Incidental Mutation 'R4688:Prrc2c'
ID |
353808 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Prrc2c
|
Ensembl Gene |
ENSMUSG00000040225 |
Gene Name |
proline-rich coiled-coil 2C |
Synonyms |
9630039I18Rik, Bat2d, 1810043M20Rik, Bat2l2 |
MMRRC Submission |
041939-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.410)
|
Stock # |
R4688 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
162499354-162568125 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 162525256 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Glutamine
at position 450
(P450Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138698
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028016]
[ENSMUST00000182149]
[ENSMUST00000182393]
[ENSMUST00000182593]
[ENSMUST00000182660]
[ENSMUST00000183223]
|
AlphaFold |
no structure available at present |
Predicted Effect |
unknown
Transcript: ENSMUST00000028016
AA Change: P1874Q
|
SMART Domains |
Protein: ENSMUSP00000028016 Gene: ENSMUSG00000040225 AA Change: P1874Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
164 |
7.7e-56 |
PFAM |
internal_repeat_2
|
167 |
349 |
4.39e-5 |
PROSPERO |
internal_repeat_1
|
336 |
391 |
2.14e-5 |
PROSPERO |
low complexity region
|
407 |
414 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
447 |
591 |
2e-5 |
SMART |
low complexity region
|
649 |
669 |
N/A |
INTRINSIC |
low complexity region
|
733 |
745 |
N/A |
INTRINSIC |
coiled coil region
|
996 |
1026 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1186 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1222 |
N/A |
INTRINSIC |
internal_repeat_1
|
1240 |
1295 |
2.14e-5 |
PROSPERO |
low complexity region
|
1308 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1409 |
N/A |
INTRINSIC |
low complexity region
|
1715 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1765 |
1803 |
N/A |
INTRINSIC |
low complexity region
|
1815 |
1832 |
N/A |
INTRINSIC |
low complexity region
|
1844 |
1909 |
N/A |
INTRINSIC |
internal_repeat_2
|
1962 |
2148 |
4.39e-5 |
PROSPERO |
low complexity region
|
2163 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2252 |
N/A |
INTRINSIC |
low complexity region
|
2272 |
2286 |
N/A |
INTRINSIC |
low complexity region
|
2321 |
2338 |
N/A |
INTRINSIC |
low complexity region
|
2427 |
2438 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2576 |
N/A |
INTRINSIC |
low complexity region
|
2811 |
2828 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182149
AA Change: P1876Q
|
SMART Domains |
Protein: ENSMUSP00000138548 Gene: ENSMUSG00000040225 AA Change: P1876Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
167 |
5.6e-73 |
PFAM |
internal_repeat_1
|
336 |
391 |
1.49e-5 |
PROSPERO |
low complexity region
|
407 |
414 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
447 |
591 |
2e-5 |
SMART |
low complexity region
|
649 |
669 |
N/A |
INTRINSIC |
low complexity region
|
733 |
745 |
N/A |
INTRINSIC |
internal_repeat_3
|
754 |
925 |
9.16e-5 |
PROSPERO |
coiled coil region
|
996 |
1026 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1186 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1222 |
