Incidental Mutation 'R7743:Ptprd'
ID |
596642 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ptprd
|
Ensembl Gene |
ENSMUSG00000028399 |
Gene Name |
protein tyrosine phosphatase receptor type D |
Synonyms |
1110002J03Rik, B230219D21Rik, 3000002J10Rik |
MMRRC Submission |
045799-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7743 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
75859475-78130198 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 76004326 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Isoleucine
at position 143
(K143I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133832
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050757]
[ENSMUST00000098005]
[ENSMUST00000102834]
[ENSMUST00000107289]
[ENSMUST00000173376]
[ENSMUST00000173662]
[ENSMUST00000174023]
[ENSMUST00000174180]
[ENSMUST00000174531]
[ENSMUST00000174831]
[ENSMUST00000212365]
|
AlphaFold |
Q64487 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000050757
|
SMART Domains |
Protein: ENSMUSP00000058466 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
208 |
1.38e-15 |
SMART |
IGc2
|
238 |
299 |
8.13e-4 |
SMART |
FN3
|
313 |
392 |
7.92e-14 |
SMART |
FN3
|
408 |
491 |
5.73e-11 |
SMART |
IG_like
|
499 |
593 |
8.34e1 |
SMART |
FN3
|
506 |
584 |
9.1e-14 |
SMART |
FN3
|
597 |
674 |
1.21e0 |
SMART |
transmembrane domain
|
847 |
869 |
N/A |
INTRINSIC |
low complexity region
|
870 |
882 |
N/A |
INTRINSIC |
PTPc
|
949 |
1207 |
6.38e-134 |
SMART |
PTPc
|
1236 |
1498 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000098005
|
SMART Domains |
Protein: ENSMUSP00000095614 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
214 |
8.5e-16 |
SMART |
low complexity region
|
225 |
237 |
N/A |
INTRINSIC |
IGc2
|
248 |
309 |
8.13e-4 |
SMART |
FN3
|
323 |
402 |
7.92e-14 |
SMART |
FN3
|
418 |
501 |
5.73e-11 |
SMART |
IG_like
|
509 |
603 |
8.34e1 |
SMART |
FN3
|
516 |
594 |
9.1e-14 |
SMART |
FN3
|
607 |
684 |
1.21e0 |
SMART |
transmembrane domain
|
857 |
879 |
N/A |
INTRINSIC |
low complexity region
|
886 |
897 |
N/A |
INTRINSIC |
PTPc
|
950 |
1208 |
6.38e-134 |
SMART |
PTPc
|
1237 |
1499 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000102834
|
SMART Domains |
Protein: ENSMUSP00000099898 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
1 |
62 |
8.13e-4 |
SMART |
FN3
|
76 |
155 |
7.92e-14 |
SMART |
FN3
|
171 |
254 |
5.73e-11 |
SMART |
IG_like
|
262 |
356 |
8.34e1 |
SMART |
FN3
|
269 |
347 |
9.1e-14 |
SMART |
FN3
|
360 |
437 |
1.21e0 |
SMART |
transmembrane domain
|
610 |
632 |
N/A |
INTRINSIC |
low complexity region
|
633 |
645 |
N/A |
INTRINSIC |
PTPc
|
698 |
956 |
6.38e-134 |
SMART |
PTPc
|
985 |
1247 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000107289
AA Change: K993I
PolyPhen 2
Score 0.964 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000102910 Gene: ENSMUSG00000028399 AA Change: K993I
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
214 |
8.5e-16 |
SMART |
low complexity region
|
225 |
237 |
N/A |
INTRINSIC |
IGc2
|
248 |
309 |
8.13e-4 |
SMART |
FN3
|
323 |
402 |
7.92e-14 |
SMART |
FN3
|
418 |
501 |
