Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110082J24Rik |
G |
A |
5: 30,310,198 (GRCm39) |
R54* |
probably null |
Het |
Acsl6 |
A |
T |
11: 54,227,819 (GRCm39) |
M350L |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,243,564 (GRCm39) |
T6279A |
probably damaging |
Het |
Ago3 |
A |
T |
4: 126,262,296 (GRCm39) |
M418K |
probably benign |
Het |
Ascc2 |
G |
A |
11: 4,596,653 (GRCm39) |
R58H |
probably benign |
Het |
Brinp3 |
A |
G |
1: 146,603,378 (GRCm39) |
|
probably benign |
Het |
Carmil3 |
T |
C |
14: 55,738,778 (GRCm39) |
|
probably null |
Het |
Ccdc47 |
T |
A |
11: 106,094,430 (GRCm39) |
H7L |
probably benign |
Het |
Ccndbp1 |
A |
T |
2: 120,839,003 (GRCm39) |
T5S |
probably benign |
Het |
Cdr2 |
A |
T |
7: 120,557,644 (GRCm39) |
F294I |
probably benign |
Het |
Chd8 |
C |
A |
14: 52,442,825 (GRCm39) |
C575F |
probably damaging |
Het |
Ctsll3 |
G |
A |
13: 60,948,209 (GRCm39) |
T156I |
probably damaging |
Het |
Dgcr8 |
G |
A |
16: 18,076,174 (GRCm39) |
R4* |
probably null |
Het |
Dnah1 |
T |
A |
14: 30,985,436 (GRCm39) |
K3818N |
probably damaging |
Het |
Dok2 |
C |
T |
14: 71,015,314 (GRCm39) |
P347L |
probably benign |
Het |
Elf1 |
T |
A |
14: 79,818,183 (GRCm39) |
N567K |
probably benign |
Het |
Emsy |
T |
C |
7: 98,295,686 (GRCm39) |
N72S |
possibly damaging |
Het |
Fam76a |
A |
G |
4: 132,643,501 (GRCm39) |
Y78H |
probably damaging |
Het |
Fam76a |
A |
T |
4: 132,629,428 (GRCm39) |
|
probably null |
Het |
Fbn1 |
A |
T |
2: 125,166,839 (GRCm39) |
C2026S |
probably damaging |
Het |
Fbxo4 |
T |
C |
15: 3,998,523 (GRCm39) |
T312A |
probably benign |
Het |
Fhip1a |
G |
T |
3: 85,595,877 (GRCm39) |
T115K |
probably damaging |
Het |
Flnb |
A |
T |
14: 7,905,701 (GRCm38) |
E1150D |
probably benign |
Het |
Galt |
T |
C |
4: 41,758,189 (GRCm39) |
V318A |
probably damaging |
Het |
Git1 |
T |
G |
11: 77,390,663 (GRCm39) |
L133R |
probably damaging |
Het |
Gm11168 |
G |
A |
9: 3,006,915 (GRCm39) |
M213I |
probably benign |
Het |
Gm7233 |
A |
G |
14: 43,037,423 (GRCm39) |
E25G |
probably benign |
Het |
Golga2 |
T |
A |
2: 32,187,168 (GRCm39) |
N89K |
probably damaging |
Het |
Grin1 |
T |
A |
2: 25,182,393 (GRCm39) |
H956L |
possibly damaging |
Het |
Hlcs |
C |
T |
16: 94,069,398 (GRCm39) |
V164I |
possibly damaging |
Het |
Hmgcr |
G |
A |
13: 96,802,701 (GRCm39) |
T66M |
probably damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,432 (GRCm39) |
H521Q |
probably benign |
Het |
Lgals3bp |
G |
A |
11: 118,284,340 (GRCm39) |
T413I |
probably damaging |
Het |
Lrrc7 |
A |
G |
3: 157,832,850 (GRCm39) |
|
probably null |
Het |
Mapk11 |
T |
C |
15: 89,033,691 (GRCm39) |
Y9C |
probably damaging |
Het |
Mccc1 |
C |
A |
3: 36,030,022 (GRCm39) |
M429I |
probably damaging |
Het |
Metrnl |
A |
G |
11: 121,598,750 (GRCm39) |
E40G |
probably benign |
Het |
Mrgpra1 |
A |
G |
7: 46,985,218 (GRCm39) |
S154P |
probably damaging |
Het |
Myh13 |
A |
T |
11: 67,232,096 (GRCm39) |
I459F |
probably damaging |
Het |
Nalf1 |
T |
C |
8: 9,258,026 (GRCm39) |
Y374C |
probably damaging |
Het |
Nedd4l |
C |
A |
18: 65,305,998 (GRCm39) |
D424E |
probably damaging |
Het |
Nid1 |
C |
T |
13: 13,674,326 (GRCm39) |
R902W |
probably damaging |
