Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atg2a |
T |
C |
19: 6,299,959 (GRCm39) |
|
probably null |
Het |
Bfsp1 |
T |
C |
2: 143,704,566 (GRCm39) |
T96A |
probably benign |
Het |
Btnl1 |
A |
G |
17: 34,601,239 (GRCm39) |
E322G |
possibly damaging |
Het |
Cand2 |
T |
C |
6: 115,766,568 (GRCm39) |
V391A |
probably damaging |
Het |
Ccdc169 |
A |
G |
3: 55,078,702 (GRCm39) |
M188V |
probably benign |
Het |
Cngb1 |
T |
C |
8: 95,968,987 (GRCm39) |
I1174V |
probably benign |
Het |
Cpeb4 |
T |
C |
11: 31,822,316 (GRCm39) |
V10A |
possibly damaging |
Het |
Cpt1b |
T |
C |
15: 89,307,942 (GRCm39) |
T206A |
probably benign |
Het |
Dapk3 |
T |
C |
10: 81,025,999 (GRCm39) |
S97P |
probably benign |
Het |
Drc3 |
T |
C |
11: 60,261,404 (GRCm39) |
L185P |
probably damaging |
Het |
Efr3b |
T |
C |
12: 4,042,923 (GRCm39) |
|
probably null |
Het |
Erbb3 |
T |
A |
10: 128,409,088 (GRCm39) |
I742F |
probably damaging |
Het |
Fktn |
A |
G |
4: 53,720,181 (GRCm39) |
Y65C |
probably benign |
Het |
Fstl5 |
G |
A |
3: 76,496,302 (GRCm39) |
G355D |
probably damaging |
Het |
Grm8 |
A |
T |
6: 27,363,115 (GRCm39) |
I800N |
probably damaging |
Het |
Gss |
C |
T |
2: 155,409,773 (GRCm39) |
R221H |
probably benign |
Het |
H2-M10.4 |
A |
T |
17: 36,771,359 (GRCm39) |
V273D |
probably damaging |
Het |
Large1 |
C |
A |
8: 73,774,945 (GRCm39) |
W255L |
possibly damaging |
Het |
Meig1 |
T |
C |
2: 3,410,288 (GRCm39) |
K71E |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,619,396 (GRCm39) |
N1760D |
probably benign |
Het |
Ncapd2 |
A |
T |
6: 125,166,781 (GRCm39) |
N24K |
probably damaging |
Het |
Papolg |
T |
G |
11: 23,841,869 (GRCm39) |
H18P |
probably damaging |
Het |
Psd |
T |
C |
19: 46,308,098 (GRCm39) |
H667R |
possibly damaging |
Het |
Rita1 |
C |
T |
5: 120,747,858 (GRCm39) |
A147T |
probably damaging |
Het |
Rtp1 |
T |
C |
16: 23,249,943 (GRCm39) |
S103P |
probably damaging |
Het |
Snx21 |
T |
C |
2: 164,634,310 (GRCm39) |
|
probably benign |
Het |
Spmip3 |
A |
T |
1: 177,570,867 (GRCm39) |
Q67L |
probably benign |
Het |
Tiam1 |
G |
T |
16: 89,596,924 (GRCm39) |
H301N |
probably benign |
Het |
Trcg1 |
A |
T |
9: 57,147,676 (GRCm39) |
I11F |
possibly damaging |
Het |
Trpm6 |
A |
G |
19: 18,831,581 (GRCm39) |
K1482R |
probably benign |
Het |
Tyw1 |
G |
T |
5: 130,295,921 (GRCm39) |
G116V |
probably benign |
Het |
Zfp341 |
T |
C |
2: 154,474,224 (GRCm39) |
C343R |
possibly damaging |
Het |
|
Other mutations in Nphp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01707:Nphp3
|
APN |
9 |
103,895,357 (GRCm39) |
missense |
possibly damaging |
0.75 |
lithograph
|
UTSW |
9 |
103,919,189 (GRCm39) |
missense |
probably damaging |
1.00 |
quartzite
|
UTSW |
9 |
103,913,376 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Nphp3
|
UTSW |
9 |
103,913,093 (GRCm39) |
critical splice donor site |
probably null |
|
FR4548:Nphp3
|
UTSW |
9 |
103,903,138 (GRCm39) |
small deletion |
probably benign |
|
FR4589:Nphp3
|
UTSW |
9 |
103,903,138 (GRCm39) |
small deletion |
probably benign |
|
R0112:Nphp3
|
UTSW |
9 |
103,914,547 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0555:Nphp3
|
UTSW |
9 |
103,900,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Nphp3
|
UTSW |
9 |
103,895,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Nphp3
|
UTSW |
9 |
103,913,481 (GRCm39) |
critical splice donor site |
probably null |
|
R0743:Nphp3
|
UTSW |
9 |
103,899,967 (GRCm39) |
small deletion |
probably benign |
|
R0853:Nphp3
|
UTSW |
9 |
103,909,132 (GRCm39) |
missense |
probably benign |
0.03 |
R0920:Nphp3
|
UTSW |
9 |
103,909,106 (GRCm39) |
missense |
probably benign |
0.00 |
R1420:Nphp3
|
UTSW |
9 |
103,913,092 (GRCm39) |
critical splice donor site |
probably null |
|
R1464:Nphp3
|
UTSW |
9 |
103,909,078 (GRCm39) |
splice site |
probably benign |
|
R1476:Nphp3
|
UTSW |
9 |
103,903,126 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1585:Nphp3
|
UTSW |
9 |
103,886,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Nphp3
|
UTSW |
9 |
103,913,039 (GRCm39) |
missense |
probably benign |
0.30 |
R1688:Nphp3
|
UTSW |
9 |
103,880,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Nphp3
|
UTSW |
9 |
103,880,010 (GRCm39) |
missense |
probably benign |
|
R1807:Nphp3
|
UTSW |
9 |
103,897,940 (GRCm39) |
missense |
probably benign |
0.01 |
R1857:Nphp3
|
UTSW |
9 |
103,898,493 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1962:Nphp3
|
UTSW |
9 |
103,898,537 (GRCm39) |
