Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
G |
A |
7: 119,784,986 (GRCm38) |
|
probably null |
Het |
Adam20 |
T |
A |
8: 40,794,948 (GRCm38) |
Y32N |
probably benign |
Het |
Adm |
T |
C |
7: 110,628,289 (GRCm38) |
V4A |
probably benign |
Het |
Anpep |
G |
A |
7: 79,839,464 (GRCm38) |
T320I |
possibly damaging |
Het |
Atp8b1 |
T |
C |
18: 64,539,270 (GRCm38) |
S1008G |
possibly damaging |
Het |
B9d1 |
T |
A |
11: 61,505,243 (GRCm38) |
M12K |
possibly damaging |
Het |
Cad |
T |
C |
5: 31,072,094 (GRCm38) |
L1435P |
probably damaging |
Het |
Cat |
T |
C |
2: 103,471,812 (GRCm38) |
D180G |
probably damaging |
Het |
Cntln |
C |
T |
4: 84,974,000 (GRCm38) |
T374M |
probably damaging |
Het |
Cyp2a5 |
G |
A |
7: 26,840,979 (GRCm38) |
R339Q |
probably benign |
Het |
Defa22 |
T |
C |
8: 21,162,336 (GRCm38) |
L6P |
probably damaging |
Het |
Dr1 |
T |
A |
5: 108,269,738 (GRCm38) |
I50K |
probably damaging |
Het |
Eln |
C |
T |
5: 134,737,178 (GRCm38) |
G57E |
unknown |
Het |
Fat4 |
T |
C |
3: 38,889,004 (GRCm38) |
I682T |
probably benign |
Het |
Fat4 |
C |
A |
3: 38,982,357 (GRCm38) |
A3386E |
probably damaging |
Het |
Fcgr3 |
T |
A |
1: 171,057,750 (GRCm38) |
Y102F |
probably damaging |
Het |
Gm5930 |
A |
T |
14: 44,336,536 (GRCm38) |
L115M |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,479,009 (GRCm38) |
V3748D |
probably damaging |
Het |
Ino80d |
A |
G |
1: 63,085,986 (GRCm38) |
S106P |
probably benign |
Het |
Kcns3 |
C |
T |
12: 11,092,748 (GRCm38) |
|
probably benign |
Het |
Kndc1 |
T |
A |
7: 139,932,917 (GRCm38) |
L1527Q |
probably damaging |
Het |
Lepr |
T |
G |
4: 101,779,983 (GRCm38) |
S690A |
probably benign |
Het |
Lrfn5 |
T |
C |
12: 61,843,557 (GRCm38) |
F544S |
probably damaging |
Het |
Mapkap1 |
C |
A |
2: 34,619,849 (GRCm38) |
H450Q |
probably damaging |
Het |
Mdm1 |
A |
G |
10: 118,158,540 (GRCm38) |
T485A |
probably benign |
Het |
Megf10 |
T |
C |
18: 57,277,688 (GRCm38) |
C690R |
probably damaging |
Het |
Myo7a |
A |
G |
7: 98,063,599 (GRCm38) |
M1723T |
probably benign |
Het |
Nrip3 |
A |
T |
7: 109,765,507 (GRCm38) |
C137* |
probably null |
Het |
Or5w22 |
T |
A |
2: 87,532,780 (GRCm38) |
I249N |
probably damaging |
Het |
Pde4a |
T |
A |
9: 21,211,001 (GRCm38) |
M731K |
probably benign |
Het |
Pebp1 |
A |
G |
5: 117,283,462 (GRCm38) |
L117P |
probably damaging |
Het |
Phc2 |
T |
C |
4: 128,705,202 (GRCm38) |
Y51H |
probably damaging |
Het |
Ppp2r5b |
A |
G |
19: 6,234,683 (GRCm38) |
F50S |
probably benign |
Het |
Prpf4b |
A |
G |
13: 34,899,842 (GRCm38) |
S865G |
probably benign |
Het |
Ptpn5 |
C |
T |
7: 47,088,606 (GRCm38) |
V243M |
probably benign |
Het |
Rora |
T |
C |
9: 69,364,559 (GRCm38) |
L273P |
