Incidental Mutation 'R5135:Myo16'
| ID |
396132 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Myo16
|
| Ensembl Gene |
ENSMUSG00000039057 |
| Gene Name |
myosin XVI |
| Synonyms |
C230040D10Rik, BM140241, Nyap3 |
| MMRRC Submission |
043261-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.265)
|
| Stock # |
R5135 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
8 |
| Chromosomal Location |
10203911-10684742 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 10526114 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Leucine
at position 885
(V885L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049345
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042103]
[ENSMUST00000207204]
[ENSMUST00000207477]
|
| AlphaFold |
Q5DU14 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000042103
AA Change: V885L
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000049345
Gene: ENSMUSG00000039057
AA Change: V885L
| Domain | Start | End | E-Value | Type |
|---|
|
ANK
|
92 |
121 |
1.65e-1 |
SMART |
|
ANK
|
125 |
154 |
3.46e-4 |
SMART |
|
ANK
|
158 |
189 |
2.11e2 |
SMART |
|
ANK
|
221 |
250 |
2.85e-5 |
SMART |
|
ANK
|
254 |
283 |
3.51e-5 |
SMART |
|
low complexity region
|
333 |
349 |
N/A |
INTRINSIC |
|
MYSc
|
394 |
1144 |
2.27e-144 |
SMART |
|
IQ
|
1144 |
1166 |
4.06e-2 |
SMART |
|
Pfam:NYAP_N
|
1207 |
1591 |
4.1e-135 |
PFAM |
|
low complexity region
|
1670 |
1690 |
N/A |
INTRINSIC |
|
low complexity region
|
1841 |
1860 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000207204
AA Change: V829L
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000207477
AA Change: V885L
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.1%
|
| Validation Efficiency |
98% (82/84) |
| MGI Phenotype |
PHENOTYPE: Triple KO of Nyap1, Nyap2 and Myo16 results in decreased brain weight and cortex and striatum size and reduced neurite length in cortical neurons. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(3) : Targeted(2) Gene trapped(1)
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700056E22Rik |
T |
C |
1: 183,765,703 (GRCm39) |
S119G |
probably benign |
Het |
| 4930553M12Rik |
G |
T |
4: 88,786,508 (GRCm39) |
H37N |
unknown |
Het |
| Adam10 |
T |
A |
9: 70,673,356 (GRCm39) |
C496S |
probably damaging |
Het |
| Aldh18a1 |
A |
C |
19: 40,543,261 (GRCm39) |
|
probably benign |
Het |
| Alox5 |
A |
G |
6: 116,390,747 (GRCm39) |
F468S |
probably benign |
Het |
| Ankrd50 |
T |
C |
3: 38,509,952 (GRCm39) |
H805R |
probably damaging |
Het |
| Ap2s1 |
T |
A |
7: 16,481,248 (GRCm39) |
D72E |
probably damaging |
Het |
| Apaf1 |
T |
C |
10: 90,895,956 (GRCm39) |
Y372C |
probably damaging |
Het |
| Apob |
C |
T |
12: 8,060,086 (GRCm39) |
T2823I |
probably damaging |
Het |
| Bhmt |
A |
G |
13: 93,763,831 (GRCm39) |
V70A |
probably damaging |
Het |
| Bltp3b |
T |
C |
10: 89,625,217 (GRCm39) |
I48T |
probably damaging |
Het |
| Cdc42bpg |
T |
A |
19: 6,370,648 (GRCm39) |
L1247H |
probably damaging |
Het |
| Cel |
A |
G |
2: 28,449,435 (GRCm39) |
V264A |
probably benign |
Het |
| Celsr2 |
T |
C |
3: 108,305,975 (GRCm39) |
N2043S |
probably damaging |
Het |
| Clca4a |
A |
T |
3: 144,660,707 (GRCm39) |
W706R |
probably damaging |
Het |
| Col22a1 |
G |
T |
15: 71,671,186 (GRCm39) |
P1058Q |
unknown |
Het |
| Cyp4a14 |
A |
G |
4: 115,347,157 (GRCm39) |
|
probably null |
Het |
| Dhx30 |
T |
G |
9: 109,927,863 (GRCm39) |
R55S |
probably damaging |
Het |
| Dlgap5 |
C |
T |
14: 47,637,122 (GRCm39) |
R452H |
