Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
C |
A |
10: 76,293,899 (GRCm39) |
F252L |
possibly damaging |
Het |
4930447A16Rik |
T |
G |
15: 37,440,742 (GRCm39) |
|
probably benign |
Het |
Abca14 |
A |
T |
7: 119,815,408 (GRCm39) |
M219L |
probably benign |
Het |
Abi3bp |
A |
G |
16: 56,498,159 (GRCm39) |
T918A |
probably damaging |
Het |
Acss3 |
C |
T |
10: 106,772,068 (GRCm39) |
S669N |
probably benign |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adamtsl4 |
A |
G |
3: 95,588,412 (GRCm39) |
Y559H |
probably damaging |
Het |
Adgrg5 |
T |
A |
8: 95,661,108 (GRCm39) |
M106K |
probably damaging |
Het |
Akt1 |
T |
C |
12: 112,626,059 (GRCm39) |
N71S |
probably damaging |
Het |
Amer2 |
A |
C |
14: 60,615,894 (GRCm39) |
K30Q |
probably damaging |
Het |
Anapc5 |
T |
C |
5: 122,938,587 (GRCm39) |
K383E |
probably damaging |
Het |
Ano1 |
A |
G |
7: 144,207,987 (GRCm39) |
L258P |
probably damaging |
Het |
Arb2a |
A |
G |
13: 78,147,756 (GRCm39) |
T321A |
possibly damaging |
Het |
Arhgef10l |
A |
G |
4: 140,271,695 (GRCm39) |
S560P |
probably damaging |
Het |
Arhgef40 |
T |
A |
14: 52,241,162 (GRCm39) |
L1395Q |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,409,145 (GRCm39) |
D1787E |
unknown |
Het |
Ces2h |
T |
C |
8: 105,745,030 (GRCm39) |
L388P |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,852,466 (GRCm39) |
N880I |
probably benign |
Het |
Cryz |
T |
C |
3: 154,327,320 (GRCm39) |
V116A |
probably damaging |
Het |
Csrp1 |
G |
A |
1: 135,678,366 (GRCm39) |
A159T |
probably damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,434,517 (GRCm39) |
F447S |
probably damaging |
Het |
Cyp4a12a |
A |
T |
4: 115,184,702 (GRCm39) |
I328F |
probably damaging |
Het |
Cyth4 |
T |
G |
15: 78,492,371 (GRCm39) |
H133Q |
probably damaging |
Het |
Ddah2 |
A |
G |
17: 35,279,402 (GRCm39) |
I88V |
possibly damaging |
Het |
Dmbt1 |
T |
G |
7: 130,712,718 (GRCm39) |
I1563S |
possibly damaging |
Het |
Dnajc22 |
T |
C |
15: 98,999,114 (GRCm39) |
S100P |
probably benign |
Het |
Fancl |
T |
A |
11: 26,372,459 (GRCm39) |
D123E |
probably damaging |
Het |
Fbxo30 |
A |
G |
10: 11,166,772 (GRCm39) |
Q498R |
probably damaging |
Het |
Fgd4 |
T |
C |
16: 16,253,824 (GRCm39) |
H581R |
probably benign |
Het |
Gm2663 |
T |
C |
6: 40,974,900 (GRCm39) |
Q57R |
probably benign |
Het |
Gm7247 |
A |
T |
14: 51,602,804 (GRCm39) |
M47L |
possibly damaging |
Het |
Gsdmc2 |
T |
A |
15: 63,699,975 (GRCm39) |
|
probably null |
Het |
Hc |
A |
C |
2: 34,903,540 (GRCm39) |
F1038C |
probably damaging |
Het |
Heatr1 |
C |
A |
13: 12,429,359 (GRCm39) |
Q890K |
possibly damaging |
Het |
Hipk4 |
C |
A |
7: 27,228,429 (GRCm39) |
T293K |
probably damaging |
Het |
Hp1bp3 |
C |
A |
4: 137,948,943 (GRCm39) |
A2E |
probably damaging |
Het |
Il6 |
T |
C |
5: 30,219,945 (GRCm39) |
|
probably null |
Het |
Itga6 |
A |
G |
2: 71,648,828 (GRCm39) |
D104G |
probably benign |
Het |
Krt24 |
A |
G |
11: 99,173,277 (GRCm39) |
S293P |
probably damaging |
Het |
Krt4 |
C |
T |
15: 101,829,086 (GRCm39) |
R309Q |
probably damaging |
Het |
Krt40 |
A |
T |
11: 99,430,913 (GRCm39) |
W199R |
probably damaging |
Het |
Lamc1 |
T |
C |
1: 153,118,378 (GRCm39) |
E931G |
probably benign |
Het |
Lamp3 |
A |
T |
16: 19,519,961 (GRCm39) |
M74K |
probably benign |
Het |
Lgalsl2 |
A |
G |
7: 5,362,573 (GRCm39) |
D68G |
probably benign |
Het |
Magel2 |
G |
A |
7: 62,028,844 (GRCm39) |
V583I |
unknown |
Het |
