Incidental Mutation 'R4883:Ptprk'
ID |
375425 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ptprk
|
Ensembl Gene |
ENSMUSG00000019889 |
Gene Name |
protein tyrosine phosphatase receptor type K |
Synonyms |
RPTPkappa, PTPk |
MMRRC Submission |
042491-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4883 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
10 |
Chromosomal Location |
27950816-28473393 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 28464928 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Phenylalanine
at position 1244
(Y1244F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000151986
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166468]
[ENSMUST00000218276]
[ENSMUST00000218359]
[ENSMUST00000220357]
|
AlphaFold |
P35822 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000166468
AA Change: Y1256F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000126279 Gene: ENSMUSG00000019889 AA Change: Y1256F
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
MAM
|
30 |
193 |
1.61e-73 |
SMART |
IG
|
200 |
288 |
2.16e-8 |
SMART |
FN3
|
290 |
373 |
1.48e-4 |
SMART |
FN3
|
389 |
475 |
4.24e1 |
SMART |
FN3
|
491 |
579 |
3.32e-7 |
SMART |
transmembrane domain
|
753 |
774 |
N/A |
INTRINSIC |
PTPc
|
898 |
1161 |
3.56e-132 |
SMART |
PTPc
|
1190 |
1455 |
2.68e-86 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000218276
AA Change: Y1270F
PolyPhen 2
Score 0.096 (Sensitivity: 0.93; Specificity: 0.85)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000218359
AA Change: Y1244F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000220357
AA Change: Y191F
PolyPhen 2
Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000220404
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.2%
|
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, a single transmembrane region, and two tandem catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP mu (MAM) domain, an Ig-like domain and four fibronectin type III-like repeats. This PTP was shown to mediate homophilic intercellular interaction, possibly through the interaction with beta- and gamma-catenin at adherens junctions. Expression of this gene was found to be stimulated by TGF-beta 1, which may be important for the inhibition of keratinocyte proliferation. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
C |
11: 110,217,457 (GRCm39) |
D133G |
probably damaging |
Het |
Abcg4 |
G |
T |
9: 44,190,616 (GRCm39) |
H55Q |
probably damaging |
Het |
Acaca |
T |
A |
11: 84,142,116 (GRCm39) |
V641E |
probably benign |
Het |
Adam28 |
T |
C |
14: 68,875,552 (GRCm39) |
I229V |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,837,493 (GRCm39) |
I793N |
probably damaging |
Het |
Akr1d1 |
A |
T |
6: 37,535,336 (GRCm39) |
D240V |
possibly damaging |
Het |
Arhgef25 |
T |
C |
10: 127,018,802 (GRCm39) |
D548G |
probably benign |
Het |
Asl |
A |
G |
5: 130,042,802 (GRCm39) |
|
probably null |
Het |
Atg14 |
C |
T |
14: 47,788,771 (GRCm39) |
R194Q |
probably damaging |
Het |
BC004004 |
T |
A |
17: 29,501,166 (GRCm39) |
F38L |
probably damaging |
Het |
Btg1 |
T |
C |
10: 96,453,259 (GRCm39) |
F25L |
probably benign |
Het |
Btrc |
C |
T |
19: 45,445,026 (GRCm39) |
P35S |
probably benign |
Het |
Calcr |
T |
A |
6: 3,714,705 (GRCm39) |
N142Y |
probably damaging |
Het |
Ccdc138 |
A |
G |
10: 58,397,818 (GRCm39) |
I553V |
probably benign |
Het |
