Incidental Mutation 'R5068:Myo9b'
ID |
388452 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo9b
|
Ensembl Gene |
ENSMUSG00000004677 |
Gene Name |
myosin IXb |
Synonyms |
|
MMRRC Submission |
042658-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.852)
|
Stock # |
R5068 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
71725358-71813357 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 71801699 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Histidine
at position 1275
(Y1275H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148316
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071935]
[ENSMUST00000168839]
[ENSMUST00000170242]
[ENSMUST00000212935]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000071935
AA Change: Y1274H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000071827 Gene: ENSMUSG00000004677 AA Change: Y1274H
Domain | Start | End | E-Value | Type |
RA
|
15 |
114 |
3.7e-30 |
SMART |
MYSc
|
140 |
954 |
N/A |
SMART |
IQ
|
955 |
977 |
1.2e-3 |
SMART |
IQ
|
978 |
1000 |
1.6e-5 |
SMART |
IQ
|
1001 |
1022 |
4.3e-5 |
SMART |
IQ
|
1023 |
1045 |
8.4e-5 |
SMART |
low complexity region
|
1050 |
1064 |
N/A |
INTRINSIC |
low complexity region
|
1127 |
1145 |
N/A |
INTRINSIC |
low complexity region
|
1211 |
1222 |
N/A |
INTRINSIC |
low complexity region
|
1232 |
1246 |
N/A |
INTRINSIC |
Blast:MYSc
|
1247 |
1323 |
3e-19 |
BLAST |
low complexity region
|
1348 |
1359 |
N/A |
INTRINSIC |
coiled coil region
|
1563 |
1590 |
N/A |
INTRINSIC |
C1
|
1591 |
1639 |
1.7e-14 |
SMART |
RhoGAP
|
1668 |
1843 |
4.7e-71 |
SMART |
coiled coil region
|
1901 |
1925 |
N/A |
INTRINSIC |
low complexity region
|
1940 |
1952 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000168839
AA Change: Y1285H
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000131635 Gene: ENSMUSG00000004677 AA Change: Y1285H
Domain | Start | End | E-Value | Type |
RA
|
15 |
114 |
5.79e-28 |
SMART |
MYSc
|
140 |
954 |
N/A |
SMART |
IQ
|
955 |
977 |
2.46e-1 |
SMART |
IQ
|
978 |
1000 |
3.35e-3 |
SMART |
IQ
|
1001 |
1022 |
8.84e-3 |
SMART |
IQ
|
1023 |
1045 |
1.77e-2 |
SMART |
low complexity region
|
1050 |
1064 |
N/A |
INTRINSIC |
low complexity region
|
1127 |
1145 |
N/A |
INTRINSIC |
low complexity region
|
1211 |
1222 |
N/A |
INTRINSIC |
low complexity region
|
1234 |
1257 |
N/A |
INTRINSIC |
Blast:MYSc
|
1258 |
1334 |
3e-19 |
BLAST |
low complexity region
|
1361 |
1372 |
N/A |
INTRINSIC |
low complexity region
|
1581 |
1601 |
N/A |
INTRINSIC |
C1
|
1605 |
1653 |
3.58e-12 |
SMART |
RhoGAP
|
1682 |
1857 |
7.78e-69 |
SMART |
coiled coil region
|
1915 |
1939 |
N/A |
INTRINSIC |
low complexity region
|
1954 |
1966 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000170242
AA Change: Y1285H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000129220 Gene: ENSMUSG00000004677 AA Change: Y1285H
Domain | Start | End | E-Value | Type |
RA
|
15 |
114 |
5.79e-28 |
SMART |
MYSc
|
140 |
954 |
N/A |
SMART |
IQ
|
955 |
977 |
2.46e-1 |
SMART |
IQ
|
978 |
1000 |
3.35e-3 |
SMART |
IQ
|
1001 |
1022 |
8.84e-3 |
SMART |
IQ
|
1023 |
1045 |
1.77e-2 |
SMART |
low complexity region
|
1050 |
1064 |
N/A |
INTRINSIC |
low complexity region