possibly damaging |
Het |
Rtp4 |
T |
A |
16: 23,613,454 (GRCm38) |
S245R |
probably benign |
Het |
Scgb2b20 |
C |
T |
7: 33,364,560 (GRCm38) |
G95D |
probably benign |
Het |
Sec24b |
A |
G |
3: 129,994,391 (GRCm38) |
V820A |
probably benign |
Het |
Sim2 |
A |
G |
16: 94,094,309 (GRCm38) |
D62G |
possibly damaging |
Het |
Slc17a4 |
A |
T |
13: 23,900,514 (GRCm38) |
V429D |
probably benign |
Het |
Sp2 |
T |
C |
11: 96,961,973 (GRCm38) |
T42A |
probably damaging |
Het |
Spata3 |
G |
A |
1: 86,024,447 (GRCm38) |
R141Q |
unknown |
Het |
Sptbn2 |
A |
T |
19: 4,745,577 (GRCm38) |
E1658D |
probably benign |
Het |
Tcaf1 |
T |
C |
6: 42,678,539 (GRCm38) |
H501R |
probably benign |
Het |
Tec |
G |
A |
5: 72,773,835 (GRCm38) |
T262M |
possibly damaging |
Het |
Timm9 |
A |
T |
12: 71,125,531 (GRCm38) |
N22K |
possibly damaging |
Het |
Tmbim4 |
A |
G |
10: 120,217,624 (GRCm38) |
I109M |
probably benign |
Het |
Tmc7 |
T |
C |
7: 118,564,343 (GRCm38) |
K110E |
probably benign |
Het |
Tmem107 |
C |
T |
11: 69,072,573 (GRCm38) |
P136L |
probably benign |
Het |
Ttc21b |
T |
C |
2: 66,231,219 (GRCm38) |
|
probably null |
Het |
Ubd |
A |
C |
17: 37,195,444 (GRCm38) |
T74P |
probably damaging |
Het |
Vps11 |
A |
G |
9: 44,358,189 (GRCm38) |
V255A |
possibly damaging |
Het |
Vsnl1 |
T |
C |
12: 11,326,447 (GRCm38) |
T146A |
probably benign |
Het |
Wdr38 |
G |
T |
2: 38,999,972 (GRCm38) |
|
probably null |
Het |
Yes1 |
T |
A |
5: 32,684,625 (GRCm38) |
S498T |
possibly damaging |
Het |
Zc3h13 |
G |
A |
14: 75,331,883 (GRCm38) |
R1390H |
probably damaging |
Het |
Zscan4b |
A |
G |
7: 10,902,022 (GRCm38) |
V126A |
possibly damaging |
Het |
|
Other mutations in Tln1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Tln1
|
APN |
4 |
43,542,719 (GRCm38) |
missense |
probably benign |
0.22 |
IGL00987:Tln1
|
APN |
4 |
43,551,297 (GRCm38) |
unclassified |
probably benign |
|
IGL01345:Tln1
|
APN |
4 |
43,536,281 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01456:Tln1
|
APN |
4 |
43,543,432 (GRCm38) |
unclassified |
probably benign |
|
IGL01715:Tln1
|
APN |
4 |
43,555,890 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01750:Tln1
|
APN |
4 |
43,545,435 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01933:Tln1
|
APN |
4 |
43,555,894 (GRCm38) |
missense |
possibly damaging |
0.52 |
IGL01933:Tln1
|
APN |
4 |
43,539,508 (GRCm38) |
missense |
probably benign |
|
IGL02119:Tln1
|
APN |
4 |
43,546,760 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02148:Tln1
|
APN |
4 |
43,555,388 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02153:Tln1
|
APN |
4 |
43,546,857 (GRCm38) |
missense |
possibly damaging |
0.76 |
IGL02522:Tln1
|
APN |
4 |
43,540,612 (GRCm38) |
