Incidental Mutation 'R8260:Myo1c'
| ID |
640023 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Myo1c
|
| Ensembl Gene |
ENSMUSG00000017774 |
| Gene Name |
myosin IC |
| Synonyms |
myr2, mm1beta, C80397, myosin-Ibeta |
| MMRRC Submission |
067685-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.697)
|
| Stock # |
R8260 (G1)
|
| Quality Score |
131.008 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
75541330-75564736 bp(+) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
C to T
at 75546942 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000121267
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000069057]
[ENSMUST00000102504]
[ENSMUST00000102505]
[ENSMUST00000108431]
[ENSMUST00000136935]
|
| AlphaFold |
Q9WTI7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000069057
|
| SMART Domains |
Protein: ENSMUSP00000070388
Gene: ENSMUSG00000017774
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
5 |
697 |
N/A |
SMART |
|
IQ
|
698 |
720 |
3.85e-3 |
SMART |
|
IQ
|
721 |
743 |
2.09e-4 |
SMART |
|
Blast:MYSc
|
751 |
780 |
5e-9 |
BLAST |
|
low complexity region
|
804 |
815 |
N/A |
INTRINSIC |
|
Pfam:Myosin_TH1
|
838 |
1024 |
1.9e-41 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102504
|
| SMART Domains |
Protein: ENSMUSP00000099562
Gene: ENSMUSG00000017774
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
5 |
697 |
N/A |
SMART |
|
IQ
|
698 |
720 |
3.85e-3 |
SMART |
|
IQ
|
721 |
743 |
2.09e-4 |
SMART |
|
Blast:MYSc
|
751 |
780 |
5e-9 |
BLAST |
|
low complexity region
|
804 |
815 |
N/A |
INTRINSIC |
|
Pfam:Myosin_TH1
|
838 |
1024 |
1.9e-41 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102505
|
| SMART Domains |
Protein: ENSMUSP00000099563
Gene: ENSMUSG00000017774
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
40 |
732 |
N/A |
SMART |
|
IQ
|
733 |
755 |
3.85e-3 |
SMART |
|
IQ
|
756 |
778 |
2.09e-4 |
SMART |
|
Blast:MYSc
|
786 |
815 |
6e-9 |
BLAST |
|
low complexity region
|
839 |
850 |
N/A |
INTRINSIC |
|
Pfam:Myosin_TH1
|
874 |
1052 |
2.9e-29 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108431
|
| SMART Domains |
Protein: ENSMUSP00000104069
Gene: ENSMUSG00000017774
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
21 |
713 |
N/A |
SMART |
|
IQ
|
714 |
736 |
3.85e-3 |
SMART |
|
IQ
|
737 |
759 |
2.09e-4 |
SMART |
|
Blast:MYSc
|
767 |
796 |
5e-9 |
BLAST |
|
low complexity region
|
820 |
831 |
N/A |
INTRINSIC |
|
Pfam:Myosin_TH1
|
854 |
1040 |
3.3e-41 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136935
|
| SMART Domains |
Protein: ENSMUSP00000121267
Gene: ENSMUSG00000017774
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
7 |
18 |
N/A |
INTRINSIC |
|
PDB:4BYF|C
|
39 |
80 |
5e-21 |
PDB |
|
Blast:MYSc
|
43 |
80 |
9e-19 |
BLAST |
|
SCOP:d1lkxa_
|
50 |
80 |
3e-7 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the unconventional myosin protein family, which are actin-based molecular motors. The protein is found in the cytoplasm, and one isoform with a unique N-terminus is also found in the nucleus. The protein functions in intracellular vesicle transport to the plasma membrane. The nuclear isoform associates with RNA polymerase I and II and functions in transcription initiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-in (Y61G) mutation that sensitizes to N6-modified ADP analogs display altered fast adaption in vestibular hair cells. Mice homozygous for a nuclear isoform-specifc knock-out allele exhibit minor changes in bone marrow density and red blood cells. [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 |