5.73e-11 |
SMART |
IG_like
|
509 |
603 |
8.34e1 |
SMART |
FN3
|
516 |
594 |
9.1e-14 |
SMART |
FN3
|
609 |
696 |
2.72e-12 |
SMART |
FN3
|
712 |
809 |
2.87e-11 |
SMART |
FN3
|
824 |
904 |
4.96e-6 |
SMART |
FN3
|
919 |
1003 |
4.12e-12 |
SMART |
FN3
|
1018 |
1095 |
1.95e0 |
SMART |
transmembrane domain
|
1268 |
1290 |
N/A |
INTRINSIC |
low complexity region
|
1291 |
1303 |
N/A |
INTRINSIC |
PTPc
|
1356 |
1614 |
6.38e-134 |
SMART |
PTPc
|
1643 |
1905 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000173376
|
SMART Domains |
Protein: ENSMUSP00000133468 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
43 |
112 |
8.57e-12 |
SMART |
IGc2
|
145 |
221 |
8.5e-16 |
SMART |
low complexity region
|
232 |
244 |
N/A |
INTRINSIC |
IGc2
|
255 |
316 |
8.13e-4 |
SMART |
FN3
|
330 |
409 |
7.92e-14 |
SMART |
FN3
|
425 |
508 |
5.73e-11 |
SMART |
IG_like
|
516 |
610 |
8.34e1 |
SMART |
FN3
|
523 |
601 |
9.1e-14 |
SMART |
FN3
|
614 |
691 |
1.21e0 |
SMART |
transmembrane domain
|
864 |
886 |
N/A |
INTRINSIC |
low complexity region
|
887 |
899 |
N/A |
INTRINSIC |
PTPc
|
952 |
1210 |
6.38e-134 |
SMART |
PTPc
|
1239 |
1501 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000173662
AA Change: K143I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000133832 Gene: ENSMUSG00000028399 AA Change: K143I
Domain | Start | End | E-Value | Type |
Blast:FN3
|
1 |
54 |
4e-31 |
BLAST |
SCOP:d1cfb_2
|
1 |
66 |
8e-4 |
SMART |
PDB:2DN7|A
|
1 |
67 |
7e-17 |
PDB |
FN3
|
69 |
153 |
4.12e-12 |
SMART |
FN3
|
169 |
246 |
1.8e0 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174023
|
SMART Domains |
Protein: ENSMUSP00000133562 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
211 |
4.88e-16 |
SMART |
low complexity region
|
222 |
234 |
N/A |
INTRINSIC |
IGc2
|
245 |
306 |
8.13e-4 |
SMART |
FN3
|
320 |
399 |
7.92e-14 |
SMART |
FN3
|
415 |
498 |
5.73e-11 |
SMART |
IG_like
|
506 |
600 |
8.34e1 |
SMART |
FN3
|
513 |
591 |
9.1e-14 |
SMART |
FN3
|
604 |
681 |
1.21e0 |
SMART |
transmembrane domain
|
853 |
875 |
N/A |
INTRINSIC |
low complexity region
|
882 |
893 |
N/A |
INTRINSIC |
PTPc
|
946 |
1204 |
6.38e-134 |
SMART |
PTPc
|
1233 |
1495 |
9.17e-135 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000174180
AA Change: K971I
PolyPhen 2
Score 0.634 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000133973 Gene: ENSMUSG00000028399 AA Change: K971I
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
205 |
2.09e-15 |
SMART |
IGc2
|
235 |
296 |
8.13e-4 |
SMART |
FN3
|
310 |
389 |
7.92e-14 |
SMART |
FN3
|
405 |
488 |
5.73e-11 |
SMART |
IG_like
|
496 |
590 |
8.34e1 |
SMART |
FN3
|
503 |
581 |
9.1e-14 |
SMART |
FN3
|
596 |
683 |
2.72e-12 |
SMART |
FN3
|
699 |
787 |
6.15e-11 |
SMART |
FN3
|
802 |
882 |
4.96e-6 |
SMART |
FN3
|
897 |
981 |
4.12e-12 |
SMART |
FN3
|
996 |
1073 |
1.95e0 |
SMART |
transmembrane domain
|
1246 |
1268 |
N/A |
INTRINSIC |
low complexity region
|
1269 |
1281 |
N/A |
INTRINSIC |
PTPc
|
1334 |
1592 |
6.38e-134 |
SMART |
PTPc
|
1621 |
1883 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174531
|
SMART Domains |
