Incidental Mutation 'R1470:Myo18b'
ID |
165791 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Myo18b
|
Ensembl Gene |
ENSMUSG00000072720 |
Gene Name |
myosin XVIIIb |
Synonyms |
4932408L24Rik, 4933411E19Rik |
MMRRC Submission |
039523-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1470 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
112836742-113044228 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 112840899 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Leucine
at position 2298
(R2298L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000083810
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086617]
|
AlphaFold |
E9PV66 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000086617
AA Change: R2298L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000083810 Gene: ENSMUSG00000072720 AA Change: R2298L
Domain | Start | End | E-Value | Type |
low complexity region
|
20 |
28 |
N/A |
INTRINSIC |
low complexity region
|
43 |
59 |
N/A |
INTRINSIC |
low complexity region
|
86 |
100 |
N/A |
INTRINSIC |
low complexity region
|
185 |
200 |
N/A |
INTRINSIC |
low complexity region
|
273 |
290 |
N/A |
INTRINSIC |
low complexity region
|
291 |
304 |
N/A |
INTRINSIC |
low complexity region
|
355 |
372 |
N/A |
INTRINSIC |
low complexity region
|
377 |
419 |
N/A |
INTRINSIC |
MYSc
|
605 |
1374 |
8.78e-30 |
SMART |
IQ
|
1375 |
1397 |
5.92e-4 |
SMART |
Pfam:Myosin_tail_1
|
1423 |
1875 |
5e-12 |
PFAM |
low complexity region
|
1965 |
1985 |
N/A |
INTRINSIC |
coiled coil region
|
2052 |
2126 |
N/A |
INTRINSIC |
low complexity region
|
2184 |
2199 |
N/A |
INTRINSIC |
low complexity region
|
2325 |
2336 |
N/A |
INTRINSIC |
low complexity region
|
2408 |
2424 |
N/A |
INTRINSIC |
low complexity region
|
2544 |
2558 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182189
|
Meta Mutation Damage Score |
0.2396 |
Coding Region Coverage |
- 1x: 99.7%
- 3x: 98.4%
- 10x: 90.6%
- 20x: 68.6%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene may regulate muscle-specific genes when in the nucleus and may influence intracellular trafficking when in the cytoplasm. The encoded protein functions as a homodimer and may interact with F actin. Mutations in this gene are associated with lung cancer. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a null mutation display embryonic lethality during organogenesis with internal hemorrhage, pericaridal effusion, enlargement of the right atrium, and cardiac myofibril abnormalities. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
A |
6: 86,944,337 (GRCm39) |
S749T |
unknown |
Het |
Abcb4 |
A |
T |
5: 8,990,968 (GRCm39) |
I843F |
probably damaging |
Het |
Actr8 |
T |
A |
14: 29,708,926 (GRCm39) |
H244Q |
possibly damaging |
Het |
Adgrv1 |
A |
G |
13: 81,530,417 (GRCm39) |
Y5886H |
probably benign |
Het |
Agk |
T |
A |
6: 40,363,751 (GRCm39) |
W244R |
probably damaging |
Het |
Ankrd11 |
C |
A |
8: 123,626,463 (GRCm39) |
V161L |
probably damaging |
Het |
Arap3 |
T |
C |
18: 38,122,249 (GRCm39) |
|
probably null |
Het |
Armc3 |
A |
G |
2: 19,243,547 (GRCm39) |
M88V |
probably benign |
Het |
Atp13a5 |
G |
T |
16: 29,167,833 (GRCm39) |
P109T |
probably benign |
Het |
Avpr1b |
T |
A |
1: 131,528,323 (GRCm39) |
V282D |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,808,890 (GRCm39) |
K120E |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 37,052,480 (GRCm39) |
