Incidental Mutation 'R7232:Ticrr'
ID |
562554 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ticrr
|
Ensembl Gene |
ENSMUSG00000046591 |
Gene Name |
TOPBP1-interacting checkpoint and replication regulator |
Synonyms |
5730590G19Rik |
MMRRC Submission |
045303-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.949)
|
Stock # |
R7232 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
7 |
Chromosomal Location |
79309944-79347896 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 79343490 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Asparagine
at position 1118
(K1118N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000041377
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035977]
[ENSMUST00000059836]
[ENSMUST00000178048]
[ENSMUST00000183846]
[ENSMUST00000184137]
[ENSMUST00000206591]
[ENSMUST00000206622]
|
AlphaFold |
Q8BQ33 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000035977
AA Change: K1118N
PolyPhen 2
Score 0.959 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000041377 Gene: ENSMUSG00000046591 AA Change: K1118N
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
31 |
N/A |
INTRINSIC |
Pfam:Treslin_N
|
211 |
1005 |
N/A |
PFAM |
low complexity region
|
1186 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1220 |
1235 |
N/A |
INTRINSIC |
low complexity region
|
1339 |
1359 |
N/A |
INTRINSIC |
low complexity region
|
1472 |
1480 |
N/A |
INTRINSIC |
low complexity region
|
1496 |
1514 |
N/A |
INTRINSIC |
low complexity region
|
1630 |
1643 |
N/A |
INTRINSIC |
low complexity region
|
1694 |
1707 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000059836
|
SMART Domains |
Protein: ENSMUSP00000061806 Gene: ENSMUSG00000050382
Domain | Start | End | E-Value | Type |
KISc
|
13 |
357 |
2.88e-143 |
SMART |
low complexity region
|
391 |
410 |
N/A |
INTRINSIC |
Blast:KISc
|
413 |
481 |
1e-19 |
BLAST |
Blast:KISc
|
482 |
518 |
3e-11 |
BLAST |
low complexity region
|
523 |
540 |
N/A |
INTRINSIC |
low complexity region
|
543 |
557 |
N/A |
INTRINSIC |
low complexity region
|
621 |
636 |
N/A |
INTRINSIC |
low complexity region
|
669 |
685 |
N/A |
INTRINSIC |
Blast:KISc
|
780 |
879 |
2e-15 |
BLAST |
low complexity region
|
927 |
944 |
N/A |
INTRINSIC |
low complexity region
|
979 |
993 |
N/A |
INTRINSIC |
low complexity region
|
1049 |
1061 |
N/A |
INTRINSIC |
coiled coil region
|
1113 |
1139 |
N/A |
INTRINSIC |
coiled coil region
|
1186 |
1205 |
N/A |
INTRINSIC |
low complexity region
|
1293 |
1304 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000178048
|
SMART Domains |
Protein: ENSMUSP00000136993 Gene: ENSMUSG00000050382
Domain | Start | End | E-Value | Type |
KISc
|
13 |
357 |
2.88e-143 |
SMART |
low complexity region
|
391 |
410 |
N/A |
INTRINSIC |
Blast:KISc
|
413 |
481 |
1e-19 |
BLAST |
Blast:KISc
|
482 |
518 |
3e-11 |
BLAST |
low complexity region
|
523 |
540 |
N/A |
INTRINSIC |
low complexity region
|
543 |
557 |
N/A |
INTRINSIC |
low complexity region
|
621 |
636 |
N/A |
INTRINSIC |
low complexity region
|
669 |
685 |
N/A |
INTRINSIC |
Blast:KISc
|
780 |
879 |
2e-15 |
BLAST |
low complexity region
|
908 |
918 |
N/A |
INTRINSIC |
low complexity region
|
928 |
945 |
N/A |
INTRINSIC |
