Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
G |
6: 128,543,958 (GRCm39) |
F528L |
probably benign |
Het |
Aadacl3 |
T |
G |
4: 144,182,778 (GRCm39) |
D230A |
probably damaging |
Het |
Adgrf3 |
T |
A |
5: 30,403,579 (GRCm39) |
|
probably benign |
Het |
Agtr1a |
A |
C |
13: 30,565,357 (GRCm39) |
T141P |
probably damaging |
Het |
Ankfy1 |
T |
A |
11: 72,621,300 (GRCm39) |
D195E |
probably benign |
Het |
AY074887 |
G |
A |
9: 54,857,786 (GRCm39) |
T113I |
probably damaging |
Het |
Cacna1c |
G |
A |
6: 119,034,314 (GRCm39) |
A71V |
|
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,003,351 (GRCm39) |
V78E |
probably benign |
Het |
Cyp2c67 |
T |
A |
19: 39,627,155 (GRCm39) |
Y225F |
probably benign |
Het |
Cyp2j13 |
T |
A |
4: 95,933,777 (GRCm39) |
H369L |
probably benign |
Het |
Dagla |
T |
C |
19: 10,225,587 (GRCm39) |
E859G |
probably benign |
Het |
Duox1 |
C |
A |
2: 122,168,152 (GRCm39) |
S1092R |
possibly damaging |
Het |
Elfn2 |
C |
A |
15: 78,556,561 (GRCm39) |
S662I |
probably benign |
Het |
Epor |
A |
T |
9: 21,870,741 (GRCm39) |
C380S |
probably benign |
Het |
Fsd2 |
T |
C |
7: 81,190,090 (GRCm39) |
E564G |
probably benign |
Het |
Hace1 |
C |
T |
10: 45,481,694 (GRCm39) |
T117I |
unknown |
Het |
Ift172 |
A |
G |
5: 31,412,985 (GRCm39) |
M1488T |
probably benign |
Het |
Insyn1 |
A |
G |
9: 58,406,623 (GRCm39) |
T178A |
probably damaging |
Het |
Kdm3b |
A |
G |
18: 34,952,840 (GRCm39) |
E1070G |
probably damaging |
Het |
Lrp6 |
A |
G |
6: 134,434,711 (GRCm39) |
F1331L |
probably benign |
Het |
Lrrc74a |
G |
A |
12: 86,783,253 (GRCm39) |
E33K |
probably damaging |
Het |
Magel2 |
T |
C |
7: 62,027,420 (GRCm39) |
M108T |
unknown |
Het |
Mief1 |
T |
C |
15: 80,132,584 (GRCm39) |
S127P |
probably benign |
Het |
Mprip |
T |
C |
11: 59,650,526 (GRCm39) |
V1410A |
probably benign |
Het |
Muc1 |
G |
A |
3: 89,138,821 (GRCm39) |
V477M |
possibly damaging |
Het |
Nat8f3 |
A |
T |
6: 85,738,687 (GRCm39) |
M25K |
possibly damaging |
Het |
Neb |
T |
G |
2: 52,073,781 (GRCm39) |
H5942P |
probably damaging |
Het |
Nf2 |
A |
T |
11: 4,766,099 (GRCm39) |
Y144N |
probably damaging |
Het |
Nipbl |
T |
A |
15: 8,368,225 (GRCm39) |
M1166L |
probably benign |
Het |
Npnt |
A |
T |
3: 132,614,136 (GRCm39) |
L206Q |
probably damaging |
Het |
Or10ak13 |
T |
C |
4: 118,638,996 (GRCm39) |
Y262C |
probably damaging |
Het |
Or4g7 |
A |
G |
2: 111,309,992 (GRCm39) |
T288A |
probably damaging |
Het |
Or6c65 |
T |
A |
10: 129,604,127 (GRCm39) |
I254N |
probably damaging |
Het |
Parg |
A |
G |
14: 31,932,492 (GRCm39) |
K444R |
probably benign |
Het |
Pcbp4 |
A |
T |
9: 106,337,202 (GRCm39) |
|
probably null |
Het |
Pcdhgb4 |
A |
G |
18: 37,853,847 (GRCm39) |
S81G |
probably benign |
Het |
Plat |
G |
T |
8: 23,262,248 (GRCm39) |
G91W |
probably damaging |
Het |
Plekho2 |
T |
C |
9: 65,464,058 (GRCm39) |
N264D |
probably benign |
Het |
Pmpca |
T |
A |
2: 26,281,893 (GRCm39) |
M182K |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,252,695 (GRCm39) |
H476R |
probably benign |
Het |
Prxl2a |
G |
A |
14: 40,720,836 (GRCm39) |
P126S |
possibly damaging |
Het |
Rab7 |
T |
C |
6: 87,989,369 (GRCm39) |
S34G |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,368,695 (GRCm39) |