M3060T |
probably benign |
Het |
Cacng6 |
G |
A |
7: 3,473,404 (GRCm39) |
C76Y |
probably damaging |
Het |
Cactin |
G |
T |
10: 81,158,985 (GRCm39) |
E279* |
probably null |
Het |
Car9 |
A |
G |
4: 43,510,222 (GRCm39) |
Y268C |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,524,564 (GRCm39) |
I263F |
probably damaging |
Het |
Cdh16 |
T |
G |
8: 105,345,003 (GRCm39) |
S429R |
probably benign |
Het |
Cep250 |
A |
G |
2: 155,832,995 (GRCm39) |
E1639G |
probably damaging |
Het |
Ces1d |
A |
T |
8: 93,921,649 (GRCm39) |
V38D |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,946,545 (GRCm39) |
Q97L |
possibly damaging |
Het |
Ciita |
G |
A |
16: 10,332,332 (GRCm39) |
D898N |
possibly damaging |
Het |
Clstn1 |
A |
G |
4: 149,719,179 (GRCm39) |
N336S |
possibly damaging |
Het |
Cntnap5a |
A |
G |
1: 116,187,249 (GRCm39) |
D607G |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col20a1 |
C |
T |
2: 180,636,753 (GRCm39) |
H245Y |
probably benign |
Het |
Coq8b |
A |
T |
7: 26,951,734 (GRCm39) |
T399S |
probably benign |
Het |
Cpn2 |
A |
G |
16: 30,079,003 (GRCm39) |
S233P |
probably benign |
Het |
Cryz |
G |
A |
3: 154,312,113 (GRCm39) |
G70D |
probably damaging |
Het |
Def6 |
T |
A |
17: 28,444,956 (GRCm39) |
D451E |
possibly damaging |
Het |
Dnah8 |
T |
A |
17: 30,966,251 (GRCm39) |
C2480* |
probably null |
Het |
Dnah9 |
T |
C |
11: 65,818,648 (GRCm39) |
N3230S |
probably benign |
Het |
Dyrk4 |
G |
T |
6: 126,893,337 (GRCm39) |
S15* |
probably null |
Het |
Erc1 |
T |
C |
6: 119,671,563 (GRCm39) |
R917G |
probably damaging |
Het |
Frem3 |
G |
T |
8: 81,337,820 (GRCm39) |
V38L |
probably benign |
Het |
Gas2l3 |
T |
C |
10: 89,249,796 (GRCm39) |
I441V |
probably benign |
Het |
Gm14393 |
T |
A |
2: 174,905,774 (GRCm39) |
Y6F |
probably damaging |
Het |
Gm1527 |
A |
G |
3: 28,969,417 (GRCm39) |
K256E |
possibly damaging |
Het |
Gm21905 |
G |
T |
5: 68,103,740 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,424,656 (GRCm39) |
|
probably null |
Het |
Hmces |
C |
A |
6: 87,913,121 (GRCm39) |
T292K |
probably benign |
Het |
Hpse2 |
G |
A |
19: 43,376,692 (GRCm39) |
S20L |
probably benign |
Het |
Ift70b |
G |
T |
2: 75,768,155 (GRCm39) |
S199R |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,204,224 (GRCm39) |
V23E |
probably null |
Het |
Ino80 |
A |
T |
2: 119,210,130 (GRCm39) |
V1387E |
probably damaging |
Het |
Islr |
G |
T |
9: 58,064,589 (GRCm39) |
A306D |
probably damaging |
Het |
Jakmip1 |
G |
A |
5: 37,258,182 (GRCm39) |
G276D |
probably damaging |
Het |
Jchain |
A |
G |
5: 88,673,979 (GRCm39) |
V55A |
probably benign |
Het |
Kalrn |
T |
C |
16: 34,007,841 (GRCm39) |
K1350E |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,841,156 (GRCm39) |
Q48R |
possibly damaging |
Het |
Kmt5a |
T |
C |
5: 124,585,334 (GRCm39) |
L23P |
probably damaging |
Het |
Lrba |
C |
T |
3: 86,644,449 (GRCm39) |
H381Y |
probably damaging |
Het |
Lrrc32 |
T |
C |
7: 98,148,564 (GRCm39) |
V448A |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,848,301 (GRCm39) |
M617T |
probably damaging |
Het |
Mfap1a |
T |
C |
2: 121,333,282 (GRCm39) |
M50V |
probably benign |
Het |
Mgam |
G |
T |
6: 40,736,062 (GRCm39) |
A854S |
probably damaging |
Het |
Myo1h |
T |
A |
5: 114,457,765 (GRCm39) |
M92K |
probably damaging |
Het |
Nlrp2 |
T |
A |
7: 5,303,950 (GRCm39) |
