Incidental Mutation 'R7146:D430041D05Rik'
ID |
553759 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
D430041D05Rik
|
Ensembl Gene |
ENSMUSG00000068373 |
Gene Name |
RIKEN cDNA D430041D05 gene |
Synonyms |
G2 |
MMRRC Submission |
045251-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.236)
|
Stock # |
R7146 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
103973418-104241358 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 104088698 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 131
(T131A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000106756
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000089726]
[ENSMUST00000136156]
[ENSMUST00000141159]
[ENSMUST00000230671]
|
AlphaFold |
A0A2R8VKG2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000089726
AA Change: T131A
PolyPhen 2
Score 0.062 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000106756 Gene: ENSMUSG00000068373 AA Change: T131A
Domain | Start | End | E-Value | Type |
low complexity region
|
55 |
70 |
N/A |
INTRINSIC |
low complexity region
|
206 |
215 |
N/A |
INTRINSIC |
low complexity region
|
218 |
230 |
N/A |
INTRINSIC |
low complexity region
|
234 |
253 |
N/A |
INTRINSIC |
Pfam:DUF3827
|
498 |
1134 |
2.4e-282 |
PFAM |
low complexity region
|
1196 |
1217 |
N/A |
INTRINSIC |
low complexity region
|
1331 |
1351 |
N/A |
INTRINSIC |
low complexity region
|
1360 |
1372 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136156
AA Change: T131A
PolyPhen 2
Score 0.102 (Sensitivity: 0.93; Specificity: 0.86)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141159
|
SMART Domains |
Protein: ENSMUSP00000117041 Gene: ENSMUSG00000068373
Domain | Start | End | E-Value | Type |
low complexity region
|
55 |
70 |
N/A |
INTRINSIC |
low complexity region
|
91 |
100 |
N/A |
INTRINSIC |
low complexity region
|
103 |
115 |
N/A |
INTRINSIC |
low complexity region
|
119 |
138 |
N/A |
INTRINSIC |
Pfam:DUF3827
|
383 |
1020 |
8.2e-280 |
PFAM |
low complexity region
|
1082 |
1103 |
N/A |
INTRINSIC |
low complexity region
|
1217 |
1237 |
N/A |
INTRINSIC |
low complexity region
|
1246 |
1258 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000230671
AA Change: T93A
PolyPhen 2
Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.2%
|
Validation Efficiency |
95% (99/104) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
T |
7: 119,854,520 (GRCm39) |
I895F |
probably benign |
Het |
Abca16 |
A |
G |
7: 120,126,974 (GRCm39) |
N1222D |
possibly damaging |
Het |
Abcc4 |
A |
T |
14: 118,852,593 (GRCm39) |
Y499N |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,550,605 (GRCm39) |
C702W |
probably damaging |
Het |
Adk |
C |
A |
14: 21,376,682 (GRCm39) |
P27H |
|
Het |
Ankrd13a |
T |
C |
5: 114,913,293 (GRCm39) |
S2P |
probably damaging |
Het |
Ano1 |
T |
C |
7: 144,209,393 (GRCm39) |
H269R |
probably benign |
Het |
Aox3 |
T |
A |
1: 58,197,688 (GRCm39) |
|
probably null |
Het |
Asl |
G |
A |
5: 130,053,290 (GRCm39) |
|
probably benign |
Het |
Asxl2 |
A |
T |
12: 3,507,066 (GRCm39) |
D86V |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,083,508 (GRCm39) |
|
probably null |
Het |
Bach2 |
A |
G |
4: 32,562,670 (GRCm39) |
D379G |
probably damaging |
Het |
Bdkrb1 |
T |
A |
12: 105,571,142 (GRCm39) |
L236Q |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 29,443,654 (GRCm39) |
Y24C |
unknown |
Het |
Cage1 |
G |
T |
13: 38,207,025 (GRCm39) |
N273K |
probably benign |
Het |
Ccdc51 |
T |
A |
9: 108,920,848 (GRCm39) |
I245N |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,456,325 (GRCm39) |
I229V |
probably benign |
Het |
Chst4 |
T |
A |
8: 110,757,363 (GRCm39) |
S167C |
probably damaging |
Het |
Cntnap4 |
A |
T |
8: 113,537,268 (GRCm39) |
Y713F |
probably damaging |
Het |
Cntnap5b |
G |
A |
1: 99,978,519 (GRCm39) |
|
probably null |
Het |
Cog8 |
G |
T |
8: 107,779,005 (GRCm39) |
T424K |
possibly damaging |
Het |
Cop1 |
T |
