Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
C |
2: 69,117,010 (GRCm39) |
Q546R |
probably null |
Het |
Acr |
T |
G |
15: 89,458,144 (GRCm39) |
V275G |
probably damaging |
Het |
Adam5 |
A |
G |
8: 25,303,448 (GRCm39) |
Y160H |
probably benign |
Het |
Adcy5 |
T |
A |
16: 35,089,438 (GRCm39) |
M545K |
probably damaging |
Het |
Aoc2 |
A |
G |
11: 101,216,379 (GRCm39) |
E154G |
possibly damaging |
Het |
Atg2a |
T |
G |
19: 6,296,608 (GRCm39) |
L338R |
probably damaging |
Het |
Atp2a1 |
T |
C |
7: 126,049,590 (GRCm39) |
|
probably benign |
Het |
Bbs7 |
A |
G |
3: 36,644,866 (GRCm39) |
S436P |
probably benign |
Het |
Bpnt1 |
T |
C |
1: 185,070,355 (GRCm39) |
Y16H |
probably benign |
Het |
Cbll1 |
A |
T |
12: 31,542,091 (GRCm39) |
F90Y |
probably damaging |
Het |
Cbs |
G |
T |
17: 31,836,216 (GRCm39) |
Q411K |
probably benign |
Het |
Cdca2 |
A |
C |
14: 67,935,411 (GRCm39) |
F435V |
probably damaging |
Het |
Cdh13 |
T |
G |
8: 120,040,786 (GRCm39) |
S664A |
probably damaging |
Het |
Cdk17 |
T |
A |
10: 93,073,702 (GRCm39) |
V438E |
probably benign |
Het |
Cep295 |
T |
C |
9: 15,266,032 (GRCm39) |
D40G |
possibly damaging |
Het |
Col6a1 |
T |
C |
10: 76,545,952 (GRCm39) |
H840R |
unknown |
Het |
Cpa1 |
A |
G |
6: 30,645,250 (GRCm39) |
T409A |
probably benign |
Het |
Crlf1 |
G |
A |
8: 70,951,739 (GRCm39) |
|
probably benign |
Het |
E2f2 |
T |
A |
4: 135,907,855 (GRCm39) |
I184N |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,045,886 (GRCm39) |
D596G |
probably damaging |
Het |
Elapor2 |
A |
G |
5: 9,495,367 (GRCm39) |
R724G |
probably benign |
Het |
Ets2 |
A |
G |
16: 95,517,267 (GRCm39) |
Y333C |
probably damaging |
Het |
Fam178b |
A |
G |
1: 36,671,487 (GRCm39) |
|
probably benign |
Het |
Fndc3b |
A |
G |
3: 27,515,928 (GRCm39) |
V626A |
probably benign |
Het |
Gart |
G |
T |
16: 91,436,337 (GRCm39) |
A140E |
probably damaging |
Het |
Gbp7 |
T |
C |
3: 142,251,274 (GRCm39) |
S477P |
possibly damaging |
Het |
Gm16380 |
T |
C |
9: 53,791,453 (GRCm39) |
|
noncoding transcript |
Het |
Hmcn1 |
C |
A |
1: 150,674,565 (GRCm39) |
R579M |
possibly damaging |
Het |
Hoxb8 |
A |
C |
11: 96,173,937 (GRCm39) |
H50P |
probably damaging |
Het |
Hspa4 |
C |
T |
11: 53,163,706 (GRCm39) |
|
probably null |
Het |
Hspa4l |
G |
A |
3: 40,711,429 (GRCm39) |
|
probably benign |
Het |
Hyal4 |
A |
T |
6: 24,756,670 (GRCm39) |
Y296F |
probably damaging |
Het |
Igsf8 |
C |
A |
1: 172,145,066 (GRCm39) |
T131K |
probably damaging |
Het |
Ilvbl |
C |
T |
10: 78,415,373 (GRCm39) |
P298L |
probably damaging |
Het |
Jak2 |
T |
A |
19: 29,259,788 (GRCm39) |
I229N |
possibly damaging |
Het |
Kif1b |
T |
C |
4: 149,288,688 (GRCm39) |
D1205G |
possibly damaging |
Het |
Lrrc63 |
T |
C |
14: 75,363,910 (GRCm39) |
R74G |
probably benign |
Het |
Lvrn |
A |
G |
18: 47,013,760 (GRCm39) |
T481A |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,244,810 (GRCm39) |
T7312S |
probably damaging |
Het |
Magel2 |
C |
T |
7: 62,030,299 (GRCm39) |
Q1068* |
probably null |
Het |
Mrpl3 |
A |
G |
9: 104,941,302 (GRCm39) |
Y203C |
probably damaging |
Het |
Nek2 |
T |
A |
1: 191,559,473 (GRCm39) |
