Incidental Mutation 'R5677:Myo9b'
ID |
442804 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo9b
|
Ensembl Gene |
ENSMUSG00000004677 |
Gene Name |
myosin IXb |
Synonyms |
|
MMRRC Submission |
043316-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.852)
|
Stock # |
R5677 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
71725358-71813357 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 71796330 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Valine
at position 857
(A857V)
|
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 |
probably damaging
Transcript: ENSMUST00000071935
AA Change: A857V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000071827 Gene: ENSMUSG00000004677 AA Change: A857V
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: A857V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000131635 Gene: ENSMUSG00000004677 AA Change: A857V
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: A857V
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000129220 Gene: ENSMUSG00000004677 AA Change: A857V
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 |
noncoding transcript
Transcript: ENSMUST00000212173
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000212935
AA Change: A858V
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.5%
- 20x: 95.9%
|
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: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
C |
T |
10: 28,862,225 (GRCm39) |
V22I |
probably benign |
Het |
Abca8a |
A |
T |
11: 109,929,225 (GRCm39) |
V1296D |
possibly damaging |
Het |
Abca8b |
C |
T |
11: 109,831,687 (GRCm39) |
S1328N |
probably damaging |
Het |
Adcy1 |
G |
A |
11: 7,111,914 (GRCm39) |
M926I |
probably damaging |
Het |
Aff4 |
G |
T |
11: 53,291,102 (GRCm39) |
M687I |
possibly damaging |
Het |
Agbl2 |
T |
A |
2: 90,638,322 (GRCm39) |
Y636N |
possibly damaging |
Het |
Agtr1a |
A |
T |
13: 30,565,567 (GRCm39) |
I211F |
probably damaging |
Het |
Alkbh8 |
T |
G |
9: 3,385,147 (GRCm39) |
S480A |
possibly damaging |
Het |
Ankrd13b |
A |
T |
11: 77,368,370 (GRCm39) |
V84E |
probably damaging |
Het |
Ap3b1 |
C |
T |
13: 94,664,704 (GRCm39) |
T881I |
unknown |
Het |
Apbb1 |
A |
C |
7: 105,208,453 (GRCm39) |
D617E |
probably damaging |
Het |
Apobec4 |
A |
G |
1: 152,633,033 (GRCm39) |
R354G |
probably benign |
Het |
Brdt |
T |
G |
5: 107,496,483 (GRCm39) |
C198W |
possibly damaging |
Het |
Cacna1b |
G |
T |
2: 24,569,370 (GRCm39) |
H851Q |
possibly damaging |
Het |
Car2 |
G |
T |
3: 14,963,115 (GRCm39) |
V217F |
possibly damaging |
Het |
Ccdc24 |
A |
C |
4: 117,727,077 (GRCm39) |
|
probably benign |
Het |
Chodl |
C |
A |
16: 78,738,203 (GRCm39) |
A57E |
probably damaging |
Het |
Clgn |
G |
T |
8: 84,136,167 (GRCm39) |
C185F |
probably damaging |
Het |
Cltc |
G |
T |
11: 86,596,068 (GRCm39) |
N1223K |
probably damaging |
Het |
Cnot10 |
T |
C |
9: 114,458,161 (GRCm39) |
N115S |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,606,603 (GRCm39) |
R607G |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,690,651 (GRCm39) |
V835A |
probably benign |
Het |
Cplane2 |
C |
T |
4: 140,947,177 (GRCm39) |
P186L |
probably benign |
Het |
Csmd3 |
G |
C |
15: 48,485,447 (GRCm39) |
L153V |
probably damaging |
Het |
Ctr9 |
A |
G |
7: 110,643,209 (GRCm39) |
H527R |
probably benign |
Het |
Cwc22 |
G |
A |
2: 77,759,787 (GRCm39) |
R87W |
probably damaging |
Het |
D930020B18Rik |
T |
A |
10: 121,505,106 (GRCm39) |
N107K |
