Incidental Mutation 'R1695:Mprip'
ID |
192151 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mprip
|
Ensembl Gene |
ENSMUSG00000005417 |
Gene Name |
myosin phosphatase Rho interacting protein |
Synonyms |
p116 Rho interacting protein, p116Rip, Gm34094, RIP3, Rhoip3 |
MMRRC Submission |
039728-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.669)
|
Stock # |
R1695 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
59552973-59671686 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 59643357 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Isoleucine
at position 505
(T505I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112072
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000066330]
[ENSMUST00000072031]
[ENSMUST00000108751]
[ENSMUST00000116371]
[ENSMUST00000133861]
|
AlphaFold |
P97434 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000066330
AA Change: T469I
PolyPhen 2
Score 0.845 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000071081 Gene: ENSMUSG00000005417 AA Change: T469I
Domain | Start | End | E-Value | Type |
PH
|
44 |
152 |
3.33e-10 |
SMART |
low complexity region
|
179 |
190 |
N/A |
INTRINSIC |
low complexity region
|
221 |
234 |
N/A |
INTRINSIC |
Blast:PH
|
249 |
320 |
1e-10 |
BLAST |
PH
|
351 |
448 |
3.76e-18 |
SMART |
low complexity region
|
492 |
501 |
N/A |
INTRINSIC |
low complexity region
|
536 |
555 |
N/A |
INTRINSIC |
coiled coil region
|
636 |
671 |
N/A |
INTRINSIC |
Blast:PAC
|
806 |
848 |
2e-10 |
BLAST |
low complexity region
|
1005 |
1023 |
N/A |
INTRINSIC |
low complexity region
|
1047 |
1059 |
N/A |
INTRINSIC |
low complexity region
|
1114 |
1128 |
N/A |
INTRINSIC |
low complexity region
|
1183 |
1200 |
N/A |
INTRINSIC |
coiled coil region
|
1267 |
1300 |
N/A |
INTRINSIC |
coiled coil region
|
1617 |
1642 |
N/A |
INTRINSIC |
coiled coil region
|
1729 |
1779 |
N/A |
INTRINSIC |
coiled coil region
|
1899 |
1936 |
N/A |
INTRINSIC |
coiled coil region
|
1960 |
2110 |
N/A |
INTRINSIC |
coiled coil region
|
2132 |
2206 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000072031
AA Change: T505I
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000071914 Gene: ENSMUSG00000005417 AA Change: T505I
Domain | Start | End | E-Value | Type |
PH
|
44 |
152 |
3.33e-10 |
SMART |
low complexity region
|
179 |
190 |
N/A |
INTRINSIC |
low complexity region
|
221 |
234 |
N/A |
INTRINSIC |
Blast:PH
|
254 |
320 |
1e-10 |
BLAST |
PH
|
387 |
484 |
3.76e-18 |
SMART |
low complexity region
|
528 |
537 |
N/A |
INTRINSIC |
low complexity region
|
572 |
591 |
N/A |
INTRINSIC |
coiled coil region
|
672 |
707 |
N/A |
INTRINSIC |
coiled coil region
|
728 |
878 |
N/A |
INTRINSIC |
coiled coil region
|
900 |
974 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000108751
AA Change: T467I
PolyPhen 2
Score 0.915 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000104382 Gene: ENSMUSG00000005417 AA Change: T467I
Domain | Start | End | E-Value | Type |
PH
|
44 |
152 |
3.33e-10 |
SMART |
low complexity region
|
183 |
196 |
N/A |
INTRINSIC |
Blast:PH
|
216 |
282 |
1e-10 |
BLAST |
PH
|
349 |
446 |
3.76e-18 |
SMART |
low complexity region
|
490 |
499 |
N/A |
INTRINSIC |
low complexity region
|
534 |
553 |
N/A |
INTRINSIC |
coiled coil region
|
634 |
669 |
N/A |
INTRINSIC |
coiled coil region
|
690 |
840 |
N/A |
INTRINSIC |
coiled coil region
|
862 |
936 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000116371
AA Change: T505I
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000112072 Gene: ENSMUSG00000005417 AA Change: T505I
Domain | Start | End | E-Value | Type |
PH
|
44 |
