Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,483,479 (GRCm39) |
M1659K |
probably benign |
Het |
Ace |
C |
A |
11: 105,864,958 (GRCm39) |
Q544K |
probably damaging |
Het |
Agpat4 |
A |
G |
17: 12,429,168 (GRCm39) |
E140G |
possibly damaging |
Het |
Akap12 |
A |
G |
10: 4,303,640 (GRCm39) |
D150G |
probably benign |
Het |
Akap6 |
A |
G |
12: 53,115,894 (GRCm39) |
Y999C |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,607,076 (GRCm39) |
I1326V |
possibly damaging |
Het |
Apold1 |
T |
A |
6: 134,960,999 (GRCm39) |
L151Q |
probably damaging |
Het |
Bmal1 |
A |
G |
7: 112,898,487 (GRCm39) |
D305G |
possibly damaging |
Het |
Brsk2 |
A |
G |
7: 141,552,133 (GRCm39) |
S564G |
probably damaging |
Het |
Ceacam18 |
T |
C |
7: 43,294,915 (GRCm39) |
V325A |
possibly damaging |
Het |
Clstn2 |
T |
C |
9: 97,464,654 (GRCm39) |
Y167C |
probably damaging |
Het |
Cyp11a1 |
G |
T |
9: 57,928,141 (GRCm39) |
V324L |
possibly damaging |
Het |
Ddx27 |
A |
G |
2: 166,861,950 (GRCm39) |
T151A |
possibly damaging |
Het |
Dhrs4 |
A |
G |
14: 55,727,306 (GRCm39) |
I252M |
possibly damaging |
Het |
Dlg2 |
A |
G |
7: 91,360,900 (GRCm39) |
D6G |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,927,333 (GRCm39) |
E1330K |
probably benign |
Het |
Ehd3 |
A |
G |
17: 74,137,391 (GRCm39) |
E520G |
probably benign |
Het |
Epha5 |
A |
G |
5: 84,479,731 (GRCm39) |
V91A |
possibly damaging |
Het |
Fam20c |
C |
A |
5: 138,743,676 (GRCm39) |
H237Q |
probably benign |
Het |
Fam217a |
C |
T |
13: 35,094,662 (GRCm39) |
G366S |
probably damaging |
Het |
Fancf |
T |
C |
7: 51,511,359 (GRCm39) |
E215G |
probably benign |
Het |
Fermt3 |
A |
T |
19: 6,980,664 (GRCm39) |
I301N |
probably damaging |
Het |
Fyco1 |
A |
T |
9: 123,660,350 (GRCm39) |
|
probably null |
Het |
Gen1 |
T |
C |
12: 11,311,068 (GRCm39) |
N55D |
probably damaging |
Het |
Gm20604 |
A |
T |
12: 102,709,636 (GRCm39) |
C75S |
unknown |
Het |
Gm3045 |
T |
A |
13: 56,578,160 (GRCm39) |
V199D |
unknown |
Het |
Gm49368 |
A |
G |
7: 127,712,178 (GRCm39) |
T805A |
possibly damaging |
Het |
Hgf |
T |
C |
5: 16,809,921 (GRCm39) |
|
probably null |
Het |
Hnrnpul2 |
T |
A |
19: 8,798,080 (GRCm39) |
H145Q |
probably benign |
Het |
Ift140 |
A |
G |
17: 25,313,753 (GRCm39) |
M1395V |
probably benign |
Het |
Il17rc |
T |
G |
6: 113,457,780 (GRCm39) |
|
probably null |
Het |
Kansl1l |
T |
A |
1: 66,840,347 (GRCm39) |
T318S |
probably benign |
Het |
Kcnc1 |
A |
T |
7: 46,077,034 (GRCm39) |
N279Y |
probably damaging |
Het |
Khdrbs2 |
T |
A |
1: 32,511,828 (GRCm39) |
H264Q |
probably benign |
Het |
Klf12 |
A |
G |
14: 100,260,144 (GRCm39) |
V195A |
possibly damaging |
Het |
Lhfpl2 |
A |
G |
13: 94,328,539 (GRCm39) |
E200G |
probably damaging |
Het |
Lmna |
T |
C |
3: 88,393,548 (GRCm39) |
D300G |
probably damaging |
Het |
Lrif1 |
A |
G |
3: 106,641,674 (GRCm39) |
T17A |
possibly damaging |
Het |
Mdm1 |
A |
G |
10: 117,982,523 (GRCm39) |
I53V |
probably damaging |
Het |
Mga |
T |
A |
2: 119,733,518 (GRCm39) |
I122N |
probably damaging |
Het |
Mos |
A |
G |
4: 3,871,763 (GRCm39) |
S18P |
probably benign |
Het |
Mterf3 |
C |
T |
13: 67,062,852 (GRCm39) |
V295I |
possibly damaging |
Het |
Muc16 |
G |
A |
9: 18,571,511 (GRCm39) |
T336I |
unknown |
Het |
Myo15a |
T |
C |
11: 60,374,555 (GRCm39) |
S136P |
|
Het |
Nav3 |
T |
A |
10: 109,738,955 (GRCm39) |
I128F |
probably damaging |
Het |
Nphs1 |
A |
G |
7: 30,170,594 (GRCm39) |
D928G |
probably damaging |
Het |
Or52z15 |
A |
G |
7: 103,332,464 (GRCm39) |
I180V |
probably damaging |
Het |