I326N |
probably benign |
Het |
Nlrc4 |
A |
C |
17: 74,752,915 (GRCm39) |
N489K |
probably damaging |
Het |
Nlrp4f |
A |
T |
13: 65,342,732 (GRCm39) |
S304R |
possibly damaging |
Het |
Ogfr |
C |
G |
2: 180,235,492 (GRCm39) |
R189G |
probably damaging |
Het |
Or52b4i |
T |
A |
7: 102,191,899 (GRCm39) |
L252H |
probably damaging |
Het |
Or5p78 |
T |
A |
7: 108,212,162 (GRCm39) |
I216N |
probably benign |
Het |
Or5w8 |
A |
T |
2: 87,688,401 (GRCm39) |
N294I |
probably damaging |
Het |
Orm3 |
A |
G |
4: 63,275,885 (GRCm39) |
S145G |
probably benign |
Het |
Pclo |
A |
G |
5: 14,731,716 (GRCm39) |
E3406G |
unknown |
Het |
Pcx |
T |
G |
19: 4,651,638 (GRCm39) |
F4C |
probably benign |
Het |
Pgd |
C |
A |
4: 149,238,339 (GRCm39) |
G364V |
probably damaging |
Het |
Pla2g12a |
C |
A |
3: 129,684,045 (GRCm39) |
D102E |
probably benign |
Het |
Pnpo |
A |
T |
11: 96,833,253 (GRCm39) |
C82* |
probably null |
Het |
Prdm1 |
T |
C |
10: 44,315,805 (GRCm39) |
N792S |
probably damaging |
Het |
Prim2 |
A |
T |
1: 33,523,757 (GRCm39) |
|
probably benign |
Het |
Proca1 |
C |
A |
11: 78,096,094 (GRCm39) |
P242Q |
probably benign |
Het |
Psmc5 |
A |
G |
11: 106,152,370 (GRCm39) |
N129S |
probably benign |
Het |
Ptchd4 |
A |
G |
17: 42,688,150 (GRCm39) |
T231A |
possibly damaging |
Het |
Qrfpr |
C |
T |
3: 36,235,201 (GRCm39) |
|
probably benign |
Het |
Rab44 |
G |
A |
17: 29,364,344 (GRCm39) |
|
probably benign |
Het |
Racgap1 |
T |
C |
15: 99,526,508 (GRCm39) |
|
probably benign |
Het |
Rapgef4 |
A |
G |
2: 71,861,385 (GRCm39) |
E25G |
probably damaging |
Het |
Rpl8 |
G |
C |
15: 76,789,246 (GRCm39) |
|
probably benign |
Het |
Samd12 |
G |
A |
15: 53,583,116 (GRCm39) |
P73S |
possibly damaging |
Het |
Sdk1 |
T |
C |
5: 141,948,476 (GRCm39) |
V607A |
probably benign |
Het |
Slc25a19 |
A |
G |
11: 115,508,401 (GRCm39) |
Y196H |
probably damaging |
Het |
Slc39a3 |
A |
T |
10: 80,869,621 (GRCm39) |
M12K |
possibly damaging |
Het |
Slc5a4a |
T |
C |
10: 76,018,556 (GRCm39) |
I501T |
possibly damaging |
Het |
Sp4 |
A |
T |
12: 118,262,408 (GRCm39) |
V546D |
possibly damaging |
Het |
Ssh3 |
C |
T |
19: 4,313,727 (GRCm39) |
V511M |
possibly damaging |
Het |
Stard9 |
T |
G |
2: 120,526,788 (GRCm39) |
V1015G |
probably benign |
Het |
Thoc5 |
G |
T |
11: 4,871,978 (GRCm39) |
V516F |
possibly damaging |
Het |
Ttc21a |
T |
A |
9: 119,783,628 (GRCm39) |
I570N |
probably damaging |
Het |
Ttc4 |
T |
C |
4: 106,524,770 (GRCm39) |
|
probably null |
Het |
Ugt1a1 |
AT |
A |
1: 88,140,093 (GRCm39) |
|
probably null |
Het |
Yipf3 |
A |
G |
17: 46,562,411 (GRCm39) |
E298G |
possibly damaging |
Het |
Zbtb34 |
C |
A |
2: 33,301,060 (GRCm39) |
E494* |
probably null |
Het |
Zfhx3 |
A |
G |
8: 109,677,878 (GRCm39) |
Y2976C |
probably damaging |
Het |
|
Other mutations in Samd9l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00538:Samd9l
|
APN |
6 |
3,376,779 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00550:Samd9l
|
APN |
6 |
3,374,594 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01100:Samd9l
|
APN |
6 |
3,375,863 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01321:Samd9l