S409R |
probably damaging |
Het |
Ryr1 |
C |
A |
7: 28,751,753 (GRCm39) |
R3680L |
probably benign |
Het |
Sbno1 |
T |
C |
5: 124,512,618 (GRCm39) |
S1384G |
possibly damaging |
Het |
Shmt1 |
T |
C |
11: 60,685,763 (GRCm39) |
D271G |
probably benign |
Het |
Sin3a |
C |
T |
9: 57,034,510 (GRCm39) |
R1228W |
probably damaging |
Het |
Slc25a39 |
T |
C |
11: 102,294,620 (GRCm39) |
R294G |
probably benign |
Het |
Smcr8 |
T |
A |
11: 60,670,254 (GRCm39) |
S467R |
probably damaging |
Het |
Spaca7 |
A |
G |
8: 12,636,480 (GRCm39) |
Y102C |
probably damaging |
Het |
Tacr1 |
A |
G |
6: 82,380,706 (GRCm39) |
Y39C |
probably damaging |
Het |
Tenm3 |
G |
A |
8: 48,752,680 (GRCm39) |
S894L |
possibly damaging |
Het |
Tmem115 |
T |
A |
9: 107,415,132 (GRCm39) |
M307K |
possibly damaging |
Het |
Tnn |
A |
G |
1: 159,943,846 (GRCm39) |
V989A |
possibly damaging |
Het |
Trabd2b |
T |
A |
4: 114,460,186 (GRCm39) |
N441K |
probably damaging |
Het |
Ttll1 |
T |
C |
15: 83,373,709 (GRCm39) |
K368R |
probably benign |
Het |
Tubgcp2 |
C |
T |
7: 139,576,705 (GRCm39) |
V858I |
probably benign |
Het |
Ufsp2 |
G |
T |
8: 46,436,614 (GRCm39) |
V122L |
probably benign |
Het |
Wdr26 |
A |
G |
1: 181,011,913 (GRCm39) |
C470R |
possibly damaging |
Het |
Xab2 |
T |
C |
8: 3,663,845 (GRCm39) |
H358R |
probably benign |
Het |
Xrcc5 |
A |
G |
1: 72,422,905 (GRCm39) |
I697V |
probably benign |
Het |
|
Other mutations in Rbp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01364:Rbp3
|
APN |
14 |
33,676,145 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01643:Rbp3
|
APN |
14 |
33,678,793 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01665:Rbp3
|
APN |
14 |
33,678,088 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01809:Rbp3
|
APN |
14 |
33,677,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01975:Rbp3
|
APN |
14 |
33,680,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02349:Rbp3
|
APN |
14 |
33,677,676 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02447:Rbp3
|
APN |
14 |
33,676,460 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03192:Rbp3
|
APN |
14 |
33,680,540 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL03302:Rbp3
|
APN |
14 |
33,676,616 (GRCm39) |
missense |
probably damaging |
0.97 |
Behagt
|
UTSW |
14 |
33,676,411 (GRCm39) |
missense |
probably benign |
0.00 |
jagt
|
UTSW |
14 |
33,678,439 (GRCm39) |
missense |
probably damaging |
0.97 |
muntre
|
UTSW |
14 |
33,678,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
Rotwild
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
P4717OSA:Rbp3
|
UTSW |
14 |
33,677,456 (GRCm39) |
missense |
probably damaging |
0.96 |
R0234:Rbp3
|
UTSW |
14 |
33,677,858 (GRCm39) |
missense |
probably damaging |
0.98 |
R0234:Rbp3
|
UTSW |
14 |
33,677,858 (GRCm39) |
missense |
probably damaging |
0.98 |
R0432:Rbp3
|
UTSW |
14 |
33,676,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R0469:Rbp3
|
UTSW |
14 |
33,684,376 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0652:Rbp3
|
UTSW |
14 |
33,680,605 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0739:Rbp3
|
UTSW |
14 |
33,680,604 (GRCm39) |
missense |
probably benign |
0.28 |
