or51v8
|
APN |
7 |
103,319,682 (GRCm39) |
nonsense |
probably null |
|
IGL02536:Or51v8
|
APN |
7 |
103,320,164 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02684:Or51v8
|
APN |
7 |
103,319,591 (GRCm39) |
missense |
probably benign |
0.06 |
FR4548:Or51v8
|
UTSW |
7 |
103,320,174 (GRCm39) |
nonsense |
probably null |
|
FR4548:Or51v8
|
UTSW |
7 |
103,320,167 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Or51v8
|
UTSW |
7 |
103,320,173 (GRCm39) |
small insertion |
probably benign |
|
R0295:Or51v8
|
UTSW |
7 |
103,319,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R0518:Or51v8
|
UTSW |
7 |
103,319,696 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0521:Or51v8
|
UTSW |
7 |
103,319,696 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1352:Or51v8
|
UTSW |
7 |
103,319,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Or51v8
|
UTSW |
7 |
103,319,845 (GRCm39) |
missense |
probably benign |
0.15 |
R1878:Or51v8
|
UTSW |
7 |
103,319,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R1965:Or51v8
|
UTSW |
7 |
103,320,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Or51v8
|
UTSW |
7 |
103,319,674 (GRCm39) |
missense |
probably damaging |
0.97 |
R3792:Or51v8
|
UTSW |
7 |
103,319,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Or51v8
|
UTSW |
7 |
103,319,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R4120:Or51v8
|
UTSW |
7 |
103,320,221 (GRCm39) |
missense |
probably benign |
|
R4183:Or51v8
|
UTSW |
7 |
103,320,178 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4853:Or51v8
|
UTSW |
7 |
103,320,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Or51v8
|
UTSW |
7 |
103,320,163 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7717:Or51v8
|
UTSW |
7 |
103,320,152 (GRCm39) |
missense |
probably benign |
|
R9091:Or51v8
|
UTSW |
7 |
103,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R9270:Or51v8
|
UTSW |
7 |
103,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Or51v8
|
UTSW |
7 |
103,319,633 (GRCm39) |
missense |
probably benign |
0.03 |
R9378:Or51v8
|
UTSW |
7 |
103,319,389 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Or51v8
|
UTSW |
7 |
103,319,602 (GRCm39) |
missense |
probably benign |
|
|