Incidental Mutation 'R5070:Igsf10'
ID |
388622 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Igsf10
|
Ensembl Gene |
ENSMUSG00000036334 |
Gene Name |
immunoglobulin superfamily, member 10 |
Synonyms |
6530405F15Rik, CMF608, Adlican2 |
MMRRC Submission |
042660-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.193)
|
Stock # |
R5070 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
3 |
Chromosomal Location |
59224156-59251815 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 59235714 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Leucine
at position 1489
(H1489L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000141391
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039419]
[ENSMUST00000193455]
[ENSMUST00000194546]
|
AlphaFold |
Q3V1M1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000039419
AA Change: H1489L
PolyPhen 2
Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000037246 Gene: ENSMUSG00000036334 AA Change: H1489L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
LRRNT
|
28 |
61 |
3.24e-4 |
SMART |
LRR
|
57 |
79 |
9.24e1 |
SMART |
LRR
|
80 |
103 |
2.02e-1 |
SMART |
LRR
|
104 |
127 |
7.16e0 |
SMART |
LRR_TYP
|
128 |
151 |
1.2e-3 |
SMART |
LRR
|
152 |
175 |
1.25e-1 |
SMART |
LRR
|
188 |
207 |
2.33e2 |
SMART |
LRRCT
|
219 |
280 |
4.19e-4 |
SMART |
IGc2
|
488 |
558 |
2.34e-4 |
SMART |
IGc2
|
586 |
652 |
7.88e-11 |
SMART |
low complexity region
|
917 |
930 |
N/A |
INTRINSIC |
low complexity region
|
1175 |
1185 |
N/A |
INTRINSIC |
low complexity region
|
1245 |
1263 |
N/A |
INTRINSIC |
low complexity region
|
1311 |
1321 |
N/A |
INTRINSIC |
low complexity region
|
1449 |
1465 |
N/A |
INTRINSIC |
IGc2
|
1632 |
1701 |
7.69e-14 |
SMART |
IGc2
|
1729 |
1798 |
5.07e-14 |
SMART |
IGc2
|
1826 |
1895 |
2.19e-9 |
SMART |
IGc2
|
1925 |
1994 |
4.59e-12 |
SMART |
IGc2
|
2022 |
2097 |
1.33e-8 |
SMART |
IGc2
|
2125 |
2191 |
2.96e-15 |
SMART |
IGc2
|
2223 |
2291 |
2.03e-4 |
SMART |
IGc2
|
2321 |
2389 |
9.99e-13 |
SMART |
IGc2
|
2416 |
2484 |
3.03e-12 |
SMART |
IGc2
|
2512 |
2583 |
7.76e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193455
AA Change: H1489L
PolyPhen 2
Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000141971 Gene: ENSMUSG00000036334 AA Change: H1489L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
LRRNT
|
28 |
61 |
3.24e-4 |
SMART |
LRR
|
57 |
79 |
9.24e1 |
SMART |
LRR
|
80 |
103 |
2.02e-1 |
SMART |
LRR
|
104 |
127 |
7.16e0 |
SMART |
LRR_TYP
|
128 |
151 |
1.2e-3 |
SMART |
LRR
|
152 |
175 |
1.25e-1 |
SMART |
LRR
|
188 |
207 |
2.33e2 |
SMART |
LRRCT
|
219 |
280 |
4.19e-4 |
SMART |
IGc2
|
488 |
558 |
2.34e-4 |
SMART |
IGc2
|
586 |
652 |
7.88e-11 |
SMART |
low complexity region
|
917 |
930 |
N/A |
INTRINSIC |
low complexity region
|
1175 |
1185 |
N/A |
INTRINSIC |
low complexity region
|
1245 |
1263 |
N/A |
INTRINSIC |
low complexity region
|
1311 |
1321 |
N/A |
INTRINSIC |
low complexity region
|
1449 |
1465 |
N/A |
INTRINSIC |
IGc2
|
1632 |
1701 |
7.69e-14 |
SMART |
IGc2
|
1729 |
1798 |
5.07e-14 |
SMART |
IGc2
|
1826 |
1895 |
2.19e-9 |
SMART |
IGc2
|
1925 |
1994 |
4.59e-12 |
SMART |
IGc2
|
2022 |
2097 |
1.33e-8 |
SMART |
IGc2
|
2125 |
2191 |
2.96e-15 |
SMART |
IGc2
|
2223 |
2291 |
