Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J11Rik |
A |
T |
9: 39,961,994 (GRCm39) |
|
noncoding transcript |
Het |
Adcy1 |
G |
A |
11: 7,080,369 (GRCm39) |
V371M |
probably damaging |
Het |
Adgrb2 |
C |
T |
4: 129,902,146 (GRCm39) |
A509V |
probably benign |
Het |
Adgrg6 |
T |
A |
10: 14,312,525 (GRCm39) |
Q754L |
probably damaging |
Het |
Agap2 |
T |
C |
10: 126,927,082 (GRCm39) |
I1008T |
probably damaging |
Het |
Aph1c |
T |
G |
9: 66,735,051 (GRCm39) |
H150P |
probably damaging |
Het |
Atcay |
T |
C |
10: 81,048,361 (GRCm39) |
R242G |
possibly damaging |
Het |
Atg2a |
G |
A |
19: 6,308,985 (GRCm39) |
V1724M |
probably damaging |
Het |
Bbs12 |
T |
C |
3: 37,373,369 (GRCm39) |
V54A |
possibly damaging |
Het |
Card14 |
A |
G |
11: 119,224,784 (GRCm39) |
M604V |
possibly damaging |
Het |
Cd28 |
A |
T |
1: 60,802,393 (GRCm39) |
H104L |
probably benign |
Het |
Cntn5 |
A |
T |
9: 10,048,776 (GRCm39) |
D262E |
probably damaging |
Het |
Col6a3 |
A |
G |
1: 90,749,736 (GRCm39) |
V366A |
probably benign |
Het |
Csnk1d |
G |
A |
11: 120,855,800 (GRCm39) |
|
probably benign |
Het |
Dcaf11 |
T |
A |
14: 55,803,063 (GRCm39) |
|
probably benign |
Het |
Dpy19l4 |
G |
A |
4: 11,304,053 (GRCm39) |
T119M |
possibly damaging |
Het |
Eif3f |
T |
C |
7: 108,540,153 (GRCm39) |
V316A |
possibly damaging |
Het |
Fbrsl1 |
G |
A |
5: 110,526,932 (GRCm39) |
|
probably benign |
Het |
Fbxo10 |
C |
T |
4: 45,043,693 (GRCm39) |
R710H |
probably damaging |
Het |
Fbxw9 |
G |
A |
8: 85,786,829 (GRCm39) |
D25N |
probably damaging |
Het |
Gm14295 |
C |
T |
2: 176,501,386 (GRCm39) |
T292I |
possibly damaging |
Het |
Gm4884 |
C |
G |
7: 40,692,687 (GRCm39) |
Q219E |
probably benign |
Het |
Gpr150 |
A |
G |
13: 76,204,273 (GRCm39) |
V224A |
probably benign |
Het |
Hps1 |
A |
T |
19: 42,750,935 (GRCm39) |
I355N |
probably damaging |
Het |
Lmbr1l |
A |
G |
15: 98,804,178 (GRCm39) |
S374P |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,289,782 (GRCm39) |
N5458K |
probably damaging |
Het |
Man1b1 |
C |
G |
2: 25,222,867 (GRCm39) |
|
probably benign |
Het |
Morc3 |
A |
G |
16: 93,671,645 (GRCm39) |
|
probably null |
Het |
Mrgpra4 |
T |
C |
7: 47,631,539 (GRCm39) |
T21A |
probably benign |
Het |
Myo1a |
G |
T |
10: 127,546,327 (GRCm39) |
V277L |
probably benign |
Het |
Nkain4 |
C |
G |
2: 180,596,415 (GRCm39) |
M1I |
probably null |
Het |
Nktr |
T |
C |
9: 121,577,962 (GRCm39) |
|
probably benign |
Het |
Nrxn3 |
T |
C |
12: 90,171,515 (GRCm39) |
S276P |
probably damaging |
Het |
Oas2 |
A |
T |
5: 120,879,220 (GRCm39) |
D373E |
possibly damaging |
Het |
Or8g37 |
T |
A |
9: 39,731,870 (GRCm39) |
*312R |
probably null |
Het |
Oser1 |
T |
A |
2: 163,257,500 (GRCm39) |
E11V |
probably null |
Het |
Oser1 |
C |
T |
2: 163,257,501 (GRCm39) |
E11K |
probably damaging |
Het |
Pacsin3 |
A |
G |
2: 91,093,288 (GRCm39) |
|
probably null |
Het |
Pcdh20 |
T |
C |
14: 88,706,434 (GRCm39) |
S289G |
probably benign |
Het |
Phlpp1 |
A |
G |
1: 106,314,176 (GRCm39) |
D1183G |
probably damaging |
Het |
Pign |
T |
C |
1: 105,575,945 (GRCm39) |
K232E |
probably benign |
Het |
Polk |
A |
G |
13: 96,630,413 (GRCm39) |
S383P |
probably damaging |
Het |
Prom2 |
C |
A |
2: 127,382,111 (GRCm39) |
R101L |
probably benign |
Het |
Rest |
T |
C |
5: 77,429,027 (GRCm39) |
V482A |
probably benign |
Het |
Rexo1 |
A |
T |
10: 80,378,492 (GRCm39) |
S476T |
probably damaging |
Het |
Rnf31 |
T |
A |
14: 55,840,777 (GRCm39) |
Y1015N |
probably damaging |
Het |
Spata3 |
T |
C |
1: 85,954,152 (GRCm39) |
Y305H |
probably benign |
Het |
Sv2a |
G |
A |
3: 96,099,810 (GRCm39) |
V587M |
probably benign |
Het |
Synj1 |
A |
G |
16: 90,766,069 (GRCm39) |
|
probably null |
Het |
Syt17 |
A |
G |
7: 118,036,040 (GRCm39) |
|
probably null |
Het |
Taf2 |
T |
C |
15: 54,922,276 (GRCm39) |