Protein: ENSMUSP00000134229 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
208 |
1.38e-15 |
SMART |
low complexity region
|
219 |
231 |
N/A |
INTRINSIC |
IGc2
|
242 |
303 |
8.13e-4 |
SMART |
FN3
|
317 |
396 |
7.92e-14 |
SMART |
FN3
|
412 |
495 |
5.73e-11 |
SMART |
IG_like
|
503 |
597 |
8.34e1 |
SMART |
FN3
|
510 |
588 |
9.1e-14 |
SMART |
FN3
|
601 |
678 |
1.21e0 |
SMART |
transmembrane domain
|
851 |
873 |
N/A |
INTRINSIC |
low complexity region
|
874 |
886 |
N/A |
INTRINSIC |
PTPc
|
939 |
1197 |
6.38e-134 |
SMART |
PTPc
|
1226 |
1488 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000174831
|
SMART Domains |
Protein: ENSMUSP00000133328 Gene: ENSMUSG00000028399
Domain | Start | End | E-Value | Type |
IGc2
|
36 |
105 |
8.57e-12 |
SMART |
IGc2
|
138 |
214 |
8.5e-16 |
SMART |
low complexity region
|
225 |
237 |
N/A |
INTRINSIC |
IGc2
|
248 |
309 |
8.13e-4 |
SMART |
FN3
|
323 |
402 |
7.92e-14 |
SMART |
FN3
|
418 |
501 |
5.73e-11 |
SMART |
IG_like
|
509 |
603 |
8.34e1 |
SMART |
FN3
|
516 |
594 |
9.1e-14 |
SMART |
FN3
|
607 |
684 |
1.21e0 |
SMART |
transmembrane domain
|
856 |
878 |
N/A |
INTRINSIC |
low complexity region
|
885 |
896 |
N/A |
INTRINSIC |
PTPc
|
949 |
1207 |
6.38e-134 |
SMART |
PTPc
|
1236 |
1498 |
9.17e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000212365
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
Validation Efficiency |
97% (77/79) |
MGI Phenotype |
PHENOTYPE: Homozygotes for a targeted null mutation exhibit impaired learning of spatial tasks, enhanced long-term potentiation at hippocampal synapses, and high mortality associated with reduced food intake. [provided by MGI curators]
|
Allele List at MGI |
All alleles(9) : Targeted(4) Gene trapped(5)
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
G |
3: 137,774,516 (GRCm39) |
E1235G |
probably damaging |
Het |
Abtb3 |
A |
T |
10: 85,460,813 (GRCm39) |
I569F |
possibly damaging |
Het |
Adam6a |
A |
G |
12: 113,508,152 (GRCm39) |
D175G |
probably benign |
Het |
Adgrf4 |
A |
T |
17: 42,983,453 (GRCm39) |
C76* |
probably null |
Het |
Agbl3 |
C |
T |
6: 34,823,765 (GRCm39) |
T815I |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,748,383 (GRCm39) |
V488A |
not run |
Het |
Akip1 |
T |
A |
7: 109,311,035 (GRCm39) |
S192T |
probably benign |
Het |
Apc2 |
G |
A |
10: 80,140,749 (GRCm39) |
M201I |
probably damaging |
Het |
Arel1 |
G |
T |
12: 84,987,043 (GRCm39) |
N124K |
probably damaging |
Het |
Atp10a |
A |
T |
7: 58,453,457 (GRCm39) |
H845L |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,599,634 (GRCm39) |
Y586H |
probably benign |
Het |
BC051019 |
A |
G |
7: 109,315,266 (GRCm39) |
Y330H |
probably damaging |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Chek2 |
T |
G |
5: 110,987,916 (GRCm39) |
|
probably null |
Het |
Cldn14 |
A |
G |
16: 93,716,615 (GRCm39) |
L77S |
probably damaging |
Het |
Cox15 |
T |
C |
19: 43,728,380 (GRCm39) |
K298E |
possibly damaging |
Het |
Cpt1b |
G |
T |
15: 89,305,607 (GRCm39) |
D369E |
probably benign |
Het |
Cpxm1 |
T |
C |
2: 130,235,342 (GRCm39) |
N550S |
probably benign |
Het |
Csdc2 |
A |
G |
15: 81,833,399 (GRCm39) |
