Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
C |
T |
17: 9,226,839 (GRCm39) |
R465* |
probably null |
Het |
Abcg3 |
A |
T |
5: 105,114,649 (GRCm39) |
D289E |
probably damaging |
Het |
Ablim2 |
G |
T |
5: 36,024,115 (GRCm39) |
|
probably null |
Het |
Acp1 |
A |
T |
12: 30,955,078 (GRCm39) |
V36D |
probably benign |
Het |
Adgrb1 |
T |
A |
15: 74,449,348 (GRCm39) |
|
probably benign |
Het |
Akap6 |
G |
A |
12: 52,933,329 (GRCm39) |
V274I |
probably damaging |
Het |
Arhgap39 |
T |
C |
15: 76,609,715 (GRCm39) |
|
probably benign |
Het |
Bmp1 |
G |
A |
14: 70,717,605 (GRCm39) |
R789W |
probably damaging |
Het |
Catspere2 |
A |
T |
1: 177,976,474 (GRCm39) |
|
probably benign |
Het |
Cfhr2 |
T |
A |
1: 139,749,520 (GRCm39) |
Y154F |
possibly damaging |
Het |
Cilp2 |
T |
C |
8: 70,336,015 (GRCm39) |
Y358C |
probably damaging |
Het |
Cyp1a2 |
T |
A |
9: 57,584,516 (GRCm39) |
K513* |
probably null |
Het |
Dennd4a |
G |
T |
9: 64,796,210 (GRCm39) |
K745N |
possibly damaging |
Het |
Dlg1 |
T |
A |
16: 31,655,085 (GRCm39) |
S542T |
probably benign |
Het |
Dmbt1 |
A |
T |
7: 130,696,465 (GRCm39) |
I893F |
possibly damaging |
Het |
Dnhd1 |
A |
T |
7: 105,353,130 (GRCm39) |
E2761V |
possibly damaging |
Het |
F11 |
T |
C |
8: 45,708,341 (GRCm39) |
T40A |
probably benign |
Het |
Fam227a |
T |
C |
15: 79,520,936 (GRCm39) |
D296G |
possibly damaging |
Het |
Fance |
C |
T |
17: 28,534,589 (GRCm39) |
|
probably benign |
Het |
Gaa |
A |
G |
11: 119,167,669 (GRCm39) |
D149G |
probably damaging |
Het |
Gapt |
A |
G |
13: 110,490,522 (GRCm39) |
M47T |
possibly damaging |
Het |
Gm1110 |
T |
C |
9: 26,813,774 (GRCm39) |
N202D |
probably damaging |
Het |
Gm7535 |
T |
C |
17: 18,131,809 (GRCm39) |
|
probably benign |
Het |
Gm973 |
T |
A |
1: 59,601,859 (GRCm39) |
M491K |
probably benign |
Het |
Gmnc |
A |
G |
16: 26,782,695 (GRCm39) |
V27A |
probably benign |
Het |
Kif27 |
T |
C |
13: 58,440,915 (GRCm39) |
T1167A |
possibly damaging |
Het |
Klrg1 |
T |
A |
6: 122,248,331 (GRCm39) |
*189C |
probably null |
Het |
Lime1 |
T |
A |
2: 181,024,640 (GRCm39) |
M98K |
probably benign |
Het |
Lrp1 |
C |
A |
10: 127,391,965 (GRCm39) |
A2867S |
probably benign |
Het |
Lrrd1 |
G |
A |
5: 3,908,735 (GRCm39) |
S669N |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,976,456 (GRCm39) |
N520S |
probably damaging |
Het |
Mrpl48 |
A |
C |
7: 100,198,535 (GRCm39) |
L206V |
probably damaging |
Het |
Nagpa |
C |
T |
16: 5,021,596 (GRCm39) |
A52T |
probably benign |
Het |
Or1o3 |
A |
G |
17: 37,573,919 (GRCm39) |
V212A |
probably benign |
Het |
Or4c3 |
T |
G |
2: 89,851,528 (GRCm39) |
D294A |
probably benign |
Het |
Orai2 |
A |
G |
5: 136,190,355 (GRCm39) |
S71P |
probably damaging |
Het |
Pcbp1 |
A |
T |
6: 86,502,209 (GRCm39) |
I230N |
probably damaging |
Het |
Pcdh15 |
T |
C |
10: 74,138,986 (GRCm39) |
L349P |
probably damaging |
Het |
Pcdhb16 |
T |
C |
18: 37,613,011 (GRCm39) |
V657A |
probably benign |
Het |
Prdm15 |
G |
T |
16: 97,609,875 (GRCm39) |
H590N |
probably damaging |
Het |
Psg18 |
T |
C |
7: 18,079,874 (GRCm39) |
I442M |
probably damaging |
Het |
Pygm |
C |
A |
19: 6,439,494 (GRCm39) |
D279E |
probably benign |
Het |
Rrn3 |
T |
A |
16: 13,610,798 (GRCm39) |
|
probably null |
Het |
Sass6 |
T |
C |
3: 116,407,702 (GRCm39) |
S273P |
possibly damaging |
Het |
Schip1 |
A |
G |
3: 68,402,270 (GRCm39) |
M116V |
probably benign |
Het |
Sdc3 |
G |
A |
4: 130,546,087 (GRCm39) |
