Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5330417H12Rik |
T |
C |
7: 107,223,897 (GRCm39) |
|
probably benign |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Adgrf2 |
T |
C |
17: 43,022,084 (GRCm39) |
I247V |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,418,857 (GRCm39) |
|
probably null |
Het |
Ankrd22 |
T |
A |
19: 34,126,752 (GRCm39) |
K26I |
possibly damaging |
Het |
Arhgap32 |
T |
A |
9: 32,156,552 (GRCm39) |
|
probably null |
Het |
Armc10 |
A |
G |
5: 21,866,522 (GRCm39) |
Y262C |
probably damaging |
Het |
Arrb2 |
A |
G |
11: 70,330,725 (GRCm39) |
D374G |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,625,227 (GRCm39) |
R1675C |
probably damaging |
Het |
Atg5 |
T |
C |
10: 44,239,046 (GRCm39) |
*276R |
probably null |
Het |
Bcl11b |
G |
A |
12: 107,882,968 (GRCm39) |
T377M |
probably damaging |
Het |
C1s2 |
C |
A |
6: 124,612,073 (GRCm39) |
E104* |
probably null |
Het |
Carf |
A |
T |
1: 60,180,526 (GRCm39) |
H316L |
probably damaging |
Het |
Ccdc77 |
A |
T |
6: 120,311,796 (GRCm39) |
I234N |
probably damaging |
Het |
Cd300c2 |
A |
T |
11: 114,887,826 (GRCm39) |
V192E |
possibly damaging |
Het |
Cep72 |
G |
A |
13: 74,207,584 (GRCm39) |
R62C |
probably damaging |
Het |
Clasp1 |
T |
A |
1: 118,436,640 (GRCm39) |
L308* |
probably null |
Het |
Clec2g |
A |
G |
6: 128,956,411 (GRCm39) |
S25G |
probably benign |
Het |
Cngb1 |
T |
C |
8: 95,978,601 (GRCm39) |
M1046V |
probably damaging |
Het |
Cobll1 |
A |
T |
2: 64,928,037 (GRCm39) |
D1095E |
probably benign |
Het |
Cpeb2 |
A |
G |
5: 43,402,005 (GRCm39) |
H662R |
possibly damaging |
Het |
Cps1 |
A |
T |
1: 67,178,922 (GRCm39) |
T45S |
probably benign |
Het |
Cspp1 |
A |
G |
1: 10,152,553 (GRCm39) |
Q368R |
possibly damaging |
Het |
Dcaf6 |
C |
A |
1: 165,239,032 (GRCm39) |
|
probably null |
Het |
Dcst1 |
T |
C |
3: 89,257,814 (GRCm39) |
Y652C |
possibly damaging |
Het |
Elf5 |
T |
G |
2: 103,279,918 (GRCm39) |
Y225* |
probably null |
Het |
Ermap |
A |
C |
4: 119,046,015 (GRCm39) |
|
probably benign |
Het |
Fam186b |
A |
T |
15: 99,169,202 (GRCm39) |
V915D |
probably damaging |
Het |
Fbxo34 |
C |
A |
14: 47,766,911 (GRCm39) |
N90K |
probably benign |
Het |
Flnc |
A |
G |
6: 29,447,524 (GRCm39) |
E1109G |
probably damaging |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Gabpb2 |
A |
G |
3: 95,097,947 (GRCm39) |
V242A |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm21798 |
A |
T |
15: 64,689,732 (GRCm39) |
|
probably benign |
Het |
Gusb |
A |
T |
5: 130,026,959 (GRCm39) |
F377L |
probably damaging |
Het |
Hnrnpu |
T |
C |
1: 178,156,938 (GRCm39) |
|
probably benign |
Het |
Htr3b |
C |
T |
9: 48,848,348 (GRCm39) |
|
probably null |
Het |
Iqub |
A |
T |
6: 24,501,368 (GRCm39) |
V194D |
probably damaging |
Het |
Itga2b |
A |
G |
11: 102,351,985 (GRCm39) |
V504A |
probably benign |
Het |
Itga4 |
T |
A |
2: 79,118,592 (GRCm39) |
F430L |
probably damaging |
Het |
Jcad |
C |
A |
18: 4,673,762 (GRCm39) |
P508H |
probably damaging |
Het |
Jph1 |
T |
C |
1: 17,161,835 (GRCm39) |
T276A |
probably damaging |
Het |
Kansl2 |
A |
G |
15: 98,429,771 (GRCm39) |
F87S |
possibly damaging |
Het |
Kdm1b |
T |
C |
13: 47,216,620 (GRCm39) |
|
probably null |
Het |
Kif5b |
C |
T |
18: 6,220,930 (GRCm39) |
D393N |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,747,420 (GRCm39) |
|
probably benign |
Het |
Krt75 |
A |
G |
15: 101,478,674 (GRCm39) |
I320T |
