Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox3 |
A |
G |
1: 58,177,568 (GRCm39) |
Y261C |
probably benign |
Het |
Arhgef10 |
T |
C |
8: 15,047,632 (GRCm39) |
V1165A |
probably damaging |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Bhmt2 |
G |
A |
13: 93,799,833 (GRCm39) |
A201V |
probably damaging |
Het |
Ccdc115 |
A |
T |
1: 34,476,895 (GRCm39) |
S115T |
possibly damaging |
Het |
Clca4b |
A |
G |
3: 144,617,100 (GRCm39) |
V850A |
probably benign |
Het |
Commd8 |
A |
T |
5: 72,318,350 (GRCm39) |
H144Q |
probably benign |
Het |
Creb3l1 |
C |
T |
2: 91,822,231 (GRCm39) |
|
probably null |
Het |
Csnka2ip |
T |
C |
16: 64,298,262 (GRCm39) |
K701E |
unknown |
Het |
Cyb5d2 |
A |
G |
11: 72,669,702 (GRCm39) |
C219R |
|
Het |
Ep400 |
T |
C |
5: 110,877,730 (GRCm39) |
T835A |
unknown |
Het |
Fam169a |
A |
G |
13: 97,246,543 (GRCm39) |
Y228C |
possibly damaging |
Het |
Fam169a |
A |
G |
13: 97,250,695 (GRCm39) |
D342G |
possibly damaging |
Het |
Fbxw21 |
A |
T |
9: 108,968,612 (GRCm39) |
C455S |
probably benign |
Het |
Fbxw26 |
A |
G |
9: 109,561,625 (GRCm39) |
S190P |
probably damaging |
Het |
Gabra5 |
A |
G |
7: 57,058,440 (GRCm39) |
I436T |
|
Het |
Gm9767 |
G |
A |
10: 25,954,916 (GRCm39) |
G156D |
|
Het |
Grid1 |
G |
A |
14: 35,043,664 (GRCm39) |
D340N |
probably damaging |
Het |
Gsn |
T |
C |
2: 35,186,227 (GRCm39) |
|
probably null |
Het |
Hao1 |
A |
G |
2: 134,396,204 (GRCm39) |
S17P |
probably benign |
Het |
Hspa1l |
A |
G |
17: 35,196,735 (GRCm39) |
N258S |
probably benign |
Het |
Isyna1 |
C |
T |
8: 71,048,193 (GRCm39) |
R200C |
probably damaging |
Het |
Itgb2 |
A |
T |
10: 77,396,942 (GRCm39) |
K659M |
probably benign |
Het |
Klf11 |
T |
C |
12: 24,705,029 (GRCm39) |
M161T |
probably benign |
Het |
Ktn1 |
A |
T |
14: 47,962,174 (GRCm39) |
K1114N |
probably damaging |
Het |
Lrrc26 |
C |
T |
2: 25,180,571 (GRCm39) |
P191S |
probably benign |
Het |
Ogdh |
T |
C |
11: 6,297,854 (GRCm39) |
I576T |
possibly damaging |
Het |
Or10al4 |
T |
C |
17: 38,036,986 (GRCm39) |
S24P |
probably damaging |
Het |
Or14c45 |
T |
C |
7: 86,176,285 (GRCm39) |
C107R |
possibly damaging |
Het |
Or14j4 |
A |
G |
17: 37,920,718 (GRCm39) |
F308S |
probably damaging |
Het |
Or4k40 |
A |
T |
2: 111,251,013 (GRCm39) |
F94L |
probably damaging |
Het |
Or4p20 |
T |
C |
2: 88,253,677 (GRCm39) |
R231G |
probably damaging |
Het |
Or7g20 |
G |
A |
9: 18,946,730 (GRCm39) |
V104I |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,217,963 (GRCm39) |
V2104A |
probably benign |
Het |
Pds5a |
G |
A |
5: 65,792,747 (GRCm39) |
R729W |
probably damaging |
Het |
Pgap1 |
G |
A |
1: 54,582,275 (GRCm39) |
Q191* |
probably null |
Het |
Pglyrp3 |
A |
G |
3: 91,935,310 (GRCm39) |
I187V |
probably benign |
Het |
Pkdrej |
T |
A |
15: 85,699,571 (GRCm39) |
I2122F |
possibly damaging |
Het |
Pold1 |
G |
A |
7: 44,191,079 (GRCm39) |
R251W |
probably damaging |
Het |
Prr22 |
A |
G |
17: 57,078,335 (GRCm39) |
M163V |
probably benign |
Het |
Ptprc |
A |
T |
1: 138,001,388 (GRCm39) |
N814K |
probably benign |
Het |
Rapgef2 |
G |
A |
3: 79,019,495 (GRCm39) |
L59F |
probably damaging |
Het |
Rbm22 |
T |
C |
18: 60,699,492 (GRCm39) |
L147P |
probably damaging |
Het |
Rgsl1 |
G |
A |
1: 153,657,445 (GRCm39) |
S391F |
unknown |
Het |
Rnf13 |
A |
T |
3: 57,727,983 (GRCm39) |
D221V |
possibly damaging |
Het |
Senp2 |
T |
A |
16: 21,842,398 (GRCm39) |
L154Q |
probably damaging |
Het |
Srfbp1 |
