Incidental Mutation 'R4898:Mgam'
ID |
375892 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mgam
|
Ensembl Gene |
ENSMUSG00000068587 |
Gene Name |
maltase-glucoamylase |
Synonyms |
6030407P20Rik |
MMRRC Submission |
042502-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.237)
|
Stock # |
R4898 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
40605765-40746057 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 40619988 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Leucine
at position 26
(I26L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000143946
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071535]
[ENSMUST00000201148]
[ENSMUST00000202636]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000071535
AA Change: I26L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000071466 Gene: ENSMUSG00000068587 AA Change: I26L
Domain | Start | End | E-Value | Type |
transmembrane domain
|
12 |
34 |
N/A |
INTRINSIC |
low complexity region
|
47 |
59 |
N/A |
INTRINSIC |
PD
|
63 |
111 |
1.81e-8 |
SMART |
Pfam:NtCtMGAM_N
|
124 |
233 |
6.2e-36 |
PFAM |
Pfam:Glyco_hydro_31
|
323 |
795 |
3.4e-145 |
PFAM |
PD
|
924 |
977 |
4.52e-9 |
SMART |
Pfam:NtCtMGAM_N
|
988 |
1101 |
1.5e-30 |
PFAM |
Blast:ANK
|
1141 |
1171 |
1e-7 |
BLAST |
Pfam:Glyco_hydro_31
|
1189 |
1691 |
2e-139 |
PFAM |
low complexity region
|
1776 |
1791 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201148
AA Change: I26L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000143946 Gene: ENSMUSG00000068587 AA Change: I26L
Domain | Start | End | E-Value | Type |
transmembrane domain
|
12 |
34 |
N/A |
INTRINSIC |
low complexity region
|
47 |
59 |
N/A |
INTRINSIC |
PD
|
63 |
111 |
1.81e-8 |
SMART |
Pfam:NtCtMGAM_N
|
124 |
233 |
6.2e-36 |
PFAM |
Pfam:Glyco_hydro_31
|
323 |
795 |
3.4e-145 |
PFAM |
PD
|
924 |
977 |
4.52e-9 |
SMART |
Pfam:NtCtMGAM_N
|
988 |
1101 |
1.5e-30 |
PFAM |
Blast:ANK
|
1141 |
1171 |
1e-7 |
BLAST |
Pfam:Glyco_hydro_31
|
1189 |
1691 |
2e-139 |
PFAM |
low complexity region
|
1776 |
1791 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202636
|
SMART Domains |
Protein: ENSMUSP00000144652 Gene: ENSMUSG00000068587
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
22 |
N/A |
INTRINSIC |
Pfam:Trefoil
|
28 |
70 |
3.6e-12 |
PFAM |
Pfam:NtCtMGAM_N
|
87 |
196 |
1.4e-36 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes maltase-glucoamylase, which is a brush border membrane enzyme that plays a role in the final steps of digestion of starch. The protein has two catalytic sites identical to those of sucrase-isomaltase, but the proteins are only 59% homologous. Both are members of glycosyl hydrolase family 31, which has a variety of substrate specificities. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a null allele display abnormalities in starch digestion and prandial glucose homeostasis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
T |
C |
7: 45,639,111 (GRCm39) |
Y944C |
probably damaging |
Het |
Acacb |
T |
C |
5: 114,370,999 (GRCm39) |
V1747A |
probably benign |
Het |
Acad8 |
C |
T |
9: 26,889,698 (GRCm39) |
R332H |
probably damaging |
Het |
Acrbp |
A |
C |
6: 125,027,501 (GRCm39) |
T50P |
probably damaging |
Het |
Ahctf1 |
G |
T |
1: 179,583,077 (GRCm39) |
N1500K |
probably benign |
Het |
Aoc1l3 |
A |
G |
6: 48,964,651 (GRCm39) |
T220A |
possibly damaging |
Het |
Arfgef1 |
A |
G |
1: 10,229,798 (GRCm39) |
I1301T |
possibly damaging |
Het |
Arhgef15 |
T |
C |
11: 68,842,171 (GRCm39) |
S478G |
probably benign |
Het |
Armh1 |
T |
C |
4: 117,094,977 (GRCm39) |
