Other mutations in this stock |
Total: 131 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
T |
C |
8: 60,982,479 (GRCm39) |
|
probably benign |
Het |
Afap1l2 |
T |
C |
19: 56,904,517 (GRCm39) |
E594G |
probably benign |
Het |
Ak8 |
T |
G |
2: 28,625,677 (GRCm39) |
I240S |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,264,744 (GRCm39) |
V174A |
probably damaging |
Het |
Alppl2 |
G |
A |
1: 87,017,095 (GRCm39) |
T66I |
probably damaging |
Het |
Ankrd61 |
T |
A |
5: 143,831,697 (GRCm39) |
I36F |
probably damaging |
Het |
Antxrl |
T |
A |
14: 33,780,758 (GRCm39) |
|
probably null |
Het |
Arhgef2 |
G |
C |
3: 88,541,743 (GRCm39) |
V244L |
probably damaging |
Het |
Arid1a |
A |
G |
4: 133,416,481 (GRCm39) |
I1098T |
unknown |
Het |
Atr |
T |
C |
9: 95,756,830 (GRCm39) |
V903A |
possibly damaging |
Het |
B3gnt6 |
C |
A |
7: 97,842,899 (GRCm39) |
A354S |
probably benign |
Het |
Bnc1 |
A |
T |
7: 81,624,114 (GRCm39) |
I371N |
probably damaging |
Het |
Camsap1 |
A |
T |
2: 25,823,659 (GRCm39) |
S1464T |
probably damaging |
Het |
Cand2 |
G |
A |
6: 115,780,766 (GRCm39) |
E1217K |
probably damaging |
Het |
Cass4 |
T |
C |
2: 172,274,331 (GRCm39) |
I728T |
probably damaging |
Het |
Ccdc88a |
A |
T |
11: 29,443,752 (GRCm39) |
M1378L |
probably damaging |
Het |
Ccdc9 |
C |
A |
7: 16,012,384 (GRCm39) |
W266L |
probably damaging |
Het |
Cct6b |
C |
A |
11: 82,627,914 (GRCm39) |
|
probably null |
Het |
Cd177 |
T |
C |
7: 24,456,111 (GRCm39) |
E219G |
probably benign |
Het |
Cdkal1 |
A |
T |
13: 29,538,667 (GRCm39) |
Y497* |
probably null |
Het |
Chmp2a |
T |
C |
7: 12,766,371 (GRCm39) |
E107G |
probably damaging |
Het |
Chrna2 |
T |
G |
14: 66,386,757 (GRCm39) |
V301G |
probably benign |
Het |
Chrna7 |
A |
G |
7: 62,749,391 (GRCm39) |
C364R |
probably benign |
Het |
Cltc |
G |
T |
11: 86,603,439 (GRCm39) |
L796I |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,610,658 (GRCm39) |
T249A |
probably damaging |
Het |
Col13a1 |
G |
A |
10: 61,723,129 (GRCm39) |
Q270* |
probably null |
Het |
Col6a1 |
C |
T |
10: 76,545,569 (GRCm39) |
V968M |
probably benign |
Het |
Copb1 |
C |
A |
7: 113,832,517 (GRCm39) |
V511F |
probably benign |
Het |
Daw1 |
C |
G |
1: 83,174,981 (GRCm39) |
S160R |
probably damaging |
Het |
Ddx46 |
A |
G |
13: 55,787,590 (GRCm39) |
|
probably benign |
Het |
Depdc7 |
T |
C |
2: 104,552,332 (GRCm39) |
K492E |
possibly damaging |
Het |
Dmbt1 |
C |
T |
7: 130,699,383 (GRCm39) |
A1004V |
possibly damaging |
Het |
Dnah7b |
G |
A |
1: 46,280,152 (GRCm39) |
V2694I |
probably benign |
Het |
Dnhd1 |
T |
A |
7: 105,300,831 (GRCm39) |
F63I |
probably benign |
Het |
Edc4 |
C |
A |
8: 106,617,424 (GRCm39) |
A1052E |
possibly damaging |
Het |
Eif2s2 |
T |
A |
2: 154,726,278 (GRCm39) |
K129M |
probably damaging |
Het |
Emx2 |
A |
G |
19: 59,452,460 (GRCm39) |
D248G |
probably damaging |
Het |
Erich6b |
T |
C |
14: 75,896,449 (GRCm39) |
|
probably benign |
Het |
Exoc3l4 |
A |
G |
12: 111,394,400 (GRCm39) |
K507E |
probably benign |
Het |
Fanci |
T |
A |
7: 79,055,953 (GRCm39) |
V195E |
probably damaging |
Het |
Fgfr2 |
T |
G |
7: 129,828,969 (GRCm39) |
|
probably benign |
Het |
Frem1 |
A |
G |
4: 82,890,402 (GRCm39) |
S1007P |
probably damaging |
Het |
Fry |
T |
C |
5: 150,419,817 (GRCm39) |
I993T |
possibly damaging |
Het |
Fst |
A |
G |
13: 114,591,038 (GRCm39) |
S244P |
possibly damaging |
Het |
Gcc1 |
