Incidental Mutation 'R1912:Mgam'
ID |
210380 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mgam
|
Ensembl Gene |
ENSMUSG00000068587 |
Gene Name |
maltase-glucoamylase |
Synonyms |
6030407P20Rik |
MMRRC Submission |
039930-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.237)
|
Stock # |
R1912 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
40605765-40746057 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
C to T
at 40741119 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamine to Stop codon
at position 959
(Q959*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000144680
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071535]
[ENSMUST00000201148]
[ENSMUST00000202779]
[ENSMUST00000202966]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000071535
AA Change: Q1705*
|
SMART Domains |
Protein: ENSMUSP00000071466 Gene: ENSMUSG00000068587 AA Change: Q1705*
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 null
Transcript: ENSMUST00000201148
AA Change: Q1705*
|
SMART Domains |
Protein: ENSMUSP00000143946 Gene: ENSMUSG00000068587 AA Change: Q1705*
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 |
noncoding transcript
Transcript: ENSMUST00000202775
|
Predicted Effect |
probably null
Transcript: ENSMUST00000202779
AA Change: Q1078*
|
SMART Domains |
Protein: ENSMUSP00000144627 Gene: ENSMUSG00000068587 AA Change: Q1078*
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 null
Transcript: ENSMUST00000202966
AA Change: Q959*
|
SMART Domains |
Protein: ENSMUSP00000144680 Gene: ENSMUSG00000068587 AA Change: Q959*
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: 97.3%
- 3x: 96.8%
- 10x: 95.3%
- 20x: 92.8%
|
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: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
A |
G |
7: 12,288,582 (GRCm39) |
M132V |
probably benign |
Het |
4921524L21Rik |
T |
A |
18: 6,620,205 (GRCm39) |
I45N |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,156,599 (GRCm39) |
V55A |
probably benign |
Het |
Adam28 |
A |
T |
14: 68,881,780 (GRCm39) |
D105E |
probably benign |
Het |
Ahnak |
T |
C |
19: 8,995,245 (GRCm39) |
S5510P |
probably damaging |
Het |
Aldh3b1 |
T |
G |
19: 3,971,187 (GRCm39) |
D159A |
probably damaging |
Het |
Alx1 |
A |
G |
10: 102,861,222 (GRCm39) |
L102P |
probably damaging |
Het |
Ankrd50 |
C |
T |
3: 38,510,925 (GRCm39) |
V481I |
probably benign |
Het |
Aox4 |
G |
T |
1: 58,303,561 (GRCm39) |
G1200W |
probably damaging |
Het |
Arhgap45 |
A |
C |
10: 79,856,524 (GRCm39) |
D24A |
probably benign |
Het |
Arhgef16 |
A |
T |
4: 154,364,780 (GRCm39) |
|
probably null |
Het |
Asic4 |
A |
T |
1: 75,445,876 (GRCm39) |
Y235F |
possibly damaging |
Het |
Asph |
T |
C |
4: 9,453,335 (GRCm39) |
E646G |
probably damaging |
Het |
Atg4d |
A |
G |
9: 21,183,935 (GRCm39) |