Marchf7 |
T |
A |
2: 60,059,384 (GRCm39) |
Y37* |
probably null |
Het |
Mrpl36 |
A |
G |
13: 73,479,687 (GRCm39) |
K66E |
probably damaging |
Het |
Mrps35 |
G |
T |
6: 146,962,982 (GRCm39) |
E229* |
probably null |
Het |
Mtmr6 |
T |
C |
14: 60,536,441 (GRCm39) |
M557T |
probably benign |
Het |
Myocd |
A |
T |
11: 65,077,854 (GRCm39) |
I647N |
probably damaging |
Het |
Myom2 |
A |
C |
8: 15,181,151 (GRCm39) |
L1350F |
probably damaging |
Het |
Nhsl3 |
A |
G |
4: 129,116,148 (GRCm39) |
S884P |
probably damaging |
Het |
Nosip |
T |
A |
7: 44,726,033 (GRCm39) |
S197T |
probably benign |
Het |
Npat |
A |
G |
9: 53,473,791 (GRCm39) |
K528E |
probably benign |
Het |
Nyap2 |
A |
G |
1: 81,169,587 (GRCm39) |
T115A |
probably benign |
Het |
Obi1 |
T |
A |
14: 104,759,978 (GRCm39) |
K24M |
probably damaging |
Het |
Or10al6 |
A |
G |
17: 38,083,467 (GRCm39) |
R317G |
probably benign |
Het |
Or4a72 |
A |
G |
2: 89,405,737 (GRCm39) |
V111A |
probably damaging |
Het |
Or4c109 |
G |
T |
2: 88,818,489 (GRCm39) |
P19Q |
probably benign |
Het |
Or51b6 |
T |
A |
7: 103,556,249 (GRCm39) |
V201D |
possibly damaging |
Het |
Or5m3 |
A |
T |
2: 85,838,567 (GRCm39) |
Y149F |
probably damaging |
Het |
Or8g55 |
A |
G |
9: 39,785,354 (GRCm39) |
Q261R |
probably benign |
Het |
Orc1 |
T |
C |
4: 108,447,897 (GRCm39) |
V48A |
possibly damaging |
Het |
Pde6d |
T |
C |
1: 86,474,438 (GRCm39) |
E69G |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,216,406 (GRCm39) |
D1088V |
possibly damaging |
Het |
Peg12 |
A |
G |
7: 62,113,386 (GRCm39) |
V237A |
probably benign |
Het |
Phf8-ps |
T |
C |
17: 33,285,941 (GRCm39) |
N287S |
probably benign |
Het |
Piezo1 |
A |
G |
8: 123,209,451 (GRCm39) |
F2371L |
probably benign |
Het |
Podn |
T |
A |
4: 107,880,570 (GRCm39) |
S27C |
probably damaging |
Het |
Pom121l2 |
A |
G |
13: 22,166,904 (GRCm39) |
M392V |
possibly damaging |
Het |
Ppm1b |
A |
G |
17: 85,301,630 (GRCm39) |
K170R |
probably damaging |
Het |
Rab18 |
A |
T |
18: 6,770,113 (GRCm39) |
|
probably null |
Het |
Raet1d |
G |
A |
10: 22,246,911 (GRCm39) |
A80T |
probably damaging |
Het |
Rfx7 |
T |
A |
9: 72,524,967 (GRCm39) |
V719E |
probably benign |
Het |
Ror1 |
C |
T |
4: 100,265,038 (GRCm39) |
Q171* |
probably null |
Het |
Rufy4 |
G |
A |
1: 74,180,106 (GRCm39) |
V454M |
possibly damaging |
Het |
Ryr2 |
C |
T |
13: 11,866,074 (GRCm39) |
G292D |
possibly damaging |
Het |
Ryr3 |
G |
T |
2: 112,611,410 (GRCm39) |
N2257K |
probably benign |
Het |
Saal1 |
A |
G |
7: 46,348,913 (GRCm39) |
F306S |
possibly damaging |
Het |
Sap18 |
A |
G |
14: 58,036,021 (GRCm39) |
N69S |
probably damaging |
Het |
Sar1b |
A |
T |
11: 51,670,514 (GRCm39) |
|
probably null |
Het |
Serpina3n |
G |
T |
12: 104,375,473 (GRCm39) |
V182L |
probably damaging |
Het |
Setd3 |
A |
T |
12: 108,084,513 (GRCm39) |
H279Q |
probably damaging |
Het |
Slc18a2 |
C |
A |
19: 59,264,937 (GRCm39) |
A307E |
possibly damaging |
Het |
Slc4a10 |
A |
T |
2: 62,064,725 (GRCm39) |
D193V |
probably damaging |
Het |
Spire2 |
T |
C |
8: 124,059,657 (GRCm39) |
C52R |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,121,353 (GRCm39) |
I5940F |
probably damaging |
Het |
Sytl1 |
C |
T |
4: 132,983,471 (GRCm39) |
S355N |
probably damaging |
Het |
Tarbp1 |
C |
T |
8: 127,154,853 (GRCm39) |
V1424I |
probably damaging |
Het |
Tatdn3 |
A |
T |
1: 190,781,477 (GRCm39) |
|
probably null |
Het |
Tbpl1 |
T |
A |
10: 22,583,576 (GRCm39) |
E131D |
