Incidental Mutation 'R7134:Ptprj'
ID |
552884 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ptprj
|
Ensembl Gene |
ENSMUSG00000025314 |
Gene Name |
protein tyrosine phosphatase receptor type J |
Synonyms |
Byp, RPTPJ, Scc1, CD148, DEP-1, Scc-1 |
MMRRC Submission |
045219-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.223)
|
Stock # |
R7134 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
90260098-90410939 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 90294822 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Histidine
at position 462
(L462H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129592
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000111493]
[ENSMUST00000111495]
[ENSMUST00000168621]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000111493
AA Change: L276H
PolyPhen 2
Score 0.244 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000107119 Gene: ENSMUSG00000025314 AA Change: L276H
Domain | Start | End | E-Value | Type |
low complexity region
|
34 |
46 |
N/A |
INTRINSIC |
FN3
|
47 |
182 |
3.76e-6 |
SMART |
FN3
|
194 |
271 |
4.56e-5 |
SMART |
FN3
|
282 |
357 |
5.32e-6 |
SMART |
FN3
|
368 |
446 |
2.19e-7 |
SMART |
FN3
|
455 |
531 |
5e-2 |
SMART |
FN3
|
546 |
628 |
2.77e1 |
SMART |
low complexity region
|
637 |
650 |
N/A |
INTRINSIC |
Blast:PTPc
|
714 |
797 |
8e-26 |
BLAST |
PTPc
|
867 |
1127 |
3.37e-133 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000111495
AA Change: L369H
PolyPhen 2
Score 0.313 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000107121 Gene: ENSMUSG00000025314 AA Change: L369H
Domain | Start | End | E-Value | Type |
low complexity region
|
14 |
25 |
N/A |
INTRINSIC |
FN3
|
59 |
131 |
2.85e-6 |
SMART |
FN3
|
140 |
275 |
3.76e-6 |
SMART |
FN3
|
287 |
364 |
4.56e-5 |
SMART |
FN3
|
375 |
450 |
5.32e-6 |
SMART |
FN3
|
461 |
539 |
2.19e-7 |
SMART |
FN3
|
548 |
624 |
5e-2 |
SMART |
FN3
|
639 |
721 |
2.77e1 |
SMART |
low complexity region
|
730 |
743 |
N/A |
INTRINSIC |
Blast:PTPc
|
807 |
890 |
1e-25 |
BLAST |
PTPc
|
960 |
1220 |
3.37e-133 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000168621
AA Change: L462H
PolyPhen 2
Score 0.158 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000129592 Gene: ENSMUSG00000025314 AA Change: L462H
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
16 |
N/A |
INTRINSIC |
low complexity region
|
26 |
94 |
N/A |
INTRINSIC |
low complexity region
|
133 |
140 |
N/A |
INTRINSIC |
FN3
|
152 |
224 |
2.85e-6 |
SMART |
FN3
|
233 |
368 |
3.76e-6 |
SMART |
FN3
|
380 |
457 |
4.56e-5 |
SMART |
FN3
|
468 |
543 |
5.32e-6 |
SMART |
FN3
|
554 |
632 |
2.19e-7 |
SMART |
FN3
|
641 |
717 |
5e-2 |
SMART |
FN3
|
732 |
814 |
2.77e1 |
SMART |
low complexity region
|
823 |
836 |
N/A |
INTRINSIC |
Blast:PTPc
|
900 |
983 |
1e-25 |
BLAST |
PTPc
|
1053 |
1313 |
3.37e-133 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
99% (84/85) |
