Incidental Mutation 'R1902:Mug1'
ID |
212329 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mug1
|
Ensembl Gene |
ENSMUSG00000059908 |
Gene Name |
murinoglobulin 1 |
Synonyms |
|
MMRRC Submission |
039922-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1902 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
121815500-121866016 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 121858780 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 1166
(D1166G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000032228
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000032228]
|
AlphaFold |
P28665 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000032228
AA Change: D1166G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000032228 Gene: ENSMUSG00000059908 AA Change: D1166G
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
Pfam:A2M_N
|
128 |
221 |
5e-21 |
PFAM |
A2M_N_2
|
449 |
599 |
2.55e-41 |
SMART |
A2M
|
740 |
830 |
5.43e-36 |
SMART |
Pfam:Thiol-ester_cl
|
963 |
992 |
1e-18 |
PFAM |
Pfam:A2M_comp
|
1012 |
1268 |
5.4e-94 |
PFAM |
A2M_recep
|
1378 |
1465 |
4.14e-41 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148563
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000204210
|
Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.7%
- 10x: 94.9%
- 20x: 91.7%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele are viable, fertile and phenotypically normal under standard conditions but show increased mortality in response to diet-induced acute pancreatitis along with hepatic cell necrosis and inflammatory infiltration, andincreased plasma amylase and lipase levels. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 128 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730507C01Rik |
C |
T |
12: 18,584,004 (GRCm39) |
Q355* |
probably null |
Het |
Acacb |
A |
T |
5: 114,303,795 (GRCm39) |
R73* |
probably null |
Het |
Adra1a |
T |
C |
14: 66,875,684 (GRCm39) |
S220P |
probably benign |
Het |
Ano2 |
A |
T |
6: 125,849,647 (GRCm39) |
E126D |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Arhgap45 |
C |
A |
10: 79,861,300 (GRCm39) |
Q488K |
probably damaging |
Het |
Arhgef7 |
C |
A |
8: 11,858,713 (GRCm39) |
|
probably null |
Het |
Atxn7l3b |
A |
G |
10: 112,764,578 (GRCm39) |
I17T |
probably benign |
Het |
Bpifb9a |
A |
T |
2: 154,103,911 (GRCm39) |
N118I |
probably benign |
Het |
Btbd9 |
A |
T |
17: 30,749,202 (GRCm39) |
D37E |
probably damaging |
Het |
C8a |
T |
C |
4: 104,713,798 (GRCm39) |
|
probably null |
Het |
Capn13 |
G |
A |
17: 73,633,356 (GRCm39) |
S535F |
probably damaging |
Het |
Carns1 |
G |
T |
19: 4,216,337 (GRCm39) |
P615Q |
probably damaging |
Het |
Casz1 |
T |
C |
4: 149,020,652 (GRCm39) |
I479T |
possibly damaging |
Het |
Ccdc88a |
G |
T |
11: 29,411,788 (GRCm39) |
M532I |
probably benign |
Het |
Cdc42bpb |
T |
G |
12: 111,292,450 (GRCm39) |
S362R |
probably damaging |
Het |
Ceacam11 |
A |
T |
7: 17,709,252 (GRCm39) |
H150L |
probably benign |
Het |
Cfap44 |
A |
C |
16: 44,242,737 (GRCm39) |
T714P |
probably benign |
Het |
Cnot1 |
T |
C |
8: 96,469,749 (GRCm39) |
I1369V |
possibly damaging |
Het |
Cpeb1 |
T |
C |
7: 81,021,867 (GRCm39) |
D92G |
probably benign |
Het |
Cped1 |
T |
A |
6: 22,120,980 (GRCm39) |
|
probably null |
Het |
Csf1r |