2.03e-4 |
SMART |
IGc2
|
2321 |
2389 |
9.99e-13 |
SMART |
IGc2
|
2416 |
2484 |
3.03e-12 |
SMART |
IGc2
|
2512 |
2583 |
7.76e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194546
AA Change: H1489L
PolyPhen 2
Score 0.022 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000141391 Gene: ENSMUSG00000036334 AA Change: H1489L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
LRRNT
|
28 |
61 |
3.24e-4 |
SMART |
LRR
|
57 |
79 |
9.24e1 |
SMART |
LRR
|
80 |
103 |
2.02e-1 |
SMART |
LRR
|
104 |
127 |
7.16e0 |
SMART |
LRR_TYP
|
128 |
151 |
1.2e-3 |
SMART |
LRR
|
152 |
175 |
1.25e-1 |
SMART |
LRR
|
188 |
207 |
2.33e2 |
SMART |
LRRCT
|
219 |
280 |
4.19e-4 |
SMART |
IGc2
|
488 |
558 |
2.34e-4 |
SMART |
IGc2
|
586 |
652 |
7.88e-11 |
SMART |
low complexity region
|
917 |
930 |
N/A |
INTRINSIC |
low complexity region
|
1175 |
1185 |
N/A |
INTRINSIC |
low complexity region
|
1245 |
1263 |
N/A |
INTRINSIC |
low complexity region
|
1311 |
1321 |
N/A |
INTRINSIC |
low complexity region
|
1449 |
1465 |
N/A |
INTRINSIC |
IGc2
|
1632 |
1701 |
7.69e-14 |
SMART |
IGc2
|
1729 |
1798 |
5.07e-14 |
SMART |
IGc2
|
1826 |
1895 |
2.19e-9 |
SMART |
IGc2
|
1925 |
1994 |
4.59e-12 |
SMART |
IGc2
|
2022 |
2097 |
1.33e-8 |
SMART |
IGc2
|
2125 |
2191 |
2.96e-15 |
SMART |
IGc2
|
2223 |
2291 |
2.03e-4 |
SMART |
IGc2
|
2321 |
2389 |
9.99e-13 |
SMART |
IGc2
|
2416 |
2484 |
3.03e-12 |
SMART |
IGc2
|
2512 |
2583 |
7.76e-10 |
SMART |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.6%
- 20x: 93.0%
|
Validation Efficiency |
|
Allele List at MGI |
All alleles(2) : Targeted, other(2) |
Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,383,749 (GRCm39) |
S739P |
possibly damaging |
Het |
Acacb |
T |
C |
5: 114,384,089 (GRCm39) |
I2206T |
possibly damaging |
Het |
Actn2 |
A |
G |
13: 12,303,408 (GRCm39) |
I464T |
possibly damaging |
Het |
AI987944 |
C |
T |
7: 41,024,748 (GRCm39) |
G77D |
probably benign |
Het |
Ankar |
T |
C |
1: 72,719,369 (GRCm39) |
|
probably null |
Het |
Armc9 |
A |
T |
1: 86,184,959 (GRCm39) |
H670L |
probably benign |
Het |
Arvcf |
A |
G |
16: 18,217,736 (GRCm39) |
Y412C |
probably damaging |
Het |
Baiap3 |
A |
T |
17: 25,468,082 (GRCm39) |
C283S |
probably damaging |
Het |
Bend3 |
A |
T |
10: 43,369,681 (GRCm39) |
E11D |
probably damaging |
Het |
Birc6 |
C |
T |
17: 74,872,967 (GRCm39) |
R409C |
probably damaging |
Het |
Cds2 |
T |
A |
2: 132,144,008 (GRCm39) |
Y4* |
probably null |
Het |
Celsr1 |
G |
T |
15: 85,823,335 (GRCm39) |
P1691Q |
possibly damaging |
Het |
Chmp1a |
A |
T |
8: 123,933,054 (GRCm39) |
V133E |
probably benign |
Het |
Cnbd2 |
T |
C |
2: 156,177,318 (GRCm39) |
V92A |
probably damaging |
Het |
Comp |
G |
A |
8: 70,829,145 (GRCm39) |
G272S |
probably benign |
Het |
Csnk1a1 |
T |
A |
18: 61,688,852 (GRCm39) |
F11I |
probably benign |
Het |
Ctse |
A |
G |
1: 131,595,917 (GRCm39) |
D203G |
probably damaging |
Het |
Cyp1b1 |
T |
A |
17: 80,018,040 (GRCm39) |
M372L |
probably benign |
Het |
Cyp2c66 |
T |
A |
19: 39,151,914 (GRCm39) |
S210T |
probably benign |
Het |
Dnah1 |
G |
A |
14: 31,004,375 (GRCm39) |
P2385S |
probably benign |
Het |
Dsp |
A |
C |
13: 38,381,099 (GRCm39) |
T2615P |
possibly damaging |
Het |
Eif4g3 |
A |
G |