N/A |
INTRINSIC |
internal_repeat_1
|
1240 |
1295 |
1.49e-5 |
PROSPERO |
low complexity region
|
1308 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1409 |
N/A |
INTRINSIC |
low complexity region
|
1715 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1765 |
1803 |
N/A |
INTRINSIC |
low complexity region
|
1815 |
1832 |
N/A |
INTRINSIC |
low complexity region
|
1844 |
1909 |
N/A |
INTRINSIC |
internal_repeat_2
|
1962 |
2148 |
3.08e-5 |
PROSPERO |
internal_repeat_3
|
1983 |
2153 |
9.16e-5 |
PROSPERO |
low complexity region
|
2163 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2252 |
N/A |
INTRINSIC |
low complexity region
|
2272 |
2286 |
N/A |
INTRINSIC |
low complexity region
|
2321 |
2338 |
N/A |
INTRINSIC |
low complexity region
|
2427 |
2438 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2576 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182393
AA Change: P592Q
|
SMART Domains |
Protein: ENSMUSP00000138451 Gene: ENSMUSG00000040225 AA Change: P592Q
Domain | Start | End | E-Value | Type |
low complexity region
|
24 |
51 |
N/A |
INTRINSIC |
low complexity region
|
104 |
125 |
N/A |
INTRINSIC |
low complexity region
|
431 |
462 |
N/A |
INTRINSIC |
low complexity region
|
481 |
519 |
N/A |
INTRINSIC |
low complexity region
|
531 |
548 |
N/A |
INTRINSIC |
low complexity region
|
560 |
625 |
N/A |
INTRINSIC |
low complexity region
|
879 |
893 |
N/A |
INTRINSIC |
low complexity region
|
946 |
968 |
N/A |
INTRINSIC |
low complexity region
|
988 |
1002 |
N/A |
INTRINSIC |
low complexity region
|
1037 |
1054 |
N/A |
INTRINSIC |
low complexity region
|
1143 |
1154 |
N/A |
INTRINSIC |
low complexity region
|
1274 |
1297 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182593
AA Change: P1874Q
|
SMART Domains |
Protein: ENSMUSP00000138674 Gene: ENSMUSG00000040225 AA Change: P1874Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
165 |
4.1e-70 |
PFAM |
internal_repeat_1
|
334 |
389 |
9.57e-6 |
PROSPERO |
low complexity region
|
405 |
412 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
445 |
589 |
3e-5 |
SMART |
low complexity region
|
647 |
667 |
N/A |
INTRINSIC |
low complexity region
|
731 |
743 |
N/A |
INTRINSIC |
internal_repeat_3
|
752 |
923 |
6.11e-5 |
PROSPERO |
coiled coil region
|
994 |
1024 |
N/A |
INTRINSIC |
low complexity region
|
1155 |
1184 |
N/A |
INTRINSIC |
low complexity region
|
1210 |
1220 |
N/A |
INTRINSIC |
internal_repeat_1
|
1238 |
1293 |
9.57e-6 |
PROSPERO |
low complexity region
|
1306 |
1333 |
N/A |
INTRINSIC |
low complexity region
|
1386 |
1407 |
N/A |
INTRINSIC |
low complexity region
|
1713 |
1744 |
N/A |
INTRINSIC |
low complexity region
|
1763 |
1801 |
N/A |
INTRINSIC |
low complexity region
|
1813 |
1830 |
N/A |
INTRINSIC |
low complexity region
|
1842 |
1907 |
N/A |
INTRINSIC |
internal_repeat_2
|
1960 |
2146 |
2.01e-5 |
PROSPERO |
internal_repeat_3
|
1981 |
2151 |
6.11e-5 |
PROSPERO |
low complexity region
|
2161 |
2175 |
N/A |
INTRINSIC |
low complexity region
|
2228 |
2250 |
N/A |
INTRINSIC |
low complexity region
|
2270 |
2284 |
N/A |
INTRINSIC |
low complexity region
