Incidental Mutation 'R4983:Ptprj'
ID |
385690 |
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 |
042577-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.223)
|
Stock # |
R4983 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
90260098-90410939 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 90290876 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Serine
at position 528
(I528S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000107121
(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: I435S
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000107119 Gene: ENSMUSG00000025314 AA Change: I435S
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: I528S
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000107121 Gene: ENSMUSG00000025314 AA Change: I528S
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: I621S
PolyPhen 2
Score 0.970 (Sensitivity: 0.77; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000129592 Gene: ENSMUSG00000025314 AA Change: I621S
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 |
|
Meta Mutation Damage Score |
0.5873 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.0%
|
Validation Efficiency |
97% (103/106) |
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 |
4933411K16Rik |
T |
G |
19: 42,041,515 (GRCm39) |
S215R |
possibly damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,867 (GRCm39) |
M388V |
probably benign |
Het |
Acbd6 |
A |
C |
1: 155,477,275 (GRCm39) |
T154P |
probably benign |
Het |
Ago1 |
T |
C |
4: 126,347,447 (GRCm39) |
D434G |
probably damaging |
Het |
Ankib1 |
A |
T |
5: 3,819,652 (GRCm39) |
M89K |
probably benign |
Het |
Arap2 |
A |
T |
5: 62,833,868 (GRCm39) |
H866Q |
probably damaging |
Het |
Armh3 |
T |
C |
19: 45,939,146 (GRCm39) |
T335A |
probably benign |
Het |
Capn12 |
A |
T |
7: 28,589,795 (GRCm39) |
H622L |
probably benign |
Het |
Capns2 |
T |
G |
8: 93,628,530 (GRCm39) |
F140V |
probably damaging |
Het |
Catsper1 |
T |
G |
19: 5,385,991 (GRCm39) |
F75V |
probably benign |
Het |
Ccdc24 |
T |
C |
4: 117,729,297 (GRCm39) |
N16S |
probably benign |
Het |
Cdkn2aip |
A |
T |
8: 48,165,964 (GRCm39) |
L114Q |
probably damaging |
Het |
Cenpe |
T |
A |
3: 134,940,689 (GRCm39) |
S649R |
probably damaging |
Het |
Chgb |
A |
T |
2: 132,635,602 (GRCm39) |
R515W |
probably damaging |
Het |
Chrnb1 |
A |
G |
11: 69,684,804 (GRCm39) |
F123S |
probably damaging |
Het |
Copz2 |
A |
T |
11: 96,748,377 (GRCm39) |
|
probably null |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Daw1 |
C |
A |
1: 83,165,719 (GRCm39) |
A178E |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
Epb41l5 |
T |
C |
1: 119,482,801 (GRCm39) |
D629G |
probably benign |
Het |
Erap1 |
A |
G |
13: 74,838,829 (GRCm39) |
E925G |
probably benign |
Het |
Exoc7 |
A |
C |
11: 116,180,095 (GRCm39) |
F657V |