4: 137,873,610 (GRCm39) |
T682A |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,727,450 (GRCm39) |
Y513C |
probably damaging |
Het |
Ercc6 |
T |
C |
14: 32,292,020 (GRCm39) |
V1128A |
probably benign |
Het |
Fam136b-ps |
C |
T |
15: 31,276,862 (GRCm39) |
|
probably benign |
Het |
Fbxl7 |
T |
A |
15: 26,789,640 (GRCm39) |
H29L |
probably benign |
Het |
Fbxw22 |
A |
G |
9: 109,214,183 (GRCm39) |
V211A |
probably benign |
Het |
Frk |
A |
T |
10: 34,360,280 (GRCm39) |
K94* |
probably null |
Het |
G0s2 |
T |
A |
1: 192,954,870 (GRCm39) |
E71D |
probably damaging |
Het |
Gfpt1 |
A |
G |
6: 87,030,727 (GRCm39) |
|
probably null |
Het |
Gga1 |
A |
G |
15: 78,776,217 (GRCm39) |
D420G |
possibly damaging |
Het |
Gldc |
T |
C |
19: 30,095,998 (GRCm39) |
Q671R |
possibly damaging |
Het |
Gpc6 |
A |
G |
14: 117,424,181 (GRCm39) |
T90A |
probably benign |
Het |
Gucy2g |
C |
A |
19: 55,218,219 (GRCm39) |
V410F |
probably damaging |
Het |
Ifnlr1 |
T |
C |
4: 135,431,509 (GRCm39) |
S233P |
probably benign |
Het |
Ighv1-9 |
A |
T |
12: 114,547,377 (GRCm39) |
W55R |
probably damaging |
Het |
Il17re |
T |
C |
6: 113,435,971 (GRCm39) |
L39P |
probably damaging |
Het |
Irag1 |
A |
G |
7: 110,524,519 (GRCm39) |
S208P |
probably benign |
Het |
Kcna2 |
T |
A |
3: 107,011,953 (GRCm39) |
V178D |
probably damaging |
Het |
Kcnk3 |
A |
G |
5: 30,779,730 (GRCm39) |
H260R |
possibly damaging |
Het |
Kctd19 |
T |
C |
8: 106,118,631 (GRCm39) |
Y287C |
probably damaging |
Het |
Klhl28 |
A |
T |
12: 65,004,486 (GRCm39) |
M9K |
probably benign |
Het |
Lama2 |
A |
G |
10: 27,226,247 (GRCm39) |
|
probably null |
Het |
Lrrc27 |
A |
T |
7: 138,794,715 (GRCm39) |
D26V |
probably damaging |
Het |
Mcm4 |
A |
G |
16: 15,443,434 (GRCm39) |
S830P |
probably damaging |
Het |
Mei1 |
T |
A |
15: 81,961,804 (GRCm39) |
C188S |
possibly damaging |
Het |
Mettl13 |
C |
T |
1: 162,373,468 (GRCm39) |
R261H |
possibly damaging |
Het |
Mex3a |
A |
T |
3: 88,443,694 (GRCm39) |
I257F |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,793,002 (GRCm39) |
E646G |
probably damaging |
Het |
Mier2 |
T |
C |
10: 79,385,411 (GRCm39) |
D139G |
probably benign |
Het |
Mmp14 |
T |
A |
14: 54,676,570 (GRCm39) |
Y372N |
probably damaging |
Het |
Myh14 |
A |
G |
7: 44,265,672 (GRCm39) |
V1569A |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,909,212 (GRCm39) |
E1977G |
probably damaging |
Het |
Myo3b |
T |
C |
2: 70,083,456 (GRCm39) |
L675P |
probably damaging |
Het |
N4bp1 |
A |
G |
8: 87,587,165 (GRCm39) |
V591A |
probably damaging |
Het |
Nedd9 |
C |
A |
13: 41,470,074 (GRCm39) |
V360L |
probably benign |
Het |
Oit3 |
C |
T |
10: 59,259,849 (GRCm39) |
R518H |
probably damaging |
Het |
Or10ag57 |
T |
G |
2: 87,218,507 (GRCm39) |
C153G |
probably damaging |
Het |
Or11g2 |
A |
G |
14: 50,855,931 (GRCm39) |
N84S |
probably benign |
Het |
Or11g2 |
T |
A |
14: 50,856,197 (GRCm39) |
C173S |
probably damaging |
Het |
Or11h4 |
C |
A |
14: 50,974,531 (GRCm39) |
L29F |
probably benign |
Het |
Or1j14 |
T |
A |
2: 36,417,778 (GRCm39) |
M118K |
probably damaging |
Het |
Or2aj6 |
A |
G |
16: 19,443,742 (GRCm39) |
I36T |
possibly damaging |
Het |
Or2j6 |
A |
G |
7: 139,980,482 (GRCm39) |
V159A |
probably benign |
Het |
