Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
A |
G |
9: 44,190,980 (GRCm39) |
|
probably benign |
Het |
Abhd14a |
G |
T |
9: 106,321,033 (GRCm39) |
D107E |
probably damaging |
Het |
Acat1 |
T |
A |
9: 53,494,807 (GRCm39) |
K362* |
probably null |
Het |
Adad2 |
T |
A |
8: 120,339,528 (GRCm39) |
S3R |
probably benign |
Het |
Adcy8 |
C |
A |
15: 64,687,199 (GRCm39) |
R435M |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,567,508 (GRCm39) |
S5222T |
probably benign |
Het |
Ankk1 |
A |
T |
9: 49,331,748 (GRCm39) |
M182K |
probably benign |
Het |
Apba1 |
C |
T |
19: 23,870,957 (GRCm39) |
P263L |
probably damaging |
Het |
Arhgap39 |
G |
A |
15: 76,649,694 (GRCm39) |
S26L |
possibly damaging |
Het |
Ccng1 |
G |
A |
11: 40,643,093 (GRCm39) |
T118I |
possibly damaging |
Het |
Cenpe |
T |
C |
3: 134,974,826 (GRCm39) |
S2329P |
probably damaging |
Het |
Chil4 |
A |
G |
3: 106,111,013 (GRCm39) |
Y294H |
possibly damaging |
Het |
Chst8 |
A |
C |
7: 34,374,670 (GRCm39) |
S390A |
probably benign |
Het |
Dars1 |
T |
C |
1: 128,301,710 (GRCm39) |
D308G |
probably benign |
Het |
Dlec1 |
A |
C |
9: 118,972,469 (GRCm39) |
Q1458P |
possibly damaging |
Het |
Dvl2 |
G |
A |
11: 69,897,233 (GRCm39) |
E312K |
probably damaging |
Het |
Fchsd1 |
T |
C |
18: 38,099,537 (GRCm39) |
H219R |
probably damaging |
Het |
Foxd4 |
A |
C |
19: 24,877,007 (GRCm39) |
C398G |
probably damaging |
Het |
Gm10719 |
T |
A |
9: 3,018,970 (GRCm39) |
F72I |
probably damaging |
Het |
Gm5414 |
T |
C |
15: 101,536,422 (GRCm39) |
I68V |
probably benign |
Het |
Gmip |
C |
T |
8: 70,270,049 (GRCm39) |
T684I |
probably damaging |
Het |
Gpr137c |
T |
C |
14: 45,516,151 (GRCm39) |
I295T |
possibly damaging |
Het |
Hivep1 |
T |
A |
13: 42,311,804 (GRCm39) |
M1348K |
probably damaging |
Het |
Igkv6-23 |
T |
C |
6: 70,237,597 (GRCm39) |
D48G |
probably benign |
Het |
Il3 |
G |
A |
11: 54,157,958 (GRCm39) |
T40M |
possibly damaging |
Het |
Ing2 |
T |
C |
8: 48,122,248 (GRCm39) |
E100G |
probably damaging |
Het |
Itpr3 |
C |
A |
17: 27,326,308 (GRCm39) |
H1359Q |
probably benign |
Het |
Lama1 |
T |
A |
17: 68,087,889 (GRCm39) |
Y1502* |
probably null |
Het |
Mamdc2 |
C |
A |
19: 23,288,302 (GRCm39) |
G579W |
probably damaging |
Het |
Mapk6 |
G |
A |
9: 75,300,598 (GRCm39) |
|
probably benign |
Het |
Mapk8ip2 |
C |
T |
15: 89,343,007 (GRCm39) |
R616W |
probably damaging |
Het |
Mc5r |
T |
A |
18: 68,472,748 (GRCm39) |
L369H |
possibly damaging |
Het |
Meis1 |
T |
C |
11: 18,938,260 (GRCm39) |
|
probably benign |
Het |
Mmp8 |
A |
G |
9: 7,560,644 (GRCm39) |
K107R |
probably benign |
Het |
Mn1 |
C |
T |
5: 111,569,635 (GRCm39) |
H1202Y |
possibly damaging |
Het |
Naip2 |
A |
G |
13: 100,291,422 (GRCm39) |
L1172P |
probably damaging |
Het |
Nek9 |
C |
T |
12: 85,374,219 (GRCm39) |
D273N |
probably benign |
Het |
Nlrp4e |
A |
T |
7: 23,021,190 (GRCm39) |
D559V |
probably benign |
Het |
Nlrp4g |
T |
C |
9: 124,350,020 (GRCm38) |
|
noncoding transcript |
Het |
Oit3 |
G |
T |
10: 59,271,736 (GRCm39) |
A207E |
probably benign |
Het |
Or13j1 |
A |
T |
4: 43,705,788 (GRCm39) |
M260K |
possibly damaging |
