Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
T |
8: 73,203,303 (GRCm39) |
P244S |
possibly damaging |
Het |
4930562C15Rik |
A |
G |
16: 4,653,633 (GRCm39) |
I61V |
unknown |
Het |
Abcb11 |
C |
T |
2: 69,130,211 (GRCm39) |
D282N |
probably damaging |
Het |
Acbd3 |
A |
G |
1: 180,562,064 (GRCm39) |
E181G |
probably benign |
Het |
Ano3 |
T |
C |
2: 110,587,412 (GRCm39) |
Y43C |
probably damaging |
Het |
Aspa |
T |
A |
11: 73,210,716 (GRCm39) |
|
probably null |
Het |
AU018091 |
A |
T |
7: 3,206,170 (GRCm39) |
N620K |
probably damaging |
Het |
Bicc1 |
G |
T |
10: 70,779,216 (GRCm39) |
T724K |
probably benign |
Het |
Bmper |
T |
C |
9: 23,395,300 (GRCm39) |
I677T |
probably damaging |
Het |
C3 |
T |
A |
17: 57,528,162 (GRCm39) |
T686S |
probably benign |
Het |
Cc2d2a |
G |
T |
5: 43,887,332 (GRCm39) |
R1315L |
probably damaging |
Het |
Ccdc150 |
G |
T |
1: 54,339,541 (GRCm39) |
E462* |
probably null |
Het |
Ccdc88c |
C |
A |
12: 100,911,209 (GRCm39) |
R875L |
possibly damaging |
Het |
Cdh23 |
A |
T |
10: 60,151,471 (GRCm39) |
Y2471* |
probably null |
Het |
Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
Cmbl |
A |
T |
15: 31,590,002 (GRCm39) |
Y244F |
probably benign |
Het |
Dcaf10 |
T |
C |
4: 45,373,919 (GRCm39) |
V448A |
probably damaging |
Het |
Ddr2 |
A |
G |
1: 169,825,533 (GRCm39) |
W356R |
probably damaging |
Het |
Depdc1a |
A |
G |
3: 159,228,849 (GRCm39) |
I534V |
probably benign |
Het |
Dhtkd1 |
T |
A |
2: 5,922,717 (GRCm39) |
I481L |
probably benign |
Het |
Dlst |
A |
T |
12: 85,175,089 (GRCm39) |
I260L |
probably benign |
Het |
Dnajc13 |
T |
G |
9: 104,061,905 (GRCm39) |
K1350Q |
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,184,943 (GRCm39) |
Y520C |
probably damaging |
Het |
Dr1 |
C |
A |
5: 108,423,594 (GRCm39) |
A127E |
unknown |
Het |
Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,752,770 (GRCm39) |
C628R |
probably damaging |
Het |
Edem3 |
T |
A |
1: 151,688,365 (GRCm39) |
|
probably null |
Het |
Efcab15 |
T |
C |
11: 103,098,944 (GRCm39) |
|
probably null |
Het |
Fam20a |
T |
A |
11: 109,564,168 (GRCm39) |
Q528H |
possibly damaging |
Het |
Fanca |
T |
C |
8: 124,007,952 (GRCm39) |
E981G |
probably benign |
Het |
Fbp2 |
A |
G |
13: 62,985,012 (GRCm39) |
V303A |
possibly damaging |
Het |
Flii |
C |
T |
11: 60,611,945 (GRCm39) |
V353M |
possibly damaging |
Het |
Gm10277 |
T |
A |
11: 77,676,584 (GRCm39) |
Y129F |
unknown |
Het |
Gm3159 |
A |
T |
14: 4,398,525 (GRCm38) |
H72L |
probably benign |
Het |
Gm5114 |
T |
G |
7: 39,058,768 (GRCm39) |
T284P |
possibly damaging |
Het |
Gm7168 |
T |
C |
17: 14,170,147 (GRCm39) |
S505P |
probably damaging |
Het |
Gnal |
T |
C |
18: 67,344,142 (GRCm39) |
V239A |
possibly damaging |
Het |
Gtf2i |
C |
T |
5: 134,294,603 (GRCm39) |
E370K |
probably damaging |
Het |
Hivep3 |
CGG |
CG |
4: 119,955,108 (GRCm39) |
1141 |
probably null |
Het |
Il3 |
T |
A |
11: 54,156,709 (GRCm39) |
R93S |
probably benign |
Het |
Itsn1 |
A |
G |
16: 91,705,338 (GRCm39) |
E1573G |
unknown |
Het |
Kif26a |
G |
A |
12: 112,129,976 (GRCm39) |
|
probably null |
Het |
Klb |
T |
C |
5: 65,529,774 (GRCm39) |
