Incidental Mutation 'R6505:Myo9b'
ID |
523745 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo9b
|
Ensembl Gene |
ENSMUSG00000004677 |
Gene Name |
myosin IXb |
Synonyms |
|
MMRRC Submission |
044637-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.852)
|
Stock # |
R6505 (G1)
|
Quality Score |
185.009 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
71725358-71813357 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 71808501 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 1715
(T1715A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129220
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000071935]
[ENSMUST00000168839]
[ENSMUST00000170242]
[ENSMUST00000212935]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000071935
AA Change: T1701A
PolyPhen 2
Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000071827 Gene: ENSMUSG00000004677 AA Change: T1701A
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 |
possibly damaging
Transcript: ENSMUST00000168839
AA Change: T1715A
PolyPhen 2
Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000131635 Gene: ENSMUSG00000004677 AA Change: T1715A
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 |
possibly damaging
Transcript: ENSMUST00000170242
AA Change: T1715A
PolyPhen 2
Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000129220 Gene: ENSMUSG00000004677 AA Change: T1715A
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: T510A
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212935
AA Change: T1703A
PolyPhen 2
Score 0.855 (Sensitivity: 0.83; Specificity: 0.93)
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.6%
- 20x: 96.2%
|
Validation Efficiency |
100% (84/84) |
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: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
A |
T |
17: 9,220,772 (GRCm39) |
I424L |
probably benign |
Het |
2610028H24Rik |
C |
T |
10: 76,285,115 (GRCm39) |
A8V |
probably benign |
Het |
Ago1 |
G |
A |
4: 126,357,628 (GRCm39) |
P16S |
probably benign |
Het |
Ak5 |
C |
T |
3: 152,187,306 (GRCm39) |
E394K |
probably benign |
Het |
Aldh7a1 |
T |
C |
18: 56,660,068 (GRCm39) |
Y498C |
probably damaging |
Het |
Alox12 |
T |
A |
11: 70,141,030 (GRCm39) |
D335V |
probably damaging |
Het |
Alx4 |
A |
T |
2: 93,498,904 (GRCm39) |
Y212F |
probably damaging |
Het |
Asb16 |
A |
G |
11: 102,167,303 (GRCm39) |
E223G |
probably damaging |
Het |
Atg9b |
C |
T |
5: 24,595,575 (GRCm39) |
V235M |
probably damaging |
Het |
BB014433 |
A |
G |
8: 15,092,304 (GRCm39) |
V183A |
probably benign |
Het |
Brca1 |
T |
A |
11: 101,414,367 (GRCm39) |
M1256L |
probably benign |
Het |
Bst1 |
A |
G |
5: 43,977,932 (GRCm39) |
I94V |
probably benign |
Het |
C3ar1 |
A |
G |
6: 122,827,599 (GRCm39) |
L206P |
probably benign |
Het |
Cabs1 |
T |
A |
5: 88,128,522 (GRCm39) |
M391K |
possibly damaging |
Het |
Cars1 |
C |
T |
7: 143,118,744 (GRCm39) |
R599Q |
probably damaging |
Het |
Ccdc190 |
T |
A |
1: 169,760,592 (GRCm39) |
Y73* |
probably null |
Het |
Cd177 |
A |
C |
7: 24,443,671 (GRCm39) |
L809W |
probably benign |
Het |
Cemip |
C |
A |
7: 83,600,805 (GRCm39) |
G939* |
probably null |
Het |
Clca3b |
T |
A |
3: 144,531,020 (GRCm39) |
I777F |
probably benign |
Het |
Cma2 |
T |
C |
14: 56,211,236 (GRCm39) |
I176T |
probably damaging |
Het |
Col12a1 |
T |
A |
9: 79,554,887 (GRCm39) |
T2064S |
probably damaging |
Het |
Csf1r |
A |
G |
18: 61,262,805 (GRCm39) |
N860S |
probably damaging |
Het |
Dab1 |
T |
A |
4: 104,369,461 (GRCm39) |
C3S |
probably benign |
Het |
Dennd4b |
A |
G |
3: 90,174,918 (GRCm39) |
E50G |
probably damaging |
Het |
Dis3l |
A |
T |
9: 64,214,795 (GRCm39) |
S925T |
probably benign |
Het |
Disp1 |
T |
C |
1: 182,868,076 (GRCm39) |
N1448S |
probably benign |
Het |
Dpp10 |
T |
C |
1: 123,264,580 (GRCm39) |
I747M |
probably damaging |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Ephx4 |
A |
T |
5: 107,551,522 (GRCm39) |
K36* |
probably null |
Het |
Fam135a |
C |
T |
1: 24,053,953 (GRCm39) |
V1195I |
probably damaging |
Het |
Fap |
A |
T |
2: 62,376,947 (GRCm39) |
Y234* |
probably null |
Het |
Fem1c |
A |
T |
18: 46,638,942 (GRCm39) |
N353K |
possibly damaging |
Het |
Furin |
C |
A |
7: 80,043,365 (GRCm39) |
R282L |
probably damaging |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm5930 |