missense |
probably benign |
0.00 |
R2127:Nphp3
|
UTSW |
9 |
103,885,442 (GRCm39) |
missense |
probably damaging |
0.98 |
R2138:Nphp3
|
UTSW |
9 |
103,903,102 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2233:Nphp3
|
UTSW |
9 |
103,914,575 (GRCm39) |
missense |
probably benign |
0.02 |
R2234:Nphp3
|
UTSW |
9 |
103,914,575 (GRCm39) |
missense |
probably benign |
0.02 |
R3861:Nphp3
|
UTSW |
9 |
103,916,525 (GRCm39) |
unclassified |
probably benign |
|
R3928:Nphp3
|
UTSW |
9 |
103,888,929 (GRCm39) |
missense |
probably damaging |
0.99 |
R3961:Nphp3
|
UTSW |
9 |
103,880,241 (GRCm39) |
nonsense |
probably null |
|
R4182:Nphp3
|
UTSW |
9 |
103,915,663 (GRCm39) |
missense |
probably benign |
0.06 |
R4294:Nphp3
|
UTSW |
9 |
103,899,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4387:Nphp3
|
UTSW |
9 |
103,907,219 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4625:Nphp3
|
UTSW |
9 |
103,913,358 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4628:Nphp3
|
UTSW |
9 |
103,880,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R4696:Nphp3
|
UTSW |
9 |
103,899,931 (GRCm39) |
missense |
probably benign |
0.01 |
R4865:Nphp3
|
UTSW |
9 |
103,909,169 (GRCm39) |
missense |
probably benign |
|
R4886:Nphp3
|
UTSW |
9 |
103,880,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Nphp3
|
UTSW |
9 |
103,909,198 (GRCm39) |
missense |
probably benign |
|
R5445:Nphp3
|
UTSW |
9 |
103,881,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5451:Nphp3
|
UTSW |
9 |
103,919,221 (GRCm39) |
missense |
probably benign |
|
R5520:Nphp3
|
UTSW |
9 |
103,901,872 (GRCm39) |
missense |
probably benign |
0.30 |
R5641:Nphp3
|
UTSW |
9 |
103,913,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Nphp3
|
UTSW |
9 |
103,880,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5928:Nphp3
|
UTSW |
9 |
103,912,996 (GRCm39) |
missense |
probably benign |
0.01 |
R5931:Nphp3
|
UTSW |
9 |
103,897,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6161:Nphp3
|
UTSW |
9 |
103,909,105 (GRCm39) |
missense |
probably benign |
0.11 |
R6298:Nphp3
|
UTSW |
9 |
103,892,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R6890:Nphp3
|
UTSW |
9 |
103,919,153 (GRCm39) |
missense |
probably damaging |
0.96 |
R7009:Nphp3
|
UTSW |
9 |
103,893,315 (GRCm39) |
missense |
probably null |
0.00 |
R7065:Nphp3
|
UTSW |
9 |
103,919,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7146:Nphp3
|
UTSW |
9 |
103,882,036 (GRCm39) |
nonsense |
probably null |
|
R7198:Nphp3
|
UTSW |
9 |
103,881,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7360:Nphp3
|
UTSW |
9 |
103,893,277 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7369:Nphp3
|
UTSW |
9 |
103,895,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R7554:Nphp3
|
UTSW |
9 |
103,919,270 (GRCm39) |
missense |
probably damaging |
0.98 |
R7591:Nphp3
|
UTSW |
9 |
103,895,477 (GRCm39) |
critical splice donor site |
probably null |
|
R7665:Nphp3
|
UTSW |
9 |
103,882,592 (GRCm39) |
splice site |
probably null |
|
R7672:Nphp3
|
UTSW |
9 |
103,909,159 (GRCm39) |
missense |
probably benign |
|
R7675:Nphp3
|
UTSW |
9 |
103,893,287 (GRCm39) |
missense |
probably benign |
|
R8039:Nphp3
|
UTSW |
9 |
103,909,162 (GRCm39) |
missense |
probably benign |
|
R8145:Nphp3
|
UTSW |
9 |
103,913,050 (GRCm39) |
missense |
probably benign |
0.16 |
R8211:Nphp3
|
UTSW |
9 |
103,909,096 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8882:Nphp3
|
UTSW |
9 |
103,882,793 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9020:Nphp3
|
UTSW |
9 |
103,909,150 (GRCm39) |
missense |
probably benign |
0.00 |
R9132:Nphp3
|
UTSW |
9 |
103,897,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R9135:Nphp3
|
UTSW |
9 |
103,909,214 (GRCm39) |
missense |
probably damaging |
0.99 |
R9159:Nphp3
|
UTSW |
9 |
103,897,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:Nphp3
|
UTSW |
9 |
103,919,305 (GRCm39) |
missense |
probably benign |
|
R9226:Nphp3
|
UTSW |
9 |
103,885,328 (GRCm39) |
missense |
probably benign |
0.00 |
R9229:Nphp3
|
UTSW |
9 |
103,913,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Nphp3
|
UTSW |
9 |
103,913,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R9678:Nphp3
|
UTSW |
9 |
103,900,686 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9731:Nphp3
|
UTSW |
9 |
103,886,369 (GRCm39) |
missense |
probably damaging |
1.00 |
V7583:Nphp3
|
UTSW |
9 |
103,913,093 (GRCm39) |
critical splice donor site |
probably null |
|
|