Incidental Mutation 'R8815:Ptprf'
ID |
672654 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ptprf
|
Ensembl Gene |
ENSMUSG00000033295 |
Gene Name |
protein tyrosine phosphatase receptor type F |
Synonyms |
RPTP-LAR, LAR |
MMRRC Submission |
068650-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.657)
|
Stock # |
R8815 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
118065410-118148602 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 118095125 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Leucine
at position 254
(V254L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000039368
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049074]
[ENSMUST00000222620]
|
AlphaFold |
A2A8L5 |
PDB Structure |
Tandem Ig domains of tyrosine phosphatase LAR [X-RAY DIFFRACTION]
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000049074
AA Change: V254L
PolyPhen 2
Score 0.523 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000039368 Gene: ENSMUSG00000033295 AA Change: V254L
Domain | Start | End | E-Value | Type |
IGc2
|
45 |
114 |
2.64e-12 |
SMART |
IGc2
|
147 |
214 |
1.48e-15 |
SMART |
IG
|
238 |
316 |
1.06e-11 |
SMART |
FN3
|
319 |
398 |
6.9e-14 |
SMART |
FN3
|
414 |
497 |
5.73e-11 |
SMART |
FN3
|
512 |
591 |
4.06e-11 |
SMART |
FN3
|
606 |
693 |
8.69e-11 |
SMART |
FN3
|
709 |
797 |
8.83e-12 |
SMART |
FN3
|
812 |
892 |
3.2e-9 |
SMART |
FN3
|
907 |
988 |
2.53e-12 |
SMART |
FN3
|
1003 |
1079 |
3.48e-1 |
SMART |
coiled coil region
|
1146 |
1175 |
N/A |
INTRINSIC |
transmembrane domain
|
1253 |
1275 |
N/A |
INTRINSIC |
PTPc
|
1342 |
1600 |
1.12e-138 |
SMART |
PTPc
|
1629 |
1891 |
3.4e-129 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000124758
|
SMART Domains |
Protein: ENSMUSP00000119954 Gene: ENSMUSG00000033295
Domain | Start | End | E-Value | Type |
FN3
|
37 |
116 |
4.06e-11 |
SMART |
FN3
|
132 |
220 |
8.83e-12 |
SMART |
FN3
|
235 |
315 |
3.2e-9 |
SMART |
FN3
|
330 |
411 |
2.53e-12 |
SMART |
FN3
|
426 |
502 |
3.48e-1 |
SMART |
coiled coil region
|
568 |
597 |
N/A |
INTRINSIC |
transmembrane domain
|
676 |
698 |
N/A |
INTRINSIC |
PTPc
|
776 |
1034 |
1.12e-138 |
SMART |
PTPc
|
1063 |
1325 |
3.4e-129 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000150096
|
SMART Domains |
Protein: ENSMUSP00000117313 Gene: ENSMUSG00000033295
Domain | Start | End | E-Value | Type |
FN3
|
14 |
66 |
2.7e1 |
SMART |
FN3
|
82 |
165 |
5.73e-11 |
SMART |
FN3
|
180 |
259 |
4.06e-11 |
SMART |
FN3
|
275 |
372 |
6.69e-12 |
SMART |
FN3
|
385 |
461 |
2.83e-1 |
SMART |
coiled coil region
|
527 |
556 |
N/A |
INTRINSIC |
transmembrane domain
|
635 |
657 |
N/A |
INTRINSIC |
PTPc
|
735 |
993 |
1.12e-138 |
SMART |
PTPc
|
1022 |
1284 |
3.4e-129 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000222620
AA Change: V260L
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.8%
- 20x: 99.3%
|
Validation Efficiency |
