Incidental Mutation 'R4660:Prrc2c'
ID |
377786 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Prrc2c
|
Ensembl Gene |
ENSMUSG00000040225 |
Gene Name |
proline-rich coiled-coil 2C |
Synonyms |
9630039I18Rik, Bat2d, 1810043M20Rik, Bat2l2 |
MMRRC Submission |
041920-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.410)
|
Stock # |
R4660 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
162499354-162568125 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 162508464 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Leucine
at position 1091
(P1091L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138451
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028016]
[ENSMUST00000182149]
[ENSMUST00000182393]
[ENSMUST00000182593]
[ENSMUST00000182660]
[ENSMUST00000183223]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000028016
AA Change: P2373L
PolyPhen 2
Score 0.930 (Sensitivity: 0.81; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000028016 Gene: ENSMUSG00000040225 AA Change: P2373L
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 |
probably damaging
Transcript: ENSMUST00000182149
AA Change: P2375L
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000138548 Gene: ENSMUSG00000040225 AA Change: P2375L
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 |
probably damaging
Transcript: ENSMUST00000182393
AA Change: P1091L
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000138451 Gene: ENSMUSG00000040225 AA Change: P1091L
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 |
noncoding transcript
Transcript: ENSMUST00000182535
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182593
AA Change: P2373L
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000138674 Gene: ENSMUSG00000040225 AA Change: P2373L
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 |
probably damaging
Transcript: ENSMUST00000182660
AA Change: P2375L
PolyPhen 2
Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000138433 Gene: ENSMUSG00000040225 AA Change: P2375L
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 |
probably damaging
Transcript: ENSMUST00000183223
AA Change: P884L
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000138698 Gene: ENSMUSG00000040225 AA Change: P884L
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 |
|
Meta Mutation Damage Score |
0.1804 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 95.0%
|
Validation Efficiency |
96% (102/106) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adra1d |
T |
C |
2: 131,403,062 (GRCm39) |
T343A |
probably damaging |
Het |
Angptl4 |
A |
T |
17: 33,996,249 (GRCm39) |
|
probably benign |
Het |
Antxr2 |
A |
T |
5: 98,151,913 (GRCm39) |
|
probably null |
Het |
Ap1b1 |
T |
A |
11: 4,966,760 (GRCm39) |
V145E |
probably damaging |
Het |
Asns |
G |
T |
6: 7,678,012 (GRCm39) |
N355K |
probably benign |
Het |
Asxl3 |
A |
G |
18: 22,649,534 (GRCm39) |
T508A |
probably benign |
Het |
B4galt7 |
T |
A |
13: 55,752,111 (GRCm39) |
V54D |
possibly damaging |
Het |
Bach2 |
C |
T |
4: 32,562,777 (GRCm39) |
P415S |
probably benign |
Het |
Bbs9 |
G |
A |
9: 22,490,063 (GRCm39) |
R278Q |
probably benign |
Het |
Blzf1 |
C |
T |
1: 164,134,062 (GRCm39) |
|
probably benign |
Het |
Btd |
A |
T |