E132G |
possibly damaging |
Het |
Cyb5d2 |
A |
T |
11: 72,669,702 (GRCm39) |
C219S |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,367,278 (GRCm39) |
T480A |
probably benign |
Het |
Fndc1 |
G |
A |
17: 7,983,969 (GRCm39) |
T1319I |
unknown |
Het |
Gm5773 |
T |
G |
3: 93,680,565 (GRCm39) |
V79G |
probably damaging |
Het |
Hsf2 |
G |
A |
10: 57,387,431 (GRCm39) |
|
probably null |
Het |
Itgb2l |
T |
C |
16: 96,238,608 (GRCm39) |
T64A |
probably damaging |
Het |
Kifc5b |
T |
C |
17: 27,143,176 (GRCm39) |
V316A |
probably damaging |
Het |
Ktn1 |
A |
G |
14: 47,907,750 (GRCm39) |
D279G |
probably damaging |
Het |
Lonrf1 |
T |
C |
8: 36,716,206 (GRCm39) |
E143G |
possibly damaging |
Het |
Mroh9 |
C |
T |
1: 162,852,122 (GRCm39) |
E856K |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,568,773 (GRCm39) |
T1249A |
unknown |
Het |
Myh6 |
G |
A |
14: 55,194,607 (GRCm39) |
R721W |
probably damaging |
Het |
Myo6 |
A |
T |
9: 80,183,611 (GRCm39) |
I669F |
unknown |
Het |
N4bp2 |
A |
G |
5: 65,965,802 (GRCm39) |
T1284A |
probably damaging |
Het |
Npr3 |
A |
G |
15: 11,905,724 (GRCm39) |
M1T |
probably null |
Het |
Obscn |
C |
T |
11: 58,990,603 (GRCm39) |
V1657M |
probably damaging |
Het |
Olfr908 |
A |
G |
9: 38,427,624 (GRCm39) |
T99A |
possibly damaging |
Het |
Or52a20 |
A |
G |
7: 103,366,560 (GRCm39) |
E253G |
possibly damaging |
Het |
Or52p2 |
A |
T |
7: 102,237,638 (GRCm39) |
F104Y |
probably benign |
Het |
Otud6b |
C |
A |
4: 14,818,389 (GRCm39) |
A171S |
possibly damaging |
Het |
Pdcd2l |
A |
C |
7: 33,892,256 (GRCm39) |
D204E |
probably benign |
Het |
Pdia2 |
T |
C |
17: 26,417,842 (GRCm39) |
S56G |
probably benign |
Het |
Plcxd1 |
G |
A |
5: 110,250,369 (GRCm39) |
E237K |
possibly damaging |
Het |
Plekha5 |
A |
T |
6: 140,501,712 (GRCm39) |
R633S |
probably damaging |
Het |
Pnpla6 |
T |
C |
8: 3,586,594 (GRCm39) |
F937L |
possibly damaging |
Het |
Pth2 |
A |
T |
7: 44,830,733 (GRCm39) |
M6L |
probably benign |
Het |
Rhbdf2 |
T |
C |
11: 116,492,427 (GRCm39) |
D487G |
probably benign |
Het |
Rhbdf2 |
A |
T |
11: 116,494,775 (GRCm39) |
D300E |
probably benign |
Het |
Rock2 |
G |
A |
12: 17,026,048 (GRCm39) |
V1265I |
probably damaging |
Het |
Rsf1 |
CGGC |
CGGCGGCGGAGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Rtn4 |
T |
A |
11: 29,683,790 (GRCm39) |
Y1027* |
probably null |
Het |
Rxfp3 |
A |
G |
15: 11,037,216 (GRCm39) |
L52P |
probably damaging |
Het |
Sel1l3 |
A |
G |
5: 53,293,227 (GRCm39) |
Y830H |
probably benign |
Het |
Serpinb3d |
C |
T |
1: 107,007,088 (GRCm39) |
V207I |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 126,190,972 (GRCm39) |
E1006G |
probably damaging |
Het |
Slc22a19 |
C |
T |
19: 7,661,201 (GRCm39) |
M324I |
possibly damaging |
Het |
Slc37a1 |
T |
A |
17: 31,535,159 (GRCm39) |
F106I |
probably damaging |
Het |
Snx14 |
A |
T |
9: 88,280,402 (GRCm39) |
S518T |
probably benign |
Het |
Sp2 |
T |
C |
11: 96,851,935 (GRCm39) |
T330A |
probably damaging |
Het |
Spata13 |
A |
T |
14: 60,993,698 (GRCm39) |
H1050L |
probably damaging |
Het |
Sptssa |
A |
C |
12: 54,703,201 (GRCm39) |
V23G |