99% (70/71) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains three Ig-like domains, and nine non-Ig like domains similar to that of neural-cell adhesion molecule. This PTP was shown to function in the regulation of epithelial cell-cell contacts at adherents junctions, as well as in the control of beta-catenin signaling. An increased expression level of this protein was found in the insulin-responsive tissue of obese, insulin-resistant individuals, and may contribute to the pathogenesis of insulin resistance. Two alternatively spliced transcript variants of this gene, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008] PHENOTYPE: Homozygous null females have premature involution of the mammary glands leading to an inability to feed pups. Other characteristics of null mice include defective nerve regeneration and hyperactivity. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
A |
T |
1: 57,421,943 (GRCm39) |
Q106H |
probably damaging |
Het |
Acad9 |
T |
C |
3: 36,139,590 (GRCm39) |
C397R |
probably damaging |
Het |
Ankfn1 |
T |
G |
11: 89,282,602 (GRCm39) |
R348S |
probably damaging |
Het |
Ankrd61 |
A |
G |
5: 143,831,336 (GRCm39) |
C28R |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,194,548 (GRCm39) |
R94* |
probably null |
Het |
Apela |
A |
T |
8: 65,489,590 (GRCm39) |
F10I |
unknown |
Het |
Arhgap31 |
T |
C |
16: 38,429,790 (GRCm39) |
S362G |
probably benign |
Het |
Arhgef18 |
C |
A |
8: 3,430,410 (GRCm39) |
H94Q |
probably benign |
Het |
Astn2 |
A |
T |
4: 65,830,834 (GRCm39) |
L585Q |
possibly damaging |
Het |
Atf3 |
G |
T |
1: 190,909,564 (GRCm39) |
A35D |
probably benign |
Het |
Atp10b |
A |
T |
11: 43,093,978 (GRCm39) |
R507S |
possibly damaging |
Het |
Brip1 |
A |
C |
11: 86,080,598 (GRCm39) |
V156G |
probably benign |
Het |
Ccdc27 |
T |
A |
4: 154,111,205 (GRCm39) |
M636L |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,493,285 (GRCm39) |
N769K |
possibly damaging |
Het |
Cklf |
C |
T |
8: 104,977,560 (GRCm39) |
|
probably benign |
Het |
Cpeb4 |
G |
A |
11: 31,870,546 (GRCm39) |
V474M |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,673,834 (GRCm39) |
C1091* |
probably null |
Het |
Eef1akmt4 |
T |
A |
16: 20,437,288 (GRCm39) |
I210N |
possibly damaging |
Het |
Fbxo38 |
A |
T |
18: 62,666,587 (GRCm39) |
H195Q |
probably damaging |
Het |
Fbxw14 |
G |
A |
9: 109,105,305 (GRCm39) |
R287* |
probably null |
Het |
Fes |
A |
G |
7: 80,033,619 (GRCm39) |
S211P |
possibly damaging |
Het |
Fry |
G |
T |
5: 150,317,603 (GRCm39) |
R861L |
possibly damaging |
Het |
Galnt12 |
A |
G |
4: 47,113,908 (GRCm39) |
|
probably benign |
Het |
Gm14226 |
G |
A |
2: 154,866,538 (GRCm39) |
W165* |
probably null |
Het |
Gm40460 |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
GCAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAGCAGGGCTTACAGCAGCTGGACTGGCAGCAG |
7: 141,794,171 (GRCm39) |
|
probably benign |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Gprc6a |
A |
G |
10: 51,497,079 (GRCm39) |
V488A |
probably benign |
Het |
Haus8 |
A |
T |
8: 71,705,910 (GRCm39) |
|
probably benign |
Het |
Helb |
A |
T |
10: 119,948,692 (GRCm39) |
C26S |
possibly damaging |
Het |
Icam1 |
A |
T |
9: 20,937,862 (GRCm39) |
I300F |
probably benign |
Het |
Ip6k1 |
A |
G |
9: 107,918,211 (GRCm39) |
N181S |
probably benign |
Het |
Itga2b |
C |
A |
11: 102,351,687 (GRCm39) |
R546L |
possibly damaging |
Het |
Kif27 |
A |
T |
13: 58,476,818 (GRCm39) |
Y611N |
probably damaging |
Het |
Lpcat2 |
A |
G |
8: 93,640,979 (GRCm39) |
I475V |
possibly damaging |
Het |
Lrit2 |
A |
G |
14: 36,794,487 (GRCm39) |
K517R |
probably benign |
Het |
Lrp1b |
A |
T |
2: 40,555,171 (GRCm39) |
I4085N |
|
Het |
Lrrc32 |
T |
A |
7: 98,148,242 (GRCm39) |
S341T |
probably damaging |
Het |
Lrrn2 |
