Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,667,536 (GRCm39) |
F309S |
unknown |
Het |
A630001G21Rik |
C |
T |
1: 85,646,761 (GRCm39) |
V167M |
probably damaging |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ano4 |
A |
G |
10: 88,948,697 (GRCm39) |
F138L |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,883,681 (GRCm39) |
V519A |
possibly damaging |
Het |
Arhgef37 |
A |
T |
18: 61,631,310 (GRCm39) |
Y558* |
probably null |
Het |
Atxn3 |
T |
A |
12: 101,914,638 (GRCm39) |
S29C |
probably damaging |
Het |
Bbs2 |
T |
C |
8: 94,796,788 (GRCm39) |
|
probably benign |
Het |
Bicral |
A |
T |
17: 47,136,502 (GRCm39) |
I236N |
probably damaging |
Het |
Cabcoco1 |
A |
G |
10: 68,377,599 (GRCm39) |
V30A |
probably benign |
Het |
Cap2 |
A |
G |
13: 46,684,497 (GRCm39) |
M1V |
probably null |
Het |
Ccdc153 |
T |
C |
9: 44,152,305 (GRCm39) |
M1T |
probably null |
Het |
Ccnf |
A |
T |
17: 24,449,311 (GRCm39) |
V489D |
probably damaging |
Het |
Cdin1 |
A |
C |
2: 115,500,539 (GRCm39) |
H159P |
probably damaging |
Het |
Cntnap3 |
T |
C |
13: 64,935,520 (GRCm39) |
T448A |
probably benign |
Het |
Cpa4 |
G |
A |
6: 30,590,814 (GRCm39) |
D371N |
probably benign |
Het |
Csl |
T |
A |
10: 99,594,402 (GRCm39) |
Y221F |
possibly damaging |
Het |
Dalrd3 |
T |
C |
9: 108,448,635 (GRCm39) |
|
probably benign |
Het |
Dennd4a |
T |
A |
9: 64,803,872 (GRCm39) |
N1070K |
probably benign |
Het |
Dipk2a |
C |
T |
9: 94,419,630 (GRCm39) |
R100H |
probably damaging |
Het |
Dmwd |
A |
T |
7: 18,814,472 (GRCm39) |
D374V |
probably damaging |
Het |
Eea1 |
G |
T |
10: 95,831,475 (GRCm39) |
A189S |
probably benign |
Het |
Fasn |
A |
G |
11: 120,703,138 (GRCm39) |
V1629A |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,842,225 (GRCm39) |
|
probably benign |
Het |
Fndc1 |
T |
C |
17: 7,990,471 (GRCm39) |
D1075G |
unknown |
Het |
Fsip2 |
A |
G |
2: 82,805,202 (GRCm39) |
N507S |
possibly damaging |
Het |
Gabra5 |
T |
G |
7: 57,063,413 (GRCm39) |
E337A |
probably damaging |
Het |
Gsg1l |
A |
G |
7: 125,490,841 (GRCm39) |
Y288H |
probably benign |
Het |
H2-M11 |
A |
T |
17: 36,858,401 (GRCm39) |
D65V |
probably benign |
Het |
Hmgxb3 |
A |
T |
18: 61,279,606 (GRCm39) |
C736S |
possibly damaging |
Het |
Hsd3b3 |
A |
T |
3: 98,649,960 (GRCm39) |
I121N |
probably damaging |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Itpr1 |
G |
A |
6: 108,459,867 (GRCm39) |
A2054T |
probably damaging |
Het |
Lamp3 |
T |
A |
16: 19,474,220 (GRCm39) |
I385F |
probably damaging |
Het |
Limch1 |
G |
A |
5: 67,039,270 (GRCm39) |
V66I |
possibly damaging |
Het |
Lmod2 |
A |
G |
6: 24,604,278 (GRCm39) |
R418G |
probably benign |
Het |
Ly6g6c |
A |
T |
17: 35,288,416 (GRCm39) |
D96V |
probably damaging |
Het |
Map2k2 |
G |
A |
10: 80,950,947 (GRCm39) |
V131M |
probably damaging |
Het |
Mapk9 |
T |
C |
11: 49,745,152 (GRCm39) |
V22A |
probably damaging |
Het |
Mettl2 |
T |
C |
11: 105,019,894 (GRCm39) |
I177T |
probably damaging |
Het |
Mob4 |
C |
T |
1: 55,191,995 (GRCm39) |
|
probably benign |
Het |
Mybpc1 |
A |
T |
10: 88,372,286 (GRCm39) |
N781K |
probably benign |
Het |
Mybpc1 |
T |
C |
10: 88,358,853 (GRCm39) |
I1113V |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,384,405 (GRCm39) |
T707A |
probably damaging |
Het |
Ncam2 |
G |
A |
16: 81,287,234 (GRCm39) |
A383T |
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,715,915 (GRCm39) |
S761P |
probably damaging |
Het |
Nsd3 |
T |
A |
8: 26,181,161 (GRCm39) |
S921T |
possibly damaging |
Het |
Omp |
A |
T |
7: 97,794,233 (GRCm39) |
D131E |
probably benign |
Het |
Or10d1c |
A |
T |
9: 38,893,922 (GRCm39) |
C139* |
probably null |
Het |
Or4f7d-ps1 |
C |
G |
2: 111,675,040 (GRCm39) |
|
noncoding transcript |
Het |
Or8d4 |
C |
T |
9: 40,038,514 (GRCm39) |
V248I |
probably damaging |
Het |
Pard3 |
T |
C |
8: 128,287,950 (GRCm39) |