D21G |
probably damaging |
Het |
Atp13a4 |
A |
T |
16: 29,227,779 (GRCm39) |
L1045* |
probably null |
Het |
Atp2a3 |
T |
A |
11: 72,873,506 (GRCm39) |
L793H |
probably damaging |
Het |
B4galnt4 |
C |
A |
7: 140,648,173 (GRCm39) |
P563Q |
probably benign |
Het |
Bcl2a1b |
A |
T |
9: 89,081,713 (GRCm39) |
K94* |
probably null |
Het |
Bod1 |
T |
A |
11: 31,616,853 (GRCm39) |
Q136L |
possibly damaging |
Het |
C2cd3 |
A |
G |
7: 100,055,166 (GRCm39) |
K443R |
probably damaging |
Het |
Cadps |
A |
G |
14: 12,411,588 (GRCm38) |
V1250A |
possibly damaging |
Het |
Car12 |
T |
A |
9: 66,671,600 (GRCm39) |
Y332* |
probably null |
Het |
Ccdc186 |
A |
T |
19: 56,790,432 (GRCm39) |
|
probably null |
Het |
Cdh6 |
T |
C |
15: 13,034,774 (GRCm39) |
T629A |
probably damaging |
Het |
Cep112 |
T |
A |
11: 108,397,471 (GRCm39) |
D353E |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,428,301 (GRCm39) |
S777G |
probably benign |
Het |
Clec4b2 |
A |
C |
6: 123,181,163 (GRCm39) |
K183Q |
probably benign |
Het |
Cngb3 |
T |
C |
4: 19,395,926 (GRCm39) |
Y323H |
probably benign |
Het |
Cnp |
G |
T |
11: 100,467,202 (GRCm39) |
E48D |
probably benign |
Het |
Ctrb1 |
T |
A |
8: 112,413,783 (GRCm39) |
I194F |
probably benign |
Het |
Cyp2d11 |
T |
A |
15: 82,275,224 (GRCm39) |
D241V |
probably benign |
Het |
D5Ertd579e |
T |
A |
5: 36,772,285 (GRCm39) |
E703D |
probably damaging |
Het |
Dlg1 |
T |
C |
16: 31,676,764 (GRCm39) |
V731A |
probably damaging |
Het |
Dlgap5 |
T |
C |
14: 47,651,276 (GRCm39) |
S86G |
probably benign |
Het |
Dock3 |
A |
G |
9: 106,807,266 (GRCm39) |
F1354L |
probably damaging |
Het |
Dock3 |
C |
A |
9: 106,870,171 (GRCm39) |
V638F |
possibly damaging |
Het |
Eif3c |
A |
T |
7: 126,156,626 (GRCm39) |
M407K |
probably benign |
Het |
Eif4a3l1 |
A |
T |
6: 136,305,737 (GRCm39) |
Q66L |
possibly damaging |
Het |
Epha4 |
T |
A |
1: 77,366,712 (GRCm39) |
K578* |
probably null |
Het |
Erc2 |
C |
T |
14: 27,375,285 (GRCm39) |
L168F |
probably damaging |
Het |
Esyt2 |
A |
G |
12: 116,305,708 (GRCm39) |
I313V |
probably benign |
Het |
Far1 |
T |
A |
7: 113,167,432 (GRCm39) |
Y506N |
probably damaging |
Het |
Fbxw26 |
T |
A |
9: 109,547,037 (GRCm39) |
N463Y |
possibly damaging |
Het |
Fgg |
A |
G |
3: 82,915,847 (GRCm39) |
D96G |
probably benign |
Het |
Gfer |
A |
G |
17: 24,914,274 (GRCm39) |
S130P |
probably damaging |
Het |
Hdac10 |
A |
T |
15: 89,012,650 (GRCm39) |
M1K |
probably null |
Het |
Hsd3b1 |
A |
T |
3: 98,760,642 (GRCm39) |
S110R |
probably benign |
Het |
Ints15 |
A |
G |
5: 143,287,592 (GRCm39) |
S438P |
probably benign |
Het |
Itga6 |
T |
C |
2: 71,668,717 (GRCm39) |
L552P |
possibly damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Llgl1 |
C |
T |
11: 60,600,394 (GRCm39) |
P581L |
probably benign |
Het |
Lrrc8a |
A |
G |
2: 30,147,214 (GRCm39) |
K676R |
probably benign |
Het |
Lrrc8b |
A |
T |
5: 105,628,080 (GRCm39) |
Y142F |
probably benign |
Het |
Lyz2 |
T |
A |
10: 117,114,614 (GRCm39) |
D105V |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,460,035 (GRCm39) |
D76G |
probably damaging |
Het |
Map7d1 |
T |
C |
4: 126,127,018 (GRCm39) |
K731E |
unknown |
Het |
Mmp13 |
A |
T |
9: 7,272,953 (GRCm39) |
E104D |
probably benign |
Het |
Morc2a |
C |
T |
11: 3,626,664 (GRCm39) |
R241* |
probably null |
Het |
Mtfmt |
C |
A |
9: 65,359,386 (GRCm39) |
H354N |
probably benign |
Het |
Myh3 |
T |
C |
11: 66,990,233 (GRCm39) |
I1626T |
probably benign |
Het |
Ndst1 |
A |
T |
18: 60,825,059 (GRCm39) |
V753D |
probably benign |
Het |
Neurl4 |
A |
G |
11: 69,793,997 (GRCm39) |
D151G |