Het |
Nphp4 |
G |
A |
4: 152,639,003 (GRCm39) |
R878K |
probably benign |
Het |
Numa1 |
A |
G |
7: 101,662,773 (GRCm39) |
T1997A |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,079,281 (GRCm39) |
A878V |
probably benign |
Het |
Nxf1 |
G |
A |
19: 8,744,162 (GRCm39) |
A339T |
probably benign |
Het |
Oas1b |
C |
A |
5: 120,952,578 (GRCm39) |
Q90K |
probably benign |
Het |
Optn |
T |
C |
2: 5,059,438 (GRCm39) |
M27V |
probably benign |
Het |
Or1r1 |
A |
G |
11: 73,874,834 (GRCm39) |
F200S |
probably damaging |
Het |
Or2t35 |
A |
C |
14: 14,407,729 (GRCm38) |
Y167S |
possibly damaging |
Het |
Or4f56 |
A |
T |
2: 111,703,395 (GRCm39) |
D268E |
possibly damaging |
Het |
Or5ac17 |
G |
T |
16: 59,036,222 (GRCm39) |
F251L |
probably damaging |
Het |
Or5d45 |
A |
G |
2: 88,153,500 (GRCm39) |
I183T |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,282 (GRCm39) |
T133A |
probably benign |
Het |
Or5h18 |
G |
T |
16: 58,848,260 (GRCm39) |
D3E |
probably benign |
Het |
Oxgr1 |
T |
C |
14: 120,259,776 (GRCm39) |
I144V |
probably benign |
Het |
Pax5 |
T |
A |
4: 44,570,086 (GRCm39) |
T127S |
probably damaging |
Het |
Pcsk2 |
T |
C |
2: 143,529,599 (GRCm39) |
|
probably null |
Het |
Pdxk |
A |
G |
10: 78,300,626 (GRCm39) |
V19A |
possibly damaging |
Het |
Pik3c2a |
A |
T |
7: 116,017,060 (GRCm39) |
S232R |
probably damaging |
Het |
Ppip5k1 |
T |
C |
2: 121,171,329 (GRCm39) |
D620G |
possibly damaging |
Het |
Ppp4r4 |
T |
A |
12: 103,557,117 (GRCm39) |
|
probably null |
Het |
Psmd1 |
A |
G |
1: 86,006,434 (GRCm39) |
N267D |
probably damaging |
Het |
Pudp |
A |
G |
18: 50,701,136 (GRCm39) |
V199A |
probably damaging |
Het |
Rasal3 |
T |
A |
17: 32,615,755 (GRCm39) |
D361V |
probably damaging |
Het |
Rbm12 |
T |
C |
2: 155,938,484 (GRCm39) |
D596G |
possibly damaging |
Het |
Rbm6 |
T |
C |
9: 107,730,102 (GRCm39) |
D182G |
probably damaging |
Het |
Rif1 |
T |
C |
2: 52,002,759 (GRCm39) |
V2071A |
probably damaging |
Het |
Rilp |
C |
T |
11: 75,401,467 (GRCm39) |
A110V |
possibly damaging |
Het |
Rprd2 |
A |
G |
3: 95,681,645 (GRCm39) |
V332A |
probably benign |
Het |
Sbpl |
T |
A |
17: 24,172,304 (GRCm39) |
D205V |
unknown |
Het |
Scn9a |
T |
C |
2: 66,370,967 (GRCm39) |
I538V |
probably benign |
Het |
Serpina1d |
T |
C |
12: 103,734,083 (GRCm39) |
S74G |
possibly damaging |
Het |
Serpina3n |
T |
C |
12: 104,375,369 (GRCm39) |
I147T |
possibly damaging |
Het |
Serpinb8 |
A |
G |
1: 107,532,472 (GRCm39) |
N188S |
probably benign |
Het |
Sipa1l3 |
A |
G |
7: 29,077,066 (GRCm39) |
V902A |
probably damaging |
Het |
Slc25a47 |
T |
A |
12: 108,821,260 (GRCm39) |
L123Q |
probably damaging |
Het |
Slc30a2 |
A |
T |
4: 134,071,317 (GRCm39) |
|
probably null |
Het |
Slc66a1 |
G |
T |
4: 139,027,312 (GRCm39) |
H343Q |
probably benign |
Het |
Tbc1d9b |
A |
G |
11: 50,062,125 (GRCm39) |
N1211S |
probably benign |
Het |
Tdrd3 |
T |
A |
14: 87,709,537 (GRCm39) |
I67N |
probably damaging |
Het |
Thbs1 |
T |
C |
2: 117,945,273 (GRCm39) |
V282A |
probably benign |
Het |
Tmc8 |
A |
G |
11: 117,682,431 (GRCm39) |
|
probably null |
Het |
Trim11 |
T |
A |
11: 58,879,750 (GRCm39) |
F284Y |
probably null |
Het |
Ttn |
G |
T |
