Incidental Mutation 'R1883:Musk'
| ID |
209228 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Musk
|
| Ensembl Gene |
ENSMUSG00000057280 |
| Gene Name |
muscle, skeletal, receptor tyrosine kinase |
| Synonyms |
Nsk1, MDK4, Nsk2, Nsk3 |
| MMRRC Submission |
039904-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1883 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
4 |
| Chromosomal Location |
58285960-58374303 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 58373189 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Proline to Threonine
at position 697
(P697T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000095667
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081919]
[ENSMUST00000084578]
[ENSMUST00000098057]
[ENSMUST00000098059]
[ENSMUST00000102893]
[ENSMUST00000177951]
[ENSMUST00000179951]
|
| AlphaFold |
Q61006 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000081919
AA Change: P695T
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000080590
Gene: ENSMUSG00000057280
AA Change: P695T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
224 |
289 |
4.67e-4 |
SMART |
|
Pfam:Fz
|
317 |
448 |
1.1e-27 |
PFAM |
|
transmembrane domain
|
495 |
517 |
N/A |
INTRINSIC |
|
low complexity region
|
518 |
529 |
N/A |
INTRINSIC |
|
low complexity region
|
558 |
567 |
N/A |
INTRINSIC |
|
TyrKc
|
574 |
855 |
2.96e-140 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000084578
AA Change: P695T
PolyPhen 2
Score 0.070 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000081625
Gene: ENSMUSG00000057280
AA Change: P695T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
224 |
289 |
4.67e-4 |
SMART |
|
Pfam:Fz
|
317 |
448 |
1.2e-28 |
PFAM |
|
transmembrane domain
|
495 |
517 |
N/A |
INTRINSIC |
|
low complexity region
|
518 |
529 |
N/A |
INTRINSIC |
|
low complexity region
|
558 |
567 |
N/A |
INTRINSIC |
|
TyrKc
|
574 |
855 |
2.96e-140 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000098057
AA Change: P720T
PolyPhen 2
Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000095665
Gene: ENSMUSG00000057280
AA Change: P720T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
234 |
299 |
4.67e-4 |
SMART |
|
Pfam:Fz
|
342 |
467 |
1.4e-15 |
PFAM |
|
transmembrane domain
|
520 |
542 |
N/A |
INTRINSIC |
|
low complexity region
|
543 |
554 |
N/A |
INTRINSIC |
|
low complexity region
|
583 |
592 |
N/A |
INTRINSIC |
|
TyrKc
|
599 |
880 |
2.96e-140 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000098059
AA Change: P697T
PolyPhen 2
Score 0.183 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000095667
Gene: ENSMUSG00000057280
AA Change: P697T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
234 |
299 |
4.67e-4 |
SMART |
|
low complexity region
|
303 |
318 |
N/A |
INTRINSIC |
|
Pfam:Fz
|
327 |
458 |
2.1e-28 |
PFAM |
|
transmembrane domain
|
497 |
519 |
N/A |
INTRINSIC |
|
low complexity region
|
520 |
531 |
N/A |
INTRINSIC |
|
low complexity region
|
560 |
569 |
N/A |
INTRINSIC |
|
TyrKc
|
576 |
857 |
2.96e-140 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000102893
AA Change: P687T
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000099957
Gene: ENSMUSG00000057280
AA Change: P687T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
224 |
289 |
4.67e-4 |
SMART |
|
Pfam:Fz
|
317 |
448 |
1.1e-27 |
PFAM |
|
transmembrane domain
|
487 |
509 |
N/A |
INTRINSIC |
|
low complexity region
|
510 |
521 |
N/A |
INTRINSIC |
|
low complexity region
|
550 |
559 |
N/A |
INTRINSIC |
|
TyrKc
|
566 |
847 |