low complexity region
|
980 |
994 |
N/A |
INTRINSIC |
low complexity region
|
1050 |
1062 |
N/A |
INTRINSIC |
coiled coil region
|
1114 |
1140 |
N/A |
INTRINSIC |
coiled coil region
|
1187 |
1206 |
N/A |
INTRINSIC |
low complexity region
|
1294 |
1305 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000183846
|
SMART Domains |
Protein: ENSMUSP00000139359 Gene: ENSMUSG00000050382
Domain | Start | End | E-Value | Type |
KISc
|
13 |
357 |
2.88e-143 |
SMART |
low complexity region
|
391 |
410 |
N/A |
INTRINSIC |
Blast:KISc
|
413 |
481 |
1e-19 |
BLAST |
Blast:KISc
|
482 |
518 |
3e-11 |
BLAST |
low complexity region
|
523 |
540 |
N/A |
INTRINSIC |
low complexity region
|
543 |
557 |
N/A |
INTRINSIC |
low complexity region
|
621 |
636 |
N/A |
INTRINSIC |
low complexity region
|
669 |
685 |
N/A |
INTRINSIC |
Blast:KISc
|
780 |
879 |
2e-15 |
BLAST |
low complexity region
|
908 |
918 |
N/A |
INTRINSIC |
low complexity region
|
928 |
945 |
N/A |
INTRINSIC |
low complexity region
|
980 |
994 |
N/A |
INTRINSIC |
low complexity region
|
1050 |
1062 |
N/A |
INTRINSIC |
coiled coil region
|
1114 |
1140 |
N/A |
INTRINSIC |
coiled coil region
|
1187 |
1206 |
N/A |
INTRINSIC |
low complexity region
|
1294 |
1305 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000184137
|
SMART Domains |
Protein: ENSMUSP00000139224 Gene: ENSMUSG00000050382
Domain | Start | End | E-Value | Type |
KISc
|
13 |
357 |
2.88e-143 |
SMART |
low complexity region
|
391 |
410 |
N/A |
INTRINSIC |
Blast:KISc
|
413 |
481 |
1e-19 |
BLAST |
Blast:KISc
|
482 |
518 |
3e-11 |
BLAST |
low complexity region
|
523 |
540 |
N/A |
INTRINSIC |
low complexity region
|
543 |
557 |
N/A |
INTRINSIC |
low complexity region
|
621 |
636 |
N/A |
INTRINSIC |
low complexity region
|
669 |
685 |
N/A |
INTRINSIC |
Blast:KISc
|
780 |
879 |
2e-15 |
BLAST |
low complexity region
|
927 |
944 |
N/A |
INTRINSIC |
low complexity region
|
979 |
993 |
N/A |
INTRINSIC |
low complexity region
|
1049 |
1061 |
N/A |
INTRINSIC |
coiled coil region
|
1113 |
1139 |
N/A |
INTRINSIC |
coiled coil region
|
1186 |
1205 |
N/A |
INTRINSIC |
low complexity region
|
1293 |
1304 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000206591
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000206622
|
Meta Mutation Damage Score |
0.1000 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
Validation Efficiency |
99% (80/81) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Treslin is involved in the initiation of DNA replication (Kumagai et al., 2010 [PubMed 20116089]).[supplied by OMIM, Apr 2010] PHENOTYPE: Mice homozygous for an ENU-induced allele are mostly hairless, with only a light patch of hair around the face and tail. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
G |
A |
7: 40,642,603 (GRCm39) |
G91S |
probably damaging |
Het |
Adam21 |
T |
G |
12: 81,607,330 (GRCm39) |
N144T |
probably damaging |
Het |
Adgrg7 |
T |
C |
16: 56,597,515 (GRCm39) |
|
probably null |
Het |
Angpt4 |
T |
C |
2: 151,771,460 (GRCm39) |
S259P |
possibly damaging |
Het |
Aqr |
A |
C |
2: 113,936,363 (GRCm39) |
L1320R |
probably damaging |
Het |
Arhgef10 |
G |
A |
8: 14,990,323 (GRCm39) |
G266D |
probably benign |
Het |
Bop1 |
