Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
T |
A |
4: 122,701,177 (GRCm38) |
|
probably benign |
Het |
Abcc2 |
G |
A |
19: 43,821,605 (GRCm38) |
|
probably benign |
Het |
Abcc8 |
C |
G |
7: 46,122,173 (GRCm38) |
G838A |
probably damaging |
Het |
Akr1c21 |
G |
A |
13: 4,581,200 (GRCm38) |
A245T |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,673,277 (GRCm38) |
E47G |
probably damaging |
Het |
Apoa1 |
A |
G |
9: 46,229,842 (GRCm38) |
T79A |
probably benign |
Het |
Atp6v1b1 |
A |
G |
6: 83,756,921 (GRCm38) |
H378R |
possibly damaging |
Het |
C4b |
A |
G |
17: 34,735,614 (GRCm38) |
|
probably benign |
Het |
Catsperd |
A |
T |
17: 56,662,821 (GRCm38) |
E638D |
probably benign |
Het |
Cckar |
C |
T |
5: 53,706,253 (GRCm38) |
|
probably null |
Het |
Cfap100 |
C |
T |
6: 90,405,339 (GRCm38) |
|
probably benign |
Het |
Chd1 |
G |
T |
17: 15,749,894 (GRCm38) |
G970C |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,446,259 (GRCm38) |
|
probably benign |
Het |
Col17a1 |
C |
T |
19: 47,663,824 (GRCm38) |
V698M |
probably damaging |
Het |
Cpeb1 |
T |
C |
7: 81,361,725 (GRCm38) |
D156G |
possibly damaging |
Het |
Cryl1 |
A |
G |
14: 57,303,775 (GRCm38) |
Y151H |
possibly damaging |
Het |
Csmd3 |
C |
A |
15: 47,657,573 (GRCm38) |
V1881L |
probably damaging |
Het |
Ctnnal1 |
C |
T |
4: 56,847,921 (GRCm38) |
A73T |
probably damaging |
Het |
Cyp2c37 |
T |
C |
19: 39,994,506 (GRCm38) |
S180P |
probably damaging |
Het |
Cyp2c54 |
T |
C |
19: 40,072,169 (GRCm38) |
T123A |
possibly damaging |
Het |
Dennd6b |
T |
C |
15: 89,187,214 (GRCm38) |
D304G |
probably damaging |
Het |
Dnmt3l |
T |
C |
10: 78,051,916 (GRCm38) |
|
probably benign |
Het |
Eci1 |
G |
A |
17: 24,433,260 (GRCm38) |
|
probably null |
Het |
Efhc1 |
A |
G |
1: 20,960,188 (GRCm38) |
Y115C |
probably damaging |
Het |
Ern1 |
T |
A |
11: 106,407,178 (GRCm38) |
K706* |
probably null |
Het |
Fam129c |
T |
A |
8: 71,602,499 (GRCm38) |
|
probably benign |
Het |
Ghrl |
T |
C |
6: 113,719,338 (GRCm38) |
E31G |
probably damaging |
Het |
Gpr108 |
A |
C |
17: 57,243,101 (GRCm38) |
V179G |
probably benign |
Het |
Henmt1 |
A |
G |
3: 108,958,535 (GRCm38) |
|
probably benign |
Het |
Ift172 |
A |
G |
5: 31,286,667 (GRCm38) |
V69A |
probably damaging |
Het |
Il17ra |
T |
C |
6: 120,476,979 (GRCm38) |
|
probably benign |
Het |
Il17rb |
T |
C |
14: 30,004,347 (GRCm38) |
N95D |
probably benign |
Het |
Il17rb |
G |
T |
14: 30,006,155 (GRCm38) |
|
probably null |
Het |
Iqub |
G |
A |
6: 24,446,155 (GRCm38) |
L757F |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,378,167 (GRCm38) |
V473A |
probably benign |
Het |
Itpr2 |
T |
G |
6: 146,229,773 (GRCm38) |
N1978H |
probably damaging |
Het |
Klk1b26 |
T |
A |
7: 44,012,727 (GRCm38) |
F3Y |
probably damaging |
Het |
Lars |
A |
G |
18: 42,251,363 (GRCm38) |
V50A |
probably benign |
Het |
Lax1 |
G |
T |
1: 133,680,066 (GRCm38) |
H312Q |
probably benign |
Het |
Lctl |
T |
C |
9: 64,122,314 (GRCm38) |
|
probably benign |
Het |
Lrp2 |
G |
A |
2: 69,460,337 (GRCm38) |
|
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,456,858 (GRCm38) |
D3745V |