missense |
probably benign |
0.07 |
IGL02691:Tln1
|
APN |
4 |
43,539,544 (GRCm38) |
missense |
probably benign |
0.42 |
IGL02882:Tln1
|
APN |
4 |
43,539,522 (GRCm38) |
missense |
probably benign |
0.45 |
IGL02892:Tln1
|
APN |
4 |
43,555,679 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03061:Tln1
|
APN |
4 |
43,545,694 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03102:Tln1
|
APN |
4 |
43,532,861 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL03183:Tln1
|
APN |
4 |
43,539,084 (GRCm38) |
splice site |
probably benign |
|
H8786:Tln1
|
UTSW |
4 |
43,544,589 (GRCm38) |
missense |
probably damaging |
0.97 |
PIT4576001:Tln1
|
UTSW |
4 |
43,539,998 (GRCm38) |
missense |
probably damaging |
1.00 |
R0206:Tln1
|
UTSW |
4 |
43,549,151 (GRCm38) |
missense |
probably damaging |
1.00 |
R0208:Tln1
|
UTSW |
4 |
43,549,151 (GRCm38) |
missense |
probably damaging |
1.00 |
R0454:Tln1
|
UTSW |
4 |
43,553,504 (GRCm38) |
missense |
probably benign |
|
R0539:Tln1
|
UTSW |
4 |
43,543,434 (GRCm38) |
critical splice donor site |
probably null |
|
R0548:Tln1
|
UTSW |
4 |
43,542,709 (GRCm38) |
missense |
possibly damaging |
0.79 |
R0561:Tln1
|
UTSW |
4 |
43,550,304 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0606:Tln1
|
UTSW |
4 |
43,547,756 (GRCm38) |
missense |
probably benign |
0.34 |
R0607:Tln1
|
UTSW |
4 |
43,553,071 (GRCm38) |
missense |
probably damaging |
1.00 |
R0609:Tln1
|
UTSW |
4 |
43,544,645 (GRCm38) |
missense |
possibly damaging |
0.63 |
R0847:Tln1
|
UTSW |
4 |
43,555,333 (GRCm38) |
missense |
probably damaging |
1.00 |
R0993:Tln1
|
UTSW |
4 |
43,549,825 (GRCm38) |
missense |
probably benign |
0.22 |
R1255:Tln1
|
UTSW |
4 |
43,538,044 (GRCm38) |
missense |
probably damaging |
1.00 |
R1292:Tln1
|
UTSW |
4 |
43,534,578 (GRCm38) |
critical splice donor site |
probably null |
|
R1752:Tln1
|
UTSW |
4 |
43,536,311 (GRCm38) |
missense |
probably damaging |
1.00 |
R2169:Tln1
|
UTSW |
4 |
43,548,005 (GRCm38) |
missense |
probably damaging |
1.00 |
R2172:Tln1
|
UTSW |
4 |
43,545,721 (GRCm38) |
missense |
probably benign |
|
R2202:Tln1
|
UTSW |
4 |
43,553,083 (GRCm38) |
splice site |
probably null |
|
R2680:Tln1
|
UTSW |
4 |
43,539,668 (GRCm38) |
missense |
probably damaging |
1.00 |
R3012:Tln1
|
UTSW |
4 |
43,542,525 (GRCm38) |
missense |
probably benign |
|
R3714:Tln1
|
UTSW |
4 |
43,540,597 (GRCm38) |
missense |
probably damaging |
1.00 |
R3735:Tln1
|
UTSW |
4 |
43,549,370 (GRCm38) |
missense |
probably damaging |
0.97 |
R3794:Tln1
|
UTSW |
4 |
43,536,295 (GRCm38) |
missense |
probably damaging |
1.00 |
R3825:Tln1
|
UTSW |
4 |
43,536,413 (GRCm38) |
splice site |
probably benign |
|
R3983:Tln1
|
UTSW |
4 |
43,553,030 (GRCm38) |