Or9s23 |
T |
A |
1: 92,501,135 (GRCm39) |
S81T |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pask |
A |
T |
1: 93,258,596 (GRCm39) |
C251S |
probably damaging |
Het |
Pdzk1 |
A |
T |
3: 96,757,637 (GRCm39) |
D31V |
probably benign |
Het |
Pmfbp1 |
A |
T |
8: 110,256,787 (GRCm39) |
Q497L |
probably damaging |
Het |
Pofut1 |
T |
C |
2: 153,103,486 (GRCm39) |
|
probably benign |
Het |
Polr2h |
A |
G |
16: 20,540,716 (GRCm39) |
N95S |
probably damaging |
Het |
Pou2f3 |
A |
G |
9: 43,056,578 (GRCm39) |
V93A |
possibly damaging |
Het |
Ppfia1 |
G |
A |
7: 144,068,210 (GRCm39) |
Q446* |
probably null |
Het |
Prkd1 |
A |
T |
12: 50,441,405 (GRCm39) |
L327* |
probably null |
Het |
Prrt4 |
T |
C |
6: 29,177,511 (GRCm39) |
E86G |
probably benign |
Het |
Psen2 |
T |
C |
1: 180,056,422 (GRCm39) |
I393V |
probably benign |
Het |
Psma2 |
G |
A |
13: 14,790,613 (GRCm39) |
V20I |
probably benign |
Het |
Qser1 |
C |
T |
2: 104,617,627 (GRCm39) |
V1062I |
possibly damaging |
Het |
Rab11b |
G |
T |
17: 33,967,855 (GRCm39) |
A114D |
probably damaging |
Het |
Rag1 |
A |
T |
2: 101,472,656 (GRCm39) |
W829R |
probably damaging |
Het |
Rgl3 |
A |
G |
9: 21,899,340 (GRCm39) |
|
probably null |
Het |
Rgs8 |
C |
T |
1: 153,541,650 (GRCm39) |
T3I |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,743,385 (GRCm39) |
V1317A |
probably damaging |
Het |
Rps6kb2 |
A |
T |
19: 4,213,227 (GRCm39) |
D6E |
probably damaging |
Het |
Shisal1 |
G |
T |
15: 84,304,364 (GRCm39) |
A14E |
possibly damaging |
Het |
Skint5 |
T |
A |
4: 113,652,735 (GRCm39) |
I630F |
unknown |
Het |
Skint7 |
T |
C |
4: 111,841,331 (GRCm39) |
L257P |
probably damaging |
Het |
Slc11a1 |
G |
A |
1: 74,424,343 (GRCm39) |
A434T |
probably damaging |
Het |
Slc5a8 |
A |
T |
10: 88,722,460 (GRCm39) |
I98F |
possibly damaging |
Het |
Sorl1 |
T |
C |
9: 41,943,114 (GRCm39) |
K921E |
possibly damaging |
Het |
Stub1 |
A |
G |
17: 26,051,112 (GRCm39) |
L90P |
probably damaging |
Het |
Sycp1 |
A |
T |
3: 102,827,881 (GRCm39) |
S289T |
probably damaging |
Het |
Taar7b |
T |
G |
10: 23,876,359 (GRCm39) |
S175A |
probably benign |
Het |
Tead3 |
T |
C |
17: 28,560,451 (GRCm39) |
K51R |
probably benign |
Het |
Tmed11 |
T |
A |
5: 108,943,089 (GRCm39) |
I30L |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,893,986 (GRCm39) |
I139T |
probably damaging |
Het |
Tmem191 |
A |
G |
16: 17,095,559 (GRCm39) |
Q206R |
probably null |
Het |
Tph2 |
T |
A |
10: 114,987,079 (GRCm39) |
Y237F |
probably benign |
Het |
Trim35 |
C |
T |
14: 66,546,421 (GRCm39) |
|
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,655,750 (GRCm39) |
I661T |
probably benign |
Het |
Ttc27 |
T |
A |
17: 75,106,337 (GRCm39) |
H541Q |
probably damaging |
Het |
Uqcrq |
A |
G |
11: 53,320,954 (GRCm39) |
|
probably null |
Het |
Vmn1r215 |
T |
A |
13: 23,260,666 (GRCm39) |
S235R |
probably benign |
Het |
Vmn1r70 |
T |
C |
7: 10,368,325 (GRCm39) |
V271A |
probably benign |
Het |
Vps13a |
G |
A |
19: 16,631,848 (GRCm39) |
R2596C |
probably benign |
Het |
Vwa7 |
G |
A |
17: 35,243,166 (GRCm39) |
V615I |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,307 (GRCm39) |
T1650A |
probably damaging |
Het |
Zbtb32 |
T |
A |
7: 30,290,891 (GRCm39) |
M135L |
