Incidental Mutation 'IGL02066:Ptpra'
| ID |
185658 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ptpra
|
| Ensembl Gene |
ENSMUSG00000027303 |
| Gene Name |
protein tyrosine phosphatase receptor type A |
| Synonyms |
PTP[a], RPTRalpha, PTPalpha, RPTPalpha, Ptpa |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02066
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
130292198-130396220 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 30333308 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 3
(T3A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000116268
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042055]
[ENSMUST00000113601]
[ENSMUST00000113603]
[ENSMUST00000131476]
[ENSMUST00000136009]
|
| AlphaFold |
P18052 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000042055
AA Change: T265A
PolyPhen 2
Score 0.231 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000046837
Gene: ENSMUSG00000039515
AA Change: T265A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
8 |
20 |
N/A |
INTRINSIC |
|
Pfam:PTPA
|
26 |
319 |
1.5e-126 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113601
AA Change: T46A
PolyPhen 2
Score 0.290 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000109231
Gene: ENSMUSG00000039515
AA Change: T46A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
8 |
20 |
N/A |
INTRINSIC |
|
Pfam:PTPA
|
38 |
104 |
5.7e-28 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113603
AA Change: T223A
PolyPhen 2
Score 0.141 (Sensitivity: 0.92; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000109233
Gene: ENSMUSG00000039515
AA Change: T223A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
8 |
20 |
N/A |
INTRINSIC |
|
Pfam:PTPA
|
64 |
280 |
5.7e-90 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000125561
AA Change: T78A
|
| SMART Domains |
Protein: ENSMUSP00000114290
Gene: ENSMUSG00000039515
AA Change: T78A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PTPA
|
1 |
125 |
6.1e-57 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125743
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130741
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000131476
AA Change: T3A
PolyPhen 2
Score 0.830 (Sensitivity: 0.84; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000116268
Gene: ENSMUSG00000039515
AA Change: T3A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PTPA
|
1 |
61 |
8.3e-28 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136009
AA Change: T3A
PolyPhen 2
Score 0.231 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000114985
Gene: ENSMUSG00000039515
AA Change: T3A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:PTPA
|
1 |
61 |
8.3e-28 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137741
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135105
|
| Coding Region Coverage |
|
| 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 contains an extracellular domain, a single transmembrane segment and two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. This PTP has been shown to dephosphorylate and activate Src family tyrosine kinases, and is implicated in the regulation of integrin signaling, cell adhesion and proliferation. Three alternatively spliced variants of this gene, which encode two distinct isoforms, have been reported. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit deficits in Morris water maze learning, reduced locomotor activity, and decreased anxiety. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2m |
T |
A |
6: 121,626,854 (GRCm39) |
C569S |
probably damaging |
Het |
| Adck5 |
T |
C |
15: 76,479,406 (GRCm39) |
V487A |
probably damaging |
Het |
| Agfg1 |
A |
G |
1: 82,871,279 (GRCm39) |
T483A |
probably damaging |
Het |
| Akr1c12 |
T |
C |
13: 4,326,236 (GRCm39) |
T82A |
probably damaging |
Het |
| Ano2 |
T |
A |
6: 125,667,702 (GRCm39) |
L6Q |
probably benign |
Het |
| Anp32a |
G |
A |
9: 62,284,615 (GRCm39) |
|
probably benign |
Het |
| Bltp2 |
G |
A |
11: 78,164,058 (GRCm39) |
R1133H |
probably damaging |
Het |
| Cep250 |
C |
A |
2: 155,818,441 (GRCm39) |
A871D |
probably damaging |
Het |
| Chl1 |
T |
C |
6: 103,675,185 (GRCm39) |
V624A |
probably benign |
Het |
| Clasp1 |
G |
A |
1: 118,492,990 (GRCm39) |
|
probably null |
Het |
| Clca3a2 |
T |
G |
3: 144,519,216 (GRCm39) |
D320A |
