Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Abhd6 |
T |
C |
14: 8,028,329 (GRCm38) |
I20T |
possibly damaging |
Het |
Adamts1 |
A |
G |
16: 85,599,505 (GRCm39) |
S32P |
probably benign |
Het |
Ak7 |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
12: 105,676,448 (GRCm39) |
|
probably benign |
Het |
Arhgap21 |
A |
T |
2: 20,886,397 (GRCm39) |
V270E |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,916,064 (GRCm39) |
L1660Q |
probably benign |
Het |
Blvrb |
A |
G |
7: 27,158,786 (GRCm39) |
D62G |
probably benign |
Het |
Ccdc68 |
T |
A |
18: 70,089,113 (GRCm39) |
S219T |
probably damaging |
Het |
Cnbp |
A |
G |
6: 87,822,108 (GRCm39) |
Y139H |
probably damaging |
Het |
Csmd3 |
T |
A |
15: 48,655,356 (GRCm39) |
|
probably benign |
Het |
Cyp2c66 |
T |
C |
19: 39,172,246 (GRCm39) |
V387A |
probably damaging |
Het |
Cyp2j7 |
C |
T |
4: 96,115,840 (GRCm39) |
R202H |
probably damaging |
Het |
Edrf1 |
A |
G |
7: 133,240,742 (GRCm39) |
D73G |
probably damaging |
Het |
Ercc6 |
C |
T |
14: 32,284,525 (GRCm39) |
R763C |
probably damaging |
Het |
Gm8159 |
T |
A |
14: 15,850,264 (GRCm39) |
I161K |
probably damaging |
Het |
Gramd1c |
A |
T |
16: 43,807,294 (GRCm39) |
M356K |
probably damaging |
Het |
Has2 |
T |
C |
15: 56,531,090 (GRCm39) |
K542E |
probably benign |
Het |
Hipk3 |
T |
C |
2: 104,301,850 (GRCm39) |
N114S |
probably benign |
Het |
Hs3st6 |
T |
C |
17: 24,977,228 (GRCm39) |
L236P |
probably damaging |
Het |
Il15 |
T |
A |
8: 83,061,177 (GRCm39) |
H100L |
probably benign |
Het |
Kcnh5 |
T |
C |
12: 75,023,334 (GRCm39) |
Y578C |
probably benign |
Het |
Lctl |
A |
G |
9: 64,025,049 (GRCm39) |
I12V |
probably benign |
Het |
Mark2 |
G |
T |
19: 7,263,263 (GRCm39) |
T201N |
possibly damaging |
Het |
Mef2c |
A |
G |
13: 83,810,461 (GRCm39) |
N371S |
probably benign |
Het |
Mgst3 |
T |
C |
1: 167,205,871 (GRCm39) |
Y36C |
probably damaging |
Het |
Ndst1 |
G |
T |
18: 60,845,931 (GRCm39) |
T126K |
probably damaging |
Het |
Nid1 |
T |
A |
13: 13,677,045 (GRCm39) |
I995N |
probably damaging |
Het |
Nr2e1 |
A |
T |
10: 42,447,487 (GRCm39) |
M175K |
probably benign |
Het |
Nrxn1 |
T |
C |
17: 90,937,450 (GRCm39) |
K669R |
probably damaging |
Het |
Or5d14 |
C |
T |
2: 87,880,509 (GRCm39) |
W153* |
probably null |
Het |
Or6k4 |
A |
T |
1: 173,964,885 (GRCm39) |
T192S |
probably benign |
Het |
Pbx1 |
T |
C |
1: 168,258,910 (GRCm39) |
D55G |
possibly damaging |
Het |
Pck2 |
T |
A |
14: 55,780,081 (GRCm39) |
I110N |
probably damaging |
Het |
Pkn2 |
T |
C |
3: 142,499,594 (GRCm39) |
D977G |
probably damaging |
Het |
Pyroxd2 |
A |
G |
19: 42,719,756 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
A |
G |
2: 72,008,561 (GRCm39) |
I246M |
probably benign |
Het |
Rnasel |
T |
A |
1: 153,630,673 (GRCm39) |
N396K |
possibly damaging |
Het |
Scaf1 |
A |
G |
7: 44,658,351 (GRCm39) |
L176P |
probably damaging |
Het |
Scgb1b12 |
C |
A |
7: 32,033,974 (GRCm39) |
A78E |
probably benign |
Het |
Scgb2b19 |
A |
G |
7: 32,979,198 (GRCm39) |
F28S |
probably damaging |
Het |
Skint5 |
C |
T |
4: 113,798,052 (GRCm39) |
C177Y |
possibly damaging |
Het |
Slitrk5 |
C |
T |
14: 111,916,496 (GRCm39) |
T40I |
probably benign |
Het |
Slu7 |
G |
A |
11: 43,329,095 (GRCm39) |
V106I |
probably benign |
Het |
Sorbs1 |
G |
A |
19: 40,361,923 (GRCm39) |
R154* |
probably null |
Het |
Stc2 |
A |
G |
11: 31,310,332 (GRCm39) |
S235P |
probably benign |
Het |
Stt3a |
T |
C |
9: 36,645,675 (GRCm39) |
D672G |
probably benign |
Het |
Tcerg1l |
T |
C |
7: 137,995,998 (GRCm39) |
D170G |
possibly damaging |
Het |
Tcf15 |
T |
C |
2: 151,986,039 (GRCm39) |
L165P |
probably damaging |
Het |
Tgm1 |
T |
C |