M434T |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,314,150 (GRCm39) |
R2194W |
probably damaging |
Het |
Lrp6 |
G |
T |
6: 134,427,781 (GRCm39) |
P1604T |
probably damaging |
Het |
Mak16 |
A |
G |
8: 31,656,127 (GRCm39) |
Y119H |
possibly damaging |
Het |
Map3k19 |
T |
A |
1: 127,745,192 (GRCm39) |
M1421L |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,164,580 (GRCm39) |
I1186V |
probably benign |
Het |
Mboat1 |
T |
A |
13: 30,386,345 (GRCm39) |
C120S |
possibly damaging |
Het |
Mctp2 |
T |
A |
7: 71,908,962 (GRCm39) |
D117V |
probably benign |
Het |
Mocos |
C |
A |
18: 24,809,673 (GRCm39) |
N425K |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,203,951 (GRCm39) |
|
probably null |
Het |
Ngfr |
A |
T |
11: 95,465,255 (GRCm39) |
W198R |
possibly damaging |
Het |
Nr4a3 |
T |
G |
4: 48,051,290 (GRCm39) |
S15A |
possibly damaging |
Het |
Obsl1 |
T |
C |
1: 75,479,608 (GRCm39) |
S596G |
probably damaging |
Het |
Or2ag1 |
G |
T |
7: 106,472,603 (GRCm39) |
P283Q |
probably damaging |
Het |
Or51g1 |
A |
T |
7: 102,633,723 (GRCm39) |
I216K |
probably damaging |
Het |
Or52e3 |
T |
G |
7: 102,869,740 (GRCm39) |
Y272D |
probably benign |
Het |
Or5v1b |
T |
A |
17: 37,841,708 (GRCm39) |
V280D |
probably damaging |
Het |
Or6b3 |
A |
G |
1: 92,439,400 (GRCm39) |
S117P |
possibly damaging |
Het |
Pithd1 |
T |
C |
4: 135,714,361 (GRCm39) |
Y29C |
probably benign |
Het |
Plcb3 |
T |
C |
19: 6,939,389 (GRCm39) |
T530A |
probably benign |
Het |
Prss40 |
A |
T |
1: 34,598,952 (GRCm39) |
Y70* |
probably null |
Het |
Ralgps1 |
T |
C |
2: 33,214,700 (GRCm39) |
M61V |
possibly damaging |
Het |
Rbp4 |
C |
T |
19: 38,113,410 (GRCm39) |
R36H |
possibly damaging |
Het |
Rnf125 |
A |
G |
18: 21,107,490 (GRCm39) |
N7S |
not run |
Het |
Rpe65 |
G |
A |
3: 159,330,366 (GRCm39) |
S511N |
probably benign |
Het |
Rspo4 |
A |
T |
2: 151,709,793 (GRCm39) |
Y66F |
probably damaging |
Het |
Ruvbl2 |
A |
G |
7: 45,071,573 (GRCm39) |
S437P |
probably benign |
Het |
Sele |
C |
A |
1: 163,876,288 (GRCm39) |
R12S |
probably benign |
Het |
Sgo2b |
T |
A |
8: 64,391,451 (GRCm39) |
K139* |
probably null |
Het |
Shroom3 |
C |
A |
5: 93,112,465 (GRCm39) |
S1942* |
probably null |
Het |
Slc12a9 |
G |
A |
5: 137,326,885 (GRCm39) |
R191* |
probably null |
Het |
Spag9 |
G |
T |
11: 93,999,347 (GRCm39) |
V1088L |
possibly damaging |
Het |
Sptb |
T |
G |
12: 76,650,968 (GRCm39) |
D1669A |
probably damaging |
Het |
Sptlc2 |
A |
G |
12: 87,360,823 (GRCm39) |
|
probably null |
Het |
Sult2a8 |
A |
T |
7: 14,150,254 (GRCm39) |
|
probably null |
Het |
Synpo2 |
A |
G |
3: 122,907,690 (GRCm39) |
V542A |
probably damaging |
Het |
Tecpr2 |
T |
C |
12: 110,881,914 (GRCm39) |
|
probably null |
Het |
Tektip1 |
T |
C |
10: 81,200,025 (GRCm39) |
D165G |
possibly damaging |
Het |
Tenm2 |
T |
C |
11: 35,960,241 (GRCm39) |
T1029A |
probably benign |
Het |
Tgoln1 |
G |
C |
6: 72,593,261 (GRCm39) |
T73R |
probably benign |
Het |
Tnfaip8l1 |
C |
A |
17: 56,478,897 (GRCm39) |
N62K |
probably damaging |
Het |
Tollip |
A |
G |
7: 141,443,334 (GRCm39) |
S174P |
probably benign |
Het |
Trp53tg5 |
A |
G |
2: 164,313,027 (GRCm39) |
I216T |