missense |
probably damaging |
1.00 |
R4061:Tln1
|
UTSW |
4 |
43,549,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R4249:Tln1
|
UTSW |
4 |
43,536,104 (GRCm38) |
missense |
probably damaging |
1.00 |
R4287:Tln1
|
UTSW |
4 |
43,543,509 (GRCm38) |
missense |
probably benign |
0.01 |
R4471:Tln1
|
UTSW |
4 |
43,551,018 (GRCm38) |
missense |
probably benign |
0.03 |
R4562:Tln1
|
UTSW |
4 |
43,533,598 (GRCm38) |
missense |
probably damaging |
1.00 |
R4654:Tln1
|
UTSW |
4 |
43,535,954 (GRCm38) |
missense |
probably null |
1.00 |
R4737:Tln1
|
UTSW |
4 |
43,540,588 (GRCm38) |
missense |
probably benign |
0.00 |
R4936:Tln1
|
UTSW |
4 |
43,547,522 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5225:Tln1
|
UTSW |
4 |
43,539,406 (GRCm38) |
missense |
probably benign |
0.06 |
R5288:Tln1
|
UTSW |
4 |
43,540,661 (GRCm38) |
missense |
probably benign |
0.06 |
R5421:Tln1
|
UTSW |
4 |
43,533,609 (GRCm38) |
missense |
possibly damaging |
0.80 |
R5445:Tln1
|
UTSW |
4 |
43,543,905 (GRCm38) |
missense |
probably benign |
0.26 |
R5660:Tln1
|
UTSW |
4 |
43,547,732 (GRCm38) |
missense |
probably damaging |
1.00 |
R5772:Tln1
|
UTSW |
4 |
43,545,191 (GRCm38) |
missense |
probably benign |
0.13 |
R6012:Tln1
|
UTSW |
4 |
43,539,508 (GRCm38) |
missense |
probably benign |
|
R6038:Tln1
|
UTSW |
4 |
43,555,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R6038:Tln1
|
UTSW |
4 |
43,555,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R6039:Tln1
|
UTSW |
4 |
43,555,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R6039:Tln1
|
UTSW |
4 |
43,555,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R6052:Tln1
|
UTSW |
4 |
43,555,052 (GRCm38) |
missense |
probably damaging |
0.99 |
R6145:Tln1
|
UTSW |
4 |
43,538,030 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6157:Tln1
|
UTSW |
4 |
43,534,744 (GRCm38) |
missense |
probably benign |
0.06 |
R6242:Tln1
|
UTSW |
4 |
43,533,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R6454:Tln1
|
UTSW |
4 |
43,533,866 (GRCm38) |
missense |
probably damaging |
0.99 |
R6467:Tln1
|
UTSW |
4 |
43,543,165 (GRCm38) |
missense |
probably benign |
0.42 |
R6548:Tln1
|
UTSW |
4 |
43,547,525 (GRCm38) |
missense |
probably damaging |
0.98 |
R6576:Tln1
|
UTSW |
4 |
43,555,419 (GRCm38) |
splice site |
probably null |
|
R6722:Tln1
|
UTSW |
4 |
43,547,618 (GRCm38) |
missense |
probably damaging |
1.00 |
R6968:Tln1
|
UTSW |
4 |
43,550,217 (GRCm38) |
missense |
probably benign |
0.02 |
R7000:Tln1
|
UTSW |
4 |
43,556,302 (GRCm38) |
missense |
probably damaging |
0.96 |
R7137:Tln1
|
UTSW |
4 |
43,540,616 (GRCm38) |
missense |
probably damaging |
1.00 |
R7242:Tln1
|
UTSW |
4 |
43,542,602 (GRCm38) |
missense |