T |
C |
6: 28,421,009 (GRCm39) |
T103A |
probably damaging |
Het |
Gdf2 |
C |
T |
14: 33,663,178 (GRCm39) |
P24L |
probably damaging |
Het |
Gja3 |
T |
C |
14: 57,274,219 (GRCm39) |
D51G |
possibly damaging |
Het |
Gm10305 |
A |
G |
4: 99,161,313 (GRCm39) |
D74G |
unknown |
Het |
Gm12689 |
G |
T |
4: 99,184,258 (GRCm39) |
G37V |
unknown |
Het |
Gm5424 |
C |
T |
10: 61,907,313 (GRCm39) |
|
noncoding transcript |
Het |
Hephl1 |
T |
C |
9: 14,995,820 (GRCm39) |
E434G |
probably benign |
Het |
Hoatz |
T |
A |
9: 51,013,253 (GRCm39) |
R6S |
probably benign |
Het |
Htatip2 |
T |
C |
7: 49,423,059 (GRCm39) |
C205R |
possibly damaging |
Het |
Igf2r |
T |
C |
17: 12,936,161 (GRCm39) |
|
probably null |
Het |
Ints2 |
T |
C |
11: 86,124,022 (GRCm39) |
I589V |
probably benign |
Het |
Itgae |
T |
A |
11: 73,005,733 (GRCm39) |
V299D |
probably damaging |
Het |
Kcnma1 |
T |
C |
14: 23,559,852 (GRCm39) |
|
probably benign |
Het |
Kif11 |
A |
G |
19: 37,401,565 (GRCm39) |
|
probably benign |
Het |
Kif13a |
A |
G |
13: 46,932,364 (GRCm39) |
|
probably benign |
Het |
Kif18a |
T |
A |
2: 109,128,667 (GRCm39) |
|
probably benign |
Het |
Klhl29 |
T |
C |
12: 5,144,883 (GRCm39) |
T406A |
probably benign |
Het |
Litaf |
A |
T |
16: 10,784,276 (GRCm39) |
|
probably benign |
Het |
Lmntd1 |
T |
A |
6: 145,375,726 (GRCm39) |
I71F |
probably benign |
Het |
Lrit3 |
A |
C |
3: 129,582,204 (GRCm39) |
C594W |
probably damaging |
Het |
Lrp6 |
T |
A |
6: 134,456,738 (GRCm39) |
Q842L |
possibly damaging |
Het |
Lrrcc1 |
T |
A |
3: 14,605,179 (GRCm39) |
|
probably benign |
Het |
Macf1 |
A |
T |
4: 123,349,317 (GRCm39) |
L1829* |
probably null |
Het |
Mapk1ip1 |
T |
C |
7: 138,437,684 (GRCm39) |
T249A |
possibly damaging |
Het |
Mfap4 |
T |
C |
11: 61,378,006 (GRCm39) |
F173L |
probably damaging |
Het |
Mfsd9 |
C |
A |
1: 40,829,634 (GRCm39) |
|
probably benign |
Het |
Mgat4b |
T |
C |
11: 50,121,590 (GRCm39) |
S69P |
probably damaging |
Het |
Mki67 |
A |
T |
7: 135,306,117 (GRCm39) |
V620D |
probably damaging |
Het |
Moxd1 |
C |
T |
10: 24,128,852 (GRCm39) |
T201I |
probably damaging |
Het |
Msh4 |
G |
C |
3: 153,572,057 (GRCm39) |
D774E |
probably benign |
Het |
Myg1 |
C |
T |
15: 102,240,284 (GRCm39) |
R37C |
probably benign |
Het |
Myrf |
C |
A |
19: 10,206,246 (GRCm39) |
A57S |
probably benign |
Het |
Ndst1 |
G |
A |
18: 60,833,431 (GRCm39) |
|
probably benign |
Het |
Nedd4l |
A |
T |
18: 65,341,574 (GRCm39) |
|
probably benign |
Het |
Neil2 |
T |
A |
14: 63,420,849 (GRCm39) |
I281F |
possibly damaging |
Het |
Nfatc2 |
T |
A |
2: 168,432,035 (GRCm39) |
D26V |
probably benign |
Het |
Nt5c |
A |
G |
11: 115,381,540 (GRCm39) |
|
probably null |
Het |
Or13a24 |
T |
G |
7: 140,154,420 (GRCm39) |
M118R |
probably damaging |
Het |
Or2w1b |
G |
T |
13: 21,300,078 (GRCm39) |
C72F |
probably damaging |
Het |
Or2z8 |
T |
A |
8: 72,812,166 (GRCm39) |
I214N |
probably damaging |
Het |
Or5ac20 |
A |
G |
16: 59,104,570 (GRCm39) |
C97R |
possibly damaging |
Het |
Or5t15 |
T |
C |
2: 86,681,311 (GRCm39) |
T244A |
probably benign |
Het |
Ovch2 |
A |
G |
7: 107,381,228 (GRCm39) |
S557P |
probably benign |
Het |
Pik3cg |
A |
G |
12: 32,255,202 (GRCm39) |
S262P |
probably benign |
Het |
Pla2g6 |
T |
A |
15: 79,190,596 (GRCm39) |
H322L |
probably damaging |
Het |
Plch1 |
A |
T |
3: 63,606,640 (GRCm39) |
L1079Q |
probably benign |
Het |
Plekhg4 |
T |
A |