A |
G |
15: 76,337,546 (GRCm39) |
V693A |
probably damaging |
Het |
Cd86 |
CA |
CAA |
16: 36,426,917 (GRCm39) |
|
probably null |
Het |
Cdc5l |
A |
G |
17: 45,738,863 (GRCm39) |
|
probably null |
Het |
Cfap46 |
C |
A |
7: 139,197,493 (GRCm39) |
R2126L |
unknown |
Het |
Chek2 |
T |
C |
5: 111,008,781 (GRCm39) |
V304A |
probably damaging |
Het |
Cntnap4 |
T |
A |
8: 113,391,731 (GRCm39) |
|
probably null |
Het |
Ctps1 |
C |
A |
4: 120,405,321 (GRCm39) |
G374C |
probably damaging |
Het |
Defa27 |
A |
T |
8: 21,805,625 (GRCm39) |
I22F |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,584,928 (GRCm39) |
S3220P |
probably damaging |
Het |
Dop1b |
T |
G |
16: 93,557,373 (GRCm39) |
|
probably null |
Het |
Dpysl5 |
G |
A |
5: 30,949,642 (GRCm39) |
V471I |
probably benign |
Het |
Duoxa1 |
T |
A |
2: 122,135,728 (GRCm39) |
I124F |
probably damaging |
Het |
Eif4enif1 |
A |
G |
11: 3,165,678 (GRCm39) |
E85G |
possibly damaging |
Het |
Eogt |
T |
A |
6: 97,096,944 (GRCm39) |
I355F |
probably damaging |
Het |
Epha7 |
T |
A |
4: 28,951,279 (GRCm39) |
V800E |
probably damaging |
Het |
Evi5l |
A |
G |
8: 4,255,906 (GRCm39) |
Q633R |
possibly damaging |
Het |
Fam170a |
T |
C |
18: 50,414,728 (GRCm39) |
Y125H |
probably damaging |
Het |
Fbxo15 |
T |
C |
18: 84,980,747 (GRCm39) |
Y241H |
probably damaging |
Het |
Gbe1 |
T |
C |
16: 70,233,828 (GRCm39) |
I235T |
possibly damaging |
Het |
Gfra3 |
C |
T |
18: 34,844,234 (GRCm39) |
R102Q |
probably damaging |
Het |
Gjd4 |
C |
T |
18: 9,280,380 (GRCm39) |
G233S |
probably damaging |
Het |
Gm29106 |
C |
T |
1: 118,127,291 (GRCm39) |
P328S |
probably damaging |
Het |
Hgfac |
G |
T |
5: 35,204,258 (GRCm39) |
R507L |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,609,355 (GRCm39) |
K153R |
probably benign |
Het |
Kcnc1 |
T |
A |
7: 46,077,383 (GRCm39) |
V395E |
probably damaging |
Het |
Krt6b |
T |
C |
15: 101,586,577 (GRCm39) |
D304G |
probably damaging |
Het |
Ldha |
T |
C |
7: 46,500,323 (GRCm39) |
Y174H |
probably benign |
Het |
Lgi4 |
G |
A |
7: 30,766,776 (GRCm39) |
V268M |
possibly damaging |
Het |
Lpar3 |
T |
G |
3: 145,947,061 (GRCm39) |
|
probably null |
Het |
Lrp3 |
T |
C |
7: 34,905,477 (GRCm39) |
D103G |
probably damaging |
Het |
Marchf5 |
G |
A |
19: 37,194,713 (GRCm39) |
|
probably null |
Het |
Muc5b |
A |
T |
7: 141,419,866 (GRCm39) |
H4115L |
possibly damaging |
Het |
Myh13 |
G |
A |
11: 67,239,672 (GRCm39) |
D741N |
probably damaging |
Het |
Naglu |
A |
T |
11: 100,967,252 (GRCm39) |
I401F |
probably damaging |
Het |
Ncam2 |
T |
A |
16: 81,309,759 (GRCm39) |
N416K |
probably damaging |
Het |
Ncan |
A |
G |
8: 70,564,738 (GRCm39) |
L292S |
probably damaging |
Het |
Nkiras1 |
T |
C |
14: 18,276,732 (GRCm38) |
V7A |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,068,708 (GRCm39) |
L203* |
probably null |
Het |
Nscme3l |
A |
T |
19: 5,553,659 (GRCm39) |
S41T |
possibly damaging |
Het |
Onecut2 |
T |
A |
18: 64,474,633 (GRCm39) |
W395R |
probably damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,062 (GRCm39) |
I9K |
probably benign |
Het |
Pak6 |
T |
A |
2: 118,524,003 (GRCm39) |
V386E |
probably damaging |
Het |
Pias2 |
A |
G |
18: 77,220,931 (GRCm39) |
S396G |
probably benign |