probably benign |
Het |
| Cnot9 |
A |
G |
1: 74,566,212 (GRCm39) |
Q201R |
possibly damaging |
Het |
| Cox4i2 |
C |
T |
2: 152,602,602 (GRCm39) |
R99C |
probably damaging |
Het |
| Csmd1 |
A |
T |
8: 15,976,594 (GRCm39) |
F2875I |
probably damaging |
Het |
| Dpagt1 |
A |
G |
9: 44,243,203 (GRCm39) |
Y246C |
probably damaging |
Het |
| Dsc1 |
A |
G |
18: 20,241,860 (GRCm39) |
|
probably benign |
Het |
| Eef1d |
G |
A |
15: 75,768,704 (GRCm39) |
T464I |
probably benign |
Het |
| Efna2 |
C |
T |
10: 80,024,500 (GRCm39) |
|
probably benign |
Het |
| Entrep3 |
C |
T |
3: 89,095,903 (GRCm39) |
R545* |
probably null |
Het |
| Etaa1 |
C |
A |
11: 17,896,687 (GRCm39) |
V477L |
probably benign |
Het |
| Fam83d |
C |
T |
2: 158,627,793 (GRCm39) |
T494M |
probably benign |
Het |
| Fbxo24 |
C |
T |
5: 137,611,132 (GRCm39) |
V553M |
probably damaging |
Het |
| Gal3st2 |
A |
G |
1: 93,801,379 (GRCm39) |
T12A |
probably damaging |
Het |
| Gba2 |
G |
A |
4: 43,570,175 (GRCm39) |
T373I |
probably benign |
Het |
| Kitl |
T |
A |
10: 99,912,744 (GRCm39) |
C154S |
probably damaging |
Het |
| Lrp1b |
A |
T |
2: 41,001,091 (GRCm39) |
C2044* |
probably null |
Het |
| Lrp6 |
G |
T |
6: 134,427,900 (GRCm39) |
S1564* |
probably null |
Het |
| Manea |
A |
T |
4: 26,340,965 (GRCm39) |
|
probably benign |
Het |
| Myt1 |
T |
C |
2: 181,438,982 (GRCm39) |
L168P |
probably damaging |
Het |
| Notch1 |
T |
C |
2: 26,350,408 (GRCm39) |
E2244G |
possibly damaging |
Het |
| Nsd3 |
T |
G |
8: 26,203,515 (GRCm39) |
V1343G |
probably damaging |
Het |
| Nup155 |
T |
C |
15: 8,187,250 (GRCm39) |
|
probably benign |
Het |
| Obox6 |
T |
C |
7: 15,568,628 (GRCm39) |
I83V |
probably benign |
Het |
| Or12k5 |
A |
T |
2: 36,895,321 (GRCm39) |
F102I |
probably damaging |
Het |
| Or13a24 |
A |
T |
7: 140,154,413 (GRCm39) |
T116S |
possibly damaging |
Het |
| Pdgfra |
T |
C |
5: 75,331,241 (GRCm39) |
V282A |
possibly damaging |
Het |
| Pkd1l2 |
A |
G |
8: 117,736,303 (GRCm39) |
|
probably benign |
Het |
| Pmfbp1 |
A |
T |
8: 110,268,365 (GRCm39) |
I971F |
possibly damaging |
Het |
| Ppp6c |
T |
C |
2: 39,089,683 (GRCm39) |
T199A |
probably benign |
Het |
| Rb1 |
A |
T |
14: 73,435,974 (GRCm39) |
M897K |
probably benign |
Het |
| Rptn |
A |
C |
3: 93,304,436 (GRCm39) |
S590R |
probably benign |
Het |
| Rreb1 |
A |
G |
13: 38,115,482 (GRCm39) |
D947G |
probably benign |
Het |
| Samd9l |
T |
C |
6: 3,376,575 (GRCm39) |
T229A |
probably damaging |
Het |
| Slc5a9 |
A |
T |
4: 111,744,719 (GRCm39) |
M423K |
probably damaging |
Het |
| Slc6a12 |
T |
A |
6: 121,329,015 (GRCm39) |
I111N |
probably damaging |
Het |
| Slc6a15 |
T |
A |
10: 103,252,519 (GRCm39) |
L561I |
probably damaging |
Het |
| Spag5 |
A |
G |
11: 78,195,358 (GRCm39) |
N222D |
probably benign |
Het |
| Spp2 |
G |
A |
1: 88,344,965 (GRCm39) |
M54I |
probably benign |
Het |
| Sptbn4 |
T |
C |
7: 27,063,940 (GRCm39) |
E847G |
possibly damaging |
Het |
| Timd2 |
T |
A |
11: 46,569,050 (GRCm39) |
N203Y |
probably damaging |
Het |
| Togaram1 |
G |
T |
12: 65,030,195 (GRCm39) |
D1000Y |
probably damaging |
Het |
| Usp47 |
C |
T |
7: 111,663,604 (GRCm39) |
R258C |
probably damaging |
Het |
| Uts2r |
A |
C |
11: 121,051,523 (GRCm39) |
D129A |
probably damaging |
Het |
| Vmn2r102 |
G |
A |
17: 19,914,191 (GRCm39) |
M585I |
probably benign |
Het |
| Vmn2r77 |
A |
T |
7: 86,452,836 (GRCm39) |
R518* |
probably null |
Het |
| Wdfy4 |
C |
T |
14: 32,871,523 (GRCm39) |
R296K |
probably benign |
Het |
| Xirp2 |
A |
T |
2: 67,356,415 (GRCm39) |
K3725N |
probably benign |
Het |
| Xntrpc |
T |
C |
7: 101,727,036 (GRCm39) |
S142P |
probably benign |
Het |
| Zfat |
T |
C |
15: 68,052,678 (GRCm39) |
H372R |
probably damaging |
Het |
|
| Other mutations in Ptpra |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01411:Ptpra
|
APN |
2 |
130,386,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01734:Ptpra
|
APN |
2 |
130,385,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02073:Ptpra
|
APN |
2 |
30,333,362 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02201:Ptpra
|
APN |
2 |
30,336,389 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL02218:Ptpra
|
APN |
2 |
130,394,255 (GRCm39) |
splice site |
probably benign |
|
|
IGL02385:Ptpra
|
APN |
2 |
130,382,393 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02480:Ptpra