2: 76,552,141 (GRCm39) |
Y29419* |
probably null |
Het |
Ttn |
A |
G |
2: 76,599,947 (GRCm39) |
Y19076H |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,149,044 (GRCm39) |
S448P |
possibly damaging |
Het |
Ugt2b34 |
T |
C |
5: 87,039,332 (GRCm39) |
E443G |
probably damaging |
Het |
Usp29 |
A |
G |
7: 6,964,390 (GRCm39) |
T78A |
probably damaging |
Het |
Vmn1r227 |
A |
G |
17: 20,955,396 (GRCm39) |
|
noncoding transcript |
Het |
Vmn1r85 |
A |
T |
7: 12,818,788 (GRCm39) |
W119R |
probably damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,234,379 (GRCm39) |
V611E |
probably damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,149,550 (GRCm39) |
M313L |
probably benign |
Het |
Zap70 |
T |
C |
1: 36,818,254 (GRCm39) |
Y314H |
probably damaging |
Het |
Zfp667 |
T |
A |
7: 6,308,684 (GRCm39) |
F451I |
possibly damaging |
Het |
|
Other mutations in Snx13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Snx13
|
APN |
12 |
35,148,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01143:Snx13
|
APN |
12 |
35,182,159 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01446:Snx13
|
APN |
12 |
35,174,479 (GRCm39) |
nonsense |
probably null |
|
IGL01519:Snx13
|
APN |
12 |
35,188,471 (GRCm39) |
unclassified |
probably benign |
|
IGL01902:Snx13
|
APN |
12 |
35,183,306 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01903:Snx13
|
APN |
12 |
35,135,968 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02146:Snx13
|
APN |
12 |
35,151,078 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02175:Snx13
|
APN |
12 |
35,182,061 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02197:Snx13
|
APN |
12 |
35,156,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02200:Snx13
|
APN |
12 |
35,136,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02476:Snx13
|
APN |
12 |
35,136,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03171:Snx13
|
APN |
12 |
35,150,539 (GRCm39) |
missense |
probably benign |
0.28 |
resistance
|
UTSW |
12 |
35,162,444 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Snx13
|
UTSW |
12 |
35,182,126 (GRCm39) |
missense |
possibly damaging |
0.48 |
P0042:Snx13
|
UTSW |
12 |
35,157,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R0047:Snx13
|
UTSW |
12 |
35,151,123 (GRCm39) |
splice site |
probably benign |
|
R0047:Snx13
|
UTSW |
12 |
35,151,123 (GRCm39) |
splice site |
probably benign |
|
R0344:Snx13
|
UTSW |
12 |
35,136,899 (GRCm39) |
nonsense |
probably null |
|
R1240:Snx13
|
UTSW |
12 |
35,141,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R1335:Snx13
|
UTSW |
12 |
35,182,123 (GRCm39) |
missense |
probably benign |
0.16 |
R1451:Snx13
|
UTSW |
12 |
35,128,983 (GRCm39) |
missense |
probably benign |
0.00 |
R1617:Snx13
|
UTSW |
12 |
35,136,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R2065:Snx13
|
UTSW |
12 |
35,188,065 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2111:Snx13
|
UTSW |
12 |
35,188,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R2385:Snx13
|
UTSW |
12 |
35,169,792 (GRCm39) |
missense |
probably benign |
0.36 |
R2437:Snx13
|
UTSW |
12 |
35,132,926 (GRCm39) |
missense |
probably benign |
0.14 |
R2511:Snx13
|
UTSW |
12 |
35,188,080 (GRCm39) |