152 |
3.33e-10 |
SMART |
low complexity region
|
179 |
190 |
N/A |
INTRINSIC |
low complexity region
|
221 |
234 |
N/A |
INTRINSIC |
Blast:PH
|
254 |
320 |
1e-10 |
BLAST |
PH
|
387 |
484 |
3.76e-18 |
SMART |
low complexity region
|
528 |
537 |
N/A |
INTRINSIC |
low complexity region
|
572 |
591 |
N/A |
INTRINSIC |
coiled coil region
|
672 |
707 |
N/A |
INTRINSIC |
coiled coil region
|
728 |
878 |
N/A |
INTRINSIC |
coiled coil region
|
900 |
974 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000132620
AA Change: T315I
|
SMART Domains |
Protein: ENSMUSP00000119422 Gene: ENSMUSG00000005417 AA Change: T315I
Domain | Start | End | E-Value | Type |
low complexity region
|
26 |
37 |
N/A |
INTRINSIC |
low complexity region
|
68 |
81 |
N/A |
INTRINSIC |
Blast:PH
|
101 |
167 |
9e-11 |
BLAST |
PH
|
198 |
295 |
3.76e-18 |
SMART |
low complexity region
|
339 |
348 |
N/A |
INTRINSIC |
low complexity region
|
383 |
402 |
N/A |
INTRINSIC |
coiled coil region
|
482 |
517 |
N/A |
INTRINSIC |
coiled coil region
|
538 |
688 |
N/A |
INTRINSIC |
coiled coil region
|
710 |
784 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000133861
AA Change: T491I
PolyPhen 2
Score 0.982 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000119562 Gene: ENSMUSG00000005417 AA Change: T491I
Domain | Start | End | E-Value | Type |
low complexity region
|
18 |
29 |
N/A |
INTRINSIC |
low complexity region
|
47 |
58 |
N/A |
INTRINSIC |
low complexity region
|
89 |
102 |
N/A |
INTRINSIC |
low complexity region
|
152 |
162 |
N/A |
INTRINSIC |
low complexity region
|
259 |
269 |
N/A |
INTRINSIC |
PH
|
373 |
470 |
3.76e-18 |
SMART |
low complexity region
|
514 |
523 |
N/A |
INTRINSIC |
low complexity region
|
558 |
577 |
N/A |
INTRINSIC |
coiled coil region
|
658 |
693 |
N/A |
INTRINSIC |
coiled coil region
|
714 |
864 |
N/A |
INTRINSIC |
coiled coil region
|
886 |
960 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153531
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.2%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
T |
A |
5: 121,638,970 (GRCm39) |
T692S |
probably benign |
Het |
Adgrf3 |
T |
A |
5: 30,408,553 (GRCm39) |
N75I |
probably benign |
Het |
Adgrg5 |
A |
G |
8: 95,664,373 (GRCm39) |
M328V |
probably damaging |
Het |
Adk |
A |
G |
14: 21,431,668 (GRCm39) |
D286G |
probably benign |
Het |
Ankrd28 |
T |
A |
14: 31,429,201 (GRCm39) |
D917V |
probably damaging |
Het |
Appl2 |
C |
T |
10: 83,457,446 (GRCm39) |
D141N |
probably damaging |
Het |
Arfgef2 |
T |
C |
2: 166,706,632 (GRCm39) |
V952A |
probably damaging |
Het |
Arpc2 |
T |
A |
1: 74,287,391 (GRCm39) |
H70Q |
probably damaging |
Het |
Bpifa5 |
T |
C |
2: 154,009,580 (GRCm39) |
L261P |
probably damaging |
Het |
Brca1 |
G |
T |
11: 101,415,281 (GRCm39) |
T951K |
probably damaging |
Het |
Ccdc73 |
A |
T |
2: 104,822,450 (GRCm39) |
S800C |
probably damaging |
Het |
Cdh15 |
C |
G |
8: 123,588,755 (GRCm39) |
D276E |
probably benign |
Het |
Cfap119 |
A |
G |
7: 127,186,745 (GRCm39) |
|
probably null |
Het |
Cfap418 |
T |
A |
4: 10,874,644 (GRCm39) |
D10E |
probably damaging |
Het |
Cfh |
T |
C |
1: 140,030,575 (GRCm39) |
I551V |
probably damaging |
Het |
Chd7 |
T |
A |
4: 8,833,960 (GRCm39) |
L1238Q |
probably damaging |
Het |
Chd9 |
T |
G |
8: 91,728,410 (GRCm39) |
F1275L |
probably damaging |
Het |
Chrnb3 |
A |
G |
8: 27,883,728 (GRCm39) |
Y155C |
probably damaging |
Het |
Cltc |
C |
A |
11: 86,591,886 (GRCm39) |
|
probably null |
Het |
Ctsll3 |
T |
A |
13: 60,948,791 (GRCm39) |
N55Y |
probably damaging |
Het |
Cysltr2 |
T |
C |
14: 73,267,321 (GRCm39) |
M130V |
probably benign |