probably benign |
Het |
Zc2hc1c |
A |
G |
12: 85,337,288 (GRCm39) |
D315G |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,254,688 (GRCm39) |
C1427* |
probably null |
Het |
Zfp30 |
A |
G |
7: 29,485,691 (GRCm39) |
|
probably benign |
Het |
Zfp428 |
T |
A |
7: 24,214,550 (GRCm39) |
D55E |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,302,135 (GRCm39) |
N1820K |
probably damaging |
Het |
Zw10 |
C |
A |
9: 48,988,759 (GRCm39) |
S675* |
probably null |
Het |
|
Other mutations in Igsf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00773:Igsf10
|
APN |
3 |
59,238,960 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00790:Igsf10
|
APN |
3 |
59,226,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00916:Igsf10
|
APN |
3 |
59,238,548 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00928:Igsf10
|
APN |
3 |
59,238,018 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01066:Igsf10
|
APN |
3 |
59,235,203 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01107:Igsf10
|
APN |
3 |
59,238,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01420:Igsf10
|
APN |
3 |
59,227,071 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01533:Igsf10
|
APN |
3 |
59,226,651 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01537:Igsf10
|
APN |
3 |
59,237,452 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01676:Igsf10
|
APN |
3 |
59,236,756 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01676:Igsf10
|
APN |
3 |
59,233,432 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01960:Igsf10
|
APN |
3 |
59,226,158 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02123:Igsf10
|
APN |
3 |
59,226,081 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02198:Igsf10
|
APN |
3 |
59,233,399 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02268:Igsf10
|
APN |
3 |
59,238,573 (GRCm39) |
nonsense |
probably null |
|
IGL02313:Igsf10
|
APN |
3 |
59,238,111 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02368:Igsf10
|
APN |
3 |
59,235,652 (GRCm39) |
missense |
probably benign |
|
IGL02494:Igsf10
|
APN |
3 |
59,235,427 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02549:Igsf10
|
APN |
3 |
59,236,662 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02616:Igsf10
|
APN |
3 |
59,226,027 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02957:Igsf10
|
APN |
3 |
59,238,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03067:Igsf10
|
APN |
3 |
59,226,339 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03104:Igsf10
|
APN |
3 |
59,226,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03124:Igsf10
|
APN |
3 |
59,227,086 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03212:Igsf10
|
APN |
3 |
59,235,586 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03347:Igsf10
|
APN |
3 |
59,239,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03357:Igsf10
|
APN |
3 |
59,243,632 (GRCm39) |
missense |
probably benign |
0.35 |
F6893:Igsf10
|
UTSW |
3 |
59,238,481 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Igsf10
|
UTSW |
3 |
59,226,531 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Igsf10
|
UTSW |
3 |
59,235,579 (GRCm39) |
missense |
probably benign |
0.06 |
PIT4402001:Igsf10
|
UTSW |
3 |
