Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arap3 |
T |
A |
18: 37,990,560 (GRCm38) |
E441V |
probably damaging |
Het |
Arfip2 |
T |
A |
7: 105,637,988 (GRCm38) |
D64V |
probably damaging |
Het |
Atg9a |
C |
A |
1: 75,185,685 (GRCm38) |
R527L |
probably damaging |
Het |
Atp1a1 |
T |
G |
3: 101,590,548 (GRCm38) |
I308L |
probably benign |
Het |
Bcan |
T |
A |
3: 87,996,581 (GRCm38) |
Y199F |
probably damaging |
Het |
Bsn |
T |
C |
9: 108,109,992 (GRCm38) |
|
probably benign |
Het |
Ccdc158 |
A |
T |
5: 92,632,508 (GRCm38) |
L902H |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,124,512 (GRCm38) |
Y492C |
probably benign |
Het |
Dnah9 |
G |
T |
11: 66,072,779 (GRCm38) |
H1783N |
probably damaging |
Het |
Dpep2 |
A |
G |
8: 105,988,998 (GRCm38) |
V320A |
possibly damaging |
Het |
Dsc2 |
A |
G |
18: 20,045,502 (GRCm38) |
Y282H |
probably damaging |
Het |
Egfr |
C |
T |
11: 16,911,562 (GRCm38) |
P1114S |
probably benign |
Het |
Fastkd1 |
A |
G |
2: 69,700,133 (GRCm38) |
S560P |
probably damaging |
Het |
Gm14295 |
G |
A |
2: 176,811,102 (GRCm38) |
R795Q |
possibly damaging |
Het |
Gpr155 |
C |
T |
2: 73,382,127 (GRCm38) |
V51I |
probably benign |
Het |
Gsap |
G |
A |
5: 21,222,440 (GRCm38) |
|
probably null |
Het |
Hecw1 |
T |
A |
13: 14,377,706 (GRCm38) |
I103F |
probably damaging |
Het |
Herc3 |
T |
A |
6: 58,887,437 (GRCm38) |
N685K |
probably damaging |
Het |
Hnrnph1 |
T |
A |
11: 50,382,816 (GRCm38) |
D244E |
probably benign |
Het |
Hydin |
A |
G |
8: 110,582,049 (GRCm38) |
E3989G |
probably benign |
Het |
Ibsp |
T |
C |
5: 104,310,430 (GRCm38) |
Y278H |
probably damaging |
Het |
Ift57 |
T |
G |
16: 49,759,340 (GRCm38) |
N291K |
probably benign |
Het |
Il15ra |
A |
G |
2: 11,723,571 (GRCm38) |
T149A |
possibly damaging |
Het |
Ints5 |
C |
T |
19: 8,896,282 (GRCm38) |
T535I |
possibly damaging |
Het |
Jarid2 |
T |
C |
13: 44,902,539 (GRCm38) |
L268P |
probably damaging |
Het |
Klhdc7a |
T |
A |
4: 139,965,810 (GRCm38) |
T609S |
probably benign |
Het |
Lrrc49 |
A |
G |
9: 60,602,682 (GRCm38) |
V429A |
probably benign |
Het |
Lsm3 |
T |
C |
6: 91,522,272 (GRCm38) |
V87A |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,703,438 (GRCm38) |
P11R |
probably damaging |
Het |
Map1a |
G |
T |
2: 121,307,932 (GRCm38) |
V2726L |
probably damaging |
Het |
Marveld3 |
A |
C |
8: 109,961,846 (GRCm38) |
S88A |
probably benign |
Het |
Mcm9 |
T |
C |
10: 53,548,574 (GRCm38) |
D640G |
probably damaging |
Het |
Mettl4 |
A |
G |
17: 94,733,163 (GRCm38) |
I399T |
probably benign |
Het |
Mmp27 |
T |
A |
9: 7,577,378 (GRCm38) |
L274* |
probably null |
Het |
Nacc2 |
A |
C |
2: 26,060,223 (GRCm38) |
D500E |
probably benign |
Het |
Nprl3 |
T |
A |
11: 32,234,894 (GRCm38) |
M372L |
probably benign |
Het |
Or5p6 |
A |
T |
7: 108,031,467 (GRCm38) |
I292N |
probably damaging |
Het |
Otud7b |
T |
G |
3: 96,153,520 (GRCm38) |
|
probably null |
Het |
Pcx |
G |
A |
19: 4,620,881 (GRCm38) |
R1070H |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,590,994 (GRCm38) |
W1560* |
probably null |
Het |
Puf60 |
A |
T |
15: 76,070,464 (GRCm38) |
I520N |
probably damaging |
Het |
Qars1 |
C |
T |
9: 108,509,200 (GRCm38) |
R143C |
probably damaging |
Het |
Rfx3 |
G |
A |
19: 27,815,494 (GRCm38) |
Q322* |
probably null |
Het |
Samd14 |
G |
T |
11: 95,014,391 (GRCm38) |
V10L |
probably benign |
Het |
Setd2 |
G |
A |
9: 110,549,844 (GRCm38) |
R909Q |
probably benign |
Het |
Sh2d4a |
T |
C |
8: 68,296,664 (GRCm38) |
S117P |
probably benign |
Het |
Sharpin |
C |
A |
15: 76,350,666 (GRCm38) |
|
probably benign |
Het |
Skor1 |
C |
A |
9: 63,145,122 (GRCm38) |
A494S |
possibly damaging |
Het |
Slc41a2 |
T |
C |
10: 83,283,774 (GRCm38) |
T375A |
probably benign |
Het |
Sparc |
G |
A |
11: 55,395,801 (GRCm38) |
Q324* |
probably null |
Het |
Spopfm2 |
T |
G |
3: 94,176,298 (GRCm38) |
K69Q |
possibly damaging |
Het |
Srebf1 |
T |
C |
11: 60,206,502 (GRCm38) |
T171A |
probably benign |
Het |
Srrd |
A |
G |
5: 112,341,122 (GRCm38) |
I54T |
possibly damaging |
Het |
Tecpr1 |
A |
T |
5: 144,211,456 (GRCm38) |
V377E |
probably benign |
Het |
Tecpr1 |
G |
T |
5: 144,196,417 (GRCm38) |
Q1072K |
probably damaging |
Het |
Tm9sf3 |
C |
T |
19: 41,217,420 (GRCm38) |
S516N |
probably damaging |
Het |
Trpa1 |
T |
A |
1: 14,881,656 (GRCm38) |
T940S |
probably benign |
Het |
Trpv4 |
G |
A |
5: 114,644,710 (GRCm38) |
R64C |
probably damaging |
Het |
Tufm |
A |
G |
7: 126,488,847 (GRCm38) |
E174G |
probably benign |
Het |
Urb2 |
A |
G |
8: 124,031,102 (GRCm38) |
T1183A |
probably damaging |
Het |
Virma |
A |
T |
4: 11,527,843 (GRCm38) |
M1245L |
possibly damaging |
Het |
Vmn2r32 |
T |
C |
7: 7,474,615 (GRCm38) |
Y259C |
probably damaging |
Het |
Zfp329 |
A |
G |
7: 12,810,767 (GRCm38) |
F277L |
probably damaging |
Het |
Zfp683 |
C |
T |
4: 134,055,795 (GRCm38) |
T190I |
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 |
PIT4696001:Tln1
|
UTSW |
4 |
43,542,701 (GRCm38) |
critical splice donor site |
probably null |
|
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 |
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 |
|