Het |
Daglb |
T |
C |
5: 143,480,361 (GRCm39) |
M455T |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,624,521 (GRCm39) |
S343P |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,405,517 (GRCm39) |
D665V |
possibly damaging |
Het |
Dusp6 |
T |
A |
10: 99,099,555 (GRCm39) |
M1K |
probably null |
Het |
Eif3m |
T |
C |
2: 104,847,298 (GRCm39) |
E12G |
probably damaging |
Het |
Epha2 |
T |
C |
4: 141,033,828 (GRCm39) |
V29A |
possibly damaging |
Het |
Farp2 |
T |
A |
1: 93,488,047 (GRCm39) |
N91K |
probably damaging |
Het |
Ferd3l |
C |
A |
12: 33,978,971 (GRCm39) |
S161R |
probably benign |
Het |
Fgd2 |
A |
T |
17: 29,587,219 (GRCm39) |
D315V |
possibly damaging |
Het |
Fhip2a |
T |
C |
19: 57,367,603 (GRCm39) |
W337R |
probably damaging |
Het |
Fstl4 |
T |
A |
11: 53,056,705 (GRCm39) |
|
probably null |
Het |
Grm5 |
A |
G |
7: 87,685,311 (GRCm39) |
D476G |
possibly damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hdlbp |
A |
G |
1: 93,364,922 (GRCm39) |
L115P |
probably damaging |
Het |
Hk2 |
T |
A |
6: 82,721,932 (GRCm39) |
N136Y |
probably damaging |
Het |
Hs2st1 |
G |
T |
3: 144,140,415 (GRCm39) |
A302E |
probably benign |
Het |
Htr7 |
T |
C |
19: 35,947,136 (GRCm39) |
N293D |
probably benign |
Het |
Ikbkb |
T |
A |
8: 23,163,496 (GRCm39) |
E271D |
probably benign |
Het |
Il5ra |
A |
T |
6: 106,715,335 (GRCm39) |
Y166* |
probably null |
Het |
Il9r |
T |
A |
11: 32,143,227 (GRCm39) |
H244L |
probably benign |
Het |
Itih4 |
T |
C |
14: 30,613,456 (GRCm39) |
|
probably null |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Large1 |
A |
T |
8: 73,544,710 (GRCm39) |
D689E |
probably damaging |
Het |
Limk2 |
A |
G |
11: 3,303,275 (GRCm39) |
|
probably null |
Het |
Med15 |
A |
G |
16: 17,540,644 (GRCm39) |
F34S |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,623,364 (GRCm39) |
N2071K |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,408,729 (GRCm39) |
L2522P |
probably damaging |
Het |
Myd88 |
A |
T |
9: 119,166,908 (GRCm39) |
|
probably null |
Het |
Myo7a |
A |
C |
7: 97,741,703 (GRCm39) |
F484V |
possibly damaging |
Het |
Nme1 |
A |
C |
11: 93,851,593 (GRCm39) |
L81R |
probably benign |
Het |
Ntn4 |
T |
A |
10: 93,569,464 (GRCm39) |
|
probably null |
Het |
Or2y13 |
T |
C |
11: 49,415,162 (GRCm39) |
V204A |
probably benign |
Het |
Or4p19 |
T |
C |
2: 88,242,444 (GRCm39) |
D186G |
probably damaging |
Het |
Or51l4 |
A |
T |
7: 103,404,131 (GRCm39) |
Y220* |
probably null |
Het |
Otogl |
T |
G |
10: 107,649,878 (GRCm39) |
N1159T |
probably damaging |
Het |
Pabpc6 |
G |
A |
17: 9,887,003 (GRCm39) |
T516I |
probably benign |
Het |
Pcdh1 |
C |
T |
18: 38,335,921 (GRCm39) |
R238H |
probably damaging |
Het |
Pex5l |
T |
A |
3: 33,008,531 (GRCm39) |
N151I |
probably benign |
Het |
Plekha7 |
T |
C |
7: 115,727,920 (GRCm39) |
N980S |
probably damaging |
Het |
Reg4 |
C |
T |
3: 98,143,677 (GRCm39) |
T157I |
probably benign |
Het |
Rev3l |
A |
T |
10: 39,700,612 (GRCm39) |
E1703V |
probably damaging |
Het |
Rev3l |
G |
T |
10: 39,700,611 (GRCm39) |
E1703* |
probably null |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Saal1 |
T |
C |
7: 46,342,340 (GRCm39) |
K368E |
probably damaging |
Het |
Scn9a |
C |
T |
2: 66,335,220 (GRCm39) |
W1245* |
probably null |
Het |
Slc38a11 |
T |
A |
2: 65,147,315 (GRCm39) |
L387F |
probably damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Sptb |
C |
A |
12: 76,667,641 (GRCm39) |
V819L |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,086,124 (GRCm39) |
T1195A |
probably benign |
Het |
Ssna1 |
C |
A |
2: 25,162,024 (GRCm39) |
V57F |
possibly damaging |