probably damaging |
Het |
| Dnah12 |
T |
A |
14: 26,492,434 (GRCm39) |
D1191E |
probably damaging |
Het |
| Dock3 |
A |
T |
9: 106,810,196 (GRCm39) |
I164N |
probably damaging |
Het |
| Edrf1 |
T |
A |
7: 133,252,773 (GRCm39) |
M436K |
probably benign |
Het |
| Eif2ak2 |
T |
A |
17: 79,173,774 (GRCm39) |
Y268F |
probably damaging |
Het |
| Evi2a |
G |
A |
11: 79,418,277 (GRCm39) |
T111M |
possibly damaging |
Het |
| Fzd4 |
A |
G |
7: 89,056,709 (GRCm39) |
E252G |
probably damaging |
Het |
| Gcm2 |
A |
G |
13: 41,256,435 (GRCm39) |
V438A |
probably benign |
Het |
| Gm10722 |
T |
C |
9: 3,000,937 (GRCm39) |
C6R |
probably benign |
Het |
| Gm4787 |
G |
C |
12: 81,424,604 (GRCm39) |
T518S |
probably benign |
Het |
| Gm4846 |
T |
C |
1: 166,311,551 (GRCm39) |
D436G |
probably damaging |
Het |
| Gm5414 |
T |
A |
15: 101,536,203 (GRCm39) |
I141F |
probably damaging |
Het |
| Gm6185 |
T |
A |
1: 161,025,801 (GRCm39) |
|
noncoding transcript |
Het |
| Grip2 |
T |
C |
6: 91,750,897 (GRCm39) |
E776G |
possibly damaging |
Het |
| H2-Ob |
T |
A |
17: 34,462,490 (GRCm39) |
V160E |
probably benign |
Het |
| Hormad1 |
T |
C |
3: 95,492,531 (GRCm39) |
|
probably benign |
Het |
| Ighv2-1 |
A |
T |
12: 113,538,082 (GRCm39) |
|
probably benign |
Het |
| Igkv4-92 |
A |
T |
6: 68,732,538 (GRCm39) |
C14S |
probably benign |
Het |
| Iqsec3 |
T |
C |
6: 121,360,878 (GRCm39) |
I993M |
probably damaging |
Het |
| Kdm5b |
T |
A |
1: 134,516,484 (GRCm39) |
|
probably benign |
Het |
| Kitl |
T |
C |
10: 99,924,084 (GRCm39) |
|
probably null |
Het |
| Klhl26 |
G |
T |
8: 70,905,368 (GRCm39) |
R100S |
probably benign |
Het |
| Kpna4 |
C |
T |
3: 69,000,142 (GRCm39) |
|
probably null |
Het |
| Lama5 |
T |
A |
2: 179,844,013 (GRCm39) |
N383Y |
possibly damaging |
Het |
| Large1 |
T |
G |
8: 73,544,724 (GRCm39) |
I685L |
probably benign |
Het |
| Larp4b |
A |
G |
13: 9,220,773 (GRCm39) |
E590G |
probably damaging |
Het |
| Liph |
A |
T |
16: 21,774,915 (GRCm39) |
C425* |
probably null |
Het |
| Lrrc31 |
A |
T |
3: 30,739,039 (GRCm39) |
C327* |
probably null |
Het |
| Lrrc36 |
T |
C |
8: 106,190,530 (GRCm39) |
V733A |
probably benign |
Het |
| Mmel1 |
T |
A |
4: 154,966,781 (GRCm39) |
I83K |
probably benign |
Het |
| Naip2 |
A |
T |
13: 100,315,948 (GRCm39) |
N277K |
probably damaging |
Het |
| Ncapg2 |
T |
A |
12: 116,391,406 (GRCm39) |
I485N |
possibly damaging |
Het |
| Npc1l1 |
A |
T |
11: 6,174,245 (GRCm39) |
Y687N |
possibly damaging |
Het |
| Obscn |
A |
T |
11: 59,020,479 (GRCm39) |
V922E |
probably damaging |
Het |
| Oc90 |
A |
G |
15: 65,755,679 (GRCm39) |
S223P |
probably benign |
Het |
| Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
| Or4a80 |
A |
T |
2: 89,582,239 (GRCm39) |
L311H |
possibly damaging |
Het |
| Or4e1 |
T |
C |
14: 52,701,311 (GRCm39) |
I52V |
probably benign |
Het |
| Pakap |
G |
T |
4: 57,855,912 (GRCm39) |
A414S |
probably benign |
Het |
| Pdlim5 |
C |
T |
3: 142,010,126 (GRCm39) |
R174H |
probably benign |
Het |
| Pex5l |
G |
T |
3: 33,009,980 (GRCm39) |
A386E |
probably damaging |
Het |
| Plcxd1 |
T |
A |
5: 110,249,229 (GRCm39) |
|
probably benign |
Het |
| Pramel12 |
T |
G |
4: 143,145,579 (GRCm39) |
S349R |
probably benign |
Het |
| Prl8a1 |
A |
T |
13: 27,763,802 (GRCm39) |
|
probably null |
Het |
| Ryr2 |
G |
T |
13: 11,677,016 (GRCm39) |
N3278K |
probably benign |
Het |
| Sacm1l |
A |
G |
9: 123,406,090 (GRCm39) |
M324V |
probably benign |
Het |
| Sdad1 |
T |
C |
5: 92,451,793 (GRCm39) |