probably damaging |
Het |
Telo2 |
A |
T |
17: 25,324,382 (GRCm39) |
M501K |
probably damaging |
Het |
Terb1 |
A |
G |
8: 105,179,331 (GRCm39) |
V619A |
probably benign |
Het |
Tmem132e |
A |
G |
11: 82,335,989 (GRCm39) |
T1024A |
probably benign |
Het |
Tmem30a |
T |
C |
9: 79,681,500 (GRCm39) |
D223G |
probably damaging |
Het |
Tmprss11d |
A |
G |
5: 86,487,413 (GRCm39) |
V19A |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,890,724 (GRCm39) |
S356G |
probably benign |
Het |
Tob2 |
T |
C |
15: 81,735,400 (GRCm39) |
K190E |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,049,433 (GRCm39) |
V1240A |
possibly damaging |
Het |
Trim13 |
T |
A |
14: 61,842,335 (GRCm39) |
C117* |
probably null |
Het |
Trpv4 |
G |
A |
5: 114,772,666 (GRCm39) |
R308C |
probably damaging |
Het |
Ttn |
C |
G |
2: 76,585,676 (GRCm39) |
D21987H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,656,418 (GRCm39) |
|
probably null |
Het |
Upp1 |
A |
T |
11: 9,083,240 (GRCm39) |
M111L |
possibly damaging |
Het |
Vmn1r206 |
A |
T |
13: 22,804,358 (GRCm39) |
V283E |
probably damaging |
Het |
Vmn2r79 |
G |
T |
7: 86,651,634 (GRCm39) |
L344F |
probably benign |
Het |
Vmn2r93 |
T |
G |
17: 18,546,324 (GRCm39) |
I732S |
probably damaging |
Het |
Vmn2r96 |
G |
T |
17: 18,804,263 (GRCm39) |
M504I |
probably benign |
Het |
Vps39 |
T |
C |
2: 120,173,708 (GRCm39) |
Y147C |
probably damaging |
Het |
Zbtb20 |
T |
A |
16: 43,398,015 (GRCm39) |
C35S |
possibly damaging |
Het |
Zfp871 |
A |
T |
17: 32,993,751 (GRCm39) |
C475S |
probably damaging |
Het |
|
Other mutations in Tnks |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Tnks
|
APN |
8 |
35,328,843 (GRCm39) |
splice site |
probably benign |
|
IGL00901:Tnks
|
APN |
8 |
35,305,549 (GRCm39) |
nonsense |
probably null |
|
IGL01448:Tnks
|
APN |
8 |
35,307,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01455:Tnks
|
APN |
8 |
35,408,054 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01962:Tnks
|
APN |
8 |
35,336,678 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Tnks
|
APN |
8 |
35,307,148 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02260:Tnks
|
APN |
8 |
35,310,137 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02454:Tnks
|
APN |
8 |
35,298,882 (GRCm39) |
unclassified |
probably benign |
|
IGL02486:Tnks
|
APN |
8 |
35,318,352 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02612:Tnks
|
APN |
8 |
35,316,453 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03179:Tnks
|
APN |
8 |
35,315,824 (GRCm39) |
missense |
probably benign |
0.38 |
IGL03404:Tnks
|
APN |
8 |
35,407,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0256:Tnks
|
UTSW |
8 |
35,328,701 (GRCm39) |
missense |
probably benign |
0.07 |
R0265:Tnks
|
UTSW |
8 |
35,307,124 (GRCm39) |
nonsense |
probably null |
|
R0334:Tnks
|
UTSW |
8 |
35,320,413 (GRCm39) |
nonsense |
probably null |
|
R0414:Tnks
|
UTSW |
8 |
35,320,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Tnks
|
UTSW |
8 |
35,320,457 (GRCm39) |
missense |
probably benign |
0.23 |
R0622:Tnks
|
UTSW |
8 |
35,407,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Tnks
|
UTSW |
8 |
35,301,757 (GRCm39) |
splice site |
probably benign |
|
R1618:Tnks
|
UTSW |
8 |
35,342,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Tnks
|
UTSW |
8 |
35,324,672 (GRCm39) |
missense |
probably benign |
0.18 |
R1919:Tnks
|
UTSW |
8 |
35,342,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Tnks