Het |
Plxna2 |
T |
A |
1: 194,394,568 (GRCm39) |
L483H |
probably damaging |
Het |
Prss36 |
G |
T |
7: 127,534,763 (GRCm39) |
R484S |
probably benign |
Het |
Ptpn21 |
A |
T |
12: 98,654,996 (GRCm39) |
V657E |
probably benign |
Het |
Rassf2 |
T |
C |
2: 131,838,332 (GRCm39) |
E318G |
probably damaging |
Het |
Rp1 |
A |
C |
1: 4,298,824 (GRCm39) |
S623A |
unknown |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Scn11a |
T |
A |
9: 119,588,982 (GRCm39) |
E1308V |
probably damaging |
Het |
Serpina3c |
A |
T |
12: 104,115,771 (GRCm39) |
S258T |
possibly damaging |
Het |
Slit3 |
A |
G |
11: 35,501,516 (GRCm39) |
T417A |
possibly damaging |
Het |
Sostdc1 |
C |
A |
12: 36,367,310 (GRCm39) |
A162E |
possibly damaging |
Het |
Sox13 |
A |
T |
1: 133,312,129 (GRCm39) |
|
probably null |
Het |
Sox8 |
G |
T |
17: 25,786,514 (GRCm39) |
S396R |
probably benign |
Het |
Sult2a3 |
A |
T |
7: 13,816,685 (GRCm39) |
F164L |
possibly damaging |
Het |
Susd2 |
T |
C |
10: 75,475,685 (GRCm39) |
Y438C |
probably damaging |
Het |
Tas2r106 |
T |
G |
6: 131,655,810 (GRCm39) |
T14P |
probably damaging |
Het |
Tcf25 |
T |
A |
8: 124,127,800 (GRCm39) |
|
probably null |
Het |
Tenm3 |
G |
A |
8: 48,688,970 (GRCm39) |
R2206W |
probably damaging |
Het |
Tep1 |
A |
G |
14: 51,081,789 (GRCm39) |
L471P |
unknown |
Het |
Tlr5 |
G |
A |
1: 182,801,064 (GRCm39) |
E123K |
probably benign |
Het |
Ttn |
ATATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTG |
ATATCTCTCCAGAGCCTCCCCTGGAGGAGTGGAGTATCTCTCCAGAGCCTCCCCTG |
2: 76,746,150 (GRCm39) |
|
probably benign |
Het |
U2surp |
A |
G |
9: 95,375,770 (GRCm39) |
V141A |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,100,734 (GRCm39) |
S2050T |
possibly damaging |
Het |
Usp13 |
A |
G |
3: 32,920,020 (GRCm39) |
D235G |
probably benign |
Het |
Vcam1 |
T |
C |
3: 115,919,628 (GRCm39) |
T213A |
possibly damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,786,166 (GRCm39) |
I323N |
possibly damaging |
Het |
Vps13b |
A |
G |
15: 35,877,703 (GRCm39) |
I2892M |
probably damaging |
Het |
Wnt5a |
T |
A |
14: 28,240,329 (GRCm39) |
S160T |
probably benign |
Het |
Zar1 |
G |
A |
5: 72,738,294 (GRCm39) |
P36L |
possibly damaging |
Het |
Zfp773 |
A |
T |
7: 7,135,984 (GRCm39) |
M204K |
probably benign |
Het |
Zhx1 |
T |
C |
15: 57,916,465 (GRCm39) |
T594A |
probably benign |
Het |
|
Other mutations in Ticrr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Ticrr
|
APN |
7 |
79,327,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00596:Ticrr
|
APN |
7 |
79,327,041 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01327:Ticrr
|
APN |
7 |
79,344,209 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01525:Ticrr
|
APN |
7 |
79,332,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01565:Ticrr
|
APN |
7 |
79,344,296 (GRCm39) |
missense |
probably benign |
|
IGL01936:Ticrr
|
APN |
7 |
79,344,297 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02160:Ticrr
|
APN |
7 |
79,343,767 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02246:Ticrr
|
APN |
7 |
79,325,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02487:Ticrr
|
APN |
7 |
79,332,769 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02593:Ticrr