|
2319 |
2336 |
N/A |
INTRINSIC |
low complexity region
|
2425 |
2436 |
N/A |
INTRINSIC |
low complexity region
|
2551 |
2574 |
N/A |
INTRINSIC |
low complexity region
|
2671 |
2682 |
N/A |
INTRINSIC |
low complexity region
|
2730 |
2747 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182660
AA Change: P1876Q
|
SMART Domains |
Protein: ENSMUSP00000138433 Gene: ENSMUSG00000040225 AA Change: P1876Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
167 |
7e-73 |
PFAM |
internal_repeat_1
|
336 |
391 |
2.14e-5 |
PROSPERO |
low complexity region
|
407 |
414 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
447 |
591 |
2e-5 |
SMART |
low complexity region
|
649 |
669 |
N/A |
INTRINSIC |
low complexity region
|
733 |
745 |
N/A |
INTRINSIC |
coiled coil region
|
996 |
1026 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1186 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1222 |
N/A |
INTRINSIC |
internal_repeat_1
|
1240 |
1295 |
2.14e-5 |
PROSPERO |
low complexity region
|
1308 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1409 |
N/A |
INTRINSIC |
low complexity region
|
1715 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1765 |
1803 |
N/A |
INTRINSIC |
low complexity region
|
1815 |
1832 |
N/A |
INTRINSIC |
low complexity region
|
1844 |
1909 |
N/A |
INTRINSIC |
internal_repeat_2
|
1962 |
2148 |
4.39e-5 |
PROSPERO |
low complexity region
|
2163 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2252 |
N/A |
INTRINSIC |
low complexity region
|
2272 |
2286 |
N/A |
INTRINSIC |
low complexity region
|
2321 |
2338 |
N/A |
INTRINSIC |
low complexity region
|
2427 |
2438 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2576 |
N/A |
INTRINSIC |
low complexity region
|
2811 |
2828 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000183223
AA Change: P450Q
|
SMART Domains |
Protein: ENSMUSP00000138698 Gene: ENSMUSG00000040225 AA Change: P450Q
Domain | Start | End | E-Value | Type |
low complexity region
|
289 |
320 |
N/A |
INTRINSIC |
low complexity region
|
339 |
377 |
N/A |
INTRINSIC |
low complexity region
|
389 |
406 |
N/A |
INTRINSIC |
low complexity region
|
418 |
483 |
N/A |
INTRINSIC |
low complexity region
|
739 |
761 |
N/A |
INTRINSIC |
low complexity region
|
781 |
795 |
N/A |
INTRINSIC |
low complexity region
|
830 |
847 |
N/A |
INTRINSIC |
low complexity region
|
936 |
947 |
N/A |
INTRINSIC |
low complexity region
|
1062 |
1085 |
N/A |
INTRINSIC |
low complexity region
|
1182 |
1193 |
N/A |
INTRINSIC |
low complexity region
|
1241 |
1258 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
G |
6: 83,139,680 (GRCm39) |
N535S |
probably damaging |
Het |
Abcc12 |
T |
C |
8: 87,275,323 (GRCm39) |
S452G |
possibly damaging |
Het |
Acacb |
C |
A |
5: 114,342,824 (GRCm39) |
Q897K |
probably benign |
Het |
Acot3 |
C |
A |
12: 84,100,691 (GRCm39) |
R145S |
probably damaging |
Het |
Ankrd54 |
A |
T |
15: 78,938,782 (GRCm39) |
Y247N |
probably damaging |
Het |
Arl11 |
G |
A |
14: 61,548,546 (GRCm39) |
V119I |
probably benign |
Het |
Atosb |
A |
G |
4: 43,034,663 (GRCm39) |
F352S |
probably damaging |
Het |
Atxn7 |
