Incidental Mutation 'R7849:Ptprj'
ID |
606777 |
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 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.223)
|
Stock # |
R7849 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
90260098-90410939 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 90274804 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Aspartic acid
at position 1186
(V1186D)
|
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 damaging
Transcript: ENSMUST00000111493
AA Change: V1000D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000107119 Gene: ENSMUSG00000025314 AA Change: V1000D
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 damaging
Transcript: ENSMUST00000111495
AA Change: V1093D
PolyPhen 2
Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000107121 Gene: ENSMUSG00000025314 AA Change: V1093D
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 damaging
Transcript: ENSMUST00000168621
AA Change: V1186D
PolyPhen 2
Score 0.982 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000129592 Gene: ENSMUSG00000025314 AA Change: V1186D
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: 99.6%
- 20x: 98.7%
|
Validation Efficiency |
|
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: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agap1 |
T |
C |
1: 89,558,141 (GRCm39) |
V143A |
probably damaging |
Het |
Agmo |
A |
G |
12: 37,292,044 (GRCm39) |
R2G |
probably benign |
Het |
Alms1 |
A |
T |
6: 85,598,479 (GRCm39) |
I1102L |
possibly damaging |
Het |
Ankrd13a |
T |
C |
5: 114,929,343 (GRCm39) |
I140T |
possibly damaging |
Het |
Arhgef10l |
T |
A |
4: 140,311,245 (GRCm39) |
|
probably null |
Het |
Atxn2l |
A |
T |
7: 126,092,345 (GRCm39) |
H967Q |
possibly damaging |
Het |
B3galnt2 |
A |
T |
13: 14,169,077 (GRCm39) |
N370I |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,080,477 (GRCm39) |
I325N |
|
Het |
Cacna1e |
C |
T |
1: 154,509,464 (GRCm39) |
D264N |
probably damaging |
Het |
Ccdc112 |
A |
T |
18: 46,429,390 (GRCm39) |
Y103N |
probably benign |
Het |
Ccdc68 |
A |
C |
18: 70,080,246 (GRCm39) |
E197A |
probably damaging |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
T |
C |
6: 102,242,392 (GRCm39) |
M418V |
probably benign |
Het |
Cpne4 |
T |
A |
9: 104,563,718 (GRCm39) |
C32S |
probably damaging |
Het |
Csf2rb2 |
A |
T |
15: 78,168,621 (GRCm39) |
S845T |
probably benign |
Het |
Ctnnd2 |
T |
G |
15: 31,027,733 (GRCm39) |
V1219G |
probably damaging |
Het |
Cyp4f14 |
G |
A |
17: 33,128,325 (GRCm39) |
A230V |
probably benign |
Het |
Cyth1 |
TGGGCAA |
T |
11: 118,074,749 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
T |
A |
18: 50,094,214 (GRCm39) |
C2897S |
probably benign |
Het |
Elavl2 |
T |
A |
4: 91,260,280 (GRCm39) |
|
probably benign |
Het |
Elp1 |
A |
T |
4: 56,758,968 (GRCm39) |
S1191T |
possibly damaging |
Het |
Fam135a |
T |
C |
1: 24,083,331 (GRCm39) |