T192S |
probably benign |
Het |
Nr2f1 |
A |
T |
13: 78,346,284 (GRCm39) |
Y137N |
possibly damaging |
Het |
Nup98 |
T |
A |
7: 101,796,513 (GRCm39) |
D841V |
probably damaging |
Het |
Nvl |
A |
G |
1: 180,966,827 (GRCm39) |
V59A |
probably damaging |
Het |
Ogdhl |
C |
A |
14: 32,068,745 (GRCm39) |
N948K |
probably damaging |
Het |
Or11g27 |
T |
C |
14: 50,771,159 (GRCm39) |
S97P |
possibly damaging |
Het |
Or12j3 |
A |
G |
7: 139,953,026 (GRCm39) |
S166P |
probably benign |
Het |
Or13a24 |
A |
G |
7: 140,154,662 (GRCm39) |
T199A |
probably benign |
Het |
Or51g1 |
A |
C |
7: 102,633,530 (GRCm39) |
Y280* |
probably null |
Het |
Osgin1 |
G |
A |
8: 120,171,704 (GRCm39) |
R166H |
probably damaging |
Het |
Palb2 |
A |
T |
7: 121,706,746 (GRCm39) |
F741I |
probably benign |
Het |
Palb2 |
G |
T |
7: 121,706,747 (GRCm39) |
Y740* |
probably null |
Het |
Parvb |
G |
A |
15: 84,155,509 (GRCm39) |
D65N |
probably benign |
Het |
Parvb |
G |
A |
15: 84,155,453 (GRCm39) |
G46D |
probably damaging |
Het |
Pcsk2 |
A |
T |
2: 143,388,438 (GRCm39) |
K10* |
probably null |
Het |
Pde3a |
C |
T |
6: 141,411,932 (GRCm39) |
A502V |
probably benign |
Het |
Pfas |
T |
C |
11: 68,882,185 (GRCm39) |
I893V |
probably benign |
Het |
Pla2g4a |
A |
T |
1: 149,716,471 (GRCm39) |
D663E |
probably damaging |
Het |
Prickle2 |
G |
A |
6: 92,435,583 (GRCm39) |
P6L |
probably damaging |
Het |
Prx |
T |
A |
7: 27,217,026 (GRCm39) |
M648K |
probably benign |
Het |
Ptpn21 |
T |
C |
12: 98,654,735 (GRCm39) |
N744S |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,554,435 (GRCm39) |
V97M |
probably damaging |
Het |
Pvr |
T |
C |
7: 19,652,549 (GRCm39) |
E122G |
possibly damaging |
Het |
Racgap1 |
T |
C |
15: 99,537,656 (GRCm39) |
K15E |
probably damaging |
Het |
Rock1 |
C |
T |
18: 10,136,091 (GRCm39) |
|
probably null |
Het |
Rorc |
T |
A |
3: 94,304,609 (GRCm39) |
Y331* |
probably null |
Het |
Rpl37 |
T |
C |
15: 5,148,096 (GRCm39) |
V91A |
probably benign |
Het |
Rrp36 |
T |
A |
17: 46,983,306 (GRCm39) |
K103* |
probably null |
Het |
Ryr3 |
T |
A |
2: 112,483,352 (GRCm39) |
M4142L |
probably benign |
Het |
Sash1 |
A |
T |
10: 8,665,357 (GRCm39) |
L125H |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,365,541 (GRCm39) |
M369V |
possibly damaging |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Sfi1 |
C |
CT |
11: 3,096,255 (GRCm39) |
|
probably null |
Het |
Siglec1 |
A |
T |
2: 130,912,307 (GRCm39) |
N1678K |
probably benign |
Het |
Slc15a5 |
A |
T |
6: 138,049,992 (GRCm39) |
V141E |
probably benign |
Het |
Slc8a3 |
A |
T |
12: 81,246,484 (GRCm39) |
H856Q |
probably benign |
Het |
Sptlc2 |
T |
A |
12: 87,402,414 (GRCm39) |
M171L |
probably benign |
Het |
Srcap |
T |
A |
7: 127,158,899 (GRCm39) |
|
probably benign |
Het |
St6gal2 |
A |
G |
17: 55,797,944 (GRCm39) |
D310G |
probably damaging |
Het |
Susd2 |
T |
A |
10: 75,473,888 (GRCm39) |
D689V |
probably damaging |
Het |
Suz12 |
A |
T |
11: 79,910,558 (GRCm39) |
E303V |
possibly damaging |
Het |
Taldo1 |
C |
A |
7: 140,978,500 (GRCm39) |
T150K |
probably damaging |
Het |
Tg |
T |
A |
15: 66,721,312 (GRCm39) |
F274I |
possibly damaging |
Het |
Tmem151b |
T |
C |
17: 45,856,663 (GRCm39) |
D259G |
probably damaging |
Het |
Tmem179 |
G |
T |
12: 112,468,288 (GRCm39) |
H64Q |
probably benign |
Het |
Tmem236 |
A |
G |
2: 14,223,732 (GRCm39) |
T174A |
