Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700102P08Rik |
A |
C |
9: 108,274,605 (GRCm39) |
D236A |
probably damaging |
Het |
Adamts7 |
C |
T |
9: 90,077,298 (GRCm39) |
P1322S |
probably damaging |
Het |
AI661453 |
A |
T |
17: 47,778,676 (GRCm39) |
T801S |
unknown |
Het |
Alpk1 |
A |
G |
3: 127,489,310 (GRCm39) |
V123A |
probably benign |
Het |
Ap2b1 |
T |
C |
11: 83,280,554 (GRCm39) |
V827A |
probably benign |
Het |
Aqp5 |
T |
A |
15: 99,492,059 (GRCm39) |
I219N |
probably benign |
Het |
Astn1 |
G |
A |
1: 158,495,105 (GRCm39) |
W1051* |
probably null |
Het |
Atp8b1 |
T |
C |
18: 64,706,376 (GRCm39) |
D211G |
possibly damaging |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
Bsn |
A |
G |
9: 107,988,189 (GRCm39) |
V2521A |
unknown |
Het |
Car7 |
T |
C |
8: 105,275,069 (GRCm39) |
V169A |
probably damaging |
Het |
Catip |
T |
A |
1: 74,408,121 (GRCm39) |
D484E |
unknown |
Het |
Ccdc18 |
T |
C |
5: 108,376,915 (GRCm39) |
|
probably null |
Het |
Cdyl |
T |
C |
13: 36,055,634 (GRCm39) |
V518A |
probably damaging |
Het |
Cep350 |
A |
T |
1: 155,754,767 (GRCm39) |
C1949* |
probably null |
Het |
Cinp |
A |
G |
12: 110,850,447 (GRCm39) |
V18A |
possibly damaging |
Het |
Clec14a |
A |
G |
12: 58,315,314 (GRCm39) |
C103R |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,256,404 (GRCm39) |
I1955V |
probably benign |
Het |
Dnah8 |
G |
C |
17: 31,004,081 (GRCm39) |
E3655Q |
probably damaging |
Het |
Dnajc11 |
T |
C |
4: 152,053,068 (GRCm39) |
I164T |
probably damaging |
Het |
Dnajc13 |
A |
T |
9: 104,039,566 (GRCm39) |
M2101K |
probably benign |
Het |
Ephb4 |
A |
G |
5: 137,370,365 (GRCm39) |
D864G |
probably damaging |
Het |
Fads2b |
T |
A |
2: 85,330,581 (GRCm39) |
H242L |
probably benign |
Het |
Fkbp5 |
T |
C |
17: 28,647,335 (GRCm39) |
T167A |
probably benign |
Het |
Foxf2 |
C |
A |
13: 31,810,087 (GRCm39) |
P9T |
unknown |
Het |
Frmpd2 |
C |
A |
14: 33,222,920 (GRCm39) |
H105N |
possibly damaging |
Het |
Gal3st3 |
C |
A |
19: 5,357,434 (GRCm39) |
R270S |
probably damaging |
Het |
Galnt13 |
A |
G |
2: 54,747,829 (GRCm39) |
I237V |
probably damaging |
Het |
Gata5 |
G |
T |
2: 179,975,790 (GRCm39) |
Q125K |
possibly damaging |
Het |
Gm10036 |
T |
A |
18: 15,966,346 (GRCm39) |
F166I |
possibly damaging |
Het |
Gon4l |
A |
G |
3: 88,802,413 (GRCm39) |
N1008S |
probably benign |
Het |
Got1l1 |
G |
A |
8: 27,687,962 (GRCm39) |
L356F |
probably damaging |
Het |
Gse1 |
A |
G |
8: 121,299,634 (GRCm39) |
E888G |
unknown |
Het |
Hmx1 |
C |
A |
5: 35,549,583 (GRCm39) |
P292Q |
possibly damaging |
Het |
Igkv7-33 |
A |
T |
6: 70,036,138 (GRCm39) |
S16T |
probably benign |
Het |
Itga2b |
C |
T |
11: 102,352,582 (GRCm39) |
G424D |
probably damaging |
Het |
Itga6 |
A |
T |
2: 71,673,577 (GRCm39) |
K870N |
probably benign |
Het |
Lama4 |
A |
T |
10: 38,968,184 (GRCm39) |
Q1442L |
probably benign |
Het |
Lamc1 |
C |
T |
1: 153,124,806 (GRCm39) |
R655H |
probably damaging |
Het |
Lclat1 |
C |
T |
17: 73,468,931 (GRCm39) |
S37L |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,013,609 (GRCm39) |
|
probably null |
Het |
Map3k20 |
T |
C |
2: 72,232,348 (GRCm39) |
S335P |
probably benign |
Het |
Micu3 |
A |
G |
8: 40,819,275 (GRCm39) |
D318G |
possibly damaging |
Het |
Mmp16 |
T |
C |
4: 18,054,382 (GRCm39) |
I296T |
probably benign |
Het |
Mmp20 |
A |
T |
9: 7,639,335 (GRCm39) |
I168L |
probably benign |
Het |
Mpp3 |
T |
C |
11: 101,916,209 (GRCm39) |
K48E |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,359,413 (GRCm39) |