E298G |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,151,405 (GRCm39) |
I2534N |
probably damaging |
Het |
Fibin |
A |
G |
2: 110,192,825 (GRCm39) |
S106P |
probably damaging |
Het |
Fndc3a |
C |
T |
14: 72,802,100 (GRCm39) |
V568M |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,479,795 (GRCm39) |
F1966S |
probably damaging |
Het |
Gata4 |
T |
G |
14: 63,442,174 (GRCm39) |
E216A |
possibly damaging |
Het |
Gmps |
T |
A |
3: 63,922,984 (GRCm39) |
V649E |
probably benign |
Het |
Golga4 |
A |
T |
9: 118,388,379 (GRCm39) |
N1834Y |
possibly damaging |
Het |
Gpr89 |
A |
T |
3: 96,778,806 (GRCm39) |
Y422* |
probably null |
Het |
Gzmc |
A |
T |
14: 56,469,829 (GRCm39) |
F157Y |
probably benign |
Het |
Hdhd2 |
A |
G |
18: 77,052,962 (GRCm39) |
D204G |
probably damaging |
Het |
Hspa4 |
T |
G |
11: 53,171,530 (GRCm39) |
T225P |
possibly damaging |
Het |
Klhl30 |
T |
A |
1: 91,287,059 (GRCm39) |
D448E |
probably benign |
Het |
Kptn |
A |
G |
7: 15,853,966 (GRCm39) |
Y28C |
probably damaging |
Het |
Krt10 |
A |
T |
11: 99,278,432 (GRCm39) |
N242K |
probably damaging |
Het |
Krt6b |
A |
T |
15: 101,587,009 (GRCm39) |
N254K |
probably damaging |
Het |
Lama5 |
G |
T |
2: 179,843,605 (GRCm39) |
D447E |
probably damaging |
Het |
Lgr6 |
T |
C |
1: 134,915,419 (GRCm39) |
Y720C |
probably damaging |
Het |
Macf1 |
G |
C |
4: 123,301,392 (GRCm39) |
P1037A |
probably benign |
Het |
Map3k19 |
C |
T |
1: 127,751,383 (GRCm39) |
G656D |
probably benign |
Het |
Mroh7 |
A |
C |
4: 106,578,287 (GRCm39) |
N130K |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,551,801 (GRCm39) |
T4831A |
probably benign |
Het |
Nfkb1 |
A |
T |
3: 135,291,173 (GRCm39) |
L533H |
|
Het |
Oaf |
G |
A |
9: 43,134,077 (GRCm39) |
R215C |
probably damaging |
Het |
Or4x11 |
A |
G |
2: 89,867,626 (GRCm39) |
Y121C |
probably damaging |
Het |
Or51k1 |
C |
A |
7: 103,661,510 (GRCm39) |
R133L |
possibly damaging |
Het |
Or5m3b |
G |
A |
2: 85,871,949 (GRCm39) |
V97I |
probably benign |
Het |
Or8a1 |
A |
G |
9: 37,642,003 (GRCm39) |
I92T |
probably damaging |
Het |
Or8g2b |
A |
G |
9: 39,751,618 (GRCm39) |
D296G |
possibly damaging |
Het |
Otub1 |
T |
C |
19: 7,177,425 (GRCm39) |
D74G |
probably damaging |
Het |
Oxct2b |
A |
G |
4: 123,010,680 (GRCm39) |
E200G |
probably damaging |
Het |
Pcdh1 |
T |
C |
18: 38,322,662 (GRCm39) |
D1057G |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,805,174 (GRCm39) |
V3242E |
probably damaging |
Het |
Pkd1l3 |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
8: 110,350,420 (GRCm39) |
|
probably benign |
Het |
Pla2g4e |
T |
A |
2: 120,015,803 (GRCm39) |
D247V |
probably benign |
Het |
Pole |
T |
A |
5: 110,480,414 (GRCm39) |
M1995K |
probably benign |
Het |
Ppargc1a |
T |
C |
5: 51,705,855 (GRCm39) |
E76G |
probably benign |
Het |
Pten |
G |
T |
19: 32,777,396 (GRCm39) |
R130L |
probably damaging |
Het |
Rab4a |
T |
A |
8: 124,532,876 (GRCm39) |
M1K |
probably null |
Het |
Rapgef3 |
C |
A |