D337G |
possibly damaging |
Het |
Tcaf1 |
A |
C |
6: 42,656,248 (GRCm39) |
S243A |
probably benign |
Het |
Tmem9 |
A |
G |
1: 135,955,234 (GRCm39) |
T123A |
probably benign |
Het |
Trav4-4-dv10 |
T |
C |
14: 53,921,187 (GRCm39) |
|
probably benign |
Het |
Trbv15 |
G |
A |
6: 41,118,493 (GRCm39) |
R83Q |
probably damaging |
Het |
Trim27 |
A |
G |
13: 21,374,056 (GRCm39) |
I268V |
probably benign |
Het |
Tubgcp6 |
T |
A |
15: 88,987,857 (GRCm39) |
S1031C |
probably damaging |
Het |
Vmn1r89 |
C |
A |
7: 12,953,799 (GRCm39) |
H110Q |
probably benign |
Het |
Vmn2r30 |
T |
C |
7: 7,320,091 (GRCm39) |
N545S |
probably damaging |
Het |
Wls |
G |
A |
3: 159,603,020 (GRCm39) |
M144I |
probably benign |
Het |
Yme1l1 |
T |
C |
2: 23,076,344 (GRCm39) |
|
probably null |
Het |
Zeb2 |
A |
T |
2: 44,913,023 (GRCm39) |
L56Q |
probably damaging |
Het |
|
Other mutations in Accsl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02336:Accsl
|
APN |
2 |
93,696,253 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02511:Accsl
|
APN |
2 |
93,692,111 (GRCm39) |
unclassified |
probably benign |
|
IGL03248:Accsl
|
APN |
2 |
93,693,129 (GRCm39) |
unclassified |
probably benign |
|
IGL03338:Accsl
|
APN |
2 |
93,686,092 (GRCm39) |
missense |
probably benign |
0.34 |
R0323:Accsl
|
UTSW |
2 |
93,691,425 (GRCm39) |
missense |
probably benign |
0.27 |
R0449:Accsl
|
UTSW |
2 |
93,696,419 (GRCm39) |
missense |
probably benign |
0.00 |
R1172:Accsl
|
UTSW |
2 |
93,696,589 (GRCm39) |
splice site |
probably benign |
|
R1173:Accsl
|
UTSW |
2 |
93,696,589 (GRCm39) |
splice site |
probably benign |
|
R1175:Accsl
|
UTSW |
2 |
93,696,589 (GRCm39) |
splice site |
probably benign |
|
R1752:Accsl
|
UTSW |
2 |
93,688,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1952:Accsl
|
UTSW |
2 |
93,689,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R2877:Accsl
|
UTSW |
2 |
93,689,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R2878:Accsl
|
UTSW |
2 |
93,689,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R4472:Accsl
|
UTSW |
2 |
93,694,337 (GRCm39) |
splice site |
probably null |
|
R5400:Accsl
|
UTSW |
2 |
93,689,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R5502:Accsl
|
UTSW |
2 |
93,687,289 (GRCm39) |
critical splice donor site |
probably null |
|
R5610:Accsl
|
UTSW |
2 |
93,692,118 (GRCm39) |
critical splice donor site |
probably null |
|
R5636:Accsl
|
UTSW |
2 |
93,699,370 (GRCm39) |
missense |
probably benign |
0.41 |
R5799:Accsl
|
UTSW |
2 |
93,694,748 (GRCm39) |
splice site |
probably null |
|
R6376:Accsl
|
UTSW |
2 |
93,687,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Accsl
|
UTSW |
2 |
93,696,488 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7311:Accsl
|
UTSW |
2 |
93,696,160 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7564:Accsl
|
UTSW |
2 |
93,688,501 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7731:Accsl
|
UTSW |
2 |
93,691,363 (GRCm39) |
missense |
probably benign |
0.01 |
R7835:Accsl
|
UTSW |
2 |
93,696,329 (GRCm39) |
nonsense |
probably null |
|
R8184:Accsl
|
UTSW |
2 |
93,686,086 (GRCm39) |
missense |
probably benign |
0.19 |
R8305:Accsl
|
UTSW |
2 |
93,696,423 (GRCm39) |
missense |
probably benign |
0.00 |
R8824:Accsl
|
UTSW |
2 |
93,693,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R8868:Accsl
|
UTSW |
2 |
93,696,490 (GRCm39) |
missense |
probably benign |
0.00 |
R8954:Accsl
|
UTSW |
2 |
93,688,299 (GRCm39) |
missense |
probably benign |
0.06 |
R9172:Accsl
|
UTSW |
2 |
93,691,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9473:Accsl
|
UTSW |
2 |
93,686,092 (GRCm39) |
missense |
probably benign |
0.03 |
R9513:Accsl
|
UTSW |
2 |
93,699,498 (GRCm39) |
unclassified |
probably benign |
|
Z1088:Accsl
|
UTSW |
2 |
93,696,293 (GRCm39) |
missense |
probably benign |
0.00 |
|