|---|
| 4930578I06Rik |
G |
C |
14: 64,223,633 (GRCm39) |
L48V |
probably benign |
Het |
| Acbd3 |
T |
C |
1: 180,566,095 (GRCm39) |
Y263H |
probably damaging |
Het |
| Acot4 |
C |
A |
12: 84,088,809 (GRCm39) |
P219Q |
possibly damaging |
Het |
| Adcy6 |
A |
G |
15: 98,498,919 (GRCm39) |
F294S |
probably damaging |
Het |
| Ahcyl |
T |
C |
16: 45,974,786 (GRCm39) |
E197G |
probably damaging |
Het |
| Aplf |
T |
C |
6: 87,606,987 (GRCm39) |
R476G |
probably benign |
Het |
| Arid1b |
A |
G |
17: 5,382,788 (GRCm39) |
T1292A |
probably benign |
Het |
| Atp2c1 |
T |
A |
9: 105,295,778 (GRCm39) |
I649F |
probably damaging |
Het |
| Bbs10 |
C |
T |
10: 111,136,104 (GRCm39) |
Q406* |
probably null |
Het |
| Bcas3 |
T |
A |
11: 85,400,372 (GRCm39) |
M447K |
possibly damaging |
Het |
| Bmal1 |
A |
T |
7: 112,884,258 (GRCm39) |
I92F |
probably damaging |
Het |
| Cars1 |
T |
C |
7: 143,139,446 (GRCm39) |
D214G |
probably benign |
Het |
| Ccdc88a |
A |
T |
11: 29,443,934 (GRCm39) |
I1410F |
probably benign |
Het |
| Cd55b |
A |
T |
1: 130,316,415 (GRCm39) |
L378H |
probably damaging |
Het |
| Cdh1 |
G |
A |
8: 107,330,979 (GRCm39) |
E37K |
probably benign |
Het |
| Cep72 |
T |
C |
13: 74,206,465 (GRCm39) |
Y119C |
probably damaging |
Het |
| Ctnnd2 |
A |
G |
15: 30,634,879 (GRCm39) |
T176A |
possibly damaging |
Het |
| D630045J12Rik |
T |
A |
6: 38,119,846 (GRCm39) |
|
probably null |
Het |
| Ddi1 |
A |
T |
9: 6,265,524 (GRCm39) |
C282S |
probably damaging |
Het |
| Ddit4 |
T |
C |
10: 59,787,277 (GRCm39) |
T20A |
probably benign |
Het |
| Dpp10 |
T |
A |
1: 123,614,024 (GRCm39) |
T102S |
probably benign |
Het |
| Ep400 |
T |
A |
5: 110,903,478 (GRCm39) |
K374* |
probably null |
Het |
| Epha3 |
A |
G |
16: 63,403,917 (GRCm39) |
L728P |
probably damaging |
Het |
| Fbxw21 |
C |
A |
9: 108,975,614 (GRCm39) |
|
probably null |
Het |
| Frmpd1 |
A |
G |
4: 45,244,638 (GRCm39) |
E109G |
probably damaging |
Het |
| Ggt1 |
C |
T |
10: 75,417,245 (GRCm39) |
P332L |
probably damaging |
Het |
| Gm4779 |
G |
C |
X: 100,837,390 (GRCm39) |
T171S |
possibly damaging |
Het |
| Gm5431 |
A |
T |
11: 48,785,556 (GRCm39) |
I273K |
probably benign |
Het |
| Gon4l |
A |
G |
3: 88,799,937 (GRCm39) |
N861D |
probably damaging |
Het |
| Grm5 |
T |
C |
7: 87,724,340 (GRCm39) |
|
probably null |
Het |
| Helt |
T |
C |
8: 46,745,745 (GRCm39) |
N84S |
possibly damaging |
Het |
| Hnrnpa0 |
G |
T |
13: 58,275,228 (GRCm39) |
Y300* |
probably null |
Het |
| Ints1 |
T |
C |
5: 139,750,968 (GRCm39) |
T810A |
|
Het |
| Irf2bp1 |
C |
T |
7: 18,740,079 (GRCm39) |
A573V |
possibly damaging |
Het |
| Itgbl1 |
C |
A |
14: 124,065,246 (GRCm39) |
D133E |
probably benign |
Het |
| Kctd15 |
A |
G |
7: 34,344,267 (GRCm39) |
F128S |
possibly damaging |
Het |
| Klra17 |
T |
A |
6: 129,808,421 (GRCm39) |
N271Y |
probably damaging |
Het |
| Kmt2c |
T |
A |
5: 25,610,514 (GRCm39) |
E197D |
possibly damaging |
Het |
| Larp1 |
C |
A |