Or5b114-ps1 |
A |
T |
19: 13,352,553 (GRCm39) |
T76S |
possibly damaging |
Het |
Or5m13b |
T |
A |
2: 85,753,819 (GRCm39) |
V69E |
probably damaging |
Het |
Or5p70 |
A |
G |
7: 107,995,259 (GRCm39) |
K311E |
probably benign |
Het |
Or8u10 |
T |
C |
2: 85,915,911 (GRCm39) |
D70G |
possibly damaging |
Het |
Parvb |
T |
C |
15: 84,155,523 (GRCm39) |
|
probably null |
Het |
Ppp2r1a |
A |
G |
17: 21,181,877 (GRCm39) |
N465S |
probably benign |
Het |
Pramel34 |
T |
A |
5: 93,786,697 (GRCm39) |
E24V |
probably damaging |
Het |
Senp6 |
A |
G |
9: 80,046,379 (GRCm39) |
K950E |
possibly damaging |
Het |
Septin12 |
T |
C |
16: 4,805,481 (GRCm39) |
H304R |
probably damaging |
Het |
Septin3 |
T |
C |
15: 82,167,914 (GRCm39) |
V110A |
probably damaging |
Het |
Slc25a35 |
G |
T |
11: 68,862,076 (GRCm39) |
V170L |
probably benign |
Het |
Slco3a1 |
A |
T |
7: 73,934,153 (GRCm39) |
L673Q |
possibly damaging |
Het |
Smim35 |
A |
G |
9: 45,154,271 (GRCm39) |
N44S |
possibly damaging |
Het |
Tcp1 |
A |
G |
17: 13,136,687 (GRCm39) |
M23V |
probably benign |
Het |
Thg1l |
T |
C |
11: 45,845,288 (GRCm39) |
|
probably benign |
Het |
Tiam2 |
G |
A |
17: 3,471,923 (GRCm39) |
E522K |
probably benign |
Het |
Tie1 |
G |
A |
4: 118,341,867 (GRCm39) |
T194I |
possibly damaging |
Het |
Vmn2r49 |
T |
A |
7: 9,718,674 (GRCm39) |
E463D |
probably benign |
Het |
Wdr1 |
C |
A |
5: 38,697,355 (GRCm39) |
|
probably null |
Het |
Zbtb38 |
A |
T |
9: 96,567,649 (GRCm39) |
M1145K |
probably damaging |
Het |
|
Other mutations in Patj |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Patj
|
APN |
4 |
98,353,343 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00095:Patj
|
APN |
4 |
98,423,799 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00517:Patj
|
APN |
4 |
98,329,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00802:Patj
|
APN |
4 |
98,312,643 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01064:Patj
|
APN |
4 |
98,385,210 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01110:Patj
|
APN |
4 |
98,301,261 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01407:Patj
|
APN |
4 |
98,301,287 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01821:Patj
|
APN |
4 |
98,344,448 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02399:Patj
|
APN |
4 |
98,480,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02494:Patj
|
APN |
4 |
98,592,224 (GRCm39) |
splice site |
probably benign |
|
IGL02803:Patj
|
APN |
4 |
98,314,301 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02931:Patj
|
APN |
4 |
98,299,410 (GRCm39) |
splice site |
probably benign |
|
IGL03017:Patj
|
APN |
4 |
98,353,264 (GRCm39) |
splice site |
probably benign |
|
IGL03115:Patj
|
APN |
4 |
98,332,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03209:Patj
|
APN |
4 |
98,353,377 (GRCm39) |
missense |
probably null |
1.00 |
IGL03377:Patj
|
APN |
4 |
98,353,341 (GRCm39) |
missense |
probably damaging |
1.00 |
D4186:Patj
|
UTSW |
4 |
98,526,999 (GRCm39) |
missense |
probably benign |
0.17 |
PIT4531001:Patj
|
UTSW |
4 |
98,329,327 (GRCm39) |
missense |
probably damaging |
0.98 |
R0136:Patj
|
UTSW |
4 |
98,555,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R0294:Patj
|
UTSW |
4 |
98,385,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R0376:Patj
|
UTSW |
4 |
98,457,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Patj
|
UTSW |
4 |
98,562,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R0465:Patj
|
UTSW |
4 |
98,423,744 (GRCm39) |
splice site |
probably null |
|
R0466:Patj