probably damaging |
Het |
Nlrx1 |
T |
C |
9: 44,168,194 (GRCm39) |
S568G |
probably benign |
Het |
Or10g3b |
G |
C |
14: 52,586,999 (GRCm39) |
P168R |
probably damaging |
Het |
Or2t45 |
T |
C |
11: 58,669,132 (GRCm39) |
Y60H |
possibly damaging |
Het |
Or2t46 |
T |
G |
11: 58,472,546 (GRCm39) |
L292R |
probably damaging |
Het |
Or4c52 |
T |
C |
2: 89,845,762 (GRCm39) |
F163L |
probably damaging |
Het |
Or52s1 |
A |
G |
7: 102,861,747 (GRCm39) |
I216V |
probably damaging |
Het |
Or6c66 |
A |
T |
10: 129,461,468 (GRCm39) |
I154N |
probably benign |
Het |
Or8b42 |
A |
T |
9: 38,342,111 (GRCm39) |
M178L |
probably benign |
Het |
Osbpl7 |
A |
G |
11: 96,950,976 (GRCm39) |
I608V |
probably damaging |
Het |
Pard3b |
T |
C |
1: 61,807,159 (GRCm39) |
I58T |
probably damaging |
Het |
Pcare |
A |
G |
17: 72,058,066 (GRCm39) |
M537T |
probably damaging |
Het |
Pcdhga1 |
A |
C |
18: 37,795,407 (GRCm39) |
E137A |
possibly damaging |
Het |
Pde6c |
G |
A |
19: 38,139,072 (GRCm39) |
V301I |
possibly damaging |
Het |
Pdia5 |
G |
C |
16: 35,230,786 (GRCm39) |
N338K |
possibly damaging |
Het |
Pex11g |
T |
C |
8: 3,514,042 (GRCm39) |
Y40C |
probably damaging |
Het |
Plekhg3 |
A |
G |
12: 76,610,899 (GRCm39) |
Y183C |
probably damaging |
Het |
Pole |
A |
C |
5: 110,438,090 (GRCm39) |
|
probably null |
Het |
Ppfia1 |
A |
G |
7: 144,045,313 (GRCm39) |
L948P |
probably damaging |
Het |
Prdm2 |
A |
T |
4: 142,860,761 (GRCm39) |
V843E |
probably damaging |
Het |
Prss56 |
C |
A |
1: 87,115,708 (GRCm39) |
F527L |
probably damaging |
Het |
Psmd11 |
T |
C |
11: 80,329,146 (GRCm39) |
L88P |
probably damaging |
Het |
Ptx3 |
G |
C |
3: 66,132,412 (GRCm39) |
G311A |
probably damaging |
Het |
Rars1 |
A |
T |
11: 35,699,385 (GRCm39) |
L636H |
probably damaging |
Het |
Rnft2 |
A |
G |
5: 118,375,507 (GRCm39) |
S81P |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Rxra |
T |
A |
2: 27,631,195 (GRCm39) |
I142N |
probably damaging |
Het |
Scin |
T |
C |
12: 40,154,931 (GRCm39) |
M221V |
probably benign |
Het |
Sfmbt2 |
G |
A |
2: 10,584,069 (GRCm39) |
V809I |
possibly damaging |
Het |
Sirt1 |
T |
A |
10: 63,157,783 (GRCm39) |
I505F |
probably benign |
Het |
Six5 |
T |
C |
7: 18,829,096 (GRCm39) |
Y179H |
probably damaging |
Het |
Slc12a4 |
A |
C |
8: 106,671,241 (GRCm39) |
M982R |
probably damaging |
Het |
Slco4c1 |
T |
A |
1: 96,765,237 (GRCm39) |
L404F |
probably damaging |
Het |
Smn1 |
T |
C |
13: 100,268,931 (GRCm39) |
L259P |
probably damaging |
Het |
Sorl1 |
T |
G |
9: 41,952,935 (GRCm39) |
D702A |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,065,400 (GRCm39) |
E1983G |
possibly damaging |
Het |
Srsf1 |
T |
A |
11: 87,940,788 (GRCm39) |
|
probably null |
Het |
Stard9 |
C |
T |
2: 120,536,900 (GRCm39) |
R4224* |
probably null |
Het |
Sybu |
T |
G |
15: 44,538,895 (GRCm39) |
M383L |
probably benign |
Het |
Tbx15 |
A |
C |
3: 99,259,583 (GRCm39) |
N485H |
possibly damaging |
Het |
Tcerg1l |
A |
T |
7: 137,819,786 (GRCm39) |
F485I |
probably damaging |
Het |
Tdrd7 |
C |
A |
4: 46,005,616 (GRCm39) |
T474N |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,755,470 (GRCm39) |
|
probably null |
Het |
Tnik |
A |
T |
3: 28,704,235 (GRCm39) |
I1020F |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,914,566 (GRCm39) |
D1884G |
possibly damaging |
Het |
Tprn |
T |
C |
2: 25,158,845 (GRCm39) |
M623T |
probably damaging |
Het |
Trdn |
T |
A |
10: 33,350,413 (GRCm39) |
Y661N |
probably damaging |
Het |
Ttc41 |
T |
C |
10: 86,612,056 (GRCm39) |
S1110P |
possibly damaging |
Het |
Ttc6 |
A |
C |
12: 57,707,026 (GRCm39) |
