Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
G |
A |
3: 137,889,470 (GRCm39) |
P49L |
probably benign |
Het |
Adam34l |
T |
A |
8: 44,079,970 (GRCm39) |
R85* |
probably null |
Het |
Anapc2 |
C |
T |
2: 25,163,303 (GRCm39) |
T180I |
probably benign |
Het |
Ankib1 |
A |
T |
5: 3,756,276 (GRCm39) |
H556Q |
probably damaging |
Het |
Aox1 |
A |
T |
1: 58,378,777 (GRCm39) |
K1009* |
probably null |
Het |
Apob |
C |
T |
12: 8,047,925 (GRCm39) |
P968L |
probably damaging |
Het |
Bpi |
T |
A |
2: 158,116,608 (GRCm39) |
F335Y |
probably benign |
Het |
Cabcoco1 |
T |
C |
10: 68,272,719 (GRCm39) |
Y222C |
probably damaging |
Het |
Camk2b |
G |
T |
11: 5,939,332 (GRCm39) |
C273* |
probably null |
Het |
Catsperd |
G |
A |
17: 56,968,252 (GRCm39) |
D546N |
probably benign |
Het |
Cenpb |
C |
T |
2: 131,021,463 (GRCm39) |
G112S |
probably damaging |
Het |
Col6a5 |
A |
G |
9: 105,739,178 (GRCm39) |
L2585P |
probably damaging |
Het |
Cop1 |
A |
G |
1: 159,147,339 (GRCm39) |
E555G |
probably damaging |
Het |
Coro1b |
T |
C |
19: 4,203,392 (GRCm39) |
V411A |
probably benign |
Het |
Cyfip2 |
G |
A |
11: 46,176,920 (GRCm39) |
R87C |
probably damaging |
Het |
Dthd1 |
A |
C |
5: 63,045,410 (GRCm39) |
I725L |
probably benign |
Het |
Dydc1 |
A |
C |
14: 40,800,054 (GRCm39) |
E20A |
probably damaging |
Het |
Ermp1 |
T |
C |
19: 29,609,845 (GRCm39) |
I317V |
probably benign |
Het |
Fat4 |
A |
G |
3: 38,942,556 (GRCm39) |
N483S |
possibly damaging |
Het |
Fbxo33 |
A |
G |
12: 59,251,095 (GRCm39) |
|
probably null |
Het |
Fcgbp |
G |
T |
7: 27,803,198 (GRCm39) |
E1601* |
probably null |
Het |
Fer1l5 |
A |
T |
1: 36,449,999 (GRCm39) |
S1118C |
probably null |
Het |
Fer1l6 |
T |
C |
15: 58,494,230 (GRCm39) |
V1141A |
probably benign |
Het |
Flnb |
C |
T |
14: 7,818,219 (GRCm38) |
T23M |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,815,574 (GRCm39) |
L3769P |
possibly damaging |
Het |
Gna11 |
T |
C |
10: 81,370,942 (GRCm39) |
K98R |
|
Het |
Gpat3 |
A |
T |
5: 101,032,230 (GRCm39) |
T176S |
probably benign |
Het |
Gprc5b |
A |
G |
7: 118,583,542 (GRCm39) |
L109P |
probably damaging |
Het |
Hadha |
A |
T |
5: 30,340,038 (GRCm39) |
N246K |
probably benign |
Het |
Haus3 |
G |
A |
5: 34,324,835 (GRCm39) |
Q275* |
probably null |
Het |
Higd1b |
A |
G |
11: 102,728,090 (GRCm39) |
Y44C |
possibly damaging |
Het |
Igkv1-131 |
T |
C |
6: 67,743,218 (GRCm39) |
K55R |
probably benign |
Het |
Igtp |
G |
T |
11: 58,098,091 (GRCm39) |
E421* |
probably null |
Het |
Kcnk3 |
G |
T |
5: 30,745,532 (GRCm39) |
|
probably benign |
Het |
Krtap4-13 |
A |
T |
11: 99,700,165 (GRCm39) |
C165S |
unknown |
Het |
Lrfn4 |
T |
C |
19: 4,663,353 (GRCm39) |
R394G |
probably benign |
Het |
Lrrc7 |
A |
C |
3: 157,867,011 (GRCm39) |
L910R |
possibly damaging |
Het |
Mbtd1 |
A |
G |
11: 93,823,218 (GRCm39) |
D568G |
probably damaging |
Het |
Mettl16 |
T |
A |
11: 74,693,826 (GRCm39) |
I279N |
probably benign |
Het |
Mmrn2 |
A |
G |