|
UTSW |
8 |
35,305,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Tnks
|
UTSW |
8 |
35,340,221 (GRCm39) |
missense |
probably benign |
0.29 |
R2198:Tnks
|
UTSW |
8 |
35,315,803 (GRCm39) |
missense |
probably benign |
|
R2925:Tnks
|
UTSW |
8 |
35,432,815 (GRCm39) |
missense |
unknown |
|
R3828:Tnks
|
UTSW |
8 |
35,340,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Tnks
|
UTSW |
8 |
35,340,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R3916:Tnks
|
UTSW |
8 |
35,320,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R3917:Tnks
|
UTSW |
8 |
35,320,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R3930:Tnks
|
UTSW |
8 |
35,407,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R4659:Tnks
|
UTSW |
8 |
35,316,465 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4760:Tnks
|
UTSW |
8 |
35,318,937 (GRCm39) |
missense |
probably benign |
0.38 |
R5091:Tnks
|
UTSW |
8 |
35,308,963 (GRCm39) |
missense |
probably benign |
0.40 |
R5419:Tnks
|
UTSW |
8 |
35,432,720 (GRCm39) |
missense |
unknown |
|
R5558:Tnks
|
UTSW |
8 |
35,432,819 (GRCm39) |
start codon destroyed |
probably null |
|
R5582:Tnks
|
UTSW |
8 |
35,408,015 (GRCm39) |
missense |
probably benign |
0.14 |
R6035:Tnks
|
UTSW |
8 |
35,385,615 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6035:Tnks
|
UTSW |
8 |
35,385,615 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6495:Tnks
|
UTSW |
8 |
35,307,120 (GRCm39) |
critical splice donor site |
probably null |
|
R6527:Tnks
|
UTSW |
8 |
35,340,247 (GRCm39) |
missense |
probably benign |
0.36 |
R6991:Tnks
|
UTSW |
8 |
35,301,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7015:Tnks
|
UTSW |
8 |
35,305,701 (GRCm39) |
missense |
probably benign |
0.04 |
R7038:Tnks
|
UTSW |
8 |
35,318,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R7057:Tnks
|
UTSW |
8 |
35,307,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R7167:Tnks
|
UTSW |
8 |
35,316,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7250:Tnks
|
UTSW |
8 |
35,318,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R7475:Tnks
|
UTSW |
8 |
35,298,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Tnks
|
UTSW |
8 |
35,328,694 (GRCm39) |
missense |
probably benign |
0.01 |
R7818:Tnks
|
UTSW |
8 |
35,340,182 (GRCm39) |
missense |
probably benign |
0.03 |
R7909:Tnks
|
UTSW |
8 |
35,407,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R7970:Tnks
|
UTSW |
8 |
35,323,080 (GRCm39) |
critical splice donor site |
probably null |
|
R8341:Tnks
|
UTSW |
8 |
35,340,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8343:Tnks
|
UTSW |
8 |
35,301,738 (GRCm39) |
missense |
probably benign |
0.03 |
R8870:Tnks
|
UTSW |
8 |
35,314,433 (GRCm39) |
critical splice donor site |
probably null |
|
R8936:Tnks
|
UTSW |
8 |
35,320,501 (GRCm39) |
nonsense |
probably null |
|
R9049:Tnks
|
UTSW |
8 |
35,308,932 (GRCm39) |
missense |
probably damaging |
0.96 |
R9080:Tnks
|
UTSW |
8 |
35,432,466 (GRCm39) |
small deletion |
probably benign |
|
R9182:Tnks
|
UTSW |
8 |
35,308,905 (GRCm39) |
critical splice donor site |
probably null |
|
R9211:Tnks
|
UTSW |
8 |
35,316,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R9425:Tnks
|
UTSW |
8 |
35,340,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9649:Tnks
|
UTSW |
8 |
35,306,089 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Tnks
|
UTSW |
8 |
35,432,299 (GRCm39) |
missense |
probably benign |
0.04 |
|