A |
G |
18: 52,621,332 (GRCm39) |
Q131R |
possibly damaging |
Het |
Tmprss11a |
A |
T |
5: 86,562,402 (GRCm39) |
Y314* |
probably null |
Het |
Ttn |
G |
T |
2: 76,666,286 (GRCm39) |
P11590Q |
unknown |
Het |
Txnrd3 |
C |
T |
6: 89,640,084 (GRCm39) |
T266M |
possibly damaging |
Het |
Zfp810 |
T |
C |
9: 22,194,497 (GRCm39) |
S64G |
possibly damaging |
Het |
|
Other mutations in Lonrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Lonrf1
|
APN |
8 |
36,697,231 (GRCm39) |
splice site |
probably benign |
|
IGL02195:Lonrf1
|
APN |
8 |
36,687,102 (GRCm39) |
nonsense |
probably null |
|
IGL03087:Lonrf1
|
APN |
8 |
36,692,705 (GRCm39) |
splice site |
probably null |
|
IGL03163:Lonrf1
|
APN |
8 |
36,697,484 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03225:Lonrf1
|
APN |
8 |
36,689,855 (GRCm39) |
missense |
probably damaging |
0.96 |
BB009:Lonrf1
|
UTSW |
8 |
36,690,070 (GRCm39) |
missense |
probably benign |
0.17 |
BB019:Lonrf1
|
UTSW |
8 |
36,690,070 (GRCm39) |
missense |
probably benign |
0.17 |
R0480:Lonrf1
|
UTSW |
8 |
36,689,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Lonrf1
|
UTSW |
8 |
36,698,313 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0557:Lonrf1
|
UTSW |
8 |
36,697,574 (GRCm39) |
missense |
probably benign |
0.12 |
R1489:Lonrf1
|
UTSW |
8 |
36,690,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Lonrf1
|
UTSW |
8 |
36,701,126 (GRCm39) |
missense |
probably benign |
0.02 |
R2225:Lonrf1
|
UTSW |
8 |
36,703,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R2345:Lonrf1
|
UTSW |
8 |
36,690,016 (GRCm39) |
critical splice donor site |
probably null |
|
R4821:Lonrf1
|
UTSW |
8 |
36,687,126 (GRCm39) |
missense |
probably benign |
|
R4934:Lonrf1
|
UTSW |
8 |
36,701,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Lonrf1
|
UTSW |
8 |
36,690,178 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6124:Lonrf1
|
UTSW |
8 |
36,696,354 (GRCm39) |
missense |
probably damaging |
0.97 |
R6485:Lonrf1
|
UTSW |
8 |
36,696,288 (GRCm39) |
critical splice donor site |
probably null |
|
R6603:Lonrf1
|
UTSW |
8 |
36,690,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R6886:Lonrf1
|
UTSW |
8 |
36,696,191 (GRCm39) |
splice site |
probably null |
|
R7113:Lonrf1
|
UTSW |
8 |
36,697,664 (GRCm39) |
missense |
probably benign |
0.01 |
R7689:Lonrf1
|
UTSW |
8 |
36,715,918 (GRCm39) |
nonsense |
probably null |
|
R7711:Lonrf1
|
UTSW |
8 |
36,716,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R7743:Lonrf1
|
UTSW |
8 |
36,716,206 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7932:Lonrf1
|
UTSW |
8 |
36,690,070 (GRCm39) |
missense |
probably benign |
0.17 |
R8085:Lonrf1
|
UTSW |
8 |
36,715,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8183:Lonrf1
|
UTSW |
8 |
36,689,819 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8500:Lonrf1
|
UTSW |
8 |
36,698,292 (GRCm39) |
missense |
probably benign |
0.00 |
R8527:Lonrf1
|
UTSW |
8 |
36,686,986 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8993:Lonrf1
|
UTSW |
8 |
36,696,392 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9100:Lonrf1
|
UTSW |
8 |
36,715,919 (GRCm39) |
small deletion |
probably benign |
|
R9464:Lonrf1
|
UTSW |
8 |
36,690,024 (GRCm39) |
missense |
probably benign |
0.01 |
R9717:Lonrf1
|
UTSW |
8 |
36,701,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Lonrf1
|
UTSW |
8 |
36,703,235 (GRCm39) |
missense |
probably damaging |
0.99 |
|