|
APN |
7 |
79,345,214 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02970:Ticrr
|
APN |
7 |
79,344,919 (GRCm39) |
missense |
probably benign |
0.01 |
FR4304:Ticrr
|
UTSW |
7 |
79,344,059 (GRCm39) |
intron |
probably benign |
|
PIT4305001:Ticrr
|
UTSW |
7 |
79,328,771 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4791001:Ticrr
|
UTSW |
7 |
79,319,386 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0016:Ticrr
|
UTSW |
7 |
79,343,540 (GRCm39) |
missense |
probably benign |
0.01 |
R0062:Ticrr
|
UTSW |
7 |
79,317,654 (GRCm39) |
missense |
probably benign |
0.01 |
R0062:Ticrr
|
UTSW |
7 |
79,317,654 (GRCm39) |
missense |
probably benign |
0.01 |
R0067:Ticrr
|
UTSW |
7 |
79,327,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Ticrr
|
UTSW |
7 |
79,327,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Ticrr
|
UTSW |
7 |
79,327,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Ticrr
|
UTSW |
7 |
79,344,236 (GRCm39) |
missense |
probably damaging |
0.99 |
R0595:Ticrr
|
UTSW |
7 |
79,345,311 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1118:Ticrr
|
UTSW |
7 |
79,343,701 (GRCm39) |
missense |
probably benign |
0.23 |
R1119:Ticrr
|
UTSW |
7 |
79,343,701 (GRCm39) |
missense |
probably benign |
0.23 |
R1572:Ticrr
|
UTSW |
7 |
79,331,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Ticrr
|
UTSW |
7 |
79,345,297 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1757:Ticrr
|
UTSW |
7 |
79,328,794 (GRCm39) |
nonsense |
probably null |
|
R1757:Ticrr
|
UTSW |
7 |
79,325,071 (GRCm39) |
missense |
probably damaging |
0.99 |
R1862:Ticrr
|
UTSW |
7 |
79,344,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R1869:Ticrr
|
UTSW |
7 |
79,328,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Ticrr
|
UTSW |
7 |
79,325,142 (GRCm39) |
missense |
probably damaging |
0.98 |
R1966:Ticrr
|
UTSW |
7 |
79,344,483 (GRCm39) |
nonsense |
probably null |
|
R2006:Ticrr
|
UTSW |
7 |
79,343,821 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2178:Ticrr
|
UTSW |
7 |
79,315,433 (GRCm39) |
missense |
probably benign |
0.12 |
R3404:Ticrr
|
UTSW |
7 |
79,344,539 (GRCm39) |
missense |
probably benign |
0.06 |
R3405:Ticrr
|
UTSW |
7 |
79,344,539 (GRCm39) |
missense |
probably benign |
0.06 |
R3941:Ticrr
|
UTSW |
7 |
79,343,445 (GRCm39) |
intron |
probably benign |
|
R3950:Ticrr
|
UTSW |
7 |
79,331,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R3951:Ticrr
|
UTSW |
7 |
79,331,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R3952:Ticrr
|
UTSW |
7 |
79,331,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Ticrr
|
UTSW |
7 |
79,310,158 (GRCm39) |
missense |
probably damaging |
0.99 |
R4972:Ticrr
|
UTSW |
7 |
79,319,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R5259:Ticrr
|
UTSW |
7 |
79,344,471 (GRCm39) |
missense |
probably benign |
0.01 |
R5272:Ticrr
|
UTSW |
7 |
79,319,353 (GRCm39) |
missense |
probably benign |
0.44 |
R5374:Ticrr
|
UTSW |
7 |
79,340,690 (GRCm39) |
nonsense |
probably null |
|
R5480:Ticrr
|
UTSW |
7 |
79,310,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Ticrr
|
UTSW |
7 |
79,345,044 (GRCm39) |
nonsense |
probably null |
|
R5568:Ticrr
|
UTSW |
7 |
79,339,715 (GRCm39) |
