Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
A |
G |
6: 86,914,049 (GRCm39) |
I173V |
possibly damaging |
Het |
Abca14 |
G |
T |
7: 119,807,202 (GRCm39) |
E83* |
probably null |
Het |
Abcc5 |
T |
C |
16: 20,152,437 (GRCm39) |
T1370A |
probably damaging |
Het |
Abtb2 |
A |
G |
2: 103,541,580 (GRCm39) |
T828A |
probably benign |
Het |
Agap1 |
T |
A |
1: 89,653,741 (GRCm39) |
V370D |
probably damaging |
Het |
Ankhd1 |
T |
C |
18: 36,777,680 (GRCm39) |
V1621A |
probably benign |
Het |
Atp2a2 |
T |
C |
5: 122,611,315 (GRCm39) |
I168V |
probably benign |
Het |
Atxn2 |
G |
A |
5: 121,885,509 (GRCm39) |
V239I |
probably damaging |
Het |
B230219D22Rik |
C |
A |
13: 55,847,283 (GRCm39) |
A132E |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,979,223 (GRCm39) |
E697G |
probably damaging |
Het |
Ccdc162 |
T |
G |
10: 41,488,944 (GRCm39) |
|
probably null |
Het |
Chd7 |
A |
G |
4: 8,752,210 (GRCm39) |
S236G |
unknown |
Het |
Csmd2 |
A |
G |
4: 128,091,112 (GRCm39) |
E217G |
|
Het |
Cyp2j7 |
T |
A |
4: 96,105,740 (GRCm39) |
K257* |
probably null |
Het |
D630003M21Rik |
C |
T |
2: 158,042,883 (GRCm39) |
A886T |
probably damaging |
Het |
D630044L22Rik |
A |
G |
17: 26,180,856 (GRCm39) |
H102R |
possibly damaging |
Het |
Dact3 |
G |
A |
7: 16,620,013 (GRCm39) |
V503I |
unknown |
Het |
Dcn |
G |
T |
10: 97,343,643 (GRCm39) |
R201L |
probably damaging |
Het |
Dmxl1 |
T |
C |
18: 50,024,567 (GRCm39) |
V1747A |
possibly damaging |
Het |
Dnajc14 |
T |
A |
10: 128,652,743 (GRCm39) |
|
probably null |
Het |
Dner |
A |
G |
1: 84,673,193 (GRCm39) |
V86A |
probably benign |
Het |
Dspp |
A |
T |
5: 104,322,760 (GRCm39) |
|
probably null |
Het |
Gphn |
T |
C |
12: 78,674,036 (GRCm39) |
|
probably null |
Het |
Gpr158 |
A |
G |
2: 21,373,042 (GRCm39) |
|
probably benign |
Het |
Grip1 |
G |
T |
10: 119,780,961 (GRCm39) |
L203F |
probably damaging |
Het |
Hgfac |
T |
C |
5: 35,202,133 (GRCm39) |
W345R |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,051,697 (GRCm39) |
L250P |
probably damaging |
Het |
Ighv1-24 |
T |
C |
12: 114,736,663 (GRCm39) |
Y79C |
possibly damaging |
Het |
Katnip |
T |
C |
7: 125,469,848 (GRCm39) |
L1439P |
probably damaging |
Het |
Kif21a |
C |
T |
15: 90,854,030 (GRCm39) |
R779Q |
probably damaging |
Het |
Klkb1 |
T |
C |
8: 45,742,067 (GRCm39) |
T71A |
probably benign |
Het |
Lama2 |
A |
G |
10: 27,298,685 (GRCm39) |
V137A |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,333,891 (GRCm39) |
D1450G |
probably benign |
Het |
Lrrc8c |
T |
A |
5: 105,756,356 (GRCm39) |
Y710* |
probably null |
Het |
Mixl1 |
A |
G |
1: 180,522,258 (GRCm39) |
S208P |
probably benign |
Het |
Mroh1 |
A |
G |
15: 76,292,215 (GRCm39) |
H229R |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,557,467 (GRCm39) |
