Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
A |
6: 128,553,223 (GRCm39) |
N178I |
probably damaging |
Het |
Aadacl2fm3 |
T |
C |
3: 59,772,769 (GRCm39) |
V91A |
probably damaging |
Het |
Adgrl2 |
T |
C |
3: 148,596,124 (GRCm39) |
I71V |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,729,846 (GRCm39) |
T212A |
possibly damaging |
Het |
Aopep |
T |
A |
13: 63,357,963 (GRCm39) |
C656S |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Apaf1 |
A |
T |
10: 90,896,027 (GRCm39) |
Y348* |
probably null |
Het |
Apobr |
A |
G |
7: 126,186,378 (GRCm39) |
T630A |
probably benign |
Het |
Arhgap23 |
A |
G |
11: 97,342,387 (GRCm39) |
D223G |
possibly damaging |
Het |
Asic1 |
A |
T |
15: 99,569,756 (GRCm39) |
T26S |
possibly damaging |
Het |
Atp13a2 |
T |
A |
4: 140,732,327 (GRCm39) |
M864K |
probably damaging |
Het |
Atrnl1 |
G |
A |
19: 57,643,426 (GRCm39) |
G438D |
probably damaging |
Het |
Bbc3 |
T |
C |
7: 16,046,268 (GRCm39) |
V68A |
possibly damaging |
Het |
Birc6 |
T |
C |
17: 74,966,149 (GRCm39) |
|
probably benign |
Het |
Btnl9 |
A |
G |
11: 49,071,523 (GRCm39) |
F100S |
probably damaging |
Het |
Castor2 |
G |
A |
5: 134,164,992 (GRCm39) |
C187Y |
probably damaging |
Het |
Ccpg1 |
A |
G |
9: 72,920,440 (GRCm39) |
N685S |
probably damaging |
Het |
Ces3b |
T |
A |
8: 105,819,607 (GRCm39) |
|
probably null |
Het |
Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
Clhc1 |
A |
G |
11: 29,507,663 (GRCm39) |
I126V |
probably benign |
Het |
Crocc |
T |
C |
4: 140,756,413 (GRCm39) |
I1071V |
probably benign |
Het |
Dbt |
T |
A |
3: 116,332,773 (GRCm39) |
D16E |
probably damaging |
Het |
Dnajc8 |
T |
C |
4: 132,271,370 (GRCm39) |
S62P |
possibly damaging |
Het |
Dpyd |
T |
C |
3: 118,468,217 (GRCm39) |
V77A |
probably benign |
Het |
Dram2 |
T |
A |
3: 106,478,076 (GRCm39) |
M136K |
possibly damaging |
Het |
Dtx2 |
T |
A |
5: 136,040,894 (GRCm39) |
F100I |
probably damaging |
Het |
Dync2h1 |
A |
T |
9: 7,011,253 (GRCm39) |
W3654R |
probably damaging |
Het |
Fbxw10 |
T |
A |
11: 62,750,683 (GRCm39) |
I422N |
probably damaging |
Het |
Fgf17 |
T |
C |
14: 70,875,927 (GRCm39) |
R102G |
probably damaging |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gm6578 |
C |
A |
6: 12,100,186 (GRCm39) |
|
noncoding transcript |
Het |
Gm8374 |
T |
C |
14: 18,537,078 (GRCm39) |
T49A |
probably damaging |
Het |
Gm9797 |
G |
T |
10: 11,485,113 (GRCm39) |
|
noncoding transcript |
Het |
Golga3 |
T |
C |
5: 110,350,805 (GRCm39) |
|
probably null |
Het |
Golim4 |
A |
T |
3: 75,815,456 (GRCm39) |
V116D |
probably damaging |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Insrr |
G |
A |
3: 87,717,879 (GRCm39) |
|
probably null |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Isoc2b |
A |
T |
7: 4,854,438 (GRCm39) |
I31N |
probably damaging |
Het |
Kif5c |
T |
A |
2: 49,648,817 (GRCm39) |
|
probably benign |
Het |
Krtap16-1 |
A |
T |
11: 99,876,602 (GRCm39) |
C267* |
probably null |
Het |
Lamc2 |
T |
A |
1: 153,002,870 (GRCm39) |
D1037V |
probably damaging |
Het |
Lhfpl2 |
A |
G |
13: 94,328,557 (GRCm39) |
D206G |
possibly damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Mgat2 |
T |
C |
12: 69,232,068 (GRCm39) |
F214S |
probably damaging |
Het |
Mki67 |
T |
A |
7: 135,305,970 (GRCm39) |
|
probably null |
Het |
Mpo |
A |
G |
11: 87,688,187 (GRCm39) |
D282G |
possibly damaging |
Het |
Myh10 |
A |
G |
11: 68,698,115 (GRCm39) |
|
probably benign |
Het |
Myo15b |
G |
A |
11: 115,762,469 (GRCm39) |
V1229I |
probably benign |
Het |
Nfatc2ip |
A |
G |
7: 125,989,634 (GRCm39) |
V250A |
probably benign |
Het |
Niban2 |
A |
G |
2: 32,813,659 (GRCm39) |
K624R |
probably benign |
Het |
Nrp1 |
A |
T |
8: 129,224,997 (GRCm39) |
E782D |
probably damaging |
Het |
Olfml3 |
T |
A |
3: 103,643,185 (GRCm39) |
M399L |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or56a5 |
T |
A |
7: 104,792,757 (GRCm39) |
I254F |
probably benign |
Het |
Plekha6 |
C |
A |
1: 133,207,103 (GRCm39) |
|
probably null |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Psph |
T |
A |
5: 129,864,603 (GRCm39) |
|
probably null |
Het |
Ptpro |
A |
G |
6: 137,388,114 (GRCm39) |
|
probably null |
Het |
Pzp |
T |
C |
6: 128,468,124 (GRCm39) |
|
probably null |
Het |
Qrich2 |
C |
T |
11: 116,339,243 (GRCm39) |