probably damaging |
Het |
Lhfpl7 |
T |
A |
5: 113,386,036 (GRCm39) |
M161K |
probably benign |
Het |
Lipo5 |
T |
C |
19: 33,443,348 (GRCm39) |
N156S |
unknown |
Het |
Mblac2 |
A |
C |
13: 81,859,706 (GRCm39) |
Q19P |
probably null |
Het |
Mdfic2 |
A |
T |
6: 98,215,080 (GRCm39) |
M181K |
probably damaging |
Het |
Mfsd4b3-ps |
T |
C |
10: 39,824,056 (GRCm39) |
H68R |
probably damaging |
Het |
Mzb1 |
A |
T |
18: 35,781,006 (GRCm39) |
|
probably null |
Het |
Nup210l |
T |
A |
3: 90,077,337 (GRCm39) |
I891N |
probably benign |
Het |
Nwd1 |
G |
A |
8: 73,398,841 (GRCm39) |
R667Q |
probably damaging |
Het |
Oas1h |
C |
T |
5: 121,005,172 (GRCm39) |
Q207* |
probably null |
Het |
Or13c7d |
A |
T |
4: 43,770,476 (GRCm39) |
F178L |
possibly damaging |
Het |
Pcdh15 |
C |
T |
10: 74,340,625 (GRCm39) |
R1120* |
probably null |
Het |
Pfkl |
A |
G |
10: 77,824,144 (GRCm39) |
L748P |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,571,758 (GRCm39) |
K473N |
probably damaging |
Het |
Rapgef6 |
G |
A |
11: 54,443,662 (GRCm39) |
V82I |
probably damaging |
Het |
Rfc3 |
A |
T |
5: 151,570,960 (GRCm39) |
L112Q |
probably damaging |
Het |
Rsph6a |
T |
A |
7: 18,801,997 (GRCm39) |
C349S |
possibly damaging |
Het |
Sec16a |
A |
T |
2: 26,331,979 (GRCm39) |
|
probably benign |
Het |
Septin14 |
T |
A |
5: 129,770,030 (GRCm39) |
Y222F |
probably benign |
Het |
Skor2 |
T |
C |
18: 76,947,990 (GRCm39) |
S571P |
possibly damaging |
Het |
Slc13a5 |
T |
A |
11: 72,148,244 (GRCm39) |
M264L |
probably damaging |
Het |
Slc45a3 |
T |
A |
1: 131,909,315 (GRCm39) |
V504E |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,751,631 (GRCm39) |
|
probably benign |
Het |
Smim20 |
A |
G |
5: 53,434,503 (GRCm39) |
N45S |
probably null |
Het |
Spp2 |
A |
T |
1: 88,339,991 (GRCm39) |
S111C |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,442,664 (GRCm39) |
|
probably null |
Het |
Sycp2 |
C |
T |
2: 178,045,450 (GRCm39) |
|
probably null |
Het |
Tas2r113 |
A |
G |
6: 132,870,521 (GRCm39) |
N183S |
possibly damaging |
Het |
Tcaf2 |
A |
T |
6: 42,606,679 (GRCm39) |
M425K |
probably benign |
Het |
Tdrp |
A |
G |
8: 14,003,845 (GRCm39) |
V164A |
possibly damaging |
Het |
Tmbim1 |
A |
G |
1: 74,328,568 (GRCm39) |
F298S |
probably damaging |
Het |
Tmem89 |
A |
G |
9: 108,743,829 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
G |
T |
10: 77,768,023 (GRCm39) |
C825* |
probably null |
Het |
Tsc1 |
A |
G |
2: 28,565,201 (GRCm39) |
E421G |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,245,834 (GRCm39) |
I1364T |
probably benign |
Het |
Vmn1r52 |
G |
A |
6: 90,155,930 (GRCm39) |
G78E |
possibly damaging |
Het |
Vmn2r73 |
T |
G |
7: 85,506,829 (GRCm39) |
I828L |
probably damaging |
Het |
Vwa5b1 |
A |
T |
4: 138,338,058 (GRCm39) |
D87E |
probably benign |
Het |
Zfp1010 |
T |
C |
2: 176,957,223 (GRCm39) |
T92A |
possibly damaging |
Het |
Zfp451 |
A |
T |
1: 33,844,465 (GRCm39) |
D47E |
probably damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,841 (GRCm39) |
E278G |
probably damaging |
Het |
Zfp930 |
A |
T |
8: 69,681,597 (GRCm39) |
T430S |
probably benign |
Het |
Zfp994 |
G |
T |
17: 22,419,448 (GRCm39) |
Y500* |
probably null |
Het |
Zmat3 |
A |
T |
3: 32,397,836 (GRCm39) |
I142N |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,792,214 (GRCm39) |
I2266N |
probably damaging |
Het |
|
Other mutations in Gpr179 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01088:Gpr179