Ccdc198 |
T |
A |
14: 49,482,560 (GRCm39) |
N52I |
probably damaging |
Het |
Cdc42 |
T |
A |
4: 137,056,115 (GRCm39) |
N132I |
probably benign |
Het |
Ces1e |
A |
G |
8: 93,950,716 (GRCm39) |
S22P |
probably benign |
Het |
Clmn |
G |
T |
12: 104,748,307 (GRCm39) |
D413E |
probably benign |
Het |
Cramp1 |
T |
C |
17: 25,201,293 (GRCm39) |
T730A |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,343,784 (GRCm39) |
M2395L |
probably benign |
Het |
Ephx1 |
G |
T |
1: 180,829,488 (GRCm39) |
S20Y |
possibly damaging |
Het |
Exoc5 |
T |
G |
14: 49,289,821 (GRCm39) |
E19A |
probably damaging |
Het |
Fam120b |
T |
C |
17: 15,623,294 (GRCm39) |
L424P |
probably benign |
Het |
Fam89a |
G |
A |
8: 125,467,823 (GRCm39) |
T163I |
possibly damaging |
Het |
Fcrl2 |
G |
A |
3: 87,166,922 (GRCm39) |
L24F |
possibly damaging |
Het |
Fgd6 |
G |
T |
10: 93,975,715 (GRCm39) |
V1377L |
probably benign |
Het |
Glud1 |
T |
A |
14: 34,057,347 (GRCm39) |
I337K |
possibly damaging |
Het |
Gm6370 |
T |
A |
5: 146,430,736 (GRCm39) |
I303N |
probably benign |
Het |
Gm7995 |
T |
C |
14: 42,133,383 (GRCm39) |
Y88H |
probably damaging |
Het |
Gsdma3 |
T |
C |
11: 98,520,393 (GRCm39) |
|
probably null |
Het |
Gsdmc2 |
T |
C |
15: 63,707,614 (GRCm39) |
D60G |
probably damaging |
Het |
Hcn1 |
T |
A |
13: 118,039,431 (GRCm39) |
|
probably null |
Het |
Hectd1 |
A |
T |
12: 51,831,030 (GRCm39) |
C936* |
probably null |
Het |
Herc4 |
T |
A |
10: 63,121,433 (GRCm39) |
S358T |
probably benign |
Het |
Hk3 |
A |
G |
13: 55,158,735 (GRCm39) |
C515R |
probably benign |
Het |
Ighg1 |
A |
G |
12: 113,291,138 (GRCm39) |
|
probably benign |
Het |
Iqgap3 |
T |
A |
3: 88,014,842 (GRCm39) |
C853S |
probably benign |
Het |
Irx4 |
G |
A |
13: 73,415,750 (GRCm39) |
A180T |
probably damaging |
Het |
Kif20b |
A |
G |
19: 34,943,522 (GRCm39) |
T1441A |
probably benign |
Het |
Lifr |
A |
G |
15: 7,215,106 (GRCm39) |
K738E |
possibly damaging |
Het |
Lmntd2 |
A |
T |
7: 140,792,531 (GRCm39) |
S218T |
probably damaging |
Het |
Lnx1 |
A |
T |
5: 74,768,530 (GRCm39) |
W353R |
probably benign |
Het |
Lrfn3 |
G |
T |
7: 30,055,238 (GRCm39) |
P569Q |
possibly damaging |
Het |
Mamstr |
A |
G |
7: 45,293,838 (GRCm39) |
I11V |
probably benign |
Het |
Med31 |
T |
C |
11: 72,104,975 (GRCm39) |
N32S |
possibly damaging |
Het |
Mob3c |
A |
T |
4: 115,690,928 (GRCm39) |
I173F |
probably benign |
Het |
Morc3 |
A |
G |
16: 93,667,250 (GRCm39) |
|
probably null |
Het |
Mphosph9 |
T |
C |
5: 124,437,108 (GRCm39) |
K412R |
probably damaging |
Het |
Mtcl3 |
A |
T |
10: 29,072,537 (GRCm39) |
N610Y |
probably damaging |
Het |
Mthfd1l |
C |
T |
10: 3,957,775 (GRCm39) |
P271S |
probably benign |
Het |
Ncam1 |
C |
T |
9: 49,453,183 (GRCm39) |
|
probably null |
Het |
Ncbp3 |
T |
A |
11: 72,960,578 (GRCm39) |
Y279N |
probably damaging |
Het |
Ncoa6 |
G |
A |
2: 155,248,687 (GRCm39) |
T1539I |
probably benign |
Het |
Nedd4 |
G |
A |
9: 72,647,515 (GRCm39) |
|
probably null |
Het |
Neil1 |
A |
G |
9: 57,054,206 (GRCm39) |
V38A |
probably damaging |
Het |
Ngf |
T |
A |
3: 102,427,961 (GRCm39) |
F237I |
probably damaging |
Het |
Nol3 |
A |
G |
8: 106,005,888 (GRCm39) |
Q94R |
possibly damaging |
Het |
Obox1 |
A |
G |
7: 15,290,263 (GRCm39) |
N202S |
probably damaging |
Het |
Odc1 |
T |
A |
12: 17,597,386 (GRCm39) |
N29K |
possibly damaging |
Het |
Or2b7 |
C |
T |
13: 21,739,658 (GRCm39) |
R178H |