15: 97,656,271 (GRCm39) |
|
probably null |
Het |
Rarb |
C |
A |
14: 16,548,473 (GRCm38) |
V83F |
probably damaging |
Het |
Rgs22 |
A |
T |
15: 36,099,858 (GRCm39) |
F410I |
probably damaging |
Het |
Rhpn2 |
A |
C |
7: 35,080,912 (GRCm39) |
E459A |
probably benign |
Het |
Rims4 |
A |
T |
2: 163,705,974 (GRCm39) |
L220Q |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,770,132 (GRCm39) |
T531A |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 109,971,717 (GRCm39) |
H839R |
probably damaging |
Het |
Setbp1 |
T |
C |
18: 78,900,068 (GRCm39) |
R1200G |
probably benign |
Het |
Slc12a8 |
C |
A |
16: 33,444,930 (GRCm39) |
P275T |
probably damaging |
Het |
Slc23a1 |
G |
T |
18: 35,757,554 (GRCm39) |
T239N |
probably benign |
Het |
Slc37a3 |
T |
A |
6: 39,341,517 (GRCm39) |
T40S |
possibly damaging |
Het |
Speer4c1 |
T |
C |
5: 15,915,925 (GRCm39) |
|
probably null |
Het |
Tet1 |
A |
T |
10: 62,655,252 (GRCm39) |
H1556Q |
possibly damaging |
Het |
Tfcp2l1 |
T |
A |
1: 118,603,325 (GRCm39) |
D454E |
probably damaging |
Het |
Timd6 |
T |
A |
11: 46,468,058 (GRCm39) |
I44K |
not run |
Het |
Tmem123 |
A |
T |
9: 7,790,890 (GRCm39) |
M64L |
probably benign |
Het |
Tmem62 |
A |
T |
2: 120,814,853 (GRCm39) |
H172L |
probably benign |
Het |
Trim15 |
T |
G |
17: 37,177,764 (GRCm39) |
Y77S |
probably benign |
Het |
Trim37 |
T |
A |
11: 87,092,270 (GRCm39) |
V693E |
possibly damaging |
Het |
Trim65 |
A |
G |
11: 116,017,082 (GRCm39) |
L460S |
probably damaging |
Het |
Ttc39a |
T |
C |
4: 109,279,687 (GRCm39) |
V109A |
probably benign |
Het |
Ttc7 |
A |
G |
17: 87,600,374 (GRCm39) |
M163V |
probably null |
Het |
Vps13b |
T |
C |
15: 35,423,378 (GRCm39) |
S233P |
probably damaging |
Het |
Vwf |
T |
C |
6: 125,633,766 (GRCm39) |
L2084P |
|
Het |
Wasl |
A |
G |
6: 24,633,922 (GRCm39) |
V114A |
possibly damaging |
Het |
Wdr5 |
A |
G |
2: 27,409,463 (GRCm39) |
S62G |
probably damaging |
Het |
Wfdc11 |
G |
T |
2: 164,507,445 (GRCm39) |
S4* |
probably null |
Het |
Wfikkn2 |
C |
A |
11: 94,129,810 (GRCm39) |
M110I |
probably benign |
Het |
Wiz |
T |
G |
17: 32,576,760 (GRCm39) |
E588A |
probably benign |
Het |
Xylt1 |
A |
G |
7: 117,255,891 (GRCm39) |
H821R |
probably benign |
Het |
Zbtb7c |
A |
T |
18: 76,278,772 (GRCm39) |
H410L |
probably benign |
Het |
Zc3h18 |
T |
A |
8: 123,110,710 (GRCm39) |
D186E |
probably damaging |
Het |
Zfp687 |
G |
T |
3: 94,917,673 (GRCm39) |
L700I |
possibly damaging |
Het |
Zmym2 |
T |
A |
14: 57,184,020 (GRCm39) |
M994K |
probably benign |
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 |
R7134:Ptprj
|
UTSW |
2 |
90,294,822 (GRCm39) |
missense |
probably benign |
0.16 |
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 |
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'- GTGTCATTGCCATGCTCGAAAG -3'
(R):5'- GACTGAGCAGTTAGTTCCCC -3'
Sequencing Primer
(F):5'- TGCCATGCTCGAAAGACTCATTTAC -3'
(R):5'- TGAGCAGTTAGTTCCCCATGACAG -3'
|
Posted On |
2019-12-20 |