Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts8 |
T |
C |
9: 30,873,224 (GRCm39) |
S810P |
probably benign |
Het |
Adcy7 |
A |
T |
8: 89,052,124 (GRCm39) |
I931F |
probably damaging |
Het |
Alcam |
G |
T |
16: 52,111,356 (GRCm39) |
Q248K |
probably benign |
Het |
Astn1 |
A |
C |
1: 158,429,507 (GRCm39) |
R750S |
probably damaging |
Het |
Atp1a2 |
A |
T |
1: 172,114,797 (GRCm39) |
N329K |
probably damaging |
Het |
Bcl6 |
A |
G |
16: 23,791,556 (GRCm39) |
V266A |
probably benign |
Het |
Bdp1 |
A |
G |
13: 100,228,794 (GRCm39) |
V278A |
probably benign |
Het |
Ccdc162 |
T |
C |
10: 41,437,111 (GRCm39) |
E493G |
probably damaging |
Het |
Cpvl |
T |
C |
6: 53,909,413 (GRCm39) |
Y241C |
probably damaging |
Het |
Ddx55 |
T |
C |
5: 124,704,913 (GRCm39) |
M390T |
probably benign |
Het |
Ero1b |
A |
G |
13: 12,594,139 (GRCm39) |
E102G |
probably benign |
Het |
Etnk1 |
A |
G |
6: 143,143,164 (GRCm39) |
D273G |
probably benign |
Het |
Exoc3 |
A |
G |
13: 74,347,643 (GRCm39) |
V109A |
probably damaging |
Het |
F830016B08Rik |
T |
A |
18: 60,433,091 (GRCm39) |
I58N |
probably damaging |
Het |
Fancd2 |
T |
A |
6: 113,538,672 (GRCm39) |
V589E |
probably benign |
Het |
Fbll1 |
G |
A |
11: 35,689,159 (GRCm39) |
R35C |
unknown |
Het |
Fnbp1 |
A |
G |
2: 30,938,211 (GRCm39) |
|
probably null |
Het |
Glce |
G |
T |
9: 61,967,426 (GRCm39) |
A575D |
probably damaging |
Het |
Ift20 |
T |
A |
11: 78,430,867 (GRCm39) |
M70K |
possibly damaging |
Het |
Impg2 |
T |
C |
16: 56,078,499 (GRCm39) |
V487A |
probably damaging |
Het |
Isx |
A |
G |
8: 75,619,426 (GRCm39) |
D206G |
probably benign |
Het |
Jak3 |
A |
G |
8: 72,136,875 (GRCm39) |
I684V |
possibly damaging |
Het |
Kdm5d |
G |
A |
Y: 941,306 (GRCm39) |
S1169N |
probably benign |
Het |
Krt35 |
A |
T |
11: 99,986,639 (GRCm39) |
L125Q |
probably damaging |
Het |
Lama4 |
G |
A |
10: 38,948,855 (GRCm39) |
A873T |
probably benign |
Het |
Lrch4 |
T |
C |
5: 137,632,127 (GRCm39) |
S74P |
possibly damaging |
Het |
Maneal |
A |
T |
4: 124,750,966 (GRCm39) |
Y263* |
probably null |
Het |
Mcat |
C |
T |
15: 83,432,116 (GRCm39) |
A251T |
probably benign |
Het |
Mup3 |
T |
G |
4: 62,004,244 (GRCm39) |
T90P |
probably benign |
Het |
Mybpc2 |
G |
A |
7: 44,156,515 (GRCm39) |
A812V |
probably damaging |
Het |
Naa15 |
T |
C |
3: 51,367,485 (GRCm39) |
F503L |
probably damaging |
Het |
Nudt8 |
T |
C |
19: 4,050,727 (GRCm39) |
L25S |
possibly damaging |
Het |
Oas1e |
A |
T |
5: 120,926,972 (GRCm39) |
V245D |
probably damaging |
Het |
Ofcc1 |
A |
G |
13: 40,417,054 (GRCm39) |
M109T |
possibly damaging |
Het |
Or4c58 |
A |
G |
2: 89,674,735 (GRCm39) |
V194A |
possibly damaging |
Het |
Or4p18 |
A |
T |
2: 88,232,535 (GRCm39) |
F248I |
probably damaging |
Het |
Phkb |
G |
T |
8: 86,748,076 (GRCm39) |
|
probably null |
Het |
Pidd1 |
A |
C |
7: 141,021,183 (GRCm39) |
L365R |
probably damaging |
Het |
Pira12 |
G |
A |
7: 3,900,621 (GRCm39) |
T43I |
probably damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,750,795 (GRCm39) |
R1739C |
probably benign |
Het |
Pkdrej |
A |
T |
15: 85,702,497 (GRCm39) |
D1146E |
possibly damaging |
Het |
Pkhd1l1 |
G |
T |
15: 44,390,159 (GRCm39) |
W1425L |
probably damaging |
Het |
Plxna4 |
A |
G |
6: 32,494,181 (GRCm39) |
L145P |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,945,649 (GRCm39) |
D941E |
probably benign |
Het |
Prdm13 |
G |
T |
4: 21,683,894 (GRCm39) |
Q126K |
unknown |
Het |
Rbm25 |
T |
A |
12: 83,728,362 (GRCm39) |
V837E |
probably damaging |
Het |
Rcc2 |
T |
A |
4: 140,444,379 (GRCm39) |
Y357N |
probably damaging |
Het |
Siglec1 |
A |
T |
2: 130,919,884 (GRCm39) |
N882K |
probably damaging |
Het |
Sox13 |
A |
G |
1: 133,311,627 (GRCm39) |
I535T |
probably benign |
Het |
Srrm2 |
T |
C |
17: 24,040,291 (GRCm39) |
S2408P |
probably benign |
Het |
Stat3 |
G |
A |
11: 100,794,556 (GRCm39) |
T251I |
probably benign |
Het |
Sulf1 |
A |
T |
1: 12,929,039 (GRCm39) |
D102V |
possibly damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,629,912 (GRCm39) |
G252R |
probably benign |
Het |
Tmem145 |
G |
T |
7: 25,007,618 (GRCm39) |
L208F |
possibly damaging |
Het |
Trim17 |
A |
T |
11: 58,859,506 (GRCm39) |
E240V |
probably damaging |
Het |
Trim43b |
A |
T |
9: 88,967,451 (GRCm39) |
I395K |
possibly damaging |
Het |
Trmt61a |
C |
A |
12: 111,647,292 (GRCm39) |
H130N |
probably damaging |
Het |
Unc5b |
A |
C |
10: 60,608,138 (GRCm39) |
L654R |
probably damaging |
Het |
Vmn1r66 |
A |
T |
7: 10,008,269 (GRCm39) |
S255T |
probably benign |
Het |
Zbtb10 |
T |
C |
3: 9,345,109 (GRCm39) |
F677S |
probably benign |
Het |
Zfp493 |
T |
A |
13: 67,934,717 (GRCm39) |
C223* |
probably null |
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 |
|
R4156:Ylpm1
|
UTSW |
12 |
85,104,177 (GRCm39) |
intron |
probably benign |
|
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 |
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 |
|