D350G |
probably damaging |
Het |
Auts2 |
T |
C |
5: 131,472,412 (GRCm39) |
T347A |
probably damaging |
Het |
Bsnd |
A |
T |
4: 106,345,227 (GRCm39) |
L73* |
probably null |
Het |
Cachd1 |
A |
T |
4: 100,810,366 (GRCm39) |
S323C |
probably damaging |
Het |
Cacna1e |
A |
G |
1: 154,312,195 (GRCm39) |
I1290T |
probably damaging |
Het |
Cdh8 |
T |
A |
8: 99,825,502 (GRCm39) |
N498Y |
probably damaging |
Het |
Cdkn3 |
A |
G |
14: 47,007,291 (GRCm39) |
|
probably null |
Het |
Celf2 |
A |
T |
2: 6,620,564 (GRCm39) |
M40K |
probably damaging |
Het |
Cfap57 |
A |
C |
4: 118,472,207 (GRCm39) |
S57R |
probably damaging |
Het |
Cfh |
A |
G |
1: 140,063,879 (GRCm39) |
|
probably null |
Het |
Chdh |
A |
G |
14: 29,754,745 (GRCm39) |
S252G |
probably benign |
Het |
Col8a1 |
T |
A |
16: 57,448,287 (GRCm39) |
I408F |
unknown |
Het |
Corin |
C |
T |
5: 72,515,746 (GRCm39) |
C303Y |
probably damaging |
Het |
Crlf2 |
C |
T |
5: 109,705,007 (GRCm39) |
C66Y |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 16,284,012 (GRCm39) |
|
probably null |
Het |
Cyp4f16 |
T |
C |
17: 32,764,018 (GRCm39) |
V270A |
probably damaging |
Het |
Defa29 |
T |
A |
8: 21,816,028 (GRCm39) |
H113L |
possibly damaging |
Het |
Dhx35 |
A |
T |
2: 158,684,227 (GRCm39) |
N501Y |
probably damaging |
Het |
Dipk1b |
A |
G |
2: 26,522,716 (GRCm39) |
E55G |
probably damaging |
Het |
Dst |
A |
G |
1: 34,330,931 (GRCm39) |
R4690G |
probably damaging |
Het |
Elac2 |
T |
A |
11: 64,885,089 (GRCm39) |
D439E |
probably benign |
Het |
Ercc6 |
A |
G |
14: 32,298,760 (GRCm39) |
R1383G |
probably damaging |
Het |
Fat3 |
T |
A |
9: 15,881,284 (GRCm39) |
Y3196F |
probably damaging |
Het |
Fbxw13 |
A |
T |
9: 109,010,611 (GRCm39) |
D342E |
probably benign |
Het |
Fmod |
A |
G |
1: 133,968,458 (GRCm39) |
N166S |
possibly damaging |
Het |
Folh1 |
A |
G |
7: 86,412,175 (GRCm39) |
S199P |
possibly damaging |
Het |
Fv1 |
A |
G |
4: 147,954,235 (GRCm39) |
N267S |
possibly damaging |
Het |
Fyn |
T |
C |
10: 39,402,828 (GRCm39) |
V200A |
possibly damaging |
Het |
Gfus |
A |
T |
15: 75,797,498 (GRCm39) |
D278E |
possibly damaging |
Het |
Ggnbp2 |
T |
C |
11: 84,753,122 (GRCm39) |
N39S |
probably benign |
Het |
Gm10509 |
A |
T |
17: 21,909,831 (GRCm39) |
I53F |
possibly damaging |
Het |
Gpr139 |
A |
T |
7: 118,744,102 (GRCm39) |
I161N |
possibly damaging |
Het |
Grhl2 |
C |
T |
15: 37,358,651 (GRCm39) |
T148I |
probably damaging |
Het |
Hmcn1 |
C |
A |
1: 150,480,633 (GRCm39) |
M4514I |
probably benign |
Het |
Igsf10 |
T |
G |
3: 59,236,993 (GRCm39) |
T1063P |
probably benign |
Het |
Itgav |
A |
G |
2: 83,625,830 (GRCm39) |
Y792C |
possibly damaging |
Het |
Itgb2l |
T |
C |
16: 96,228,135 (GRCm39) |
Q456R |
probably benign |
Het |
Jph4 |
G |
A |
14: 55,345,818 (GRCm39) |
A613V |
probably benign |
Het |
Kcna2 |