Het |
Or14a257 |
A |
T |
7: 86,137,839 (GRCm39) |
C307S |
probably benign |
Het |
Or4d2b |
A |
T |
11: 87,780,545 (GRCm39) |
M59K |
probably damaging |
Het |
Or5w16 |
A |
G |
2: 87,577,406 (GRCm39) |
I289V |
probably benign |
Het |
Pde4c |
T |
C |
8: 71,200,031 (GRCm39) |
|
probably null |
Het |
Ppp1r26 |
A |
G |
2: 28,341,438 (GRCm39) |
E356G |
probably benign |
Het |
Pramel13 |
A |
G |
4: 144,122,541 (GRCm39) |
M1T |
probably null |
Het |
Ptges3-ps |
T |
A |
6: 85,821,303 (GRCm39) |
|
noncoding transcript |
Het |
Reps1 |
T |
C |
10: 17,979,982 (GRCm39) |
S114P |
probably damaging |
Het |
Scarf2 |
T |
A |
16: 17,621,466 (GRCm39) |
|
probably null |
Het |
Sdha |
A |
T |
13: 74,498,218 (GRCm39) |
|
probably benign |
Het |
Secisbp2l |
A |
T |
2: 125,594,897 (GRCm39) |
V146D |
possibly damaging |
Het |
Slc26a8 |
T |
A |
17: 28,873,833 (GRCm39) |
T385S |
probably benign |
Het |
Slc4a1 |
G |
A |
11: 102,244,092 (GRCm39) |
T679M |
probably benign |
Het |
Tbc1d14 |
T |
A |
5: 36,677,896 (GRCm39) |
E353V |
probably damaging |
Het |
Thap2 |
T |
A |
10: 115,208,665 (GRCm39) |
K152* |
probably null |
Het |
Thbd |
A |
T |
2: 148,249,655 (GRCm39) |
I71N |
probably damaging |
Het |
V1ra8 |
T |
A |
6: 90,180,036 (GRCm39) |
W80R |
probably damaging |
Het |
Vmn1r218 |
A |
G |
13: 23,320,743 (GRCm39) |
Y30C |
probably benign |
Het |
Vmn2r60 |
C |
A |
7: 41,845,049 (GRCm39) |
T804K |
probably damaging |
Het |
Vmn2r68 |
A |
T |
7: 84,882,926 (GRCm39) |
D275E |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,858,721 (GRCm39) |
I2724V |
probably benign |
Het |
Xrcc5 |
C |
A |
1: 72,385,430 (GRCm39) |
P507Q |
probably damaging |
Het |
Zfp120 |
A |
T |
2: 149,959,499 (GRCm39) |
Y274* |
probably null |
Het |
Zfp780b |
C |
A |
7: 27,674,173 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ptpn13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Ptpn13
|
APN |
5 |
103,698,924 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00569:Ptpn13
|
APN |
5 |
103,738,872 (GRCm39) |
splice site |
probably benign |
|
IGL00764:Ptpn13
|
APN |
5 |
103,745,584 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00805:Ptpn13
|
APN |
5 |
103,702,595 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00922:Ptpn13
|
APN |
5 |
103,735,954 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00959:Ptpn13
|
APN |
5 |
103,665,437 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01090:Ptpn13
|
APN |
5 |
103,689,180 (GRCm39) |
missense |
probably null |
0.80 |
IGL01352:Ptpn13
|
APN |
5 |
103,634,641 (GRCm39) |
splice site |
probably null |
|
IGL01510:Ptpn13
|
APN |
5 |
103,710,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01515:Ptpn13
|
APN |
5 |
103,703,979 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01896:Ptpn13
|
APN |
5 |
103,649,389 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02094:Ptpn13
|
APN |
5 |
103,742,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02561:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02562:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Ptpn13
|
APN |
5 |