D1291V |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,359,490 (GRCm39) |
T1317S |
possibly damaging |
Het |
Myl10 |
A |
T |
5: 136,729,718 (GRCm39) |
M119L |
probably benign |
Het |
Myo5b |
T |
A |
18: 74,713,467 (GRCm39) |
V104E |
probably damaging |
Het |
Nek10 |
G |
A |
14: 14,850,932 (GRCm38) |
V326M |
probably benign |
Het |
Or11l3 |
T |
A |
11: 58,515,990 (GRCm39) |
E107D |
unknown |
Het |
Or6c2 |
A |
T |
10: 129,362,551 (GRCm39) |
M152L |
probably benign |
Het |
Or6z1 |
G |
A |
7: 6,504,581 (GRCm39) |
L221F |
probably benign |
Het |
Pcnx1 |
A |
G |
12: 81,965,899 (GRCm39) |
T161A |
|
Het |
Peg10 |
T |
C |
6: 4,754,938 (GRCm39) |
S240P |
probably damaging |
Het |
Pex6 |
G |
A |
17: 47,034,943 (GRCm39) |
V822M |
probably damaging |
Het |
Pla2r1 |
T |
A |
2: 60,365,106 (GRCm39) |
T155S |
probably benign |
Het |
Pld5 |
A |
T |
1: 175,821,416 (GRCm39) |
|
probably null |
Het |
Plxna4 |
A |
G |
6: 32,473,676 (GRCm39) |
V447A |
probably damaging |
Het |
Pou2af1 |
T |
C |
9: 51,144,283 (GRCm39) |
S66P |
probably benign |
Het |
Pramel26 |
T |
C |
4: 143,536,987 (GRCm39) |
E448G |
probably damaging |
Het |
Prl2c2 |
T |
C |
13: 13,171,928 (GRCm39) |
D147G |
probably damaging |
Het |
Prune1 |
A |
G |
3: 95,162,596 (GRCm39) |
L359P |
probably damaging |
Het |
Rab4b |
A |
T |
7: 26,875,642 (GRCm39) |
V13E |
probably damaging |
Het |
Rbbp6 |
T |
G |
7: 122,575,231 (GRCm39) |
V80G |
possibly damaging |
Het |
Reep5 |
C |
T |
18: 34,482,853 (GRCm39) |
G119S |
possibly damaging |
Het |
Rem1 |
G |
C |
2: 152,476,585 (GRCm39) |
R281P |
probably damaging |
Het |
Rnf215 |
C |
T |
11: 4,089,989 (GRCm39) |
R309C |
probably damaging |
Het |
Scn4a |
C |
A |
11: 106,215,458 (GRCm39) |
V1173F |
probably damaging |
Het |
Serpine3 |
A |
T |
14: 62,910,464 (GRCm39) |
I186F |
possibly damaging |
Het |
Slc7a1 |
A |
G |
5: 148,289,046 (GRCm39) |
V67A |
probably damaging |
Het |
Smco2 |
A |
T |
6: 146,761,507 (GRCm39) |
E142V |
possibly damaging |
Het |
Spata25 |
G |
A |
2: 164,669,889 (GRCm39) |
P41S |
probably benign |
Het |
Specc1l |
A |
G |
10: 75,112,638 (GRCm39) |
D955G |
probably damaging |
Het |
Spns3 |
C |
T |
11: 72,429,860 (GRCm39) |
|
probably null |
Het |
Sptbn2 |
C |
T |
19: 4,794,235 (GRCm39) |
R1480C |
probably damaging |
Het |
Taf1a |
T |
C |
1: 183,189,253 (GRCm39) |
|
probably null |
Het |
Tas2r107 |
G |
T |
6: 131,636,563 (GRCm39) |
T162K |
possibly damaging |
Het |
Tcea1 |
T |
C |
1: 4,959,774 (GRCm39) |
S139P |
probably benign |
Het |
Tecta |
C |
T |
9: 42,242,283 (GRCm39) |
V2102I |
probably benign |
Het |
Tpbpb |
A |
G |
13: 61,049,925 (GRCm39) |
V68A |
probably benign |
Het |
Ttc27 |
A |
T |
17: 75,025,710 (GRCm39) |
N61I |
probably benign |
Het |
Ttn |
T |
C |
2: 76,580,021 (GRCm39) |
N23624S |
probably damaging |
Het |
Tut7 |
T |
C |
13: 59,947,904 (GRCm39) |
K806E |
probably benign |
Het |
Usp2 |
T |
C |
9: 43,978,519 (GRCm39) |
|
probably null |
Het |
Vmn1r10 |
A |
G |
6: 57,091,026 (GRCm39) |
H206R |
probably benign |
Het |
Vmn1r234 |
T |
C |
17: 21,449,479 (GRCm39) |
I131T |
probably damaging |
Het |
Vwf |
G |
T |
6: 125,659,697 (GRCm39) |
R2632L |
|
Het |
Wdr36 |
T |
C |
18: 32,983,578 (GRCm39) |
L443P |
probably benign |
Het |
Zfp143 |
T |
C |
7: 109,688,025 (GRCm39) |
V489A |
probably benign |
Het |
Zfp383 |
G |
A |
7: 29,614,696 (GRCm39) |
R317Q |
probably damaging |
Het |
Zswim8 |
A |
G |
14: 20,766,368 (GRCm39) |
T839A |
probably damaging |
Het |
|
Other mutations in Tmem131 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00561:Tmem131