A |
G |
18: 61,263,213 (GRCm39) |
T896A |
probably damaging |
Het |
Csf3r |
T |
C |
4: 125,936,711 (GRCm39) |
F658S |
probably damaging |
Het |
Cts6 |
A |
T |
13: 61,349,329 (GRCm39) |
Y126* |
probably null |
Het |
Cul7 |
T |
C |
17: 46,966,666 (GRCm39) |
L365P |
probably damaging |
Het |
Cxcl5 |
T |
C |
5: 90,907,644 (GRCm39) |
V72A |
probably damaging |
Het |
Cyp4v3 |
T |
A |
8: 45,759,989 (GRCm39) |
H521L |
probably benign |
Het |
Dct |
T |
C |
14: 118,271,690 (GRCm39) |
N380S |
probably benign |
Het |
Dnah1 |
T |
C |
14: 31,041,716 (GRCm39) |
D85G |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,574,637 (GRCm39) |
D1709G |
probably damaging |
Het |
Dnai1 |
A |
T |
4: 41,625,319 (GRCm39) |
K428* |
probably null |
Het |
Dsc1 |
A |
T |
18: 20,229,045 (GRCm39) |
V415D |
probably damaging |
Het |
E2f8 |
T |
C |
7: 48,520,920 (GRCm39) |
H467R |
probably benign |
Het |
Eddm3b |
T |
A |
14: 51,354,321 (GRCm39) |
I103N |
probably damaging |
Het |
Gal3st2c |
T |
G |
1: 93,936,611 (GRCm39) |
N185K |
probably damaging |
Het |
Ganc |
T |
C |
2: 120,276,963 (GRCm39) |
L675P |
probably damaging |
Het |
Garin3 |
A |
T |
11: 46,297,838 (GRCm39) |
T381S |
probably benign |
Het |
Gdf9 |
G |
A |
11: 53,327,780 (GRCm39) |
M245I |
probably benign |
Het |
Gm21886 |
G |
A |
18: 80,132,633 (GRCm39) |
T175I |
probably damaging |
Het |
Gria2 |
A |
G |
3: 80,629,415 (GRCm39) |
L269P |
probably damaging |
Het |
Grm8 |
T |
C |
6: 27,429,481 (GRCm39) |
Y471C |
probably damaging |
Het |
Gucy2g |
T |
A |
19: 55,198,669 (GRCm39) |
T825S |
probably benign |
Het |
H2-T13 |
A |
T |
17: 36,394,845 (GRCm39) |
M16K |
probably damaging |
Het |
Iffo2 |
T |
C |
4: 139,335,012 (GRCm39) |
S124P |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,850,997 (GRCm39) |
Y931H |
possibly damaging |
Het |
Il22ra1 |
A |
T |
4: 135,478,219 (GRCm39) |
Q430L |
probably damaging |
Het |
Il23r |
A |
C |
6: 67,400,718 (GRCm39) |
D537E |
probably benign |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Itgb4 |
T |
C |
11: 115,871,564 (GRCm39) |
V179A |
probably damaging |
Het |
Itpr2 |
T |
A |
6: 146,131,201 (GRCm39) |
H1968L |
probably damaging |
Het |
Kdm4a |
A |
G |
4: 118,017,596 (GRCm39) |
V490A |
probably benign |
Het |
Kif13a |
A |
T |
13: 46,941,638 (GRCm39) |
D946E |
probably benign |
Het |
Klhl22 |
T |
A |
16: 17,589,651 (GRCm39) |
I104N |
probably damaging |
Het |
Klk6 |
A |
C |
7: 43,475,481 (GRCm39) |
M1L |
probably benign |
Het |
Krt78 |
A |
T |
15: 101,855,398 (GRCm39) |
C804* |
probably null |
Het |
Larp7 |
A |
T |
3: 127,334,227 (GRCm39) |
N533K |
probably damaging |
Het |
Lrit3 |
T |
C |
3: 129,584,895 (GRCm39) |
T288A |
probably benign |
Het |
Lrp11 |
T |
A |
10: 7,499,544 (GRCm39) |
L245Q |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,750,673 (GRCm39) |
S2964G |
probably damaging |
Het |
Lrrc66 |
C |
T |
5: 73,764,965 (GRCm39) |
V693M |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,364,958 (GRCm39) |
M3268L |
probably benign |
Het |
Mad1l1 |
A |
G |
5: 140,289,443 (GRCm39) |
S161P |
possibly damaging |
Het |
Mettl25 |
A |
G |
10: 105,661,948 (GRCm39) |
S341P |
probably damaging |
Het |
Morc3 |
A |
G |
16: 93,667,385 (GRCm39) |
T588A |
probably damaging |
Het |
Mospd3 |
A |
G |
5: 137,598,677 (GRCm39) |
S21P |
