Incidental Mutation 'R7570:Mgam'
ID |
585701 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mgam
|
Ensembl Gene |
ENSMUSG00000068587 |
Gene Name |
maltase-glucoamylase |
Synonyms |
6030407P20Rik |
MMRRC Submission |
045631-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.231)
|
Stock # |
R7570 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
40605765-40746057 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 40723367 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Leucine
at position 491
(I491L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144627
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071535]
[ENSMUST00000201148]
[ENSMUST00000202779]
[ENSMUST00000202966]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000071535
|
SMART Domains |
Protein: ENSMUSP00000071466 Gene: ENSMUSG00000068587
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
|
SMART Domains |
Protein: ENSMUSP00000143946 Gene: ENSMUSG00000068587
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: ENSMUST00000202779
AA Change: I491L
PolyPhen 2
Score 0.157 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000144627 Gene: ENSMUSG00000068587 AA Change: I491L
Domain | Start | End | E-Value | Type |
Pfam:Glyco_hydro_31
|
2 |
170 |
1.4e-53 |
PFAM |
PD
|
297 |
350 |
1.4e-14 |
SMART |
Pfam:NtCtMGAM_N
|
361 |
474 |
1.5e-26 |
PFAM |
Blast:ANK
|
514 |
544 |
7e-8 |
BLAST |
Pfam:Glyco_hydro_31
|
562 |
1064 |
2.2e-137 |
PFAM |
low complexity region
|
1149 |
1164 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202966
AA Change: I372L
PolyPhen 2
Score 0.091 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000144680 Gene: ENSMUSG00000068587 AA Change: I372L
Domain | Start | End | E-Value | Type |
internal_repeat_1
|
2 |
88 |
2.6e-19 |
PROSPERO |
PD
|
178 |
231 |
1.4e-14 |
SMART |
Pfam:NtCtMGAM_N
|
242 |
355 |
1.1e-26 |
PFAM |
Blast:ANK
|
395 |
425 |
6e-8 |
BLAST |
Pfam:Glyco_hydro_31
|
443 |
945 |
1.3e-137 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
98% (104/106) |
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: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
C |
T |
6: 91,911,591 (GRCm39) |
T613I |
probably benign |
Het |
Ajuba |
T |
C |
14: 54,813,859 (GRCm39) |
E288G |
probably damaging |
Het |
Ankrd12 |
C |
T |
17: 66,292,355 (GRCm39) |
R1026K |
probably benign |
Het |
Apol7b |
T |
C |
15: 77,307,674 (GRCm39) |
T274A |
probably benign |
Het |
Arid4a |
A |
T |
12: 71,109,916 (GRCm39) |
R86* |
probably null |
Het |
Asnsd1 |
C |
T |
1: 53,387,417 (GRCm39) |
G70D |
probably damaging |
Het |
Atg4c |
T |
A |
4: 99,116,797 (GRCm39) |
V313D |
possibly damaging |
Het |
Atp13a5 |
A |
C |
16: 29,085,715 (GRCm39) |
C885G |
probably damaging |
Het |
Bpifb9a |
A |
T |
2: 154,104,183 (GRCm39) |
I209F |
possibly damaging |
Het |
Bsn |
T |
C |
9: 107,990,742 (GRCm39) |
D1670G |
probably damaging |
Het |
Cct8 |
T |
A |
16: 87,288,210 (GRCm39) |
I121F |
probably benign |
Het |
Cd209a |
T |
G |
8: 3,794,151 (GRCm39) |
D217A |
probably damaging |
Het |
Cdk19 |
C |
T |
10: 40,353,954 (GRCm39) |
S456L |
possibly damaging |
Het |
Chd9 |
C |
T |
8: 91,721,208 (GRCm39) |
H999Y |
unknown |
Het |
Col5a1 |
G |
A |
2: 27,841,395 (GRCm39) |
V339M |
unknown |
Het |
Cr2 |
G |
A |
1: 194,851,648 (GRCm39) |
R115* |
probably null |
Het |
Cyb561 |
A |
T |
11: 105,828,470 (GRCm39) |
F62I |
probably damaging |
Het |
Cyp2c38 |
A |
T |
19: 39,393,187 (GRCm39) |
N293K |
possibly damaging |
Het |
Cyp2c69 |
A |
T |