T |
A |
1: 132,866,831 (GRCm39) |
I632K |
possibly damaging |
Het |
Mettl22 |
A |
G |
16: 8,300,178 (GRCm39) |
Q194R |
probably benign |
Het |
Mfhas1 |
T |
A |
8: 36,057,394 (GRCm39) |
V623E |
probably damaging |
Het |
Mitd1 |
T |
C |
1: 37,929,315 (GRCm39) |
D26G |
probably damaging |
Het |
Myo1a |
C |
T |
10: 127,546,043 (GRCm39) |
T222M |
probably benign |
Het |
Naf1 |
A |
G |
8: 67,317,333 (GRCm39) |
K275R |
possibly damaging |
Het |
Nf1 |
T |
C |
11: 79,332,491 (GRCm39) |
L765P |
probably damaging |
Het |
Or12k7 |
G |
T |
2: 36,958,429 (GRCm39) |
M37I |
probably benign |
Het |
Or52a5 |
A |
G |
7: 103,427,063 (GRCm39) |
L163P |
possibly damaging |
Het |
Or5ac16 |
T |
A |
16: 59,022,264 (GRCm39) |
H175L |
possibly damaging |
Het |
Or9r3 |
T |
A |
10: 129,947,808 (GRCm39) |
I284F |
probably damaging |
Het |
Pappa |
A |
G |
4: 65,099,347 (GRCm39) |
H622R |
probably benign |
Het |
Pcdhb4 |
A |
T |
18: 37,442,055 (GRCm39) |
Y455F |
probably damaging |
Het |
Pepd |
A |
G |
7: 34,671,116 (GRCm39) |
Y220C |
probably damaging |
Het |
Pias3 |
T |
C |
3: 96,607,381 (GRCm39) |
I172T |
probably damaging |
Het |
Polq |
T |
A |
16: 36,853,893 (GRCm39) |
H415Q |
probably damaging |
Het |
Pp2d1 |
A |
T |
17: 53,814,897 (GRCm39) |
M609K |
probably benign |
Het |
Ppm1m |
G |
A |
9: 106,076,237 (GRCm39) |
|
probably benign |
Het |
Prss22 |
T |
A |
17: 24,215,662 (GRCm39) |
T87S |
probably benign |
Het |
Ripply3 |
A |
G |
16: 94,136,723 (GRCm39) |
E128G |
possibly damaging |
Het |
Rrm2 |
A |
C |
12: 24,760,470 (GRCm39) |
I185L |
possibly damaging |
Het |
Sbsn |
T |
A |
7: 30,454,227 (GRCm39) |
|
probably benign |
Het |
Sdc3 |
T |
A |
4: 130,546,336 (GRCm39) |
S232T |
probably benign |
Het |
Slx4 |
G |
C |
16: 3,803,458 (GRCm39) |
P1119A |
probably benign |
Het |
Smc5 |
C |
T |
19: 23,221,422 (GRCm39) |
R369Q |
probably damaging |
Het |
Speer4a3 |
A |
G |
5: 26,158,191 (GRCm39) |
S54P |
probably damaging |
Het |
Spns1 |
G |
A |
7: 125,971,593 (GRCm39) |
S319F |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,106,657 (GRCm39) |
Q924* |
probably null |
Het |
Srcap |
G |
C |
7: 127,158,037 (GRCm39) |
D2638H |
unknown |
Het |
Srsf12 |
T |
C |
4: 33,226,045 (GRCm39) |
S103P |
possibly damaging |
Het |
Tanc1 |
A |
G |
2: 59,621,185 (GRCm39) |
T335A |
possibly damaging |
Het |
Them4 |
C |
T |
3: 94,231,610 (GRCm39) |
T149I |
probably damaging |
Het |
Trpc7 |
T |
C |
13: 56,970,312 (GRCm39) |
Y424C |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,628,364 (GRCm39) |
D14599N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,698,244 (GRCm39) |
L186H |
|
Het |
Usp17lc |
T |
C |
7: 103,067,524 (GRCm39) |
F273S |
probably benign |
Het |
Vwa5b2 |
T |
C |
16: 20,419,516 (GRCm39) |
S620P |
probably damaging |
Het |
|
Other mutations in Ptprf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Ptprf
|
APN |
4 |
118,080,417 (GRCm39) |
splice site |
probably benign |
|
IGL01337:Ptprf
|
APN |
4 |
118,093,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01482:Ptprf
|
APN |
4 |
118,069,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01743:Ptprf
|
APN |
4 |
118,106,095 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01987:Ptprf
|
APN |
4 |
118,134,567 (GRCm39) |
missense |
probably benign |
|
IGL02189:Ptprf
|
APN |
4 |
118,070,839 (GRCm39) |
splice site |