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 containing five fibronectin type III repeats, a single transmembrane region, and a single intracytoplasmic catalytic domain, and thus represents a receptor-type PTP. This protein is present in all hematopoietic lineages, and was shown to negatively regulate T cell receptor signaling possibly through interfering with the phosphorylation of Phospholipase C Gamma 1 and Linker for Activation of T Cells. This protein can also dephosphorylate the PDGF beta receptor, and may be involved in UV-induced signal transduction. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a null allele die in utero displaying severe growth retardation and cardiovascular defects. Homozygotes for a second null allele are viable, fertile and healthy with no spontaneous tumor formation. Homozygotes for a third null allele show sterility and a block B cell development. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf1 |
A |
G |
17: 36,270,144 (GRCm39) |
F638S |
possibly damaging |
Het |
Actl6b |
T |
A |
5: 137,562,762 (GRCm39) |
N159K |
probably damaging |
Het |
Adam6a |
T |
G |
12: 113,508,655 (GRCm39) |
S343A |
probably benign |
Het |
Ankrd17 |
G |
A |
5: 90,380,173 (GRCm39) |
T2505I |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,433,382 (GRCm39) |
T728A |
probably benign |
Het |
Asap2 |
G |
T |
12: 21,315,964 (GRCm39) |
E919* |
probably null |
Het |
Atp10b |
A |
T |
11: 43,136,291 (GRCm39) |
I1140F |
probably damaging |
Het |
Cep126 |
A |
T |
9: 8,103,383 (GRCm39) |
V209E |
probably damaging |
Het |
Cfap65 |
C |
T |
1: 74,965,792 (GRCm39) |
R406Q |
probably benign |
Het |
Cldn1 |
T |
C |
16: 26,190,376 (GRCm39) |
M1V |
probably null |
Het |
Cryl1 |
C |
T |
14: 57,512,956 (GRCm39) |
D304N |
probably benign |
Het |
D3Ertd751e |
T |
C |
3: 41,708,212 (GRCm39) |
|
probably null |
Het |
D630044L22Rik |
A |
T |
17: 26,181,090 (GRCm39) |
M156L |
probably benign |
Het |
Ddx21 |
T |
C |
10: 62,427,634 (GRCm39) |
D423G |
possibly damaging |
Het |
Dock2 |
T |
A |
11: 34,260,363 (GRCm39) |
M993L |
probably benign |
Het |
Dusp29 |
A |
T |
14: 21,727,129 (GRCm39) |
I173N |
probably damaging |
Het |
Eif4g1 |
C |
T |
16: 20,500,252 (GRCm39) |
A675V |
probably damaging |
Het |
Eml1 |
C |
T |
12: 108,472,810 (GRCm39) |
S206L |
probably benign |
Het |
Farp2 |
A |
C |
1: 93,531,181 (GRCm39) |
I560L |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,223,969 (GRCm39) |
D593E |
probably benign |
Het |
Fetub |
A |
G |
16: 22,748,007 (GRCm39) |
D61G |
possibly damaging |
Het |
Fpgs |
T |
C |
2: 32,576,641 (GRCm39) |
K329E |
probably benign |
Het |
Fpgt |
T |
C |
3: 154,797,120 (GRCm39) |
Y45C |
probably damaging |
Het |
Gas2l1 |
A |
T |
11: 5,011,106 (GRCm39) |
C574* |
probably null |
Het |
Gm9747 |
G |
T |
1: 82,211,837 (GRCm39) |
C12F |
unknown |
Het |
H2-T23 |
T |
C |
17: 36,342,709 (GRCm39) |
Y143C |
probably damaging |
Het |
Hhip |
A |
T |
8: 80,719,142 (GRCm39) |
S462T |
probably benign |
Het |
Hnf1a |
C |
T |
5: 115,091,446 (GRCm39) |
G416R |
probably damaging |
Het |
Hoxa5 |
C |
T |
6: 52,181,023 (GRCm39) |
C103Y |
probably damaging |
Het |
Kansl3 |
G |
T |
1: 36,390,848 (GRCm39) |
D395E |
possibly damaging |
Het |
Marchf10 |
A |
G |
11: 105,299,502 (GRCm39) |
S116P |
probably benign |
Het |
Med12l |
C |
T |
3: 59,001,180 (GRCm39) |
Q748* |
probably null |
Het |
Mroh7 |
T |
A |
4: 106,577,791 (GRCm39) |
N296Y |
probably damaging |
Het |
Mtbp |
T |
G |
15: 55,421,961 (GRCm39) |
D61E |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,411,391 (GRCm39) |
I1446L |
unknown |
Het |
Myh15 |
T |
C |
16: 48,901,705 (GRCm39) |
V266A |
possibly damaging |
Het |
Nap1l1 |
G |
A |
10: 111,330,655 (GRCm39) |
|
probably null |
Het |
Napsa |
A |
G |
7: 44,235,159 (GRCm39) |
T315A |
probably benign |
Het |
Nlrc5 |