11: 57,949,515 (GRCm39) |
T1048K |
probably benign |
Het |
| Macf1 |
A |
G |
4: 123,365,863 (GRCm39) |
V2966A |
probably benign |
Het |
| Magi3 |
A |
G |
3: 103,922,625 (GRCm39) |
L1364P |
probably benign |
Het |
| Malrd1 |
T |
C |
2: 15,619,017 (GRCm39) |
S294P |
|
Het |
| Med13l |
C |
T |
5: 118,886,794 (GRCm39) |
T1565I |
possibly damaging |
Het |
| Mov10l1 |
A |
G |
15: 88,896,313 (GRCm39) |
D719G |
probably benign |
Het |
| Mtcl3 |
T |
A |
10: 29,024,270 (GRCm39) |
H395Q |
possibly damaging |
Het |
| Muc4 |
CAC |
CACTAC |
16: 32,575,367 (GRCm39) |
|
probably benign |
Het |
| Myh14 |
T |
C |
7: 44,264,800 (GRCm39) |
E1654G |
probably damaging |
Het |
| Myo9a |
A |
G |
9: 59,817,961 (GRCm39) |
T2343A |
probably benign |
Het |
| Or1j12 |
A |
G |
2: 36,342,897 (GRCm39) |
Q100R |
probably damaging |
Het |
| Or2ag18 |
A |
T |
7: 106,405,234 (GRCm39) |
V145E |
possibly damaging |
Het |
| Or2d2b |
A |
T |
7: 106,706,062 (GRCm39) |
M2K |
probably benign |
Het |
| Or4m1 |
T |
C |
14: 50,557,615 (GRCm39) |
K226E |
probably benign |
Het |
| Or52m2 |
T |
A |
7: 102,263,432 (GRCm39) |
I255F |
possibly damaging |
Het |
| Or52n5 |
T |
A |
7: 104,587,879 (GRCm39) |
Y49N |
probably damaging |
Het |
| Or6c2 |
T |
A |
10: 129,362,957 (GRCm39) |
I287N |
possibly damaging |
Het |
| Or8k53 |
T |
A |
2: 86,177,276 (GRCm39) |
Y278F |
possibly damaging |
Het |
| Or9g3 |
A |
T |
2: 85,589,820 (GRCm39) |
L300Q |
probably damaging |
Het |
| Osmr |
A |
T |
15: 6,844,897 (GRCm39) |
D957E |
probably benign |
Het |
| Pappa |
T |
A |
4: 65,234,419 (GRCm39) |
V1408E |
probably damaging |
Het |
| Pcnx3 |
C |
T |
19: 5,715,412 (GRCm39) |
G1946E |
probably damaging |
Het |
| Pdcd6ip |
A |
T |
9: 113,501,865 (GRCm39) |
D464E |
probably benign |
Het |
| Pde1c |
T |
C |
6: 56,114,404 (GRCm39) |
Y503C |
probably benign |
Het |
| Potefam3d |
A |
T |
8: 69,972,400 (GRCm39) |
D116E |
possibly damaging |
Het |
| Prob1 |
T |
A |
18: 35,787,210 (GRCm39) |
E348V |
possibly damaging |
Het |
| Rnls |
A |
G |
19: 33,180,048 (GRCm39) |
L134S |
probably damaging |
Het |
| Scrn3 |
T |
C |
2: 73,166,202 (GRCm39) |
Y412H |
probably damaging |
Het |
| Serpina3g |
T |
C |
12: 104,205,362 (GRCm39) |
S34P |
probably benign |
Het |
| Sertad3 |
G |
A |
7: 27,175,784 (GRCm39) |
A73T |
probably benign |
Het |
| Sez6l |
C |
T |
5: 112,609,122 (GRCm39) |
A576T |
probably benign |
Het |
| Sh3tc2 |
G |
A |
18: 62,146,137 (GRCm39) |
R1172H |
probably damaging |
Het |
| Sirt3 |
A |
G |
7: 140,456,319 (GRCm39) |
V110A |
|
Het |
| Smpd3 |
A |
T |
8: 106,984,047 (GRCm39) |
D557E |
probably benign |
Het |
| Sptssb |
A |
T |
3: 69,728,305 (GRCm39) |
M44K |
probably damaging |
Het |
| Tars2 |
A |
G |
3: 95,662,132 (GRCm39) |
W7R |
probably damaging |
Het |
| Tbc1d9b |
A |
G |
11: 50,055,013 (GRCm39) |
D964G |
probably benign |
Het |
| Tiam2 |
A |
T |
17: 3,568,594 (GRCm39) |
D1580V |
possibly damaging |
Het |
| Tmeff2 |
T |
A |
1: 50,977,478 (GRCm39) |
V130D |
probably damaging |
Het |
| Top2a |
T |
A |
11: 98,891,595 (GRCm39) |
E1176V |
probably null |
Het |
| Trappc9 |
C |
A |
15: 72,813,758 (GRCm39) |
E680* |
probably null |
Het |
| Trip10 |
A |
G |
17: 57,564,314 (GRCm39) |
N355S |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,596,337 (GRCm39) |