T143A |
probably benign |
Het |
| Sec11a |
A |
T |
7: 80,572,812 (GRCm39) |
|
probably benign |
Het |
| Sema6a |
A |
G |
18: 47,424,239 (GRCm39) |
V223A |
probably damaging |
Het |
| Serpinb6c |
A |
G |
13: 34,064,080 (GRCm39) |
V325A |
probably damaging |
Het |
| Slc4a2 |
G |
A |
5: 24,635,125 (GRCm39) |
A177T |
possibly damaging |
Het |
| Slc5a4a |
A |
G |
10: 75,983,428 (GRCm39) |
N22D |
unknown |
Het |
| Stard13 |
C |
T |
5: 150,986,232 (GRCm39) |
W308* |
probably null |
Het |
| Tanc2 |
C |
T |
11: 105,748,379 (GRCm39) |
L504F |
possibly damaging |
Het |
| Tfap2e |
G |
T |
4: 126,614,337 (GRCm39) |
N282K |
probably damaging |
Het |
| Usp36 |
G |
T |
11: 118,155,731 (GRCm39) |
T682K |
possibly damaging |
Het |
| Zc3h11a |
T |
C |
1: 133,561,527 (GRCm39) |
T315A |
probably benign |
Het |
| Zfa-ps |
T |
A |
10: 52,419,118 (GRCm39) |
|
noncoding transcript |
Het |
| Zfp1002 |
A |
T |
2: 150,097,410 (GRCm39) |
Y34* |
probably null |
Het |
| Zfp663 |
A |
T |
2: 165,195,590 (GRCm39) |
C210S |
possibly damaging |
Het |
| Zfp747 |
T |
C |
7: 126,973,566 (GRCm39) |
I201M |
probably damaging |
Het |
| Zic4 |
C |
T |
9: 91,266,205 (GRCm39) |
T276M |
probably damaging |
Het |
|
| Other mutations in Myo16 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00421:Myo16
|
APN |
8 |
10,488,889 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00567:Myo16
|
APN |
8 |
10,512,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00671:Myo16
|
APN |
8 |
10,411,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00897:Myo16
|
APN |
8 |
10,365,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01458:Myo16
|
APN |
8 |
10,485,853 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01523:Myo16
|
APN |
8 |
10,420,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01532:Myo16
|
APN |
8 |
10,450,551 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01680:Myo16
|
APN |
8 |
10,322,630 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01747:Myo16
|
APN |
8 |
10,654,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02084:Myo16
|
APN |
8 |
10,411,088 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02203:Myo16
|
APN |
8 |
10,620,132 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
IGL02506:Myo16
|
APN |
8 |
10,440,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02819:Myo16
|
APN |
8 |
10,372,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02935:Myo16
|
APN |
8 |
10,582,990 (GRCm39) |
missense |
probably benign |
0.41 |
|
IGL02943:Myo16
|
APN |
8 |
10,450,595 (GRCm39) |
splice site |
probably benign |
|
|
IGL03347:Myo16
|
APN |
8 |
10,426,120 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
3-1:Myo16
|
UTSW |
8 |
10,488,869 (GRCm39) |
missense |
probably damaging |
0.99 |
|
P0016:Myo16
|
UTSW |
8 |
10,450,596 (GRCm39) |
splice site |
probably benign |
|
|
R0006:Myo16
|
UTSW |
8 |
10,525,988 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0006:Myo16
|
UTSW |
8 |
10,525,988 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0033:Myo16
|
UTSW |
8 |
10,420,955 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0033:Myo16
|
UTSW |
8 |
10,420,955 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0142:Myo16
|
UTSW |
8 |
10,619,790 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0195:Myo16
|
UTSW |
8 |
10,365,538 (GRCm39) |
splice site |
probably benign |
|
|
R0418:Myo16
|
UTSW |
8 |
10,619,918 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0576:Myo16
|
UTSW |
8 |