probably benign |
0.01 |
R7294:Tln1
|
UTSW |
4 |
43,534,399 (GRCm38) |
missense |
probably benign |
0.02 |
R7312:Tln1
|
UTSW |
4 |
43,545,922 (GRCm38) |
missense |
probably damaging |
1.00 |
R7547:Tln1
|
UTSW |
4 |
43,545,206 (GRCm38) |
missense |
possibly damaging |
0.80 |
R7836:Tln1
|
UTSW |
4 |
43,554,309 (GRCm38) |
missense |
probably benign |
0.01 |
R7874:Tln1
|
UTSW |
4 |
43,555,606 (GRCm38) |
missense |
probably damaging |
1.00 |
R7874:Tln1
|
UTSW |
4 |
43,538,041 (GRCm38) |
missense |
probably damaging |
1.00 |
R8030:Tln1
|
UTSW |
4 |
43,535,737 (GRCm38) |
critical splice donor site |
probably null |
|
R8105:Tln1
|
UTSW |
4 |
43,538,231 (GRCm38) |
missense |
probably benign |
0.32 |
R8212:Tln1
|
UTSW |
4 |
43,555,918 (GRCm38) |
missense |
probably damaging |
1.00 |
R8416:Tln1
|
UTSW |
4 |
43,540,116 (GRCm38) |
missense |
probably benign |
0.01 |
R8419:Tln1
|
UTSW |
4 |
43,536,397 (GRCm38) |
missense |
probably damaging |
1.00 |
R8680:Tln1
|
UTSW |
4 |
43,553,041 (GRCm38) |
missense |
possibly damaging |
0.52 |
R8708:Tln1
|
UTSW |
4 |
43,534,769 (GRCm38) |
splice site |
probably benign |
|
R8725:Tln1
|
UTSW |
4 |
43,555,911 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8727:Tln1
|
UTSW |
4 |
43,555,911 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8830:Tln1
|
UTSW |
4 |
43,556,383 (GRCm38) |
missense |
probably benign |
|
R8865:Tln1
|
UTSW |
4 |
43,538,281 (GRCm38) |
missense |
possibly damaging |
0.93 |
R9049:Tln1
|
UTSW |
4 |
43,549,786 (GRCm38) |
nonsense |
probably null |
|
R9050:Tln1
|
UTSW |
4 |
43,549,786 (GRCm38) |
nonsense |
probably null |
|
R9145:Tln1
|
UTSW |
4 |
43,536,024 (GRCm38) |
missense |
probably damaging |
1.00 |
R9210:Tln1
|
UTSW |
4 |
43,536,119 (GRCm38) |
missense |
probably damaging |
1.00 |
R9337:Tln1
|
UTSW |
4 |
43,532,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R9346:Tln1
|
UTSW |
4 |
43,546,895 (GRCm38) |
missense |
probably damaging |
0.97 |
R9358:Tln1
|
UTSW |
4 |
43,532,084 (GRCm38) |
missense |
possibly damaging |
0.68 |
R9487:Tln1
|
UTSW |
4 |
43,542,893 (GRCm38) |
missense |
probably damaging |
1.00 |
R9631:Tln1
|
UTSW |
4 |
43,545,694 (GRCm38) |
missense |
probably damaging |
1.00 |
R9650:Tln1
|
UTSW |
4 |
43,545,912 (GRCm38) |
missense |
probably damaging |
1.00 |
R9666:Tln1
|
UTSW |
4 |
43,542,957 (GRCm38) |
missense |
probably damaging |
0.96 |
RF021:Tln1
|
UTSW |
4 |
43,555,890 (GRCm38) |
missense |
probably damaging |
1.00 |
X0052:Tln1
|
UTSW |
4 |
43,533,125 (GRCm38) |
critical splice donor site |
probably null |
|
X0063:Tln1
|
UTSW |
4 |
43,548,015 (GRCm38) |
nonsense |
probably null |
|
Z1176:Tln1
|
UTSW |
4 |
43,543,211 (GRCm38) |
missense |
probably benign |
0.31 |
|