Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
C |
T |
8: 60,993,158 (GRCm39) |
T373I |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,241,653 (GRCm39) |
L1172P |
possibly damaging |
Het |
Abcg2 |
A |
G |
6: 58,661,326 (GRCm39) |
Y459C |
probably benign |
Het |
AC125199.3 |
T |
C |
16: 88,609,061 (GRCm39) |
N4D |
possibly damaging |
Het |
Acad8 |
A |
G |
9: 26,910,785 (GRCm39) |
M3T |
probably benign |
Het |
Acsbg3 |
A |
C |
17: 57,189,218 (GRCm39) |
I209L |
probably benign |
Het |
Adcyap1r1 |
C |
T |
6: 55,474,080 (GRCm39) |
T472I |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,840,671 (GRCm39) |
K1890N |
possibly damaging |
Het |
Asic1 |
G |
A |
15: 99,569,826 (GRCm39) |
C49Y |
probably benign |
Het |
Atp1a1 |
T |
C |
3: 101,498,547 (GRCm39) |
N215S |
probably damaging |
Het |
C87436 |
A |
G |
6: 86,422,774 (GRCm39) |
Y116C |
probably damaging |
Het |
Car5a |
T |
C |
8: 122,671,519 (GRCm39) |
D5G |
probably benign |
Het |
Ccdc169 |
T |
C |
3: 55,058,368 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
A |
G |
1: 121,426,970 (GRCm39) |
R586G |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,238,007 (GRCm39) |
V131A |
probably damaging |
Het |
Cox5a |
A |
G |
9: 57,436,329 (GRCm39) |
D60G |
possibly damaging |
Het |
Cpne6 |
A |
T |
14: 55,750,104 (GRCm39) |
E78D |
probably benign |
Het |
Cyp2u1 |
T |
C |
3: 131,089,114 (GRCm39) |
E390G |
probably damaging |
Het |
Dab2 |
C |
A |
15: 6,465,271 (GRCm39) |
N707K |
|
Het |
Dock10 |
A |
T |
1: 80,483,147 (GRCm39) |
D2101E |
probably benign |
Het |
Duoxa2 |
G |
A |
2: 122,132,357 (GRCm39) |
|
probably null |
Het |
Eif4a3 |
T |
C |
11: 119,190,758 (GRCm39) |
D22G |
probably benign |
Het |
Fhip1b |
T |
C |
7: 105,037,477 (GRCm39) |
T369A |
possibly damaging |
Het |
Fubp3 |
A |
G |
2: 31,482,476 (GRCm39) |
|
probably null |
Het |
Gm10330 |
A |
G |
12: 23,829,887 (GRCm39) |
L98P |
probably benign |
Het |
Gm5108 |
A |
G |
5: 68,134,299 (GRCm39) |
*102W |
probably null |
Het |
Gpr149 |
A |
C |
3: 62,438,478 (GRCm39) |
S560A |
probably damaging |
Het |
Haspin |
T |
C |
11: 73,027,430 (GRCm39) |
D553G |
probably benign |
Het |
Hsf1 |
C |
T |
15: 76,382,051 (GRCm39) |
H104Y |
probably benign |
Het |
Ifi203 |
T |
C |
1: 173,756,494 (GRCm39) |
T430A |
unknown |
Het |
Itih2 |
G |
A |
2: 10,102,822 (GRCm39) |
Q771* |
probably null |
Het |
Kazald1 |
T |
A |
19: 45,065,395 (GRCm39) |
L92Q |
probably damaging |
Het |
Krt19 |
T |
C |
11: 100,031,980 (GRCm39) |
E324G |
probably damaging |
Het |
Lrrc28 |
A |
T |
7: 67,268,833 (GRCm39) |
V79E |
possibly damaging |
Het |
Ltn1 |
T |
A |
16: 87,178,381 (GRCm39) |
Q1616L |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,158,843 (GRCm39) |
K408E |
probably benign |
Het |
Nalcn |
A |
T |
14: 123,561,284 (GRCm39) |
M738K |
probably benign |
Het |
Ncoa4 |
T |
C |
14: 31,894,848 (GRCm39) |
L125P |
probably damaging |
Het |
Ncor2 |
G |
T |
5: 125,106,253 (GRCm39) |
R810S |
|
Het |
Neb |
C |
T |
2: 52,127,141 (GRCm39) |
G348D |
|
Het |
Nfat5 |
T |
A |
8: 108,095,228 (GRCm39) |
F1156L |
probably damaging |
Het |
Oit3 |
G |
A |
10: 59,277,468 (GRCm39) |
T13I |
unknown |
Het |
Opa1 |
A |
C |
16: 29,424,340 (GRCm39) |
Q230P |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,044,064 (GRCm39) |
I282T |
probably damaging |
Het |
Or52k2 |
T |
A |
7: 102,253,711 (GRCm39) |
I50N |
probably damaging |
Het |
Or5p66 |
A |
G |
7: 107,886,289 (GRCm39) |
F15L |
probably damaging |
Het |
Or5w12 |
A |
C |
2: 87,502,567 (GRCm39) |
L48W |
probably damaging |
Het |
Or6c5b |
G |
T |
10: 129,246,082 (GRCm39) |
M282I |
probably benign |
Het |
Parpbp |
T |
C |
10: 87,946,189 (GRCm39) |
H410R |
probably null |
Het |
Pex5l |
A |
G |
3: 33,007,333 (GRCm39) |
V481A |
probably damaging |
Het |
Plekhh3 |
C |
A |
11: 101,057,225 (GRCm39) |
R344L |
probably benign |
Het |
Prrc2b |
T |
C |
2: 32,104,953 (GRCm39) |
V1477A |
probably benign |
Het |
Ptp4a2 |
G |
A |
4: 129,738,945 (GRCm39) |
G94S |
possibly damaging |
Het |
Ptprk |
T |
A |
