Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
C |
9: 53,336,971 (GRCm39) |
T92P |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,243,810 (GRCm39) |
V1891A |
probably benign |
Het |
Abcc1 |
T |
A |
16: 14,228,791 (GRCm39) |
I346N |
probably damaging |
Het |
Afdn |
G |
T |
17: 14,105,770 (GRCm39) |
|
probably null |
Het |
Ahrr |
G |
A |
13: 74,431,143 (GRCm39) |
|
probably benign |
Het |
Akap13 |
A |
G |
7: 75,264,678 (GRCm39) |
D507G |
probably damaging |
Het |
Akap8 |
A |
T |
17: 32,535,234 (GRCm39) |
M260K |
possibly damaging |
Het |
Akr1b8 |
T |
C |
6: 34,342,194 (GRCm39) |
V265A |
probably benign |
Het |
Alpk3 |
C |
G |
7: 80,728,358 (GRCm39) |
P496R |
possibly damaging |
Het |
Ankrd13b |
A |
G |
11: 77,363,571 (GRCm39) |
V249A |
possibly damaging |
Het |
Arid4a |
T |
C |
12: 71,122,604 (GRCm39) |
V995A |
probably benign |
Het |
Ascc3 |
G |
T |
10: 50,625,022 (GRCm39) |
V1637L |
probably benign |
Het |
Atad2 |
G |
A |
15: 57,977,653 (GRCm39) |
A499V |
probably damaging |
Het |
Barhl2 |
G |
T |
5: 106,605,253 (GRCm39) |
A152E |
possibly damaging |
Het |
Bbs12 |
T |
A |
3: 37,375,194 (GRCm39) |
D547E |
probably damaging |
Het |
Btaf1 |
A |
G |
19: 36,981,934 (GRCm39) |
M1655V |
probably damaging |
Het |
Ccdc50 |
T |
A |
16: 27,225,408 (GRCm39) |
H40Q |
probably damaging |
Het |
Cdh15 |
A |
G |
8: 123,592,175 (GRCm39) |
D654G |
probably damaging |
Het |
Cebpz |
T |
C |
17: 79,233,553 (GRCm39) |
D758G |
probably damaging |
Het |
Cgn |
C |
T |
3: 94,672,960 (GRCm39) |
R906K |
possibly damaging |
Het |
Chil3 |
T |
A |
3: 106,067,839 (GRCm39) |
M109L |
possibly damaging |
Het |
Cntnap4 |
A |
T |
8: 113,569,148 (GRCm39) |
|
probably null |
Het |
Cyp4f18 |
C |
T |
8: 72,754,856 (GRCm39) |
|
probably benign |
Het |
Daam2 |
A |
G |
17: 49,770,952 (GRCm39) |
|
probably null |
Het |
Ddost |
T |
A |
4: 138,037,922 (GRCm39) |
H220Q |
probably benign |
Het |
Dennd2a |
C |
T |
6: 39,441,135 (GRCm39) |
|
probably benign |
Het |
Depdc1b |
G |
A |
13: 108,510,375 (GRCm39) |
V296I |
possibly damaging |
Het |
Dnaaf4 |
A |
T |
9: 72,879,618 (GRCm39) |
D386V |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,299,256 (GRCm39) |
R1539S |
probably benign |
Het |
Dusp22 |
T |
C |
13: 30,889,641 (GRCm39) |
I74T |
probably damaging |
Het |
Epc1 |
A |
G |
18: 6,440,202 (GRCm39) |
|
probably benign |
Het |
Epha7 |
A |
G |
4: 28,961,301 (GRCm39) |
I845V |
probably benign |
Het |
Fanci |
C |
T |
7: 79,057,165 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
T |
A |
2: 125,205,564 (GRCm39) |
E1104V |
probably damaging |
Het |
Fbxo8 |
T |
A |
8: 57,043,132 (GRCm39) |
F205L |
probably damaging |
Het |
Fcgbpl1 |
G |
T |
7: 27,841,699 (GRCm39) |
V545L |
probably benign |
Het |
Fetub |
T |
C |
16: 22,748,506 (GRCm39) |
|
probably benign |
Het |
Frs3 |
T |
C |
17: 48,014,747 (GRCm39) |
V480A |
probably benign |
Het |
Gne |
C |
A |
4: 44,060,157 (GRCm39) |
E79* |
probably null |
Het |
Hrc |
T |
A |
7: 44,985,921 (GRCm39) |
H357Q |
probably benign |
Het |
Idh1 |
T |
C |
1: 65,201,079 (GRCm39) |
M291V |
probably damaging |
Het |
Il22b |
T |
A |
10: 118,129,090 (GRCm39) |
H133L |
probably benign |
Het |
Ino80b |
T |
C |
6: 83,101,072 (GRCm39) |
E165G |
probably damaging |
Het |
Inppl1 |
A |
T |
7: 101,477,706 (GRCm39) |
|
probably benign |
Het |
Ints15 |
G |
T |
5: 143,293,643 (GRCm39) |
T278K |
probably benign |
Het |
Ip6k2 |
T |
C |
9: 108,676,432 (GRCm39) |
|
probably benign |
Het |
Itga11 |
A |
T |
9: 62,667,628 (GRCm39) |
I654F |
probably damaging |
Het |
Jag2 |