probably benign |
Het |
Dgkg |
C |
A |
16: 22,388,921 (GRCm39) |
V418L |
probably benign |
Het |
Dhx40 |
A |
G |
11: 86,691,789 (GRCm39) |
|
probably null |
Het |
Diaph1 |
A |
T |
18: 37,989,004 (GRCm39) |
M910K |
probably damaging |
Het |
Diras2 |
T |
A |
13: 52,661,711 (GRCm39) |
M199L |
possibly damaging |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dock5 |
T |
A |
14: 68,015,052 (GRCm39) |
Q1302H |
probably benign |
Het |
Dync1i2 |
T |
C |
2: 71,058,967 (GRCm39) |
S90P |
probably benign |
Het |
E2f8 |
A |
T |
7: 48,516,943 (GRCm39) |
V812E |
probably damaging |
Het |
Egfem1 |
C |
A |
3: 29,744,323 (GRCm39) |
Q521K |
probably damaging |
Het |
Fbxl18 |
A |
T |
5: 142,864,475 (GRCm39) |
C699* |
probably null |
Het |
Fgf3 |
C |
T |
7: 144,392,520 (GRCm39) |
R26* |
probably null |
Het |
Fpr-rs7 |
T |
G |
17: 20,334,365 (GRCm39) |
I42L |
probably benign |
Het |
Gm3159 |
T |
A |
14: 4,398,582 (GRCm38) |
M91K |
probably damaging |
Het |
Gprin3 |
A |
G |
6: 59,330,877 (GRCm39) |
S477P |
possibly damaging |
Het |
Grm8 |
A |
T |
6: 27,761,203 (GRCm39) |
|
probably null |
Het |
Hepacam2 |
A |
T |
6: 3,466,142 (GRCm39) |
D420E |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,485,529 (GRCm39) |
W4358R |
probably benign |
Het |
Ifna6 |
G |
A |
4: 88,745,956 (GRCm39) |
A102T |
probably benign |
Het |
Ighv2-2 |
T |
C |
12: 113,552,142 (GRCm39) |
Q32R |
probably benign |
Het |
Igkv1-131 |
T |
A |
6: 67,743,242 (GRCm39) |
Q47L |
possibly damaging |
Het |
Il16 |
T |
C |
7: 83,323,761 (GRCm39) |
E263G |
probably damaging |
Het |
Kansl1 |
A |
T |
11: 104,225,974 (GRCm39) |
C981S |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,410,298 (GRCm39) |
F1483I |
probably damaging |
Het |
Ltf |
T |
C |
9: 110,849,980 (GRCm39) |
M1T |
probably null |
Het |
Ly75 |
C |
T |
2: 60,129,426 (GRCm39) |
R1653H |
probably benign |
Het |
Macrod2 |
T |
C |
2: 142,018,587 (GRCm39) |
F240S |
probably damaging |
Het |
Man1c1 |
T |
C |
4: 134,296,371 (GRCm39) |
E433G |
probably damaging |
Het |
Mansc4 |
A |
T |
6: 146,983,047 (GRCm39) |
M130K |
probably benign |
Het |
Mccc1 |
C |
T |
3: 36,044,197 (GRCm39) |
|
probably null |
Het |
Mink1 |
G |
T |
11: 70,495,991 (GRCm39) |
R75L |
possibly damaging |
Het |
Mst1 |
A |
G |
9: 107,958,485 (GRCm39) |
D65G |
probably damaging |
Het |
Ndufa4 |
A |
G |
6: 11,900,574 (GRCm39) |
V70A |
probably benign |
Het |
Npat |
T |
A |
9: 53,466,400 (GRCm39) |
S230T |
probably benign |
Het |
Nr1d1 |
A |
G |
11: 98,662,134 (GRCm39) |
Y167H |
probably damaging |
Het |
Oca2 |
A |
G |
7: 56,064,210 (GRCm39) |
D735G |
probably damaging |
Het |
Odr4 |
G |
A |
1: 150,250,588 (GRCm39) |
L319F |
probably damaging |
Het |
Or2a7 |
T |
C |
6: 43,151,265 (GRCm39) |
V115A |
probably benign |
Het |
Or2b2 |
C |
T |
13: 21,887,393 (GRCm39) |
T74I |
probably benign |
Het |
Or2y13 |
A |
G |
11: 49,414,771 (GRCm39) |
T74A |
probably damaging |
Het |
Or7g20 |
T |
A |
9: 18,946,854 (GRCm39) |
I145N |
possibly damaging |
Het |
Otop1 |
A |
G |
5: 38,457,507 (GRCm39) |
Y422C |
probably damaging |
Het |
Pde4dip |
G |
A |
3: 97,748,964 (GRCm39) |
R126* |
probably null |
Het |
Pdp2 |
C |
T |
8: 105,321,320 (GRCm39) |
P390S |
probably damaging |
Het |
Pds5b |
A |
T |
5: 150,639,926 (GRCm39) |
T14S |
possibly damaging |
Het |
Pfkp |
T |
C |
13: 6,638,631 (GRCm39) |
E580G |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,250,767 (GRCm39) |
L212Q |
possibly damaging |
Het |
Piezo2 |
G |
C |