|
probably benign |
Het |
Parg |
A |
G |
14: 31,993,625 (GRCm39) |
T286A |
probably damaging |
Het |
Parp1 |
T |
A |
1: 180,396,600 (GRCm39) |
M1K |
probably null |
Het |
Pclo |
T |
A |
5: 14,861,694 (GRCm39) |
S4882R |
unknown |
Het |
Pcnx2 |
C |
T |
8: 126,498,847 (GRCm39) |
E1551K |
probably damaging |
Het |
Pcyox1l |
A |
G |
18: 61,832,565 (GRCm39) |
Y161H |
probably damaging |
Het |
Pdzd8 |
A |
T |
19: 59,289,236 (GRCm39) |
C721* |
probably null |
Het |
Piwil4 |
T |
C |
9: 14,651,761 (GRCm39) |
D90G |
probably benign |
Het |
Plxdc2 |
T |
A |
2: 16,708,129 (GRCm39) |
C306S |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,326,083 (GRCm39) |
F6I |
probably benign |
Het |
Prkaa1 |
T |
C |
15: 5,203,886 (GRCm39) |
M265T |
probably benign |
Het |
Prrc2b |
T |
C |
2: 32,104,212 (GRCm39) |
V1230A |
probably benign |
Het |
Rfx2 |
T |
C |
17: 57,091,706 (GRCm39) |
E329G |
probably benign |
Het |
Scg2 |
T |
C |
1: 79,413,636 (GRCm39) |
I322M |
probably damaging |
Het |
Scly |
T |
A |
1: 91,247,850 (GRCm39) |
N399K |
probably damaging |
Het |
Sec23b |
T |
A |
2: 144,428,281 (GRCm39) |
|
probably null |
Het |
Sephs2 |
A |
T |
7: 126,872,219 (GRCm39) |
Y291* |
probably null |
Het |
Slc45a3 |
T |
C |
1: 131,909,285 (GRCm39) |
I494T |
possibly damaging |
Het |
Slc6a21 |
C |
A |
7: 44,929,535 (GRCm39) |
Y76* |
probably null |
Het |
Slfn14 |
T |
A |
11: 83,167,098 (GRCm39) |
I806L |
possibly damaging |
Het |
Slfn4 |
T |
A |
11: 83,077,844 (GRCm39) |
S211T |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,071,577 (GRCm39) |
V1624A |
probably damaging |
Het |
Sugp1 |
T |
A |
8: 70,523,834 (GRCm39) |
M567K |
probably damaging |
Het |
Tmem121 |
A |
T |
12: 113,152,348 (GRCm39) |
M189L |
probably benign |
Het |
Tmem201 |
A |
G |
4: 149,806,727 (GRCm39) |
S444P |
probably damaging |
Het |
Tmem63a |
T |
C |
1: 180,800,751 (GRCm39) |
V744A |
probably benign |
Het |
Tnrc18 |
G |
A |
5: 142,717,380 (GRCm39) |
S2358F |
unknown |
Het |
Ubash3b |
A |
G |
9: 40,929,405 (GRCm39) |
V404A |
probably benign |
Het |
Unc13c |
A |
T |
9: 73,656,821 (GRCm39) |
C1127S |
probably damaging |
Het |
Unc5a |
T |
C |
13: 55,145,042 (GRCm39) |
V253A |
probably benign |
Het |
Vmn1r-ps123 |
C |
T |
13: 23,180,535 (GRCm39) |
|
noncoding transcript |
Het |
Wdr74 |
A |
G |
19: 8,716,849 (GRCm39) |
E253G |
possibly damaging |
Het |
Wwox |
T |
C |
8: 115,174,988 (GRCm39) |
Y107H |
probably damaging |
Het |
Zdhhc22 |
A |
T |
12: 87,035,012 (GRCm39) |
Y147N |
probably damaging |
Het |
Zfp131 |
T |
C |
13: 120,250,491 (GRCm39) |
H44R |
possibly damaging |
Het |
Zfp235 |
A |
G |
7: 23,840,384 (GRCm39) |
T268A |
probably benign |
Het |
Zfp280d |
T |
C |
9: 72,206,140 (GRCm39) |
|
probably benign |
Het |
Zfp358 |
T |
C |
8: 3,546,170 (GRCm39) |
S251P |
probably damaging |
Het |
|
Other mutations in Il16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Il16
|
APN |
7 |
83,301,666 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01743:Il16
|
APN |
7 |
83,301,507 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01770:Il16
|
APN |
7 |
83,322,234 (GRCm39) |
splice site |
probably benign |
|
IGL02025:Il16
|
APN |
7 |
83,302,056 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02317:Il16
|
APN |
7 |
83,316,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02412:Il16
|
APN |
7 |
83,301,899 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02550:Il16
|
APN |
7 |
83,323,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02568:Il16
|
APN |
7 |
83,310,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02578:Il16
|
APN |
7 |
83,327,194 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02815:Il16
|
APN |
7 |
83,300,249 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03157:Il16
|
APN |
7 |
83,371,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03161:Il16