|
probably benign |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rfwd3 |
A |
T |
8: 112,024,034 (GRCm39) |
V96E |
probably benign |
Het |
Rnf17 |
T |
C |
14: 56,730,811 (GRCm39) |
V1205A |
probably damaging |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Senp1 |
T |
A |
15: 97,973,848 (GRCm39) |
T132S |
probably benign |
Het |
Sgo2b |
T |
C |
8: 64,380,181 (GRCm39) |
R884G |
probably benign |
Het |
Slc10a5 |
G |
T |
3: 10,400,278 (GRCm39) |
D127E |
probably benign |
Het |
Slc25a35 |
T |
G |
11: 68,859,791 (GRCm39) |
S101R |
possibly damaging |
Het |
Slc6a13 |
T |
C |
6: 121,302,000 (GRCm39) |
L194P |
possibly damaging |
Het |
Snw1 |
T |
G |
12: 87,499,473 (GRCm39) |
|
probably benign |
Het |
Sort1 |
T |
A |
3: 108,259,002 (GRCm39) |
F678Y |
probably benign |
Het |
Srsf12 |
C |
T |
4: 33,225,764 (GRCm39) |
|
probably benign |
Het |
Ssxa1 |
T |
A |
X: 20,985,581 (GRCm39) |
|
probably benign |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
Tacr3 |
T |
C |
3: 134,637,941 (GRCm39) |
V366A |
probably benign |
Het |
Tasor |
T |
A |
14: 27,168,345 (GRCm39) |
Y296N |
probably damaging |
Het |
Tasor |
A |
G |
14: 27,198,571 (GRCm39) |
N1301S |
possibly damaging |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,113,888 (GRCm39) |
M457L |
possibly damaging |
Het |
Tmem98 |
A |
G |
11: 80,708,348 (GRCm39) |
E106G |
probably damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Trim41 |
C |
A |
11: 48,698,419 (GRCm39) |
G516W |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,572,861 (GRCm39) |
T24265A |
possibly damaging |
Het |
Usp37 |
A |
G |
1: 74,500,815 (GRCm39) |
V582A |
probably damaging |
Het |
Vps13b |
T |
A |
15: 35,671,546 (GRCm39) |
I1683N |
probably benign |
Het |
Vps13d |
C |
T |
4: 144,882,671 (GRCm39) |
R968H |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Vwf |
C |
T |
6: 125,634,020 (GRCm39) |
T166I |
probably damaging |
Het |
Zfp280d |
T |
C |
9: 72,215,287 (GRCm39) |
F133L |
probably damaging |
Het |
Zfp459 |
A |
T |
13: 67,556,395 (GRCm39) |
H229Q |
probably benign |
Het |
Zfyve26 |
T |
A |
12: 79,315,208 (GRCm39) |
I1423F |
possibly damaging |
Het |
Zmynd19 |
T |
A |
2: 24,842,648 (GRCm39) |
Y15* |
probably null |
Het |
|
Other mutations in Tkfc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01066:Tkfc
|
APN |
19 |
10,571,892 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01149:Tkfc
|
APN |
19 |
10,578,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Tkfc
|
APN |
19 |
10,573,576 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03069:Tkfc
|
APN |
19 |
10,576,518 (GRCm39) |
missense |
probably benign |
|
R1367:Tkfc
|
UTSW |
19 |
10,570,838 (GRCm39) |
missense |
probably benign |
0.19 |
R1476:Tkfc
|
UTSW |
19 |
10,572,690 (GRCm39) |
missense |
probably null |
0.55 |
R2081:Tkfc
|
UTSW |
19 |
10,574,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Tkfc
|
UTSW |
19 |
10,576,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R2443:Tkfc
|
UTSW |
19 |
10,571,902 (GRCm39) |
missense |
probably damaging |
0.97 |
R3104:Tkfc
|
UTSW |
19 |
10,574,357 (GRCm39) |
nonsense |
probably null |
|
R3105:Tkfc
|
UTSW |
19 |
10,574,357 (GRCm39) |
nonsense |
probably null |
|
R3106:Tkfc
|
UTSW |
19 |
10,574,357 (GRCm39) |
nonsense |
probably null |
|
R5027:Tkfc
|
UTSW |
19 |
10,570,023 (GRCm39) |
splice site |
probably null |
|
R5601:Tkfc
|
UTSW |
19 |
10,571,927 (GRCm39) |
missense |
probably benign |
|
R5637:Tkfc
|
UTSW |
19 |
10,571,897 (GRCm39) |
missense |
probably benign |
0.00 |
R5933:Tkfc
|
UTSW |
19 |
10,574,711 (GRCm39) |
missense |
probably benign |
0.17 |
R6792:Tkfc
|
UTSW |
19 |
10,571,888 (GRCm39) |
missense |
probably benign |
|
R6845:Tkfc
|
UTSW |
19 |
10,576,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R6909:Tkfc
|
UTSW |
19 |
10,573,630 (GRCm39) |
missense |
probably benign |
0.06 |
R7007:Tkfc
|
UTSW |
19 |
10,573,727 (GRCm39) |
missense |
probably benign |
|
R7883:Tkfc
|
UTSW |
19 |
10,572,394 (GRCm39) |
splice site |
probably null |
|
R8962:Tkfc
|
UTSW |
19 |
10,570,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R9039:Tkfc
|
UTSW |
19 |
10,573,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R9254:Tkfc
|
UTSW |
19 |
10,574,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|