19: 39,848,342 (GRCm39) |
D293E |
probably damaging |
Het |
Dcbld2 |
T |
A |
16: 58,244,932 (GRCm39) |
C69S |
possibly damaging |
Het |
Dcdc2a |
T |
C |
13: 25,303,356 (GRCm39) |
S296P |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,027,024 (GRCm39) |
I2044K |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,347,098 (GRCm39) |
D2527G |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,126,413 (GRCm39) |
T1305A |
probably benign |
Het |
Dnajc9 |
A |
G |
14: 20,438,712 (GRCm39) |
V47A |
probably benign |
Het |
Dnmt3b |
A |
G |
2: 153,518,619 (GRCm39) |
Y594C |
probably damaging |
Het |
Dph7 |
A |
G |
2: 24,855,642 (GRCm39) |
D147G |
probably damaging |
Het |
Drap1 |
T |
C |
19: 5,473,380 (GRCm39) |
H164R |
possibly damaging |
Het |
Dsg3 |
T |
A |
18: 20,660,837 (GRCm39) |
V392E |
possibly damaging |
Het |
Dxo |
A |
G |
17: 35,056,616 (GRCm39) |
D81G |
probably benign |
Het |
E230025N22Rik |
G |
T |
18: 36,828,645 (GRCm39) |
T11K |
probably benign |
Het |
Esyt1 |
A |
G |
10: 128,354,801 (GRCm39) |
V533A |
possibly damaging |
Het |
Etv3 |
T |
A |
3: 87,443,338 (GRCm39) |
C307* |
probably null |
Het |
Fam114a1 |
T |
A |
5: 65,187,402 (GRCm39) |
|
probably null |
Het |
Fam3c |
T |
A |
6: 22,326,404 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
G |
T |
2: 125,239,772 (GRCm39) |
T305K |
probably benign |
Het |
Ggt1 |
A |
T |
10: 75,421,428 (GRCm39) |
I484F |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 34,993,237 (GRCm39) |
D536G |
probably damaging |
Het |
Gpx4 |
T |
C |
10: 79,890,875 (GRCm39) |
I189T |
probably damaging |
Het |
Gsr |
T |
A |
8: 34,159,193 (GRCm39) |
C85S |
probably damaging |
Het |
Gsta5 |
A |
T |
9: 78,211,751 (GRCm39) |
D171V |
possibly damaging |
Het |
Havcr1 |
T |
A |
11: 46,661,369 (GRCm39) |
|
probably null |
Het |
Heatr4 |
T |
C |
12: 84,026,418 (GRCm39) |
T280A |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,313,923 (GRCm39) |
E3532D |
probably benign |
Het |
Hnrnpc |
T |
C |
14: 52,312,556 (GRCm39) |
N308S |
possibly damaging |
Het |
Ighv8-9 |
A |
G |
12: 115,432,358 (GRCm39) |
V13A |
probably benign |
Het |
Itgb2l |
A |
T |
16: 96,227,439 (GRCm39) |
F535I |
probably benign |
Het |
Kdm5a |
T |
G |
6: 120,404,803 (GRCm39) |
D1348E |
probably damaging |
Het |
Kndc1 |
CT |
C |
7: 139,503,691 (GRCm39) |
|
probably null |
Het |
Ky |
A |
G |
9: 102,419,528 (GRCm39) |
I512V |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,119,021 (GRCm39) |
F866Y |
possibly damaging |
Het |
Lbx1 |
C |
A |
19: 45,223,687 (GRCm39) |
|
probably benign |
Het |
Magel2 |
A |
G |
7: 62,028,658 (GRCm39) |
T521A |
possibly damaging |
Het |
Mitd1 |
T |
C |
1: 37,929,273 (GRCm39) |
E40G |
probably damaging |
Het |
Mpzl3 |
A |
G |
9: 44,981,985 (GRCm39) |
T218A |
probably benign |
Het |
Mrpl42 |
A |
G |
10: 95,316,827 (GRCm39) |
S77P |
probably benign |
Het |
Mup5 |
C |
T |
4: 61,752,911 (GRCm39) |
W37* |
probably null |
Het |
Myh14 |
T |
C |
7: 44,281,850 (GRCm39) |
I803V |
probably benign |
Het |
Ncor2 |
T |
A |
5: 125,107,153 (GRCm39) |
T744S |
|
Het |
Ndufv3 |
A |
G |
17: 31,746,596 (GRCm39) |
D162G |
probably damaging |
Het |
Nostrin |
A |
G |
2: 69,006,150 (GRCm39) |
E278G |
probably damaging |
Het |
Nrxn1 |
T |
G |
17: 90,469,807 (GRCm39) |
E1288A |
probably benign |
Het |
Or4c11c |
A |
G |
2: 88,661,472 (GRCm39) |
N4D |
possibly damaging |
Het |
Or51b6b |
C |
A |
7: 103,310,088 (GRCm39) |
R123L |
probably damaging |
Het |
Or52h1 |
T |
A |
7: 103,828,955 (GRCm39) |
Y220F |
probably damaging |