R644S |
probably benign |
Het |
Ttyh1 |
A |
T |
7: 4,136,735 (GRCm39) |
M448L |
probably benign |
Het |
Unc79 |
G |
T |
12: 103,128,079 (GRCm39) |
C2250F |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,358,805 (GRCm39) |
I2110M |
probably benign |
Het |
Uvssa |
G |
T |
5: 33,571,257 (GRCm39) |
E634* |
probably null |
Het |
Vac14 |
A |
C |
8: 111,372,440 (GRCm39) |
T384P |
probably benign |
Het |
Wdr11 |
A |
G |
7: 129,235,445 (GRCm39) |
E1169G |
probably benign |
Het |
Zfp36l1 |
T |
A |
12: 80,157,298 (GRCm39) |
T28S |
probably benign |
Het |
Zfp715 |
A |
T |
7: 42,949,106 (GRCm39) |
Y285N |
possibly damaging |
Het |
Zfp91 |
A |
T |
19: 12,747,424 (GRCm39) |
D566E |
probably damaging |
Het |
Zgrf1 |
G |
A |
3: 127,396,085 (GRCm39) |
V544M |
probably damaging |
Het |
|
Other mutations in Mgam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Mgam
|
APN |
6 |
40,619,944 (GRCm39) |
missense |
probably benign |
|
IGL01065:Mgam
|
APN |
6 |
40,639,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01402:Mgam
|
APN |
6 |
40,621,879 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01404:Mgam
|
APN |
6 |
40,621,879 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01413:Mgam
|
APN |
6 |
40,638,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01546:Mgam
|
APN |
6 |
40,631,627 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01596:Mgam
|
APN |
6 |
40,635,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02133:Mgam
|
APN |
6 |
40,620,010 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02734:Mgam
|
APN |
6 |
40,639,628 (GRCm39) |
missense |
probably damaging |
1.00 |
BB002:Mgam
|
UTSW |
6 |
40,735,985 (GRCm39) |
missense |
probably damaging |
0.99 |
BB012:Mgam
|
UTSW |
6 |
40,735,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R0012:Mgam
|
UTSW |
6 |
40,742,190 (GRCm39) |
splice site |
probably null |
|
R0116:Mgam
|
UTSW |
6 |
40,635,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R0310:Mgam
|
UTSW |
6 |
40,737,969 (GRCm39) |
splice site |
probably benign |
|
R0452:Mgam
|
UTSW |
6 |
40,736,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R0497:Mgam
|
UTSW |
6 |
40,641,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Mgam
|
UTSW |
6 |
40,619,953 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0738:Mgam
|
UTSW |
6 |
40,731,869 (GRCm39) |
missense |
probably benign |
0.01 |
R1033:Mgam
|
UTSW |
6 |
40,657,558 (GRCm39) |
missense |
probably benign |
0.07 |
R1403:Mgam
|
UTSW |
6 |
40,643,815 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1403:Mgam
|
UTSW |
6 |
40,643,815 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1430:Mgam
|
UTSW |
6 |
40,733,305 (GRCm39) |
missense |
probably benign |
0.08 |
R1432:Mgam
|
UTSW |
6 |
40,733,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R1443:Mgam
|
UTSW |
6 |
40,736,714 (GRCm39) |
nonsense |
probably null |
|
R1470:Mgam
|
UTSW |
6 |
40,736,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Mgam
|
UTSW |
6 |
40,736,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:Mgam
|
UTSW |
6 |
40,638,617 (GRCm39) |
missense |
probably benign |
0.45 |
R1654:Mgam
|
UTSW |
6 |
40,734,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Mgam
|
UTSW |
6 |
40,653,978 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1730:Mgam
|
UTSW |
6 |
40,641,794 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1781:Mgam
|
UTSW |
6 |
40,646,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Mgam
|
UTSW |
6 |
40,641,794 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1829:Mgam
|
UTSW |
6 |
