Incidental Mutation 'R0415:Adgb'
| ID |
40254 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Adgb
|
| Ensembl Gene |
ENSMUSG00000050994 |
| Gene Name |
androglobin |
| Synonyms |
9130014G24Rik |
| MMRRC Submission |
038617-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0415 (G1)
|
| Quality Score |
199 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
10335703-10472326 bp(-) (GRCm38) |
| Type of Mutation |
splice site (4 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 10431067 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000146658
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045328]
[ENSMUST00000132573]
[ENSMUST00000172530]
[ENSMUST00000179956]
[ENSMUST00000179956]
[ENSMUST00000208717]
|
| AlphaFold |
G3UZ78 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000045328
|
| SMART Domains |
Protein: ENSMUSP00000045452
Gene: ENSMUSG00000050994
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:CysPc
|
11 |
257 |
1e-165 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000132573
|
| SMART Domains |
Protein: ENSMUSP00000120422
Gene: ENSMUSG00000050994
| Domain | Start | End | E-Value | Type |
|---|
|
CysPc
|
56 |
655 |
2.7e-2 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000172530
|
| SMART Domains |
Protein: ENSMUSP00000134378
Gene: ENSMUSG00000050994
| Domain | Start | End | E-Value | Type |
|---|
|
CysPc
|
56 |
655 |
2.7e-2 |
SMART |
|
IQ
|
904 |
926 |
6.41e0 |
SMART |
|
low complexity region
|
1179 |
1190 |
N/A |
INTRINSIC |
|
low complexity region
|
1318 |
1335 |
N/A |
INTRINSIC |
|
coiled coil region
|
1534 |
1559 |
N/A |
INTRINSIC |
|
low complexity region
|
1616 |
1633 |
N/A |
INTRINSIC |
|
low complexity region
|
1649 |
1657 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000179956
|
| SMART Domains |
Protein: ENSMUSP00000136386
Gene: ENSMUSG00000050994
| Domain | Start | End | E-Value | Type |
|---|
|
CysPc
|
56 |
657 |
5.36e-2 |
SMART |
|
IQ
|
906 |
928 |
6.41e0 |
SMART |
|
low complexity region
|
1181 |
1192 |
N/A |
INTRINSIC |
|
low complexity region
|
1321 |
1338 |
N/A |
INTRINSIC |
|
coiled coil region
|
1537 |
1562 |
N/A |
INTRINSIC |
|
low complexity region
|
1619 |
1636 |
N/A |
INTRINSIC |
|
low complexity region
|
1652 |
1660 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000179956
|
| SMART Domains |
Protein: ENSMUSP00000136386
Gene: ENSMUSG00000050994
| Domain | Start | End | E-Value | Type |
|---|
|
CysPc
|
56 |
657 |
5.36e-2 |
SMART |
|
IQ
|
906 |
928 |
6.41e0 |
SMART |
|
low complexity region
|
1181 |
1192 |
N/A |
INTRINSIC |
|
low complexity region
|
1321 |
1338 |
N/A |
INTRINSIC |
|
coiled coil region
|
1537 |
1562 |
N/A |
INTRINSIC |
|
low complexity region
|
1619 |
1636 |
N/A |
INTRINSIC |
|
low complexity region
|
1652 |
1660 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000208717
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.6%
|
| Validation Efficiency |
97% (99/102) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 98 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933427G23Rik |
A |
T |
5: 23,831,050 (GRCm38) |
|
noncoding transcript |
Het |
| Acox2 |
A |
G |