V55I |
unknown |
Het |
Serpinb8 |
T |
A |
1: 107,525,201 (GRCm39) |
M1K |
probably null |
Het |
Slc24a5 |
T |
C |
2: 124,927,739 (GRCm39) |
I346T |
probably damaging |
Het |
Slc35f3 |
T |
A |
8: 127,117,846 (GRCm39) |
I335N |
probably damaging |
Het |
Snapc2 |
T |
A |
8: 4,305,299 (GRCm39) |
V147E |
probably damaging |
Het |
Snx2 |
T |
C |
18: 53,322,784 (GRCm39) |
S56P |
possibly damaging |
Het |
Sptbn5 |
A |
G |
2: 119,915,812 (GRCm39) |
|
probably benign |
Het |
Stk19 |
A |
T |
17: 35,040,400 (GRCm39) |
|
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,911,702 (GRCm39) |
E692G |
probably benign |
Het |
Tet1 |
C |
T |
10: 62,674,450 (GRCm39) |
V1209I |
probably damaging |
Het |
Tmem135 |
G |
T |
7: 88,845,335 (GRCm39) |
Y165* |
probably null |
Het |
Tmprss6 |
T |
C |
15: 78,336,707 (GRCm39) |
T398A |
probably damaging |
Het |
Ube4a |
C |
T |
9: 44,851,258 (GRCm39) |
|
probably null |
Het |
Vmn1r227 |
T |
C |
17: 20,955,499 (GRCm39) |
|
noncoding transcript |
Het |
Wdhd1 |
T |
C |
14: 47,488,273 (GRCm39) |
S745G |
probably benign |
Het |
Xylt1 |
A |
G |
7: 117,191,263 (GRCm39) |
H353R |
probably damaging |
Het |
Zfp788 |
A |
G |
7: 41,298,980 (GRCm39) |
T539A |
probably benign |
Het |
Zfp866 |
A |
T |
8: 70,218,091 (GRCm39) |
F510I |
possibly damaging |
Het |
|
Other mutations in Tln1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Tln1
|
APN |
4 |
43,542,719 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00987:Tln1
|
APN |
4 |
43,551,297 (GRCm39) |
unclassified |
probably benign |
|
IGL01345:Tln1
|
APN |
4 |
43,536,281 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01456:Tln1
|
APN |
4 |
43,543,432 (GRCm39) |
unclassified |
probably benign |
|
IGL01715:Tln1
|
APN |
4 |
43,555,890 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01750:Tln1
|
APN |
4 |
43,545,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Tln1
|
APN |
4 |
43,555,894 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01933:Tln1
|
APN |
4 |
43,539,508 (GRCm39) |
missense |
probably benign |
|
IGL02119:Tln1
|
APN |
4 |
43,546,760 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02148:Tln1
|
APN |
4 |
43,555,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02153:Tln1
|
APN |
4 |
43,546,857 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02522:Tln1
|
APN |
4 |
43,540,612 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02691:Tln1
|
APN |
4 |
43,539,544 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02882:Tln1
|
APN |
4 |
43,539,522 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02892:Tln1
|
APN |
4 |
43,555,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Tln1
|
APN |
4 |
43,545,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03102:Tln1
|
APN |
4 |
43,532,861 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03183:Tln1
|
APN |
4 |
43,539,084 (GRCm39) |
splice site |
probably benign |
|
H8786:Tln1
|
UTSW |
4 |
43,544,589 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4576001:Tln1
|
UTSW |
4 |
43,539,998 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4696001:Tln1
|
UTSW |
4 |
43,542,701 (GRCm39) |
critical splice donor site |
probably null |
|
R0206:Tln1
|
UTSW |
4 |
43,549,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Tln1
|
UTSW |
4 |
43,549,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Tln1
|
UTSW |
4 |
43,553,504 (GRCm39) |
missense |
probably benign |
|
R0539:Tln1
|
UTSW |
4 |