|
1127 |
1145 |
N/A |
INTRINSIC |
low complexity region
|
1211 |
1222 |
N/A |
INTRINSIC |
low complexity region
|
1234 |
1257 |
N/A |
INTRINSIC |
Blast:MYSc
|
1258 |
1334 |
3e-19 |
BLAST |
low complexity region
|
1361 |
1372 |
N/A |
INTRINSIC |
low complexity region
|
1581 |
1601 |
N/A |
INTRINSIC |
C1
|
1605 |
1653 |
3.58e-12 |
SMART |
RhoGAP
|
1682 |
1857 |
7.78e-69 |
SMART |
coiled coil region
|
1931 |
1955 |
N/A |
INTRINSIC |
low complexity region
|
1970 |
1982 |
N/A |
INTRINSIC |
low complexity region
|
1992 |
2003 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000212412
AA Change: Y82H
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212935
AA Change: Y1275H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.6%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the myosin family of actin-based molecular motor heavy chain proteins. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). The protein has four IQ motifs located in the neck domain that bind calmodulin, which serves as a light chain. The protein complex has a single-headed structure and exhibits processive movement on actin filaments toward the minus-end. The protein also has rho-GTPase activity. Polymorphisms in this gene are associated with celiac disease and ulcerative colitis susceptibility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] PHENOTYPE: Homozygous null mutants breed normal, but shows defect in macrophage motility and chemotaxis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,383,749 (GRCm39) |
S739P |
possibly damaging |
Het |
6030468B19Rik |
A |
G |
11: 117,693,701 (GRCm39) |
Y56C |
possibly damaging |
Het |
Actn2 |
A |
G |
13: 12,303,408 (GRCm39) |
I464T |
possibly damaging |
Het |
Add2 |
T |
A |
6: 86,084,440 (GRCm39) |
L496Q |
probably damaging |
Het |
Akt1s1 |
T |
C |
7: 44,499,432 (GRCm39) |
|
probably null |
Het |
Als2 |
G |
T |
1: 59,250,433 (GRCm39) |
P437Q |
probably benign |
Het |
Ankar |
T |
C |
1: 72,719,369 (GRCm39) |
|
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,402,667 (GRCm39) |
R1464G |
probably damaging |
Het |
Ankrd24 |
T |
C |
10: 81,475,699 (GRCm39) |
S121P |
possibly damaging |
Het |
Arvcf |
A |
G |
16: 18,217,736 (GRCm39) |
Y412C |
probably damaging |
Het |
Birc6 |
C |
T |
17: 74,872,967 (GRCm39) |
R409C |
probably damaging |
Het |
Bnip3l |
T |
C |
14: 67,237,081 (GRCm39) |
E57G |
possibly damaging |
Het |
Calcoco1 |
A |
G |
15: 102,619,527 (GRCm39) |
L354P |
probably damaging |
Het |
Cc2d1b |
T |
C |
4: 108,480,661 (GRCm39) |
V27A |
possibly damaging |
Het |
Cdc37 |
T |
C |
9: 21,061,099 (GRCm39) |
T19A |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,413,736 (GRCm39) |
I1199V |
probably benign |
Het |
Chd6 |
G |
T |
2: 160,808,289 (GRCm39) |
L1642I |
possibly damaging |
Het |
Chst13 |
T |
C |
6: 90,286,551 (GRCm39) |
E137G |
possibly damaging |
Het |
Cnrip1 |
A |
G |
11: 17,004,687 (GRCm39) |
D79G |
probably damaging |
Het |
Dars2 |
A |
T |
1: 160,869,483 (GRCm39) |
C589S |
probably benign |
Het |
Dhx15 |
T |
G |
5: 52,327,409 (GRCm39) |
I102L |
possibly damaging |
Het |
Dip2a |
A |
G |
10: 76,153,877 (GRCm39) |
L151P |
possibly damaging |
Het |
Dlc1 |
T |
C |