Het |
Or8g55 |
A |
T |
9: 39,784,751 (GRCm39) |
Y60F |
possibly damaging |
Het |
Patj |
T |
A |
4: 98,312,737 (GRCm39) |
|
probably null |
Het |
Pcm1 |
T |
G |
8: 41,720,381 (GRCm39) |
I314R |
possibly damaging |
Het |
Pcsk6 |
A |
G |
7: 65,683,646 (GRCm39) |
T754A |
probably benign |
Het |
Pde2a |
A |
T |
7: 101,152,041 (GRCm39) |
N326I |
probably benign |
Het |
Plekhg4 |
T |
C |
8: 106,105,316 (GRCm39) |
S594P |
possibly damaging |
Het |
Plekhm3 |
T |
C |
1: 64,977,065 (GRCm39) |
D135G |
probably damaging |
Het |
Plin4 |
A |
T |
17: 56,413,776 (GRCm39) |
M283K |
probably benign |
Het |
Ppfia3 |
T |
C |
7: 44,990,172 (GRCm39) |
|
probably null |
Het |
Prdm9 |
T |
C |
17: 15,775,914 (GRCm39) |
N179S |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,471,449 (GRCm39) |
S908G |
probably damaging |
Het |
Psg22 |
C |
A |
7: 18,456,660 (GRCm39) |
S181Y |
possibly damaging |
Het |
Rcor3 |
C |
A |
1: 191,822,173 (GRCm39) |
G8V |
probably damaging |
Het |
Rp1l1 |
T |
A |
14: 64,269,023 (GRCm39) |
C1536* |
probably null |
Het |
Rpp25l |
T |
C |
4: 41,712,529 (GRCm39) |
H82R |
probably damaging |
Het |
Rps3a1 |
T |
A |
3: 86,046,396 (GRCm39) |
M172L |
probably benign |
Het |
Rtbdn |
T |
C |
8: 85,679,556 (GRCm39) |
L110P |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,778,010 (GRCm39) |
Q2169L |
probably damaging |
Het |
Scn4a |
A |
T |
11: 106,211,299 (GRCm39) |
C1573S |
possibly damaging |
Het |
Sec16b |
A |
T |
1: 157,358,965 (GRCm39) |
|
probably null |
Het |
Serpina1a |
A |
T |
12: 103,820,096 (GRCm39) |
D383E |
possibly damaging |
Het |
Sh3gl3 |
T |
C |
7: 81,934,285 (GRCm39) |
M262T |
probably benign |
Het |
Sos2 |
G |
A |
12: 69,637,654 (GRCm39) |
T1052M |
probably damaging |
Het |
Spag16 |
G |
A |
1: 70,036,000 (GRCm39) |
V343I |
probably benign |
Het |
Spocd1 |
T |
G |
4: 129,823,957 (GRCm39) |
D251E |
|
Het |
Stc2 |
G |
T |
11: 31,317,798 (GRCm39) |
N74K |
probably damaging |
Het |
Tasor2 |
A |
G |
13: 3,623,621 (GRCm39) |
Y2110H |
probably damaging |
Het |
Thbs3 |
C |
T |
3: 89,126,359 (GRCm39) |
Q227* |
probably null |
Het |
Tmem92 |
A |
C |
11: 94,669,816 (GRCm39) |
I105R |
probably benign |
Het |
Tmod1 |
T |
A |
4: 46,083,632 (GRCm39) |
N20K |
probably benign |
Het |
Tns1 |
T |
C |
1: 73,992,638 (GRCm39) |
D53G |
probably damaging |
Het |
Tspan33 |
T |
A |
6: 29,717,337 (GRCm39) |
L246Q |
probably damaging |
Het |
Ttc16 |
A |
G |
2: 32,658,980 (GRCm39) |
L392P |
probably damaging |
Het |
Uggt1 |
T |
A |
1: 36,224,919 (GRCm39) |
T572S |
probably benign |
Het |
Usp17la |
A |
T |
7: 104,509,604 (GRCm39) |
T70S |
probably damaging |
Het |
Usp31 |
C |
T |
7: 121,274,186 (GRCm39) |
R370H |
probably damaging |
Het |
Wdr83 |
C |
T |
8: 85,806,463 (GRCm39) |
V112M |
probably damaging |
Het |
Zbtb25 |
T |
A |
12: 76,416,366 (GRCm39) |
|
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,583,267 (GRCm39) |
N638K |
possibly damaging |
Het |
Zfp747l1 |
T |
A |
7: 126,984,455 (GRCm39) |
S216C |
probably benign |
Het |
Zfp820 |
T |
C |
17: 22,037,994 (GRCm39) |
T445A |
probably benign |
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 |
R4898:Mgam
|
UTSW |
6 |
40,619,988 (GRCm39) |
missense |
probably benign |
|
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 |
|
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'- ATGGATGGTGACTACCCGGC -3'
(R):5'- TGTCCATTTGCCTAAAAGTAGAAG -3'
Sequencing Primer
(F):5'- TGACTACCCGGCCATTGATG -3'
(R):5'- CATTTGCCTAAAAGTAGAAGAGACC -3'
|
Posted On |
2019-10-17 |