probably benign |
Het |
Tnc |
A |
T |
4: 63,884,811 (GRCm39) |
N1821K |
probably damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,752,773 (GRCm39) |
N261S |
probably damaging |
Het |
Trank1 |
C |
A |
9: 111,172,300 (GRCm39) |
F96L |
possibly damaging |
Het |
Trim56 |
T |
A |
5: 137,142,017 (GRCm39) |
I500F |
probably damaging |
Het |
Ttll5 |
A |
G |
12: 85,926,168 (GRCm39) |
I321V |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,608,367 (GRCm39) |
W17852L |
probably damaging |
Het |
Twnk |
G |
A |
19: 44,997,820 (GRCm39) |
V450M |
probably damaging |
Het |
Uba52 |
A |
G |
8: 70,962,206 (GRCm39) |
I127T |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,148,537 (GRCm39) |
|
probably null |
Het |
Uggt1 |
A |
T |
1: 36,215,877 (GRCm39) |
M130K |
probably benign |
Het |
Ulk4 |
T |
A |
9: 120,910,722 (GRCm39) |
T1101S |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,548,902 (GRCm39) |
S2269P |
probably benign |
Het |
Ush2a |
G |
T |
1: 188,132,403 (GRCm39) |
R875L |
probably benign |
Het |
Usp9y |
T |
A |
Y: 1,332,471 (GRCm39) |
H1624L |
probably benign |
Het |
Vipr1 |
T |
C |
9: 121,494,586 (GRCm39) |
L308S |
possibly damaging |
Het |
Xdh |
T |
G |
17: 74,198,107 (GRCm39) |
K1260T |
probably damaging |
Het |
Yipf4 |
A |
G |
17: 74,800,963 (GRCm39) |
I94V |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,478,206 (GRCm39) |
*3582W |
probably null |
Het |
Zfp58 |
T |
C |
13: 67,640,144 (GRCm39) |
N116D |
possibly damaging |
Het |
Zfp750 |
C |
A |
11: 121,402,819 (GRCm39) |
R643L |
probably benign |
Het |
Znfx1 |
A |
G |
2: 166,884,507 (GRCm39) |
V51A |
possibly damaging |
Het |
|
Other mutations in Myo18b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Myo18b
|
APN |
5 |
113,021,997 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00847:Myo18b
|
APN |
5 |
112,978,255 (GRCm39) |
splice site |
probably benign |
|
IGL00848:Myo18b
|
APN |
5 |
113,019,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00969:Myo18b
|
APN |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
IGL01018:Myo18b
|
APN |
5 |
112,957,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01448:Myo18b
|
APN |
5 |
112,959,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Myo18b
|
APN |
5 |
112,957,566 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01556:Myo18b
|
APN |
5 |
112,905,315 (GRCm39) |
splice site |
probably benign |
|
IGL01637:Myo18b
|
APN |
5 |
112,988,495 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01819:Myo18b
|
APN |
5 |
113,025,916 (GRCm39) |
missense |
unknown |
|
IGL02007:Myo18b
|
APN |
5 |
113,022,838 (GRCm39) |
unclassified |
probably benign |
|
IGL02146:Myo18b
|
APN |
5 |
112,991,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02229:Myo18b
|
APN |
5 |
113,025,976 (GRCm39) |
missense |
unknown |
|
IGL02319:Myo18b
|
APN |
5 |
112,939,005 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02398:Myo18b
|
APN |
5 |
112,978,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02420:Myo18b
|
APN |
5 |
112,975,852 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02626:Myo18b
|
APN |
5 |
113,025,951 (GRCm39) |
missense |
unknown |
|
IGL02815:Myo18b
|
APN |
5 |
112,957,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Myo18b
|
APN |
5 |
112,923,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02852:Myo18b
|
APN |
5 |
