Incidental Mutation 'IGL01019:Myo1f'
| ID |
54055 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Myo1f
|
| Ensembl Gene |
ENSMUSG00000024300 |
| Gene Name |
myosin IF |
| Synonyms |
C330006B10Rik |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.143)
|
| Stock # |
IGL01019
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
17 |
| Chromosomal Location |
33774681-33826738 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 33811977 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Histidine
at position 592
(R592H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134715
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000087605]
[ENSMUST00000173372]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000087605
AA Change: R592H
PolyPhen 2
Score 0.615 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000084887
Gene: ENSMUSG00000024300
AA Change: R592H
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
11 |
691 |
N/A |
SMART |
|
IQ
|
692 |
714 |
7.57e0 |
SMART |
|
Pfam:Myosin_TH1
|
717 |
909 |
1.7e-51 |
PFAM |
|
low complexity region
|
939 |
952 |
N/A |
INTRINSIC |
|
low complexity region
|
973 |
987 |
N/A |
INTRINSIC |
|
low complexity region
|
991 |
1001 |
N/A |
INTRINSIC |
|
SH3
|
1044 |
1098 |
2.09e-19 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000173372
AA Change: R592H
PolyPhen 2
Score 0.929 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000134715
Gene: ENSMUSG00000024300
AA Change: R592H
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
11 |
691 |
N/A |
SMART |
|
IQ
|
692 |
714 |
7.57e0 |
SMART |
|
Pfam:Myosin_TH1
|
716 |
780 |
6e-23 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173426
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Myosins are molecular motors that use the energy from ATP hydrolysis to generate force on actin filaments. The protein encoded by this gene is an unconventional myosin that may be involved in the intracellular movement of membrane-enclosed compartments. There is evidence to suggest that mutations in this gene can result in hearing loss. [provided by RefSeq, Jan 2017]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired neutrophil migration and adhesion. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 50 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9930022D16Rik |
T |
C |
11: 109,308,737 (GRCm39) |
|
probably benign |
Het |
| Aatk |
T |
C |
11: 119,903,101 (GRCm39) |
S375G |
probably benign |
Het |
| Abcg8 |
T |
C |
17: 84,999,423 (GRCm39) |
M173T |
probably benign |
Het |
| B3galt2 |
A |
C |
1: 143,522,495 (GRCm39) |
R210S |
probably benign |
Het |
| Bltp1 |
G |
T |
3: 37,061,133 (GRCm39) |
|
probably null |
Het |
| Capn5 |
C |
T |
7: 97,784,971 (GRCm39) |
A168T |
probably damaging |
Het |
| Cbx7 |
C |
T |
15: 79,814,829 (GRCm39) |
G24D |
probably damaging |
Het |
| Ccdc7a |
A |
T |
8: 129,788,099 (GRCm39) |
S77T |
probably benign |
Het |
| Cd200r2 |
T |
A |
16: 44,729,832 (GRCm39) |
|
probably benign |
Het |
| Cdh11 |
T |
C |
8: 103,406,377 (GRCm39) |
H32R |
probably benign |
Het |
| Chdh |
A |
T |
14: 29,753,289 (GRCm39) |
N66I |
probably benign |
Het |
| Clca3a2 |
G |
A |
3: 144,519,388 (GRCm39) |
Q263* |
probably null |
Het |
| Dcc |
T |
C |
18: 71,942,161 (GRCm39) |
I319V |
probably benign |
Het |
| Depdc5 |
G |
T |
5: 33,050,745 (GRCm39) |
M170I |
probably damaging |
Het |
| Dop1b |
T |
A |
16: 93,607,117 (GRCm39) |
L2140Q |
probably benign |
Het |
| Frem3 |
G |
A |
8: 81,341,763 (GRCm39) |
G1352E |
probably benign |
Het |
| Fsd1l |
T |
A |
4: 53,694,742 (GRCm39) |
C389S |
probably damaging |
Het |
| Grin2c |
C |
T |
11: 115,148,936 (GRCm39) |
A221T |
possibly damaging |
Het |
| Gstz1 |
C |
A |
12: 87,210,575 (GRCm39) |