G |
1: 159,071,922 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
A |
G |
4: 96,434,019 (GRCm39) |
I97T |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 117,972,936 (GRCm39) |
D1999G |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,863,591 (GRCm39) |
D250G |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,988,618 (GRCm39) |
V3196A |
possibly damaging |
Het |
Dscam |
A |
T |
16: 96,631,117 (GRCm39) |
Y299* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,858,578 (GRCm39) |
N3879S |
unknown |
Het |
Efcab3 |
A |
C |
11: 104,913,764 (GRCm39) |
D4594A |
probably benign |
Het |
Ephb1 |
A |
G |
9: 101,841,157 (GRCm39) |
S774P |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,403,962 (GRCm39) |
V238I |
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,776,785 (GRCm39) |
M234I |
probably benign |
Het |
Fmnl2 |
C |
T |
2: 52,958,552 (GRCm39) |
S212L |
|
Het |
Frem1 |
T |
C |
4: 82,840,532 (GRCm39) |
N1798S |
possibly damaging |
Het |
Gabrd |
T |
A |
4: 155,469,863 (GRCm39) |
M449L |
probably benign |
Het |
Gad1 |
T |
C |
2: 70,417,706 (GRCm39) |
F302L |
probably benign |
Het |
Gm10800 |
A |
AC |
2: 98,497,378 (GRCm39) |
|
probably null |
Het |
Gm21886 |
GGGCCTGCAGACAGTAGGTGCTCACTAGGGCCTGTAAATAGTAGGTGCTCACTGAGGCCTGTAGACAGTAGGTGCTCA |
GGGCCTGTAGACAGTAGGTGCTCA |
18: 80,132,697 (GRCm39) |
|
probably benign |
Het |
Gnb3 |
C |
T |
6: 124,813,887 (GRCm39) |
|
probably null |
Het |
Gtf3c1 |
A |
T |
7: 125,271,993 (GRCm39) |
M642K |
possibly damaging |
Het |
Hps3 |
A |
T |
3: 20,063,050 (GRCm39) |
W838R |
probably damaging |
Het |
Ide |
A |
T |
19: 37,273,343 (GRCm39) |
W527R |
|
Het |
Ighe |
A |
T |
12: 113,235,975 (GRCm39) |
I117N |
|
Het |
Ighv1-50 |
T |
C |
12: 115,083,396 (GRCm39) |
E108G |
probably benign |
Het |
Ivl |
G |
A |
3: 92,479,538 (GRCm39) |
P176S |
probably damaging |
Het |
Lamb2 |
T |
A |
9: 108,361,283 (GRCm39) |
L605Q |
possibly damaging |
Het |
Lgi3 |
G |
A |
14: 70,770,832 (GRCm39) |
R157H |
probably damaging |
Het |
Lrp1b |
G |
T |
2: 41,266,006 (GRCm39) |
C1053* |
probably null |
Het |
Mcpt9 |
A |
T |
14: 56,264,445 (GRCm39) |
S217T |
probably damaging |
Het |
Mgat4c |
T |
G |
10: 102,224,357 (GRCm39) |
N190K |
probably damaging |
Het |
Mknk1 |
T |
A |
4: 115,721,789 (GRCm39) |
V111D |
probably damaging |
Het |
Mmp11 |
T |
C |
10: 75,764,280 (GRCm39) |
T62A |
probably benign |
Het |
Mmp1b |
C |
A |
9: 7,385,014 (GRCm39) |
V212F |
probably damaging |
Het |
Mmp7 |
A |
G |
9: 7,697,587 (GRCm39) |
|
probably null |
Het |
Muc5b |
C |
T |
7: 141,417,704 (GRCm39) |
T3550M |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nphp3 |
A |
T |
9: 103,882,036 (GRCm39) |
K169* |
probably null |
Het |
Npy6r |
G |
T |
18: 44,408,788 (GRCm39) |
V70F |
probably benign |
Het |
Nsun2 |
T |
A |
13: 69,774,672 (GRCm39) |
|
probably null |
Het |
Oplah |
T |
A |
15: 76,186,860 (GRCm39) |
I652F |
probably benign |
Het |
Pcdh18 |
T |
C |
3: 49,710,271 (GRCm39) |
N348S |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,409 (GRCm39) |
V263D |
probably damaging |
Het |
Pcdhga1 |
C |
A |
18: 37,795,164 (GRCm39) |
T56N |
probably benign |
Het |
Pdk4 |
A |
G |
6: 5,491,068 (GRCm39) |
|
probably null |
Het |
Pfkp |
C |
A |
13: 6,652,817 (GRCm39) |
V434F |
probably benign |
Het |
Phospho1 |
G |
A |
11: 95,721,732 (GRCm39) |
R134H |
probably damaging |
Het |
Polg2 |
G |
T |
11: 106,663,572 (GRCm39) |
Q374K |
probably benign |
Het |
Ptpra |
T |
C |
2: 130,379,571 (GRCm39) |
|
probably null |
Het |
Rassf3 |
C |
T |
10: 121,252,052 (GRCm39) |
E120K |
probably benign |
Het |
Reln |
A |
T |
5: 22,311,095 (GRCm39) |
S273T |
probably damaging |
Het |
Scarb1 |
C |
T |
5: 125,361,089 (GRCm39) |
A133T |
probably benign |
Het |
Scn3a |
T |
A |
2: 65,313,486 (GRCm39) |
K1142N |
probably damaging |
Het |
Sema3c |
G |
A |
5: 17,899,701 (GRCm39) |
V398I |
probably benign |
Het |
Serpine1 |
C |
A |
5: 137,099,918 (GRCm39) |