|
APN |
11 |
97,228,627 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01152:Gpr179
|
APN |
11 |
97,228,237 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01402:Gpr179
|
APN |
11 |
97,229,012 (GRCm39) |
nonsense |
probably null |
|
IGL01404:Gpr179
|
APN |
11 |
97,229,012 (GRCm39) |
nonsense |
probably null |
|
IGL01773:Gpr179
|
APN |
11 |
97,232,192 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02682:Gpr179
|
APN |
11 |
97,242,691 (GRCm39) |
missense |
probably benign |
|
IGL02728:Gpr179
|
APN |
11 |
97,228,726 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03243:Gpr179
|
APN |
11 |
97,242,301 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03272:Gpr179
|
APN |
11 |
97,227,419 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03347:Gpr179
|
APN |
11 |
97,242,664 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Gpr179
|
APN |
11 |
97,228,434 (GRCm39) |
missense |
possibly damaging |
0.57 |
PIT4280001:Gpr179
|
UTSW |
11 |
97,234,941 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Gpr179
|
UTSW |
11 |
97,227,677 (GRCm39) |
missense |
probably benign |
|
R0042:Gpr179
|
UTSW |
11 |
97,225,757 (GRCm39) |
missense |
probably benign |
0.04 |
R0042:Gpr179
|
UTSW |
11 |
97,225,757 (GRCm39) |
missense |
probably benign |
0.04 |
R0080:Gpr179
|
UTSW |
11 |
97,242,295 (GRCm39) |
missense |
probably benign |
0.08 |
R0255:Gpr179
|
UTSW |
11 |
97,226,892 (GRCm39) |
missense |
probably benign |
0.24 |
R0412:Gpr179
|
UTSW |
11 |
97,229,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Gpr179
|
UTSW |
11 |
97,240,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R0612:Gpr179
|
UTSW |
11 |
97,229,264 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0786:Gpr179
|
UTSW |
11 |
97,234,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Gpr179
|
UTSW |
11 |
97,237,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Gpr179
|
UTSW |
11 |
97,225,932 (GRCm39) |
missense |
probably benign |
0.00 |
R1796:Gpr179
|
UTSW |
11 |
97,227,382 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1969:Gpr179
|
UTSW |
11 |
97,228,784 (GRCm39) |
missense |
probably benign |
|
R2240:Gpr179
|
UTSW |
11 |
97,242,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R3855:Gpr179
|
UTSW |
11 |
97,232,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Gpr179
|
UTSW |
11 |
97,225,591 (GRCm39) |
missense |
probably benign |
0.01 |
R4484:Gpr179
|
UTSW |
11 |
97,226,537 (GRCm39) |
missense |
probably benign |
0.28 |
R4806:Gpr179
|
UTSW |
11 |
97,240,610 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4816:Gpr179
|
UTSW |
11 |
97,230,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R4945:Gpr179
|
UTSW |
11 |
97,240,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5191:Gpr179
|
UTSW |
11 |
97,228,975 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5273:Gpr179
|
UTSW |
11 |
97,238,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5317:Gpr179
|
UTSW |
11 |
97,228,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R5459:Gpr179
|
UTSW |
11 |
97,227,483 (GRCm39) |
missense |
probably benign |
0.00 |
R5507:Gpr179
|
UTSW |
11 |
97,229,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R5523:Gpr179
|
UTSW |
11 |
97,227,608 (GRCm39) |
missense |
probably benign |
0.37 |
R5536:Gpr179
|
UTSW |
11 |
97,234,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5591:Gpr179
|
UTSW |
11 |