T |
A |
14: 14,089,288 (GRCm38) |
M268K |
probably benign |
Het |
Bms1 |
G |
A |
6: 118,369,667 (GRCm39) |
R934C |
probably damaging |
Het |
Brd10 |
A |
G |
19: 29,694,501 (GRCm39) |
I1664T |
probably benign |
Het |
Chrnb3 |
T |
C |
8: 27,884,147 (GRCm39) |
S295P |
probably damaging |
Het |
Cic |
TCCCCC |
TCCCCCCC |
7: 24,991,095 (GRCm39) |
|
probably null |
Het |
Cnr1 |
A |
T |
4: 33,944,571 (GRCm39) |
I320F |
probably benign |
Het |
Cntn4 |
C |
T |
6: 106,414,910 (GRCm39) |
P147L |
probably damaging |
Het |
Col24a1 |
G |
A |
3: 145,020,144 (GRCm39) |
V172I |
probably benign |
Het |
Col9a3 |
A |
G |
2: 180,249,424 (GRCm39) |
D262G |
probably damaging |
Het |
Csrnp2 |
A |
G |
15: 100,380,241 (GRCm39) |
V350A |
probably damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,173,592 (GRCm39) |
V192A |
possibly damaging |
Het |
Deptor |
A |
G |
15: 55,072,177 (GRCm39) |
M219V |
probably benign |
Het |
Dmrtb1 |
A |
T |
4: 107,541,247 (GRCm39) |
L38Q |
probably damaging |
Het |
Dvl2 |
G |
A |
11: 69,898,344 (GRCm39) |
R367Q |
possibly damaging |
Het |
Dync1h1 |
T |
G |
12: 110,621,962 (GRCm39) |
I3435S |
probably damaging |
Het |
Ecpas |
A |
G |
4: 58,840,757 (GRCm39) |
V667A |
probably damaging |
Het |
Eif2b3 |
A |
G |
4: 116,916,046 (GRCm39) |
N218D |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,046,292 (GRCm39) |
D497G |
probably benign |
Het |
Epha7 |
G |
T |
4: 28,821,367 (GRCm39) |
L177F |
probably damaging |
Het |
Fam98c |
C |
T |
7: 28,854,666 (GRCm39) |
E147K |
probably damaging |
Het |
Fbxo17 |
A |
G |
7: 28,431,979 (GRCm39) |
T19A |
probably benign |
Het |
Fbxo47 |
A |
G |
11: 97,747,049 (GRCm39) |
F339S |
probably damaging |
Het |
Frmd4a |
G |
T |
2: 4,542,122 (GRCm39) |
V234L |
possibly damaging |
Het |
Gal3st2 |
A |
G |
1: 93,800,245 (GRCm39) |
D32G |
probably damaging |
Het |
Gpr135 |
T |
C |
12: 72,117,720 (GRCm39) |
T16A |
probably benign |
Het |
Gpr160 |
A |
T |
3: 30,950,835 (GRCm39) |
R302S |
probably benign |
Het |
Hrh2 |
C |
A |
13: 54,368,820 (GRCm39) |
N265K |
probably benign |
Het |
Htatip2 |
C |
A |
7: 49,423,171 (GRCm39) |
A242E |
probably damaging |
Het |
Igfbp7 |
T |
C |
5: 77,555,482 (GRCm39) |
Y127C |
probably damaging |
Het |
Igkv16-104 |
A |
G |
6: 68,402,878 (GRCm39) |
Q57R |
possibly damaging |
Het |
Ino80c |
A |
G |
18: 24,241,903 (GRCm39) |
S161P |
probably damaging |
Het |
Itprid1 |
G |
A |
6: 55,944,132 (GRCm39) |
|
probably null |
Het |
Kcnc1 |
A |
G |
7: 46,047,259 (GRCm39) |
D53G |
probably benign |
Het |
Khdc4 |
T |
A |
3: 88,593,824 (GRCm39) |
M71K |
probably damaging |
Het |
Lce1h |
G |
T |
3: 92,670,874 (GRCm39) |
R93S |
unknown |
Het |
Lce1k |
T |
C |
3: 92,713,951 (GRCm39) |
S78G |
unknown |
Het |
Lhcgr |
T |
A |
17: 89,072,580 (GRCm39) |
I156F |
probably damaging |
Het |
Lpl |
T |
C |
8: 69,352,077 (GRCm39) |
Y343H |
probably damaging |
Het |
Lrp6 |
G |
T |
6: 134,456,706 (GRCm39) |
R853S |
probably damaging |
Het |
Lrrc7 |
A |
G |
3: 157,854,242 (GRCm39) |
V1322A |
probably damaging |
Het |
Lrrc74a |
C |
T |
12: 86,784,472 (GRCm39) |
Q67* |
probably null |
Het |
Megf6 |
A |
T |
4: 154,338,271 (GRCm39) |