P153T |
probably damaging |
Het |
| Itgb2 |
T |
C |
10: 77,378,237 (GRCm39) |
S22P |
possibly damaging |
Het |
| Krt87 |
G |
T |
15: 101,336,312 (GRCm39) |
Q114K |
possibly damaging |
Het |
| Krtap5-4 |
A |
C |
7: 141,857,647 (GRCm39) |
S106R |
unknown |
Het |
| Lats1 |
T |
C |
10: 7,581,435 (GRCm39) |
V740A |
probably damaging |
Het |
| Mcm9 |
C |
A |
10: 53,506,041 (GRCm39) |
G78C |
probably damaging |
Het |
| Mn1 |
G |
A |
5: 111,569,413 (GRCm39) |
E1128K |
possibly damaging |
Het |
| Nfat5 |
G |
T |
8: 108,094,146 (GRCm39) |
A277S |
probably damaging |
Het |
| Nfkbia |
T |
A |
12: 55,537,327 (GRCm39) |
Y254F |
probably damaging |
Het |
| Nr3c2 |
A |
T |
8: 77,635,843 (GRCm39) |
N315Y |
probably damaging |
Het |
| Otof |
T |
C |
5: 30,562,560 (GRCm39) |
M258V |
probably benign |
Het |
| Panx3 |
C |
T |
9: 37,572,767 (GRCm39) |
C261Y |
probably damaging |
Het |
| Pdia2 |
C |
A |
17: 26,417,896 (GRCm39) |
G38W |
probably damaging |
Het |
| Psg19 |
G |
T |
7: 18,527,971 (GRCm39) |
Y257* |
probably null |
Het |
| Ptpre |
A |
T |
7: 135,280,054 (GRCm39) |
K586* |
probably null |
Het |
| Reps1 |
A |
G |
10: 18,000,643 (GRCm39) |
R752G |
probably damaging |
Het |
| Rpgrip1 |
T |
A |
14: 52,368,633 (GRCm39) |
D277E |
possibly damaging |
Het |
| Rpl21-ps6 |
A |
G |
17: 56,222,671 (GRCm39) |
|
noncoding transcript |
Het |
| Serpinf2 |
T |
A |
11: 75,327,333 (GRCm39) |
E198V |
possibly damaging |
Het |
| Sh3tc1 |
A |
G |
5: 35,860,719 (GRCm39) |
L1046P |
probably damaging |
Het |
| Snw1 |
T |
C |
12: 87,497,711 (GRCm39) |
E426G |
probably benign |
Het |
| Sord |
T |
A |
2: 122,094,564 (GRCm39) |
N317K |
probably benign |
Het |
| Taar3 |
A |
T |
10: 23,826,330 (GRCm39) |
D292V |
probably damaging |
Het |
| Tdrd3 |
C |
A |
14: 87,709,618 (GRCm39) |
T94K |
probably damaging |
Het |
| Ttn |
C |
A |
2: 76,687,165 (GRCm39) |
E736* |
probably null |
Het |
| Usp32 |
A |
G |
11: 84,930,091 (GRCm39) |
V562A |
probably damaging |
Het |
| Vmn1r169 |
T |
G |
7: 23,276,611 (GRCm39) |
M1R |
probably null |
Het |
| Vmn2r3 |
C |
T |
3: 64,167,304 (GRCm39) |
C609Y |
probably damaging |
Het |
| Vmn2r69 |
T |
C |
7: 85,055,739 (GRCm39) |
T800A |
probably benign |
Het |
| Vmn2r72 |
G |
A |
7: 85,387,542 (GRCm39) |
T674I |
probably benign |
Het |
| Zfp160 |
T |
A |
17: 21,241,088 (GRCm39) |
M52K |
possibly damaging |
Het |
| Zfp607a |
T |
A |
7: 27,578,042 (GRCm39) |
C371S |
probably damaging |
Het |
|
| Other mutations in Myo1f |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00851:Myo1f
|
APN |
17 |
33,800,938 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01524:Myo1f
|
APN |
17 |
33,798,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01744:Myo1f
|
APN |
17 |
33,802,654 (GRCm39) |
splice site |
probably benign |
|
|
IGL01951:Myo1f
|
APN |
17 |
33,816,991 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL02132:Myo1f
|
APN |
17 |
33,798,945 (GRCm39) |
missense |
probably benign |
0.10 |
|
IGL02170:Myo1f
|
APN |
17 |
33,797,246 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL02173:Myo1f
|
APN |
17 |
33,826,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02277:Myo1f
|
APN |
17 |
33,798,835 (GRCm39) |
splice site |
probably null |
|
|
IGL02550:Myo1f
|
APN |
17 |
33,799,124 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02550:Myo1f
|
APN |
17 |
33,807,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02615:Myo1f
|
APN |
17 |
33,823,630 (GRCm39) |
missense |
probably benign |
|
|
IGL02801:Myo1f
|
APN |
17 |
33,797,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02817:Myo1f
|
APN |
17 |
33,823,532 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02904:Myo1f
|
APN |
17 |
33,804,632 (GRCm39) |
nonsense |
probably null |
|