Q80H |
probably damaging |
Het |
Sh3gl1 |
G |
A |
17: 56,324,646 (GRCm39) |
T334M |
probably damaging |
Het |
Smg7 |
T |
C |
1: 152,737,576 (GRCm39) |
N122D |
probably benign |
Het |
Speer4b |
T |
C |
5: 27,703,708 (GRCm39) |
I144V |
probably benign |
Het |
Spire2 |
T |
A |
8: 124,095,989 (GRCm39) |
D671E |
probably benign |
Het |
Sspo |
A |
T |
6: 48,478,029 (GRCm39) |
H5144L |
probably benign |
Het |
Sstr2 |
A |
T |
11: 113,516,179 (GRCm39) |
Q366L |
probably damaging |
Het |
Ssu72 |
T |
C |
4: 155,815,850 (GRCm39) |
F98S |
probably damaging |
Het |
Syde2 |
C |
T |
3: 145,712,870 (GRCm39) |
Q1003* |
probably null |
Het |
Tapbp |
G |
A |
17: 34,144,461 (GRCm39) |
A186T |
possibly damaging |
Het |
Tcf12 |
T |
A |
9: 71,790,385 (GRCm39) |
|
probably null |
Het |
Tnfrsf22 |
A |
T |
7: 143,194,556 (GRCm39) |
C124S |
probably damaging |
Het |
Txlnb |
A |
T |
10: 17,703,546 (GRCm39) |
T235S |
possibly damaging |
Het |
Uaca |
T |
C |
9: 60,777,695 (GRCm39) |
L694P |
probably damaging |
Het |
Unc13a |
T |
A |
8: 72,083,197 (GRCm39) |
N1620Y |
probably damaging |
Het |
Vmn2r10 |
C |
T |
5: 109,151,200 (GRCm39) |
C138Y |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,484,495 (GRCm39) |
E568D |
probably benign |
Het |
Vmn2r57 |
A |
T |
7: 41,097,895 (GRCm39) |
H57Q |
possibly damaging |
Het |
Vwa5b1 |
A |
G |
4: 138,308,923 (GRCm39) |
S756P |
probably benign |
Het |
Washc5 |
C |
A |
15: 59,224,350 (GRCm39) |
E470* |
probably null |
Het |
Xpot |
A |
T |
10: 121,442,678 (GRCm39) |
V508D |
probably damaging |
Het |
Zfp616 |
A |
T |
11: 73,976,087 (GRCm39) |
K785N |
possibly damaging |
Het |
Zfp653 |
T |
C |
9: 21,977,195 (GRCm39) |
N119D |
probably damaging |
Het |
Zfp729b |
A |
G |
13: 67,741,495 (GRCm39) |
S257P |
probably damaging |
Het |
Zfp82 |
T |
A |
7: 29,755,592 (GRCm39) |
T497S |
probably benign |
Het |
Znrf4 |
T |
G |
17: 56,819,305 (GRCm39) |
M1L |
probably benign |
Het |
|
Other mutations in D430041D05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:D430041D05Rik
|
APN |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01114:D430041D05Rik
|
APN |
2 |
104,088,511 (GRCm39) |
nonsense |
probably null |
|
IGL01669:D430041D05Rik
|
APN |
2 |
104,085,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02015:D430041D05Rik
|
APN |
2 |
104,060,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:D430041D05Rik
|
APN |
2 |
104,038,559 (GRCm39) |
splice site |
probably benign |
|
IGL02268:D430041D05Rik
|
APN |
2 |
104,071,500 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02294:D430041D05Rik
|
APN |
2 |
104,085,351 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02457:D430041D05Rik
|
APN |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02601:D430041D05Rik
|
APN |
2 |
104,060,631 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02647:D430041D05Rik
|
APN |
2 |
104,078,611 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:D430041D05Rik
|
APN |
2 |
104,060,650 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02926:D430041D05Rik
|
APN |
2 |
104,044,604 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03171:D430041D05Rik
|
APN |
2 |
104,071,508 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03178:D430041D05Rik
|
APN |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03371:D430041D05Rik
|
APN |
2 |
104,078,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:D430041D05Rik
|
UTSW |
2 |
104,085,389 (GRCm39) |
missense |
probably benign |
|
R0064:D430041D05Rik
|
UTSW |
2 |
104,079,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:D430041D05Rik
|
UTSW |
2 |
104,085,379 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0227:D430041D05Rik
|
UTSW |
2 |
104,035,545 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0265:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:D430041D05Rik
|
UTSW |
2 |
104,031,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:D430041D05Rik