97,236,581 (GRCm39) |
missense |
probably benign |
0.17 |
R5679:Gpr179
|
UTSW |
11 |
97,227,571 (GRCm39) |
missense |
probably benign |
0.20 |
R5738:Gpr179
|
UTSW |
11 |
97,242,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R5829:Gpr179
|
UTSW |
11 |
97,226,524 (GRCm39) |
missense |
probably benign |
0.11 |
R5836:Gpr179
|
UTSW |
11 |
97,229,882 (GRCm39) |
missense |
probably benign |
0.03 |
R6007:Gpr179
|
UTSW |
11 |
97,226,628 (GRCm39) |
nonsense |
probably null |
|
R6047:Gpr179
|
UTSW |
11 |
97,229,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Gpr179
|
UTSW |
11 |
97,235,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Gpr179
|
UTSW |
11 |
97,227,973 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6674:Gpr179
|
UTSW |
11 |
97,238,231 (GRCm39) |
critical splice donor site |
probably null |
|
R6712:Gpr179
|
UTSW |
11 |
97,226,993 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6835:Gpr179
|
UTSW |
11 |
97,238,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Gpr179
|
UTSW |
11 |
97,225,684 (GRCm39) |
missense |
probably benign |
0.38 |
R7044:Gpr179
|
UTSW |
11 |
97,240,616 (GRCm39) |
missense |
probably benign |
0.19 |
R7121:Gpr179
|
UTSW |
11 |
97,225,556 (GRCm39) |
missense |
probably benign |
0.00 |
R7307:Gpr179
|
UTSW |
11 |
97,229,672 (GRCm39) |
missense |
probably benign |
0.36 |
R7406:Gpr179
|
UTSW |
11 |
97,242,420 (GRCm39) |
missense |
probably damaging |
0.99 |
R7467:Gpr179
|
UTSW |
11 |
97,226,115 (GRCm39) |
missense |
probably benign |
0.02 |
R7477:Gpr179
|
UTSW |
11 |
97,226,665 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7725:Gpr179
|
UTSW |
11 |
97,242,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Gpr179
|
UTSW |
11 |
97,228,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R8165:Gpr179
|
UTSW |
11 |
97,242,364 (GRCm39) |
missense |
probably benign |
0.12 |
R8262:Gpr179
|
UTSW |
11 |
97,226,983 (GRCm39) |
missense |
probably benign |
0.00 |
R8674:Gpr179
|
UTSW |
11 |
97,225,873 (GRCm39) |
missense |
probably benign |
0.00 |
R8695:Gpr179
|
UTSW |
11 |
97,227,124 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8731:Gpr179
|
UTSW |
11 |
97,234,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8791:Gpr179
|
UTSW |
11 |
97,242,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R8889:Gpr179
|
UTSW |
11 |
97,226,590 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8892:Gpr179
|
UTSW |
11 |
97,226,590 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8898:Gpr179
|
UTSW |
11 |
97,242,329 (GRCm39) |
nonsense |
probably null |
|
R8940:Gpr179
|
UTSW |
11 |
97,228,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R9266:Gpr179
|
UTSW |
11 |
97,227,766 (GRCm39) |
missense |
probably benign |
|
R9332:Gpr179
|
UTSW |
11 |
97,229,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R9440:Gpr179
|
UTSW |
11 |
97,229,315 (GRCm39) |
missense |
probably benign |
0.11 |
R9557:Gpr179
|
UTSW |
11 |
97,235,029 (GRCm39) |
missense |
probably damaging |
0.97 |
R9594:Gpr179
|
UTSW |
11 |
97,225,727 (GRCm39) |
missense |
probably benign |
0.13 |
R9723:Gpr179
|
UTSW |
11 |
97,225,546 (GRCm39) |
missense |
possibly damaging |
0.93 |
X0065:Gpr179
|
UTSW |
11 |
97,238,264 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Gpr179
|
UTSW |
11 |
97,227,474 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Gpr179
|
UTSW |
11 |
97,242,065 (GRCm39) |
missense |
probably damaging |
1.00 |
|