8: 37,405,184 (GRCm39) |
T202A |
probably benign |
Het |
Dlg1 |
G |
T |
16: 31,503,113 (GRCm39) |
|
probably null |
Het |
Dlgap4 |
T |
C |
2: 156,549,031 (GRCm39) |
F464L |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,632,013 (GRCm39) |
H1314R |
probably benign |
Het |
Dsp |
A |
C |
13: 38,381,099 (GRCm39) |
T2615P |
possibly damaging |
Het |
Dthd1 |
C |
A |
5: 62,976,059 (GRCm39) |
D244E |
probably benign |
Het |
Dtl |
A |
T |
1: 191,300,485 (GRCm39) |
D126E |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,911,737 (GRCm39) |
N341S |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,727,450 (GRCm39) |
Y513C |
probably damaging |
Het |
Erbb4 |
A |
T |
1: 68,083,061 (GRCm39) |
|
probably null |
Het |
Erc2 |
A |
T |
14: 28,024,900 (GRCm39) |
H593L |
possibly damaging |
Het |
Ercc6 |
T |
C |
14: 32,292,020 (GRCm39) |
V1128A |
probably benign |
Het |
Fyn |
A |
G |
10: 39,402,839 (GRCm39) |
K204E |
probably damaging |
Het |
Gm4847 |
A |
T |
1: 166,465,953 (GRCm39) |
F212Y |
possibly damaging |
Het |
Gpc5 |
T |
C |
14: 115,654,676 (GRCm39) |
*499R |
probably null |
Het |
Hcn4 |
T |
C |
9: 58,767,304 (GRCm39) |
L955P |
unknown |
Het |
Hook2 |
C |
A |
8: 85,720,028 (GRCm39) |
L111I |
possibly damaging |
Het |
Hook3 |
C |
T |
8: 26,585,785 (GRCm39) |
|
probably null |
Het |
Hvcn1 |
T |
C |
5: 122,371,544 (GRCm39) |
F28S |
probably damaging |
Het |
Igkv6-32 |
A |
G |
6: 70,051,267 (GRCm39) |
F30L |
possibly damaging |
Het |
Inpp5b |
G |
A |
4: 124,636,442 (GRCm39) |
|
probably null |
Het |
Itgb2 |
G |
A |
10: 77,384,595 (GRCm39) |
A239T |
probably damaging |
Het |
Kcnrg |
T |
C |
14: 61,845,266 (GRCm39) |
L102P |
probably damaging |
Het |
Kif16b |
A |
T |
2: 142,553,627 (GRCm39) |
M1068K |
probably benign |
Het |
Kifc3 |
T |
C |
8: 95,836,844 (GRCm39) |
R109G |
possibly damaging |
Het |
Klhl28 |
A |
T |
12: 65,004,486 (GRCm39) |
M9K |
probably benign |
Het |
Kptn |
T |
C |
7: 15,857,027 (GRCm39) |
Y172H |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,793,002 (GRCm39) |
E646G |
probably damaging |
Het |
Mmp14 |
T |
A |
14: 54,676,570 (GRCm39) |
Y372N |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,311,327 (GRCm39) |
M868K |
probably benign |
Het |
Mterf1a |
T |
C |
5: 3,941,854 (GRCm39) |
N5D |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,412,345 (GRCm39) |
S1764P |
unknown |
Het |
Nek1 |
T |
C |
8: 61,469,330 (GRCm39) |
I129T |
probably damaging |
Het |
Net1 |
G |
A |
13: 3,936,740 (GRCm39) |
A221V |
probably benign |
Het |
Nuak2 |
A |
T |
1: 132,259,509 (GRCm39) |
D429V |
probably benign |
Het |
Nup98 |
T |
C |
7: 101,794,862 (GRCm39) |
T882A |
probably benign |
Het |
Or11g2 |
T |
A |
14: 50,856,197 (GRCm39) |
C173S |
probably damaging |
Het |
Or11h4 |
C |
A |
14: 50,974,531 (GRCm39) |
L29F |
probably benign |
Het |
Or52ab4 |
A |
T |
7: 102,987,229 (GRCm39) |
|
probably null |
Het |
Or52h1 |
T |
A |
7: 103,829,448 (GRCm39) |
S56C |
probably damaging |
Het |
Or8b42 |
T |
C |
9: 38,341,760 (GRCm39) |
Y61H |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pcdh7 |
T |
C |
5: 57,879,508 (GRCm39) |
V1021A |
probably damaging |
Het |
Pclo |
G |
C |
5: 14,729,087 (GRCm39) |
|
probably benign |