probably damaging |
Het |
Mrpl57 |
T |
A |
14: 58,064,186 (GRCm39) |
F71L |
probably damaging |
Het |
Mtbp |
T |
C |
15: 55,470,111 (GRCm39) |
L594S |
probably damaging |
Het |
Mthfd2 |
T |
C |
6: 83,283,713 (GRCm39) |
N323S |
probably damaging |
Het |
Muc5b |
G |
T |
7: 141,417,842 (GRCm39) |
S3596I |
possibly damaging |
Het |
Nav1 |
T |
G |
1: 135,400,148 (GRCm39) |
N474T |
probably benign |
Het |
Ncoa1 |
A |
T |
12: 4,389,049 (GRCm39) |
D75E |
possibly damaging |
Het |
Ncor1 |
A |
C |
11: 62,228,984 (GRCm39) |
I958S |
probably damaging |
Het |
Nefm |
T |
C |
14: 68,361,563 (GRCm39) |
S234G |
probably benign |
Het |
Nlrp4c |
T |
C |
7: 6,068,818 (GRCm39) |
S240P |
probably damaging |
Het |
Nox3 |
C |
T |
17: 3,720,292 (GRCm39) |
V298M |
probably damaging |
Het |
Ntn4 |
A |
G |
10: 93,543,234 (GRCm39) |
D320G |
possibly damaging |
Het |
Nudt13 |
C |
G |
14: 20,360,709 (GRCm39) |
T174R |
probably damaging |
Het |
Odr4 |
T |
A |
1: 150,264,360 (GRCm39) |
|
probably null |
Het |
Opn1sw |
T |
A |
6: 29,379,803 (GRCm39) |
N144Y |
possibly damaging |
Het |
Or10al3 |
T |
A |
17: 38,012,312 (GRCm39) |
H250Q |
probably damaging |
Het |
Or10g3 |
T |
G |
14: 52,610,174 (GRCm39) |
Q112P |
possibly damaging |
Het |
Or1l8 |
T |
C |
2: 36,817,197 (GRCm39) |
I310V |
probably benign |
Het |
Or2a52 |
T |
A |
6: 43,144,657 (GRCm39) |
|
probably null |
Het |
Or4a72 |
A |
T |
2: 89,405,947 (GRCm39) |
L41Q |
possibly damaging |
Het |
Or5ac25 |
A |
T |
16: 59,182,526 (GRCm39) |
D18E |
probably benign |
Het |
Or5g25 |
T |
C |
2: 85,478,201 (GRCm39) |
S155G |
possibly damaging |
Het |
Or6c216 |
G |
T |
10: 129,678,375 (GRCm39) |
P179T |
probably benign |
Het |
Or6n2 |
T |
C |
1: 173,897,692 (GRCm39) |
V276A |
probably damaging |
Het |
Or8g4 |
T |
C |
9: 39,662,102 (GRCm39) |
V140A |
probably benign |
Het |
Osbpl5 |
T |
C |
7: 143,256,918 (GRCm39) |
D404G |
possibly damaging |
Het |
Parp14 |
C |
T |
16: 35,673,888 (GRCm39) |
|
probably null |
Het |
Pde3a |
C |
A |
6: 141,444,496 (GRCm39) |
N1101K |
probably benign |
Het |
Plcb1 |
G |
A |
2: 134,655,533 (GRCm39) |
V38I |
possibly damaging |
Het |
Plec |
T |
A |
15: 76,059,751 (GRCm39) |
E3417D |
probably damaging |
Het |
Ppfibp2 |
C |
T |
7: 107,345,585 (GRCm39) |
P869L |
probably damaging |
Het |
Ppp1r12a |
T |
A |
10: 108,034,752 (GRCm39) |
I99N |
probably damaging |
Het |
Pramel5 |
G |
A |
4: 144,000,433 (GRCm39) |
Q48* |
probably null |
Het |
Prr13 |
C |
A |
15: 102,369,133 (GRCm39) |
|
probably benign |
Het |
Psg22 |
T |
A |
7: 18,458,363 (GRCm39) |
Y312* |
probably null |
Het |
Ptchd4 |
A |
T |
17: 42,814,507 (GRCm39) |
I803L |
probably benign |
Het |
Rasa4 |
A |
G |
5: 136,120,092 (GRCm39) |
D56G |
probably benign |
Het |
Rif1 |
T |
A |
2: 52,006,685 (GRCm39) |
N2206K |
possibly damaging |
Het |
Robo1 |
A |
G |
16: 72,757,092 (GRCm39) |
Q351R |
probably null |
Het |
Samd4 |
T |
C |
14: 47,311,585 (GRCm39) |
F81S |
probably damaging |
Het |
Sh3pxd2b |
T |
C |
11: 32,373,559 (GRCm39) |
*909Q |
probably null |
Het |
Slc25a45 |
A |
G |
19: 5,934,550 (GRCm39) |
R173G |
probably damaging |
Het |
Smarca1 |
G |
A |
X: 46,938,840 (GRCm39) |
Q723* |
probably null |
Het |
Smoc1 |
T |
C |
12: 81,151,445 (GRCm39) |
I54T |
probably benign |
Het |
Spef2 |
G |
T |
15: 9,607,463 (GRCm39) |