10,612,318 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0627:Myo16
|
UTSW |
8 |
10,489,689 (GRCm39) |
missense |
probably benign |
0.15 |
|
R0826:Myo16
|
UTSW |
8 |
10,426,285 (GRCm39) |
splice site |
probably benign |
|
|
R0835:Myo16
|
UTSW |
8 |
10,322,766 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1015:Myo16
|
UTSW |
8 |
10,440,183 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1052:Myo16
|
UTSW |
8 |
10,620,181 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1180:Myo16
|
UTSW |
8 |
10,446,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1185:Myo16
|
UTSW |
8 |
10,683,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1185:Myo16
|
UTSW |
8 |
10,683,624 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1474:Myo16
|
UTSW |
8 |
10,552,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1484:Myo16
|
UTSW |
8 |
10,610,145 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1503:Myo16
|
UTSW |
8 |
10,552,817 (GRCm39) |
missense |
probably benign |
0.44 |
|
R1733:Myo16
|
UTSW |
8 |
10,492,283 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1873:Myo16
|
UTSW |
8 |
10,322,789 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1885:Myo16
|
UTSW |
8 |
10,372,656 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1943:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2013:Myo16
|
UTSW |
8 |
10,552,796 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2019:Myo16
|
UTSW |
8 |
10,426,260 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2022:Myo16
|
UTSW |
8 |
10,322,633 (GRCm39) |
missense |
probably benign |
0.08 |
|
R2214:Myo16
|
UTSW |
8 |
10,488,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2228:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2351:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2352:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2357:Myo16
|
UTSW |
8 |
10,644,905 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2566:Myo16
|
UTSW |
8 |
10,644,820 (GRCm39) |
missense |
probably benign |
0.43 |
|
R3402:Myo16
|
UTSW |
8 |
10,434,719 (GRCm39) |
missense |
probably benign |
|
|
R3870:Myo16
|
UTSW |
8 |
10,492,239 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4080:Myo16
|
UTSW |
8 |
10,612,240 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4498:Myo16
|
UTSW |
8 |
10,485,869 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4631:Myo16
|
UTSW |
8 |
10,556,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4689:Myo16
|
UTSW |
8 |
10,488,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4736:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4738:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4739:Myo16
|
UTSW |
8 |
10,423,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4764:Myo16
|
UTSW |
8 |
10,485,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4778:Myo16
|
UTSW |
8 |
10,619,694 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4852:Myo16
|
UTSW |
8 |
10,423,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4885:Myo16
|
UTSW |
8 |
10,488,892 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4993:Myo16
|
UTSW |
8 |
10,526,094 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5077:Myo16
|
UTSW |
8 |
10,372,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5170:Myo16
|
UTSW |
8 |
10,619,745 (GRCm39) |
missense |
probably benign |
0.30 |
|
R5203:Myo16
|
UTSW |
8 |
10,410,995 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5246:Myo16
|
UTSW |
8 |
10,612,212 (GRCm39) |
nonsense |