possibly damaging |
Het |
Syt3 |
A |
T |
7: 44,042,091 (GRCm39) |
I317F |
probably damaging |
Het |
Tars1 |
A |
C |
15: 11,399,458 (GRCm39) |
|
probably null |
Het |
Tead3 |
T |
A |
17: 28,551,801 (GRCm39) |
T431S |
probably benign |
Het |
Tiam2 |
G |
A |
17: 3,568,431 (GRCm39) |
E1526K |
possibly damaging |
Het |
Tnni3 |
G |
A |
7: 4,524,891 (GRCm39) |
P12L |
probably benign |
Het |
Topaz1 |
A |
G |
9: 122,614,201 (GRCm39) |
H1207R |
probably benign |
Het |
Trdn |
G |
T |
10: 33,133,058 (GRCm39) |
E107* |
probably null |
Het |
Trp63 |
A |
G |
16: 25,701,375 (GRCm39) |
N483S |
probably benign |
Het |
Trpm4 |
A |
G |
7: 44,957,762 (GRCm39) |
S1009P |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,804,772 (GRCm39) |
V908A |
probably benign |
Het |
Tsen34 |
A |
T |
7: 3,697,601 (GRCm39) |
M25L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,781,827 (GRCm39) |
E1073G |
unknown |
Het |
Uaca |
A |
T |
9: 60,783,677 (GRCm39) |
I1380F |
probably damaging |
Het |
Ubr3 |
A |
G |
2: 69,774,793 (GRCm39) |
T539A |
probably benign |
Het |
Ugt1a5 |
T |
A |
1: 88,094,117 (GRCm39) |
M115K |
probably benign |
Het |
Unc45b |
A |
T |
11: 82,813,726 (GRCm39) |
I378F |
probably damaging |
Het |
Unk |
G |
A |
11: 115,940,262 (GRCm39) |
R205Q |
possibly damaging |
Het |
Ush2a |
T |
A |
1: 188,542,376 (GRCm39) |
L3314Q |
probably benign |
Het |
Vezt |
A |
G |
10: 93,816,286 (GRCm39) |
L475P |
probably damaging |
Het |
Vmn2r115 |
C |
T |
17: 23,564,772 (GRCm39) |
Q220* |
probably null |
Het |
Yap1 |
T |
C |
9: 7,962,379 (GRCm39) |
Q223R |
probably benign |
Het |
Zdhhc7 |
G |
A |
8: 120,813,467 (GRCm39) |
T114M |
possibly damaging |
Het |
Zwilch |
A |
C |
9: 64,060,217 (GRCm39) |
C374G |
probably damaging |
Het |
|
Other mutations in Ptprd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00964:Ptprd
|
APN |
4 |
75,916,793 (GRCm39) |
nonsense |
probably null |
|
IGL01067:Ptprd
|
APN |
4 |
75,977,922 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01121:Ptprd
|
APN |
4 |
75,872,438 (GRCm39) |
splice site |
probably benign |
|
IGL01531:Ptprd
|
APN |
4 |
76,003,757 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01661:Ptprd
|
APN |
4 |
75,872,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Ptprd
|
APN |
4 |
76,161,910 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01735:Ptprd
|
APN |
4 |
76,055,057 (GRCm39) |
splice site |
probably null |
|
IGL01810:Ptprd
|
APN |
4 |
76,058,744 (GRCm39) |
splice site |
probably benign |
|
IGL01834:Ptprd
|
APN |
4 |
76,046,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01835:Ptprd
|
APN |
4 |
76,165,058 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01867:Ptprd
|
APN |
4 |
76,161,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02582:Ptprd
|
APN |
4 |
75,865,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Ptprd
|
APN |
4 |
75,900,287 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02741:Ptprd
|
APN |
4 |
76,051,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02866:Ptprd
|
APN |
4 |
75,968,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02960:Ptprd
|
APN |
4 |