|
UTSW |
2 |
104,085,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R0402:D430041D05Rik
|
UTSW |
2 |
103,998,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R0436:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:D430041D05Rik
|
UTSW |
2 |
103,998,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R0540:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0747:D430041D05Rik
|
UTSW |
2 |
104,060,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0864:D430041D05Rik
|
UTSW |
2 |
104,060,773 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0980:D430041D05Rik
|
UTSW |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R1014:D430041D05Rik
|
UTSW |
2 |
104,088,674 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1254:D430041D05Rik
|
UTSW |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R1364:D430041D05Rik
|
UTSW |
2 |
103,985,363 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1456:D430041D05Rik
|
UTSW |
2 |
104,038,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:D430041D05Rik
|
UTSW |
2 |
104,051,553 (GRCm39) |
small deletion |
probably benign |
|
R1604:D430041D05Rik
|
UTSW |
2 |
104,035,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:D430041D05Rik
|
UTSW |
2 |
104,085,915 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1623:D430041D05Rik
|
UTSW |
2 |
103,983,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:D430041D05Rik
|
UTSW |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:D430041D05Rik
|
UTSW |
2 |
103,998,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1885:D430041D05Rik
|
UTSW |
2 |
104,060,800 (GRCm39) |
missense |
probably benign |
0.39 |
R2080:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:D430041D05Rik
|
UTSW |
2 |
103,979,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R2240:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2923:D430041D05Rik
|
UTSW |
2 |
104,085,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3751:D430041D05Rik
|
UTSW |
2 |
104,085,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3862:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3863:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3864:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3949:D430041D05Rik
|
UTSW |
2 |
104,087,713 (GRCm39) |
missense |
probably benign |
0.02 |
R4493:D430041D05Rik
|
UTSW |
2 |
104,086,684 (GRCm39) |
missense |
probably benign |
0.02 |
R4526:D430041D05Rik
|
UTSW |
2 |
104,022,778 (GRCm39) |
critical splice donor site |
probably null |
|
R4592:D430041D05Rik
|
UTSW |
2 |
104,063,824 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4598:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R4599:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R4647:D430041D05Rik
|
UTSW |
2 |
104,088,788 (GRCm39) |
missense |
probably damaging |
0.99 |
R4765:D430041D05Rik
|
UTSW |
2 |
104,044,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R4808:D430041D05Rik
|
UTSW |
2 |
104,031,455 (GRCm39) |
critical splice donor site |
probably null |
|
R4868:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4982:D430041D05Rik
|
UTSW |
2 |
104,085,732 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5144:D430041D05Rik
|
UTSW |
2 |
104,088,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R5255:D430041D05Rik
|
UTSW |
2 |
104,086,945 (GRCm39) |
missense |
probably benign |
0.26 |
R5356:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R5368:D430041D05Rik
|
UTSW |
2 |
104,078,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:D430041D05Rik
|
UTSW |
2 |
104,078,630 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5993:D430041D05Rik
|
UTSW |
2 |
103,998,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:D430041D05Rik
|
UTSW |
2 |
104,086,637 (GRCm39) |
missense |
probably benign |
0.01 |
R6410:D430041D05Rik
|
UTSW |
2 |
103,998,548 (GRCm39) |
splice site |
probably null |
|
R6804:D430041D05Rik
|