112,863,377 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02995:Myo18b
|
APN |
5 |
112,923,279 (GRCm39) |
splice site |
probably benign |
|
IGL03019:Myo18b
|
APN |
5 |
112,840,263 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03039:Myo18b
|
APN |
5 |
112,988,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Myo18b
|
APN |
5 |
113,021,856 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03123:Myo18b
|
APN |
5 |
113,022,804 (GRCm39) |
unclassified |
probably benign |
|
IGL03288:Myo18b
|
APN |
5 |
112,937,863 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Myo18b
|
APN |
5 |
113,022,345 (GRCm39) |
unclassified |
probably benign |
|
klippel
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4651001:Myo18b
|
UTSW |
5 |
112,982,301 (GRCm39) |
missense |
probably benign |
0.01 |
R0271:Myo18b
|
UTSW |
5 |
112,957,551 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0277:Myo18b
|
UTSW |
5 |
112,841,213 (GRCm39) |
splice site |
probably benign |
|
R0352:Myo18b
|
UTSW |
5 |
113,022,389 (GRCm39) |
unclassified |
probably benign |
|
R0504:Myo18b
|
UTSW |
5 |
113,021,442 (GRCm39) |
unclassified |
probably benign |
|
R0539:Myo18b
|
UTSW |
5 |
112,871,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Myo18b
|
UTSW |
5 |
113,013,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Myo18b
|
UTSW |
5 |
112,946,700 (GRCm39) |
missense |
probably benign |
0.38 |
R0659:Myo18b
|
UTSW |
5 |
112,908,193 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0671:Myo18b
|
UTSW |
5 |
112,840,632 (GRCm39) |
missense |
probably benign |
0.00 |
R0847:Myo18b
|
UTSW |
5 |
113,022,354 (GRCm39) |
unclassified |
probably benign |
|
R1082:Myo18b
|
UTSW |
5 |
112,908,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Myo18b
|
UTSW |
5 |
112,951,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Myo18b
|
UTSW |
5 |
112,978,185 (GRCm39) |
missense |
probably benign |
0.12 |
R1280:Myo18b
|
UTSW |
5 |
112,871,671 (GRCm39) |
critical splice donor site |
probably null |
|
R1444:Myo18b
|
UTSW |
5 |
112,923,117 (GRCm39) |
critical splice donor site |
probably null |
|
R1446:Myo18b
|
UTSW |
5 |
112,905,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Myo18b
|
UTSW |
5 |
113,023,132 (GRCm39) |
nonsense |
probably null |
|
R1601:Myo18b
|
UTSW |
5 |
113,019,364 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1903:Myo18b
|
UTSW |
5 |
112,840,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R1936:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R2008:Myo18b
|
UTSW |
5 |
113,021,423 (GRCm39) |
missense |
probably benign |
|
R2127:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Myo18b
|
UTSW |
5 |
113,021,892 (GRCm39) |
missense |
probably benign |
0.01 |
R2170:Myo18b
|
UTSW |
5 |
112,871,724 (GRCm39) |
missense |
probably benign |
0.23 |
R2258:Myo18b
|
UTSW |
5 |
113,022,529 (GRCm39) |
unclassified |
probably benign |
|
R2265:Myo18b
|
UTSW |
5 |
112,930,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Myo18b
|
UTSW |
5 |
113,006,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Myo18b
|
UTSW |
5 |
112,840,993 (GRCm39) |
missense |
probably benign |
0.01 |
R3160:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3777:Myo18b
|
UTSW |
5 |
112,905,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R4240:Myo18b
|
UTSW |
5 |
112,951,053 (GRCm39) |
critical splice donor site |
probably null |