76,047,105 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Ptprd
|
APN |
4 |
75,984,456 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03230:Ptprd
|
APN |
4 |
75,968,654 (GRCm39) |
nonsense |
probably null |
|
IGL03343:Ptprd
|
APN |
4 |
75,977,966 (GRCm39) |
missense |
probably damaging |
1.00 |
unhurried
|
UTSW |
4 |
76,018,870 (GRCm39) |
nonsense |
probably null |
|
ANU22:Ptprd
|
UTSW |
4 |
76,018,693 (GRCm39) |
missense |
probably damaging |
0.99 |
F5493:Ptprd
|
UTSW |
4 |
76,002,645 (GRCm39) |
missense |
probably damaging |
1.00 |
P0033:Ptprd
|
UTSW |
4 |
76,047,091 (GRCm39) |
nonsense |
probably null |
|
R0044:Ptprd
|
UTSW |
4 |
76,004,566 (GRCm39) |
missense |
probably benign |
0.08 |
R0044:Ptprd
|
UTSW |
4 |
76,004,566 (GRCm39) |
missense |
probably benign |
0.08 |
R0076:Ptprd
|
UTSW |
4 |
75,865,276 (GRCm39) |
splice site |
probably benign |
|
R0137:Ptprd
|
UTSW |
4 |
76,055,140 (GRCm39) |
missense |
probably benign |
0.24 |
R0358:Ptprd
|
UTSW |
4 |
75,863,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Ptprd
|
UTSW |
4 |
76,055,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R0385:Ptprd
|
UTSW |
4 |
76,046,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Ptprd
|
UTSW |
4 |
76,018,711 (GRCm39) |
missense |
probably benign |
|
R0646:Ptprd
|
UTSW |
4 |
76,002,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R0667:Ptprd
|
UTSW |
4 |
75,875,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Ptprd
|
UTSW |
4 |
75,875,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Ptprd
|
UTSW |
4 |
76,058,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R0827:Ptprd
|
UTSW |
4 |
76,047,152 (GRCm39) |
missense |
probably damaging |
0.98 |
R0932:Ptprd
|
UTSW |
4 |
76,055,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R1069:Ptprd
|
UTSW |
4 |
76,018,870 (GRCm39) |
nonsense |
probably null |
|
R1069:Ptprd
|
UTSW |
4 |
75,916,724 (GRCm39) |
splice site |
probably benign |
|
R1086:Ptprd
|
UTSW |
4 |
76,051,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Ptprd
|
UTSW |
4 |
75,984,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Ptprd
|
UTSW |
4 |
76,002,789 (GRCm39) |
missense |
probably damaging |
0.98 |
R1688:Ptprd
|
UTSW |
4 |
75,900,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Ptprd
|
UTSW |
4 |
75,865,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Ptprd
|
UTSW |
4 |
75,872,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Ptprd
|
UTSW |
4 |
76,051,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R2023:Ptprd
|
UTSW |
4 |
75,875,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R2413:Ptprd
|
UTSW |
4 |
76,051,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Ptprd
|
UTSW |
4 |
76,004,248 (GRCm39) |
critical splice donor site |
probably null |
|
R2914:Ptprd
|
UTSW |
4 |
75,865,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R2971:Ptprd
|
UTSW |
4 |
76,025,561 (GRCm39) |
missense |
probably benign |
0.10 |
R3051:Ptprd
|
UTSW |
4 |
76,018,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R3433:Ptprd
|
UTSW |
4 |
76,004,248 (GRCm39) |
critical splice donor site |