2.96e-140 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000177951
AA Change: P697T
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000136696
Gene: ENSMUSG00000057280
AA Change: P697T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
234 |
299 |
4.67e-4 |
SMART |
|
Pfam:Fz
|
327 |
458 |
1.1e-27 |
PFAM |
|
transmembrane domain
|
497 |
519 |
N/A |
INTRINSIC |
|
low complexity region
|
520 |
531 |
N/A |
INTRINSIC |
|
low complexity region
|
560 |
569 |
N/A |
INTRINSIC |
|
TyrKc
|
576 |
857 |
2.96e-140 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000179951
AA Change: P705T
PolyPhen 2
Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
|
| SMART Domains |
Protein: ENSMUSP00000137453
Gene: ENSMUSG00000057280
AA Change: P705T
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
IGc2
|
40 |
106 |
1.16e-8 |
SMART |
|
IGc2
|
133 |
197 |
1.79e-14 |
SMART |
|
IGc2
|
234 |
299 |
4.67e-4 |
SMART |
|
low complexity region
|
303 |
318 |
N/A |
INTRINSIC |
|
Pfam:Fz
|
327 |
458 |
1.2e-27 |
PFAM |
|
transmembrane domain
|
505 |
527 |
N/A |
INTRINSIC |
|
low complexity region
|
528 |
539 |
N/A |
INTRINSIC |
|
low complexity region
|
568 |
577 |
N/A |
INTRINSIC |
|
TyrKc
|
584 |
865 |
2.96e-140 |
SMART |
|
| Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.8%
- 10x: 95.4%
- 20x: 93.0%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the protein tyrosine kinase family. The encoded protein is a type 1 receptor-like protein located in muscle membrane that is activated by the heparan sulfate proteoglycan agrin released by nerve cells. The encoded protein activates signaling cascades responsible for multiple aspects of motor neuron and muscle development, including organization of the postsynaptic membrane, synaptic gene transcription, patterning of skeletal muscle, anchoring of acetylcholinesterase, and guidance of motor axons. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation lack neuromuscular synapses and spontaneous movement, and die at birth of respiratory failure. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ano9 |
T |
C |
7: 140,682,244 (GRCm39) |
E677G |
probably benign |
Het |
| Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
| Bhmt1b |
T |
C |
18: 87,774,669 (GRCm39) |
L64P |
probably damaging |
Het |
| Brs3 |
T |
C |
X: 56,092,449 (GRCm39) |
I311T |
probably benign |
Het |
| Capn9 |
A |
G |
8: 125,338,297 (GRCm39) |
K552R |
probably benign |
Het |
| Catsperg1 |
C |
T |
7: 28,881,661 (GRCm39) |
|
probably null |
Het |
| Cdc16 |
A |
G |
8: 13,825,738 (GRCm39) |
N449D |
probably damaging |
Het |
| Cdyl2 |
A |
T |
8: 117,321,902 (GRCm39) |
N208K |
probably damaging |
Het |
| Cnot4 |
C |
T |
6: 35,055,092 (GRCm39) |
V66I |
probably damaging |
Het |
| Cntn4 |
A |
G |
6: 106,656,353 (GRCm39) |
T885A |
probably benign |
Het |
| Col20a1 |
C |
T |
2: 180,634,703 (GRCm39) |
T131I |
possibly damaging |
Het |
| Crybg2 |
C |
A |
4: 133,801,594 (GRCm39) |
S918* |
probably null |
Het |
| Dact2 |
A |
T |
17: 14,418,085 (GRCm39) |
S207T |
possibly damaging |
Het |
| Dbnl |
G |
A |
11: 5,749,247 (GRCm39) |
G356E |
probably benign |
Het |
| Ddx18 |
C |
A |
1: 121,495,645 (GRCm39) |
|
probably benign |
Het |
| Dis3 |
A |
T |
14: 99,328,905 (GRCm39) |
H282Q |
probably benign |
Het |
| Dnah3 |
T |
C |
7: 119,677,142 (GRCm39) |
D453G |
probably benign |
Het |
| Dst |
T |
C |
1: 34,228,389 (GRCm39) |
V1994A |
possibly damaging |
Het |
| Dusp8 |
C |
T |
7: 141,638,085 (GRCm39) |
|
probably null |
Het |
| Eipr1 |
A |
T |
12: 28,816,850 (GRCm39) |
H69L |