critical splice donor site |
probably null |
|
R5588:Ticrr
|
UTSW |
7 |
79,328,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R5698:Ticrr
|
UTSW |
7 |
79,328,881 (GRCm39) |
missense |
probably benign |
|
R5879:Ticrr
|
UTSW |
7 |
79,346,438 (GRCm39) |
missense |
probably benign |
0.12 |
R5980:Ticrr
|
UTSW |
7 |
79,310,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R6128:Ticrr
|
UTSW |
7 |
79,343,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Ticrr
|
UTSW |
7 |
79,344,444 (GRCm39) |
missense |
probably benign |
0.00 |
R6335:Ticrr
|
UTSW |
7 |
79,344,031 (GRCm39) |
splice site |
probably null |
|
R6866:Ticrr
|
UTSW |
7 |
79,343,705 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6905:Ticrr
|
UTSW |
7 |
79,315,598 (GRCm39) |
missense |
probably benign |
0.00 |
R6923:Ticrr
|
UTSW |
7 |
79,341,601 (GRCm39) |
missense |
probably damaging |
0.98 |
R6962:Ticrr
|
UTSW |
7 |
79,315,645 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7285:Ticrr
|
UTSW |
7 |
79,310,610 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7385:Ticrr
|
UTSW |
7 |
79,341,597 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7426:Ticrr
|
UTSW |
7 |
79,343,734 (GRCm39) |
missense |
probably benign |
|
R7583:Ticrr
|
UTSW |
7 |
79,346,487 (GRCm39) |
nonsense |
probably null |
|
R7749:Ticrr
|
UTSW |
7 |
79,328,844 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7863:Ticrr
|
UTSW |
7 |
79,331,760 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7899:Ticrr
|
UTSW |
7 |
79,319,233 (GRCm39) |
missense |
probably benign |
0.23 |
R7935:Ticrr
|
UTSW |
7 |
79,331,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R8005:Ticrr
|
UTSW |
7 |
79,343,796 (GRCm39) |
missense |
probably damaging |
0.98 |
R8080:Ticrr
|
UTSW |
7 |
79,334,012 (GRCm39) |
splice site |
probably null |
|
R8181:Ticrr
|
UTSW |
7 |
79,310,728 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8349:Ticrr
|
UTSW |
7 |
79,344,428 (GRCm39) |
missense |
probably benign |
0.27 |
R8410:Ticrr
|
UTSW |
7 |
79,317,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R8449:Ticrr
|
UTSW |
7 |
79,344,428 (GRCm39) |
missense |
probably benign |
0.27 |
R9073:Ticrr
|
UTSW |
7 |
79,317,679 (GRCm39) |
missense |
probably benign |
0.01 |
R9090:Ticrr
|
UTSW |
7 |
79,310,604 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9271:Ticrr
|
UTSW |
7 |
79,310,604 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9287:Ticrr
|
UTSW |
7 |
79,343,516 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9368:Ticrr
|
UTSW |
7 |
79,330,735 (GRCm39) |
missense |
probably damaging |
0.99 |
R9469:Ticrr
|
UTSW |
7 |
79,344,511 (GRCm39) |
missense |
probably benign |
0.03 |
R9502:Ticrr
|
UTSW |
7 |
79,343,597 (GRCm39) |
missense |
probably benign |
|
R9614:Ticrr
|
UTSW |
7 |
79,345,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Ticrr
|
UTSW |
7 |
79,345,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R9779:Ticrr
|
UTSW |
7 |
79,328,802 (GRCm39) |
missense |
probably benign |
0.37 |
|
Predicted Primers |
PCR Primer
(F):5'- AGAGGGAACAGGTCACTATTCTAG -3'
(R):5'- ATCAGACTCTCTGGGTGTGC -3'
Sequencing Primer
(F):5'- GGGAACAGGTCACTATTCTAGATTCC -3'
(R):5'- GAGACTGTCTTTTGAGAAGTGAC -3'
|
Posted On |
2019-06-26 |