|
IGL03056:Myo1f
|
APN |
17 |
33,804,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03334:Myo1f
|
APN |
17 |
33,817,168 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0066:Myo1f
|
UTSW |
17 |
33,820,677 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0066:Myo1f
|
UTSW |
17 |
33,820,677 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0321:Myo1f
|
UTSW |
17 |
33,811,986 (GRCm39) |
missense |
probably benign |
0.31 |
|
R0375:Myo1f
|
UTSW |
17 |
33,820,930 (GRCm39) |
missense |
probably benign |
0.27 |
|
R0487:Myo1f
|
UTSW |
17 |
33,797,258 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0925:Myo1f
|
UTSW |
17 |
33,797,107 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1394:Myo1f
|
UTSW |
17 |
33,802,714 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1395:Myo1f
|
UTSW |
17 |
33,802,714 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1474:Myo1f
|
UTSW |
17 |
33,813,001 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R1760:Myo1f
|
UTSW |
17 |
33,805,172 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1965:Myo1f
|
UTSW |
17 |
33,817,146 (GRCm39) |
nonsense |
probably null |
|
|
R2409:Myo1f
|
UTSW |
17 |
33,795,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2432:Myo1f
|
UTSW |
17 |
33,794,823 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4610:Myo1f
|
UTSW |
17 |
33,801,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4785:Myo1f
|
UTSW |
17 |
33,817,165 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5239:Myo1f
|
UTSW |
17 |
33,820,709 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5881:Myo1f
|
UTSW |
17 |
33,799,259 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R5881:Myo1f
|
UTSW |
17 |
33,795,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6160:Myo1f
|
UTSW |
17 |
33,823,318 (GRCm39) |
missense |
probably benign |
|
|
R6210:Myo1f
|
UTSW |
17 |
33,820,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6365:Myo1f
|
UTSW |
17 |
33,805,090 (GRCm39) |
missense |
probably benign |
|
|
R6464:Myo1f
|
UTSW |
17 |
33,795,621 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6532:Myo1f
|
UTSW |
17 |
33,794,820 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6678:Myo1f
|
UTSW |
17 |
33,794,819 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7241:Myo1f
|
UTSW |
17 |
33,798,902 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7266:Myo1f
|
UTSW |
17 |
33,820,668 (GRCm39) |
missense |
probably benign |
|
|
R7513:Myo1f
|
UTSW |
17 |
33,794,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7606:Myo1f
|
UTSW |
17 |
33,795,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7779:Myo1f
|
UTSW |
17 |
33,797,247 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7853:Myo1f
|
UTSW |
17 |
33,795,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7884:Myo1f
|
UTSW |
17 |
33,817,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8507:Myo1f
|
UTSW |
17 |
33,816,992 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8807:Myo1f
|
UTSW |
17 |
33,794,879 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9009:Myo1f
|
UTSW |
17 |
33,823,662 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9083:Myo1f
|
UTSW |
17 |
33,813,036 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9227:Myo1f
|
UTSW |
17 |
33,795,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9230:Myo1f
|
UTSW |
17 |
33,795,424 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9528:Myo1f
|
UTSW |
17 |
33,797,156 (GRCm39) |
critical splice donor site |
probably null |
|
|
X0028:Myo1f
|
UTSW |
17 |
33,795,412 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
X0065:Myo1f
|
UTSW |
17 |
33,820,957 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-06-28 |
Incidental Mutation