14: 34,121,158 (GRCm39) |
H676R |
probably benign |
Het |
Mrgprg |
T |
C |
7: 143,318,350 (GRCm39) |
K254R |
probably benign |
Het |
Muc16 |
A |
C |
9: 18,554,038 (GRCm39) |
V4085G |
unknown |
Het |
Mvp |
T |
C |
7: 126,591,822 (GRCm39) |
Q456R |
probably benign |
Het |
Myf6 |
T |
C |
10: 107,329,318 (GRCm39) |
D209G |
probably benign |
Het |
Ociad1 |
A |
G |
5: 73,467,725 (GRCm39) |
D167G |
probably benign |
Het |
Or11l3 |
A |
G |
11: 58,516,062 (GRCm39) |
L270P |
probably benign |
Het |
Or51f23b |
T |
A |
7: 102,402,734 (GRCm39) |
Y134F |
probably damaging |
Het |
Or5m3 |
T |
G |
2: 85,838,325 (GRCm39) |
D68E |
probably damaging |
Het |
Or6c1b |
T |
C |
10: 129,272,858 (GRCm39) |
F59S |
probably damaging |
Het |
Phf20 |
A |
G |
2: 156,114,537 (GRCm39) |
D295G |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Ppp1r13b |
A |
T |
12: 111,811,416 (GRCm39) |
H157Q |
probably benign |
Het |
Prss3b |
A |
G |
6: 41,008,681 (GRCm39) |
L211P |
probably damaging |
Het |
Rbm26 |
C |
T |
14: 105,391,039 (GRCm39) |
R149H |
unknown |
Het |
Reg3d |
C |
T |
6: 78,355,443 (GRCm39) |
C16Y |
possibly damaging |
Het |
Rrp36 |
A |
G |
17: 46,978,980 (GRCm39) |
F193L |
possibly damaging |
Het |
Rtca |
A |
T |
3: 116,282,905 (GRCm39) |
M361K |
probably benign |
Het |
Ryr3 |
T |
G |
2: 112,491,981 (GRCm39) |
D3790A |
probably damaging |
Het |
Serpina3n |
C |
A |
12: 104,377,440 (GRCm39) |
A231E |
probably benign |
Het |
Sh2d2a |
A |
G |
3: 87,759,070 (GRCm39) |
D224G |
possibly damaging |
Het |
Sh3bp2 |
A |
T |
5: 34,718,377 (GRCm39) |
K526* |
probably null |
Het |
Slc12a2 |
A |
G |
18: 58,069,469 (GRCm39) |
T1017A |
possibly damaging |
Het |
Slc12a8 |
T |
C |
16: 33,361,397 (GRCm39) |
L93P |
probably damaging |
Het |
Slc5a6 |
A |
G |
5: 31,195,190 (GRCm39) |
I469T |
probably damaging |
Het |
Smarcc1 |
T |
A |
9: 109,964,728 (GRCm39) |
V95D |
probably damaging |
Het |
Snap29 |
T |
A |
16: 17,224,163 (GRCm39) |
S59R |
probably damaging |
Het |
Tmem121b |
T |
A |
6: 120,469,784 (GRCm39) |
Y311F |
probably damaging |
Het |
Tpcn1 |
C |
A |
5: 120,694,000 (GRCm39) |
V199L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,618,721 (GRCm39) |
I16188V |
probably benign |
Het |
Usp24 |
T |
C |
4: 106,216,247 (GRCm39) |
I366T |
possibly damaging |
Het |
Utrn |
T |
A |
10: 12,545,463 (GRCm39) |
E1727D |
probably damaging |
Het |
Vav2 |
T |
C |
2: 27,182,701 (GRCm39) |
D301G |
probably damaging |
Het |
Vmn2r104 |
T |
C |
17: 20,263,087 (GRCm39) |
T125A |
probably benign |
Het |
Vmn2r73 |
T |
G |
7: 85,507,123 (GRCm39) |
I730L |
probably benign |
Het |
Zfp352 |
A |
T |
4: 90,113,118 (GRCm39) |
K419N |
probably benign |
Het |
Zfp84 |
C |
A |
7: 29,474,873 (GRCm39) |
S48R |
probably damaging |
Het |
Zfp947 |
A |
T |
17: 22,364,386 (GRCm39) |
H429Q |
probably damaging |
Het |
|
Other mutations in Or1l4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Or1l4
|
APN |
2 |
37,091,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00943:Or1l4