A |
T |
8: 95,206,350 (GRCm39) |
I734F |
probably damaging |
Het |
Nnt |
A |
G |
13: 119,531,198 (GRCm39) |
V183A |
probably damaging |
Het |
Nploc4 |
A |
T |
11: 120,276,614 (GRCm39) |
D477E |
probably benign |
Het |
Nrip3 |
A |
G |
7: 109,364,695 (GRCm39) |
S144P |
probably damaging |
Het |
Ntng1 |
A |
T |
3: 109,842,445 (GRCm39) |
F109L |
probably benign |
Het |
Or5p61 |
A |
G |
7: 107,758,883 (GRCm39) |
Y66H |
probably damaging |
Het |
Or5v1 |
T |
A |
17: 37,809,776 (GRCm39) |
V78D |
probably damaging |
Het |
Or6aa1 |
G |
A |
7: 86,044,752 (GRCm39) |
|
probably benign |
Het |
Or8b36 |
A |
G |
9: 37,937,795 (GRCm39) |
E231G |
probably benign |
Het |
Pacsin1 |
G |
A |
17: 27,921,707 (GRCm39) |
D30N |
probably damaging |
Het |
Pbld2 |
A |
T |
10: 62,860,368 (GRCm39) |
|
probably benign |
Het |
Pcnx4 |
C |
T |
12: 72,613,750 (GRCm39) |
T565I |
probably damaging |
Het |
Pdzk1 |
A |
T |
3: 96,763,246 (GRCm39) |
T225S |
probably benign |
Het |
Phyhip |
T |
G |
14: 70,704,639 (GRCm39) |
I286S |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,813,086 (GRCm39) |
Y3903N |
probably damaging |
Het |
Plcb3 |
A |
T |
19: 6,942,698 (GRCm39) |
L222Q |
probably damaging |
Het |
Plcd4 |
T |
A |
1: 74,593,662 (GRCm39) |
H262Q |
probably benign |
Het |
Plekhh1 |
C |
T |
12: 79,109,390 (GRCm39) |
A474V |
probably benign |
Het |
Plppr3 |
T |
C |
10: 79,701,537 (GRCm39) |
E435G |
probably damaging |
Het |
Poln |
T |
A |
5: 34,276,340 (GRCm39) |
N305I |
possibly damaging |
Het |
Pou3f2 |
T |
C |
4: 22,486,874 (GRCm39) |
T420A |
probably benign |
Het |
Ppdpf |
T |
C |
2: 180,829,523 (GRCm39) |
Y17H |
probably damaging |
Het |
Prrx2 |
C |
A |
2: 30,768,485 (GRCm39) |
T104K |
probably damaging |
Het |
Radil |
T |
C |
5: 142,471,304 (GRCm39) |
T991A |
probably damaging |
Het |
Rbsn |
T |
C |
6: 92,178,608 (GRCm39) |
E147G |
probably damaging |
Het |
Ror2 |
C |
T |
13: 53,300,742 (GRCm39) |
V35M |
probably benign |
Het |
Rps6ka1 |
T |
C |
4: 133,599,373 (GRCm39) |
Q18R |
probably benign |
Het |
Setbp1 |
T |
A |
18: 78,902,734 (GRCm39) |
D311V |
possibly damaging |
Het |
Setd2 |
C |
T |
9: 110,377,865 (GRCm39) |
S560L |
possibly damaging |
Het |
Slc12a5 |
A |
T |
2: 164,816,878 (GRCm39) |
I134F |
probably damaging |
Het |
Speer1h |
C |
T |
5: 11,647,706 (GRCm39) |
T148I |
possibly damaging |
Het |
Svil |
A |
G |
18: 5,116,080 (GRCm39) |
D2035G |
probably damaging |
Het |
Syngap1 |
T |
C |
17: 27,178,985 (GRCm39) |
Y665H |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,043,519 (GRCm39) |
Y547H |
possibly damaging |
Het |
Tgm2 |
A |
G |
2: 157,980,812 (GRCm39) |
V83A |
probably benign |
Het |
Tmem233 |
T |
C |
5: 116,189,429 (GRCm39) |
I117V |
probably benign |
Het |
Tsen34 |
A |
G |
7: 3,703,640 (GRCm39) |
T293A |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,709,023 (GRCm39) |
V8752A |
unknown |
Het |
Ubac1 |
A |
G |
2: 25,904,974 (GRCm39) |
V88A |
probably benign |
Het |
Uchl4 |
T |
C |
9: 64,142,621 (GRCm39) |
V34A |
probably damaging |
Het |
Ugt2a2 |
C |
T |
5: 87,608,435 (GRCm39) |
R468H |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,749 (GRCm39) |
T255S |
probably benign |
Het |
Wdr6 |
T |
A |
9: 108,450,564 (GRCm39) |
N988I |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,903,389 (GRCm39) |
I2359N |
unknown |
Het |
Ybey |
A |
G |
10: 76,304,025 (GRCm39) |