probably benign |
Het |
Or2h15 |
T |
C |
17: 38,441,508 (GRCm39) |
T192A |
probably damaging |
Het |
Or4a69 |
C |
T |
2: 89,312,652 (GRCm39) |
V276I |
probably benign |
Het |
Or52a20 |
A |
C |
7: 103,365,914 (GRCm39) |
I38L |
probably benign |
Het |
P2rx7 |
T |
A |
5: 122,819,129 (GRCm39) |
V517E |
probably damaging |
Het |
Parm1 |
A |
G |
5: 91,741,775 (GRCm39) |
T48A |
possibly damaging |
Het |
Pcdh9 |
T |
A |
14: 94,126,164 (GRCm39) |
D2V |
possibly damaging |
Het |
Pgm3 |
G |
T |
9: 86,451,378 (GRCm39) |
T92N |
probably damaging |
Het |
Plcg2 |
G |
T |
8: 118,333,872 (GRCm39) |
G882* |
probably null |
Het |
Ptpn14 |
C |
T |
1: 189,582,997 (GRCm39) |
P615S |
probably damaging |
Het |
Rere |
G |
A |
4: 150,700,510 (GRCm39) |
A1162T |
probably damaging |
Het |
Rfx2 |
T |
C |
17: 57,090,747 (GRCm39) |
E391G |
probably damaging |
Het |
Sema4c |
A |
G |
1: 36,591,097 (GRCm39) |
V414A |
probably damaging |
Het |
Serpinb10 |
A |
T |
1: 107,468,681 (GRCm39) |
N185I |
probably damaging |
Het |
Shroom3 |
T |
G |
5: 93,098,993 (GRCm39) |
M1410R |
probably benign |
Het |
Slc13a1 |
A |
T |
6: 24,134,356 (GRCm39) |
S176T |
probably benign |
Het |
Sntb1 |
A |
T |
15: 55,506,198 (GRCm39) |
Y458* |
probably null |
Het |
Sorcs1 |
C |
T |
19: 50,220,741 (GRCm39) |
V570I |
probably benign |
Het |
Sp8 |
T |
A |
12: 118,812,805 (GRCm39) |
V220E |
probably damaging |
Het |
Spry1 |
C |
T |
3: 37,696,868 (GRCm39) |
T37M |
possibly damaging |
Het |
Sspo |
A |
T |
6: 48,437,756 (GRCm39) |
H1305L |
probably benign |
Het |
Tbc1d22a |
A |
G |
15: 86,381,117 (GRCm39) |
D509G |
possibly damaging |
Het |
Tmem108 |
A |
T |
9: 103,376,276 (GRCm39) |
V391D |
possibly damaging |
Het |
Tmem132d |
T |
A |
5: 128,346,366 (GRCm39) |
H52L |
possibly damaging |
Het |
Tmem132d |
T |
A |
5: 128,346,364 (GRCm39) |
I53F |
probably damaging |
Het |
Tnnt2 |
A |
T |
1: 135,775,496 (GRCm39) |
R87* |
probably null |
Het |
Ube3a |
A |
T |
7: 58,893,198 (GRCm39) |
M1L |
probably benign |
Het |
Unc79 |
A |
G |
12: 103,060,592 (GRCm39) |
T1119A |
probably damaging |
Het |
Usf3 |
A |
T |
16: 44,039,942 (GRCm39) |
H1474L |
probably damaging |
Het |
Vcpip1 |
G |
A |
1: 9,817,423 (GRCm39) |
T320I |
probably damaging |
Het |
Vmn1r56 |
A |
G |
7: 5,199,443 (GRCm39) |
L58P |
probably damaging |
Het |
Wdr53 |
A |
T |
16: 32,075,796 (GRCm39) |
K334* |
probably null |
Het |
Zbtb40 |
T |
A |
4: 136,728,241 (GRCm39) |
R459W |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,246,547 (GRCm39) |
L878Q |
probably damaging |
Het |
Zfp286 |
T |
C |
11: 62,671,455 (GRCm39) |
D206G |
probably benign |
Het |
Zfp46 |
T |
A |
4: 136,017,792 (GRCm39) |
C209S |
probably damaging |
Het |
Zup1 |
G |
T |
10: 33,825,038 (GRCm39) |
T148K |
probably damaging |
Het |
|
Other mutations in Ptprk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00310:Ptprk
|
APN |
10 |
28,212,506 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00533:Ptprk
|
APN |
10 |
28,461,971 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01062:Ptprk
|
APN |
10 |
28,456,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01295:Ptprk
|
APN |
10 |
28,351,174 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01372:Ptprk
|
APN |
10 |
28,445,923 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01452:Ptprk
|
APN |
10 |
28,450,913 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01829:Ptprk
|
APN |