|
APN |
1 |
36,850,508 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:Tmem131
|
APN |
1 |
36,866,086 (GRCm39) |
splice site |
probably benign |
|
IGL01107:Tmem131
|
APN |
1 |
36,868,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01401:Tmem131
|
APN |
1 |
36,838,468 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01533:Tmem131
|
APN |
1 |
36,857,803 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01701:Tmem131
|
APN |
1 |
36,847,318 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01784:Tmem131
|
APN |
1 |
36,854,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01890:Tmem131
|
APN |
1 |
36,862,237 (GRCm39) |
splice site |
probably benign |
|
IGL01969:Tmem131
|
APN |
1 |
36,864,541 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02327:Tmem131
|
APN |
1 |
36,838,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02707:Tmem131
|
APN |
1 |
36,864,560 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02743:Tmem131
|
APN |
1 |
36,832,232 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03111:Tmem131
|
APN |
1 |
36,867,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.09 |
R0063:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.09 |
R0238:Tmem131
|
UTSW |
1 |
36,867,131 (GRCm39) |
splice site |
probably benign |
|
R0239:Tmem131
|
UTSW |
1 |
36,867,131 (GRCm39) |
splice site |
probably benign |
|
R0499:Tmem131
|
UTSW |
1 |
36,880,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Tmem131
|
UTSW |
1 |
36,877,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0845:Tmem131
|
UTSW |
1 |
36,855,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R0975:Tmem131
|
UTSW |
1 |
36,893,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Tmem131
|
UTSW |
1 |
36,833,900 (GRCm39) |
missense |
probably damaging |
0.98 |
R1170:Tmem131
|
UTSW |
1 |
36,873,979 (GRCm39) |
nonsense |
probably null |
|
R1443:Tmem131
|
UTSW |
1 |
36,864,559 (GRCm39) |
missense |
probably damaging |
0.98 |
R1448:Tmem131
|
UTSW |
1 |
36,866,439 (GRCm39) |
missense |
probably benign |
0.16 |
R1472:Tmem131
|
UTSW |
1 |
36,855,322 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1530:Tmem131
|
UTSW |
1 |
36,866,090 (GRCm39) |
critical splice donor site |
probably null |
|
R1672:Tmem131
|
UTSW |
1 |
36,863,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Tmem131
|
UTSW |
1 |
36,847,008 (GRCm39) |
missense |
probably benign |
0.05 |
R1914:Tmem131
|
UTSW |
1 |
36,835,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Tmem131
|
UTSW |
1 |
36,835,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Tmem131
|
UTSW |
1 |
36,851,352 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1971:Tmem131
|
UTSW |
1 |
36,843,680 (GRCm39) |
nonsense |
probably null |
|
R2146:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2148:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2149:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2150:Tmem131
|
UTSW |
1 |
36,851,690 (GRCm39) |
missense |
probably benign |
0.13 |
R2386:Tmem131
|
UTSW |
1 |
36,868,716 (GRCm39) |
missense |
probably benign |
0.00 |
R2879:Tmem131
|
UTSW |
1 |
36,880,788 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2903:Tmem131
|
UTSW |
1 |
36,864,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Tmem131
|
UTSW |
1 |
36,847,902 (GRCm39) |
splice site |
probably benign |
|
R3821:Tmem131
|
UTSW |
1 |
36,847,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R3961:Tmem131
|
UTSW |
1 |
36,858,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R4153:Tmem131