103,710,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Ptpn13
|
APN |
5 |
103,649,769 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02679:Ptpn13
|
APN |
5 |
103,717,320 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02981:Ptpn13
|
APN |
5 |
103,676,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03131:Ptpn13
|
APN |
5 |
103,665,425 (GRCm39) |
missense |
probably benign |
|
IGL03136:Ptpn13
|
APN |
5 |
103,691,329 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03163:Ptpn13
|
APN |
5 |
103,739,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Ptpn13
|
APN |
5 |
103,610,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Ptpn13
|
APN |
5 |
103,688,943 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03328:Ptpn13
|
APN |
5 |
103,664,214 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03343:Ptpn13
|
APN |
5 |
103,702,816 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02835:Ptpn13
|
UTSW |
5 |
103,707,891 (GRCm39) |
missense |
probably damaging |
0.98 |
P0021:Ptpn13
|
UTSW |
5 |
103,676,686 (GRCm39) |
missense |
probably benign |
0.39 |
R0017:Ptpn13
|
UTSW |
5 |
103,634,638 (GRCm39) |
critical splice donor site |
probably null |
|
R0090:Ptpn13
|
UTSW |
5 |
103,717,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Ptpn13
|
UTSW |
5 |
103,728,629 (GRCm39) |
splice site |
probably benign |
|
R0183:Ptpn13
|
UTSW |
5 |
103,664,274 (GRCm39) |
missense |
probably benign |
0.00 |
R0230:Ptpn13
|
UTSW |
5 |
103,674,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Ptpn13
|
UTSW |
5 |
103,713,091 (GRCm39) |
missense |
probably benign |
|
R0360:Ptpn13
|
UTSW |
5 |
103,681,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Ptpn13
|
UTSW |
5 |
103,681,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Ptpn13
|
UTSW |
5 |
103,702,928 (GRCm39) |
missense |
probably benign |
0.31 |
R0504:Ptpn13
|
UTSW |
5 |
103,649,362 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0558:Ptpn13
|
UTSW |
5 |
103,677,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R0562:Ptpn13
|
UTSW |
5 |
103,664,291 (GRCm39) |
critical splice donor site |
probably null |
|
R0568:Ptpn13
|
UTSW |
5 |
103,637,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Ptpn13
|
UTSW |
5 |
103,704,011 (GRCm39) |
missense |
probably benign |
|
R0669:Ptpn13
|
UTSW |
5 |
103,703,975 (GRCm39) |
missense |
probably benign |
|
R0739:Ptpn13
|
UTSW |
5 |
103,722,998 (GRCm39) |
missense |
probably benign |
|
R1006:Ptpn13
|
UTSW |
5 |
103,734,655 (GRCm39) |
missense |
probably benign |
0.04 |
R1164:Ptpn13
|
UTSW |
5 |
103,637,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1274:Ptpn13
|
UTSW |
5 |
103,698,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R1501:Ptpn13
|
UTSW |
5 |
103,664,230 (GRCm39) |
missense |
probably benign |
0.01 |
R1529:Ptpn13
|
UTSW |
5 |
103,711,998 (GRCm39) |
missense |
probably benign |
0.00 |
R1533:Ptpn13
|
UTSW |
5 |
103,704,044 (GRCm39) |
nonsense |
probably null |
|
R1613:Ptpn13
|
UTSW |
5 |
103,684,737 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1616:Ptpn13
|
UTSW |
5 |
103,713,103 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1830:Ptpn13