|
APN |
6 |
3,376,259 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01553:Samd9l
|
APN |
6 |
3,375,566 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01575:Samd9l
|
APN |
6 |
3,376,734 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01896:Samd9l
|
APN |
6 |
3,375,120 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01915:Samd9l
|
APN |
6 |
3,373,864 (GRCm39) |
nonsense |
probably null |
|
IGL02063:Samd9l
|
APN |
6 |
3,372,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Samd9l
|
APN |
6 |
3,376,575 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02145:Samd9l
|
APN |
6 |
3,374,105 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02163:Samd9l
|
APN |
6 |
3,374,246 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02256:Samd9l
|
APN |
6 |
3,376,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02508:Samd9l
|
APN |
6 |
3,374,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Samd9l
|
APN |
6 |
3,375,760 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02968:Samd9l
|
APN |
6 |
3,376,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03058:Samd9l
|
APN |
6 |
3,374,980 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03068:Samd9l
|
APN |
6 |
3,375,348 (GRCm39) |
nonsense |
probably null |
|
IGL03160:Samd9l
|
APN |
6 |
3,374,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03372:Samd9l
|
APN |
6 |
3,375,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03385:Samd9l
|
APN |
6 |
3,376,208 (GRCm39) |
missense |
probably damaging |
0.99 |
boston_lager
|
UTSW |
6 |
3,375,761 (GRCm39) |
missense |
probably benign |
0.12 |
ipa
|
UTSW |
6 |
3,376,347 (GRCm39) |
missense |
probably damaging |
1.00 |
Paine
|
UTSW |
6 |
3,372,716 (GRCm39) |
missense |
probably damaging |
0.99 |
samad
|
UTSW |
6 |
3,374,032 (GRCm39) |
nonsense |
probably null |
|
IGL03054:Samd9l
|
UTSW |
6 |
3,376,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Samd9l
|
UTSW |
6 |
3,374,946 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0112:Samd9l
|
UTSW |
6 |
3,376,031 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0356:Samd9l
|
UTSW |
6 |
3,375,107 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0370:Samd9l
|
UTSW |
6 |
3,377,264 (GRCm39) |
start gained |
probably benign |
|
R0744:Samd9l
|
UTSW |
6 |
3,372,725 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0833:Samd9l
|
UTSW |
6 |
3,372,725 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0880:Samd9l
|
UTSW |
6 |
3,377,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R1110:Samd9l
|
UTSW |
6 |
3,374,267 (GRCm39) |
missense |
probably benign |
0.44 |
R1155:Samd9l
|
UTSW |
6 |
3,376,939 (GRCm39) |
missense |
probably benign |
0.01 |
R1268:Samd9l
|
UTSW |
6 |
3,376,113 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1293:Samd9l
|
UTSW |
6 |
3,373,947 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1478:Samd9l
|
UTSW |
6 |
3,376,369 (GRCm39) |
missense |
probably benign |
0.06 |
R1573:Samd9l
|
UTSW |
6 |
3,375,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R1590:Samd9l
|
UTSW |
6 |
3,375,761 (GRCm39) |
missense |
probably benign |
0.12 |
R1611:Samd9l