|
UTSW |
4 |
98,576,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Patj
|
UTSW |
4 |
98,457,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Patj
|
UTSW |
4 |
98,569,472 (GRCm39) |
splice site |
probably benign |
|
R0657:Patj
|
UTSW |
4 |
98,555,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1281:Patj
|
UTSW |
4 |
98,304,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R1393:Patj
|
UTSW |
4 |
98,312,648 (GRCm39) |
missense |
probably benign |
0.01 |
R1480:Patj
|
UTSW |
4 |
98,357,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Patj
|
UTSW |
4 |
98,301,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Patj
|
UTSW |
4 |
98,320,017 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1729:Patj
|
UTSW |
4 |
98,320,017 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1797:Patj
|
UTSW |
4 |
98,575,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Patj
|
UTSW |
4 |
98,511,885 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1835:Patj
|
UTSW |
4 |
98,379,827 (GRCm39) |
missense |
probably benign |
0.00 |
R1880:Patj
|
UTSW |
4 |
98,385,477 (GRCm39) |
missense |
probably benign |
0.00 |
R2009:Patj
|
UTSW |
4 |
98,344,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R2090:Patj
|
UTSW |
4 |
98,325,560 (GRCm39) |
unclassified |
probably benign |
|
R2120:Patj
|
UTSW |
4 |
98,344,462 (GRCm39) |
missense |
probably benign |
0.01 |
R2180:Patj
|
UTSW |
4 |
98,411,739 (GRCm39) |
critical splice donor site |
probably null |
|
R2655:Patj
|
UTSW |
4 |
98,325,687 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3156:Patj
|
UTSW |
4 |
98,562,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R3749:Patj
|
UTSW |
4 |
98,357,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R3767:Patj
|
UTSW |
4 |
98,569,456 (GRCm39) |
nonsense |
probably null |
|
R3913:Patj
|
UTSW |
4 |
98,457,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R3917:Patj
|
UTSW |
4 |
98,480,245 (GRCm39) |
nonsense |
probably null |
|
R3918:Patj
|
UTSW |
4 |
98,344,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R4299:Patj
|
UTSW |
4 |
98,565,558 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4355:Patj
|
UTSW |
4 |
98,538,691 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4471:Patj
|
UTSW |
4 |
98,423,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R4762:Patj
|
UTSW |
4 |
98,293,807 (GRCm39) |
nonsense |
probably null |
|
R4877:Patj
|
UTSW |
4 |
98,457,295 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4945:Patj
|
UTSW |
4 |
98,383,301 (GRCm39) |
missense |
probably damaging |
0.97 |
R5274:Patj
|
UTSW |
4 |
98,407,218 (GRCm39) |
missense |
probably damaging |
0.99 |
R5343:Patj
|
UTSW |
4 |
98,564,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Patj
|
UTSW |
4 |
98,342,633 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5688:Patj
|
UTSW |
4 |
98,409,047 (GRCm39) |
nonsense |
probably null |
|
R5880:Patj
|
UTSW |
4 |
98,299,382 (GRCm39) |
missense |
probably damaging |
0.96 |
R5972:Patj
|
UTSW |
4 |
98,457,290 (GRCm39) |
missense |
probably damaging |
0.98 |
R6149:Patj
|
UTSW |
4 |
98,312,562 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6192:Patj
|
UTSW |
4 |
98,344,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Patj
|
UTSW |
4 |
98,357,804 (GRCm39) |
missense |
probably benign |
0.08 |
R6350:Patj
|
UTSW |
4 |
98,293,855 (GRCm39) |
missense |
probably benign |
0.26 |
R6363:Patj
|
UTSW |
4 |
98,320,097 (GRCm39) |
missense |
probably benign |
0.25 |
R6434:Patj
|
UTSW |
4 |