43,543,434 (GRCm39) |
critical splice donor site |
probably null |
|
R0548:Tln1
|
UTSW |
4 |
43,542,709 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0561:Tln1
|
UTSW |
4 |
43,550,304 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0606:Tln1
|
UTSW |
4 |
43,547,756 (GRCm39) |
missense |
probably benign |
0.34 |
R0607:Tln1
|
UTSW |
4 |
43,553,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Tln1
|
UTSW |
4 |
43,544,645 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0847:Tln1
|
UTSW |
4 |
43,555,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R0993:Tln1
|
UTSW |
4 |
43,549,825 (GRCm39) |
missense |
probably benign |
0.22 |
R1255:Tln1
|
UTSW |
4 |
43,538,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1292:Tln1
|
UTSW |
4 |
43,534,578 (GRCm39) |
critical splice donor site |
probably null |
|
R1752:Tln1
|
UTSW |
4 |
43,536,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R2169:Tln1
|
UTSW |
4 |
43,548,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Tln1
|
UTSW |
4 |
43,545,721 (GRCm39) |
missense |
probably benign |
|
R2202:Tln1
|
UTSW |
4 |
43,553,083 (GRCm39) |
splice site |
probably null |
|
R2680:Tln1
|
UTSW |
4 |
43,539,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R3012:Tln1
|
UTSW |
4 |
43,542,525 (GRCm39) |
missense |
probably benign |
|
R3714:Tln1
|
UTSW |
4 |
43,540,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R3735:Tln1
|
UTSW |
4 |
43,549,370 (GRCm39) |
missense |
probably damaging |
0.97 |
R3794:Tln1
|
UTSW |
4 |
43,536,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R3825:Tln1
|
UTSW |
4 |
43,536,413 (GRCm39) |
splice site |
probably benign |
|
R3983:Tln1
|
UTSW |
4 |
43,553,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R4061:Tln1
|
UTSW |
4 |
43,549,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R4249:Tln1
|
UTSW |
4 |
43,536,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R4287:Tln1
|
UTSW |
4 |
43,543,509 (GRCm39) |
missense |
probably benign |
0.01 |
R4471:Tln1
|
UTSW |
4 |
43,551,018 (GRCm39) |
missense |
probably benign |
0.03 |
R4562:Tln1
|
UTSW |
4 |
43,533,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Tln1
|
UTSW |
4 |
43,535,954 (GRCm39) |
missense |
probably null |
1.00 |
R4737:Tln1
|
UTSW |
4 |
43,540,588 (GRCm39) |
missense |
probably benign |
0.00 |
R4936:Tln1
|
UTSW |
4 |
43,547,522 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5288:Tln1
|
UTSW |
4 |
43,540,661 (GRCm39) |
missense |
probably benign |
0.06 |
R5421:Tln1
|
UTSW |
4 |
43,533,609 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5445:Tln1
|
UTSW |
4 |
43,543,905 (GRCm39) |
missense |
probably benign |
0.26 |
R5660:Tln1
|
UTSW |
4 |
43,547,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Tln1
|
UTSW |
4 |
43,545,191 (GRCm39) |
missense |
probably benign |
0.13 |
R6012:Tln1
|
UTSW |
4 |
43,539,508 (GRCm39) |
missense |
probably benign |
|
R6038:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6038:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6039:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6039:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6052:Tln1
|
UTSW |
4 |
43,555,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R6145:Tln1
|
UTSW |
4 |
43,538,030 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6157:Tln1
|
UTSW |
4 |
43,534,744 (GRCm39) |
missense |
probably benign |
0.06 |
R6242:Tln1
|
UTSW |
4 |