missense |
probably benign |
0.13 |
R2860:Snx13
|
UTSW |
12 |
35,188,116 (GRCm39) |
missense |
probably benign |
0.45 |
R2861:Snx13
|
UTSW |
12 |
35,188,116 (GRCm39) |
missense |
probably benign |
0.45 |
R2862:Snx13
|
UTSW |
12 |
35,188,116 (GRCm39) |
missense |
probably benign |
0.45 |
R2992:Snx13
|
UTSW |
12 |
35,155,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Snx13
|
UTSW |
12 |
35,194,096 (GRCm39) |
missense |
probably benign |
0.10 |
R4304:Snx13
|
UTSW |
12 |
35,172,941 (GRCm39) |
missense |
probably benign |
0.10 |
R4532:Snx13
|
UTSW |
12 |
35,194,219 (GRCm39) |
missense |
probably damaging |
0.98 |
R4692:Snx13
|
UTSW |
12 |
35,136,917 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4914:Snx13
|
UTSW |
12 |
35,182,032 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5309:Snx13
|
UTSW |
12 |
35,194,324 (GRCm39) |
nonsense |
probably null |
|
R5425:Snx13
|
UTSW |
12 |
35,150,643 (GRCm39) |
nonsense |
probably null |
|
R5476:Snx13
|
UTSW |
12 |
35,156,819 (GRCm39) |
splice site |
probably null |
|
R5533:Snx13
|
UTSW |
12 |
35,173,025 (GRCm39) |
critical splice donor site |
probably null |
|
R5564:Snx13
|
UTSW |
12 |
35,174,471 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5572:Snx13
|
UTSW |
12 |
35,153,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5635:Snx13
|
UTSW |
12 |
35,190,170 (GRCm39) |
missense |
probably benign |
0.00 |
R6018:Snx13
|
UTSW |
12 |
35,097,318 (GRCm39) |
start gained |
probably benign |
|
R6612:Snx13
|
UTSW |
12 |
35,156,758 (GRCm39) |
missense |
probably benign |
0.19 |
R6618:Snx13
|
UTSW |
12 |
35,162,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Snx13
|
UTSW |
12 |
35,190,185 (GRCm39) |
missense |
probably damaging |
0.98 |
R6964:Snx13
|
UTSW |
12 |
35,169,788 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7186:Snx13
|
UTSW |
12 |
35,142,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R7372:Snx13
|
UTSW |
12 |
35,128,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7429:Snx13
|
UTSW |
12 |
35,183,357 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7430:Snx13
|
UTSW |
12 |
35,183,357 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7537:Snx13
|
UTSW |
12 |
35,135,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R7567:Snx13
|
UTSW |
12 |
35,136,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7582:Snx13
|
UTSW |
12 |
35,174,534 (GRCm39) |
nonsense |
probably null |
|
R7767:Snx13
|
UTSW |
12 |
35,157,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Snx13
|
UTSW |
12 |
35,174,527 (GRCm39) |
missense |
probably benign |
|
R7838:Snx13
|
UTSW |
12 |
35,155,174 (GRCm39) |
missense |
probably benign |
0.26 |
R7901:Snx13
|
UTSW |
12 |
35,150,624 (GRCm39) |
missense |
probably benign |
0.02 |
R8029:Snx13
|
UTSW |
12 |
35,169,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R8418:Snx13
|
UTSW |
12 |
35,148,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R8961:Snx13
|
UTSW |
12 |
35,155,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R9197:Snx13
|
UTSW |
12 |
35,155,196 (GRCm39) |
missense |
probably benign |
0.00 |
R9372:Snx13
|
UTSW |
12 |
35,151,048 (GRCm39) |
missense |
possibly damaging |
0.78 |
|