98,379,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R6496:Patj
|
UTSW |
4 |
98,304,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Patj
|
UTSW |
4 |
98,314,287 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7039:Patj
|
UTSW |
4 |
98,457,315 (GRCm39) |
missense |
probably damaging |
0.96 |
R7040:Patj
|
UTSW |
4 |
98,329,317 (GRCm39) |
missense |
probably benign |
0.02 |
R7052:Patj
|
UTSW |
4 |
98,565,497 (GRCm39) |
missense |
probably benign |
0.03 |
R7066:Patj
|
UTSW |
4 |
98,301,434 (GRCm39) |
missense |
probably benign |
0.24 |
R7236:Patj
|
UTSW |
4 |
98,299,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Patj
|
UTSW |
4 |
98,480,170 (GRCm39) |
missense |
probably benign |
0.26 |
R7260:Patj
|
UTSW |
4 |
98,304,970 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7412:Patj
|
UTSW |
4 |
98,299,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R7493:Patj
|
UTSW |
4 |
98,383,298 (GRCm39) |
missense |
probably benign |
0.41 |
R7570:Patj
|
UTSW |
4 |
98,312,737 (GRCm39) |
splice site |
probably null |
|
R7571:Patj
|
UTSW |
4 |
98,457,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:Patj
|
UTSW |
4 |
98,435,224 (GRCm39) |
missense |
probably benign |
0.35 |
R7658:Patj
|
UTSW |
4 |
98,576,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:Patj
|
UTSW |
4 |
98,385,187 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7669:Patj
|
UTSW |
4 |
98,407,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R7796:Patj
|
UTSW |
4 |
98,435,220 (GRCm39) |
start codon destroyed |
probably benign |
0.05 |
R7870:Patj
|
UTSW |
4 |
98,312,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7883:Patj
|
UTSW |
4 |
98,499,372 (GRCm39) |
missense |
probably benign |
0.00 |
R7948:Patj
|
UTSW |
4 |
98,312,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R8050:Patj
|
UTSW |
4 |
98,427,201 (GRCm39) |
missense |
probably benign |
0.00 |
R8183:Patj
|
UTSW |
4 |
98,562,466 (GRCm39) |
missense |
probably damaging |
0.96 |
R8239:Patj
|
UTSW |
4 |
98,570,308 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8483:Patj
|
UTSW |
4 |
98,312,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R8546:Patj
|
UTSW |
4 |
98,325,634 (GRCm39) |
missense |
probably benign |
0.00 |
R8746:Patj
|
UTSW |
4 |
98,394,067 (GRCm39) |
intron |
probably benign |
|
R8844:Patj
|
UTSW |
4 |
98,480,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Patj
|
UTSW |
4 |
98,385,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R8912:Patj
|
UTSW |
4 |
98,385,565 (GRCm39) |
missense |
|
|
R8959:Patj
|
UTSW |
4 |
98,480,212 (GRCm39) |
missense |
probably damaging |
0.99 |
R9083:Patj
|
UTSW |
4 |
98,401,871 (GRCm39) |
missense |
probably benign |
0.03 |
R9173:Patj
|
UTSW |
4 |
98,526,958 (GRCm39) |
missense |
probably benign |
|
R9206:Patj
|
UTSW |
4 |
98,427,310 (GRCm39) |
missense |
unknown |
|
R9208:Patj
|
UTSW |
4 |
98,427,310 (GRCm39) |
missense |
unknown |
|
R9560:Patj
|
UTSW |
4 |
98,570,289 (GRCm39) |
missense |
probably benign |
0.29 |
R9609:Patj
|
UTSW |
4 |
98,576,473 (GRCm39) |
missense |
probably benign |
0.00 |
R9617:Patj
|
UTSW |
4 |
98,393,991 (GRCm39) |
missense |
probably benign |
0.03 |
R9658:Patj
|
UTSW |
4 |
98,353,377 (GRCm39) |
missense |
probably null |
1.00 |
R9756:Patj
|
UTSW |
4 |
98,565,535 (GRCm39) |
missense |
probably benign |
|
Z1176:Patj
|
UTSW |
4 |
98,564,555 (GRCm39) |
nonsense |
probably null |
|
Z1176:Patj
|
UTSW |
4 |
98,499,367 (GRCm39) |
missense |
probably benign |
0.11 |
Z1177:Patj
|
UTSW |
4 |
98,385,411 (GRCm39) |
missense |
probably benign |
0.01 |
|