43,533,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6454:Tln1
|
UTSW |
4 |
43,533,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R6467:Tln1
|
UTSW |
4 |
43,543,165 (GRCm39) |
missense |
probably benign |
0.42 |
R6548:Tln1
|
UTSW |
4 |
43,547,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R6576:Tln1
|
UTSW |
4 |
43,555,419 (GRCm39) |
splice site |
probably null |
|
R6722:Tln1
|
UTSW |
4 |
43,547,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Tln1
|
UTSW |
4 |
43,550,217 (GRCm39) |
missense |
probably benign |
0.02 |
R7000:Tln1
|
UTSW |
4 |
43,556,302 (GRCm39) |
missense |
probably damaging |
0.96 |
R7137:Tln1
|
UTSW |
4 |
43,540,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Tln1
|
UTSW |
4 |
43,542,602 (GRCm39) |
missense |
probably benign |
0.01 |
R7294:Tln1
|
UTSW |
4 |
43,534,399 (GRCm39) |
missense |
probably benign |
0.02 |
R7312:Tln1
|
UTSW |
4 |
43,545,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7547:Tln1
|
UTSW |
4 |
43,545,206 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7836:Tln1
|
UTSW |
4 |
43,554,309 (GRCm39) |
missense |
probably benign |
0.01 |
R7874:Tln1
|
UTSW |
4 |
43,555,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R7874:Tln1
|
UTSW |
4 |
43,538,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Tln1
|
UTSW |
4 |
43,535,737 (GRCm39) |
critical splice donor site |
probably null |
|
R8105:Tln1
|
UTSW |
4 |
43,538,231 (GRCm39) |
missense |
probably benign |
0.32 |
R8212:Tln1
|
UTSW |
4 |
43,555,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R8416:Tln1
|
UTSW |
4 |
43,540,116 (GRCm39) |
missense |
probably benign |
0.01 |
R8419:Tln1
|
UTSW |
4 |
43,536,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Tln1
|
UTSW |
4 |
43,553,041 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8708:Tln1
|
UTSW |
4 |
43,534,769 (GRCm39) |
splice site |
probably benign |
|
R8725:Tln1
|
UTSW |
4 |
43,555,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8727:Tln1
|
UTSW |
4 |
43,555,911 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8830:Tln1
|
UTSW |
4 |
43,556,383 (GRCm39) |
missense |
probably benign |
|
R8865:Tln1
|
UTSW |
4 |
43,538,281 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9049:Tln1
|
UTSW |
4 |
43,549,786 (GRCm39) |
nonsense |
probably null |
|
R9050:Tln1
|
UTSW |
4 |
43,549,786 (GRCm39) |
nonsense |
probably null |
|
R9145:Tln1
|
UTSW |
4 |
43,536,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9210:Tln1
|
UTSW |
4 |
43,536,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R9337:Tln1
|
UTSW |
4 |
43,532,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Tln1
|
UTSW |
4 |
43,546,895 (GRCm39) |
missense |
probably damaging |
0.97 |
R9358:Tln1
|
UTSW |
4 |
43,532,084 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9487:Tln1
|
UTSW |
4 |
43,542,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R9631:Tln1
|
UTSW |
4 |
43,545,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Tln1
|
UTSW |
4 |
43,545,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Tln1
|
UTSW |
4 |
43,542,957 (GRCm39) |
missense |
probably damaging |
0.96 |
RF021:Tln1
|
UTSW |
4 |
43,555,890 (GRCm39) |
missense |
probably damaging |
1.00 |
X0052:Tln1
|
UTSW |
4 |
43,533,125 (GRCm39) |
critical splice donor site |
probably null |
|
X0063:Tln1
|
UTSW |
4 |
43,548,015 (GRCm39) |
nonsense |
probably null |
|
Z1176:Tln1
|
UTSW |
4 |
43,543,211 (GRCm39) |
missense |
probably benign |
0.31 |
|