|
APN |
2 |
130,346,181 (GRCm39) |
missense |
probably benign |
0.09 |
|
IGL03181:Ptpra
|
APN |
2 |
130,359,707 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0374:Ptpra
|
UTSW |
2 |
130,379,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0483:Ptpra
|
UTSW |
2 |
130,381,605 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0848:Ptpra
|
UTSW |
2 |
130,360,911 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1550:Ptpra
|
UTSW |
2 |
130,383,313 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1596:Ptpra
|
UTSW |
2 |
130,386,872 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1602:Ptpra
|
UTSW |
2 |
30,327,602 (GRCm39) |
missense |
probably benign |
0.22 |
|
R1689:Ptpra
|
UTSW |
2 |
130,345,412 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1760:Ptpra
|
UTSW |
2 |
130,391,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1943:Ptpra
|
UTSW |
2 |
130,386,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2114:Ptpra
|
UTSW |
2 |
130,381,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2115:Ptpra
|
UTSW |
2 |
130,381,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2117:Ptpra
|
UTSW |
2 |
130,381,655 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2187:Ptpra
|
UTSW |
2 |
130,346,219 (GRCm39) |
missense |
probably benign |
|
|
R2848:Ptpra
|
UTSW |
2 |
130,386,919 (GRCm39) |
missense |
probably benign |
0.06 |
|
R2849:Ptpra
|
UTSW |
2 |
130,386,919 (GRCm39) |
missense |
probably benign |
0.06 |
|
R3962:Ptpra
|
UTSW |
2 |
30,325,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4080:Ptpra
|
UTSW |
2 |
30,333,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4644:Ptpra
|
UTSW |
2 |
130,386,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4779:Ptpra
|
UTSW |
2 |
130,379,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4849:Ptpra
|
UTSW |
2 |
130,374,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4899:Ptpra
|
UTSW |
2 |
130,386,356 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5186:Ptpra
|
UTSW |
2 |
30,328,367 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5657:Ptpra
|
UTSW |
2 |
130,346,204 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6018:Ptpra
|
UTSW |
2 |
130,345,422 (GRCm39) |
missense |
probably benign |
|
|
R6234:Ptpra
|
UTSW |
2 |
130,379,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6350:Ptpra
|
UTSW |
2 |
130,382,512 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6622:Ptpra
|
UTSW |
2 |
30,327,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6856:Ptpra
|
UTSW |
2 |
130,361,301 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7072:Ptpra
|
UTSW |
2 |
130,395,350 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7146:Ptpra
|
UTSW |
2 |
130,379,571 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7220:Ptpra
|
UTSW |
2 |
130,386,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7346:Ptpra
|
UTSW |
2 |
130,395,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7819:Ptpra
|
UTSW |
2 |
130,346,126 (GRCm39) |
missense |
probably benign |
|
|
R7943:Ptpra
|
UTSW |
2 |
30,322,056 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8044:Ptpra
|
UTSW |
2 |
130,386,881 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8190:Ptpra
|
UTSW |
2 |
30,328,351 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8231:Ptpra
|
UTSW |
2 |
130,379,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8404:Ptpra
|
UTSW |
2 |
130,391,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8422:Ptpra
|
UTSW |
2 |
130,374,091 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R8502:Ptpra
|
UTSW |
2 |
130,391,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8683:Ptpra
|
UTSW |
2 |
130,394,187 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8952:Ptpra
|
UTSW |
2 |
130,386,969 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9147:Ptpra
|
UTSW |
2 |
30,328,256 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9147:Ptpra
|
UTSW |
2 |
30,328,255 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9148:Ptpra
|
UTSW |
2 |
30,328,256 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9148:Ptpra
|
UTSW |
2 |
30,328,255 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9717:Ptpra
|
UTSW |
2 |
130,384,366 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
| Posted On |
2014-05-07 |
Incidental Mutation