10 |
28,449,383 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Ptprk
|
APN |
10 |
28,259,441 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01955:Ptprk
|
APN |
10 |
28,471,861 (GRCm39) |
unclassified |
probably benign |
|
IGL02263:Ptprk
|
APN |
10 |
27,951,110 (GRCm39) |
missense |
unknown |
|
IGL02489:Ptprk
|
APN |
10 |
28,259,468 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02697:Ptprk
|
APN |
10 |
28,451,614 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02713:Ptprk
|
APN |
10 |
28,468,807 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02943:Ptprk
|
APN |
10 |
28,351,172 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03240:Ptprk
|
APN |
10 |
28,368,957 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03373:Ptprk
|
APN |
10 |
28,442,533 (GRCm39) |
missense |
probably damaging |
1.00 |
LCD18:Ptprk
|
UTSW |
10 |
28,450,983 (GRCm39) |
intron |
probably benign |
|
PIT4366001:Ptprk
|
UTSW |
10 |
28,462,015 (GRCm39) |
missense |
probably benign |
|
R0010:Ptprk
|
UTSW |
10 |
28,461,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R0021:Ptprk
|
UTSW |
10 |
28,468,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R0021:Ptprk
|
UTSW |
10 |
28,468,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Ptprk
|
UTSW |
10 |
28,139,504 (GRCm39) |
nonsense |
probably null |
|
R0035:Ptprk
|
UTSW |
10 |
28,139,504 (GRCm39) |
nonsense |
probably null |
|
R0053:Ptprk
|
UTSW |
10 |
28,351,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R0063:Ptprk
|
UTSW |
10 |
28,139,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Ptprk
|
UTSW |
10 |
28,139,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Ptprk
|
UTSW |
10 |
28,082,221 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0281:Ptprk
|
UTSW |
10 |
28,449,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Ptprk
|
UTSW |
10 |
28,230,625 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0480:Ptprk
|
UTSW |
10 |
28,461,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Ptprk
|
UTSW |
10 |
28,461,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R0585:Ptprk
|
UTSW |
10 |
28,451,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Ptprk
|
UTSW |
10 |
27,951,132 (GRCm39) |
missense |
probably damaging |
0.96 |
R0684:Ptprk
|
UTSW |
10 |
28,359,294 (GRCm39) |
splice site |
probably benign |
|
R1073:Ptprk
|
UTSW |
10 |
28,372,943 (GRCm39) |
critical splice donor site |
probably null |
|
R1377:Ptprk
|
UTSW |
10 |
28,462,022 (GRCm39) |
missense |
probably benign |
0.42 |
R1422:Ptprk
|
UTSW |
10 |
28,351,276 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1482:Ptprk
|
UTSW |
10 |
28,139,512 (GRCm39) |
missense |
probably benign |
0.24 |
R1532:Ptprk
|
UTSW |
10 |
28,461,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R1576:Ptprk
|
UTSW |
10 |
28,427,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Ptprk
|
UTSW |
10 |
28,369,166 (GRCm39) |
missense |
probably benign |
0.00 |
R1654:Ptprk
|
UTSW |
10 |
28,259,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R1701:Ptprk
|
UTSW |
10 |
28,342,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1747:Ptprk
|
UTSW |
10 |
28,230,688 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2033:Ptprk
|
UTSW |
10 |
28,468,763 (GRCm39) |
unclassified |
probably benign |
|
R2059:Ptprk
|
UTSW |
10 |
28,442,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Ptprk
|
UTSW |