14: 8,243,835 (GRCm38) |
|
probably benign |
Het |
| Adgra3 |
C |
A |
5: 49,961,757 (GRCm38) |
|
probably benign |
Het |
| Adgre4 |
G |
A |
17: 55,852,288 (GRCm38) |
V658I |
probably benign |
Het |
| Ahnak |
A |
G |
19: 9,012,871 (GRCm38) |
|
probably benign |
Het |
| Anapc2 |
A |
G |
2: 25,278,325 (GRCm38) |
T159A |
probably damaging |
Het |
| Arfgef3 |
A |
G |
10: 18,613,127 (GRCm38) |
|
probably benign |
Het |
| Atf7ip |
C |
T |
6: 136,560,012 (GRCm38) |
S81L |
possibly damaging |
Het |
| Cacna1i |
A |
G |
15: 80,368,830 (GRCm38) |
|
probably benign |
Het |
| Camk1 |
A |
T |
6: 113,341,891 (GRCm38) |
Y20* |
probably null |
Het |
| Ccdc40 |
T |
C |
11: 119,232,118 (GRCm38) |
Y249H |
possibly damaging |
Het |
| Cd109 |
T |
A |
9: 78,712,615 (GRCm38) |
S1380T |
probably benign |
Het |
| Cfap57 |
A |
T |
4: 118,569,431 (GRCm38) |
L1107Q |
possibly damaging |
Het |
| Col6a4 |
C |
T |
9: 106,075,080 (GRCm38) |
V540I |
probably damaging |
Het |
| Cst9 |
T |
A |
2: 148,838,442 (GRCm38) |
|
probably benign |
Het |
| Cul5 |
C |
T |
9: 53,667,070 (GRCm38) |
V73I |
probably benign |
Het |
| Cxcl16 |
T |
A |
11: 70,458,748 (GRCm38) |
K84* |
probably null |
Het |
| Cyp2c29 |
T |
C |
19: 39,329,095 (GRCm38) |
|
probably benign |
Het |
| D6Ertd527e |
C |
G |
6: 87,111,524 (GRCm38) |
T223S |
unknown |
Het |
| Dip2c |
C |
T |
13: 9,568,289 (GRCm38) |
|
probably benign |
Het |
| Dis3 |
A |
T |
14: 99,087,456 (GRCm38) |
I513N |
probably damaging |
Het |
| Dnajc16 |
A |
T |
4: 141,789,048 (GRCm38) |
L3* |
probably null |
Het |
| Dopey1 |
T |
A |
9: 86,506,502 (GRCm38) |
L480M |
probably damaging |
Het |
| Eml6 |
A |
G |
11: 29,749,392 (GRCm38) |
V1787A |
possibly damaging |
Het |
| Etnk1 |
A |
G |
6: 143,180,774 (GRCm38) |
N115S |
probably damaging |
Het |
| Fryl |
T |
C |
5: 73,098,414 (GRCm38) |
Y758C |
probably damaging |
Het |
| Gbp4 |
G |
A |
5: 105,121,106 (GRCm38) |
R394C |
possibly damaging |
Het |
| Ggnbp2 |
A |
C |
11: 84,833,225 (GRCm38) |
|
probably benign |
Het |
| Gm7137 |
A |
G |
10: 77,788,173 (GRCm38) |
|
probably benign |
Het |
| Gstm2 |
T |
A |
3: 107,984,006 (GRCm38) |
Q132L |
probably benign |
Het |
| Habp2 |
T |
C |
19: 56,317,717 (GRCm38) |
|
probably benign |
Het |
| Hectd2 |
T |
C |
19: 36,584,884 (GRCm38) |
|
probably benign |
Het |
| Htr6 |
A |
G |
4: 139,062,081 (GRCm38) |
I291T |
possibly damaging |
Het |
| Ighg2c |
T |
C |
12: 113,287,910 (GRCm38) |
D199G |
unknown |
Het |
| Itih2 |
A |
G |
2: 10,105,615 (GRCm38) |
|
probably benign |
Het |
| Kcnab2 |
A |
G |
4: 152,395,136 (GRCm38) |
F248S |
probably benign |
Het |
| Kcnc4 |
T |
C |
3: 107,445,433 (GRCm38) |
K610E |
probably damaging |
Het |
| Kcnk16 |
T |
A |
14: 20,262,975 (GRCm38) |
|
probably null |
Het |
| Kndc1 |
C |
T |
7: 139,930,124 (GRCm38) |
T1293I |
probably damaging |
Het |
| Lcp1 |
A |
T |
14: 75,227,006 (GRCm38) |
I556F |
possibly damaging |
Het |
| Lrrc8d |
T |
C |
5: 105,811,865 (GRCm38) |
L47P |
probably damaging |
Het |
| Lyst |
T |
C |
13: 13,711,610 (GRCm38) |
|
probably benign |
Het |
| Macrod2 |
G |
A |
2: 142,210,145 (GRCm38) |
|
probably null |
Het |
| Micalcl |
C |
T |
7: 112,381,028 (GRCm38) |
R70C |