possibly damaging |
Het |
Tssk5 |
A |
G |
15: 76,258,713 (GRCm39) |
S58P |
probably benign |
Het |
Ttc9b |
T |
C |
7: 27,354,384 (GRCm39) |
Y157H |
probably damaging |
Het |
Tuba8 |
A |
G |
6: 121,199,871 (GRCm39) |
Y185C |
probably damaging |
Het |
Ubr2 |
C |
T |
17: 47,266,771 (GRCm39) |
A1127T |
probably damaging |
Het |
Urb1 |
CACTTAC |
CAC |
16: 90,569,461 (GRCm39) |
|
probably benign |
Het |
Yipf3 |
T |
A |
17: 46,559,855 (GRCm39) |
L57Q |
possibly damaging |
Het |
Zbtb32 |
A |
C |
7: 30,289,606 (GRCm39) |
C19G |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,979 (GRCm39) |
H641L |
possibly damaging |
Het |
Zfyve28 |
A |
T |
5: 34,389,571 (GRCm39) |
Y210N |
probably damaging |
Het |
Zpr1 |
T |
A |
9: 46,184,671 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cd177 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Cd177
|
APN |
7 |
24,459,176 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL00479:Cd177
|
APN |
7 |
24,457,440 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00673:Cd177
|
APN |
7 |
24,451,442 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL00913:Cd177
|
APN |
7 |
24,455,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01445:Cd177
|
APN |
7 |
24,451,496 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02021:Cd177
|
APN |
7 |
24,444,631 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02134:Cd177
|
APN |
7 |
24,451,777 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02532:Cd177
|
APN |
7 |
24,444,674 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02821:Cd177
|
APN |
7 |
24,443,819 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02821:Cd177
|
APN |
7 |
24,443,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02888:Cd177
|
APN |
7 |
24,457,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R0506:Cd177
|
UTSW |
7 |
24,457,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Cd177
|
UTSW |
7 |
24,451,738 (GRCm39) |
missense |
probably benign |
0.00 |
R0631:Cd177
|
UTSW |
7 |
24,456,111 (GRCm39) |
missense |
probably benign |
0.03 |
R0713:Cd177
|
UTSW |
7 |
24,443,855 (GRCm39) |
missense |
probably benign |
0.25 |
R1595:Cd177
|
UTSW |
7 |
24,444,389 (GRCm39) |
missense |
probably benign |
|
R1659:Cd177
|
UTSW |
7 |
24,445,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Cd177
|
UTSW |
7 |
24,455,661 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2260:Cd177
|
UTSW |
7 |
24,455,661 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2379:Cd177
|
UTSW |
7 |
24,457,468 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2763:Cd177
|
UTSW |
7 |
24,457,462 (GRCm39) |
missense |
probably benign |
0.05 |
R2929:Cd177
|
UTSW |
7 |
24,453,704 (GRCm39) |
nonsense |
probably null |
|
R3815:Cd177
|
UTSW |
7 |
24,453,817 (GRCm39) |
missense |
probably benign |
0.00 |
R3818:Cd177
|
UTSW |
7 |
24,453,817 (GRCm39) |
missense |
probably benign |
0.00 |
R3919:Cd177
|
UTSW |
7 |
24,443,858 (GRCm39) |
missense |
probably benign |
0.15 |
R4300:Cd177
|
UTSW |
7 |
24,449,845 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4494:Cd177
|
UTSW |
7 |
24,451,428 (GRCm39) |
missense |
probably benign |