probably damaging |
Het |
Lvrn |
A |
T |
18: 46,850,466 (GRCm38) |
H92L |
probably benign |
Het |
March1 |
A |
G |
8: 66,418,973 (GRCm38) |
T385A |
probably damaging |
Het |
Marf1 |
C |
T |
16: 14,142,534 (GRCm38) |
A549T |
probably damaging |
Het |
Mbd5 |
T |
C |
2: 49,272,416 (GRCm38) |
V970A |
possibly damaging |
Het |
Mccc1 |
A |
G |
3: 35,963,570 (GRCm38) |
|
probably benign |
Het |
Mpp4 |
A |
T |
1: 59,143,829 (GRCm38) |
|
probably benign |
Het |
Mrnip |
G |
A |
11: 50,199,920 (GRCm38) |
A304T |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,865,082 (GRCm38) |
S3922P |
possibly damaging |
Het |
Myh3 |
T |
A |
11: 67,096,507 (GRCm38) |
|
probably benign |
Het |
Nbea |
A |
T |
3: 56,037,277 (GRCm38) |
H555Q |
probably damaging |
Het |
Nlrp9c |
A |
T |
7: 26,371,476 (GRCm38) |
|
probably benign |
Het |
Nmur1 |
A |
T |
1: 86,387,678 (GRCm38) |
V178E |
probably damaging |
Het |
Nod2 |
T |
G |
8: 88,663,778 (GRCm38) |
S238A |
probably benign |
Het |
Ogfod1 |
A |
T |
8: 94,063,023 (GRCm38) |
T451S |
probably damaging |
Het |
Olfr145 |
G |
A |
9: 37,897,842 (GRCm38) |
G146D |
probably benign |
Het |
Olfr23 |
T |
C |
11: 73,941,109 (GRCm38) |
F288L |
probably damaging |
Het |
Olfr372 |
C |
T |
8: 72,058,400 (GRCm38) |
T240M |
probably damaging |
Het |
Olfr716 |
T |
A |
7: 107,148,187 (GRCm38) |
Y290* |
probably null |
Het |
Pcdh20 |
T |
C |
14: 88,468,668 (GRCm38) |
I399V |
probably benign |
Het |
Pdlim1 |
G |
T |
19: 40,243,573 (GRCm38) |
H120Q |
probably damaging |
Het |
Plg |
T |
C |
17: 12,419,081 (GRCm38) |
V798A |
probably damaging |
Het |
Polr2c |
A |
G |
8: 94,857,775 (GRCm38) |
I39V |
possibly damaging |
Het |
Ppfia2 |
C |
A |
10: 106,830,714 (GRCm38) |
|
probably benign |
Het |
Ppp1r3a |
A |
T |
6: 14,719,697 (GRCm38) |
I406N |
probably benign |
Het |
Psg28 |
A |
T |
7: 18,426,173 (GRCm38) |
M366K |
probably benign |
Het |
Rad54b |
T |
C |
4: 11,601,702 (GRCm38) |
I419T |
probably damaging |
Het |
Rnf43 |
A |
G |
11: 87,731,282 (GRCm38) |
Q403R |
possibly damaging |
Het |
Sema6a |
G |
A |
18: 47,290,045 (GRCm38) |
|
probably null |
Het |
Slc28a3 |
A |
G |
13: 58,569,415 (GRCm38) |
|
probably benign |
Het |
Smad2 |
A |
T |
18: 76,289,037 (GRCm38) |
|
probably null |
Het |
Smad4 |
G |
A |
18: 73,658,649 (GRCm38) |
P274S |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,403,154 (GRCm38) |
V906D |
probably damaging |
Het |
Soat2 |
C |
A |
15: 102,158,753 (GRCm38) |
R320S |
possibly damaging |
Het |
Spata33 |
C |
T |
8: 123,221,887 (GRCm38) |
A57V |
probably damaging |
Het |
Stab1 |
A |
G |
14: 31,143,418 (GRCm38) |
L1814P |
probably benign |
Het |
Stab2 |
T |
C |
10: 86,947,144 (GRCm38) |
K680R |
probably benign |
Het |
Stil |
A |
G |
4: 115,041,172 (GRCm38) |
|
probably null |
Het |
Sympk |
T |
A |
7: 19,046,849 (GRCm38) |
L759H |
probably benign |
Het |
Tet1 |
A |
T |
10: 62,814,546 (GRCm38) |
|
probably null |
Het |
Tfpi2 |
A |
T |
6: 3,965,460 (GRCm38) |
N117K |
probably benign |
Het |
Tle3 |
A |
G |
9: 61,416,661 (GRCm38) |
Y766C |
probably damaging |
Het |
Trpt1 |
C |
A |
19: 6,997,930 (GRCm38) |
|
probably null |
