Incidental Mutation 'R5928:Adgb'
| ID |
460021 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Adgb
|
| Ensembl Gene |
ENSMUSG00000050994 |
| Gene Name |
androglobin |
| Synonyms |
9130014G24Rik |
| MMRRC Submission |
044123-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R5928 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
10211447-10348070 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 10254531 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 1118
(D1118G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000146658
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000148816]
[ENSMUST00000172530]
[ENSMUST00000179956]
[ENSMUST00000208717]
|
| AlphaFold |
G3UZ78 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000148816
|
| SMART Domains |
Protein: ENSMUSP00000133652
Gene: ENSMUSG00000050994
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:CysPc
|
1 |
41 |
1e-19 |
BLAST |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000172530
AA Change: D1142G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000134378
Gene: ENSMUSG00000050994
AA Change: D1142G
| 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 damaging
Transcript: ENSMUST00000179956
AA Change: D1144G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000136386
Gene: ENSMUSG00000050994
AA Change: D1144G
| 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 damaging
Transcript: ENSMUST00000208717
AA Change: D1118G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Meta Mutation Damage Score |
0.1430 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.5%
- 10x: 97.8%
- 20x: 93.3%
|
| Validation Efficiency |
97% (90/93) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca17 |
T |
A |
17: 24,537,159 (GRCm39) |
I475L |
probably benign |
Het |
| Abcc2 |
C |
T |
19: 43,807,797 (GRCm39) |
R813W |
probably damaging |
Het |
| Adam34 |
T |
C |
8: 44,105,067 (GRCm39) |
T193A |
probably benign |
Het |
| Adprh |
A |
C |
16: 38,267,746 (GRCm39) |
S180A |
probably benign |
Het |
| Atad5 |
A |
T |
11: 79,985,003 (GRCm39) |
D30V |
probably damaging |
Het |
| Best3 |
G |
A |
10: 116,843,532 (GRCm39) |
D303N |
probably damaging |
Het |
| Bmp2k |
G |
C |
5: 97,235,595 (GRCm39) |
|
probably benign |
Het |
| Btc |
A |
T |
5: 91,514,004 (GRCm39) |
V86E |
probably damaging |
Het |
| Cacna2d4 |
G |
T |
6: 119,258,659 (GRCm39) |
A582S |
probably benign |
Het |
| Carm1 |
A |
G |
9: 21,486,598 (GRCm39) |
|
probably benign |
Het |
| Catsperg1 |
A |
T |
7: 28,906,040 (GRCm39) |
S180T |
probably damaging |
Het |
| Ccdc185 |
A |
T |
1: 182,575,047 (GRCm39) |
H547Q |
probably benign |
Het |
| Ccl6 |
A |
G |
11: 83,479,658 (GRCm39) |
I115T |
possibly damaging |
Het |
| Cd44 |
C |
T |
2: 102,654,648 (GRCm39) |
V470M |
probably damaging |
Het |
| Cdc25a |
T |
C |
9: 109,718,861 (GRCm39) |
V354A |
probably damaging |
Het |
| Cdhr2 |
C |
A |
13: 54,881,832 (GRCm39) |
Q1122K |
probably benign |
Het |
| Cep290 |
A |
G |
10: 100,387,692 (GRCm39) |
K1958E |
probably damaging |
Het |
| Cfap53 |
C |
T |
18: 74,492,811 (GRCm39) |
P512S |
possibly damaging |
Het |
| Chrdl2 |
A |
T |
7: 99,659,200 (GRCm39) |
|
probably benign |
Het |
| Cibar1 |
A |
G |
4: 12,171,919 (GRCm39) |
|
probably benign |
Het |
| Clec7a |
A |
T |
6: 129,442,430 (GRCm39) |
F199Y |
probably damaging |
Het |
| Cracd |
A |
C |
5: 76,989,581 (GRCm39) |
|
probably benign |
Het |
| Dhx29 |
A |
G |
13: 113,101,002 (GRCm39) |
K1182E |
probably benign |
Het |
| Dnah11 |
G |
T |
12: 117,878,371 (GRCm39) |
|
probably null |
Het |
| Dnmt3a |
A |
G |
12: 3,916,096 (GRCm39) |
S94G |
possibly damaging |
Het |
| Ecpas |
A |
T |
4: 58,849,948 (GRCm39) |
M425K |
possibly damaging |
Het |
| Egfem1 |
T |
C |
3: 29,637,077 (GRCm39) |
V42A |
possibly damaging |
Het |
| Eif3e |
T |
A |
15: 43,138,728 (GRCm39) |
|
probably null |
Het |
| Exosc9 |
T |
A |
3: 36,609,774 (GRCm39) |
|
probably benign |
Het |
| Fbxw18 |
T |
A |
9: 109,529,149 (GRCm39) |
T135S |
probably damaging |
Het |
| Fbxw21 |
T |
C |
9: 108,972,893 (GRCm39) |