R1319S |
probably damaging |
Het |
Steap3 |
T |
G |
1: 120,169,464 (GRCm39) |
I240L |
probably benign |
Het |
Stmn4 |
C |
T |
14: 66,593,058 (GRCm39) |
L13F |
probably damaging |
Het |
Stxbp5 |
C |
A |
10: 9,688,042 (GRCm39) |
V420F |
possibly damaging |
Het |
Syt3 |
T |
C |
7: 44,039,940 (GRCm39) |
S58P |
possibly damaging |
Het |
Tas2r125 |
T |
C |
6: 132,887,139 (GRCm39) |
F176L |
probably benign |
Het |
Tbc1d19 |
T |
A |
5: 53,986,695 (GRCm39) |
C35S |
probably benign |
Het |
Tcaf3 |
T |
C |
6: 42,570,486 (GRCm39) |
E422G |
possibly damaging |
Het |
Tekt4 |
T |
A |
17: 25,690,832 (GRCm39) |
F46Y |
possibly damaging |
Het |
Tnfaip3 |
T |
C |
10: 18,883,937 (GRCm39) |
K148E |
probably benign |
Het |
Trrap |
T |
G |
5: 144,752,863 (GRCm39) |
I1813R |
probably damaging |
Het |
Ttc29 |
A |
G |
8: 78,978,361 (GRCm39) |
E137G |
probably benign |
Het |
Tubgcp6 |
C |
A |
15: 89,000,444 (GRCm39) |
R307L |
possibly damaging |
Het |
Tyro3 |
T |
C |
2: 119,632,176 (GRCm39) |
I81T |
possibly damaging |
Het |
Upp2 |
T |
G |
2: 58,661,464 (GRCm39) |
M71R |
probably damaging |
Het |
Utp20 |
G |
T |
10: 88,588,888 (GRCm39) |
T2427K |
probably benign |
Het |
Vcl |
T |
A |
14: 21,032,767 (GRCm39) |
L122Q |
probably damaging |
Het |
Vmn1r213 |
A |
C |
13: 23,196,476 (GRCm39) |
N353T |
possibly damaging |
Het |
Vwa5b2 |
G |
T |
16: 20,423,582 (GRCm39) |
S1165I |
possibly damaging |
Het |
Zfp869 |
T |
C |
8: 70,160,088 (GRCm39) |
K162E |
probably benign |
Het |
|
Other mutations in Mug1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Mug1
|
APN |
6 |
121,842,768 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00485:Mug1
|
APN |
6 |
121,864,375 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00816:Mug1
|
APN |
6 |
121,859,597 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01140:Mug1
|
APN |
6 |
121,859,693 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01141:Mug1
|
APN |
6 |
121,847,458 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01384:Mug1
|
APN |
6 |
121,826,433 (GRCm39) |
splice site |
probably benign |
|
IGL01659:Mug1
|
APN |
6 |
121,847,619 (GRCm39) |
splice site |
probably benign |
|
IGL02049:Mug1
|
APN |
6 |
121,848,295 (GRCm39) |
missense |
probably benign |
|
IGL02151:Mug1
|
APN |
6 |
121,861,649 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02315:Mug1
|
APN |
6 |
121,817,126 (GRCm39) |
missense |
probably benign |
|
IGL02629:Mug1
|
APN |
6 |
121,817,024 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02642:Mug1
|
APN |
6 |
121,859,544 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02807:Mug1
|
APN |
6 |
121,863,531 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02932:Mug1
|
APN |
6 |
121,864,386 (GRCm39) |
missense |
probably benign |
0.35 |
IGL03232:Mug1
|
APN |
6 |
121,855,494 (GRCm39) |
missense |
probably benign |
0.00 |
R1462_Mug1_304
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R2341_Mug1_749
|
UTSW |
6 |
121,861,588 (GRCm39) |
missense |
probably benign |
0.06 |
R4261_Mug1_652
|
UTSW |
6 |
121,850,693 (GRCm39) |
missense |
probably benign |
|
R6173_mug1_139
|
UTSW |
6 |
121,840,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03050:Mug1
|
UTSW |
6 |
121,857,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0101:Mug1
|
UTSW |
6 |