V59A |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,349,375 (GRCm39) |
C271S |
possibly damaging |
Het |
Zfp397 |
A |
G |
18: 24,090,122 (GRCm39) |
N142S |
probably benign |
Het |
Zfy1 |
A |
T |
Y: 725,788 (GRCm39) |
V659E |
probably damaging |
Het |
|
Other mutations in Ptprj |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01528:Ptprj
|
APN |
2 |
90,282,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01594:Ptprj
|
APN |
2 |
90,271,139 (GRCm39) |
splice site |
probably benign |
|
IGL01767:Ptprj
|
APN |
2 |
90,299,918 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01917:Ptprj
|
APN |
2 |
90,300,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01981:Ptprj
|
APN |
2 |
90,270,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02830:Ptprj
|
APN |
2 |
90,283,488 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02955:Ptprj
|
APN |
2 |
90,298,808 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03102:Ptprj
|
APN |
2 |
90,309,312 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03150:Ptprj
|
APN |
2 |
90,290,955 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03210:Ptprj
|
APN |
2 |
90,300,070 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02799:Ptprj
|
UTSW |
2 |
90,299,942 (GRCm39) |
missense |
probably benign |
0.00 |
R0083:Ptprj
|
UTSW |
2 |
90,300,121 (GRCm39) |
splice site |
probably null |
|
R0108:Ptprj
|
UTSW |
2 |
90,300,121 (GRCm39) |
splice site |
probably null |
|
R0579:Ptprj
|
UTSW |
2 |
90,266,913 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1130:Ptprj
|
UTSW |
2 |
90,283,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R1160:Ptprj
|
UTSW |
2 |
90,274,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1238:Ptprj
|
UTSW |
2 |
90,274,758 (GRCm39) |
splice site |
probably null |
|
R1507:Ptprj
|
UTSW |
2 |
90,301,631 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1552:Ptprj
|
UTSW |
2 |
90,301,497 (GRCm39) |
missense |
probably damaging |
0.98 |
R1607:Ptprj
|
UTSW |
2 |
90,293,664 (GRCm39) |
missense |
probably benign |
0.14 |
R1693:Ptprj
|
UTSW |
2 |
90,280,141 (GRCm39) |
nonsense |
probably null |
|
R2016:Ptprj
|
UTSW |
2 |
90,294,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2017:Ptprj
|
UTSW |
2 |
90,294,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2044:Ptprj
|
UTSW |
2 |
90,293,439 (GRCm39) |
missense |
probably damaging |
0.96 |
R2322:Ptprj
|
UTSW |
2 |
90,301,473 (GRCm39) |
missense |
probably benign |
0.06 |
R2516:Ptprj
|
UTSW |
2 |
90,305,340 (GRCm39) |
splice site |
probably benign |
|
R3106:Ptprj
|
UTSW |
2 |
90,270,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R3964:Ptprj
|
UTSW |
2 |
90,298,785 (GRCm39) |
missense |
probably benign |
0.00 |
R4201:Ptprj
|
UTSW |
2 |
90,293,439 (GRCm39) |
missense |
probably damaging |
0.99 |
R4533:Ptprj
|
UTSW |
2 |
90,270,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R4680:Ptprj
|
UTSW |
2 |
90,290,840 (GRCm39) |
missense |
probably benign |
0.00 |
R4738:Ptprj
|
UTSW |
2 |
90,270,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Ptprj
|
UTSW |
2 |
90,290,876 (GRCm39) |
missense |
probably damaging |
0.98 |
R5137:Ptprj
|
UTSW |
2 |
90,299,992 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5349:Ptprj
|
UTSW |
2 |
90,301,605 (GRCm39) |
missense |
probably benign |
0.00 |
R5369:Ptprj
|
UTSW |
2 |
90,299,985 (GRCm39) |
missense |