E347G |
possibly damaging |
Het |
| Gcm2 |
A |
G |
13: 41,256,874 (GRCm39) |
Y292H |
probably benign |
Het |
| Gltpd2 |
C |
A |
11: 70,410,179 (GRCm39) |
Q46K |
probably benign |
Het |
| Gm6741 |
A |
G |
17: 91,544,528 (GRCm39) |
Y97C |
probably damaging |
Het |
| Golgb1 |
T |
C |
16: 36,732,349 (GRCm39) |
L532S |
probably damaging |
Het |
| Hdac3 |
C |
T |
18: 38,074,394 (GRCm39) |
|
probably benign |
Het |
| Helz2 |
A |
T |
2: 180,872,177 (GRCm39) |
F2554L |
possibly damaging |
Het |
| Hmbox1 |
T |
A |
14: 65,061,122 (GRCm39) |
H384L |
possibly damaging |
Het |
| Hmcn1 |
G |
T |
1: 150,474,648 (GRCm39) |
D4746E |
possibly damaging |
Het |
| Il17rb |
C |
A |
14: 29,726,232 (GRCm39) |
|
probably null |
Het |
| Irak2 |
A |
T |
6: 113,653,587 (GRCm39) |
I252F |
probably damaging |
Het |
| Khnyn |
C |
T |
14: 56,123,344 (GRCm39) |
R33C |
probably damaging |
Het |
| Ksr1 |
G |
A |
11: 78,950,545 (GRCm39) |
P20L |
probably damaging |
Het |
| Lamc3 |
T |
C |
2: 31,811,721 (GRCm39) |
Y903H |
probably benign |
Het |
| Miga2 |
T |
C |
2: 30,258,875 (GRCm39) |
|
probably benign |
Het |
| Mroh2a |
A |
C |
1: 88,169,340 (GRCm39) |
I672L |
probably benign |
Het |
| Ncoa4 |
T |
C |
14: 31,888,678 (GRCm39) |
|
probably null |
Het |
| Nphp3 |
T |
C |
9: 103,912,996 (GRCm39) |
Y925H |
probably benign |
Het |
| Nr2c1 |
T |
G |
10: 94,024,055 (GRCm39) |
L420R |
probably damaging |
Het |
| Onecut1 |
A |
G |
9: 74,770,066 (GRCm39) |
N163S |
probably benign |
Het |
| Or5ac21 |
G |
A |
16: 59,123,521 (GRCm39) |
E2K |
probably damaging |
Het |
| Or5d47 |
T |
A |
2: 87,804,380 (GRCm39) |
S210C |
probably benign |
Het |
| Or7e166 |
A |
T |
9: 19,625,049 (GRCm39) |
T309S |
probably benign |
Het |
| Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
| Per2 |
C |
T |
1: 91,372,373 (GRCm39) |
V234I |
probably damaging |
Het |
| Pign |
A |
G |
1: 105,485,792 (GRCm39) |
V735A |
possibly damaging |
Het |
| Plekha7 |
T |
C |
7: 115,727,809 (GRCm39) |
K85R |
probably benign |
Het |
| Pnma2 |
C |
T |
14: 67,154,323 (GRCm39) |
T249I |
probably benign |
Het |
| Polr2b |
A |
G |
5: 77,493,189 (GRCm39) |
D1057G |
probably damaging |
Het |
| Polrmt |
A |
T |
10: 79,576,186 (GRCm39) |
L519H |
probably damaging |
Het |
| Ptar1 |
T |
C |
19: 23,695,277 (GRCm39) |
I248T |
probably benign |
Het |
| Ptprh |
A |
C |
7: 4,576,507 (GRCm39) |
L251R |
probably damaging |
Het |
| Purg |
T |
C |
8: 33,876,980 (GRCm39) |
M206T |
probably benign |
Het |
| Pwp2 |
A |
T |
10: 78,018,290 (GRCm39) |
F134I |
probably damaging |
Het |
| Riok3 |
T |
A |
18: 12,286,075 (GRCm39) |
H434Q |
probably benign |
Het |
| Sorbs2 |
A |
G |
8: 46,216,220 (GRCm39) |
I187V |
probably damaging |
Het |
| Tbc1d2b |
T |
C |
9: 90,101,197 (GRCm39) |
I598V |
probably benign |
Het |
| Tdg |
T |
A |
10: 82,477,204 (GRCm39) |
V85E |
probably benign |
Het |
| Tfb1m |
C |
T |
17: 3,593,422 (GRCm39) |
V166I |
probably benign |
Het |
| Tmem163 |
A |
T |
1: 127,419,383 (GRCm39) |
M274K |
probably damaging |
Het |
| Tpr |
T |
C |
1: 150,303,878 (GRCm39) |
I1343T |
probably benign |
Het |
| Ttn |
T |
A |
2: 76,719,794 (GRCm39) |
|
probably benign |
Het |
| Tut7 |
G |
A |
13: 59,969,880 (GRCm39) |
A5V |
probably benign |
Het |
| Usp34 |
A |
G |
11: 23,386,040 (GRCm39) |
T2156A |
probably damaging |
Het |
| Vmn1r215 |
A |
T |
13: 23,260,487 (GRCm39) |
T176S |
possibly damaging |
Het |
| Vps52 |
C |
T |
17: 34,180,100 (GRCm39) |
P268L |
possibly damaging |
Het |
| Xbp1 |
G |
A |
11: 5,473,514 (GRCm39) |
|
probably benign |
Het |
| Ythdc2 |
T |
A |
18: 44,966,272 (GRCm39) |
F169L |
probably benign |
Het |
| Zfyve16 |
T |
C |
13: 92,658,625 (GRCm39) |
R429G |
probably benign |
Het |
| Zzef1 |
A |
G |
11: 72,803,678 (GRCm39) |
E2504G |
probably damaging |
Het |
|
| Other mutations in Adgb |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00503:Adgb
|
APN |
10 |
10,281,843 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL01083:Adgb
|
APN |
10 |
10,283,298 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
IGL03064:Adgb