|
UTSW |
5 |
103,691,325 (GRCm39) |
missense |
probably benign |
0.00 |
R1892:Ptpn13
|
UTSW |
5 |
103,649,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1907:Ptpn13
|
UTSW |
5 |
103,728,575 (GRCm39) |
missense |
probably null |
0.45 |
R2143:Ptpn13
|
UTSW |
5 |
103,703,999 (GRCm39) |
missense |
probably benign |
|
R2145:Ptpn13
|
UTSW |
5 |
103,703,999 (GRCm39) |
missense |
probably benign |
|
R2151:Ptpn13
|
UTSW |
5 |
103,673,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Ptpn13
|
UTSW |
5 |
103,717,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2264:Ptpn13
|
UTSW |
5 |
103,637,527 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2313:Ptpn13
|
UTSW |
5 |
103,712,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Ptpn13
|
UTSW |
5 |
103,737,720 (GRCm39) |
splice site |
probably benign |
|
R3773:Ptpn13
|
UTSW |
5 |
103,624,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R3924:Ptpn13
|
UTSW |
5 |
103,698,607 (GRCm39) |
splice site |
probably benign |
|
R4289:Ptpn13
|
UTSW |
5 |
103,681,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4348:Ptpn13
|
UTSW |
5 |
103,717,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Ptpn13
|
UTSW |
5 |
103,681,273 (GRCm39) |
splice site |
probably null |
|
R4526:Ptpn13
|
UTSW |
5 |
103,649,335 (GRCm39) |
missense |
probably benign |
0.32 |
R4557:Ptpn13
|
UTSW |
5 |
103,688,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R4596:Ptpn13
|
UTSW |
5 |
103,671,558 (GRCm39) |
missense |
probably benign |
0.06 |
R4632:Ptpn13
|
UTSW |
5 |
103,717,726 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4727:Ptpn13
|
UTSW |
5 |
103,717,721 (GRCm39) |
missense |
probably benign |
|
R4780:Ptpn13
|
UTSW |
5 |
103,734,639 (GRCm39) |
missense |
probably benign |
0.04 |
R4793:Ptpn13
|
UTSW |
5 |
103,730,644 (GRCm39) |
critical splice donor site |
probably null |
|
R4812:Ptpn13
|
UTSW |
5 |
103,671,481 (GRCm39) |
missense |
probably benign |
0.00 |
R4939:Ptpn13
|
UTSW |
5 |
103,665,335 (GRCm39) |
splice site |
probably null |
|
R4951:Ptpn13
|
UTSW |
5 |
103,735,912 (GRCm39) |
missense |
probably benign |
0.00 |
R5052:Ptpn13
|
UTSW |
5 |
103,709,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5148:Ptpn13
|
UTSW |
5 |
103,640,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Ptpn13
|
UTSW |
5 |
103,688,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5545:Ptpn13
|
UTSW |
5 |
103,709,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Ptpn13
|
UTSW |
5 |
103,702,625 (GRCm39) |
missense |
probably benign |
0.20 |
R5735:Ptpn13
|
UTSW |
5 |
103,702,686 (GRCm39) |
missense |
probably benign |
0.03 |
R5815:Ptpn13
|
UTSW |
5 |
103,745,556 (GRCm39) |
splice site |
probably null |
|
R5876:Ptpn13
|
UTSW |
5 |
103,624,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R5878:Ptpn13
|
UTSW |
5 |
103,624,984 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6366:Ptpn13
|
UTSW |
5 |
103,698,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Ptpn13
|
UTSW |
5 |
103,689,150 (GRCm39) |
missense |
probably benign |
0.00 |
R6492:Ptpn13
|
UTSW |
5 |
103,649,478 (GRCm39) |