40,643,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R1833:Mgam
|
UTSW |
6 |
40,631,652 (GRCm39) |
critical splice donor site |
probably null |
|
R1872:Mgam
|
UTSW |
6 |
40,638,234 (GRCm39) |
nonsense |
probably null |
|
R1912:Mgam
|
UTSW |
6 |
40,741,119 (GRCm39) |
nonsense |
probably null |
|
R1977:Mgam
|
UTSW |
6 |
40,641,814 (GRCm39) |
missense |
probably benign |
0.01 |
R2048:Mgam
|
UTSW |
6 |
40,633,363 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2086:Mgam
|
UTSW |
6 |
40,737,962 (GRCm39) |
splice site |
probably null |
|
R2138:Mgam
|
UTSW |
6 |
40,733,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R2224:Mgam
|
UTSW |
6 |
40,741,208 (GRCm39) |
splice site |
probably null |
|
R2408:Mgam
|
UTSW |
6 |
40,663,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Mgam
|
UTSW |
6 |
40,736,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Mgam
|
UTSW |
6 |
40,638,279 (GRCm39) |
missense |
probably benign |
0.01 |
R2847:Mgam
|
UTSW |
6 |
40,629,649 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2848:Mgam
|
UTSW |
6 |
40,629,649 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2965:Mgam
|
UTSW |
6 |
40,745,154 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2966:Mgam
|
UTSW |
6 |
40,745,154 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3035:Mgam
|
UTSW |
6 |
40,640,464 (GRCm39) |
missense |
probably benign |
|
R3895:Mgam
|
UTSW |
6 |
40,736,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Mgam
|
UTSW |
6 |
40,731,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4030:Mgam
|
UTSW |
6 |
40,731,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4302:Mgam
|
UTSW |
6 |
40,740,019 (GRCm39) |
missense |
probably benign |
0.02 |
R4707:Mgam
|
UTSW |
6 |
40,691,566 (GRCm39) |
splice site |
probably null |
|
R4826:Mgam
|
UTSW |
6 |
40,657,582 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5438:Mgam
|
UTSW |
6 |
40,661,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R5492:Mgam
|
UTSW |
6 |
40,733,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R5770:Mgam
|
UTSW |
6 |
40,646,738 (GRCm39) |
missense |
probably benign |
0.01 |
R5839:Mgam
|
UTSW |
6 |
40,716,998 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5845:Mgam
|
UTSW |
6 |
40,652,257 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5847:Mgam
|
UTSW |
6 |
40,660,989 (GRCm39) |
missense |
probably benign |
0.42 |
R5891:Mgam
|
UTSW |
6 |
40,721,282 (GRCm39) |
missense |
probably benign |
|
R6158:Mgam
|
UTSW |
6 |
40,734,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Mgam
|
UTSW |
6 |
40,724,854 (GRCm39) |
nonsense |
probably null |
|
R6423:Mgam
|
UTSW |
6 |
40,653,979 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6706:Mgam
|
UTSW |
6 |
40,721,720 (GRCm39) |
missense |
probably benign |
0.00 |
R6813:Mgam
|
UTSW |
6 |
40,727,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R6863:Mgam
|
UTSW |
6 |
40,705,943 (GRCm39) |
missense |
probably benign |
0.00 |
R6906:Mgam
|
UTSW |
6 |
40,724,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7091:Mgam
|
UTSW |
6 |
40,745,210 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7099:Mgam
|
UTSW |
6 |
40,638,650 (GRCm39) |
missense |
probably benign |
0.09 |
R7282:Mgam
|
UTSW |
6 |
40,740,045 (GRCm39) |
missense |
probably benign |
|
R7282:Mgam
|
UTSW |
6 |
40,633,446 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7354:Mgam
|
UTSW |
6 |
40,721,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7374:Mgam
|
UTSW |
6 |
40,734,373 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7399:Mgam
|
UTSW |
6 |