|
APN |
10 |
10,276,316 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0080:Adgb
|
UTSW |
10 |
10,253,583 (GRCm39) |
splice site |
probably benign |
|
|
R0084:Adgb
|
UTSW |
10 |
10,272,088 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0112:Adgb
|
UTSW |
10 |
10,282,902 (GRCm39) |
splice site |
probably benign |
|
|
R0348:Adgb
|
UTSW |
10 |
10,233,623 (GRCm39) |
missense |
probably benign |
|
|
R0415:Adgb
|
UTSW |
10 |
10,306,811 (GRCm39) |
splice site |
probably null |
|
|
R0633:Adgb
|
UTSW |
10 |
10,267,473 (GRCm39) |
missense |
probably benign |
0.36 |
|
R1052:Adgb
|
UTSW |
10 |
10,318,357 (GRCm39) |
missense |
probably benign |
0.29 |
|
R1248:Adgb
|
UTSW |
10 |
10,271,054 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1278:Adgb
|
UTSW |
10 |
10,258,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1568:Adgb
|
UTSW |
10 |
10,318,409 (GRCm39) |
nonsense |
probably null |
|
|
R1647:Adgb
|
UTSW |
10 |
10,271,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1648:Adgb
|
UTSW |
10 |
10,271,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1663:Adgb
|
UTSW |
10 |
10,215,419 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1688:Adgb
|
UTSW |
10 |
10,226,061 (GRCm39) |
nonsense |
probably null |
|
|
R1758:Adgb
|
UTSW |
10 |
10,302,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1772:Adgb
|
UTSW |
10 |
10,258,465 (GRCm39) |
splice site |
probably benign |
|
|
R1850:Adgb
|
UTSW |
10 |
10,318,246 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1959:Adgb
|
UTSW |
10 |
10,270,993 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1980:Adgb
|
UTSW |
10 |
10,309,242 (GRCm39) |
missense |
probably benign |
|
|
R2179:Adgb
|
UTSW |
10 |
10,271,018 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2229:Adgb
|
UTSW |
10 |
10,311,795 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2283:Adgb
|
UTSW |
10 |
10,253,635 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2870:Adgb
|
UTSW |
10 |
10,307,025 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2870:Adgb
|
UTSW |
10 |
10,307,025 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2875:Adgb
|
UTSW |
10 |
10,298,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2876:Adgb
|
UTSW |
10 |
10,298,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2920:Adgb
|
UTSW |
10 |
10,265,987 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2931:Adgb
|
UTSW |
10 |
10,318,246 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R3722:Adgb
|
UTSW |
10 |
10,216,254 (GRCm39) |
missense |
probably benign |
0.32 |
|
R3846:Adgb
|
UTSW |
10 |
10,258,465 (GRCm39) |
splice site |
probably benign |
|
|
R3877:Adgb
|
UTSW |
10 |
10,318,227 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4210:Adgb
|
UTSW |
10 |
10,283,209 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4211:Adgb
|
UTSW |
10 |
10,283,209 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4333:Adgb
|
UTSW |
10 |
10,318,246 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R4448:Adgb
|
UTSW |
10 |
10,266,569 (GRCm39) |
missense |
probably benign |
0.32 |
|
R4470:Adgb
|
UTSW |
10 |
10,274,695 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4624:Adgb
|
UTSW |
10 |
10,278,748 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4656:Adgb
|
UTSW |
10 |
10,281,050 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4676:Adgb
|
UTSW |
10 |
10,302,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4792:Adgb
|
UTSW |
10 |
10,274,647 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4795:Adgb
|
UTSW |
10 |
10,233,616 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4858:Adgb
|
UTSW |
10 |
10,225,321 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4985:Adgb
|
UTSW |
10 |
10,276,376 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R5057:Adgb
|
UTSW |
10 |
10,233,722 (GRCm39) |
missense |
probably benign |
0.11 |
|
R5157:Adgb
|
UTSW |
10 |
10,274,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5209:Adgb
|
UTSW |
10 |
10,274,681 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R5339:Adgb