probably damaging |
Het |
| Mllt3 |
ACTGCTGCTGCTGCTGCTGCT |
ACTGCTGCTGCTGCTGCT |
4: 87,841,339 (GRCm38) |
|
probably benign |
Het |
| Msh3 |
A |
G |
13: 92,346,786 (GRCm38) |
V283A |
possibly damaging |
Het |
| Nup205 |
T |
C |
6: 35,214,634 (GRCm38) |
|
probably benign |
Het |
| Nxpe2 |
T |
C |
9: 48,326,614 (GRCm38) |
T114A |
probably damaging |
Het |
| Olfr1023 |
A |
T |
2: 85,887,438 (GRCm38) |
I213F |
possibly damaging |
Het |
| Olfr1034 |
A |
T |
2: 86,047,055 (GRCm38) |
H191L |
probably benign |
Het |
| Olfr229 |
A |
G |
9: 39,909,983 (GRCm38) |
Y60C |
probably damaging |
Het |
| Olfr78 |
C |
T |
7: 102,742,087 (GRCm38) |
M305I |
probably benign |
Het |
| Olfr893 |
A |
T |
9: 38,209,973 (GRCm38) |
M305L |
probably benign |
Het |
| Pard3 |
G |
A |
8: 127,610,566 (GRCm38) |
G1221D |
probably damaging |
Het |
| Pax5 |
G |
A |
4: 44,691,886 (GRCm38) |
A120V |
probably damaging |
Het |
| Pcsk6 |
C |
T |
7: 66,033,874 (GRCm38) |
R746C |
probably damaging |
Het |
| Pif1 |
G |
A |
9: 65,588,051 (GRCm38) |
C81Y |
probably benign |
Het |
| Plcb1 |
A |
G |
2: 135,337,499 (GRCm38) |
Y609C |
probably damaging |
Het |
| Plcd4 |
C |
A |
1: 74,552,097 (GRCm38) |
S217Y |
probably damaging |
Het |
| Plxna1 |
G |
A |
6: 89,357,336 (GRCm38) |
H104Y |
probably benign |
Het |
| Polr2k |
A |
G |
15: 36,175,456 (GRCm38) |
Y45C |
probably damaging |
Het |
| Pqlc3 |
C |
A |
12: 16,997,710 (GRCm38) |
|
probably benign |
Het |
| Prex1 |
A |
G |
2: 166,586,699 (GRCm38) |
|
probably benign |
Het |
| Pth2r |
A |
G |
1: 65,388,439 (GRCm38) |
M424V |
probably benign |
Het |
| Pygm |
A |
G |
19: 6,391,366 (GRCm38) |
R464G |
probably benign |
Het |
| Rad51c |
A |
G |
11: 87,397,655 (GRCm38) |
L234P |
probably damaging |
Het |
| Rnf145 |
A |
G |
11: 44,525,138 (GRCm38) |
Y60C |
probably damaging |
Het |
| Rnf167 |
T |
C |
11: 70,649,699 (GRCm38) |
I135T |
probably damaging |
Het |
| Rnf213 |
A |
T |
11: 119,414,469 (GRCm38) |
I509F |
probably damaging |
Het |
| Ryr2 |
T |
C |
13: 11,869,156 (GRCm38) |
S213G |
probably damaging |
Het |
| Selenbp1 |
T |
C |
3: 94,936,913 (GRCm38) |
V27A |
possibly damaging |
Het |
| Selenof |
T |
G |
3: 144,577,692 (GRCm38) |
L14R |
probably damaging |
Het |
| Sfswap |
A |
T |
5: 129,504,126 (GRCm38) |
D121V |
probably damaging |
Het |
| Slc25a34 |
C |
A |
4: 141,620,469 (GRCm38) |
M300I |
possibly damaging |
Het |
| Slc34a3 |
T |
G |
2: 25,229,110 (GRCm38) |
T583P |
probably benign |
Het |
| Smg1 |
C |
A |
7: 118,182,468 (GRCm38) |
A1199S |
probably benign |
Het |
| Spint1 |
A |
G |
2: 119,245,615 (GRCm38) |
T231A |
probably damaging |
Het |
| Sptbn1 |
A |
C |
11: 30,149,576 (GRCm38) |
N229K |
probably damaging |
Het |
| Sult2b1 |
A |
G |
7: 45,730,092 (GRCm38) |
|
probably benign |
Het |
| Tas2r123 |
A |
T |
6: 132,847,838 (GRCm38) |
M233L |
probably damaging |
Het |
| Tbcel |
C |
A |
9: 42,444,500 (GRCm38) |
C139F |
probably benign |
Het |
| Thbs2 |
A |
C |
17: 14,679,973 (GRCm38) |
S573A |
probably benign |
Het |
| Tmem132c |
A |
G |
5: 127,563,705 (GRCm38) |
E980G |
probably damaging |
Het |
| Tmem247 |
G |
T |
17: 86,922,322 (GRCm38) |
C197F |
probably damaging |
Het |