40,643,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R7406:Mgam
|
UTSW |
6 |
40,640,459 (GRCm39) |
missense |
probably benign |
0.13 |
R7446:Mgam
|
UTSW |
6 |
40,723,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Mgam
|
UTSW |
6 |
40,721,723 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Mgam
|
UTSW |
6 |
40,742,954 (GRCm39) |
missense |
probably benign |
0.01 |
R7530:Mgam
|
UTSW |
6 |
40,686,152 (GRCm39) |
splice site |
probably null |
|
R7570:Mgam
|
UTSW |
6 |
40,723,367 (GRCm39) |
missense |
probably benign |
0.16 |
R7669:Mgam
|
UTSW |
6 |
40,635,944 (GRCm39) |
missense |
probably benign |
0.00 |
R7679:Mgam
|
UTSW |
6 |
40,619,980 (GRCm39) |
missense |
probably damaging |
0.98 |
R7746:Mgam
|
UTSW |
6 |
40,645,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R7859:Mgam
|
UTSW |
6 |
40,717,113 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7925:Mgam
|
UTSW |
6 |
40,735,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R8206:Mgam
|
UTSW |
6 |
40,657,169 (GRCm39) |
missense |
probably benign |
0.00 |
R8244:Mgam
|
UTSW |
6 |
40,727,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R8309:Mgam
|
UTSW |
6 |
40,722,111 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8472:Mgam
|
UTSW |
6 |
40,671,460 (GRCm39) |
splice site |
probably null |
|
R8758:Mgam
|
UTSW |
6 |
40,705,977 (GRCm39) |
missense |
probably benign |
0.41 |
R8777:Mgam
|
UTSW |
6 |
40,632,185 (GRCm39) |
missense |
probably damaging |
0.97 |
R8777-TAIL:Mgam
|
UTSW |
6 |
40,632,185 (GRCm39) |
missense |
probably damaging |
0.97 |
R8783:Mgam
|
UTSW |
6 |
40,633,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R8939:Mgam
|
UTSW |
6 |
40,740,137 (GRCm39) |
critical splice donor site |
probably null |
|
R8968:Mgam
|
UTSW |
6 |
40,734,745 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8987:Mgam
|
UTSW |
6 |
40,706,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R9055:Mgam
|
UTSW |
6 |
40,691,663 (GRCm39) |
intron |
probably benign |
|
R9171:Mgam
|
UTSW |
6 |
40,745,146 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9252:Mgam
|
UTSW |
6 |
40,706,577 (GRCm39) |
missense |
probably damaging |
0.99 |
R9258:Mgam
|
UTSW |
6 |
40,657,121 (GRCm39) |
missense |
probably benign |
|
R9262:Mgam
|
UTSW |
6 |
40,723,422 (GRCm39) |
critical splice donor site |
probably null |
|
R9287:Mgam
|
UTSW |
6 |
40,705,905 (GRCm39) |
intron |
probably benign |
|
R9521:Mgam
|
UTSW |
6 |
40,722,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R9589:Mgam
|
UTSW |
6 |
40,727,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Mgam
|
UTSW |
6 |
40,721,311 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9784:Mgam
|
UTSW |
6 |
40,736,024 (GRCm39) |
missense |
probably damaging |
1.00 |
RF011:Mgam
|
UTSW |
6 |
40,734,370 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Mgam
|
UTSW |
6 |
40,662,243 (GRCm39) |
missense |
probably damaging |
1.00 |
RF023:Mgam
|
UTSW |
6 |
40,657,642 (GRCm39) |
missense |
probably benign |
|
X0021:Mgam
|
UTSW |
6 |
40,635,981 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Mgam
|
UTSW |
6 |
40,619,994 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Mgam
|
UTSW |
6 |
40,706,000 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mgam
|
UTSW |
6 |
40,654,578 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Mgam
|
UTSW |
6 |
40,717,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ACAGGTCGGCGACTAAATAG -3'
(R):5'- TACTGTCTGCATGCGTTCAC -3'
Sequencing Primer
(F):5'- TTACTTTTGAAAATTCAGGGGGAAGG -3'
(R):5'- GCATGCGTTCACATCCAC -3'
|
Posted On |
2016-03-17 |