probably null |
|
R3964:Ptprd
|
UTSW |
4 |
75,978,073 (GRCm39) |
splice site |
probably benign |
|
R4009:Ptprd
|
UTSW |
4 |
75,874,634 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4394:Ptprd
|
UTSW |
4 |
76,046,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R4420:Ptprd
|
UTSW |
4 |
75,957,614 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4424:Ptprd
|
UTSW |
4 |
76,021,200 (GRCm39) |
missense |
probably benign |
0.22 |
R4575:Ptprd
|
UTSW |
4 |
76,162,023 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4578:Ptprd
|
UTSW |
4 |
76,162,023 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4715:Ptprd
|
UTSW |
4 |
76,025,570 (GRCm39) |
missense |
probably benign |
0.03 |
R4782:Ptprd
|
UTSW |
4 |
76,009,769 (GRCm39) |
missense |
probably benign |
0.01 |
R4785:Ptprd
|
UTSW |
4 |
76,058,790 (GRCm39) |
missense |
probably benign |
0.05 |
R4799:Ptprd
|
UTSW |
4 |
76,009,769 (GRCm39) |
missense |
probably benign |
0.01 |
R4944:Ptprd
|
UTSW |
4 |
76,047,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R4950:Ptprd
|
UTSW |
4 |
76,058,752 (GRCm39) |
splice site |
probably null |
|
R4969:Ptprd
|
UTSW |
4 |
76,051,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Ptprd
|
UTSW |
4 |
75,930,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5164:Ptprd
|
UTSW |
4 |
76,018,995 (GRCm39) |
splice site |
probably null |
|
R5287:Ptprd
|
UTSW |
4 |
75,872,405 (GRCm39) |
nonsense |
probably null |
|
R5305:Ptprd
|
UTSW |
4 |
75,900,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Ptprd
|
UTSW |
4 |
76,047,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Ptprd
|
UTSW |
4 |
75,872,405 (GRCm39) |
nonsense |
probably null |
|
R5531:Ptprd
|
UTSW |
4 |
75,977,904 (GRCm39) |
critical splice donor site |
probably null |
|
R5543:Ptprd
|
UTSW |
4 |
75,977,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Ptprd
|
UTSW |
4 |
75,990,255 (GRCm39) |
missense |
probably benign |
0.01 |
R5719:Ptprd
|
UTSW |
4 |
75,972,839 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5884:Ptprd
|
UTSW |
4 |
75,900,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Ptprd
|
UTSW |
4 |
75,984,528 (GRCm39) |
missense |
probably benign |
0.06 |
R6250:Ptprd
|
UTSW |
4 |
76,047,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R6335:Ptprd
|
UTSW |
4 |
75,872,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Ptprd
|
UTSW |
4 |
76,009,789 (GRCm39) |
splice site |
probably null |
|
R6533:Ptprd
|
UTSW |
4 |
76,046,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R6756:Ptprd
|
UTSW |
4 |
75,873,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6782:Ptprd
|
UTSW |
4 |
76,243,377 (GRCm39) |
splice site |
probably null |
|
R7131:Ptprd
|
UTSW |
4 |
75,984,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Ptprd
|
UTSW |
4 |
75,990,199 (GRCm39) |
missense |
probably benign |
0.06 |
R7233:Ptprd
|
UTSW |
4 |
75,978,020 (GRCm39) |
missense |
probably benign |
0.00 |
R7246:Ptprd
|
UTSW |
4 |
76,046,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Ptprd
|
UTSW |
4 |
76,165,076 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Ptprd
|
UTSW |