10: 28,359,203 (GRCm39) |
Y598* |
probably null |
Het |
Rfx5 |
C |
A |
3: 94,864,475 (GRCm39) |
T207N |
probably damaging |
Het |
Rnase2b |
A |
G |
14: 51,400,347 (GRCm39) |
T143A |
possibly damaging |
Het |
Scn1a |
A |
G |
2: 66,168,330 (GRCm39) |
V92A |
probably benign |
Het |
Shank2 |
C |
A |
7: 143,965,265 (GRCm39) |
P958T |
probably damaging |
Het |
Slc13a1 |
A |
G |
6: 24,108,194 (GRCm39) |
I294T |
probably damaging |
Het |
Slc4a8 |
A |
T |
15: 100,712,421 (GRCm39) |
E1084D |
probably benign |
Het |
Smurf1 |
T |
A |
5: 144,820,422 (GRCm39) |
R549* |
probably null |
Het |
Spmip10 |
T |
C |
18: 56,725,537 (GRCm39) |
F66L |
probably damaging |
Het |
Sprr2b |
T |
C |
3: 92,225,032 (GRCm39) |
C93R |
unknown |
Het |
Tcn2 |
G |
T |
11: 3,873,569 (GRCm39) |
S259Y |
probably damaging |
Het |
Tent4a |
G |
T |
13: 69,651,828 (GRCm39) |
T531N |
possibly damaging |
Het |
Tle1 |
A |
G |
4: 72,076,525 (GRCm39) |
S168P |
possibly damaging |
Het |
Tnfrsf1b |
C |
T |
4: 144,950,150 (GRCm39) |
G264D |
probably damaging |
Het |
Tnks2 |
T |
A |
19: 36,823,088 (GRCm39) |
N118K |
probably damaging |
Het |
Topaz1 |
G |
T |
9: 122,626,930 (GRCm39) |
|
probably benign |
Het |
Traf3ip1 |
A |
G |
1: 91,443,796 (GRCm39) |
|
probably benign |
Het |
Ttk |
A |
G |
9: 83,721,322 (GRCm39) |
E69G |
probably damaging |
Het |
Tulp3 |
T |
C |
6: 128,310,966 (GRCm39) |
D87G |
probably benign |
Het |
Usp38 |
C |
T |
8: 81,708,479 (GRCm39) |
G1033D |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,693,775 (GRCm39) |
N707K |
probably benign |
Het |
Vipas39 |
T |
A |
12: 87,305,858 (GRCm39) |
R112* |
probably null |
Het |
Vmn1r185 |
A |
C |
7: 26,311,206 (GRCm39) |
S100A |
probably damaging |
Het |
Vmn1r209 |
T |
C |
13: 22,990,223 (GRCm39) |
M156V |
probably benign |
Het |
Wdr41 |
G |
A |
13: 95,151,620 (GRCm39) |
R260H |
probably benign |
Het |
Wdr90 |
G |
A |
17: 26,076,146 (GRCm39) |
R104C |
|
Het |
Wnk2 |
A |
T |
13: 49,221,711 (GRCm39) |
H1183Q |
possibly damaging |
Het |
Zfp667 |
A |
T |
7: 6,308,256 (GRCm39) |
H308L |
possibly damaging |
Het |
Zfp952 |
A |
G |
17: 33,220,628 (GRCm39) |
N18D |
possibly damaging |
Het |
|
Other mutations in Vmn1r3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03130:Vmn1r3
|
APN |
4 |
3,185,214 (GRCm39) |
missense |
possibly damaging |
0.89 |
PIT4131001:Vmn1r3
|
UTSW |
4 |
3,184,774 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4131001:Vmn1r3
|
UTSW |
4 |
3,184,691 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Vmn1r3
|
UTSW |
4 |
3,184,774 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4142001:Vmn1r3
|
UTSW |
4 |
3,184,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R0972:Vmn1r3
|
UTSW |
4 |
3,185,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R1423:Vmn1r3
|
UTSW |
4 |
3,185,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R3902:Vmn1r3
|
UTSW |
4 |
3,185,241 (GRCm39) |
missense |
probably benign |
0.41 |
R4999:Vmn1r3
|
UTSW |
4 |
3,185,009 (GRCm39) |
nonsense |
probably null |
|
R6091:Vmn1r3
|
UTSW |
4 |
3,184,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R6140:Vmn1r3
|
UTSW |
4 |
3,185,031 (GRCm39) |
missense |
probably damaging |
0.97 |
R6188:Vmn1r3
|
UTSW |
4 |
3,185,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Vmn1r3
|
UTSW |
4 |
3,185,098 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6303:Vmn1r3
|
UTSW |
4 |
3,184,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R6304:Vmn1r3
|
UTSW |
4 |
3,184,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Vmn1r3
|
UTSW |
4 |
3,184,993 (GRCm39) |
missense |
probably benign |
0.39 |
R6430:Vmn1r3
|
UTSW |
4 |
3,184,971 (GRCm39) |
missense |
probably benign |
|
R6633:Vmn1r3
|
UTSW |
4 |
3,184,971 (GRCm39) |
missense |
probably benign |
|
R9320:Vmn1r3
|
UTSW |
4 |
3,185,284 (GRCm39) |
missense |
probably benign |
0.00 |
R9357:Vmn1r3
|
UTSW |
4 |
3,185,149 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Vmn1r3
|
UTSW |
4 |
3,185,304 (GRCm39) |
start codon destroyed |
probably null |
0.60 |
|