59,233,000 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4810001:Igsf10
|
UTSW |
3 |
59,225,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Igsf10
|
UTSW |
3 |
59,238,045 (GRCm39) |
missense |
probably damaging |
0.98 |
R0095:Igsf10
|
UTSW |
3 |
59,238,617 (GRCm39) |
nonsense |
probably null |
|
R0095:Igsf10
|
UTSW |
3 |
59,238,617 (GRCm39) |
nonsense |
probably null |
|
R0112:Igsf10
|
UTSW |
3 |
59,233,429 (GRCm39) |
missense |
probably benign |
0.00 |
R0141:Igsf10
|
UTSW |
3 |
59,238,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Igsf10
|
UTSW |
3 |
59,227,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R0551:Igsf10
|
UTSW |
3 |
59,236,089 (GRCm39) |
missense |
probably benign |
0.01 |
R0556:Igsf10
|
UTSW |
3 |
59,236,296 (GRCm39) |
missense |
probably benign |
0.02 |
R0582:Igsf10
|
UTSW |
3 |
59,227,188 (GRCm39) |
missense |
probably benign |
0.00 |
R0630:Igsf10
|
UTSW |
3 |
59,233,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Igsf10
|
UTSW |
3 |
59,236,015 (GRCm39) |
missense |
probably benign |
0.14 |
R0948:Igsf10
|
UTSW |
3 |
59,238,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Igsf10
|
UTSW |
3 |
59,239,269 (GRCm39) |
missense |
probably benign |
0.03 |
R1412:Igsf10
|
UTSW |
3 |
59,235,196 (GRCm39) |
splice site |
probably benign |
|
R1473:Igsf10
|
UTSW |
3 |
59,226,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Igsf10
|
UTSW |
3 |
59,237,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Igsf10
|
UTSW |
3 |
59,233,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1660:Igsf10
|
UTSW |
3 |
59,238,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1671:Igsf10
|
UTSW |
3 |
59,235,921 (GRCm39) |
nonsense |
probably null |
|
R1748:Igsf10
|
UTSW |
3 |
59,226,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R1758:Igsf10
|
UTSW |
3 |
59,236,617 (GRCm39) |
missense |
probably benign |
0.09 |
R1856:Igsf10
|
UTSW |
3 |
59,238,693 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1912:Igsf10
|
UTSW |
3 |
59,236,993 (GRCm39) |
missense |
probably benign |
0.40 |
R2148:Igsf10
|
UTSW |
3 |
59,243,998 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2155:Igsf10
|
UTSW |
3 |
59,239,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Igsf10
|
UTSW |
3 |
59,239,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Igsf10
|
UTSW |
3 |
59,239,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Igsf10
|
UTSW |
3 |
59,232,875 (GRCm39) |
missense |
probably benign |
0.14 |
R2913:Igsf10
|
UTSW |
3 |
59,239,157 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2927:Igsf10
|
UTSW |
3 |
59,236,848 (GRCm39) |
missense |
probably benign |
|
R3547:Igsf10
|
UTSW |
3 |
59,243,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Igsf10
|
UTSW |
3 |
59,237,962 (GRCm39) |
missense |
probably benign |
0.02 |
R3548:Igsf10
|
UTSW |
3 |
59,243,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R3620:Igsf10
|
UTSW |
3 |
59,243,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Igsf10
|
UTSW |
3 |
59,233,135 (GRCm39) |
missense |
probably benign |
0.29 |
R3743:Igsf10
|
UTSW |
3 |
59,233,546 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3973:Igsf10
|
UTSW |
3 |
59,239,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R4005:Igsf10