0.06 |
R4781:Cd177
|
UTSW |
7 |
24,450,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R4819:Cd177
|
UTSW |
7 |
24,451,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Cd177
|
UTSW |
7 |
24,443,741 (GRCm39) |
missense |
probably benign |
0.03 |
R5186:Cd177
|
UTSW |
7 |
24,444,348 (GRCm39) |
missense |
probably benign |
0.31 |
R5285:Cd177
|
UTSW |
7 |
24,445,674 (GRCm39) |
missense |
probably benign |
0.00 |
R5415:Cd177
|
UTSW |
7 |
24,451,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5577:Cd177
|
UTSW |
7 |
24,444,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R5637:Cd177
|
UTSW |
7 |
24,455,748 (GRCm39) |
missense |
probably benign |
0.01 |
R5673:Cd177
|
UTSW |
7 |
24,449,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5731:Cd177
|
UTSW |
7 |
24,443,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Cd177
|
UTSW |
7 |
24,451,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5840:Cd177
|
UTSW |
7 |
24,457,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R5870:Cd177
|
UTSW |
7 |
24,455,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5872:Cd177
|
UTSW |
7 |
24,451,688 (GRCm39) |
missense |
probably null |
1.00 |
R6148:Cd177
|
UTSW |
7 |
24,443,698 (GRCm39) |
nonsense |
probably null |
|
R6505:Cd177
|
UTSW |
7 |
24,443,671 (GRCm39) |
missense |
probably benign |
0.00 |
R6897:Cd177
|
UTSW |
7 |
24,444,499 (GRCm39) |
missense |
probably benign |
0.31 |
R7023:Cd177
|
UTSW |
7 |
24,459,187 (GRCm39) |
missense |
probably benign |
0.44 |
R7088:Cd177
|
UTSW |
7 |
24,444,558 (GRCm39) |
nonsense |
probably null |
|
R7188:Cd177
|
UTSW |
7 |
24,456,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Cd177
|
UTSW |
7 |
24,449,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R8008:Cd177
|
UTSW |
7 |
24,451,774 (GRCm39) |
missense |
not run |
|
R8029:Cd177
|
UTSW |
7 |
24,455,594 (GRCm39) |
nonsense |
probably null |
|
R8030:Cd177
|
UTSW |
7 |
24,455,594 (GRCm39) |
nonsense |
probably null |
|
R8032:Cd177
|
UTSW |
7 |
24,455,594 (GRCm39) |
nonsense |
probably null |
|
R8094:Cd177
|
UTSW |
7 |
24,443,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R8121:Cd177
|
UTSW |
7 |
24,459,067 (GRCm39) |
missense |
probably benign |
|
R8192:Cd177
|
UTSW |
7 |
24,453,727 (GRCm39) |
missense |
probably benign |
0.00 |
R8314:Cd177
|
UTSW |
7 |
24,450,013 (GRCm39) |
missense |
probably benign |
0.15 |
R8682:Cd177
|
UTSW |
7 |
24,459,438 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8730:Cd177
|
UTSW |
7 |
24,457,501 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9185:Cd177
|
UTSW |
7 |
24,443,668 (GRCm39) |
missense |
probably benign |
0.00 |
R9217:Cd177
|
UTSW |
7 |
24,445,550 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9335:Cd177
|
UTSW |
7 |
24,443,711 (GRCm39) |
missense |
probably benign |
0.04 |
R9595:Cd177
|
UTSW |
7 |
24,451,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9796:Cd177
|
UTSW |
7 |
24,459,169 (GRCm39) |
missense |
probably benign |
|
Z1176:Cd177
|
UTSW |
7 |
24,445,596 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Cd177
|
UTSW |
7 |
24,459,681 (GRCm39) |
missense |
probably damaging |
1.00 |
|