probably benign |
|
IGL03067:Ptprf
|
APN |
4 |
118,067,910 (GRCm39) |
missense |
possibly damaging |
0.67 |
PIT4677001:Ptprf
|
UTSW |
4 |
118,070,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0382:Ptprf
|
UTSW |
4 |
118,080,591 (GRCm39) |
splice site |
probably benign |
|
R0788:Ptprf
|
UTSW |
4 |
118,083,663 (GRCm39) |
missense |
probably damaging |
0.97 |
R1164:Ptprf
|
UTSW |
4 |
118,114,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Ptprf
|
UTSW |
4 |
118,069,302 (GRCm39) |
nonsense |
probably null |
|
R1483:Ptprf
|
UTSW |
4 |
118,093,161 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1611:Ptprf
|
UTSW |
4 |
118,093,430 (GRCm39) |
missense |
probably benign |
0.34 |
R1721:Ptprf
|
UTSW |
4 |
118,082,096 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1817:Ptprf
|
UTSW |
4 |
118,080,462 (GRCm39) |
missense |
probably benign |
0.02 |
R1818:Ptprf
|
UTSW |
4 |
118,067,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Ptprf
|
UTSW |
4 |
118,081,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R2208:Ptprf
|
UTSW |
4 |
118,126,369 (GRCm39) |
splice site |
probably benign |
|
R2406:Ptprf
|
UTSW |
4 |
118,126,501 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2912:Ptprf
|
UTSW |
4 |
118,106,177 (GRCm39) |
missense |
probably damaging |
0.98 |
R3111:Ptprf
|
UTSW |
4 |
118,068,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R3498:Ptprf
|
UTSW |
4 |
118,082,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R3499:Ptprf
|
UTSW |
4 |
118,082,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R3615:Ptprf
|
UTSW |
4 |
118,095,080 (GRCm39) |
missense |
probably benign |
0.04 |
R3616:Ptprf
|
UTSW |
4 |
118,095,080 (GRCm39) |
missense |
probably benign |
0.04 |
R4038:Ptprf
|
UTSW |
4 |
118,114,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R4243:Ptprf
|
UTSW |
4 |
118,083,649 (GRCm39) |
critical splice donor site |
probably null |
|
R4260:Ptprf
|
UTSW |
4 |
118,083,280 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4693:Ptprf
|
UTSW |
4 |
118,068,219 (GRCm39) |
missense |
probably benign |
0.16 |
R4726:Ptprf
|
UTSW |
4 |
118,069,414 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4746:Ptprf
|
UTSW |
4 |
118,082,236 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4802:Ptprf
|
UTSW |
4 |
118,067,526 (GRCm39) |
intron |
probably benign |
|
R4857:Ptprf
|
UTSW |
4 |
118,074,394 (GRCm39) |
splice site |
probably benign |
|
R5071:Ptprf
|
UTSW |
4 |
118,069,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5221:Ptprf
|
UTSW |
4 |
118,082,305 (GRCm39) |
missense |
probably benign |
0.00 |
R5327:Ptprf
|
UTSW |
4 |
118,093,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Ptprf
|
UTSW |
4 |
118,092,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Ptprf
|
UTSW |
4 |
118,083,535 (GRCm39) |
missense |
probably benign |
0.00 |
R5373:Ptprf
|
UTSW |
4 |
118,083,238 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5555:Ptprf
|
UTSW |
4 |
118,082,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5693:Ptprf
|
UTSW |
4 |
118,093,374 (GRCm39) |
nonsense |
probably null |
|
R5860:Ptprf
|
UTSW |
4 |
118,068,486 (GRCm39) |
intron |
probably benign |
|
R5869:Ptprf
|
UTSW |
4 |
118,067,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Ptprf
|
UTSW |
4 |
118,081,932 (GRCm39) |
missense |
probably benign |
|