|
APN |
2 |
37,092,183 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01100:Or1l4
|
APN |
2 |
37,091,652 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01696:Or1l4
|
APN |
2 |
37,091,523 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02119:Or1l4
|
APN |
2 |
37,091,281 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02807:Or1l4
|
APN |
2 |
37,091,586 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03030:Or1l4
|
APN |
2 |
37,091,883 (GRCm39) |
missense |
probably benign |
0.00 |
R0388:Or1l4
|
UTSW |
2 |
37,092,196 (GRCm39) |
splice site |
probably null |
|
R0788:Or1l4
|
UTSW |
2 |
37,092,035 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1126:Or1l4
|
UTSW |
2 |
37,092,113 (GRCm39) |
missense |
probably benign |
|
R1753:Or1l4
|
UTSW |
2 |
37,091,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Or1l4
|
UTSW |
2 |
37,091,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R1837:Or1l4
|
UTSW |
2 |
37,092,114 (GRCm39) |
missense |
probably benign |
0.23 |
R3711:Or1l4
|
UTSW |
2 |
37,091,285 (GRCm39) |
missense |
probably benign |
|
R4077:Or1l4
|
UTSW |
2 |
37,092,024 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4078:Or1l4
|
UTSW |
2 |
37,092,024 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4375:Or1l4
|
UTSW |
2 |
37,091,574 (GRCm39) |
missense |
probably benign |
0.33 |
R4607:Or1l4
|
UTSW |
2 |
37,092,094 (GRCm39) |
nonsense |
probably null |
|
R4608:Or1l4
|
UTSW |
2 |
37,092,094 (GRCm39) |
nonsense |
probably null |
|
R4889:Or1l4
|
UTSW |
2 |
37,092,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Or1l4
|
UTSW |
2 |
37,091,330 (GRCm39) |
missense |
probably benign |
0.33 |
R5560:Or1l4
|
UTSW |
2 |
37,091,942 (GRCm39) |
missense |
probably benign |
0.01 |
R5670:Or1l4
|
UTSW |
2 |
37,092,006 (GRCm39) |
missense |
probably benign |
0.19 |
R6108:Or1l4
|
UTSW |
2 |
37,091,778 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6727:Or1l4
|
UTSW |
2 |
37,092,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:Or1l4
|
UTSW |
2 |
37,092,189 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7079:Or1l4
|
UTSW |
2 |
37,092,185 (GRCm39) |
missense |
probably benign |
0.00 |
R7113:Or1l4
|
UTSW |
2 |
37,091,568 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7278:Or1l4
|
UTSW |
2 |
37,092,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R7731:Or1l4
|
UTSW |
2 |
37,091,561 (GRCm39) |
missense |
probably benign |
0.07 |
R8096:Or1l4
|
UTSW |
2 |
37,092,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R9301:Or1l4
|
UTSW |
2 |
37,091,255 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R9448:Or1l4
|
UTSW |
2 |
37,091,221 (GRCm39) |
start gained |
probably benign |
|
R9562:Or1l4
|
UTSW |
2 |
37,091,575 (GRCm39) |
missense |
probably benign |
|
R9565:Or1l4
|
UTSW |
2 |
37,091,575 (GRCm39) |
missense |
probably benign |
|
R9659:Or1l4
|
UTSW |
2 |
37,091,897 (GRCm39) |
missense |
possibly damaging |
0.58 |
|