A |
G |
3: 107,012,717 (GRCm39) |
T433A |
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,697,393 (GRCm39) |
K97R |
probably benign |
Het |
Krba1 |
C |
A |
6: 48,392,699 (GRCm39) |
A871E |
probably benign |
Het |
Loxhd1 |
T |
C |
18: 77,427,833 (GRCm39) |
F468L |
probably benign |
Het |
Lpin1 |
A |
G |
12: 16,596,728 (GRCm39) |
V713A |
probably damaging |
Het |
Ltbp2 |
T |
A |
12: 84,832,637 (GRCm39) |
I67F |
probably damaging |
Het |
Mdc1 |
G |
A |
17: 36,155,430 (GRCm39) |
R35H |
probably benign |
Het |
Mdc1 |
A |
G |
17: 36,161,703 (GRCm39) |
D872G |
probably benign |
Het |
Mttp |
T |
A |
3: 137,821,788 (GRCm39) |
T260S |
probably benign |
Het |
Naalad2 |
A |
T |
9: 18,287,831 (GRCm39) |
D266E |
probably benign |
Het |
Nans |
T |
A |
4: 46,500,162 (GRCm39) |
L182H |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,616,145 (GRCm39) |
C2228S |
probably benign |
Het |
Nfix |
A |
T |
8: 85,448,306 (GRCm39) |
V407E |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,579,306 (GRCm39) |
|
probably benign |
Het |
Nlrp10 |
G |
A |
7: 108,524,602 (GRCm39) |
R293* |
probably null |
Het |
Nrxn3 |
T |
C |
12: 88,762,112 (GRCm39) |
F53S |
probably damaging |
Het |
Or11h4 |
G |
A |
14: 50,974,235 (GRCm39) |
P128L |
probably damaging |
Het |
Or12e7 |
T |
C |
2: 87,287,727 (GRCm39) |
S73P |
probably damaging |
Het |
Or1e21 |
A |
T |
11: 73,344,820 (GRCm39) |
F73I |
probably damaging |
Het |
Or2f2 |
T |
C |
6: 42,767,411 (GRCm39) |
I146T |
probably benign |
Het |
Or3a1c |
T |
C |
11: 74,046,711 (GRCm39) |
C244R |
probably damaging |
Het |
Or5ak24 |
T |
A |
2: 85,260,604 (GRCm39) |
N190Y |
probably damaging |
Het |
Or5p68 |
A |
G |
7: 107,946,014 (GRCm39) |
L58P |
probably damaging |
Het |
Or6d12 |
A |
G |
6: 116,492,950 (GRCm39) |
T71A |
probably benign |
Het |
Oxld1 |
A |
G |
11: 120,347,732 (GRCm39) |
V155A |
probably damaging |
Het |
Pamr1 |
T |
A |
2: 102,472,645 (GRCm39) |
F648Y |
probably damaging |
Het |
Parg |
T |
C |
14: 31,932,497 (GRCm39) |
W446R |
probably damaging |
Het |
Pate13 |
A |
T |
9: 35,819,915 (GRCm39) |
T23S |
probably benign |
Het |
Phf3 |
A |
T |
1: 30,843,426 (GRCm39) |
H1844Q |
probably damaging |
Het |
Phf7 |
T |
C |
14: 30,962,281 (GRCm39) |
I175V |
possibly damaging |
Het |
Pibf1 |
G |
A |
14: 99,425,245 (GRCm39) |
|
probably null |
Het |
Plcxd1 |
A |
G |
5: 110,251,308 (GRCm39) |
I295V |
probably benign |
Het |
Pole2 |
A |
C |
12: 69,256,764 (GRCm39) |
Y254D |
probably damaging |
Het |
Ppm1e |
T |
A |
11: 87,135,196 (GRCm39) |
I225F |
probably benign |
Het |
Pttg1ip2 |
C |
A |
5: 5,502,019 (GRCm39) |
W144C |
probably benign |
Het |
Rem1 |
G |
A |
2: 152,476,455 (GRCm39) |
V238M |
probably damaging |
Het |
Resf1 |
T |
A |
6: 149,230,342 (GRCm39) |
D1129E |
possibly damaging |
Het |
Rnase2b |
T |
G |
14: 51,400,357 (GRCm39) |