possibly damaging |
Het |
| Eml1 |
A |
G |
12: 108,429,911 (GRCm39) |
R65G |
probably damaging |
Het |
| Epha7 |
C |
T |
4: 28,950,362 (GRCm39) |
H722Y |
possibly damaging |
Het |
| Epyc |
A |
T |
10: 97,511,695 (GRCm39) |
K229N |
possibly damaging |
Het |
| Extl1 |
A |
G |
4: 134,091,917 (GRCm39) |
I312T |
probably benign |
Het |
| F13a1 |
G |
C |
13: 37,172,981 (GRCm39) |
A133G |
probably benign |
Het |
| Fam185a |
G |
T |
5: 21,630,242 (GRCm39) |
C26F |
possibly damaging |
Het |
| Fam186b |
T |
C |
15: 99,176,679 (GRCm39) |
N737S |
probably damaging |
Het |
| Fam78b |
A |
G |
1: 166,829,171 (GRCm39) |
I13V |
probably benign |
Het |
| Fat1 |
A |
T |
8: 45,504,184 (GRCm39) |
Q4559L |
probably benign |
Het |
| Fnip1 |
T |
C |
11: 54,406,373 (GRCm39) |
S1157P |
probably damaging |
Het |
| Foxj3 |
A |
C |
4: 119,467,226 (GRCm39) |
M190L |
probably benign |
Het |
| Heatr3 |
T |
C |
8: 88,871,221 (GRCm39) |
Y192H |
possibly damaging |
Het |
| Hexd |
T |
A |
11: 121,098,524 (GRCm39) |
S3T |
probably benign |
Het |
| Klf3 |
C |
T |
5: 64,980,224 (GRCm39) |
P5S |
probably damaging |
Het |
| Klf9 |
C |
T |
19: 23,142,101 (GRCm39) |
S187L |
probably damaging |
Het |
| Krt9 |
T |
C |
11: 100,079,523 (GRCm39) |
H623R |
unknown |
Het |
| Krtap2-4 |
G |
C |
11: 99,505,505 (GRCm39) |
|
probably benign |
Het |
| Lmtk3 |
T |
C |
7: 45,436,273 (GRCm39) |
Y84H |
probably damaging |
Het |
| Mroh3 |
G |
T |
1: 136,134,731 (GRCm39) |
A166D |
probably damaging |
Het |
| Nek9 |
A |
G |
12: 85,379,330 (GRCm39) |
L192P |
probably damaging |
Het |
| Nipbl |
A |
C |
15: 8,356,616 (GRCm39) |
F1590C |
probably damaging |
Het |
| Nrk |
G |
T |
X: 137,907,922 (GRCm39) |
V1455F |
probably damaging |
Het |
| Nsun3 |
T |
C |
16: 62,555,656 (GRCm39) |
D290G |
probably damaging |
Het |
| Obscn |
T |
C |
11: 58,969,029 (GRCm39) |
T222A |
probably damaging |
Het |
| Or2a12 |
T |
C |
6: 42,904,764 (GRCm39) |
S200P |
probably damaging |
Het |
| Or51f1d |
T |
C |
7: 102,701,189 (GRCm39) |
I228T |
probably benign |
Het |
| Or6b9 |
T |
C |
7: 106,555,981 (GRCm39) |
H54R |
probably benign |
Het |
| Osbpl11 |
T |
G |
16: 33,034,723 (GRCm39) |
H237Q |
probably benign |
Het |
| Pde10a |
A |
T |
17: 9,197,776 (GRCm39) |
T671S |
possibly damaging |
Het |
| Pkd2 |
A |
T |
5: 104,631,094 (GRCm39) |
N506I |
probably damaging |
Het |
| Ppp3cb |
A |
G |
14: 20,573,913 (GRCm39) |
V274A |
possibly damaging |
Het |
| Prex1 |
T |
C |
2: 166,425,192 (GRCm39) |
D938G |
probably benign |
Het |
| Ptch1 |
G |
A |
13: 63,659,841 (GRCm39) |
Q1134* |
probably null |
Het |
| Rasgrf2 |
A |
G |
13: 92,117,149 (GRCm39) |
V820A |
probably benign |
Het |
| Rimbp2 |
C |
T |
5: 128,880,998 (GRCm39) |
V137M |
possibly damaging |
Het |
| Rpa1 |
A |
G |
11: 75,209,309 (GRCm39) |
V137A |
probably benign |
Het |
| Rps6ka1 |
A |
C |
4: 133,591,354 (GRCm39) |
I299S |
probably damaging |
Het |
| Scn3b |
A |
C |
9: 40,190,669 (GRCm39) |
|
probably null |
Het |
| Sdha |
A |
T |
13: 74,481,255 (GRCm39) |
I317N |
probably damaging |
Het |
| Serpina1d |
T |
A |
12: 103,732,037 (GRCm39) |
D274V |
possibly damaging |
Het |
| Sik3 |
C |
G |
9: 46,132,387 (GRCm39) |
H1276Q |
probably benign |
Het |
| Snx14 |
T |
A |
9: 88,284,314 (GRCm39) |
E451D |
probably benign |
Het |
| Spmip4 |
T |
C |
6: 50,551,433 (GRCm39) |
T339A |
probably benign |
Het |
| Swt1 |
T |
A |
1: 151,299,284 (GRCm39) |
K8* |
probably null |
Het |
| Tas1r3 |
G |
T |
4: 155,946,610 (GRCm39) |
P332T |
probably damaging |
Het |
| Tas2r126 |
A |
T |
6: 42,411,961 (GRCm39) |
T165S |