D447V |
probably damaging |
Het |
Mep1a |
T |
C |
17: 43,793,139 (GRCm39) |
D355G |
possibly damaging |
Het |
Ncoa1 |
T |
C |
12: 4,365,781 (GRCm39) |
D95G |
probably benign |
Het |
Npepl1 |
A |
T |
2: 173,956,235 (GRCm39) |
I139F |
possibly damaging |
Het |
Nrcam |
T |
C |
12: 44,594,020 (GRCm39) |
S262P |
probably benign |
Het |
Nrp1 |
A |
G |
8: 129,229,047 (GRCm39) |
N842D |
probably benign |
Het |
Olfml3 |
A |
G |
3: 103,639,497 (GRCm39) |
|
probably benign |
Het |
Or1x6 |
A |
G |
11: 50,939,815 (GRCm39) |
R294G |
probably damaging |
Het |
Or4b1d |
T |
A |
2: 89,969,343 (GRCm39) |
N47Y |
possibly damaging |
Het |
Or6b6 |
T |
A |
7: 106,571,068 (GRCm39) |
Y161F |
probably benign |
Het |
Or6c204 |
G |
A |
10: 129,022,514 (GRCm39) |
P259S |
probably damaging |
Het |
Or6k8-ps1 |
T |
C |
1: 173,979,162 (GRCm39) |
Y27H |
possibly damaging |
Het |
Or8b3b |
A |
G |
9: 38,584,659 (GRCm39) |
L27P |
probably damaging |
Het |
Or9i1b |
A |
T |
19: 13,896,605 (GRCm39) |
T74S |
probably benign |
Het |
Pde2a |
A |
G |
7: 101,152,041 (GRCm39) |
N316S |
probably benign |
Het |
Pde4dip |
T |
A |
3: 97,750,993 (GRCm39) |
R74* |
probably null |
Het |
Pex13 |
A |
T |
11: 23,605,472 (GRCm39) |
W253R |
possibly damaging |
Het |
Piezo1 |
A |
T |
8: 123,215,278 (GRCm39) |
W1444R |
probably damaging |
Het |
Pla2g4e |
T |
C |
2: 119,998,414 (GRCm39) |
K843R |
possibly damaging |
Het |
Plxna2 |
C |
T |
1: 194,326,753 (GRCm39) |
P229L |
probably damaging |
Het |
Prelid3b |
G |
T |
2: 174,308,592 (GRCm39) |
T131K |
probably benign |
Het |
Pros1 |
T |
C |
16: 62,709,370 (GRCm39) |
|
probably null |
Het |
Ptbp1 |
G |
T |
10: 79,692,342 (GRCm39) |
V5F |
possibly damaging |
Het |
Ptk2 |
T |
A |
15: 73,078,074 (GRCm39) |
L997F |
probably damaging |
Het |
Rims1 |
G |
T |
1: 22,518,528 (GRCm39) |
S525* |
probably null |
Het |
Sanbr |
A |
G |
11: 23,543,449 (GRCm39) |
S530P |
probably benign |
Het |
Sh2b3 |
T |
A |
5: 121,956,697 (GRCm39) |
D318V |
probably benign |
Het |
Slc16a13 |
A |
T |
11: 70,111,101 (GRCm39) |
I88N |
probably damaging |
Het |
Slit2 |
T |
A |
5: 48,414,345 (GRCm39) |
|
probably null |
Het |
Snx10 |
A |
G |
6: 51,556,918 (GRCm39) |
N67S |
probably damaging |
Het |
Stil |
A |
G |
4: 114,898,505 (GRCm39) |
Y1045C |
probably damaging |
Het |
Stra6 |
A |
G |
9: 58,042,359 (GRCm39) |
|
probably null |
Het |
Sympk |
A |
G |
7: 18,788,335 (GRCm39) |
S1254G |
probably benign |
Het |
Syt15 |
G |
T |
14: 33,950,011 (GRCm39) |
G377V |
probably damaging |
Het |
Taar4 |
A |
T |
10: 23,836,731 (GRCm39) |
I114F |
probably damaging |
Het |
Tcaf3 |
G |
A |
6: 42,570,300 (GRCm39) |
|
probably null |
Het |
Tgm7 |
A |
T |
2: 120,924,502 (GRCm39) |
N558K |
probably benign |
Het |
Tln2 |
T |
G |
9: 67,304,935 (GRCm39) |
M1L |
probably benign |
Het |
Trim50 |
C |
T |
5: 135,395,994 (GRCm39) |
T314I |
probably damaging |
Het |
Trp53rka |
A |
T |
2: 165,333,312 (GRCm39) |
Y192* |
probably null |
Het |
Ube3b |
T |
C |
5: 114,531,139 (GRCm39) |
V211A |
probably benign |
Het |
Ush2a |
A |
G |
1: 188,132,138 (GRCm39) |
S787G |
probably benign |
Het |
Vmn1r189 |
T |
C |