121,861,206 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0194:Mug1
|
UTSW |
6 |
121,817,066 (GRCm39) |
missense |
probably damaging |
0.98 |
R0196:Mug1
|
UTSW |
6 |
121,815,684 (GRCm39) |
critical splice donor site |
probably null |
|
R0325:Mug1
|
UTSW |
6 |
121,826,801 (GRCm39) |
missense |
probably benign |
|
R0332:Mug1
|
UTSW |
6 |
121,826,856 (GRCm39) |
splice site |
probably null |
|
R0377:Mug1
|
UTSW |
6 |
121,834,320 (GRCm39) |
missense |
probably benign |
0.02 |
R0393:Mug1
|
UTSW |
6 |
121,826,809 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0414:Mug1
|
UTSW |
6 |
121,833,513 (GRCm39) |
missense |
probably benign |
0.00 |
R0457:Mug1
|
UTSW |
6 |
121,838,514 (GRCm39) |
missense |
probably benign |
0.06 |
R0479:Mug1
|
UTSW |
6 |
121,817,186 (GRCm39) |
missense |
probably benign |
|
R0519:Mug1
|
UTSW |
6 |
121,828,383 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0535:Mug1
|
UTSW |
6 |
121,828,413 (GRCm39) |
missense |
probably benign |
|
R0745:Mug1
|
UTSW |
6 |
121,864,386 (GRCm39) |
missense |
probably benign |
0.35 |
R0939:Mug1
|
UTSW |
6 |
121,861,308 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0975:Mug1
|
UTSW |
6 |
121,855,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R1033:Mug1
|
UTSW |
6 |
121,857,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R1086:Mug1
|
UTSW |
6 |
121,862,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Mug1
|
UTSW |
6 |
121,847,604 (GRCm39) |
missense |
probably benign |
|
R1131:Mug1
|
UTSW |
6 |
121,838,144 (GRCm39) |
missense |
probably benign |
0.18 |
R1249:Mug1
|
UTSW |
6 |
121,826,420 (GRCm39) |
missense |
probably benign |
0.07 |
R1364:Mug1
|
UTSW |
6 |
121,858,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Mug1
|
UTSW |
6 |
121,815,635 (GRCm39) |
missense |
probably benign |
0.00 |
R1462:Mug1
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1462:Mug1
|
UTSW |
6 |
121,859,588 (GRCm39) |
missense |
probably benign |
0.41 |
R1494:Mug1
|
UTSW |
6 |
121,856,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1639:Mug1
|
UTSW |
6 |
121,857,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Mug1
|
UTSW |
6 |
121,858,780 (GRCm39) |
missense |
probably benign |
|
R2087:Mug1
|
UTSW |
6 |
121,833,250 (GRCm39) |
missense |
probably benign |
0.00 |
R2168:Mug1
|
UTSW |
6 |
121,847,458 (GRCm39) |
missense |
probably benign |
0.08 |
R2249:Mug1
|
UTSW |
6 |
121,847,469 (GRCm39) |
missense |
probably benign |
|
R2341:Mug1
|
UTSW |
6 |
121,861,588 (GRCm39) |
missense |
probably benign |
0.06 |
R2888:Mug1
|
UTSW |
6 |
121,858,802 (GRCm39) |
missense |
probably benign |
0.44 |
R2892:Mug1
|
UTSW |
6 |
121,817,029 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3703:Mug1
|
UTSW |
6 |
121,865,515 (GRCm39) |
splice site |
probably benign |
|
R3789:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3790:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R3950:Mug1
|
UTSW |
6 |
121,855,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:Mug1
|
UTSW |
6 |
121,850,693 (GRCm39) |
missense |
probably benign |
|
R4402:Mug1
|
UTSW |
6 |
121,856,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4589:Mug1
|
UTSW |
6 |
121,834,310 (GRCm39) |
missense |
probably benign |
0.19 |
R4707:Mug1
|
UTSW |
6 |