V146G |
probably damaging |
Het |
Rnf169 |
G |
A |
7: 99,575,461 (GRCm39) |
T378I |
probably damaging |
Het |
Rpf2 |
A |
G |
10: 40,112,197 (GRCm39) |
F80L |
probably benign |
Het |
Sec11c |
T |
A |
18: 65,947,945 (GRCm39) |
D128E |
probably damaging |
Het |
Septin12 |
A |
G |
16: 4,806,417 (GRCm39) |
V248A |
probably damaging |
Het |
Serinc1 |
T |
C |
10: 57,401,547 (GRCm39) |
N82S |
probably benign |
Het |
Serpina9 |
A |
C |
12: 103,967,508 (GRCm39) |
W296G |
probably damaging |
Het |
Sgo2b |
A |
C |
8: 64,384,503 (GRCm39) |
D164E |
probably damaging |
Het |
Slc15a3 |
A |
G |
19: 10,825,977 (GRCm39) |
N223D |
probably damaging |
Het |
Slc44a3 |
A |
G |
3: 121,325,815 (GRCm39) |
Y12H |
probably benign |
Het |
Slco3a1 |
A |
G |
7: 74,154,359 (GRCm39) |
F42S |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Snx7 |
A |
T |
3: 117,623,317 (GRCm39) |
|
probably null |
Het |
Sorl1 |
A |
T |
9: 41,993,246 (GRCm39) |
D259E |
probably damaging |
Het |
Stpg2 |
G |
A |
3: 139,228,742 (GRCm39) |
|
probably null |
Het |
Strn |
T |
A |
17: 78,991,824 (GRCm39) |
Y165F |
probably damaging |
Het |
Sval2 |
T |
A |
6: 41,841,254 (GRCm39) |
*106R |
probably null |
Het |
Tcaf3 |
A |
G |
6: 42,573,622 (GRCm39) |
S197P |
possibly damaging |
Het |
Tespa1 |
C |
A |
10: 130,190,592 (GRCm39) |
T73N |
probably benign |
Het |
Tex10 |
C |
T |
4: 48,456,800 (GRCm39) |
R637Q |
probably benign |
Het |
Thoc5 |
C |
A |
11: 4,865,561 (GRCm39) |
T380K |
probably benign |
Het |
Tmprss7 |
T |
A |
16: 45,476,911 (GRCm39) |
R784* |
probably null |
Het |
Trank1 |
A |
T |
9: 111,219,777 (GRCm39) |
L2171F |
probably benign |
Het |
Trpm2 |
T |
G |
10: 77,781,710 (GRCm39) |
K303T |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,549,784 (GRCm39) |
V681M |
probably damaging |
Het |
Usp40 |
A |
G |
1: 87,874,368 (GRCm39) |
F1131L |
probably benign |
Het |
Vmn1r215 |
A |
T |
13: 23,260,673 (GRCm39) |
I238F |
possibly damaging |
Het |
Vwa3a |
A |
T |
7: 120,394,850 (GRCm39) |
Y890F |
probably damaging |
Het |
Zdhhc18 |
A |
G |
4: 133,341,171 (GRCm39) |
L234P |
probably damaging |
Het |
Zfp109 |
A |
G |
7: 23,927,676 (GRCm39) |
S578P |
probably damaging |
Het |
Zfp704 |
T |
C |
3: 9,674,418 (GRCm39) |
D121G |
unknown |
Het |
Zgrf1 |
G |
T |
3: 127,356,786 (GRCm39) |
V671L |
probably benign |
Het |
Zkscan8 |
A |
T |
13: 21,704,927 (GRCm39) |
C265* |
probably null |
Het |
Zscan26 |
T |
C |
13: 21,629,310 (GRCm39) |
I398V |
possibly 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 |
|
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 |
|
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'- GCAGTGGTCCAGTAATTTCTGC -3'
(R):5'- CTGGGGAACTGGTCATGTAG -3'
Sequencing Primer
(F):5'- CTGCATGGATGTAGAACTGCTGTAC -3'
(R):5'- AACTGGTCATGTAGTTGGAGAATG -3'
|
Posted On |
2014-06-30 |