probably benign |
0.09 |
R5718:Ptprj
|
UTSW |
2 |
90,288,613 (GRCm39) |
missense |
probably benign |
0.00 |
R5914:Ptprj
|
UTSW |
2 |
90,283,684 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6022:Ptprj
|
UTSW |
2 |
90,301,667 (GRCm39) |
missense |
probably benign |
0.14 |
R6341:Ptprj
|
UTSW |
2 |
90,288,693 (GRCm39) |
missense |
probably benign |
|
R6421:Ptprj
|
UTSW |
2 |
90,301,484 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6724:Ptprj
|
UTSW |
2 |
90,281,195 (GRCm39) |
missense |
probably benign |
0.04 |
R6831:Ptprj
|
UTSW |
2 |
90,290,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R6939:Ptprj
|
UTSW |
2 |
90,289,858 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6972:Ptprj
|
UTSW |
2 |
90,410,747 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7149:Ptprj
|
UTSW |
2 |
90,274,790 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7243:Ptprj
|
UTSW |
2 |
90,276,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R7335:Ptprj
|
UTSW |
2 |
90,271,126 (GRCm39) |
missense |
probably benign |
0.01 |
R7439:Ptprj
|
UTSW |
2 |
90,280,163 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7441:Ptprj
|
UTSW |
2 |
90,280,163 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7498:Ptprj
|
UTSW |
2 |
90,266,909 (GRCm39) |
nonsense |
probably null |
|
R7571:Ptprj
|
UTSW |
2 |
90,285,530 (GRCm39) |
missense |
probably benign |
0.24 |
R7657:Ptprj
|
UTSW |
2 |
90,282,501 (GRCm39) |
splice site |
probably null |
|
R7672:Ptprj
|
UTSW |
2 |
90,290,940 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7849:Ptprj
|
UTSW |
2 |
90,274,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R7939:Ptprj
|
UTSW |
2 |
90,295,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R7958:Ptprj
|
UTSW |
2 |
90,299,971 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8338:Ptprj
|
UTSW |
2 |
90,301,481 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8354:Ptprj
|
UTSW |
2 |
90,300,061 (GRCm39) |
missense |
probably benign |
0.43 |
R8556:Ptprj
|
UTSW |
2 |
90,271,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R8695:Ptprj
|
UTSW |
2 |
90,301,481 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8784:Ptprj
|
UTSW |
2 |
90,290,856 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8984:Ptprj
|
UTSW |
2 |
90,270,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R9054:Ptprj
|
UTSW |
2 |
90,290,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9056:Ptprj
|
UTSW |
2 |
90,288,613 (GRCm39) |
missense |
probably benign |
0.00 |
R9147:Ptprj
|
UTSW |
2 |
90,288,562 (GRCm39) |
missense |
probably benign |
0.02 |
R9148:Ptprj
|
UTSW |
2 |
90,288,562 (GRCm39) |
missense |
probably benign |
0.02 |
R9168:Ptprj
|
UTSW |
2 |
90,294,916 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9314:Ptprj
|
UTSW |
2 |
90,301,631 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9337:Ptprj
|
UTSW |
2 |
90,270,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R9546:Ptprj
|
UTSW |
2 |
90,274,805 (GRCm39) |
missense |
probably benign |
0.08 |
RF013:Ptprj
|
UTSW |
2 |
90,301,514 (GRCm39) |
nonsense |
probably null |
|
Z1177:Ptprj
|
UTSW |
2 |
90,290,913 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGAACAGAGCTCTCTTGCCTG -3'
(R):5'- TGGGTCCCGTACTTCAATTGTC -3'
Sequencing Primer
(F):5'- AGCTCTATAACTGCCAGGTTGGAC -3'
(R):5'- TGTCTACAAAATACACGTGGCTGG -3'
|
Posted On |
2019-05-15 |