G |
T |
12: 112,876,997 (GRCm39) |
|
probably benign |
Het |
Katna1 |
G |
T |
10: 7,619,513 (GRCm39) |
|
probably benign |
Het |
Kcnh4 |
G |
T |
11: 100,636,995 (GRCm39) |
S707Y |
probably benign |
Het |
Kcnn2 |
T |
G |
18: 45,693,585 (GRCm39) |
L387R |
probably damaging |
Het |
Khnyn |
A |
G |
14: 56,125,425 (GRCm39) |
T503A |
probably damaging |
Het |
Lama5 |
G |
T |
2: 179,823,359 (GRCm39) |
|
probably benign |
Het |
Lmbr1l |
A |
T |
15: 98,806,654 (GRCm39) |
|
probably benign |
Het |
Mast4 |
A |
T |
13: 102,890,669 (GRCm39) |
S870T |
possibly damaging |
Het |
Med1 |
A |
G |
11: 98,058,400 (GRCm39) |
Y266H |
probably benign |
Het |
Med13 |
A |
T |
11: 86,236,829 (GRCm39) |
N109K |
probably benign |
Het |
Mgam |
T |
C |
6: 40,737,969 (GRCm39) |
|
probably benign |
Het |
Mmp8 |
A |
G |
9: 7,561,455 (GRCm39) |
Q153R |
probably benign |
Het |
Mpeg1 |
C |
A |
19: 12,439,055 (GRCm39) |
T171N |
probably benign |
Het |
Mtus2 |
T |
C |
5: 148,043,829 (GRCm39) |
S806P |
probably benign |
Het |
Naip2 |
T |
A |
13: 100,285,350 (GRCm39) |
E1226V |
probably damaging |
Het |
Naip6 |
A |
G |
13: 100,444,721 (GRCm39) |
F246L |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,602,989 (GRCm39) |
I1187V |
possibly damaging |
Het |
Nbeal1 |
T |
C |
1: 60,344,529 (GRCm39) |
|
probably benign |
Het |
Nbeal2 |
C |
A |
9: 110,467,231 (GRCm39) |
V653L |
probably damaging |
Het |
Ndufa9 |
G |
T |
6: 126,804,495 (GRCm39) |
|
probably benign |
Het |
Nlrp5 |
G |
T |
7: 23,129,582 (GRCm39) |
C883F |
probably damaging |
Het |
Nr0b2 |
C |
A |
4: 133,283,303 (GRCm39) |
|
probably null |
Het |
Or1m1 |
T |
A |
9: 18,666,629 (GRCm39) |
M101L |
possibly damaging |
Het |
Or6c209 |
T |
A |
10: 129,483,600 (GRCm39) |
V201E |
probably damaging |
Het |
Or6c69c |
G |
A |
10: 129,910,692 (GRCm39) |
V138I |
probably benign |
Het |
Or8b101 |
T |
A |
9: 38,020,782 (GRCm39) |
S267T |
possibly damaging |
Het |
Pkhd1 |
A |
T |
1: 20,620,046 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
A |
G |
15: 44,386,134 (GRCm39) |
|
probably benign |
Het |
Ppm1l |
A |
G |
3: 69,456,794 (GRCm39) |
K237R |
probably benign |
Het |
Ppp1r18 |
T |
C |
17: 36,184,603 (GRCm39) |
|
probably benign |
Het |
Ptpn3 |
A |
T |
4: 57,204,958 (GRCm39) |
D734E |
probably benign |
Het |
Pxdn |
T |
C |
12: 30,065,528 (GRCm39) |
C1283R |
probably damaging |
Het |
Rbm12 |
A |
G |
2: 155,937,644 (GRCm39) |
|
probably benign |
Het |
Rttn |
A |
T |
18: 89,027,584 (GRCm39) |
|
probably benign |
Het |
Sgsm1 |
G |
T |
5: 113,411,571 (GRCm39) |
H431Q |
probably benign |
Het |
Siah3 |
A |
G |
14: 75,763,367 (GRCm39) |
N206S |
possibly damaging |
Het |
Slc22a15 |
G |
T |
3: 101,767,827 (GRCm39) |
D521E |
probably benign |
Het |
Sprr2k |
A |
T |
3: 92,340,770 (GRCm39) |
|
probably benign |
Het |
Stab2 |
G |
A |
10: 86,803,477 (GRCm39) |
|
probably benign |
Het |
Sval3 |
T |
A |
6: 41,945,120 (GRCm39) |
L16Q |
probably damaging |
Het |
Sycp2 |
C |
G |
2: 178,023,648 (GRCm39) |
S456T |
probably benign |
Het |
Tk1 |
T |
C |
11: 117,707,921 (GRCm39) |
|
probably benign |
Het |
Tlk2 |
C |
A |
11: 105,145,799 (GRCm39) |
A335E |
probably benign |
Het |
Tmtc1 |
T |
C |
6: 148,151,079 (GRCm39) |
K659E |
probably benign |
Het |
Tnk2 |
C |
T |
16: 32,499,408 (GRCm39) |
P907L |
probably benign |
Het |
Trim14 |
C |
A |
4: 46,522,043 (GRCm39) |
K211N |
probably damaging |
Het |
Trim15 |
A |
C |
17: 37,177,878 (GRCm39) |
L39R |
probably damaging |
Het |
Tspan15 |
T |
A |
10: 62,023,872 (GRCm39) |
T269S |
probably benign |
Het |
Ttc7 |
T |