E20192G |
probably damaging |
Het |
| Vmn2r96 |
A |
G |
17: 18,804,243 (GRCm39) |
M306V |
probably benign |
Het |
| Wdr90 |
A |
T |
17: 26,064,141 (GRCm39) |
H1860Q |
probably damaging |
Het |
| Wrnip1 |
A |
G |
13: 32,989,339 (GRCm39) |
I276V |
possibly damaging |
Het |
| Zfp608 |
T |
C |
18: 55,030,821 (GRCm39) |
K1040E |
possibly damaging |
Het |
| Zfp808 |
T |
A |
13: 62,320,552 (GRCm39) |
C594S |
probably benign |
Het |
|
| Other mutations in Myo1c |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01346:Myo1c
|
APN |
11 |
75,563,076 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02054:Myo1c
|
APN |
11 |
75,551,962 (GRCm39) |
missense |
probably benign |
0.30 |
|
IGL02115:Myo1c
|
APN |
11 |
75,552,417 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02375:Myo1c
|
APN |
11 |
75,552,400 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02878:Myo1c
|
APN |
11 |
75,559,859 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL03008:Myo1c
|
APN |
11 |
75,549,240 (GRCm39) |
missense |
probably benign |
0.13 |
|
Sweeper
|
UTSW |
11 |
75,560,856 (GRCm39) |
nonsense |
probably null |
|
|
R0070:Myo1c
|
UTSW |
11 |
75,551,076 (GRCm39) |
missense |
probably benign |
0.39 |
|
R0070:Myo1c
|
UTSW |
11 |
75,551,076 (GRCm39) |
missense |
probably benign |
0.39 |
|
R0138:Myo1c
|
UTSW |
11 |
75,551,827 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R0200:Myo1c
|
UTSW |
11 |
75,563,008 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0227:Myo1c
|
UTSW |
11 |
75,549,520 (GRCm39) |
missense |
probably benign |
0.34 |
|
R0257:Myo1c
|
UTSW |
11 |
75,556,342 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R0513:Myo1c
|
UTSW |
11 |
75,556,657 (GRCm39) |
splice site |
probably null |
|
|
R0587:Myo1c
|
UTSW |
11 |
75,548,616 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0667:Myo1c
|
UTSW |
11 |
75,559,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1469:Myo1c
|
UTSW |
11 |
75,560,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1469:Myo1c
|
UTSW |
11 |
75,560,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1793:Myo1c
|
UTSW |
11 |
75,548,415 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1922:Myo1c
|
UTSW |
11 |
75,559,055 (GRCm39) |
missense |
probably benign |
|
|
R2000:Myo1c
|
UTSW |
11 |
75,561,405 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3983:Myo1c
|
UTSW |
11 |
75,552,325 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4583:Myo1c
|
UTSW |
11 |
75,562,688 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R4599:Myo1c
|
UTSW |
11 |
75,559,019 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4671:Myo1c
|
UTSW |
11 |
75,560,856 (GRCm39) |
nonsense |
probably null |
|
|
R4682:Myo1c
|
UTSW |
11 |
75,560,856 (GRCm39) |
nonsense |
probably null |
|
|
R4708:Myo1c
|
UTSW |
11 |
75,560,856 (GRCm39) |
nonsense |
probably null |
|
|
R4709:Myo1c
|
UTSW |
11 |
75,560,856 (GRCm39) |
nonsense |
probably null |
|
|
R4742:Myo1c
|
UTSW |
11 |
75,560,856 (GRCm39) |
nonsense |
probably null |
|
|
R4770:Myo1c
|
UTSW |
11 |
75,551,139 (GRCm39) |
nonsense |
probably null |
|
|
R4888:Myo1c
|
UTSW |
11 |
75,560,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4915:Myo1c
|
UTSW |
11 |
75,547,135 (GRCm39) |
start codon destroyed |
probably null |