121,861,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Mug1
|
UTSW |
6 |
121,861,213 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Mug1
|
UTSW |
6 |
121,862,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Mug1
|
UTSW |
6 |
121,815,576 (GRCm39) |
utr 5 prime |
probably benign |
|
R4999:Mug1
|
UTSW |
6 |
121,855,902 (GRCm39) |
nonsense |
probably null |
|
R5198:Mug1
|
UTSW |
6 |
121,851,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5220:Mug1
|
UTSW |
6 |
121,838,092 (GRCm39) |
missense |
probably benign |
0.03 |
R5253:Mug1
|
UTSW |
6 |
121,865,872 (GRCm39) |
missense |
probably benign |
0.03 |
R5273:Mug1
|
UTSW |
6 |
121,850,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R5285:Mug1
|
UTSW |
6 |
121,818,066 (GRCm39) |
missense |
probably benign |
0.45 |
R5387:Mug1
|
UTSW |
6 |
121,861,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R5560:Mug1
|
UTSW |
6 |
121,838,032 (GRCm39) |
missense |
probably damaging |
0.96 |
R5652:Mug1
|
UTSW |
6 |
121,817,140 (GRCm39) |
missense |
probably benign |
|
R5704:Mug1
|
UTSW |
6 |
121,828,392 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5732:Mug1
|
UTSW |
6 |
121,855,452 (GRCm39) |
missense |
probably benign |
0.00 |
R6053:Mug1
|
UTSW |
6 |
121,842,697 (GRCm39) |
missense |
probably benign |
0.00 |
R6173:Mug1
|
UTSW |
6 |
121,840,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R6578:Mug1
|
UTSW |
6 |
121,864,411 (GRCm39) |
missense |
probably benign |
0.00 |
R6647:Mug1
|
UTSW |
6 |
121,817,200 (GRCm39) |
missense |
probably benign |
0.02 |
R6681:Mug1
|
UTSW |
6 |
121,815,683 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6925:Mug1
|
UTSW |
6 |
121,858,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Mug1
|
UTSW |
6 |
121,838,084 (GRCm39) |
missense |
probably benign |
0.22 |
R7031:Mug1
|
UTSW |
6 |
121,815,673 (GRCm39) |
missense |
probably benign |
0.00 |
R7034:Mug1
|
UTSW |
6 |
121,850,603 (GRCm39) |
missense |
probably benign |
0.00 |
R7156:Mug1
|
UTSW |
6 |
121,861,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7156:Mug1
|
UTSW |
6 |
121,857,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Mug1
|
UTSW |
6 |
121,834,379 (GRCm39) |
missense |
probably benign |
0.00 |
R7211:Mug1
|
UTSW |
6 |
121,857,498 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7318:Mug1
|
UTSW |
6 |
121,847,611 (GRCm39) |
critical splice donor site |
probably null |
|
R7462:Mug1
|
UTSW |
6 |
121,852,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7479:Mug1
|
UTSW |
6 |
121,855,467 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7588:Mug1
|
UTSW |
6 |
121,852,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R7611:Mug1
|
UTSW |
6 |
121,852,387 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7659:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7660:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7661:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7663:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7664:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7666:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7788:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7789:Mug1
|
UTSW |
6 |
121,838,179 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7794:Mug1
|
UTSW |
6 |