14: 31,389,760 (GRCm39) |
T494S |
probably benign |
Het |
Casp9 |
C |
T |
4: 141,540,934 (GRCm39) |
T434I |
probably benign |
Het |
Cavin2 |
T |
C |
1: 51,340,510 (GRCm39) |
S396P |
probably benign |
Het |
Ccnk |
C |
T |
12: 108,168,575 (GRCm39) |
|
probably benign |
Het |
Cldn8 |
G |
A |
16: 88,359,296 (GRCm39) |
H210Y |
probably benign |
Het |
Clip1 |
G |
A |
5: 123,717,437 (GRCm39) |
T1284I |
probably damaging |
Het |
Coch |
T |
C |
12: 51,642,268 (GRCm39) |
V80A |
probably benign |
Het |
Cttnbp2 |
A |
G |
6: 18,406,536 (GRCm39) |
S1052P |
probably benign |
Het |
Cyp2j7 |
C |
T |
4: 96,083,579 (GRCm39) |
R457K |
probably benign |
Het |
Dalrd3 |
T |
C |
9: 108,447,568 (GRCm39) |
S129P |
probably benign |
Het |
Ddx10 |
A |
G |
9: 53,147,698 (GRCm39) |
|
probably null |
Het |
Dnah7b |
A |
T |
1: 46,328,696 (GRCm39) |
T3143S |
probably damaging |
Het |
Dynlt1b |
A |
G |
17: 6,699,279 (GRCm39) |
T10A |
probably benign |
Het |
Eif2s2 |
G |
A |
2: 154,730,189 (GRCm39) |
T36I |
probably benign |
Het |
Fam118b |
A |
T |
9: 35,146,551 (GRCm39) |
H105Q |
possibly damaging |
Het |
Galntl5 |
T |
A |
5: 25,408,377 (GRCm39) |
I250N |
probably damaging |
Het |
Gm11544 |
C |
T |
11: 94,736,306 (GRCm39) |
|
noncoding transcript |
Het |
Gm5709 |
C |
T |
3: 59,526,124 (GRCm39) |
|
noncoding transcript |
Het |
Golgb1 |
T |
A |
16: 36,707,980 (GRCm39) |
I107N |
probably damaging |
Het |
Gpld1 |
T |
C |
13: 25,166,586 (GRCm39) |
|
probably null |
Het |
Grik1 |
T |
A |
16: 87,720,019 (GRCm39) |
T768S |
probably damaging |
Het |
H2-T23 |
T |
G |
17: 36,341,108 (GRCm39) |
Q349P |
probably damaging |
Het |
Ing3 |
A |
T |
6: 21,973,710 (GRCm39) |
|
probably benign |
Het |
Iqgap3 |
T |
G |
3: 88,027,483 (GRCm39) |
L702R |
probably damaging |
Het |
Itga8 |
A |
G |
2: 12,270,069 (GRCm39) |
V139A |
probably damaging |
Het |
Jam2 |
G |
A |
16: 84,609,840 (GRCm39) |
V151M |
probably damaging |
Het |
Kbtbd12 |
T |
C |
6: 88,594,772 (GRCm39) |
I353V |
probably benign |
Het |
Kif27 |
T |
C |
13: 58,471,730 (GRCm39) |
E786G |
probably damaging |
Het |
Lingo4 |
T |
A |
3: 94,310,672 (GRCm39) |
S537T |
probably benign |
Het |
Lipo3 |
C |
T |
19: 33,598,360 (GRCm39) |
|
probably benign |
Het |
Lrrc3 |
G |
T |
10: 77,729,866 (GRCm39) |
|
probably benign |
Het |
Ltbp3 |
T |
A |
19: 5,798,814 (GRCm39) |
|
probably null |
Het |
Lyg1 |
T |
A |
1: 37,985,942 (GRCm39) |
|
probably benign |
Het |
Mcm9 |
T |
C |
10: 53,424,623 (GRCm39) |
I656V |
probably benign |
Het |
Mfsd8 |
T |
A |
3: 40,776,372 (GRCm39) |
I427F |
probably benign |
Het |
Mga |
T |
A |
2: 119,769,104 (GRCm39) |
|
probably benign |
Het |
Miga1 |
A |
G |
3: 151,993,155 (GRCm39) |
L422P |
probably damaging |
Het |
Msantd3 |
A |
G |
4: 48,552,536 (GRCm39) |
I42V |
probably benign |
Het |
Mybbp1a |
T |
C |
11: 72,336,538 (GRCm39) |
V510A |
probably benign |
Het |
Nccrp1 |
G |
T |
7: 28,245,760 (GRCm39) |
P135T |
probably damaging |
Het |
Neb |
T |
A |
2: 52,145,600 (GRCm39) |
M2975L |
possibly damaging |
Het |
Nfxl1 |
A |
T |
5: 72,710,011 (GRCm39) |
I171N |
probably damaging |
Het |
Odad2 |
A |
G |
18: 7,211,609 (GRCm39) |
V755A |
possibly damaging |
Het |
Or10q3 |
T |
C |
19: 11,848,412 (GRCm39) |
H56R |
possibly damaging |
Het |
Or12j5 |
A |
T |
7: 140,083,933 (GRCm39) |