probably null |
|
|
R5517:Myo16
|
UTSW |
8 |
10,610,226 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5567:Myo16
|
UTSW |
8 |
10,372,676 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5694:Myo16
|
UTSW |
8 |
10,619,606 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5749:Myo16
|
UTSW |
8 |
10,463,245 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6131:Myo16
|
UTSW |
8 |
10,619,877 (GRCm39) |
missense |
probably benign |
|
|
R6213:Myo16
|
UTSW |
8 |
10,420,963 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6216:Myo16
|
UTSW |
8 |
10,365,494 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6240:Myo16
|
UTSW |
8 |
10,420,930 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6628:Myo16
|
UTSW |
8 |
10,620,638 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6935:Myo16
|
UTSW |
8 |
10,619,820 (GRCm39) |
missense |
probably benign |
0.37 |
|
R6996:Myo16
|
UTSW |
8 |
10,619,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7103:Myo16
|
UTSW |
8 |
10,619,673 (GRCm39) |
missense |
unknown |
|
|
R7164:Myo16
|
UTSW |
8 |
10,619,585 (GRCm39) |
missense |
unknown |
|
|
R7255:Myo16
|
UTSW |
8 |
10,549,169 (GRCm39) |
missense |
unknown |
|
|
R7266:Myo16
|
UTSW |
8 |
10,322,687 (GRCm39) |
missense |
unknown |
|
|
R7319:Myo16
|
UTSW |
8 |
10,526,185 (GRCm39) |
splice site |
probably null |
|
|
R7398:Myo16
|
UTSW |
8 |
10,612,183 (GRCm39) |
missense |
unknown |
|
|
R7442:Myo16
|
UTSW |
8 |
10,322,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7498:Myo16
|
UTSW |
8 |
10,450,589 (GRCm39) |
missense |
unknown |
|
|
R7539:Myo16
|
UTSW |
8 |
10,411,095 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7622:Myo16
|
UTSW |
8 |
10,426,238 (GRCm39) |
missense |
unknown |
|
|
R7794:Myo16
|
UTSW |
8 |
10,619,913 (GRCm39) |
missense |
unknown |
|
|
R7903:Myo16
|
UTSW |
8 |
10,426,265 (GRCm39) |
missense |
probably null |
|
|
R8055:Myo16
|
UTSW |
8 |
10,612,186 (GRCm39) |
missense |
unknown |
|
|
R8078:Myo16
|
UTSW |
8 |
10,612,078 (GRCm39) |
missense |
unknown |
|
|
R8081:Myo16
|
UTSW |
8 |
10,372,743 (GRCm39) |
missense |
unknown |
|
|
R8679:Myo16
|
UTSW |
8 |
10,411,042 (GRCm39) |
missense |
unknown |
|
|
R8700:Myo16
|
UTSW |
8 |
10,463,172 (GRCm39) |
missense |
unknown |
|
|
R8939:Myo16
|
UTSW |
8 |
10,524,679 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8955:Myo16
|
UTSW |
8 |
10,426,175 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8968:Myo16
|
UTSW |
8 |
10,619,700 (GRCm39) |
missense |
unknown |
|
|
R9187:Myo16
|
UTSW |
8 |
10,492,233 (GRCm39) |
missense |
unknown |
|
|
R9219:Myo16
|
UTSW |
8 |
10,492,236 (GRCm39) |
missense |
unknown |
|
|
R9287:Myo16
|
UTSW |
8 |
10,526,114 (GRCm39) |
missense |
unknown |
|
|
R9327:Myo16
|
UTSW |
8 |
10,489,705 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9763:Myo16
|
UTSW |
8 |
10,450,528 (GRCm39) |
missense |
unknown |
|
|
R9765:Myo16
|
UTSW |
8 |
10,620,401 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9790:Myo16
|
UTSW |
8 |
10,619,925 (GRCm39) |
missense |
unknown |
|
|
R9791:Myo16
|
UTSW |
8 |
10,619,925 (GRCm39) |
missense |
unknown |
|
|
X0066:Myo16
|
UTSW |
8 |
10,426,185 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Myo16
|
UTSW |
8 |
10,524,691 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GAGCGTATGTCAAGGATGCC -3'
(R):5'- ATGACTGCAGGCTGTTCATG -3'
Sequencing Primer
(F):5'- CGTATGTCAAGGATGCCAAGTG -3'
(R):5'- GGCCTTTGAATGTGGAATAGTAACAC -3'
|
| Posted On |
2016-06-21 |
Incidental Mutation