Het |
Ttc1 |
T |
C |
11: 43,738,808 (GRCm38) |
D177G |
probably damaging |
Het |
Ttc13 |
T |
A |
8: 124,674,401 (GRCm38) |
Y741F |
probably damaging |
Het |
Ulk3 |
C |
T |
9: 57,594,832 (GRCm38) |
S462L |
probably benign |
Het |
Utrn |
C |
T |
10: 12,525,333 (GRCm38) |
|
probably benign |
Het |
V1rd19 |
A |
C |
7: 24,003,585 (GRCm38) |
T159P |
probably damaging |
Het |
Vars |
T |
C |
17: 35,011,486 (GRCm38) |
V515A |
possibly damaging |
Het |
Vmn1r85 |
A |
G |
7: 13,084,588 (GRCm38) |
Y210H |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,455,978 (GRCm38) |
T262A |
probably damaging |
Het |
Vps53 |
G |
A |
11: 76,121,579 (GRCm38) |
T209I |
probably benign |
Het |
Wdfy2 |
T |
C |
14: 62,925,133 (GRCm38) |
F95L |
possibly damaging |
Het |
Wwp1 |
G |
T |
4: 19,627,911 (GRCm38) |
S694Y |
probably damaging |
Het |
Zbtb8b |
T |
A |
4: 129,432,670 (GRCm38) |
D201V |
probably damaging |
Het |
Zmym5 |
A |
C |
14: 56,804,451 (GRCm38) |
N123K |
possibly damaging |
Het |
|
Other mutations in Tshz1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01486:Tshz1
|
APN |
18 |
84,013,509 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL02934:Tshz1
|
APN |
18 |
84,013,090 (GRCm38) |
missense |
probably damaging |
1.00 |
ANU18:Tshz1
|
UTSW |
18 |
84,014,661 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4810001:Tshz1
|
UTSW |
18 |
84,013,250 (GRCm38) |
missense |
possibly damaging |
0.85 |
R0052:Tshz1
|
UTSW |
18 |
84,014,945 (GRCm38) |
missense |
possibly damaging |
0.76 |
R0052:Tshz1
|
UTSW |
18 |
84,014,945 (GRCm38) |
missense |
possibly damaging |
0.76 |
R0364:Tshz1
|
UTSW |
18 |
84,016,124 (GRCm38) |
missense |
probably benign |
0.31 |
R0515:Tshz1
|
UTSW |
18 |
84,015,965 (GRCm38) |
missense |
probably benign |
|
R0942:Tshz1
|
UTSW |
18 |
84,013,053 (GRCm38) |
missense |
probably damaging |
0.99 |
R0943:Tshz1
|
UTSW |
18 |
84,015,231 (GRCm38) |
missense |
probably benign |
0.04 |
R1472:Tshz1
|
UTSW |
18 |
84,013,805 (GRCm38) |
missense |
possibly damaging |
0.93 |
R1895:Tshz1
|
UTSW |
18 |
84,013,433 (GRCm38) |
missense |
probably damaging |
1.00 |
R2022:Tshz1
|
UTSW |
18 |
84,013,862 (GRCm38) |
missense |
probably damaging |
0.98 |
R2860:Tshz1
|
UTSW |
18 |
84,014,980 (GRCm38) |
missense |
probably damaging |
1.00 |
R2861:Tshz1
|
UTSW |
18 |
84,014,980 (GRCm38) |
missense |
probably damaging |
1.00 |
R4027:Tshz1
|
UTSW |
18 |
84,014,829 (GRCm38) |
missense |
possibly damaging |
0.74 |
R4028:Tshz1
|
UTSW |
18 |
84,014,829 (GRCm38) |
missense |
possibly damaging |
0.74 |
R4030:Tshz1
|
UTSW |
18 |
84,014,829 (GRCm38) |
missense |
possibly damaging |
0.74 |
R4031:Tshz1
|
UTSW |
18 |
84,014,829 (GRCm38) |
missense |
possibly damaging |
0.74 |
R4119:Tshz1
|
UTSW |
18 |
84,014,189 (GRCm38) |
missense |
probably benign |
0.00 |
R4233:Tshz1
|
UTSW |
18 |
84,016,195 (GRCm38) |
missense |
probably benign |
0.00 |
R4573:Tshz1
|
UTSW |
18 |
84,015,082 (GRCm38) |
missense |
probably damaging |
1.00 |
R4604:Tshz1
|
UTSW |
18 |
84,013,374 (GRCm38) |
missense |
probably damaging |
1.00 |
R4960:Tshz1
|
UTSW |
18 |
84,014,862 (GRCm38) |
missense |