probably benign |
Het |
| Tecpr1 |
A |
G |
5: 144,143,347 (GRCm39) |
V676A |
probably benign |
Het |
| Tg |
A |
G |
15: 66,543,158 (GRCm39) |
E24G |
probably damaging |
Het |
| Tlr7 |
C |
T |
X: 166,089,468 (GRCm39) |
G673S |
probably benign |
Het |
| Tnxb |
T |
A |
17: 34,908,539 (GRCm39) |
D1520E |
probably benign |
Het |
| Trabd |
A |
G |
15: 88,966,184 (GRCm39) |
E47G |
probably damaging |
Het |
| Trim29 |
T |
A |
9: 43,222,702 (GRCm39) |
I177N |
probably damaging |
Het |
| Ubxn2a |
A |
T |
12: 4,944,563 (GRCm39) |
L53* |
probably null |
Het |
| Ulk2 |
A |
G |
11: 61,721,438 (GRCm39) |
L208P |
probably damaging |
Het |
| Unc80 |
G |
A |
1: 66,564,929 (GRCm39) |
C872Y |
possibly damaging |
Het |
| Vac14 |
A |
G |
8: 111,438,319 (GRCm39) |
H644R |
probably damaging |
Het |
| Vmn1r20 |
C |
A |
6: 57,409,306 (GRCm39) |
H211N |
probably benign |
Het |
| Vmn1r31 |
C |
T |
6: 58,449,029 (GRCm39) |
V279I |
probably damaging |
Het |
| Vmn2r18 |
G |
T |
5: 151,499,190 (GRCm39) |
Q425K |
probably benign |
Het |
| Vmn2r60 |
T |
C |
7: 41,786,094 (GRCm39) |
V299A |
probably damaging |
Het |
| Vps54 |
A |
T |
11: 21,262,967 (GRCm39) |
T685S |
possibly damaging |
Het |
| Vwa5b1 |
A |
G |
4: 138,302,700 (GRCm39) |
W932R |
probably damaging |
Het |
| Wdr53 |
A |
T |
16: 32,075,316 (GRCm39) |
I174F |
possibly damaging |
Het |
| Zfp157 |
A |
G |
5: 138,443,102 (GRCm39) |
D31G |
probably damaging |
Het |
| Zfp60 |
T |
C |
7: 27,449,435 (GRCm39) |
L701P |
probably benign |
Het |
| Zfp609 |
A |
T |
9: 65,702,040 (GRCm39) |
M204K |
probably benign |
Het |
| Zfp831 |
A |
G |
2: 174,545,870 (GRCm39) |
H1325R |
possibly damaging |
Het |
| Zfp995 |
A |
T |
17: 22,099,622 (GRCm39) |
I204N |
probably benign |
Het |
| Zp2 |
C |
T |
7: 119,732,624 (GRCm39) |
D641N |
probably benign |
Het |
|
| Other mutations in Musk |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01406:Musk
|
APN |
4 |
58,367,539 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01727:Musk
|
APN |
4 |
58,303,887 (GRCm39) |
missense |
probably benign |
0.37 |
|
IGL01981:Musk
|
APN |
4 |
58,296,629 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02064:Musk
|
APN |
4 |
58,286,128 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02326:Musk
|
APN |
4 |
58,354,113 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02475:Musk
|
APN |
4 |
58,353,936 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|
IGL02585:Musk
|
APN |
4 |
58,347,849 (GRCm39) |
missense |
probably benign |
|
|
IGL02719:Musk
|
APN |
4 |
58,356,496 (GRCm39) |
missense |
probably benign |
|
|
IGL02797:Musk
|
APN |
4 |
58,366,921 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02869:Musk
|
APN |
4 |
58,354,078 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02940:Musk
|
APN |
4 |
58,373,364 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03167:Musk
|
APN |
4 |
58,366,821 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL03230:Musk
|
APN |
4 |
58,296,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB002:Musk
|
UTSW |
4 |
58,367,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB012:Musk
|
UTSW |
4 |
58,367,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0384:Musk
|
UTSW |
4 |
58,373,711 (GRCm39) |
makesense |
probably null |
|
|
R1014:Musk
|
UTSW |
4 |
58,354,156 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R1462:Musk
|
UTSW |
4 |
58,286,204 (GRCm39) |
splice site |
probably benign |
|
|
R1493:Musk
|
UTSW |
4 |
58,354,003 (GRCm39) |
missense |
probably benign |
0.19 |
|
R1739:Musk
|
UTSW |
4 |