Het |
Pds5a |
A |
C |
5: 65,772,615 (GRCm39) |
D1329E |
probably damaging |
Het |
Pex5 |
A |
G |
6: 124,390,555 (GRCm39) |
S97P |
probably benign |
Het |
Pias3 |
A |
G |
3: 96,611,171 (GRCm39) |
K431E |
probably damaging |
Het |
Piwil1 |
T |
C |
5: 128,818,678 (GRCm39) |
S158P |
probably damaging |
Het |
Plxnc1 |
A |
T |
10: 94,635,239 (GRCm39) |
I1329N |
possibly damaging |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Pnpla1 |
T |
A |
17: 29,098,397 (GRCm39) |
|
probably null |
Het |
Prdm10 |
T |
C |
9: 31,270,343 (GRCm39) |
Y827H |
probably damaging |
Het |
Prss3b |
A |
C |
6: 41,009,370 (GRCm39) |
Y155D |
probably benign |
Het |
Psma2 |
G |
A |
13: 14,790,613 (GRCm39) |
V20I |
probably benign |
Het |
Pwwp4a |
T |
C |
X: 72,171,577 (GRCm39) |
I323T |
probably damaging |
Het |
Rgl3 |
A |
G |
9: 21,899,340 (GRCm39) |
|
probably null |
Het |
Rnf17 |
T |
C |
14: 56,743,385 (GRCm39) |
V1317A |
probably damaging |
Het |
Rpp40 |
T |
C |
13: 36,082,681 (GRCm39) |
N254D |
probably benign |
Het |
Scin |
T |
A |
12: 40,174,699 (GRCm39) |
H128L |
probably damaging |
Het |
Sh3bp2 |
A |
T |
5: 34,714,311 (GRCm39) |
M225L |
probably benign |
Het |
Shisa9 |
C |
A |
16: 12,085,412 (GRCm39) |
H324Q |
possibly damaging |
Het |
Sipa1l1 |
A |
G |
12: 82,484,601 (GRCm39) |
D1585G |
probably damaging |
Het |
Slc11a1 |
G |
A |
1: 74,424,343 (GRCm39) |
A434T |
probably damaging |
Het |
Slc5a8 |
A |
T |
10: 88,722,460 (GRCm39) |
I98F |
possibly damaging |
Het |
Slc6a13 |
T |
C |
6: 121,310,301 (GRCm39) |
L320P |
probably damaging |
Het |
Spats2l |
A |
G |
1: 57,982,380 (GRCm39) |
T421A |
probably benign |
Het |
Spryd3 |
A |
T |
15: 102,037,046 (GRCm39) |
D207E |
probably benign |
Het |
Srrt |
T |
C |
5: 137,294,803 (GRCm39) |
N392S |
possibly damaging |
Het |
Stk36 |
G |
T |
1: 74,661,504 (GRCm39) |
R510S |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,288 (GRCm39) |
Y272C |
probably damaging |
Het |
Taar7b |
T |
G |
10: 23,876,359 (GRCm39) |
S175A |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,893,986 (GRCm39) |
I139T |
probably damaging |
Het |
Tph2 |
T |
A |
10: 114,987,079 (GRCm39) |
Y237F |
probably benign |
Het |
Trim35 |
C |
T |
14: 66,546,421 (GRCm39) |
|
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,655,750 (GRCm39) |
I661T |
probably benign |
Het |
Ttc27 |
T |
A |
17: 75,106,337 (GRCm39) |
H541Q |
probably damaging |
Het |
Uap1 |
G |
T |
1: 169,989,032 (GRCm39) |
P130Q |
probably damaging |
Het |
Ube3c |
T |
C |
5: 29,806,352 (GRCm39) |
|
probably null |
Het |
Umad1 |
A |
T |
6: 8,401,157 (GRCm39) |
|
probably null |
Het |
Usp34 |
T |
C |
11: 23,410,665 (GRCm39) |
V2705A |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,723,422 (GRCm39) |
S259G |
probably benign |
Het |
Vwa7 |
G |
A |
17: 35,243,166 (GRCm39) |
V615I |
probably benign |
Het |
Wdfy3 |
T |
C |
5: 102,042,803 (GRCm39) |
T1983A |
probably benign |
Het |
Wdr24 |
T |
G |
17: 26,044,753 (GRCm39) |
F203V |
possibly damaging |
Het |
Xlr4c |
T |
A |
X: 72,282,290 (GRCm39) |
K121M |
probably damaging |
Het |
Zfc3h1 |
T |
A |
10: 115,254,688 (GRCm39) |
C1427* |
probably null |
Het |
Zfp282 |
A |
C |
6: 47,854,637 (GRCm39) |
Q11P |