Q2942L |
unknown |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nup85 |
T |
C |
11: 115,469,424 (GRCm39) |
I322T |
probably benign |
Het |
Odad1 |
A |
G |
7: 45,597,116 (GRCm39) |
T456A |
probably benign |
Het |
Odad2 |
T |
C |
18: 7,265,089 (GRCm39) |
D426G |
possibly damaging |
Het |
Or10n7-ps1 |
A |
G |
9: 39,598,114 (GRCm39) |
L42P |
probably damaging |
Het |
Or5w15 |
T |
A |
2: 87,568,372 (GRCm39) |
M99L |
probably benign |
Het |
Or7e169 |
T |
A |
9: 19,757,212 (GRCm39) |
K234N |
possibly damaging |
Het |
Or8b4 |
C |
T |
9: 37,830,447 (GRCm39) |
L165F |
probably damaging |
Het |
Or9k2b |
A |
G |
10: 130,016,605 (GRCm39) |
M48T |
possibly damaging |
Het |
Pcyt1a |
G |
A |
16: 32,288,894 (GRCm39) |
R245Q |
probably benign |
Het |
Pi15 |
T |
C |
1: 17,695,180 (GRCm39) |
Y266H |
probably benign |
Het |
Plxna2 |
C |
T |
1: 194,492,474 (GRCm39) |
T1777I |
probably damaging |
Het |
Ppp3cb |
T |
C |
14: 20,581,874 (GRCm39) |
D47G |
probably benign |
Het |
Pram1 |
T |
C |
17: 33,860,441 (GRCm39) |
V336A |
probably damaging |
Het |
Prl |
T |
A |
13: 27,243,503 (GRCm39) |
I58N |
probably damaging |
Het |
Qrich2 |
T |
C |
11: 116,348,934 (GRCm39) |
D630G |
unknown |
Het |
Ralgapa1 |
G |
C |
12: 55,769,583 (GRCm39) |
P803A |
probably damaging |
Het |
Rin1 |
A |
G |
19: 5,103,249 (GRCm39) |
K513E |
probably damaging |
Het |
Rtcb |
A |
T |
10: 85,779,071 (GRCm39) |
|
probably null |
Het |
Ryr2 |
C |
T |
13: 11,898,002 (GRCm39) |
C131Y |
probably damaging |
Het |
Sspo |
G |
T |
6: 48,464,928 (GRCm39) |
V3954L |
probably damaging |
Het |
Taf4b |
C |
T |
18: 14,946,431 (GRCm39) |
T418M |
probably damaging |
Het |
Taf6 |
A |
G |
5: 138,181,952 (GRCm39) |
I92T |
possibly damaging |
Het |
Tfg |
A |
T |
16: 56,526,050 (GRCm39) |
D64E |
probably damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tmem200a |
A |
T |
10: 25,869,654 (GRCm39) |
L205Q |
probably damaging |
Het |
Trav13n-3 |
T |
G |
14: 53,574,853 (GRCm39) |
L32V |
probably damaging |
Het |
Tsen2 |
T |
A |
6: 115,553,864 (GRCm39) |
M414K |
probably damaging |
Het |
Tut7 |
T |
C |
13: 59,936,288 (GRCm39) |
Y1271C |
possibly damaging |
Het |
Txlna |
A |
T |
4: 129,530,900 (GRCm39) |
Y196N |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,688,635 (GRCm39) |
I562K |
possibly damaging |
Het |
Vmn1r24 |
T |
A |
6: 57,932,736 (GRCm39) |
I261F |
probably benign |
Het |
Vmn2r106 |
T |
C |
17: 20,496,066 (GRCm39) |
T553A |
probably damaging |
Het |
Vmn2r65 |
A |
G |
7: 84,596,650 (GRCm39) |
V135A |
probably damaging |
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 |
R2130:Tkfc
|
UTSW |
19 |
10,573,405 (GRCm39) |
missense |
probably damaging |
0.97 |
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 |
|