10 |
28,465,364 (GRCm39) |
missense |
probably damaging |
0.98 |
R2164:Ptprk
|
UTSW |
10 |
28,436,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R2260:Ptprk
|
UTSW |
10 |
28,082,145 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2394:Ptprk
|
UTSW |
10 |
28,427,713 (GRCm39) |
missense |
probably damaging |
0.98 |
R2432:Ptprk
|
UTSW |
10 |
28,468,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R2437:Ptprk
|
UTSW |
10 |
28,230,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R2495:Ptprk
|
UTSW |
10 |
28,351,074 (GRCm39) |
splice site |
probably benign |
|
R3037:Ptprk
|
UTSW |
10 |
28,456,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Ptprk
|
UTSW |
10 |
28,468,822 (GRCm39) |
missense |
probably benign |
|
R3162:Ptprk
|
UTSW |
10 |
28,468,822 (GRCm39) |
missense |
probably benign |
|
R3687:Ptprk
|
UTSW |
10 |
28,349,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3722:Ptprk
|
UTSW |
10 |
28,259,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Ptprk
|
UTSW |
10 |
28,139,617 (GRCm39) |
missense |
probably benign |
0.02 |
R3963:Ptprk
|
UTSW |
10 |
28,427,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R4077:Ptprk
|
UTSW |
10 |
28,139,508 (GRCm39) |
missense |
probably benign |
|
R4079:Ptprk
|
UTSW |
10 |
28,139,508 (GRCm39) |
missense |
probably benign |
|
R4112:Ptprk
|
UTSW |
10 |
28,351,284 (GRCm39) |
critical splice donor site |
probably null |
|
R4255:Ptprk
|
UTSW |
10 |
28,082,241 (GRCm39) |
missense |
probably benign |
0.14 |
R4523:Ptprk
|
UTSW |
10 |
28,342,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R4651:Ptprk
|
UTSW |
10 |
28,139,686 (GRCm39) |
missense |
probably damaging |
0.99 |
R4652:Ptprk
|
UTSW |
10 |
28,139,686 (GRCm39) |
missense |
probably damaging |
0.99 |
R4828:Ptprk
|
UTSW |
10 |
28,436,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Ptprk
|
UTSW |
10 |
28,456,480 (GRCm39) |
nonsense |
probably null |
|
R5004:Ptprk
|
UTSW |
10 |
28,462,059 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5013:Ptprk
|
UTSW |
10 |
28,427,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R5092:Ptprk
|
UTSW |
10 |
28,468,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5126:Ptprk
|
UTSW |
10 |
28,451,640 (GRCm39) |
splice site |
probably null |
|
R5183:Ptprk
|
UTSW |
10 |
28,351,232 (GRCm39) |
missense |
probably benign |
0.02 |
R5264:Ptprk
|
UTSW |
10 |
28,461,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Ptprk
|
UTSW |
10 |
28,468,050 (GRCm39) |
splice site |
probably null |
|
R5330:Ptprk
|
UTSW |
10 |
28,463,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R5474:Ptprk
|
UTSW |
10 |
28,372,926 (GRCm39) |
nonsense |
probably null |
|
R5516:Ptprk
|
UTSW |
10 |
28,372,926 (GRCm39) |
nonsense |
probably null |
|
R5796:Ptprk
|
UTSW |
10 |
28,259,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Ptprk
|
UTSW |
10 |
28,369,060 (GRCm39) |
missense |
probably damaging |
0.99 |
R5952:Ptprk
|
UTSW |
10 |
28,461,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R6065:Ptprk
|
UTSW |
10 |
28,351,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R6226:Ptprk
|
UTSW |
10 |
28,440,099 (GRCm39) |
missense |
probably benign |
0.02 |
R6264:Ptprk
|
UTSW |
10 |
28,442,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R6638:Ptprk
|
UTSW |
10 |
28,471,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R6843:Ptprk
|
UTSW |
10 |