UTSW |
2 |
103,979,371 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6850:D430041D05Rik
|
UTSW |
2 |
104,031,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:D430041D05Rik
|
UTSW |
2 |
104,071,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:D430041D05Rik
|
UTSW |
2 |
104,022,883 (GRCm39) |
missense |
probably damaging |
0.99 |
R7250:D430041D05Rik
|
UTSW |
2 |
104,086,961 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7251:D430041D05Rik
|
UTSW |
2 |
104,051,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:D430041D05Rik
|
UTSW |
2 |
104,085,910 (GRCm39) |
missense |
probably benign |
|
R7359:D430041D05Rik
|
UTSW |
2 |
104,044,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:D430041D05Rik
|
UTSW |
2 |
104,085,363 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7436:D430041D05Rik
|
UTSW |
2 |
104,087,447 (GRCm39) |
missense |
probably benign |
0.02 |
R7472:D430041D05Rik
|
UTSW |
2 |
104,240,484 (GRCm39) |
missense |
unknown |
|
R7492:D430041D05Rik
|
UTSW |
2 |
104,031,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R7631:D430041D05Rik
|
UTSW |
2 |
103,979,363 (GRCm39) |
nonsense |
probably null |
|
R7672:D430041D05Rik
|
UTSW |
2 |
104,071,581 (GRCm39) |
missense |
probably benign |
0.01 |
R7721:D430041D05Rik
|
UTSW |
2 |
104,088,874 (GRCm39) |
missense |
probably benign |
0.00 |
R7754:D430041D05Rik
|
UTSW |
2 |
104,087,504 (GRCm39) |
missense |
probably benign |
0.01 |
R7882:D430041D05Rik
|
UTSW |
2 |
104,087,974 (GRCm39) |
nonsense |
probably null |
|
R7896:D430041D05Rik
|
UTSW |
2 |
104,088,385 (GRCm39) |
missense |
probably benign |
0.05 |
R7986:D430041D05Rik
|
UTSW |
2 |
104,087,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8005:D430041D05Rik
|
UTSW |
2 |
104,088,599 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8016:D430041D05Rik
|
UTSW |
2 |
104,022,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:D430041D05Rik
|
UTSW |
2 |
103,985,390 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8058:D430041D05Rik
|
UTSW |
2 |
103,979,128 (GRCm39) |
makesense |
probably null |
|
R8100:D430041D05Rik
|
UTSW |
2 |
104,087,287 (GRCm39) |
missense |
probably benign |
0.00 |
R8461:D430041D05Rik
|
UTSW |
2 |
103,998,280 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8695:D430041D05Rik
|
UTSW |
2 |
104,085,299 (GRCm39) |
critical splice donor site |
probably null |
|
R8885:D430041D05Rik
|
UTSW |
2 |
104,071,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:D430041D05Rik
|
UTSW |
2 |
104,087,930 (GRCm39) |
missense |
probably benign |
0.08 |
R9009:D430041D05Rik
|
UTSW |
2 |
104,240,521 (GRCm39) |
start gained |
probably benign |
|
R9335:D430041D05Rik
|
UTSW |
2 |
104,078,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:D430041D05Rik
|
UTSW |
2 |
104,088,337 (GRCm39) |
missense |
probably benign |
0.05 |
R9384:D430041D05Rik
|
UTSW |
2 |
104,087,920 (GRCm39) |
missense |
probably benign |
|
R9483:D430041D05Rik
|
UTSW |
2 |
104,087,563 (GRCm39) |
missense |
probably benign |
0.44 |
R9489:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
R9605:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
R9613:D430041D05Rik
|
UTSW |
2 |
104,060,737 (GRCm39) |
missense |
probably benign |
0.09 |
R9698:D430041D05Rik
|
UTSW |
2 |
103,985,396 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:D430041D05Rik
|
UTSW |
2 |
104,022,911 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:D430041D05Rik
|
UTSW |
2 |
104,087,201 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:D430041D05Rik
|
UTSW |
2 |
103,985,280 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:D430041D05Rik
|
UTSW |
2 |
104,071,536 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
Predicted Primers |
PCR Primer
(F):5'- AAACCTGACATGTCCGCTGC -3'
(R):5'- CATTGCAGTGCATCCTGATCC -3'
Sequencing Primer
(F):5'- GACATGTCCGCTGCTTCTC -3'
(R):5'- AGTGCATCCTGATCCCACATC -3'
|
Posted On |
2019-05-15 |