| Tmem251 |
T |
A |
12: 102,744,876 (GRCm38) |
Y119* |
probably null |
Het |
| Tmem43 |
C |
A |
6: 91,482,318 (GRCm38) |
P257Q |
probably benign |
Het |
| Tmprss13 |
A |
G |
9: 45,337,132 (GRCm38) |
|
probably null |
Het |
| Trove2 |
G |
T |
1: 143,760,075 (GRCm38) |
N444K |
probably benign |
Het |
| Ubr5 |
T |
C |
15: 37,972,980 (GRCm38) |
T2626A |
probably damaging |
Het |
| Vmn1r196 |
T |
A |
13: 22,293,836 (GRCm38) |
V215D |
probably damaging |
Het |
| Vmn1r22 |
G |
T |
6: 57,900,332 (GRCm38) |
T220K |
probably benign |
Het |
| Vmn2r116 |
G |
A |
17: 23,387,279 (GRCm38) |
M388I |
possibly damaging |
Het |
| Vmn2r74 |
A |
C |
7: 85,961,410 (GRCm38) |
C25G |
probably damaging |
Het |
| Xndc1 |
T |
C |
7: 102,080,616 (GRCm38) |
|
probably benign |
Het |
| Zfp282 |
A |
G |
6: 47,897,881 (GRCm38) |
D340G |
probably damaging |
Het |
| Zfp282 |
T |
A |
6: 47,905,053 (GRCm38) |
I558N |
possibly damaging |
Het |
| Zfp316 |
T |
A |
5: 143,264,491 (GRCm38) |
T56S |
unknown |
Het |
| Zfp345 |
A |
G |
2: 150,474,559 (GRCm38) |
|
probably benign |
Het |
|
| Other mutations in Adgb |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00503:Adgb
|
APN |
10 |
10,406,099 (GRCm38) |
missense |
possibly damaging |
0.87 |
|
IGL01083:Adgb
|
APN |
10 |
10,407,554 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
IGL03064:Adgb
|
APN |
10 |
10,400,572 (GRCm38) |
missense |
probably benign |
0.02 |
|
R0080:Adgb
|
UTSW |
10 |
10,377,839 (GRCm38) |
splice site |
probably benign |
|
|
R0084:Adgb
|
UTSW |
10 |
10,396,344 (GRCm38) |
missense |
possibly damaging |
0.74 |
|
R0112:Adgb
|
UTSW |
10 |
10,407,158 (GRCm38) |
splice site |
probably benign |
|
|
R0348:Adgb
|
UTSW |
10 |
10,357,879 (GRCm38) |
missense |
probably benign |
|
|
R0633:Adgb
|
UTSW |
10 |
10,391,729 (GRCm38) |
missense |
probably benign |
0.36 |
|
R1052:Adgb
|
UTSW |
10 |
10,442,613 (GRCm38) |
missense |
probably benign |
0.29 |
|
R1248:Adgb
|
UTSW |
10 |
10,395,310 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R1278:Adgb
|
UTSW |
10 |
10,382,828 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1568:Adgb
|
UTSW |
10 |
10,442,665 (GRCm38) |
nonsense |
probably null |
|
|
R1647:Adgb
|
UTSW |
10 |
10,395,371 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1648:Adgb
|
UTSW |
10 |
10,395,371 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1663:Adgb
|
UTSW |
10 |
10,339,675 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R1688:Adgb
|
UTSW |
10 |
10,350,317 (GRCm38) |
nonsense |
probably null |
|
|
R1758:Adgb
|
UTSW |
10 |
10,426,605 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1772:Adgb
|
UTSW |
10 |
10,382,721 (GRCm38) |
splice site |
probably benign |
|
|
R1850:Adgb
|
UTSW |
10 |
10,442,502 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1959:Adgb
|
UTSW |
10 |
10,395,249 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1980:Adgb
|
UTSW |
10 |
10,433,498 (GRCm38) |
missense |
probably benign |
|
|
R2179:Adgb
|
UTSW |
10 |
10,395,274 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R2229:Adgb
|
UTSW |
10 |
10,436,051 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2283:Adgb
|
UTSW |
10 |