28,467,978 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6860:Ptprk
|
UTSW |
10 |
28,210,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6869:Ptprk
|
UTSW |
10 |
28,349,055 (GRCm39) |
critical splice donor site |
probably null |
|
R7214:Ptprk
|
UTSW |
10 |
28,450,905 (GRCm39) |
missense |
probably benign |
0.11 |
R7307:Ptprk
|
UTSW |
10 |
28,465,004 (GRCm39) |
nonsense |
probably null |
|
R7349:Ptprk
|
UTSW |
10 |
28,468,834 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7442:Ptprk
|
UTSW |
10 |
28,450,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Ptprk
|
UTSW |
10 |
28,436,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R7661:Ptprk
|
UTSW |
10 |
28,342,036 (GRCm39) |
missense |
probably benign |
0.00 |
R7694:Ptprk
|
UTSW |
10 |
28,465,366 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7740:Ptprk
|
UTSW |
10 |
28,372,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7810:Ptprk
|
UTSW |
10 |
28,468,853 (GRCm39) |
missense |
probably damaging |
0.97 |
R7831:Ptprk
|
UTSW |
10 |
28,444,404 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7836:Ptprk
|
UTSW |
10 |
28,449,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R8049:Ptprk
|
UTSW |
10 |
28,259,565 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8235:Ptprk
|
UTSW |
10 |
28,465,037 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8274:Ptprk
|
UTSW |
10 |
28,456,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8286:Ptprk
|
UTSW |
10 |
28,444,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Ptprk
|
UTSW |
10 |
28,230,688 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8727:Ptprk
|
UTSW |
10 |
28,442,541 (GRCm39) |
unclassified |
probably benign |
|
R8794:Ptprk
|
UTSW |
10 |
28,139,504 (GRCm39) |
nonsense |
probably null |
|
R8842:Ptprk
|
UTSW |
10 |
28,442,497 (GRCm39) |
missense |
probably damaging |
0.97 |
R8861:Ptprk
|
UTSW |
10 |
28,446,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Ptprk
|
UTSW |
10 |
28,467,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8910:Ptprk
|
UTSW |
10 |
28,368,993 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8919:Ptprk
|
UTSW |
10 |
28,359,203 (GRCm39) |
nonsense |
probably null |
|
R8976:Ptprk
|
UTSW |
10 |
28,461,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8982:Ptprk
|
UTSW |
10 |
28,436,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R9036:Ptprk
|
UTSW |
10 |
28,461,928 (GRCm39) |
missense |
probably benign |
0.01 |
R9135:Ptprk
|
UTSW |
10 |
28,456,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R9308:Ptprk
|
UTSW |
10 |
28,450,850 (GRCm39) |
missense |
probably benign |
0.15 |
R9317:Ptprk
|
UTSW |
10 |
28,230,731 (GRCm39) |
missense |
probably damaging |
0.96 |
R9475:Ptprk
|
UTSW |
10 |
28,210,476 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9585:Ptprk
|
UTSW |
10 |
28,369,147 (GRCm39) |
nonsense |
probably null |
|
R9625:Ptprk
|
UTSW |
10 |
28,462,006 (GRCm39) |
missense |
probably damaging |
0.99 |
R9700:Ptprk
|
UTSW |
10 |
28,456,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9745:Ptprk
|
UTSW |
10 |
28,139,608 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1177:Ptprk
|
UTSW |
10 |
28,369,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGCAACATTCCGGTTCCATACC -3'
(R):5'- CTGCTAGGTTGTATCCAAAAGCAC -3'
Sequencing Primer
(F):5'- CTTGGTCCTACAATGGAGTACACTG -3'
(R):5'- GGTTGTATCCAAAAGCACATTGTC -3'
|
Posted On |
2016-03-17 |