probably benign |
Het |
Zfp750 |
T |
A |
11: 121,403,021 (GRCm39) |
T576S |
probably benign |
Het |
|
Other mutations in Myo9b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Myo9b
|
APN |
8 |
71,801,379 (GRCm39) |
missense |
probably benign |
|
IGL01020:Myo9b
|
APN |
8 |
71,804,644 (GRCm39) |
missense |
probably benign |
|
IGL01479:Myo9b
|
APN |
8 |
71,811,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01704:Myo9b
|
APN |
8 |
71,812,286 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01761:Myo9b
|
APN |
8 |
71,801,796 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01766:Myo9b
|
APN |
8 |
71,743,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01834:Myo9b
|
APN |
8 |
71,807,901 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01834:Myo9b
|
APN |
8 |
71,808,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01838:Myo9b
|
APN |
8 |
71,787,034 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02318:Myo9b
|
APN |
8 |
71,806,768 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02333:Myo9b
|
APN |
8 |
71,811,637 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02340:Myo9b
|
APN |
8 |
71,743,689 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02514:Myo9b
|
APN |
8 |
71,743,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02593:Myo9b
|
APN |
8 |
71,743,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Myo9b
|
APN |
8 |
71,807,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03332:Myo9b
|
APN |
8 |
71,801,418 (GRCm39) |
missense |
possibly damaging |
0.78 |
avantgarde
|
UTSW |
8 |
71,796,806 (GRCm39) |
missense |
probably damaging |
1.00 |
Freaky
|
UTSW |
8 |
71,743,463 (GRCm39) |
missense |
probably damaging |
1.00 |
iconoclastic
|
UTSW |
8 |
71,743,119 (GRCm39) |
missense |
probably benign |
0.37 |
unconventional
|
UTSW |
8 |
71,801,241 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4418001:Myo9b
|
UTSW |
8 |
71,775,591 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4651001:Myo9b
|
UTSW |
8 |
71,795,456 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0023:Myo9b
|
UTSW |
8 |
71,786,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Myo9b
|
UTSW |
8 |
71,776,493 (GRCm39) |
splice site |
probably benign |
|
R0103:Myo9b
|
UTSW |
8 |
71,776,493 (GRCm39) |
splice site |
probably benign |
|
R0144:Myo9b
|
UTSW |
8 |
71,798,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0207:Myo9b
|
UTSW |
8 |
71,807,869 (GRCm39) |
splice site |
probably benign |
|
R0226:Myo9b
|
UTSW |
8 |
71,806,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R0227:Myo9b
|
UTSW |
8 |
71,796,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Myo9b
|
UTSW |
8 |
71,774,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0277:Myo9b
|
UTSW |
8 |
71,808,596 (GRCm39) |
splice site |
probably benign |
|
R0362:Myo9b
|
UTSW |
8 |
71,800,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Myo9b
|
UTSW |
8 |
71,783,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R0844:Myo9b
|
UTSW |
8 |
71,743,119 (GRCm39) |
missense |
probably benign |
0.37 |
R1051:Myo9b
|
UTSW |
8 |
71,808,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Myo9b
|
UTSW |
8 |
71,743,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Myo9b