8: 106,105,934 (GRCm39) |
V777D |
probably damaging |
Het |
Plekhg5 |
A |
G |
4: 152,196,876 (GRCm39) |
D747G |
possibly damaging |
Het |
Poln |
C |
A |
5: 34,276,302 (GRCm39) |
V318F |
possibly damaging |
Het |
Pou5f2 |
T |
A |
13: 78,173,873 (GRCm39) |
S272T |
probably benign |
Het |
Ppp1r3e |
T |
G |
14: 55,114,073 (GRCm39) |
S200R |
possibly damaging |
Het |
Prl7d1 |
G |
A |
13: 27,894,165 (GRCm39) |
P135S |
probably benign |
Het |
Ptgs2 |
G |
A |
1: 149,980,288 (GRCm39) |
V409I |
probably benign |
Het |
Ptk2b |
T |
C |
14: 66,415,200 (GRCm39) |
T276A |
probably damaging |
Het |
Ptpn3 |
T |
C |
4: 57,204,921 (GRCm39) |
T747A |
probably damaging |
Het |
Qrfpr |
A |
G |
3: 36,276,138 (GRCm39) |
I84T |
probably damaging |
Het |
Rab44 |
A |
G |
17: 29,358,118 (GRCm39) |
D102G |
possibly damaging |
Het |
Rimoc1 |
A |
G |
15: 4,015,971 (GRCm39) |
|
probably benign |
Het |
Rnf125 |
A |
T |
18: 21,112,140 (GRCm39) |
D57V |
possibly damaging |
Het |
Rnf145 |
T |
C |
11: 44,450,851 (GRCm39) |
F392L |
probably damaging |
Het |
Rttn |
A |
G |
18: 89,007,670 (GRCm39) |
N435S |
probably benign |
Het |
Scn8a |
A |
G |
15: 100,933,418 (GRCm39) |
T1500A |
probably damaging |
Het |
Sgsm1 |
A |
G |
5: 113,432,989 (GRCm39) |
|
probably benign |
Het |
Sgsm3 |
A |
T |
15: 80,895,937 (GRCm39) |
*751C |
probably null |
Het |
Slc35c2 |
A |
C |
2: 165,122,849 (GRCm39) |
L145R |
probably damaging |
Het |
Slc4a7 |
A |
T |
14: 14,757,382 (GRCm38) |
E396V |
probably damaging |
Het |
Smarca4 |
G |
C |
9: 21,570,280 (GRCm39) |
|
probably benign |
Het |
Snapc3 |
T |
A |
4: 83,336,039 (GRCm39) |
V17D |
probably damaging |
Het |
Snta1 |
G |
T |
2: 154,218,992 (GRCm39) |
Q448K |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,790,014 (GRCm39) |
D1334G |
probably benign |
Het |
Stard5 |
A |
G |
7: 83,281,965 (GRCm39) |
R41G |
probably damaging |
Het |
Stxbp5 |
T |
A |
10: 9,660,102 (GRCm39) |
N731I |
probably benign |
Het |
Tmem38a |
G |
A |
8: 73,333,862 (GRCm39) |
V114I |
probably benign |
Het |
Tpr |
A |
G |
1: 150,298,282 (GRCm39) |
T1057A |
probably damaging |
Het |
Ttc23l |
A |
T |
15: 10,540,066 (GRCm39) |
L139Q |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,585,640 (GRCm39) |
|
probably null |
Het |
Tuba3b |
A |
G |
6: 145,565,302 (GRCm39) |
T257A |
probably damaging |
Het |
Tubgcp6 |
A |
C |
15: 88,985,190 (GRCm39) |
Y1633D |
probably damaging |
Het |
Txnl1 |
C |
T |
18: 63,804,644 (GRCm39) |
|
probably benign |
Het |
Unc13b |
A |
G |
4: 43,182,849 (GRCm39) |
Q3186R |
possibly damaging |
Het |
Vmn2r75 |
T |
A |
7: 85,812,478 (GRCm39) |
S514C |
probably null |
Het |
Whrn |
G |
A |
4: 63,337,726 (GRCm39) |
T545I |
probably damaging |
Het |
Zdhhc20 |
T |
C |
14: 58,095,097 (GRCm39) |
H154R |
probably damaging |
Het |
Zfp462 |
A |
T |
4: 55,007,563 (GRCm39) |
M1L |
possibly damaging |
Het |
Zfp831 |
A |
G |
2: 174,487,083 (GRCm39) |
K586R |
possibly damaging |
Het |
Zfp990 |
A |
T |
4: 145,263,872 (GRCm39) |
H290L |
possibly damaging |
Het |
Zfpm1 |
C |
T |
8: 123,063,613 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Tmem135 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01459:Tmem135
|
APN |
7 |
88,800,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Tmem135
|
APN |
7 |
88,797,252 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01933:Tmem135
|
APN |
7 |
88,793,065 (GRCm39) |
unclassified |
