Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410004B18Rik |
T |
A |
3: 145,644,018 (GRCm39) |
F69I |
possibly damaging |
Het |
Acot12 |
C |
T |
13: 91,932,882 (GRCm39) |
L552F |
probably benign |
Het |
Aff4 |
T |
A |
11: 53,301,726 (GRCm39) |
|
probably benign |
Het |
Aldh18a1 |
A |
G |
19: 40,539,725 (GRCm39) |
V750A |
probably damaging |
Het |
Anapc1 |
A |
G |
2: 128,469,149 (GRCm39) |
|
probably benign |
Het |
Arl6ip1 |
AAAATAAATAAATAAATAAATAAATA |
AAAATAAATAAATAAATAAATAAATAAATA |
7: 117,721,122 (GRCm39) |
|
probably benign |
Het |
Bcl11b |
A |
T |
12: 107,883,684 (GRCm39) |
|
probably null |
Het |
Ccpg1 |
C |
A |
9: 72,919,449 (GRCm39) |
Q355K |
probably benign |
Het |
Cdc42bpb |
G |
A |
12: 111,260,573 (GRCm39) |
P1702S |
probably benign |
Het |
Ddx20 |
G |
T |
3: 105,586,249 (GRCm39) |
Q699K |
probably benign |
Het |
Ecd |
A |
G |
14: 20,374,632 (GRCm39) |
S503P |
probably damaging |
Het |
Etaa1 |
C |
T |
11: 17,890,281 (GRCm39) |
R860Q |
probably damaging |
Het |
Ffar2 |
T |
A |
7: 30,519,093 (GRCm39) |
Y149F |
probably damaging |
Het |
Gamt |
T |
A |
10: 80,096,558 (GRCm39) |
R60* |
probably null |
Het |
Gm6871 |
T |
C |
7: 41,195,510 (GRCm39) |
N302S |
probably damaging |
Het |
Hps3 |
A |
G |
3: 20,083,393 (GRCm39) |
S135P |
probably damaging |
Het |
Ifi203 |
T |
A |
1: 173,764,106 (GRCm39) |
N122I |
probably damaging |
Het |
Leng9 |
T |
C |
7: 4,152,433 (GRCm39) |
D81G |
possibly damaging |
Het |
Lrrc23 |
T |
A |
6: 124,747,804 (GRCm39) |
K262* |
probably null |
Het |
Morc2b |
T |
A |
17: 33,357,401 (GRCm39) |
T124S |
probably benign |
Het |
Mroh1 |
G |
A |
15: 76,286,326 (GRCm39) |
|
probably null |
Het |
Naxe |
T |
C |
3: 87,964,011 (GRCm39) |
K240R |
probably benign |
Het |
Ncan |
C |
A |
8: 70,562,727 (GRCm39) |
E510D |
possibly damaging |
Het |
Ndufs4 |
A |
T |
13: 114,444,390 (GRCm39) |
S129R |
probably benign |
Het |
Oog2 |
A |
G |
4: 143,920,523 (GRCm39) |
|
probably benign |
Het |
Or5h18 |
A |
T |
16: 58,847,931 (GRCm39) |
F113Y |
probably damaging |
Het |
Or8h8 |
T |
C |
2: 86,753,222 (GRCm39) |
Y218C |
probably damaging |
Het |
Or8j3c |
C |
A |
2: 86,253,544 (GRCm39) |
V159L |
possibly damaging |
Het |
Papola |
G |
A |
12: 105,767,010 (GRCm39) |
|
probably null |
Het |
Pasd1 |
T |
C |
X: 70,983,161 (GRCm39) |
C378R |
possibly damaging |
Het |
Plec |
A |
G |
15: 76,056,453 (GRCm39) |
S4517P |
probably damaging |
Het |
Rpap1 |
C |
T |
2: 119,604,660 (GRCm39) |
R416H |
probably damaging |
Het |
Rpl31-ps17 |
C |
T |
12: 54,748,397 (GRCm39) |
|
noncoding transcript |
Het |
Rxfp2 |
G |
A |
5: 149,975,020 (GRCm39) |
V210I |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,484,020 (GRCm39) |
D3909G |
probably damaging |
Het |
Spata31d1a |
T |
A |
13: 59,852,861 (GRCm39) |
K76N |
possibly damaging |
Het |
Srgn |
A |
G |
10: 62,333,613 (GRCm39) |
F55L |
possibly damaging |
Het |
Tmem54 |
G |
A |
4: 129,004,504 (GRCm39) |
R151Q |
probably damaging |
Het |
Tns1 |
T |
A |
1: 73,953,790 (GRCm39) |
N1848Y |
probably damaging |
Het |
Trim33 |
G |
T |
3: 103,217,630 (GRCm39) |
V192L |
possibly damaging |
Het |
Trpm5 |
G |
T |
7: 142,642,792 (GRCm39) |
L52I |
probably benign |
Het |
Uaca |
A |
G |
9: 60,779,035 (GRCm39) |
S1141G |
probably benign |
Het |
Vmn1r63 |
T |
C |
7: 5,806,531 (GRCm39) |
T34A |
possibly damaging |
Het |
Vmn2r50 |
T |
C |
7: 9,774,309 (GRCm39) |
K529R |
probably benign |
Het |
Vmn2r9 |
T |
C |
5: 108,995,743 (GRCm39) |
T302A |
possibly damaging |
Het |
Zfp410 |
G |
A |
12: 84,374,206 (GRCm39) |
R181H |
probably damaging |
Het |
|
Other mutations in Ylpm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00539:Ylpm1