|
UTSW |
6 |
3,373,771 (GRCm39) |
missense |
probably benign |
0.00 |
R1754:Samd9l
|
UTSW |
6 |
3,373,126 (GRCm39) |
missense |
probably damaging |
0.96 |
R1759:Samd9l
|
UTSW |
6 |
3,373,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Samd9l
|
UTSW |
6 |
3,375,264 (GRCm39) |
nonsense |
probably null |
|
R1829:Samd9l
|
UTSW |
6 |
3,375,107 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1935:Samd9l
|
UTSW |
6 |
3,376,269 (GRCm39) |
missense |
probably benign |
0.01 |
R2154:Samd9l
|
UTSW |
6 |
3,372,945 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2228:Samd9l
|
UTSW |
6 |
3,376,910 (GRCm39) |
missense |
probably benign |
0.08 |
R3622:Samd9l
|
UTSW |
6 |
3,374,032 (GRCm39) |
nonsense |
probably null |
|
R3903:Samd9l
|
UTSW |
6 |
3,376,830 (GRCm39) |
nonsense |
probably null |
|
R3904:Samd9l
|
UTSW |
6 |
3,376,830 (GRCm39) |
nonsense |
probably null |
|
R3945:Samd9l
|
UTSW |
6 |
3,377,029 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4091:Samd9l
|
UTSW |
6 |
3,376,887 (GRCm39) |
missense |
probably benign |
0.22 |
R4602:Samd9l
|
UTSW |
6 |
3,373,937 (GRCm39) |
frame shift |
probably null |
|
R4602:Samd9l
|
UTSW |
6 |
3,373,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Samd9l
|
UTSW |
6 |
3,376,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Samd9l
|
UTSW |
6 |
3,375,504 (GRCm39) |
nonsense |
probably null |
|
R4762:Samd9l
|
UTSW |
6 |
3,375,623 (GRCm39) |
missense |
probably benign |
0.01 |
R4814:Samd9l
|
UTSW |
6 |
3,372,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R4934:Samd9l
|
UTSW |
6 |
3,375,621 (GRCm39) |
nonsense |
probably null |
|
R5026:Samd9l
|
UTSW |
6 |
3,375,284 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5048:Samd9l
|
UTSW |
6 |
3,374,157 (GRCm39) |
missense |
probably benign |
0.35 |
R5130:Samd9l
|
UTSW |
6 |
3,374,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5271:Samd9l
|
UTSW |
6 |
3,376,156 (GRCm39) |
missense |
probably benign |
0.02 |
R5328:Samd9l
|
UTSW |
6 |
3,376,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R5507:Samd9l
|
UTSW |
6 |
3,373,898 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5587:Samd9l
|
UTSW |
6 |
3,373,291 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5846:Samd9l
|
UTSW |
6 |
3,376,754 (GRCm39) |
missense |
probably benign |
|
R5881:Samd9l
|
UTSW |
6 |
3,372,716 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5889:Samd9l
|
UTSW |
6 |
3,376,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Samd9l
|
UTSW |
6 |
3,377,252 (GRCm39) |
missense |
probably benign |
0.00 |
R6199:Samd9l
|
UTSW |
6 |
3,376,686 (GRCm39) |
missense |
probably benign |
0.13 |
R6298:Samd9l
|
UTSW |
6 |
3,375,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R6331:Samd9l
|
UTSW |
6 |
3,376,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Samd9l
|
UTSW |
6 |
3,376,896 (GRCm39) |
missense |
probably benign |
|
R6601:Samd9l
|
UTSW |
6 |
3,377,229 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6655:Samd9l
|
UTSW |
6 |
3,377,247 (GRCm39) |
missense |
probably benign |
0.22 |
R6803:Samd9l
|
UTSW |
6 |
3,375,446 (GRCm39) |
missense |
probably damaging |