probably benign |
|
IGL02177:Tmem135
|
APN |
7 |
88,987,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02305:Tmem135
|
APN |
7 |
88,814,331 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02747:Tmem135
|
APN |
7 |
88,793,878 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02801:Tmem135
|
APN |
7 |
88,803,333 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03353:Tmem135
|
APN |
7 |
88,791,161 (GRCm39) |
missense |
probably damaging |
1.00 |
Skim
|
UTSW |
7 |
88,845,335 (GRCm39) |
nonsense |
probably null |
|
R0657:Tmem135
|
UTSW |
7 |
88,793,890 (GRCm39) |
missense |
probably damaging |
0.96 |
R2233:Tmem135
|
UTSW |
7 |
88,803,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R3118:Tmem135
|
UTSW |
7 |
88,797,005 (GRCm39) |
missense |
probably benign |
0.02 |
R3119:Tmem135
|
UTSW |
7 |
88,797,005 (GRCm39) |
missense |
probably benign |
0.02 |
R5094:Tmem135
|
UTSW |
7 |
88,793,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R5225:Tmem135
|
UTSW |
7 |
88,845,335 (GRCm39) |
nonsense |
probably null |
|
R5248:Tmem135
|
UTSW |
7 |
88,797,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Tmem135
|
UTSW |
7 |
88,954,723 (GRCm39) |
missense |
probably benign |
0.06 |
R5372:Tmem135
|
UTSW |
7 |
88,814,382 (GRCm39) |
splice site |
probably null |
|
R5442:Tmem135
|
UTSW |
7 |
88,793,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R5789:Tmem135
|
UTSW |
7 |
88,845,330 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5863:Tmem135
|
UTSW |
7 |
88,797,176 (GRCm39) |
critical splice donor site |
probably null |
|
R6158:Tmem135
|
UTSW |
7 |
88,805,652 (GRCm39) |
missense |
probably benign |
0.12 |
R6383:Tmem135
|
UTSW |
7 |
88,793,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R6416:Tmem135
|
UTSW |
7 |
88,797,002 (GRCm39) |
missense |
probably benign |
|
R6659:Tmem135
|
UTSW |
7 |
88,956,372 (GRCm39) |
nonsense |
probably null |
|
R6659:Tmem135
|
UTSW |
7 |
88,956,371 (GRCm39) |
missense |
probably benign |
0.07 |
R6731:Tmem135
|
UTSW |
7 |
88,893,172 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7545:Tmem135
|
UTSW |
7 |
88,954,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R7626:Tmem135
|
UTSW |
7 |
88,805,718 (GRCm39) |
splice site |
probably null |
|
R8089:Tmem135
|
UTSW |
7 |
88,805,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R8447:Tmem135
|
UTSW |
7 |
88,803,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Tmem135
|
UTSW |
7 |
88,808,170 (GRCm39) |
missense |
probably benign |
0.00 |
R8750:Tmem135
|
UTSW |
7 |
88,956,456 (GRCm39) |
missense |
probably damaging |
0.99 |
R8758:Tmem135
|
UTSW |
7 |
88,954,721 (GRCm39) |
missense |
probably benign |
0.04 |
R8806:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R8807:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R8808:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R8835:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R8836:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R9093:Tmem135
|
UTSW |
7 |
88,797,204 (GRCm39) |
missense |
probably benign |
0.02 |
R9120:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R9122:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R9308:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R9649:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
R9650:Tmem135
|
UTSW |
7 |
88,797,186 (GRCm39) |
missense |
probably benign |
0.25 |
|