|
APN |
12 |
85,075,728 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00809:Ylpm1
|
APN |
12 |
85,095,968 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01508:Ylpm1
|
APN |
12 |
85,062,229 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02199:Ylpm1
|
APN |
12 |
85,080,779 (GRCm39) |
nonsense |
probably null |
|
IGL02392:Ylpm1
|
APN |
12 |
85,061,731 (GRCm39) |
missense |
unknown |
|
IGL02455:Ylpm1
|
APN |
12 |
85,077,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Ylpm1
|
APN |
12 |
85,095,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03102:Ylpm1
|
APN |
12 |
85,096,032 (GRCm39) |
splice site |
probably benign |
|
I1329:Ylpm1
|
UTSW |
12 |
85,087,654 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Ylpm1
|
UTSW |
12 |
85,091,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Ylpm1
|
UTSW |
12 |
85,075,800 (GRCm39) |
missense |
probably damaging |
0.97 |
R0090:Ylpm1
|
UTSW |
12 |
85,075,814 (GRCm39) |
intron |
probably benign |
|
R0149:Ylpm1
|
UTSW |
12 |
85,075,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R0226:Ylpm1
|
UTSW |
12 |
85,096,511 (GRCm39) |
missense |
probably benign |
0.21 |
R0375:Ylpm1
|
UTSW |
12 |
85,061,754 (GRCm39) |
missense |
unknown |
|
R0378:Ylpm1
|
UTSW |
12 |
85,043,850 (GRCm39) |
intron |
probably benign |
|
R0507:Ylpm1
|
UTSW |
12 |
85,075,886 (GRCm39) |
missense |
probably benign |
0.03 |
R0742:Ylpm1
|
UTSW |
12 |
85,075,886 (GRCm39) |
missense |
probably benign |
0.03 |
R1350:Ylpm1
|
UTSW |
12 |
85,060,856 (GRCm39) |
unclassified |
probably benign |
|
R1452:Ylpm1
|
UTSW |
12 |
85,077,157 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1500:Ylpm1
|
UTSW |
12 |
85,061,770 (GRCm39) |
missense |
unknown |
|
R1837:Ylpm1
|
UTSW |
12 |
85,076,107 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1945:Ylpm1
|
UTSW |
12 |
85,062,192 (GRCm39) |
missense |
probably damaging |
0.98 |
R1971:Ylpm1
|
UTSW |
12 |
85,087,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Ylpm1
|
UTSW |
12 |
85,091,152 (GRCm39) |
nonsense |
probably null |
|
R2213:Ylpm1
|
UTSW |
12 |
85,116,492 (GRCm39) |
missense |
probably benign |
0.25 |
R2269:Ylpm1
|
UTSW |
12 |
85,061,824 (GRCm39) |
missense |
unknown |
|
R2300:Ylpm1
|
UTSW |
12 |
85,107,093 (GRCm39) |
splice site |
probably null |
|
R2439:Ylpm1
|
UTSW |
12 |
85,060,891 (GRCm39) |
unclassified |
probably benign |
|
R2497:Ylpm1
|
UTSW |
12 |
85,043,535 (GRCm39) |
missense |
probably damaging |
0.98 |
R2890:Ylpm1
|
UTSW |
12 |
85,076,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R3111:Ylpm1
|
UTSW |
12 |
85,076,145 (GRCm39) |
missense |
probably damaging |
0.98 |
R3436:Ylpm1
|
UTSW |
12 |
85,096,644 (GRCm39) |
critical splice donor site |
probably null |
|
R3437:Ylpm1
|
UTSW |
12 |
85,096,644 (GRCm39) |
critical splice donor site |
probably null |
|
R4157:Ylpm1
|
UTSW |
12 |
85,104,177 (GRCm39) |
intron |
probably benign |
|
R4959:Ylpm1
|
UTSW |
12 |
85,096,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Ylpm1
|
UTSW |
12 |
85,061,523 (GRCm39) |
missense |
unknown |
|
R5039:Ylpm1
|
UTSW |
12 |
85,089,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Ylpm1
|
UTSW |
12 |
85,062,267 (GRCm39) |
missense |
probably damaging |
0.98 |
R5084:Ylpm1
|
UTSW |
12 |
85,076,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R5325:Ylpm1
|
UTSW |
12 |
85,060,735 (GRCm39) |
unclassified |
probably benign |
|
R5378:Ylpm1
|
UTSW |
12 |
85,077,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R5428:Ylpm1
|
UTSW |
12 |
85,077,003 (GRCm39) |
missense |
probably benign |
0.04 |
R5467:Ylpm1
|
UTSW |
12 |
85,043,633 (GRCm39) |