A |
17: 87,669,292 (GRCm39) |
D646E |
probably benign |
Het |
Ttll6 |
A |
T |
11: 96,038,382 (GRCm39) |
Q410L |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,027,666 (GRCm39) |
Q419R |
probably damaging |
Het |
Vcam1 |
A |
T |
3: 115,908,065 (GRCm39) |
Y666N |
possibly damaging |
Het |
Vmn1r10 |
A |
T |
6: 57,090,486 (GRCm39) |
Y26F |
probably damaging |
Het |
Vmn1r80 |
A |
G |
7: 11,927,775 (GRCm39) |
N295S |
probably benign |
Het |
Vmn2r114 |
A |
T |
17: 23,509,917 (GRCm39) |
H854Q |
probably benign |
Het |
Vmn2r2 |
A |
T |
3: 64,042,039 (GRCm39) |
D225E |
probably damaging |
Het |
Vmn2r4 |
A |
T |
3: 64,296,855 (GRCm39) |
Y643* |
probably null |
Het |
Vmn2r52 |
T |
A |
7: 9,893,393 (GRCm39) |
Y582F |
probably damaging |
Het |
Vmn2r60 |
G |
T |
7: 41,844,564 (GRCm39) |
L642F |
possibly damaging |
Het |
Zbtb20 |
T |
C |
16: 43,430,109 (GRCm39) |
S207P |
probably damaging |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
Zkscan7 |
G |
T |
9: 122,717,958 (GRCm39) |
E118* |
probably null |
Het |
|
Other mutations in Ccr9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Ccr9
|
APN |
9 |
123,609,109 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00983:Ccr9
|
APN |
9 |
123,608,351 (GRCm39) |
missense |
probably benign |
|
IGL02466:Ccr9
|
APN |
9 |
123,608,911 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03151:Ccr9
|
APN |
9 |
123,603,638 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03302:Ccr9
|
APN |
9 |
123,608,601 (GRCm39) |
missense |
probably damaging |
1.00 |
hamlet
|
UTSW |
9 |
123,608,504 (GRCm39) |
missense |
probably damaging |
1.00 |
Laertes
|
UTSW |
9 |
123,608,911 (GRCm39) |
missense |
probably damaging |
1.00 |
Ophelia
|
UTSW |
9 |
123,608,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Ccr9
|
UTSW |
9 |
123,609,035 (GRCm39) |
missense |
probably benign |
0.18 |
R0421:Ccr9
|
UTSW |
9 |
123,608,671 (GRCm39) |
missense |
probably benign |
|
R2069:Ccr9
|
UTSW |
9 |
123,608,429 (GRCm39) |
missense |
probably benign |
0.05 |
R3980:Ccr9
|
UTSW |
9 |
123,608,441 (GRCm39) |
missense |
probably benign |
0.14 |
R4645:Ccr9
|
UTSW |
9 |
123,608,658 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Ccr9
|
UTSW |
9 |
123,608,752 (GRCm39) |
missense |
probably damaging |
0.96 |
R4920:Ccr9
|
UTSW |
9 |
123,608,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5661:Ccr9
|
UTSW |
9 |
123,609,164 (GRCm39) |
missense |
probably benign |
0.04 |
R5964:Ccr9
|
UTSW |
9 |
123,608,499 (GRCm39) |
missense |
probably benign |
0.12 |
R7037:Ccr9
|
UTSW |
9 |
123,609,036 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7500:Ccr9
|
UTSW |
9 |
123,608,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7620:Ccr9
|
UTSW |
9 |
123,608,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R7670:Ccr9
|
UTSW |
9 |
123,608,371 (GRCm39) |
missense |
probably damaging |
0.98 |
R7762:Ccr9
|
UTSW |
9 |
123,609,022 (GRCm39) |
missense |
probably benign |
0.08 |
R8154:Ccr9
|
UTSW |
9 |
123,608,896 (GRCm39) |
missense |
probably benign |
0.00 |
R8283:Ccr9
|
UTSW |
9 |
123,608,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8525:Ccr9
|
UTSW |
9 |
123,608,732 (GRCm39) |
missense |
probably benign |
0.31 |
R9046:Ccr9
|
UTSW |
9 |
123,608,831 (GRCm39) |
missense |
probably benign |
|
R9273:Ccr9
|
UTSW |
9 |
123,609,085 (GRCm39) |
missense |
probably benign |
0.07 |
R9462:Ccr9
|
UTSW |
9 |
123,608,600 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Ccr9
|
UTSW |
9 |
123,608,566 (GRCm39) |
missense |
probably damaging |
1.00 |
|