Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5330417H12Rik |
C |
T |
7: 107,223,922 (GRCm39) |
E51K |
unknown |
Het |
Akr1c20 |
T |
C |
13: 4,561,215 (GRCm39) |
D146G |
probably benign |
Het |
Anapc4 |
T |
A |
5: 53,000,843 (GRCm39) |
C205* |
probably null |
Het |
Ap3s2 |
A |
G |
7: 79,564,911 (GRCm39) |
I86T |
probably benign |
Het |
Arih2 |
C |
G |
9: 108,488,938 (GRCm39) |
R260P |
probably damaging |
Het |
Atp9a |
C |
T |
2: 168,479,420 (GRCm39) |
|
probably null |
Het |
Bcl11b |
C |
A |
12: 107,883,163 (GRCm39) |
R384L |
probably damaging |
Het |
Bltp3a |
T |
G |
17: 28,105,887 (GRCm39) |
D804E |
possibly damaging |
Het |
Brca2 |
T |
A |
5: 150,465,208 (GRCm39) |
D1657E |
probably damaging |
Het |
Cabyr |
C |
A |
18: 12,884,077 (GRCm39) |
T188N |
probably damaging |
Het |
Capn5 |
C |
A |
7: 97,784,997 (GRCm39) |
W159L |
probably damaging |
Het |
Ccdc121rt3 |
A |
T |
5: 112,503,087 (GRCm39) |
Y206N |
probably damaging |
Het |
Ccnl1 |
A |
T |
3: 65,854,080 (GRCm39) |
S514T |
unknown |
Het |
Cdk14 |
G |
T |
5: 5,086,515 (GRCm39) |
H286Q |
possibly damaging |
Het |
Cpsf3 |
T |
A |
12: 21,345,112 (GRCm39) |
H141Q |
probably damaging |
Het |
Ddx24 |
A |
G |
12: 103,390,665 (GRCm39) |
S109P |
possibly damaging |
Het |
Dnmt3a |
A |
T |
12: 3,916,192 (GRCm39) |
R126* |
probably null |
Het |
Dpys |
C |
A |
15: 39,720,619 (GRCm39) |
R47L |
probably benign |
Het |
Dync1li2 |
A |
G |
8: 105,152,090 (GRCm39) |
V361A |
probably benign |
Het |
Epha7 |
T |
G |
4: 28,963,892 (GRCm39) |
D962E |
probably damaging |
Het |
Erh |
G |
T |
12: 80,684,282 (GRCm39) |
A65E |
probably benign |
Het |
Fyb2 |
T |
C |
4: 104,857,700 (GRCm39) |
S626P |
probably benign |
Het |
Gtpbp1 |
T |
A |
15: 79,600,393 (GRCm39) |
V442D |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,422,188 (GRCm39) |
I973F |
probably damaging |
Het |
Igkv1-99 |
A |
C |
6: 68,519,340 (GRCm39) |
K99T |
|
Het |
Igkv6-14 |
C |
T |
6: 70,412,180 (GRCm39) |
V35I |
probably benign |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Klk1b9 |
C |
T |
7: 43,628,925 (GRCm39) |
T143I |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Mettl15 |
A |
C |
2: 108,967,625 (GRCm39) |
|
probably benign |
Het |
Mki67 |
A |
G |
7: 135,299,595 (GRCm39) |
V1813A |
|
Het |
Mrps30 |
A |
G |
13: 118,523,755 (GRCm39) |
Y6H |
possibly damaging |
Het |
Mthfd1 |
T |
A |
12: 76,329,710 (GRCm39) |
I176K |
probably benign |
Het |
Nckap5l |
C |
T |
15: 99,323,761 (GRCm39) |
G914D |
probably damaging |
Het |
Nemf |
C |
A |
12: 69,363,089 (GRCm39) |
E930* |
probably null |
Het |
Nuggc |
G |
A |
14: 65,879,354 (GRCm39) |
V705I |
probably benign |
Het |
Omd |
A |
T |
13: 49,745,718 (GRCm39) |
K376M |
probably damaging |
Het |
Or10a3n |
T |
C |
7: 108,492,736 (GRCm39) |
R298G |
probably damaging |
Het |
Or2n1d |
A |
T |
17: 38,646,320 (GRCm39) |
T91S |
possibly damaging |
Het |
Or4k42 |
C |
A |
2: 111,320,004 (GRCm39) |
L166F |
probably damaging |
Het |
Or51l14 |
T |
A |
7: 103,101,090 (GRCm39) |
L182Q |
probably damaging |
Het |
Or5g27 |
A |
G |
2: 85,410,056 (GRCm39) |
T158A |
possibly damaging |
Het |
Or5p68 |
A |
G |
7: 107,945,759 (GRCm39) |
V143A |
probably benign |
Het |
Or6c200-ps1 |
C |
A |
10: 128,871,372 (GRCm39) |
M2I |
probably benign |
Het |
Pi15 |
A |
G |
1: 17,691,962 (GRCm39) |
Y217C |
probably damaging |
Het |
Pou5f1 |
T |
C |
17: 35,821,371 (GRCm39) |
S328P |
probably benign |
Het |
Pparg |
T |
A |
6: 115,440,133 (GRCm39) |
S236T |
probably benign |
Het |
Prss23 |
T |
C |
7: 89,159,854 (GRCm39) |
T72A |
probably benign |
Het |
Ptprb |
C |
A |
10: 116,158,567 (GRCm39) |
S546* |
probably null |
Het |
Ranbp9 |
A |
G |
13: 43,578,560 (GRCm39) |