|
|
R4934:Myo1c
|
UTSW |
11 |
75,562,676 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4971:Myo1c
|
UTSW |
11 |
75,562,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5319:Myo1c
|
UTSW |
11 |
75,552,852 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5589:Myo1c
|
UTSW |
11 |
75,548,414 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R5624:Myo1c
|
UTSW |
11 |
75,553,461 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5756:Myo1c
|
UTSW |
11 |
75,549,240 (GRCm39) |
missense |
probably benign |
0.42 |
|
R5959:Myo1c
|
UTSW |
11 |
75,548,345 (GRCm39) |
missense |
probably benign |
0.37 |
|
R6160:Myo1c
|
UTSW |
11 |
75,541,568 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6559:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6568:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6569:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6574:Myo1c
|
UTSW |
11 |
75,547,124 (GRCm39) |
start gained |
probably benign |
|
|
R6579:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6580:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6583:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6640:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6642:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6643:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6679:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6680:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6687:Myo1c
|
UTSW |
11 |
75,563,027 (GRCm39) |
missense |
probably benign |
|
|
R6695:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6696:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6700:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6712:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6713:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R6715:Myo1c
|
UTSW |
11 |
75,562,461 (GRCm39) |
missense |
probably benign |
0.42 |
|
R7081:Myo1c
|
UTSW |
11 |
75,551,789 (GRCm39) |
missense |
probably benign |
|
|
R7265:Myo1c
|
UTSW |
11 |
75,560,616 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R7397:Myo1c
|
UTSW |
11 |
75,562,068 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7586:Myo1c
|
UTSW |
11 |
75,548,345 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R7714:Myo1c
|
UTSW |
11 |
75,549,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8341:Myo1c
|
UTSW |
11 |
75,562,253 (GRCm39) |
missense |
probably benign |
0.42 |
|
R8466:Myo1c
|
UTSW |
11 |
75,549,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8771:Myo1c
|
UTSW |
11 |
75,556,709 (GRCm39) |
missense |
probably benign |
|
|
R8829:Myo1c
|
UTSW |
11 |
75,561,072 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8832:Myo1c
|
UTSW |
11 |
75,561,072 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9243:Myo1c
|
UTSW |
11 |
75,541,437 (GRCm39) |
unclassified |
probably benign |
|
|
R9489:Myo1c
|
UTSW |
11 |
75,559,899 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9605:Myo1c
|
UTSW |
11 |
75,559,899 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9744:Myo1c
|
UTSW |
11 |
75,562,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9782:Myo1c
|
UTSW |
11 |
75,549,273 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
|
| Posted On |
2020-07-28 |
Incidental Mutation