R5932:Ptprf
|
UTSW |
4 |
118,068,964 (GRCm39) |
missense |
probably benign |
0.10 |
R6028:Ptprf
|
UTSW |
4 |
118,070,826 (GRCm39) |
missense |
probably benign |
0.01 |
R6030:Ptprf
|
UTSW |
4 |
118,068,245 (GRCm39) |
missense |
probably benign |
0.19 |
R6030:Ptprf
|
UTSW |
4 |
118,068,245 (GRCm39) |
missense |
probably benign |
0.19 |
R6088:Ptprf
|
UTSW |
4 |
118,067,952 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6089:Ptprf
|
UTSW |
4 |
118,068,281 (GRCm39) |
missense |
probably damaging |
0.99 |
R6108:Ptprf
|
UTSW |
4 |
118,080,453 (GRCm39) |
missense |
probably benign |
0.01 |
R6320:Ptprf
|
UTSW |
4 |
118,070,011 (GRCm39) |
missense |
probably benign |
|
R6741:Ptprf
|
UTSW |
4 |
118,080,565 (GRCm39) |
missense |
probably benign |
0.00 |
R6744:Ptprf
|
UTSW |
4 |
118,093,562 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Ptprf
|
UTSW |
4 |
118,088,928 (GRCm39) |
missense |
probably benign |
0.03 |
R6906:Ptprf
|
UTSW |
4 |
118,126,474 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7021:Ptprf
|
UTSW |
4 |
118,081,101 (GRCm39) |
missense |
probably benign |
0.00 |
R7153:Ptprf
|
UTSW |
4 |
118,088,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ptprf
|
UTSW |
4 |
118,088,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R7337:Ptprf
|
UTSW |
4 |
118,068,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R7374:Ptprf
|
UTSW |
4 |
118,114,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Ptprf
|
UTSW |
4 |
118,070,011 (GRCm39) |
missense |
probably benign |
|
R7399:Ptprf
|
UTSW |
4 |
118,083,720 (GRCm39) |
missense |
probably benign |
0.28 |
R7417:Ptprf
|
UTSW |
4 |
118,069,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Ptprf
|
UTSW |
4 |
118,092,864 (GRCm39) |
missense |
probably benign |
0.03 |
R7530:Ptprf
|
UTSW |
4 |
118,069,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Ptprf
|
UTSW |
4 |
118,069,593 (GRCm39) |
missense |
probably benign |
0.00 |
R8172:Ptprf
|
UTSW |
4 |
118,068,275 (GRCm39) |
missense |
probably benign |
0.03 |
R8239:Ptprf
|
UTSW |
4 |
118,069,309 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8257:Ptprf
|
UTSW |
4 |
118,083,476 (GRCm39) |
missense |
probably damaging |
0.96 |
R8331:Ptprf
|
UTSW |
4 |
118,083,263 (GRCm39) |
missense |
probably benign |
0.27 |
R8441:Ptprf
|
UTSW |
4 |
118,075,255 (GRCm39) |
splice site |
probably benign |
|
R8681:Ptprf
|
UTSW |
4 |
118,088,844 (GRCm39) |
missense |
probably benign |
0.02 |
R8771:Ptprf
|
UTSW |
4 |
118,068,987 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8998:Ptprf
|
UTSW |
4 |
118,083,671 (GRCm39) |
missense |
probably benign |
0.00 |
R8999:Ptprf
|
UTSW |
4 |
118,083,671 (GRCm39) |
missense |
probably benign |
0.00 |
R9389:Ptprf
|
UTSW |
4 |
118,093,236 (GRCm39) |
missense |
probably benign |
|
R9508:Ptprf
|
UTSW |
4 |
118,126,776 (GRCm39) |
nonsense |
probably null |
|
R9581:Ptprf
|
UTSW |
4 |
118,092,257 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Ptprf
|
UTSW |
4 |
118,093,223 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Ptprf
|
UTSW |
4 |
118,126,812 (GRCm39) |
missense |
probably benign |
0.04 |
|
Predicted Primers |
PCR Primer
(F):5'- ACAGGCCTGAGGATCTAAAGCC -3'
(R):5'- AGAGGCTTCCTTGATGAGGG -3'
Sequencing Primer
(F):5'- TAGCTGAGGCACCGCTACAC -3'
(R):5'- TTCCTTGATGAGGGGCCCC -3'
|
Posted On |
2021-04-30 |