I171T |
probably benign |
Het |
Rap1gap2 |
A |
T |
11: 74,326,587 (GRCm39) |
L160* |
probably null |
Het |
Rfxap |
T |
C |
3: 54,715,042 (GRCm39) |
T19A |
probably benign |
Het |
Sctr |
T |
A |
1: 119,959,386 (GRCm39) |
F95I |
probably benign |
Het |
Sf3b3 |
T |
A |
8: 111,540,439 (GRCm39) |
Q994L |
probably benign |
Het |
Slfn9 |
A |
T |
11: 82,872,132 (GRCm39) |
I868N |
probably damaging |
Het |
Top3a |
A |
T |
11: 60,631,405 (GRCm39) |
C986S |
probably damaging |
Het |
Trak1 |
T |
A |
9: 121,272,847 (GRCm39) |
L245Q |
unknown |
Het |
Trim27 |
A |
G |
13: 21,364,993 (GRCm39) |
D110G |
possibly damaging |
Het |
Ubxn2a |
T |
C |
12: 4,930,754 (GRCm39) |
D202G |
probably benign |
Het |
Urb1 |
T |
C |
16: 90,607,122 (GRCm39) |
K36R |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,293,604 (GRCm39) |
T252A |
|
Het |
Vmn2r117 |
C |
T |
17: 23,679,143 (GRCm39) |
V694I |
probably benign |
Het |
Vmn2r26 |
T |
C |
6: 124,038,983 (GRCm39) |
F853L |
probably benign |
Het |
Vmn2r55 |
A |
T |
7: 12,405,024 (GRCm39) |
H126Q |
probably benign |
Het |
|
Other mutations in Vmn1r73 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01782:Vmn1r73
|
APN |
7 |
11,490,665 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02337:Vmn1r73
|
APN |
7 |
11,490,640 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02666:Vmn1r73
|
APN |
7 |
11,490,865 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02741:Vmn1r73
|
APN |
7 |
11,490,710 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02756:Vmn1r73
|
APN |
7 |
11,490,574 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03113:Vmn1r73
|
APN |
7 |
11,490,527 (GRCm39) |
missense |
probably benign |
|
IGL03195:Vmn1r73
|
APN |
7 |
11,491,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Vmn1r73
|
UTSW |
7 |
11,490,997 (GRCm39) |
missense |
probably benign |
0.43 |
R0379:Vmn1r73
|
UTSW |
7 |
11,490,773 (GRCm39) |
missense |
probably benign |
0.16 |
R3941:Vmn1r73
|
UTSW |
7 |
11,490,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R4224:Vmn1r73
|
UTSW |
7 |
11,490,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R4631:Vmn1r73
|
UTSW |
7 |
11,490,758 (GRCm39) |
missense |
probably benign |
0.22 |
R4912:Vmn1r73
|
UTSW |
7 |
11,490,596 (GRCm39) |
missense |
probably damaging |
0.99 |
R5060:Vmn1r73
|
UTSW |
7 |
11,490,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5450:Vmn1r73
|
UTSW |
7 |
11,490,376 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5609:Vmn1r73
|
UTSW |
7 |
11,490,591 (GRCm39) |
nonsense |
probably null |
|
R6059:Vmn1r73
|
UTSW |
7 |
11,490,538 (GRCm39) |
missense |
probably benign |
0.40 |
R6508:Vmn1r73
|
UTSW |
7 |
11,490,631 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6967:Vmn1r73
|
UTSW |
7 |
11,490,544 (GRCm39) |
nonsense |
probably null |
|
R7099:Vmn1r73
|
UTSW |
7 |
11,490,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7304:Vmn1r73
|
UTSW |
7 |
11,490,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Vmn1r73
|
UTSW |
7 |
11,491,082 (GRCm39) |
missense |
probably benign |
0.08 |
R7891:Vmn1r73
|
UTSW |
7 |
11,491,036 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9072:Vmn1r73
|
UTSW |
7 |
11,490,203 (GRCm39) |
missense |
probably benign |
0.00 |
R9073:Vmn1r73
|
UTSW |
7 |
11,490,203 (GRCm39) |
missense |
probably benign |
0.00 |
R9275:Vmn1r73
|
UTSW |
7 |
11,490,479 (GRCm39) |
missense |
probably benign |
0.04 |
R9632:Vmn1r73
|
UTSW |
7 |
11,490,407 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9710:Vmn1r73
|
UTSW |
7 |
11,490,407 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1176:Vmn1r73
|
UTSW |
7 |
11,490,883 (GRCm39) |
missense |
probably benign |
0.02 |
|