R0747:Rbp3
|
UTSW |
14 |
33,678,235 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0836:Rbp3
|
UTSW |
14 |
33,678,595 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1102:Rbp3
|
UTSW |
14 |
33,678,313 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1583:Rbp3
|
UTSW |
14 |
33,676,481 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1589:Rbp3
|
UTSW |
14 |
33,677,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R1595:Rbp3
|
UTSW |
14 |
33,678,155 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1720:Rbp3
|
UTSW |
14 |
33,678,866 (GRCm39) |
missense |
probably benign |
0.38 |
R1830:Rbp3
|
UTSW |
14 |
33,676,601 (GRCm39) |
missense |
probably benign |
0.31 |
R1982:Rbp3
|
UTSW |
14 |
33,676,502 (GRCm39) |
missense |
probably damaging |
0.99 |
R1985:Rbp3
|
UTSW |
14 |
33,678,418 (GRCm39) |
missense |
probably benign |
0.00 |
R1985:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2027:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2100:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Rbp3
|
UTSW |
14 |
33,678,014 (GRCm39) |
missense |
probably benign |
0.00 |
R2138:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2183:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2277:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2306:Rbp3
|
UTSW |
14 |
33,684,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2696:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2697:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2698:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2940:Rbp3
|
UTSW |
14 |
33,677,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R2971:Rbp3
|
UTSW |
14 |
33,676,411 (GRCm39) |
missense |
probably benign |
0.00 |
R3111:Rbp3
|
UTSW |
14 |
33,676,069 (GRCm39) |
missense |
probably benign |
0.01 |
R3155:Rbp3
|
UTSW |
14 |
33,679,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R3156:Rbp3
|
UTSW |
14 |
33,679,071 (GRCm39) |
missense |
probably damaging |
0.98 |
R3751:Rbp3
|
UTSW |
14 |
33,677,969 (GRCm39) |
missense |
probably damaging |
0.98 |
R3752:Rbp3
|
UTSW |
14 |
33,677,969 (GRCm39) |
missense |
probably damaging |
0.98 |
R3851:Rbp3
|
UTSW |
14 |
33,677,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R4016:Rbp3
|
UTSW |
14 |
33,677,347 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4276:Rbp3
|
UTSW |
14 |
33,680,607 (GRCm39) |
missense |
probably benign |
0.24 |
R4277:Rbp3
|
UTSW |
14 |
33,680,607 (GRCm39) |
missense |
probably benign |
0.24 |
R4278:Rbp3
|
UTSW |
14 |
33,680,607 (GRCm39) |
missense |
probably benign |
0.24 |
R4382:Rbp3
|
UTSW |
14 |
33,677,253 (GRCm39) |
missense |
probably benign |
0.12 |
R4383:Rbp3
|
UTSW |
14 |
33,677,253 (GRCm39) |
missense |
probably benign |
0.12 |
R4385:Rbp3
|
UTSW |
14 |
33,677,253 (GRCm39) |
missense |
probably benign |
0.12 |
R4625:Rbp3
|
UTSW |
14 |
33,678,056 (GRCm39) |
missense |
probably benign |
|
R4712:Rbp3
|
UTSW |
14 |
33,682,615 (GRCm39) |
missense |
probably damaging |
0.97 |
R4812:Rbp3
|
UTSW |
14 |
33,676,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Rbp3
|
UTSW |
14 |
33,677,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Rbp3
|
UTSW |
14 |
33,676,427 (GRCm39) |
missense |