4 |
76,004,705 (GRCm39) |
missense |
probably benign |
0.03 |
R7442:Ptprd
|
UTSW |
4 |
75,978,058 (GRCm39) |
nonsense |
probably null |
|
R7491:Ptprd
|
UTSW |
4 |
76,051,392 (GRCm39) |
missense |
probably benign |
0.23 |
R7526:Ptprd
|
UTSW |
4 |
75,984,564 (GRCm39) |
missense |
probably benign |
0.00 |
R7609:Ptprd
|
UTSW |
4 |
75,990,240 (GRCm39) |
missense |
probably benign |
0.03 |
R7612:Ptprd
|
UTSW |
4 |
76,004,696 (GRCm39) |
missense |
probably benign |
0.45 |
R7659:Ptprd
|
UTSW |
4 |
76,047,153 (GRCm39) |
missense |
probably benign |
0.03 |
R7748:Ptprd
|
UTSW |
4 |
76,017,741 (GRCm39) |
missense |
probably null |
0.39 |
R7788:Ptprd
|
UTSW |
4 |
75,916,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R7836:Ptprd
|
UTSW |
4 |
75,900,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R7937:Ptprd
|
UTSW |
4 |
76,013,772 (GRCm39) |
missense |
probably benign |
0.00 |
R8000:Ptprd
|
UTSW |
4 |
75,984,479 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8018:Ptprd
|
UTSW |
4 |
76,003,757 (GRCm39) |
missense |
probably damaging |
0.98 |
R8072:Ptprd
|
UTSW |
4 |
76,004,273 (GRCm39) |
missense |
probably benign |
0.01 |
R8119:Ptprd
|
UTSW |
4 |
76,047,263 (GRCm39) |
missense |
probably benign |
0.00 |
R8350:Ptprd
|
UTSW |
4 |
75,868,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8387:Ptprd
|
UTSW |
4 |
75,873,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Ptprd
|
UTSW |
4 |
75,984,496 (GRCm39) |
missense |
probably benign |
0.00 |
R8529:Ptprd
|
UTSW |
4 |
76,047,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Ptprd
|
UTSW |
4 |
75,959,629 (GRCm39) |
missense |
probably benign |
|
R8924:Ptprd
|
UTSW |
4 |
75,916,736 (GRCm39) |
critical splice donor site |
probably null |
|
R8984:Ptprd
|
UTSW |
4 |
75,863,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9024:Ptprd
|
UTSW |
4 |
75,874,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:Ptprd
|
UTSW |
4 |
75,872,315 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9206:Ptprd
|
UTSW |
4 |
75,872,315 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9259:Ptprd
|
UTSW |
4 |
75,990,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R9311:Ptprd
|
UTSW |
4 |
76,051,320 (GRCm39) |
missense |
probably benign |
0.25 |
R9417:Ptprd
|
UTSW |
4 |
75,865,335 (GRCm39) |
missense |
probably damaging |
0.99 |
R9427:Ptprd
|
UTSW |
4 |
76,051,440 (GRCm39) |
missense |
probably benign |
0.01 |
R9579:Ptprd
|
UTSW |
4 |
75,872,315 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9580:Ptprd
|
UTSW |
4 |
75,872,315 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9701:Ptprd
|
UTSW |
4 |
75,916,896 (GRCm39) |
missense |
probably damaging |
1.00 |
RF016:Ptprd
|
UTSW |
4 |
76,046,892 (GRCm39) |
missense |
probably benign |
0.01 |
RF023:Ptprd
|
UTSW |
4 |
76,046,802 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Ptprd
|
UTSW |
4 |
76,051,451 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGGCCGATCAGTTATTTACAGC -3'
(R):5'- TCTGTTCCAGAAGAAATACCAACTG -3'
Sequencing Primer
(F):5'- taccttgatccacaggca -3'
(R):5'- AACCTCTGTTCAGTTATCGTGG -3'
|
Posted On |
2019-11-26 |