10,377,891 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R2870:Adgb
|
UTSW |
10 |
10,431,281 (GRCm38) |
critical splice donor site |
probably null |
|
|
R2870:Adgb
|
UTSW |
10 |
10,431,281 (GRCm38) |
critical splice donor site |
probably null |
|
|
R2875:Adgb
|
UTSW |
10 |
10,422,719 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2876:Adgb
|
UTSW |
10 |
10,422,719 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2920:Adgb
|
UTSW |
10 |
10,390,243 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2931:Adgb
|
UTSW |
10 |
10,442,502 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R3722:Adgb
|
UTSW |
10 |
10,340,510 (GRCm38) |
missense |
probably benign |
0.32 |
|
R3846:Adgb
|
UTSW |
10 |
10,382,721 (GRCm38) |
splice site |
probably benign |
|
|
R3877:Adgb
|
UTSW |
10 |
10,442,483 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4210:Adgb
|
UTSW |
10 |
10,407,465 (GRCm38) |
missense |
probably benign |
0.06 |
|
R4211:Adgb
|
UTSW |
10 |
10,407,465 (GRCm38) |
missense |
probably benign |
0.06 |
|
R4333:Adgb
|
UTSW |
10 |
10,442,502 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R4448:Adgb
|
UTSW |
10 |
10,390,825 (GRCm38) |
missense |
probably benign |
0.32 |
|
R4470:Adgb
|
UTSW |
10 |
10,398,951 (GRCm38) |
missense |
probably benign |
0.02 |
|
R4624:Adgb
|
UTSW |
10 |
10,403,004 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4656:Adgb
|
UTSW |
10 |
10,405,306 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4676:Adgb
|
UTSW |
10 |
10,426,710 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4792:Adgb
|
UTSW |
10 |
10,398,903 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R4795:Adgb
|
UTSW |
10 |
10,357,872 (GRCm38) |
missense |
probably benign |
0.01 |
|
R4858:Adgb
|
UTSW |
10 |
10,349,577 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4985:Adgb
|
UTSW |
10 |
10,400,632 (GRCm38) |
missense |
possibly damaging |
0.69 |
|
R5057:Adgb
|
UTSW |
10 |
10,357,978 (GRCm38) |
missense |
probably benign |
0.11 |
|
R5157:Adgb
|
UTSW |
10 |
10,398,966 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5209:Adgb
|
UTSW |
10 |
10,398,937 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R5339:Adgb
|
UTSW |
10 |
10,442,606 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5376:Adgb
|
UTSW |
10 |
10,346,563 (GRCm38) |
missense |
probably benign |
0.09 |
|
R5426:Adgb
|
UTSW |
10 |
10,350,260 (GRCm38) |
missense |
probably benign |
0.14 |
|
R5516:Adgb
|
UTSW |
10 |
10,431,157 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5554:Adgb
|
UTSW |
10 |
10,340,473 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R5678:Adgb
|
UTSW |
10 |
10,431,326 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R5707:Adgb
|
UTSW |
10 |
10,391,757 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5708:Adgb
|
UTSW |
10 |
10,391,757 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5891:Adgb
|
UTSW |
10 |
10,377,847 (GRCm38) |
nonsense |
probably null |
|
|
R5928:Adgb
|
UTSW |
10 |
10,378,787 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6005:Adgb
|
UTSW |
10 |
10,395,352 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6017:Adgb
|
UTSW |