|
R4243:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4245:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4533:Myo18b
|
UTSW |
5 |
112,840,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Myo18b
|
UTSW |
5 |
112,994,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Myo18b
|
UTSW |
5 |
113,023,041 (GRCm39) |
unclassified |
probably benign |
|
R4755:Myo18b
|
UTSW |
5 |
113,022,340 (GRCm39) |
nonsense |
probably null |
|
R4771:Myo18b
|
UTSW |
5 |
112,840,093 (GRCm39) |
nonsense |
probably null |
|
R4812:Myo18b
|
UTSW |
5 |
112,957,584 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4840:Myo18b
|
UTSW |
5 |
113,021,895 (GRCm39) |
missense |
probably benign |
0.02 |
R4888:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R4995:Myo18b
|
UTSW |
5 |
112,908,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R5001:Myo18b
|
UTSW |
5 |
112,909,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R5015:Myo18b
|
UTSW |
5 |
112,937,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Myo18b
|
UTSW |
5 |
113,023,083 (GRCm39) |
unclassified |
probably benign |
|
R5070:Myo18b
|
UTSW |
5 |
112,909,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5105:Myo18b
|
UTSW |
5 |
112,988,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R5130:Myo18b
|
UTSW |
5 |
113,021,769 (GRCm39) |
missense |
probably benign |
0.06 |
R5186:Myo18b
|
UTSW |
5 |
113,019,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Myo18b
|
UTSW |
5 |
112,905,439 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5535:Myo18b
|
UTSW |
5 |
112,937,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Myo18b
|
UTSW |
5 |
113,016,161 (GRCm39) |
missense |
probably damaging |
0.96 |
R5810:Myo18b
|
UTSW |
5 |
112,982,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Myo18b
|
UTSW |
5 |
112,950,196 (GRCm39) |
splice site |
probably null |
|
R6065:Myo18b
|
UTSW |
5 |
112,840,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Myo18b
|
UTSW |
5 |
113,022,157 (GRCm39) |
unclassified |
probably benign |
|
R6113:Myo18b
|
UTSW |
5 |
113,014,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Myo18b
|
UTSW |
5 |
113,022,038 (GRCm39) |
missense |
probably benign |
0.01 |
R6167:Myo18b
|
UTSW |
5 |
113,020,373 (GRCm39) |
splice site |
probably null |
|
R6220:Myo18b
|
UTSW |
5 |
112,905,373 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6276:Myo18b
|
UTSW |
5 |
112,959,508 (GRCm39) |
missense |
probably benign |
0.31 |
R6290:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6291:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6795:Myo18b
|
UTSW |
5 |
112,994,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Myo18b
|
UTSW |
5 |
112,909,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R6817:Myo18b
|
UTSW |
5 |
112,978,104 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Myo18b
|
UTSW |
5 |
112,950,258 (GRCm39) |
missense |
probably benign |
0.12 |
R7034:Myo18b
|
UTSW |
5 |
112,871,770 (GRCm39) |
nonsense |
probably null |
|
R7097:Myo18b
|
UTSW |
5 |
113,022,271 (GRCm39) |
missense |
unknown |
|
R7145:Myo18b
|
UTSW |
5 |
112,965,545 (GRCm39) |
nonsense |
probably null |
|
R7201:Myo18b
|
UTSW |
5 |
112,863,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Myo18b
|
UTSW |
5 |
112,923,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7265:Myo18b
|
UTSW |
5 |