|
APN |
7 |
83,371,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03188:Il16
|
APN |
7 |
83,337,371 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03213:Il16
|
APN |
7 |
83,295,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03274:Il16
|
APN |
7 |
83,310,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Il16
|
UTSW |
7 |
83,371,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R0309:Il16
|
UTSW |
7 |
83,371,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Il16
|
UTSW |
7 |
83,327,183 (GRCm39) |
splice site |
probably benign |
|
R0942:Il16
|
UTSW |
7 |
83,312,349 (GRCm39) |
missense |
probably benign |
0.01 |
R1018:Il16
|
UTSW |
7 |
83,323,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Il16
|
UTSW |
7 |
83,304,520 (GRCm39) |
missense |
probably benign |
|
R1715:Il16
|
UTSW |
7 |
83,297,936 (GRCm39) |
missense |
probably benign |
0.01 |
R2179:Il16
|
UTSW |
7 |
83,337,287 (GRCm39) |
splice site |
probably null |
|
R2520:Il16
|
UTSW |
7 |
83,301,202 (GRCm39) |
missense |
probably benign |
0.03 |
R3425:Il16
|
UTSW |
7 |
83,293,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R3761:Il16
|
UTSW |
7 |
83,300,093 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3943:Il16
|
UTSW |
7 |
83,301,223 (GRCm39) |
missense |
probably damaging |
0.97 |
R4470:Il16
|
UTSW |
7 |
83,300,046 (GRCm39) |
intron |
probably benign |
|
R4530:Il16
|
UTSW |
7 |
83,330,518 (GRCm39) |
intron |
probably benign |
|
R4583:Il16
|
UTSW |
7 |
83,332,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Il16
|
UTSW |
7 |
83,300,104 (GRCm39) |
missense |
probably benign |
0.14 |
R4874:Il16
|
UTSW |
7 |
83,310,153 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5677:Il16
|
UTSW |
7 |
83,323,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Il16
|
UTSW |
7 |
83,297,936 (GRCm39) |
missense |
probably benign |
0.36 |
R5920:Il16
|
UTSW |
7 |
83,301,552 (GRCm39) |
missense |
probably benign |
0.03 |
R6115:Il16
|
UTSW |
7 |
83,301,775 (GRCm39) |
nonsense |
probably null |
|
R6459:Il16
|
UTSW |
7 |
83,371,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6459:Il16
|
UTSW |
7 |
83,371,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Il16
|
UTSW |
7 |
83,371,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6616:Il16
|
UTSW |
7 |
83,295,684 (GRCm39) |
missense |
probably benign |
0.37 |
R6642:Il16
|
UTSW |
7 |
83,337,335 (GRCm39) |
missense |
probably benign |
0.03 |
R6721:Il16
|
UTSW |
7 |
83,312,270 (GRCm39) |
critical splice donor site |
probably null |
|
R7009:Il16
|
UTSW |
7 |
83,295,596 (GRCm39) |
missense |
probably benign |
|
R7144:Il16
|
UTSW |
7 |
83,295,659 (GRCm39) |
missense |
probably damaging |
0.97 |
R7346:Il16
|
UTSW |
7 |
83,293,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7403:Il16
|
UTSW |
7 |
83,319,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7499:Il16
|
UTSW |
7 |
83,323,702 (GRCm39) |
missense |
probably damaging |
0.99 |
R7814:Il16
|
UTSW |
7 |
83,319,348 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7941:Il16
|
UTSW |
7 |
83,332,037 (GRCm39) |
missense |
probably damaging |
0.98 |
R8098:Il16
|
UTSW |
7 |
83,295,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R8317:Il16
|
UTSW |
7 |
83,304,538 (GRCm39) |
missense |
probably benign |
|
R8437:Il16
|
UTSW |
7 |
83,301,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R9094:Il16
|
UTSW |
7 |
83,301,559 (GRCm39) |
missense |
probably benign |
|
R9267:Il16
|
UTSW |
7 |
83,371,757 (GRCm39) |
missense |
probably benign |
0.01 |
R9445:Il16
|
UTSW |
7 |
83,337,380 (GRCm39) |
nonsense |
probably null |
|
R9595:Il16
|
UTSW |
7 |
83,322,273 (GRCm39) |
nonsense |
probably null |
|
R9651:Il16
|
UTSW |
7 |
83,332,064 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Il16
|
UTSW |
7 |
83,302,035 (GRCm39) |
missense |
probably benign |
0.05 |
|