18: 63,250,768 (GRCm39) |
L444V |
probably benign |
Het |
Pla2g4d |
T |
A |
2: 120,109,429 (GRCm39) |
T207S |
possibly damaging |
Het |
Plk2 |
C |
A |
13: 110,535,591 (GRCm39) |
T471K |
possibly damaging |
Het |
Potefam1 |
T |
C |
2: 111,041,910 (GRCm39) |
T342A |
probably benign |
Het |
Potegl |
T |
A |
2: 23,102,730 (GRCm39) |
L156Q |
probably damaging |
Het |
Ppp1r3g |
G |
A |
13: 36,153,245 (GRCm39) |
E222K |
probably damaging |
Het |
Pramel28 |
A |
T |
4: 143,691,708 (GRCm39) |
D338E |
possibly damaging |
Het |
Prkcg |
A |
G |
7: 3,371,974 (GRCm39) |
D480G |
probably damaging |
Het |
Pxdc1 |
T |
A |
13: 34,836,178 (GRCm39) |
T81S |
probably benign |
Het |
Rnf150 |
A |
T |
8: 83,730,228 (GRCm39) |
K253* |
probably null |
Het |
Sae1 |
T |
C |
7: 16,104,387 (GRCm39) |
|
probably null |
Het |
Scin |
C |
T |
12: 40,113,258 (GRCm39) |
D538N |
probably damaging |
Het |
Serpinb3c |
C |
A |
1: 107,199,533 (GRCm39) |
K329N |
probably damaging |
Het |
Sgo2b |
T |
A |
8: 64,380,008 (GRCm39) |
K941N |
possibly damaging |
Het |
Six1 |
C |
T |
12: 73,093,058 (GRCm39) |
S48N |
possibly damaging |
Het |
Slc39a8 |
G |
A |
3: 135,590,449 (GRCm39) |
G381R |
probably damaging |
Het |
Slc9b1 |
A |
G |
3: 135,063,320 (GRCm39) |
K35E |
unknown |
Het |
Srek1 |
C |
T |
13: 103,895,752 (GRCm39) |
A274T |
probably damaging |
Het |
Steap2 |
A |
T |
5: 5,727,497 (GRCm39) |
Y279* |
probably null |
Het |
Svil |
T |
A |
18: 5,046,823 (GRCm39) |
L110* |
probably null |
Het |
Syncrip |
T |
C |
9: 88,338,762 (GRCm39) |
|
probably benign |
Het |
Tcf20 |
A |
G |
15: 82,737,443 (GRCm39) |
I1336T |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,155,451 (GRCm39) |
K36* |
probably null |
Het |
Tenm2 |
A |
G |
11: 36,032,510 (GRCm39) |
V670A |
probably damaging |
Het |
Thbd |
G |
A |
2: 148,249,286 (GRCm39) |
T194I |
probably damaging |
Het |
Tm9sf2 |
A |
T |
14: 122,389,374 (GRCm39) |
|
probably null |
Het |
Tmtc4 |
A |
T |
14: 123,187,911 (GRCm39) |
I225N |
probably damaging |
Het |
Tpp1 |
C |
T |
7: 105,396,743 (GRCm39) |
V425M |
probably damaging |
Het |
Trbc2 |
T |
A |
6: 41,524,746 (GRCm39) |
Y144* |
probably null |
Het |
Trps1 |
T |
C |
15: 50,709,504 (GRCm39) |
D282G |
probably damaging |
Het |
Tsc22d4 |
T |
A |
5: 137,745,404 (GRCm39) |
S9R |
probably damaging |
Het |
Upp1 |
T |
A |
11: 9,086,025 (GRCm39) |
D287E |
probably benign |
Het |
Uso1 |
A |
C |
5: 92,349,158 (GRCm39) |
Q916H |
probably damaging |
Het |
Uty |
T |
A |
Y: 1,134,902 (GRCm39) |
Y884F |
probably damaging |
Het |
Vmn1r222 |
T |
C |
13: 23,416,950 (GRCm39) |
R88G |
probably damaging |
Het |
Vmn1r79 |
T |
C |
7: 11,910,928 (GRCm39) |
V270A |
possibly damaging |
Het |
Zbtb22 |
T |
C |
17: 34,136,709 (GRCm39) |
S285P |
probably benign |
Het |
Zfp385a |
A |
G |
15: 103,226,492 (GRCm39) |
V82A |
probably damaging |
Het |
Zfp59 |
T |
C |
7: 27,553,594 (GRCm39) |
F349L |
probably benign |
Het |
Zfp780b |
T |
G |
7: 27,662,224 (GRCm39) |
H777P |
probably benign |
Het |
Zfp82 |
T |
C |
7: 29,756,549 (GRCm39) |
T178A |
probably benign |
Het |
Zfp850 |
T |
C |
7: 27,688,513 (GRCm39) |
Y565C |
probably damaging |
Het |
Zfp957 |
A |
G |
14: 79,450,207 (GRCm39) |
Y531H |
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 |
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'- TGGAGTTGCAAGACCTTTGG -3'
(R):5'- TCTGGTGGCTAAAGCTTCTTCTAC -3'
Sequencing Primer
(F):5'- GACCTTTGGTCGGCTCCATG -3'
(R):5'- ACTTCAGATCCTCAGTGCTGGAATG -3'
|
Posted On |
2016-11-09 |