probably damaging |
Het |
Fam210b |
G |
C |
2: 172,187,585 (GRCm39) |
A2P |
probably damaging |
Homo |
Fry |
A |
G |
5: 150,321,719 (GRCm39) |
E1018G |
probably damaging |
Het |
Galc |
A |
T |
12: 98,209,027 (GRCm39) |
L15* |
probably null |
Het |
Gm11232 |
T |
A |
4: 71,675,138 (GRCm39) |
K121N |
possibly damaging |
Het |
Hectd1 |
A |
T |
12: 51,831,045 (GRCm39) |
D931E |
probably benign |
Het |
Hecw2 |
T |
C |
1: 53,871,830 (GRCm39) |
H1372R |
probably benign |
Het |
Ighv3-2 |
T |
A |
12: 113,997,606 (GRCm39) |
|
noncoding transcript |
Het |
Kcns2 |
T |
G |
15: 34,839,751 (GRCm39) |
S371R |
probably damaging |
Het |
Kif23 |
T |
C |
9: 61,843,985 (GRCm39) |
K175E |
probably benign |
Het |
Kmt2c |
G |
A |
5: 25,500,509 (GRCm39) |
R436W |
possibly damaging |
Het |
Lama5 |
A |
G |
2: 179,835,242 (GRCm39) |
S1317P |
probably benign |
Het |
Lce1e |
T |
C |
3: 92,615,135 (GRCm39) |
S71G |
unknown |
Het |
Lrrc37a |
T |
A |
11: 103,388,444 (GRCm39) |
E2327V |
unknown |
Het |
Map3k20 |
A |
G |
2: 72,232,411 (GRCm39) |
M356V |
probably benign |
Het |
Med12l |
C |
T |
3: 59,169,350 (GRCm39) |
A1580V |
probably damaging |
Het |
Metap2 |
G |
T |
10: 93,725,462 (GRCm39) |
T30K |
possibly damaging |
Het |
Mysm1 |
T |
A |
4: 94,861,207 (GRCm39) |
T53S |
probably benign |
Het |
Nasp |
A |
T |
4: 116,459,382 (GRCm39) |
D717E |
probably damaging |
Het |
Ndnf |
G |
A |
6: 65,680,555 (GRCm39) |
R278H |
possibly damaging |
Het |
Neb |
A |
T |
2: 52,106,273 (GRCm39) |
N4205K |
probably damaging |
Het |
Nebl |
A |
T |
2: 17,380,082 (GRCm39) |
I764N |
possibly damaging |
Het |
Nucb1 |
A |
G |
7: 45,148,313 (GRCm39) |
Y131H |
probably damaging |
Het |
Or14c39 |
A |
C |
7: 86,343,687 (GRCm39) |
T8P |
probably benign |
Het |
Or1e22 |
A |
G |
11: 73,377,623 (GRCm39) |
I9T |
probably benign |
Het |
Or5l14 |
G |
T |
2: 87,793,042 (GRCm39) |
H65N |
probably benign |
Het |
Oscp1 |
T |
A |
4: 125,970,555 (GRCm39) |
C115S |
probably benign |
Het |
Paip2 |
C |
T |
18: 35,746,412 (GRCm39) |
R59C |
possibly damaging |
Het |
Pate10 |
T |
G |
9: 35,653,465 (GRCm39) |
F90V |
probably benign |
Het |
Pcdhga4 |
G |
A |
18: 37,819,572 (GRCm39) |
D374N |
probably damaging |
Het |
Pcolce |
G |
T |
5: 137,603,936 (GRCm39) |
|
probably benign |
Het |
Pcyox1l |
T |
C |
18: 61,832,468 (GRCm39) |
E193G |
probably damaging |
Het |
Pde6b |
A |
T |
5: 108,573,196 (GRCm39) |
Q522L |
probably benign |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phf11a |
A |
G |
14: 59,521,887 (GRCm39) |
F95L |
probably benign |
Het |
Pja2 |
A |
C |
17: 64,616,053 (GRCm39) |
S281A |
probably benign |
Het |
Plekhm2 |
A |
G |
4: 141,361,687 (GRCm39) |
F272S |
probably damaging |
Het |
Pom121l2 |
T |
C |
13: 22,167,984 (GRCm39) |
S752P |
probably benign |
Het |
Ppl |
T |
C |
16: 4,906,582 (GRCm39) |
T1238A |
possibly damaging |
Het |
Prmt7 |