probably damaging |
0.98 |
R5262:Rbp3
|
UTSW |
14 |
33,676,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R5387:Rbp3
|
UTSW |
14 |
33,678,370 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5468:Rbp3
|
UTSW |
14 |
33,678,584 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5837:Rbp3
|
UTSW |
14 |
33,676,230 (GRCm39) |
missense |
probably benign |
0.00 |
R5994:Rbp3
|
UTSW |
14 |
33,676,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Rbp3
|
UTSW |
14 |
33,676,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Rbp3
|
UTSW |
14 |
33,678,439 (GRCm39) |
missense |
probably damaging |
0.97 |
R6266:Rbp3
|
UTSW |
14 |
33,676,418 (GRCm39) |
missense |
probably benign |
|
R6357:Rbp3
|
UTSW |
14 |
33,678,991 (GRCm39) |
missense |
probably damaging |
0.99 |
R6457:Rbp3
|
UTSW |
14 |
33,677,224 (GRCm39) |
nonsense |
probably null |
|
R6777:Rbp3
|
UTSW |
14 |
33,676,230 (GRCm39) |
missense |
probably benign |
0.00 |
R7158:Rbp3
|
UTSW |
14 |
33,677,513 (GRCm39) |
missense |
probably benign |
0.00 |
R7183:Rbp3
|
UTSW |
14 |
33,677,161 (GRCm39) |
missense |
probably benign |
0.02 |
R7256:Rbp3
|
UTSW |
14 |
33,684,540 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7654:Rbp3
|
UTSW |
14 |
33,677,797 (GRCm39) |
missense |
probably benign |
|
R7756:Rbp3
|
UTSW |
14 |
33,676,732 (GRCm39) |
missense |
probably benign |
0.15 |
R7758:Rbp3
|
UTSW |
14 |
33,676,732 (GRCm39) |
missense |
probably benign |
0.15 |
R7784:Rbp3
|
UTSW |
14 |
33,676,115 (GRCm39) |
missense |
probably benign |
0.41 |
R7845:Rbp3
|
UTSW |
14 |
33,678,421 (GRCm39) |
missense |
probably benign |
0.24 |
R8176:Rbp3
|
UTSW |
14 |
33,677,605 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8281:Rbp3
|
UTSW |
14 |
33,678,320 (GRCm39) |
missense |
probably benign |
0.00 |
R8393:Rbp3
|
UTSW |
14 |
33,678,156 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8552:Rbp3
|
UTSW |
14 |
33,677,621 (GRCm39) |
missense |
probably benign |
0.01 |
R8730:Rbp3
|
UTSW |
14 |
33,677,795 (GRCm39) |
missense |
probably benign |
|
R8773:Rbp3
|
UTSW |
14 |
33,684,492 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8836:Rbp3
|
UTSW |
14 |
33,680,588 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8843:Rbp3
|
UTSW |
14 |
33,676,522 (GRCm39) |
missense |
probably benign |
|
R8880:Rbp3
|
UTSW |
14 |
33,678,796 (GRCm39) |
missense |
probably benign |
0.16 |
R8941:Rbp3
|
UTSW |
14 |
33,678,486 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8971:Rbp3
|
UTSW |
14 |
33,677,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Rbp3
|
UTSW |
14 |
33,684,360 (GRCm39) |
nonsense |
probably null |
|
R8999:Rbp3
|
UTSW |
14 |
33,684,360 (GRCm39) |
nonsense |
probably null |
|
R9436:Rbp3
|
UTSW |
14 |
33,677,234 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9525:Rbp3
|
UTSW |
14 |
33,676,402 (GRCm39) |
missense |
probably benign |
0.00 |
R9563:Rbp3
|
UTSW |
14 |
33,677,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Rbp3
|
UTSW |
14 |
33,677,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R9723:Rbp3
|
UTSW |
14 |
33,677,474 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Rbp3
|
UTSW |
14 |
33,676,495 (GRCm39) |
missense |
possibly damaging |
0.58 |
|