Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
GC |
G |
11: 59,101,139 (GRCm39) |
|
probably null |
Het |
Acvr1b |
C |
A |
15: 101,092,856 (GRCm39) |
D166E |
probably benign |
Het |
Adgra2 |
T |
C |
8: 27,604,491 (GRCm39) |
I522T |
probably damaging |
Het |
Adgre4 |
C |
T |
17: 56,099,013 (GRCm39) |
S173L |
probably benign |
Het |
Akap9 |
A |
T |
5: 4,082,801 (GRCm39) |
Q1975L |
probably damaging |
Het |
Ap3d1 |
T |
A |
10: 80,546,298 (GRCm39) |
M965L |
probably benign |
Het |
Brca2 |
CATA |
CA |
5: 150,465,040 (GRCm39) |
|
probably null |
Het |
Chd6 |
T |
C |
2: 160,807,502 (GRCm39) |
N1904S |
probably benign |
Het |
Clstn3 |
A |
T |
6: 124,408,623 (GRCm39) |
S896R |
possibly damaging |
Het |
Col6a3 |
T |
A |
1: 90,755,824 (GRCm39) |
D155V |
probably damaging |
Het |
Dct |
T |
C |
14: 118,273,876 (GRCm39) |
T344A |
possibly damaging |
Het |
Dctn1 |
T |
A |
6: 83,170,673 (GRCm39) |
|
probably null |
Het |
Dgkz |
T |
C |
2: 91,776,255 (GRCm39) |
T3A |
possibly damaging |
Het |
Duoxa2 |
T |
C |
2: 122,132,332 (GRCm39) |
S249P |
possibly damaging |
Het |
Ehbp1 |
A |
T |
11: 22,189,156 (GRCm39) |
V82E |
probably damaging |
Het |
Fcho1 |
A |
T |
8: 72,165,217 (GRCm39) |
|
probably null |
Het |
Garin5b |
T |
A |
7: 4,761,143 (GRCm39) |
D523V |
probably benign |
Het |
Ifi213 |
T |
A |
1: 173,422,800 (GRCm39) |
N22Y |
probably damaging |
Het |
Kcnq1 |
T |
A |
7: 142,660,170 (GRCm39) |
|
probably benign |
Het |
Kif7 |
T |
A |
7: 79,354,388 (GRCm39) |
Q799L |
probably benign |
Het |
Lmnb1 |
T |
A |
18: 56,862,456 (GRCm39) |
L206* |
probably null |
Het |
Lonp2 |
G |
T |
8: 87,440,001 (GRCm39) |
G247V |
probably damaging |
Het |
Ly75 |
T |
C |
2: 60,206,306 (GRCm39) |
Y121C |
probably damaging |
Het |
Mboat1 |
C |
A |
13: 30,408,509 (GRCm39) |
T224K |
probably benign |
Het |
Mcm9 |
T |
C |
10: 53,492,073 (GRCm39) |
E416G |
possibly damaging |
Het |
Mtnr1b |
A |
T |
9: 15,774,093 (GRCm39) |
I322N |
probably damaging |
Het |
Nanog |
G |
A |
6: 122,690,350 (GRCm39) |
G227R |
possibly damaging |
Het |
Nbn |
T |
C |
4: 15,981,347 (GRCm39) |
S480P |
probably damaging |
Het |
Nek10 |
C |
A |
14: 14,865,633 (GRCm38) |
L638M |
probably benign |
Het |
Nelfcd |
T |
C |
2: 174,268,611 (GRCm39) |
V538A |
probably damaging |
Het |
Or1e33 |
A |
T |
11: 73,738,745 (GRCm39) |
S69T |
probably benign |
Het |
Or2b4 |
T |
G |
17: 38,116,312 (GRCm39) |
I92S |
probably damaging |
Het |
Or52a5b |
T |
C |
7: 103,417,416 (GRCm39) |
I63V |
probably benign |
Het |
Or5b97 |
T |
A |
19: 12,879,034 (GRCm39) |
T37S |
probably benign |
Het |
Phf24 |
G |
A |
4: 42,938,780 (GRCm39) |
|
probably null |
Het |
Pigz |
T |
C |
16: 31,764,528 (GRCm39) |
S529P |
probably damaging |
Het |
Pik3r5 |
A |
G |
11: 68,383,144 (GRCm39) |
E321G |
probably damaging |
Het |
Plcb3 |
G |
A |
19: 6,933,547 (GRCm39) |
T926I |
probably benign |
Het |
Pm20d2 |
G |
A |
4: 33,181,833 (GRCm39) |
P257S |
probably damaging |
Het |
Pon2 |
A |
G |
6: 5,289,057 (GRCm39) |
V34A |
probably benign |
Het |
Prkar2b |
A |
G |
12: 32,110,855 (GRCm39) |
F76S |
possibly damaging |
Het |
Prpf31 |
G |
A |
7: 3,642,668 (GRCm39) |
E414K |
probably benign |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Setbp1 |
A |
T |
18: 78,902,455 (GRCm39) |
L404Q |
probably damaging |
Het |
Slc26a11 |
C |
T |
11: 119,265,654 (GRCm39) |
A389V |
probably damaging |
Het |
Slc2a1 |
A |
T |
4: 118,993,539 (GRCm39) |
T459S |