13: 22,286,289 (GRCm39) |
M183V |
probably damaging |
Het |
Vps13d |
G |
T |
4: 144,904,782 (GRCm39) |
Q115K |
probably benign |
Het |
Zfp358 |
A |
G |
8: 3,545,493 (GRCm39) |
D25G |
probably damaging |
Het |
Zfp521 |
T |
G |
18: 13,977,647 (GRCm39) |
K922T |
probably damaging |
Het |
Zfp521 |
T |
A |
18: 13,977,648 (GRCm39) |
K922* |
probably null |
Het |
Zfp68 |
T |
A |
5: 138,614,743 (GRCm39) |
K4* |
probably null |
Het |
|
Other mutations in Prrc2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Prrc2c
|
APN |
1 |
162,548,182 (GRCm39) |
splice site |
probably null |
|
IGL00577:Prrc2c
|
APN |
1 |
162,525,685 (GRCm39) |
missense |
unknown |
|
IGL00580:Prrc2c
|
APN |
1 |
162,525,685 (GRCm39) |
missense |
unknown |
|
IGL01295:Prrc2c
|
APN |
1 |
162,510,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01554:Prrc2c
|
APN |
1 |
162,538,355 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01684:Prrc2c
|
APN |
1 |
162,534,031 (GRCm39) |
unclassified |
probably benign |
|
IGL01745:Prrc2c
|
APN |
1 |
162,552,297 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01770:Prrc2c
|
APN |
1 |
162,532,068 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01905:Prrc2c
|
APN |
1 |
162,532,898 (GRCm39) |
unclassified |
probably benign |
|
IGL02304:Prrc2c
|
APN |
1 |
162,511,705 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02389:Prrc2c
|
APN |
1 |
162,520,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Prrc2c
|
APN |
1 |
162,550,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02681:Prrc2c
|
APN |
1 |
162,533,181 (GRCm39) |
unclassified |
probably benign |
|
IGL02686:Prrc2c
|
APN |
1 |
162,535,516 (GRCm39) |
unclassified |
probably benign |
|
IGL02795:Prrc2c
|
APN |
1 |
162,541,868 (GRCm39) |
missense |
probably benign |
|
IGL02894:Prrc2c
|
APN |
1 |
162,505,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02957:Prrc2c
|
APN |
1 |
162,534,104 (GRCm39) |
unclassified |
probably benign |
|
IGL02981:Prrc2c
|
APN |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
IGL03070:Prrc2c
|
APN |
1 |
162,504,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03096:Prrc2c
|
APN |
1 |
162,529,928 (GRCm39) |
missense |
unknown |
|
R0058:Prrc2c
|
UTSW |
1 |
162,526,453 (GRCm39) |
missense |
unknown |
|
R0058:Prrc2c
|
UTSW |
1 |
162,526,453 (GRCm39) |
missense |
unknown |
|
R0135:Prrc2c
|
UTSW |
1 |
162,543,052 (GRCm39) |
splice site |
probably benign |
|
R0279:Prrc2c
|
UTSW |
1 |
162,543,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Prrc2c
|
UTSW |
1 |
162,525,380 (GRCm39) |
missense |
unknown |
|
R0436:Prrc2c
|
UTSW |
1 |
162,532,883 (GRCm39) |
unclassified |
probably benign |
|
R0605:Prrc2c
|
UTSW |
1 |
162,509,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0696:Prrc2c
|
UTSW |
1 |
162,536,421 (GRCm39) |
critical splice donor site |
probably null |
|
R0981:Prrc2c
|
UTSW |
1 |
162,533,550 (GRCm39) |
unclassified |
probably benign |
|
R1693:Prrc2c
|
UTSW |
1 |
162,546,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R1714:Prrc2c
|
UTSW |
1 |
162,504,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Prrc2c
|
UTSW |
1 |