0.97 |
R6864:Samd9l
|
UTSW |
6 |
3,374,750 (GRCm39) |
missense |
probably benign |
0.14 |
R6905:Samd9l
|
UTSW |
6 |
3,375,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R6919:Samd9l
|
UTSW |
6 |
3,376,313 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7060:Samd9l
|
UTSW |
6 |
3,372,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R7073:Samd9l
|
UTSW |
6 |
3,375,856 (GRCm39) |
nonsense |
probably null |
|
R7250:Samd9l
|
UTSW |
6 |
3,374,201 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7307:Samd9l
|
UTSW |
6 |
3,372,600 (GRCm39) |
nonsense |
probably null |
|
R7351:Samd9l
|
UTSW |
6 |
3,374,157 (GRCm39) |
missense |
probably benign |
0.35 |
R7423:Samd9l
|
UTSW |
6 |
3,374,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7610:Samd9l
|
UTSW |
6 |
3,376,754 (GRCm39) |
missense |
probably benign |
|
R7667:Samd9l
|
UTSW |
6 |
3,375,975 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7672:Samd9l
|
UTSW |
6 |
3,373,646 (GRCm39) |
missense |
probably benign |
0.16 |
R7680:Samd9l
|
UTSW |
6 |
3,376,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7680:Samd9l
|
UTSW |
6 |
3,372,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7814:Samd9l
|
UTSW |
6 |
3,374,793 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7829:Samd9l
|
UTSW |
6 |
3,374,749 (GRCm39) |
missense |
probably benign |
0.00 |
R8000:Samd9l
|
UTSW |
6 |
3,373,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R8098:Samd9l
|
UTSW |
6 |
3,375,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8698:Samd9l
|
UTSW |
6 |
3,373,843 (GRCm39) |
missense |
probably benign |
0.06 |
R8785:Samd9l
|
UTSW |
6 |
3,377,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R8795:Samd9l
|
UTSW |
6 |
3,374,221 (GRCm39) |
nonsense |
probably null |
|
R8806:Samd9l
|
UTSW |
6 |
3,376,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R8832:Samd9l
|
UTSW |
6 |
3,374,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Samd9l
|
UTSW |
6 |
3,374,577 (GRCm39) |
missense |
probably damaging |
0.98 |
R9023:Samd9l
|
UTSW |
6 |
3,373,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Samd9l
|
UTSW |
6 |
3,373,493 (GRCm39) |
missense |
probably benign |
0.16 |
R9108:Samd9l
|
UTSW |
6 |
3,373,104 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9213:Samd9l
|
UTSW |
6 |
3,376,856 (GRCm39) |
missense |
probably benign |
0.23 |
R9494:Samd9l
|
UTSW |
6 |
3,375,830 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9504:Samd9l
|
UTSW |
6 |
3,372,621 (GRCm39) |
missense |
probably benign |
0.17 |
R9655:Samd9l
|
UTSW |
6 |
3,373,578 (GRCm39) |
missense |
probably benign |
0.00 |
R9688:Samd9l
|
UTSW |
6 |
3,377,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R9696:Samd9l
|
UTSW |
6 |
3,375,078 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9721:Samd9l
|
UTSW |
6 |
3,375,854 (GRCm39) |
missense |
possibly damaging |
0.69 |
X0026:Samd9l
|
UTSW |
6 |
3,375,560 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Samd9l
|
UTSW |
6 |
3,374,477 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Samd9l
|
UTSW |
6 |
3,376,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|