121,833,247 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7809:Mug1
|
UTSW |
6 |
121,855,944 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7836:Mug1
|
UTSW |
6 |
121,847,611 (GRCm39) |
critical splice donor site |
probably null |
|
R7867:Mug1
|
UTSW |
6 |
121,850,593 (GRCm39) |
missense |
probably benign |
|
R7904:Mug1
|
UTSW |
6 |
121,828,424 (GRCm39) |
missense |
probably benign |
|
R7937:Mug1
|
UTSW |
6 |
121,838,128 (GRCm39) |
missense |
probably benign |
0.00 |
R7981:Mug1
|
UTSW |
6 |
121,858,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Mug1
|
UTSW |
6 |
121,857,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8070:Mug1
|
UTSW |
6 |
121,852,838 (GRCm39) |
missense |
probably benign |
0.26 |
R8071:Mug1
|
UTSW |
6 |
121,850,631 (GRCm39) |
missense |
probably benign |
|
R8151:Mug1
|
UTSW |
6 |
121,818,117 (GRCm39) |
missense |
probably benign |
0.01 |
R8491:Mug1
|
UTSW |
6 |
121,859,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R8714:Mug1
|
UTSW |
6 |
121,859,681 (GRCm39) |
missense |
probably benign |
0.01 |
R8734:Mug1
|
UTSW |
6 |
121,848,340 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Mug1
|
UTSW |
6 |
121,817,208 (GRCm39) |
splice site |
probably benign |
|
R8807:Mug1
|
UTSW |
6 |
121,851,434 (GRCm39) |
missense |
probably benign |
0.27 |
R8931:Mug1
|
UTSW |
6 |
121,861,296 (GRCm39) |
missense |
probably benign |
|
R8940:Mug1
|
UTSW |
6 |
121,858,642 (GRCm39) |
missense |
|
|
R9156:Mug1
|
UTSW |
6 |
121,851,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R9314:Mug1
|
UTSW |
6 |
121,834,296 (GRCm39) |
missense |
probably damaging |
0.97 |
R9315:Mug1
|
UTSW |
6 |
121,850,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9330:Mug1
|
UTSW |
6 |
121,859,723 (GRCm39) |
missense |
probably benign |
0.14 |
R9334:Mug1
|
UTSW |
6 |
121,838,490 (GRCm39) |
missense |
probably benign |
0.01 |
R9357:Mug1
|
UTSW |
6 |
121,852,450 (GRCm39) |
missense |
probably benign |
0.02 |
R9515:Mug1
|
UTSW |
6 |
121,861,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R9549:Mug1
|
UTSW |
6 |
121,858,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Mug1
|
UTSW |
6 |
121,861,587 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mug1
|
UTSW |
6 |
121,859,699 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Mug1
|
UTSW |
6 |
121,857,463 (GRCm39) |
missense |
probably benign |
0.08 |
R9681:Mug1
|
UTSW |
6 |
121,833,254 (GRCm39) |
missense |
probably benign |
0.01 |
R9777:Mug1
|
UTSW |
6 |
121,857,864 (GRCm39) |
missense |
probably damaging |
1.00 |
RF017:Mug1
|
UTSW |
6 |
121,861,533 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Mug1
|
UTSW |
6 |
121,838,174 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Mug1
|
UTSW |
6 |
121,857,452 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mug1
|
UTSW |
6 |
121,818,253 (GRCm39) |
missense |
probably benign |
0.32 |
Z1177:Mug1
|
UTSW |
6 |
121,856,258 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Mug1
|
UTSW |
6 |
121,840,767 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Mug1
|
UTSW |
6 |
121,863,527 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGCCTCCATATTTGTCCCAG -3'
(R):5'- AGACTCATTTCTTCATGGGGC -3'
Sequencing Primer
(F):5'- ATATTTGTCCCAGGATCTGCTAGGAC -3'
(R):5'- CATTTCTTCATGGGGCAGTCCAAG -3'
|
Posted On |
2014-06-30 |