Het |
Stk32a |
G |
T |
18: 43,446,485 (GRCm39) |
E312* |
probably null |
Het |
Synpo |
A |
G |
18: 60,736,459 (GRCm39) |
F496L |
probably benign |
Het |
Syt15 |
C |
T |
14: 33,944,858 (GRCm39) |
T135M |
probably benign |
Het |
Tm9sf4 |
A |
G |
2: 153,032,832 (GRCm39) |
E246G |
probably benign |
Het |
Trim44 |
T |
C |
2: 102,187,830 (GRCm39) |
M308V |
possibly damaging |
Het |
Unc119b |
T |
A |
5: 115,272,885 (GRCm39) |
K29* |
probably null |
Het |
Vim |
T |
A |
2: 13,584,921 (GRCm39) |
D367E |
probably benign |
Het |
Virma |
T |
A |
4: 11,494,814 (GRCm39) |
N38K |
probably damaging |
Het |
Vmn1r228 |
A |
T |
17: 20,996,560 (GRCm39) |
D319E |
possibly damaging |
Het |
Vmn2r32 |
T |
A |
7: 7,466,991 (GRCm39) |
I846F |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,576,667 (GRCm39) |
V1025A |
probably benign |
Het |
Vps13c |
G |
T |
9: 67,879,357 (GRCm39) |
E566* |
probably null |
Het |
|
Other mutations in Mprip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Mprip
|
APN |
11 |
59,639,417 (GRCm39) |
missense |
probably benign |
0.07 |
IGL00563:Mprip
|
APN |
11 |
59,643,443 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00905:Mprip
|
APN |
11 |
59,662,994 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00928:Mprip
|
APN |
11 |
59,635,578 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01161:Mprip
|
APN |
11 |
59,622,399 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01991:Mprip
|
APN |
11 |
59,645,838 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02491:Mprip
|
APN |
11 |
59,660,857 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03030:Mprip
|
APN |
11 |
59,631,941 (GRCm39) |
splice site |
probably null |
|
IGL03056:Mprip
|
APN |
11 |
59,662,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03293:Mprip
|
APN |
11 |
59,586,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Mprip
|
UTSW |
11 |
59,657,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R0097:Mprip
|
UTSW |
11 |
59,649,317 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0097:Mprip
|
UTSW |
11 |
59,649,317 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0147:Mprip
|
UTSW |
11 |
59,627,899 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0319:Mprip
|
UTSW |
11 |
59,587,864 (GRCm39) |
splice site |
probably benign |
|
R0471:Mprip
|
UTSW |
11 |
59,650,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Mprip
|
UTSW |
11 |
59,631,943 (GRCm39) |
splice site |
probably benign |
|
R0627:Mprip
|
UTSW |
11 |
59,660,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:Mprip
|
UTSW |
11 |
59,649,587 (GRCm39) |
missense |
probably benign |
|
R1218:Mprip
|
UTSW |
11 |
59,634,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Mprip
|
UTSW |
11 |
59,650,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Mprip
|
UTSW |
11 |
59,650,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R1698:Mprip
|
UTSW |
11 |
59,651,084 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1802:Mprip
|
UTSW |
11 |
59,645,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1837:Mprip
|
UTSW |
11 |
59,657,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R1862:Mprip
|
UTSW |
11 |
59,649,047 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2094:Mprip
|
UTSW |
11 |
59,640,334 (GRCm39) |
splice site |
probably benign |
|
R2107:Mprip
|
UTSW |
11 |
59,660,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Mprip
|
UTSW |
11 |
59,660,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Mprip
|
UTSW |
11 |
59,640,334 (GRCm39) |
splice site |
probably benign |
|
R3003:Mprip
|
UTSW |
11 |
59,618,381 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3115:Mprip