A |
G |
14: 44,568,828 (GRCm39) |
*265Q |
probably null |
Het |
Hcrtr1 |
T |
A |
4: 130,031,379 (GRCm39) |
T15S |
probably benign |
Het |
Ifnar1 |
C |
T |
16: 91,296,425 (GRCm39) |
Q309* |
probably null |
Het |
Il18r1 |
A |
T |
1: 40,528,867 (GRCm39) |
I304L |
probably benign |
Het |
Ino80 |
A |
T |
2: 119,281,922 (GRCm39) |
Y185N |
probably damaging |
Het |
Itgb2 |
G |
A |
10: 77,395,507 (GRCm39) |
C536Y |
probably damaging |
Het |
Ivns1abp |
T |
C |
1: 151,236,744 (GRCm39) |
M435T |
probably benign |
Het |
Kcnh4 |
T |
C |
11: 100,647,911 (GRCm39) |
N151D |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,628,405 (GRCm39) |
M1499T |
probably benign |
Het |
Lamb1 |
A |
T |
12: 31,373,461 (GRCm39) |
T1397S |
possibly damaging |
Het |
Leng1 |
G |
A |
7: 3,664,211 (GRCm39) |
R239* |
probably null |
Het |
Map2k4 |
A |
T |
11: 65,584,355 (GRCm39) |
N309K |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,873,768 (GRCm39) |
F784S |
probably damaging |
Het |
Mrgpra9 |
T |
A |
7: 46,884,884 (GRCm39) |
N260I |
probably benign |
Het |
Mrnip |
C |
A |
11: 50,090,679 (GRCm39) |
T281N |
possibly damaging |
Het |
Nectin3 |
A |
G |
16: 46,269,184 (GRCm39) |
I406T |
possibly damaging |
Het |
Neto1 |
A |
G |
18: 86,516,699 (GRCm39) |
T339A |
possibly damaging |
Het |
Ntn1 |
T |
C |
11: 68,104,025 (GRCm39) |
D541G |
probably damaging |
Het |
Nuak2 |
C |
A |
1: 132,244,132 (GRCm39) |
H55Q |
probably damaging |
Het |
Nufip2 |
A |
G |
11: 77,582,439 (GRCm39) |
T118A |
probably benign |
Het |
Or11i1 |
T |
G |
3: 106,729,638 (GRCm39) |
N79T |
possibly damaging |
Het |
Or12e7 |
T |
A |
2: 87,288,271 (GRCm39) |
V254E |
probably damaging |
Het |
Or51af1 |
T |
A |
7: 103,141,858 (GRCm39) |
T76S |
probably damaging |
Het |
Or52e19 |
C |
A |
7: 102,959,000 (GRCm39) |
A24D |
probably benign |
Het |
Or5d16 |
A |
T |
2: 87,773,518 (GRCm39) |
Y151* |
probably null |
Het |
Or5p59 |
T |
C |
7: 107,702,774 (GRCm39) |
V86A |
probably benign |
Het |
Or6d13 |
C |
T |
6: 116,517,561 (GRCm39) |
T49M |
probably benign |
Het |
Or7a40 |
A |
T |
16: 16,491,784 (GRCm39) |
D20E |
probably benign |
Het |
Or7g29 |
T |
C |
9: 19,286,237 (GRCm39) |
*313W |
probably null |
Het |
Pcdhb5 |
T |
A |
18: 37,453,933 (GRCm39) |
H104Q |
probably benign |
Het |
Phf11a |
T |
C |
14: 59,514,986 (GRCm39) |
R232G |
probably damaging |
Het |
Pik3r5 |
C |
T |
11: 68,383,615 (GRCm39) |
T478I |
probably benign |
Het |
Prkacb |
T |
A |
3: 146,438,401 (GRCm39) |
E380V |
probably damaging |
Het |
Prl7c1 |
G |
T |
13: 27,957,776 (GRCm39) |
D221E |
probably damaging |
Het |
Prr11 |
T |
A |
11: 86,996,950 (GRCm39) |
K5* |
probably null |
Het |
Prrc2b |
G |
A |
2: 32,112,332 (GRCm39) |
G1932D |
probably damaging |
Het |
Rexo1 |
A |
T |
10: 80,378,845 (GRCm39) |
Y1064N |
possibly damaging |
Het |
Rnf182 |
C |
T |
13: 43,822,147 (GRCm39) |
Q233* |
probably null |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Sash1 |
C |
G |
10: 8,605,291 (GRCm39) |
G1033A |
probably benign |
Het |
Sncaip |
C |
A |
18: 53,039,609 (GRCm39) |
S189* |
probably null |
Het |
Sorl1 |
T |
C |
9: 41,982,530 (GRCm39) |
Y350C |
probably damaging |
Het |
Speg |
T |
C |
1: 75,383,328 (GRCm39) |
V1141A |
possibly damaging |
Het |
Speg |
C |
A |
1: 75,406,167 (GRCm39) |
D3091E |
possibly damaging |
Het |
Sucnr1 |
A |
T |
3: 59,994,144 (GRCm39) |
D224V |
probably benign |
Het |
Tg |
G |
A |
15: 66,631,407 (GRCm39) |
A559T |
probably damaging |
Het |
Tmem132d |
A |
G |
5: 127,861,502 (GRCm39) |
I873T |
probably benign |
Het |
Tmem229a |
C |
T |
6: 24,954,920 (GRCm39) |
C278Y |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,013,364 (GRCm39) |
I205T |
possibly damaging |
Het |
Usp19 |
T |
A |
9: 108,374,082 (GRCm39) |
L713Q |
probably damaging |
Het |
Vsig10 |
A |
G |
5: 117,489,824 (GRCm39) |
D530G |
possibly damaging |
Het |
Zfp106 |
A |
G |
2: 120,364,983 (GRCm39) |
S475P |
probably damaging |
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 |
R5068:Myo9b
|
UTSW |
8 |
71,801,699 (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 |
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'- CCTTCAAGGACAGAGTAGGCAG -3'
(R):5'- CAAAAGTCATGAGTGGCTCAGG -3'
Sequencing Primer
(F):5'- ACTGCAGAAGTGGCACC -3'
(R):5'- CTCAGGCAGCTCACGAAG -3'
|
Posted On |
2018-06-22 |