missense |
probably benign |
0.02 |
R6709:Ptpn13
|
UTSW |
5 |
103,734,622 (GRCm39) |
missense |
probably benign |
0.18 |
R6759:Ptpn13
|
UTSW |
5 |
103,713,121 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6944:Ptpn13
|
UTSW |
5 |
103,624,857 (GRCm39) |
missense |
probably null |
1.00 |
R7079:Ptpn13
|
UTSW |
5 |
103,649,752 (GRCm39) |
missense |
probably benign |
0.00 |
R7253:Ptpn13
|
UTSW |
5 |
103,713,150 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7254:Ptpn13
|
UTSW |
5 |
103,742,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Ptpn13
|
UTSW |
5 |
103,688,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Ptpn13
|
UTSW |
5 |
103,674,961 (GRCm39) |
missense |
probably benign |
0.16 |
R7614:Ptpn13
|
UTSW |
5 |
103,649,331 (GRCm39) |
missense |
probably benign |
0.13 |
R7652:Ptpn13
|
UTSW |
5 |
103,677,578 (GRCm39) |
missense |
probably benign |
0.12 |
R7655:Ptpn13
|
UTSW |
5 |
103,688,849 (GRCm39) |
missense |
probably benign |
0.00 |
R7656:Ptpn13
|
UTSW |
5 |
103,688,849 (GRCm39) |
missense |
probably benign |
0.00 |
R7683:Ptpn13
|
UTSW |
5 |
103,713,018 (GRCm39) |
missense |
probably benign |
0.01 |
R7734:Ptpn13
|
UTSW |
5 |
103,709,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Ptpn13
|
UTSW |
5 |
103,640,090 (GRCm39) |
missense |
probably benign |
0.06 |
R7834:Ptpn13
|
UTSW |
5 |
103,610,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Ptpn13
|
UTSW |
5 |
103,688,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Ptpn13
|
UTSW |
5 |
103,707,803 (GRCm39) |
nonsense |
probably null |
|
R8308:Ptpn13
|
UTSW |
5 |
103,688,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R8493:Ptpn13
|
UTSW |
5 |
103,717,671 (GRCm39) |
missense |
probably benign |
0.01 |
R8493:Ptpn13
|
UTSW |
5 |
103,712,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Ptpn13
|
UTSW |
5 |
103,705,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Ptpn13
|
UTSW |
5 |
103,707,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Ptpn13
|
UTSW |
5 |
103,739,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Ptpn13
|
UTSW |
5 |
103,727,671 (GRCm39) |
missense |
probably benign |
0.00 |
R8958:Ptpn13
|
UTSW |
5 |
103,698,973 (GRCm39) |
missense |
probably benign |
0.15 |
R8975:Ptpn13
|
UTSW |
5 |
103,649,266 (GRCm39) |
missense |
probably benign |
0.32 |
R9080:Ptpn13
|
UTSW |
5 |
103,637,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R9091:Ptpn13
|
UTSW |
5 |
103,649,735 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9219:Ptpn13
|
UTSW |
5 |
103,745,632 (GRCm39) |
missense |
probably benign |
0.16 |
R9270:Ptpn13
|
UTSW |
5 |
103,649,735 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9577:Ptpn13
|
UTSW |
5 |
103,676,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R9593:Ptpn13
|
UTSW |
5 |
103,674,998 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9705:Ptpn13
|
UTSW |
5 |
103,681,221 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF017:Ptpn13
|
UTSW |
5 |
103,741,446 (GRCm39) |
missense |
probably benign |
0.45 |
Z1177:Ptpn13
|
UTSW |
5 |
103,717,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|