|
UTSW |
10 |
10,318,350 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5376:Adgb
|
UTSW |
10 |
10,222,307 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5426:Adgb
|
UTSW |
10 |
10,226,004 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5516:Adgb
|
UTSW |
10 |
10,306,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5554:Adgb
|
UTSW |
10 |
10,216,217 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5678:Adgb
|
UTSW |
10 |
10,307,070 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R5707:Adgb
|
UTSW |
10 |
10,267,501 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5708:Adgb
|
UTSW |
10 |
10,267,501 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5891:Adgb
|
UTSW |
10 |
10,253,591 (GRCm39) |
nonsense |
probably null |
|
|
R6005:Adgb
|
UTSW |
10 |
10,271,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6017:Adgb
|
UTSW |
10 |
10,325,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6049:Adgb
|
UTSW |
10 |
10,253,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6118:Adgb
|
UTSW |
10 |
10,307,035 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6175:Adgb
|
UTSW |
10 |
10,274,687 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6186:Adgb
|
UTSW |
10 |
10,298,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6234:Adgb
|
UTSW |
10 |
10,228,824 (GRCm39) |
splice site |
probably null |
|
|
R6383:Adgb
|
UTSW |
10 |
10,325,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6522:Adgb
|
UTSW |
10 |
10,253,636 (GRCm39) |
nonsense |
probably null |
|
|
R6639:Adgb
|
UTSW |
10 |
10,311,700 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R6697:Adgb
|
UTSW |
10 |
10,281,870 (GRCm39) |
nonsense |
probably null |
|
|
R6742:Adgb
|
UTSW |
10 |
10,287,593 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6745:Adgb
|
UTSW |
10 |
10,265,941 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6850:Adgb
|
UTSW |
10 |
10,270,318 (GRCm39) |
missense |
probably benign |
0.39 |
|
R7128:Adgb
|
UTSW |
10 |
10,347,985 (GRCm39) |
missense |
probably benign |
0.26 |
|
R7326:Adgb
|
UTSW |
10 |
10,276,318 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R7386:Adgb
|
UTSW |
10 |
10,253,693 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R7431:Adgb
|
UTSW |
10 |
10,267,699 (GRCm39) |
splice site |
probably null |
|
|
R7569:Adgb
|
UTSW |
10 |
10,306,996 (GRCm39) |
missense |
probably benign |
|
|
R7579:Adgb
|
UTSW |
10 |
10,286,562 (GRCm39) |
nonsense |
probably null |
|
|
R7582:Adgb
|
UTSW |
10 |
10,266,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7615:Adgb
|
UTSW |
10 |
10,311,754 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7692:Adgb
|
UTSW |
10 |
10,287,456 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7774:Adgb
|
UTSW |
10 |
10,215,404 (GRCm39) |
nonsense |
probably null |
|
|
R7808:Adgb
|
UTSW |
10 |
10,254,403 (GRCm39) |
splice site |
probably null |
|
|
R8158:Adgb
|
UTSW |
10 |
10,254,478 (GRCm39) |
missense |
probably benign |
0.22 |
|
R8386:Adgb
|
UTSW |
10 |
10,226,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8746:Adgb
|
UTSW |
10 |
10,281,028 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8785:Adgb
|
UTSW |
10 |
10,233,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9089:Adgb
|
UTSW |
10 |
10,318,432 (GRCm39) |
missense |
probably benign |
0.26 |
|
R9140:Adgb
|
UTSW |
10 |
10,216,263 (GRCm39) |
nonsense |
probably null |
|
|
R9386:Adgb
|
UTSW |
10 |
10,274,708 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9777:Adgb
|
UTSW |
10 |
10,283,214 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
X0003:Adgb
|
UTSW |
10 |
10,270,374 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
Z1176:Adgb
|
UTSW |
10 |
10,254,486 (GRCm39) |
missense |
probably benign |
0.09 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACACAAGCATCTGTTTCTGAATGG -3'
(R):5'- GCTCTTTGTCGAAGTCTGCAG -3'
Sequencing Primer
(F):5'- CTGTTTCTGAATGGAGGCCAAACTC -3'
(R):5'- CATGGGCCTTACGAAGCTGTATTAC -3'
|
| Posted On |
2017-02-28 |
Incidental Mutation