A |
G |
8: 106,976,995 (GRCm39) |
Y569C |
probably damaging |
Het |
Prss37 |
G |
A |
6: 40,493,070 (GRCm39) |
T132I |
probably benign |
Het |
Psmf1 |
A |
T |
2: 151,571,377 (GRCm39) |
|
probably benign |
Het |
Reg1 |
A |
G |
6: 78,405,196 (GRCm39) |
T140A |
possibly damaging |
Het |
Rtn4 |
A |
G |
11: 29,657,217 (GRCm39) |
N457S |
probably benign |
Het |
Rusf1 |
C |
T |
7: 127,875,645 (GRCm39) |
|
probably benign |
Het |
Scn9a |
T |
C |
2: 66,396,614 (GRCm39) |
K93R |
probably benign |
Het |
Sec16a |
A |
G |
2: 26,329,531 (GRCm39) |
V828A |
probably benign |
Het |
Sec23b |
T |
A |
2: 144,423,873 (GRCm39) |
D507E |
probably benign |
Het |
Sirt4 |
A |
T |
5: 115,620,850 (GRCm39) |
F107L |
probably benign |
Het |
Slc14a2 |
A |
T |
18: 78,193,616 (GRCm39) |
L862Q |
probably damaging |
Het |
Slc16a4 |
T |
C |
3: 107,208,176 (GRCm39) |
S229P |
probably benign |
Het |
Slc37a3 |
A |
T |
6: 39,329,651 (GRCm39) |
C185* |
probably null |
Het |
Slc5a2 |
A |
T |
7: 127,870,982 (GRCm39) |
*154C |
probably null |
Het |
Snx17 |
A |
G |
5: 31,353,138 (GRCm39) |
S42G |
possibly damaging |
Het |
Tgm6 |
T |
C |
2: 129,983,113 (GRCm39) |
V234A |
probably damaging |
Het |
Thbs4 |
A |
G |
13: 92,927,207 (GRCm39) |
M94T |
probably benign |
Het |
Thtpa |
A |
G |
14: 55,309,605 (GRCm39) |
|
probably benign |
Het |
Tie1 |
T |
C |
4: 118,340,952 (GRCm39) |
E343G |
probably damaging |
Het |
Tmem145 |
A |
G |
7: 25,008,027 (GRCm39) |
I238V |
probably benign |
Het |
Tmprss11f |
T |
C |
5: 86,685,858 (GRCm39) |
S170G |
probably benign |
Het |
Tnk2 |
T |
A |
16: 32,499,283 (GRCm39) |
D865E |
probably damaging |
Het |
Ttll8 |
T |
C |
15: 88,809,785 (GRCm39) |
E337G |
probably benign |
Het |
Ttn |
G |
A |
2: 76,697,790 (GRCm39) |
|
probably benign |
Het |
Tubgcp6 |
T |
C |
15: 88,990,494 (GRCm39) |
E710G |
probably damaging |
Het |
Txndc2 |
T |
A |
17: 65,945,055 (GRCm39) |
H374L |
probably benign |
Het |
Unc80 |
G |
T |
1: 66,713,891 (GRCm39) |
|
probably null |
Het |
Vmn2r23 |
G |
A |
6: 123,710,308 (GRCm39) |
C537Y |
probably damaging |
Het |
Vmn2r45 |
A |
G |
7: 8,486,116 (GRCm39) |
F391L |
probably damaging |
Het |
Vstm4 |
A |
T |
14: 32,641,202 (GRCm39) |
T262S |
probably benign |
Het |
Zfp180 |
C |
T |
7: 23,805,503 (GRCm39) |
R641C |
probably damaging |
Het |
Zfp979 |
A |
T |
4: 147,698,371 (GRCm39) |
S113T |
possibly damaging |
Het |
Zswim4 |
C |
T |
8: 84,953,296 (GRCm39) |
|
probably null |
Het |
Zswim5 |
T |
A |
4: 116,842,883 (GRCm39) |
M876K |
possibly 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 |
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 |
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'- TGCGCACAGTCCTACCATAC -3'
(R):5'- TGGTCAACATTAGCACCACTG -3'
Sequencing Primer
(F):5'- TACAGAAGAGCCTTTACTGAGGTTG -3'
(R):5'- TGGTCAACATTAGCACCACTGAAATG -3'
|
Posted On |
2016-05-10 |