probably benign |
0.08 |
R5085:Tshz1
|
UTSW |
18 |
84,013,928 (GRCm38) |
missense |
probably benign |
0.01 |
R5124:Tshz1
|
UTSW |
18 |
84,015,467 (GRCm38) |
missense |
probably damaging |
1.00 |
R5150:Tshz1
|
UTSW |
18 |
84,013,215 (GRCm38) |
nonsense |
probably null |
|
R5357:Tshz1
|
UTSW |
18 |
84,015,080 (GRCm38) |
missense |
probably damaging |
1.00 |
R5530:Tshz1
|
UTSW |
18 |
84,013,268 (GRCm38) |
missense |
probably damaging |
1.00 |
R5718:Tshz1
|
UTSW |
18 |
84,014,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R5750:Tshz1
|
UTSW |
18 |
84,013,961 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5778:Tshz1
|
UTSW |
18 |
84,015,680 (GRCm38) |
missense |
probably damaging |
1.00 |
R6052:Tshz1
|
UTSW |
18 |
84,014,069 (GRCm38) |
missense |
probably damaging |
1.00 |
R6279:Tshz1
|
UTSW |
18 |
84,015,311 (GRCm38) |
missense |
probably damaging |
1.00 |
R6393:Tshz1
|
UTSW |
18 |
84,013,220 (GRCm38) |
missense |
probably damaging |
1.00 |
R6407:Tshz1
|
UTSW |
18 |
84,015,966 (GRCm38) |
missense |
possibly damaging |
0.55 |
R6425:Tshz1
|
UTSW |
18 |
84,015,563 (GRCm38) |
missense |
probably damaging |
0.99 |
R6998:Tshz1
|
UTSW |
18 |
84,015,841 (GRCm38) |
missense |
probably benign |
0.00 |
R7165:Tshz1
|
UTSW |
18 |
84,015,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R7233:Tshz1
|
UTSW |
18 |
84,014,819 (GRCm38) |
missense |
possibly damaging |
0.63 |
R7330:Tshz1
|
UTSW |
18 |
84,014,831 (GRCm38) |
missense |
probably damaging |
0.96 |
R7491:Tshz1
|
UTSW |
18 |
84,015,641 (GRCm38) |
missense |
probably damaging |
1.00 |
R7579:Tshz1
|
UTSW |
18 |
84,014,665 (GRCm38) |
nonsense |
probably null |
|
R7592:Tshz1
|
UTSW |
18 |
84,014,048 (GRCm38) |
missense |
probably damaging |
1.00 |
R7659:Tshz1
|
UTSW |
18 |
84,016,075 (GRCm38) |
missense |
probably damaging |
0.97 |
R7702:Tshz1
|
UTSW |
18 |
84,014,336 (GRCm38) |
missense |
probably damaging |
1.00 |
R7844:Tshz1
|
UTSW |
18 |
84,014,171 (GRCm38) |
missense |
probably benign |
0.00 |
R7908:Tshz1
|
UTSW |
18 |
84,014,607 (GRCm38) |
nonsense |
probably null |
|
R7941:Tshz1
|
UTSW |
18 |
84,015,392 (GRCm38) |
missense |
possibly damaging |
0.91 |
R7947:Tshz1
|
UTSW |
18 |
84,015,657 (GRCm38) |
missense |
probably damaging |
1.00 |
R8435:Tshz1
|
UTSW |
18 |
84,014,024 (GRCm38) |
missense |
probably damaging |
1.00 |
R8750:Tshz1
|
UTSW |
18 |
84,015,037 (GRCm38) |
missense |
probably damaging |
1.00 |
R8774:Tshz1
|
UTSW |
18 |
84,014,976 (GRCm38) |
missense |
possibly damaging |
0.96 |
R8774-TAIL:Tshz1
|
UTSW |
18 |
84,014,976 (GRCm38) |
missense |
possibly damaging |
0.96 |
R9029:Tshz1
|
UTSW |
18 |
84,013,514 (GRCm38) |
missense |
probably damaging |
0.98 |
R9031:Tshz1
|
UTSW |
18 |
84,014,862 (GRCm38) |
missense |
probably benign |
0.08 |
R9573:Tshz1
|
UTSW |
18 |
84,014,279 (GRCm38) |
missense |
probably benign |
0.45 |
R9584:Tshz1
|
UTSW |
18 |
84,014,964 (GRCm38) |
missense |
probably damaging |
1.00 |
R9596:Tshz1
|
UTSW |
18 |
84,013,779 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9701:Tshz1
|
UTSW |
18 |
84,014,454 (GRCm38) |
missense |
possibly damaging |
0.96 |
|