|
UTSW |
1 |
36,847,874 (GRCm39) |
intron |
probably benign |
|
R4154:Tmem131
|
UTSW |
1 |
36,847,874 (GRCm39) |
intron |
probably benign |
|
R4502:Tmem131
|
UTSW |
1 |
36,864,560 (GRCm39) |
missense |
probably benign |
0.03 |
R4503:Tmem131
|
UTSW |
1 |
36,864,560 (GRCm39) |
missense |
probably benign |
0.03 |
R4795:Tmem131
|
UTSW |
1 |
36,880,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Tmem131
|
UTSW |
1 |
36,866,255 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5068:Tmem131
|
UTSW |
1 |
36,893,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Tmem131
|
UTSW |
1 |
36,893,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Tmem131
|
UTSW |
1 |
36,911,639 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5507:Tmem131
|
UTSW |
1 |
36,928,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R5569:Tmem131
|
UTSW |
1 |
36,838,419 (GRCm39) |
missense |
probably benign |
0.02 |
R5913:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.01 |
R6044:Tmem131
|
UTSW |
1 |
36,920,422 (GRCm39) |
nonsense |
probably null |
|
R6125:Tmem131
|
UTSW |
1 |
36,847,387 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6259:Tmem131
|
UTSW |
1 |
36,858,209 (GRCm39) |
missense |
probably benign |
0.09 |
R6392:Tmem131
|
UTSW |
1 |
36,920,423 (GRCm39) |
missense |
probably benign |
0.10 |
R6704:Tmem131
|
UTSW |
1 |
36,835,261 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6828:Tmem131
|
UTSW |
1 |
36,843,724 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6964:Tmem131
|
UTSW |
1 |
36,835,373 (GRCm39) |
missense |
probably damaging |
0.99 |
R7034:Tmem131
|
UTSW |
1 |
36,832,054 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7036:Tmem131
|
UTSW |
1 |
36,832,054 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7081:Tmem131
|
UTSW |
1 |
36,928,376 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7278:Tmem131
|
UTSW |
1 |
36,835,382 (GRCm39) |
missense |
probably damaging |
0.99 |
R7282:Tmem131
|
UTSW |
1 |
36,880,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Tmem131
|
UTSW |
1 |
36,893,928 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7916:Tmem131
|
UTSW |
1 |
36,862,167 (GRCm39) |
missense |
probably benign |
0.00 |
R7948:Tmem131
|
UTSW |
1 |
36,833,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Tmem131
|
UTSW |
1 |
36,847,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R8244:Tmem131
|
UTSW |
1 |
36,847,974 (GRCm39) |
missense |
probably benign |
0.08 |
R8461:Tmem131
|
UTSW |
1 |
36,833,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Tmem131
|
UTSW |
1 |
36,838,186 (GRCm39) |
splice site |
probably benign |
|
R8902:Tmem131
|
UTSW |
1 |
36,848,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8915:Tmem131
|
UTSW |
1 |
36,868,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R8984:Tmem131
|
UTSW |
1 |
36,867,228 (GRCm39) |
missense |
probably benign |
0.05 |
R8994:Tmem131
|
UTSW |
1 |
36,854,538 (GRCm39) |
missense |
probably benign |
0.29 |
R9105:Tmem131
|
UTSW |
1 |
36,854,591 (GRCm39) |
missense |
probably benign |
0.44 |
R9156:Tmem131
|
UTSW |
1 |
36,880,767 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9328:Tmem131
|
UTSW |
1 |
36,858,236 (GRCm39) |
nonsense |
probably null |
|
R9501:Tmem131
|
UTSW |
1 |
36,858,265 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9633:Tmem131
|
UTSW |
1 |
36,847,069 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Tmem131
|
UTSW |
1 |
36,835,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|