F146L |
probably benign |
Het |
Or13a19 |
T |
C |
7: 139,903,325 (GRCm39) |
F238L |
possibly damaging |
Het |
Otop1 |
T |
G |
5: 38,457,368 (GRCm39) |
S376A |
possibly damaging |
Het |
Pdgfra |
T |
C |
5: 75,322,932 (GRCm39) |
V10A |
possibly damaging |
Het |
Pgs1 |
T |
C |
11: 117,910,503 (GRCm39) |
V538A |
probably damaging |
Het |
Ppa2 |
A |
T |
3: 133,032,445 (GRCm39) |
T97S |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,380,847 (GRCm39) |
Y392F |
probably benign |
Het |
Pramel26 |
A |
G |
4: 143,538,435 (GRCm39) |
S179P |
probably benign |
Het |
Prdm10 |
G |
A |
9: 31,238,624 (GRCm39) |
C172Y |
probably damaging |
Het |
Pthlh |
G |
A |
6: 147,158,796 (GRCm39) |
R55C |
probably damaging |
Het |
Ptpn9 |
A |
T |
9: 56,943,782 (GRCm39) |
T105S |
probably benign |
Het |
Rundc1 |
T |
A |
11: 101,324,830 (GRCm39) |
V512E |
possibly damaging |
Het |
Scrib |
G |
A |
15: 75,937,185 (GRCm39) |
S307L |
probably damaging |
Het |
Sec23ip |
A |
G |
7: 128,352,010 (GRCm39) |
S26G |
probably null |
Het |
Sec61a2 |
A |
G |
2: 5,878,504 (GRCm39) |
|
probably benign |
Het |
Sema3c |
T |
C |
5: 17,877,511 (GRCm39) |
V206A |
probably damaging |
Het |
Sgk2 |
C |
T |
2: 162,839,763 (GRCm39) |
H124Y |
possibly damaging |
Het |
Slc26a6 |
C |
T |
9: 108,738,540 (GRCm39) |
T592I |
probably damaging |
Het |
Slc5a11 |
T |
C |
7: 122,864,486 (GRCm39) |
Y361H |
probably damaging |
Het |
Smc6 |
T |
C |
12: 11,324,008 (GRCm39) |
V51A |
probably damaging |
Het |
Stab1 |
A |
T |
14: 30,876,872 (GRCm39) |
N817K |
possibly damaging |
Het |
Swt1 |
A |
T |
1: 151,283,348 (GRCm39) |
D336E |
probably benign |
Het |
Taf13 |
T |
A |
3: 108,480,293 (GRCm39) |
|
probably benign |
Het |
Tmub2 |
T |
C |
11: 102,175,845 (GRCm39) |
|
probably benign |
Het |
Tnf |
A |
G |
17: 35,419,156 (GRCm39) |
S209P |
probably benign |
Het |
Try10 |
A |
G |
6: 41,334,761 (GRCm39) |
Y229C |
probably damaging |
Het |
Ttbk1 |
G |
T |
17: 46,788,714 (GRCm39) |
Y183* |
probably null |
Het |
Ttc17 |
A |
T |
2: 94,194,774 (GRCm39) |
I533N |
possibly damaging |
Het |
Tubb6 |
C |
T |
18: 67,535,016 (GRCm39) |
P305L |
probably damaging |
Het |
Tulp3 |
G |
A |
6: 128,300,017 (GRCm39) |
|
probably benign |
Het |
Usp9x |
A |
G |
X: 12,989,747 (GRCm39) |
R776G |
possibly damaging |
Het |
Virma |
T |
C |
4: 11,513,505 (GRCm39) |
V453A |
probably damaging |
Het |
Vmn2r103 |
A |
T |
17: 20,032,077 (GRCm39) |
N617I |
probably damaging |
Het |
Xirp1 |
G |
T |
9: 119,846,058 (GRCm39) |
L942M |
probably damaging |
Het |
Zc3h7b |
T |
G |
15: 81,676,451 (GRCm39) |
V731G |
probably benign |
Het |
Zfp534 |
C |
T |
4: 147,759,175 (GRCm39) |
G498D |
probably benign |
Het |
Zfp639 |
T |
C |
3: 32,574,679 (GRCm39) |
Y435H |
probably damaging |
Het |
Zxdc |
A |
G |
6: 90,355,820 (GRCm39) |
H443R |
probably damaging |
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 |
R4677:Prrc2c
|
UTSW |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
R4688:Prrc2c
|
UTSW |
1 |
162,525,256 (GRCm39) |
missense |
unknown |
|
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'- AGTTGAAATCACCAGGCACAGG -3'
(R):5'- CCAGAGTTTAGTATACCAGTGTAAGTC -3'
Sequencing Primer
(F):5'- GGCACAGGCTTGAAAATATAATGTAC -3'
(R):5'- AGTCACAGGTTAAAAACAAAATTGG -3'
|
Posted On |
2016-04-06 |