missense |
unknown |
|
R5605:Ylpm1
|
UTSW |
12 |
85,075,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R5614:Ylpm1
|
UTSW |
12 |
85,111,718 (GRCm39) |
intron |
probably benign |
|
R5748:Ylpm1
|
UTSW |
12 |
85,107,025 (GRCm39) |
splice site |
probably null |
|
R5860:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5861:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5881:Ylpm1
|
UTSW |
12 |
85,088,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6000:Ylpm1
|
UTSW |
12 |
85,044,030 (GRCm39) |
missense |
unknown |
|
R6004:Ylpm1
|
UTSW |
12 |
85,075,858 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6007:Ylpm1
|
UTSW |
12 |
85,076,064 (GRCm39) |
missense |
probably benign |
0.33 |
R6053:Ylpm1
|
UTSW |
12 |
85,043,277 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6104:Ylpm1
|
UTSW |
12 |
85,076,404 (GRCm39) |
missense |
probably benign |
0.00 |
R6197:Ylpm1
|
UTSW |
12 |
85,088,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
R6297:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
R6305:Ylpm1
|
UTSW |
12 |
85,077,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R6379:Ylpm1
|
UTSW |
12 |
85,077,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R6465:Ylpm1
|
UTSW |
12 |
85,096,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R6608:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
R6609:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
R6737:Ylpm1
|
UTSW |
12 |
85,077,620 (GRCm39) |
missense |
probably damaging |
0.98 |
R6794:Ylpm1
|
UTSW |
12 |
85,043,655 (GRCm39) |
missense |
unknown |
|
R7383:Ylpm1
|
UTSW |
12 |
85,091,242 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7514:Ylpm1
|
UTSW |
12 |
85,077,268 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7577:Ylpm1
|
UTSW |
12 |
85,043,994 (GRCm39) |
missense |
unknown |
|
R7709:Ylpm1
|
UTSW |
12 |
85,059,799 (GRCm39) |
missense |
unknown |
|
R7718:Ylpm1
|
UTSW |
12 |
85,075,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R7736:Ylpm1
|
UTSW |
12 |
85,059,757 (GRCm39) |
missense |
unknown |
|
R7758:Ylpm1
|
UTSW |
12 |
85,061,796 (GRCm39) |
missense |
unknown |
|
R7807:Ylpm1
|
UTSW |
12 |
85,060,855 (GRCm39) |
nonsense |
probably null |
|
R7838:Ylpm1
|
UTSW |
12 |
85,095,640 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7846:Ylpm1
|
UTSW |
12 |
85,104,042 (GRCm39) |
missense |
probably damaging |
0.98 |
R8170:Ylpm1
|
UTSW |
12 |
85,080,801 (GRCm39) |
missense |
probably benign |
0.40 |
R8776:Ylpm1
|
UTSW |
12 |
85,077,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R8776-TAIL:Ylpm1
|
UTSW |
12 |
85,077,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R8812:Ylpm1
|
UTSW |
12 |
85,043,566 (GRCm39) |
missense |
unknown |
|
R8847:Ylpm1
|
UTSW |
12 |
85,061,672 (GRCm39) |
missense |
unknown |
|
R8874:Ylpm1
|
UTSW |
12 |
85,116,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R9129:Ylpm1
|
UTSW |
12 |
85,104,052 (GRCm39) |
missense |
|
|
R9165:Ylpm1
|
UTSW |
12 |
85,077,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R9198:Ylpm1
|
UTSW |
12 |
85,080,689 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9564:Ylpm1
|
UTSW |
12 |
85,091,176 (GRCm39) |
missense |
probably benign |
0.30 |
R9629:Ylpm1
|
UTSW |
12 |
85,044,036 (GRCm39) |
missense |
unknown |
|
R9797:Ylpm1
|
UTSW |
12 |
85,077,109 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1088:Ylpm1
|
UTSW |
12 |
85,076,929 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1176:Ylpm1
|
UTSW |
12 |
85,077,058 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Ylpm1
|
UTSW |
12 |
85,104,057 (GRCm39) |
missense |
probably damaging |
0.98 |
|