|
UTSW |
11 |
59,656,229 (GRCm39) |
splice site |
probably null |
|
R3941:Mprip
|
UTSW |
11 |
59,622,328 (GRCm39) |
splice site |
probably benign |
|
R4347:Mprip
|
UTSW |
11 |
59,650,279 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4603:Mprip
|
UTSW |
11 |
59,622,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Mprip
|
UTSW |
11 |
59,648,846 (GRCm39) |
missense |
probably benign |
0.00 |
R5011:Mprip
|
UTSW |
11 |
59,650,721 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5338:Mprip
|
UTSW |
11 |
59,651,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R5549:Mprip
|
UTSW |
11 |
59,651,644 (GRCm39) |
missense |
probably benign |
0.00 |
R5569:Mprip
|
UTSW |
11 |
59,651,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Mprip
|
UTSW |
11 |
59,649,293 (GRCm39) |
missense |
probably benign |
|
R5615:Mprip
|
UTSW |
11 |
59,649,313 (GRCm39) |
missense |
probably benign |
0.08 |
R5846:Mprip
|
UTSW |
11 |
59,649,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R5970:Mprip
|
UTSW |
11 |
59,648,547 (GRCm39) |
missense |
probably damaging |
0.96 |
R6054:Mprip
|
UTSW |
11 |
59,649,251 (GRCm39) |
missense |
probably benign |
|
R6452:Mprip
|
UTSW |
11 |
59,643,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6457:Mprip
|
UTSW |
11 |
59,649,815 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6544:Mprip
|
UTSW |
11 |
59,648,552 (GRCm39) |
missense |
probably benign |
0.15 |
R6750:Mprip
|
UTSW |
11 |
59,586,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6843:Mprip
|
UTSW |
11 |
59,650,554 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6851:Mprip
|
UTSW |
11 |
59,649,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R6867:Mprip
|
UTSW |
11 |
59,640,456 (GRCm39) |
critical splice donor site |
probably null |
|
R7002:Mprip
|
UTSW |
11 |
59,652,016 (GRCm39) |
missense |
probably benign |
0.22 |
R7023:Mprip
|
UTSW |
11 |
59,628,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7764:Mprip
|
UTSW |
11 |
59,655,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R7765:Mprip
|
UTSW |
11 |
59,649,047 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7828:Mprip
|
UTSW |
11 |
59,627,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7866:Mprip
|
UTSW |
11 |
59,643,756 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7911:Mprip
|
UTSW |
11 |
59,651,681 (GRCm39) |
missense |
|
|
R7979:Mprip
|
UTSW |
11 |
59,657,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8292:Mprip
|
UTSW |
11 |
59,650,340 (GRCm39) |
missense |
probably benign |
0.21 |
R8481:Mprip
|
UTSW |
11 |
59,648,982 (GRCm39) |
nonsense |
probably null |
|
R8717:Mprip
|
UTSW |
11 |
59,650,526 (GRCm39) |
missense |
probably benign |
|
R8810:Mprip
|
UTSW |
11 |
59,587,851 (GRCm39) |
critical splice donor site |
probably benign |
|
R8981:Mprip
|
UTSW |
11 |
59,622,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9214:Mprip
|
UTSW |
11 |
59,650,901 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9245:Mprip
|
UTSW |
11 |
59,628,403 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9748:Mprip
|
UTSW |
11 |
59,656,348 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mprip
|
UTSW |
11 |
59,650,310 (GRCm39) |
missense |
probably benign |
0.05 |
Z1176:Mprip
|
UTSW |
11 |
59,628,230 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Mprip
|
UTSW |
11 |
59,648,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGAATAGCGGAGGCTCTTTTCCC -3'
(R):5'- AATGGTGTCCAGCATCCCAAAGCG -3'
Sequencing Primer
(F):5'- CAACTAGGTTTGAGTTCTCCAAGG -3'
(R):5'- TGGCTCGGCTTCAAGACAC -3'
|
Posted On |
2014-05-14 |