14: 55,950,933 (GRCm39) |
|
probably benign |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmco4 |
G |
A |
4: 138,779,895 (GRCm39) |
V447M |
probably damaging |
Het |
Trf |
C |
T |
9: 103,099,283 (GRCm39) |
V339I |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,717,282 (GRCm39) |
D2946G |
possibly damaging |
Het |
Vmn1r82 |
A |
G |
7: 12,039,600 (GRCm39) |
N291S |
possibly damaging |
Het |
Vmn1r86 |
A |
T |
7: 12,836,781 (GRCm39) |
Y32N |
possibly damaging |
Het |
Wdr49 |
T |
C |
3: 75,230,931 (GRCm39) |
D577G |
probably benign |
Het |
Wnt10b |
C |
A |
15: 98,670,713 (GRCm39) |
G272W |
probably damaging |
Het |
Yipf4 |
T |
C |
17: 74,806,024 (GRCm39) |
F221S |
probably damaging |
Het |
Zfp512 |
G |
A |
5: 31,623,676 (GRCm39) |
C14Y |
probably benign |
Het |
Zfp658 |
G |
T |
7: 43,222,567 (GRCm39) |
V281F |
probably benign |
Het |
Zfp827 |
T |
G |
8: 79,787,403 (GRCm39) |
W190G |
probably damaging |
Het |
Zpld2 |
G |
A |
4: 133,929,312 (GRCm39) |
P331L |
probably benign |
Het |
|
Other mutations in Ucp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4585001:Ucp1
|
UTSW |
8 |
84,020,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Ucp1
|
UTSW |
8 |
84,020,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Ucp1
|
UTSW |
8 |
84,017,233 (GRCm39) |
nonsense |
probably null |
|
R0055:Ucp1
|
UTSW |
8 |
84,017,233 (GRCm39) |
nonsense |
probably null |
|
R0505:Ucp1
|
UTSW |
8 |
84,021,936 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0590:Ucp1
|
UTSW |
8 |
84,018,232 (GRCm39) |
splice site |
probably benign |
|
R0681:Ucp1
|
UTSW |
8 |
84,021,936 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0731:Ucp1
|
UTSW |
8 |
84,024,476 (GRCm39) |
splice site |
probably benign |
|
R1606:Ucp1
|
UTSW |
8 |
84,021,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R1722:Ucp1
|
UTSW |
8 |
84,017,317 (GRCm39) |
missense |
probably benign |
0.25 |
R1809:Ucp1
|
UTSW |
8 |
84,024,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R1823:Ucp1
|
UTSW |
8 |
84,020,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Ucp1
|
UTSW |
8 |
84,017,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R4085:Ucp1
|
UTSW |
8 |
84,020,580 (GRCm39) |
missense |
probably benign |
0.43 |
R4673:Ucp1
|
UTSW |
8 |
84,021,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R4998:Ucp1
|
UTSW |
8 |
84,024,484 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5163:Ucp1
|
UTSW |
8 |
84,020,832 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5421:Ucp1
|
UTSW |
8 |
84,017,320 (GRCm39) |
missense |
probably benign |
0.12 |
R5790:Ucp1
|
UTSW |
8 |
84,024,520 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5994:Ucp1
|
UTSW |
8 |
84,020,567 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6574:Ucp1
|
UTSW |
8 |
84,020,718 (GRCm39) |
critical splice donor site |
probably null |
|
R6732:Ucp1
|
UTSW |
8 |
84,018,106 (GRCm39) |
missense |
probably benign |
0.08 |
R7282:Ucp1
|
UTSW |
8 |
84,020,531 (GRCm39) |
missense |
probably benign |
0.03 |
R7343:Ucp1
|
UTSW |
8 |
84,021,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R7878:Ucp1
|
UTSW |
8 |
84,024,521 (GRCm39) |
missense |
probably benign |
0.19 |
R8008:Ucp1
|
UTSW |
8 |
84,020,640 (GRCm39) |
missense |
probably benign |
0.32 |
R8365:Ucp1
|
UTSW |
8 |
84,020,628 (GRCm39) |
missense |
probably damaging |
0.97 |
R8899:Ucp1
|
UTSW |
8 |
84,017,216 (GRCm39) |
missense |
probably benign |
0.35 |
R9186:Ucp1
|
UTSW |
8 |
84,017,272 (GRCm39) |
nonsense |
probably null |
|
R9499:Ucp1
|
UTSW |
8 |
84,024,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9551:Ucp1
|
UTSW |
8 |
84,024,509 (GRCm39) |
missense |
probably damaging |
1.00 |
|