|
UTSW |
8 |
71,743,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Myo9b
|
UTSW |
8 |
71,808,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Myo9b
|
UTSW |
8 |
71,743,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Myo9b
|
UTSW |
8 |
71,767,836 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1645:Myo9b
|
UTSW |
8 |
71,775,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Myo9b
|
UTSW |
8 |
71,806,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Myo9b
|
UTSW |
8 |
71,786,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Myo9b
|
UTSW |
8 |
71,743,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Myo9b
|
UTSW |
8 |
71,743,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Myo9b
|
UTSW |
8 |
71,812,334 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2129:Myo9b
|
UTSW |
8 |
71,786,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Myo9b
|
UTSW |
8 |
71,780,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2869:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2872:Myo9b
|
UTSW |
8 |
71,743,610 (GRCm39) |
missense |
probably benign |
0.01 |
R2872:Myo9b
|
UTSW |
8 |
71,743,610 (GRCm39) |
missense |
probably benign |
0.01 |
R2873:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2874:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2920:Myo9b
|
UTSW |
8 |
71,778,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R2926:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2939:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2940:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3033:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3040:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3689:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3691:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3735:Myo9b
|
UTSW |
8 |
71,801,241 (GRCm39) |
missense |
probably benign |
0.00 |
R4194:Myo9b
|
UTSW |
8 |
71,812,268 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4258:Myo9b
|
UTSW |
8 |
71,808,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R4457:Myo9b
|
UTSW |
8 |
71,743,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R4478:Myo9b
|
UTSW |
8 |
71,743,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4496:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R4544:Myo9b
|
UTSW |
8 |
71,780,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Myo9b
|
UTSW |
8 |
71,767,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Myo9b
|
UTSW |
8 |
71,809,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5124:Myo9b
|
UTSW |
8 |
71,808,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5194:Myo9b
|
UTSW |
8 |
71,801,733 (GRCm39) |
missense |
probably benign |
0.01 |
R5296:Myo9b
|
UTSW |
8 |
71,786,032 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5528:Myo9b
|
UTSW |
8 |
71,775,918 (GRCm39) |
missense |
probably benign |
0.06 |
R5664:Myo9b
|
UTSW |
8 |
71,812,526 (GRCm39) |
missense |
probably benign |
0.13 |
R5677:Myo9b
|
UTSW |
8 |
71,796,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5680:Myo9b
|
UTSW |
8 |
71,743,016 (GRCm39) |
missense |
probably benign |
0.00 |
R5982:Myo9b
|
UTSW |
8 |