10 |
10,450,036 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6049:Adgb
|
UTSW |
10 |
10,378,026 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6118:Adgb
|
UTSW |
10 |
10,431,291 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6175:Adgb
|
UTSW |
10 |
10,398,943 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R6186:Adgb
|
UTSW |
10 |
10,422,758 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6234:Adgb
|
UTSW |
10 |
10,353,080 (GRCm38) |
splice site |
probably null |
|
|
R6383:Adgb
|
UTSW |
10 |
10,450,028 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6522:Adgb
|
UTSW |
10 |
10,377,892 (GRCm38) |
nonsense |
probably null |
|
|
R6639:Adgb
|
UTSW |
10 |
10,435,956 (GRCm38) |
missense |
possibly damaging |
0.51 |
|
R6697:Adgb
|
UTSW |
10 |
10,406,126 (GRCm38) |
nonsense |
probably null |
|
|
R6742:Adgb
|
UTSW |
10 |
10,411,849 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6745:Adgb
|
UTSW |
10 |
10,390,197 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6850:Adgb
|
UTSW |
10 |
10,394,574 (GRCm38) |
missense |
probably benign |
0.39 |
|
R7128:Adgb
|
UTSW |
10 |
10,472,241 (GRCm38) |
missense |
probably benign |
0.26 |
|
R7326:Adgb
|
UTSW |
10 |
10,400,574 (GRCm38) |
missense |
possibly damaging |
0.80 |
|
R7386:Adgb
|
UTSW |
10 |
10,377,949 (GRCm38) |
missense |
possibly damaging |
0.52 |
|
R7431:Adgb
|
UTSW |
10 |
10,391,955 (GRCm38) |
splice site |
probably null |
|
|
R7569:Adgb
|
UTSW |
10 |
10,431,252 (GRCm38) |
missense |
probably benign |
|
|
R7579:Adgb
|
UTSW |
10 |
10,410,818 (GRCm38) |
nonsense |
probably null |
|
|
R7582:Adgb
|
UTSW |
10 |
10,390,821 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7615:Adgb
|
UTSW |
10 |
10,436,010 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R7692:Adgb
|
UTSW |
10 |
10,411,712 (GRCm38) |
critical splice donor site |
probably null |
|
|
R7774:Adgb
|
UTSW |
10 |
10,339,660 (GRCm38) |
nonsense |
probably null |
|
|
R7808:Adgb
|
UTSW |
10 |
10,378,659 (GRCm38) |
splice site |
probably null |
|
|
R8158:Adgb
|
UTSW |
10 |
10,378,734 (GRCm38) |
missense |
probably benign |
0.22 |
|
R8386:Adgb
|
UTSW |
10 |
10,350,304 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8746:Adgb
|
UTSW |
10 |
10,405,284 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8785:Adgb
|
UTSW |
10 |
10,357,966 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9089:Adgb
|
UTSW |
10 |
10,442,688 (GRCm38) |
missense |
probably benign |
0.26 |
|
R9140:Adgb
|
UTSW |
10 |
10,340,519 (GRCm38) |
nonsense |
probably null |
|
|
R9386:Adgb
|
UTSW |
10 |
10,398,964 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9777:Adgb
|
UTSW |
10 |
10,407,470 (GRCm38) |
missense |
possibly damaging |
0.74 |
|
X0003:Adgb
|
UTSW |
10 |
10,394,630 (GRCm38) |
missense |
possibly damaging |
0.76 |
|
Z1176:Adgb
|
UTSW |
10 |
10,378,742 (GRCm38) |
missense |
probably benign |
0.09 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCCTGTGCTATTTACTAAAGGGGCG -3'
(R):5'- ACAGAAGAGCCCAGTTCTGAAAGC -3'
Sequencing Primer
(F):5'- CTATTTACTAAAGGGGCGTGACAAG -3'
(R):5'- ggatggcaaggatggcaag -3'
|
| Posted On |
2013-05-23 |
Incidental Mutation