162,532,551 (GRCm39) |
unclassified |
probably benign |
|
R1794:Prrc2c
|
UTSW |
1 |
162,533,528 (GRCm39) |
unclassified |
probably benign |
|
R1998:Prrc2c
|
UTSW |
1 |
162,532,487 (GRCm39) |
unclassified |
probably benign |
|
R2040:Prrc2c
|
UTSW |
1 |
162,525,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R2168:Prrc2c
|
UTSW |
1 |
162,537,903 (GRCm39) |
unclassified |
probably benign |
|
R2246:Prrc2c
|
UTSW |
1 |
162,535,360 (GRCm39) |
unclassified |
probably benign |
|
R2830:Prrc2c
|
UTSW |
1 |
162,536,485 (GRCm39) |
unclassified |
probably benign |
|
R2926:Prrc2c
|
UTSW |
1 |
162,533,696 (GRCm39) |
unclassified |
probably benign |
|
R3703:Prrc2c
|
UTSW |
1 |
162,538,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R3745:Prrc2c
|
UTSW |
1 |
162,525,754 (GRCm39) |
missense |
unknown |
|
R3760:Prrc2c
|
UTSW |
1 |
162,520,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Prrc2c
|
UTSW |
1 |
162,537,238 (GRCm39) |
unclassified |
probably benign |
|
R3959:Prrc2c
|
UTSW |
1 |
162,536,461 (GRCm39) |
unclassified |
probably benign |
|
R4255:Prrc2c
|
UTSW |
1 |
162,533,895 (GRCm39) |
unclassified |
probably benign |
|
R4276:Prrc2c
|
UTSW |
1 |
162,501,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4421:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R4593:Prrc2c
|
UTSW |
1 |
162,525,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Prrc2c
|
UTSW |
1 |
162,550,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Prrc2c
|
UTSW |
1 |
162,550,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Prrc2c
|
UTSW |
1 |
162,508,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Prrc2c
|
UTSW |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
R4753:Prrc2c
|
UTSW |
1 |
162,518,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Prrc2c
|
UTSW |
1 |
162,538,050 (GRCm39) |
missense |
unknown |
|
R4981:Prrc2c
|
UTSW |
1 |
162,520,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Prrc2c
|
UTSW |
1 |
162,532,879 (GRCm39) |
unclassified |
probably benign |
|
R5119:Prrc2c
|
UTSW |
1 |
162,533,009 (GRCm39) |
unclassified |
probably benign |
|
R5127:Prrc2c
|
UTSW |
1 |
162,525,415 (GRCm39) |
missense |
unknown |
|
R5291:Prrc2c
|
UTSW |
1 |
162,533,151 (GRCm39) |
unclassified |
probably benign |
|
R5474:Prrc2c
|
UTSW |
1 |
162,537,213 (GRCm39) |
unclassified |
probably benign |
|
R5543:Prrc2c
|
UTSW |
1 |
162,501,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R5579:Prrc2c
|
UTSW |
1 |
162,508,327 (GRCm39) |
critical splice donor site |
probably null |
|
R5594:Prrc2c
|
UTSW |
1 |
162,526,600 (GRCm39) |
missense |
unknown |
|
R5620:Prrc2c
|
UTSW |
1 |
162,501,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Prrc2c
|
UTSW |
1 |
162,501,725 (GRCm39) |
splice site |
probably null |
|
R6142:Prrc2c
|
UTSW |
1 |
162,537,956 (GRCm39) |
missense |
unknown |
|
R6199:Prrc2c
|
UTSW |
1 |
162,510,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Prrc2c
|
UTSW |
1 |
162,541,883 (GRCm39) |
missense |
probably benign |
|
R6504:Prrc2c
|
UTSW |
1 |
162,525,364 (GRCm39) |
missense |
unknown |
|
R6671:Prrc2c
|
UTSW |
1 |
162,525,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Prrc2c