58,293,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2230:Musk
|
UTSW |
4 |
58,333,672 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R2914:Musk
|
UTSW |
4 |
58,366,938 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3508:Musk
|
UTSW |
4 |
58,327,347 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4225:Musk
|
UTSW |
4 |
58,373,240 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4601:Musk
|
UTSW |
4 |
58,301,625 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4771:Musk
|
UTSW |
4 |
58,301,706 (GRCm39) |
missense |
probably benign |
0.16 |
|
R4793:Musk
|
UTSW |
4 |
58,373,400 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4845:Musk
|
UTSW |
4 |
58,296,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4919:Musk
|
UTSW |
4 |
58,366,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4954:Musk
|
UTSW |
4 |
58,344,222 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5596:Musk
|
UTSW |
4 |
58,373,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5715:Musk
|
UTSW |
4 |
58,333,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5894:Musk
|
UTSW |
4 |
58,373,583 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5934:Musk
|
UTSW |
4 |
58,373,613 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6230:Musk
|
UTSW |
4 |
58,367,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6335:Musk
|
UTSW |
4 |
58,366,811 (GRCm39) |
missense |
probably benign |
|
|
R6358:Musk
|
UTSW |
4 |
58,373,171 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6395:Musk
|
UTSW |
4 |
58,286,169 (GRCm39) |
missense |
probably benign |
|
|
R6652:Musk
|
UTSW |
4 |
58,368,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6764:Musk
|
UTSW |
4 |
58,354,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7233:Musk
|
UTSW |
4 |
58,373,307 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7238:Musk
|
UTSW |
4 |
58,344,312 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7271:Musk
|
UTSW |
4 |
58,373,409 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7511:Musk
|
UTSW |
4 |
58,333,672 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7925:Musk
|
UTSW |
4 |
58,367,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8085:Musk
|
UTSW |
4 |
58,373,110 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8243:Musk
|
UTSW |
4 |
58,293,600 (GRCm39) |
missense |
probably benign |
|
|
R8249:Musk
|
UTSW |
4 |
58,368,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8501:Musk
|
UTSW |
4 |
58,367,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8671:Musk
|
UTSW |
4 |
58,286,051 (GRCm39) |
start gained |
probably benign |
|
|
R8672:Musk
|
UTSW |
4 |
58,286,051 (GRCm39) |
start gained |
probably benign |
|
|
R8839:Musk
|
UTSW |
4 |
58,286,151 (GRCm39) |
missense |
probably benign |
|
|
R8927:Musk
|
UTSW |
4 |
58,301,638 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8928:Musk
|
UTSW |
4 |
58,301,638 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8988:Musk
|
UTSW |
4 |
58,354,032 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9167:Musk
|
UTSW |
4 |
58,296,687 (GRCm39) |
missense |
probably benign |
0.30 |
|
X0020:Musk
|
UTSW |
4 |
58,368,996 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0066:Musk
|
UTSW |
4 |
58,327,356 (GRCm39) |
critical splice donor site |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GGAAGGACTCGGTCTAACTATG -3'
(R):5'- ATGGCGTCATTTCCATCAGC -3'
Sequencing Primer
(F):5'- AGGACTCGGTCTAACTATGATAATG -3'
(R):5'- CCATCAGCTTTGTAGTAGTCTGCG -3'
|
| Posted On |
2014-06-30 |
Incidental Mutation