71,801,040 (GRCm39) |
missense |
probably benign |
0.05 |
R6344:Myo9b
|
UTSW |
8 |
71,780,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Myo9b
|
UTSW |
8 |
71,801,055 (GRCm39) |
missense |
probably benign |
|
R6352:Myo9b
|
UTSW |
8 |
71,801,054 (GRCm39) |
missense |
probably benign |
0.16 |
R6411:Myo9b
|
UTSW |
8 |
71,775,599 (GRCm39) |
nonsense |
probably null |
|
R6425:Myo9b
|
UTSW |
8 |
71,786,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Myo9b
|
UTSW |
8 |
71,808,501 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6743:Myo9b
|
UTSW |
8 |
71,804,803 (GRCm39) |
splice site |
probably null |
|
R6811:Myo9b
|
UTSW |
8 |
71,809,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6813:Myo9b
|
UTSW |
8 |
71,775,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Myo9b
|
UTSW |
8 |
71,743,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Myo9b
|
UTSW |
8 |
71,786,345 (GRCm39) |
nonsense |
probably null |
|
R7255:Myo9b
|
UTSW |
8 |
71,743,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Myo9b
|
UTSW |
8 |
71,778,549 (GRCm39) |
missense |
probably benign |
0.00 |
R7342:Myo9b
|
UTSW |
8 |
71,808,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Myo9b
|
UTSW |
8 |
71,804,832 (GRCm39) |
missense |
probably benign |
0.28 |
R7482:Myo9b
|
UTSW |
8 |
71,795,442 (GRCm39) |
missense |
probably benign |
0.00 |
R7508:Myo9b
|
UTSW |
8 |
71,807,445 (GRCm39) |
missense |
probably benign |
0.00 |
R7957:Myo9b
|
UTSW |
8 |
71,807,405 (GRCm39) |
missense |
probably benign |
0.12 |
R8062:Myo9b
|
UTSW |
8 |
71,774,457 (GRCm39) |
missense |
probably damaging |
0.99 |
R8108:Myo9b
|
UTSW |
8 |
71,800,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R8197:Myo9b
|
UTSW |
8 |
71,743,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Myo9b
|
UTSW |
8 |
71,812,480 (GRCm39) |
missense |
probably benign |
0.00 |
R8686:Myo9b
|
UTSW |
8 |
71,786,966 (GRCm39) |
missense |
probably benign |
0.01 |
R8731:Myo9b
|
UTSW |
8 |
71,806,486 (GRCm39) |
critical splice donor site |
probably null |
|
R8924:Myo9b
|
UTSW |
8 |
71,801,675 (GRCm39) |
missense |
probably benign |
|
R9056:Myo9b
|
UTSW |
8 |
71,804,906 (GRCm39) |
missense |
probably benign |
0.17 |
R9117:Myo9b
|
UTSW |
8 |
71,800,451 (GRCm39) |
missense |
probably benign |
0.03 |
R9151:Myo9b
|
UTSW |
8 |
71,807,871 (GRCm39) |
splice site |
probably benign |
|
R9315:Myo9b
|
UTSW |
8 |
71,801,811 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9332:Myo9b
|
UTSW |
8 |
71,812,246 (GRCm39) |
missense |
probably benign |
0.07 |
R9364:Myo9b
|
UTSW |
8 |
71,808,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:Myo9b
|
UTSW |
8 |
71,811,629 (GRCm39) |
missense |
probably benign |
|
R9581:Myo9b
|
UTSW |
8 |
71,812,543 (GRCm39) |
missense |
probably benign |
0.19 |
R9600:Myo9b
|
UTSW |
8 |
71,743,075 (GRCm39) |
missense |
possibly damaging |
0.80 |
X0066:Myo9b
|
UTSW |
8 |
71,776,542 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo9b
|
UTSW |
8 |
71,743,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GTTCAAAGCAGGCACAGGTTG -3'
(R):5'- TGCCCTCAACCCTGCATAATG -3'
Sequencing Primer
(F):5'- TCCCAGTCCCGTGCAGAG -3'
(R):5'- CCCTGCATAATGGATAGGCTTAC -3'
|
Posted On |
2016-06-06 |