|
UTSW |
1 |
162,536,670 (GRCm39) |
unclassified |
probably benign |
|
R6799:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6801:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6850:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6851:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6856:Prrc2c
|
UTSW |
1 |
162,509,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6869:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6882:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6884:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6897:Prrc2c
|
UTSW |
1 |
162,533,075 (GRCm39) |
unclassified |
probably benign |
|
R6934:Prrc2c
|
UTSW |
1 |
162,548,074 (GRCm39) |
missense |
probably benign |
0.10 |
R6976:Prrc2c
|
UTSW |
1 |
162,520,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Prrc2c
|
UTSW |
1 |
162,508,850 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7165:Prrc2c
|
UTSW |
1 |
162,501,086 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7282:Prrc2c
|
UTSW |
1 |
162,507,543 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7467:Prrc2c
|
UTSW |
1 |
162,504,932 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7915:Prrc2c
|
UTSW |
1 |
162,519,977 (GRCm39) |
missense |
probably benign |
0.39 |
R8068:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R8529:Prrc2c
|
UTSW |
1 |
162,536,663 (GRCm39) |
unclassified |
probably benign |
|
R8734:Prrc2c
|
UTSW |
1 |
162,507,081 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8735:Prrc2c
|
UTSW |
1 |
162,537,127 (GRCm39) |
missense |
unknown |
|
R8813:Prrc2c
|
UTSW |
1 |
162,532,812 (GRCm39) |
missense |
unknown |
|
R8946:Prrc2c
|
UTSW |
1 |
162,536,478 (GRCm39) |
unclassified |
probably benign |
|
R8975:Prrc2c
|
UTSW |
1 |
162,533,630 (GRCm39) |
missense |
unknown |
|
R9035:Prrc2c
|
UTSW |
1 |
162,503,295 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9185:Prrc2c
|
UTSW |
1 |
162,532,212 (GRCm39) |
missense |
unknown |
|
R9261:Prrc2c
|
UTSW |
1 |
162,505,622 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9287:Prrc2c
|
UTSW |
1 |
162,541,843 (GRCm39) |
missense |
probably benign |
0.34 |
R9289:Prrc2c
|
UTSW |
1 |
162,507,130 (GRCm39) |
missense |
probably benign |
0.33 |
R9466:Prrc2c
|
UTSW |
1 |
162,503,258 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9523:Prrc2c
|
UTSW |
1 |
162,525,298 (GRCm39) |
missense |
unknown |
|
R9542:Prrc2c
|
UTSW |
1 |
162,508,359 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9629:Prrc2c
|
UTSW |
1 |
162,519,959 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9744:Prrc2c
|
UTSW |
1 |
162,505,733 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9748:Prrc2c
|
UTSW |
1 |
162,535,435 (GRCm39) |
missense |
unknown |
|
X0020:Prrc2c
|
UTSW |
1 |
162,535,416 (GRCm39) |
unclassified |
probably benign |
|
X0039:Prrc2c
|
UTSW |
1 |
162,532,362 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- CTGTTAGAGAGCCATGGGACTG -3'
(R):5'- AGCCTCAACTACAGTCTCTGTC -3'
Sequencing Primer
(F):5'- ACTGTGAAGTGGGCATGGACTTC -3'
(R):5'- CAACTACAGTCTCTGTCCCTATTC -3'
|
Posted On |
2015-10-21 |