112,959,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Myo18b
|
UTSW |
5 |
113,021,971 (GRCm39) |
missense |
probably benign |
0.25 |
R7466:Myo18b
|
UTSW |
5 |
112,871,758 (GRCm39) |
missense |
probably benign |
0.02 |
R7487:Myo18b
|
UTSW |
5 |
112,982,299 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7571:Myo18b
|
UTSW |
5 |
112,978,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Myo18b
|
UTSW |
5 |
113,025,969 (GRCm39) |
missense |
unknown |
|
R7612:Myo18b
|
UTSW |
5 |
113,013,168 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7617:Myo18b
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
R7696:Myo18b
|
UTSW |
5 |
112,840,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myo18b
|
UTSW |
5 |
113,022,891 (GRCm39) |
missense |
unknown |
|
R8047:Myo18b
|
UTSW |
5 |
112,871,681 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8070:Myo18b
|
UTSW |
5 |
112,938,986 (GRCm39) |
missense |
probably benign |
0.01 |
R8088:Myo18b
|
UTSW |
5 |
113,027,376 (GRCm39) |
start gained |
probably benign |
|
R8247:Myo18b
|
UTSW |
5 |
112,840,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Myo18b
|
UTSW |
5 |
112,943,273 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8313:Myo18b
|
UTSW |
5 |
113,023,045 (GRCm39) |
missense |
unknown |
|
R8375:Myo18b
|
UTSW |
5 |
112,908,259 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8432:Myo18b
|
UTSW |
5 |
112,912,378 (GRCm39) |
missense |
probably benign |
0.00 |
R8475:Myo18b
|
UTSW |
5 |
113,021,422 (GRCm39) |
nonsense |
probably null |
|
R8482:Myo18b
|
UTSW |
5 |
113,019,489 (GRCm39) |
nonsense |
probably null |
|
R8671:Myo18b
|
UTSW |
5 |
113,022,609 (GRCm39) |
missense |
unknown |
|
R8681:Myo18b
|
UTSW |
5 |
113,021,429 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8918:Myo18b
|
UTSW |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
R8941:Myo18b
|
UTSW |
5 |
113,022,795 (GRCm39) |
unclassified |
probably benign |
|
R8962:Myo18b
|
UTSW |
5 |
113,006,346 (GRCm39) |
missense |
probably benign |
0.24 |
R8972:Myo18b
|
UTSW |
5 |
112,841,164 (GRCm39) |
missense |
probably benign |
0.00 |
R9116:Myo18b
|
UTSW |
5 |
112,975,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Myo18b
|
UTSW |
5 |
113,022,927 (GRCm39) |
missense |
unknown |
|
R9358:Myo18b
|
UTSW |
5 |
112,943,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9469:Myo18b
|
UTSW |
5 |
112,994,247 (GRCm39) |
missense |
probably benign |
0.15 |
R9607:Myo18b
|
UTSW |
5 |
113,022,544 (GRCm39) |
missense |
unknown |
|
R9659:Myo18b
|
UTSW |
5 |
113,022,382 (GRCm39) |
missense |
unknown |
|
Z1088:Myo18b
|
UTSW |
5 |
112,905,350 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Myo18b
|
UTSW |
5 |
112,840,809 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Myo18b
|
UTSW |
5 |
112,979,056 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myo18b
|
UTSW |
5 |
112,957,604 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
113,021,407 (GRCm39) |
nonsense |
probably null |
|
Z1177:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
112,840,765 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo18b
|
UTSW |
5 |
113,023,018 (GRCm39) |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- TTTCACCCTGGTCTTCAGCGAGAG -3'
(R):5'- ACAGCATCTTCGGCTTTGAGCG -3'
Sequencing Primer
(F):5'- AGGTCTCCCTCATCGCTACTG -3'
(R):5'- TGCCAGAGATGCCTCGAAG -3'
|
Posted On |
2014-03-28 |