possibly damaging |
Het |
Spi1 |
T |
C |
2: 90,944,685 (GRCm39) |
L135P |
probably benign |
Het |
Sspo |
T |
C |
6: 48,463,720 (GRCm39) |
L3844P |
possibly damaging |
Het |
Stxbp5 |
T |
A |
10: 9,675,772 (GRCm39) |
T616S |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,712,896 (GRCm39) |
|
probably null |
Het |
Synm |
G |
T |
7: 67,384,686 (GRCm39) |
A550D |
possibly damaging |
Het |
Tanc2 |
T |
C |
11: 105,787,373 (GRCm39) |
V891A |
possibly damaging |
Het |
Tanc2 |
G |
A |
11: 105,758,543 (GRCm39) |
R768Q |
probably damaging |
Het |
Tlx1 |
A |
T |
19: 45,144,413 (GRCm39) |
Q45L |
probably damaging |
Het |
Tmem17 |
A |
C |
11: 22,468,659 (GRCm39) |
*199C |
probably null |
Het |
Tns3 |
A |
T |
11: 8,442,578 (GRCm39) |
M595K |
possibly damaging |
Het |
Tyk2 |
A |
G |
9: 21,027,256 (GRCm39) |
V538A |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,734,727 (GRCm39) |
D3250G |
possibly damaging |
Het |
Usp4 |
A |
G |
9: 108,237,322 (GRCm39) |
H130R |
possibly damaging |
Het |
Zfhx2 |
T |
C |
14: 55,302,665 (GRCm39) |
Q1773R |
probably benign |
Het |
Zfp790 |
A |
G |
7: 29,528,970 (GRCm39) |
K552E |
possibly damaging |
Het |
Zswim5 |
G |
A |
4: 116,808,106 (GRCm39) |
R230Q |
probably damaging |
Het |
|
Other mutations in Tmem104 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Tmem104
|
APN |
11 |
115,134,763 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02948:Tmem104
|
APN |
11 |
115,088,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03010:Tmem104
|
APN |
11 |
115,134,360 (GRCm39) |
missense |
probably benign |
0.01 |
R0107:Tmem104
|
UTSW |
11 |
115,093,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Tmem104
|
UTSW |
11 |
115,092,134 (GRCm39) |
splice site |
probably benign |
|
R0534:Tmem104
|
UTSW |
11 |
115,091,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2034:Tmem104
|
UTSW |
11 |
115,134,373 (GRCm39) |
missense |
probably benign |
0.42 |
R2037:Tmem104
|
UTSW |
11 |
115,092,221 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4095:Tmem104
|
UTSW |
11 |
115,134,749 (GRCm39) |
nonsense |
probably null |
|
R4640:Tmem104
|
UTSW |
11 |
115,134,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4981:Tmem104
|
UTSW |
11 |
115,095,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Tmem104
|
UTSW |
11 |
115,134,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Tmem104
|
UTSW |
11 |
115,092,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R5522:Tmem104
|
UTSW |
11 |
115,079,149 (GRCm39) |
critical splice donor site |
probably null |
|
R5602:Tmem104
|
UTSW |
11 |
115,095,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Tmem104
|
UTSW |
11 |
115,134,819 (GRCm39) |
missense |
probably benign |
|
R6522:Tmem104
|
UTSW |
11 |
115,134,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7962:Tmem104
|
UTSW |
11 |
115,134,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R7980:Tmem104
|
UTSW |
11 |
115,134,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R8323:Tmem104
|
UTSW |
11 |
115,134,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8552:Tmem104
|
UTSW |
11 |
115,088,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Tmem104
|
UTSW |
11 |
115,092,144 (GRCm39) |
missense |
probably benign |
0.01 |
R9363:Tmem104
|
UTSW |
11 |
115,134,691 (GRCm39) |
missense |
probably benign |
0.14 |
R9507:Tmem104
|
UTSW |
11 |
115,091,699 (GRCm39) |
missense |
probably damaging |
1.00 |
|