|
UTSW |
3 |
59,235,981 (GRCm39) |
missense |
probably benign |
0.00 |
R4184:Igsf10
|
UTSW |
3 |
59,227,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R4302:Igsf10
|
UTSW |
3 |
59,226,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4404:Igsf10
|
UTSW |
3 |
59,236,972 (GRCm39) |
missense |
probably benign |
0.04 |
R4575:Igsf10
|
UTSW |
3 |
59,237,521 (GRCm39) |
missense |
probably benign |
|
R4676:Igsf10
|
UTSW |
3 |
59,233,370 (GRCm39) |
missense |
probably benign |
0.23 |
R4700:Igsf10
|
UTSW |
3 |
59,227,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R4765:Igsf10
|
UTSW |
3 |
59,237,126 (GRCm39) |
missense |
probably benign |
0.01 |
R4986:Igsf10
|
UTSW |
3 |
59,236,027 (GRCm39) |
missense |
probably benign |
0.24 |
R5012:Igsf10
|
UTSW |
3 |
59,226,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5083:Igsf10
|
UTSW |
3 |
59,233,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Igsf10
|
UTSW |
3 |
59,227,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5462:Igsf10
|
UTSW |
3 |
59,233,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Igsf10
|
UTSW |
3 |
59,235,574 (GRCm39) |
missense |
probably benign |
0.01 |
R5810:Igsf10
|
UTSW |
3 |
59,226,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5871:Igsf10
|
UTSW |
3 |
59,237,832 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5880:Igsf10
|
UTSW |
3 |
59,238,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Igsf10
|
UTSW |
3 |
59,235,578 (GRCm39) |
missense |
probably benign |
0.12 |
R5979:Igsf10
|
UTSW |
3 |
59,243,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Igsf10
|
UTSW |
3 |
59,239,077 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6222:Igsf10
|
UTSW |
3 |
59,226,336 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6224:Igsf10
|
UTSW |
3 |
59,232,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Igsf10
|
UTSW |
3 |
59,235,928 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6283:Igsf10
|
UTSW |
3 |
59,226,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R6336:Igsf10
|
UTSW |
3 |
59,237,760 (GRCm39) |
missense |
probably benign |
0.00 |
R6490:Igsf10
|
UTSW |
3 |
59,236,992 (GRCm39) |
missense |
probably benign |
0.06 |
R6785:Igsf10
|
UTSW |
3 |
59,226,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Igsf10
|
UTSW |
3 |
59,235,865 (GRCm39) |
missense |
probably benign |
|
R6889:Igsf10
|
UTSW |
3 |
59,239,354 (GRCm39) |
missense |
probably benign |
|
R7024:Igsf10
|
UTSW |
3 |
59,239,122 (GRCm39) |
missense |
probably benign |
0.00 |
R7056:Igsf10
|
UTSW |
3 |
59,238,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7128:Igsf10
|
UTSW |
3 |
59,236,326 (GRCm39) |
missense |
probably benign |
|
R7251:Igsf10
|
UTSW |
3 |
59,226,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Igsf10
|
UTSW |
3 |
59,236,837 (GRCm39) |
missense |
probably benign |
0.05 |
R7340:Igsf10
|
UTSW |
3 |
59,233,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Igsf10
|
UTSW |
3 |
59,239,222 (GRCm39) |
missense |
probably benign |
0.39 |
R7506:Igsf10
|
UTSW |
3 |
59,226,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Igsf10
|
UTSW |
3 |
59,226,761 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7695:Igsf10
|
UTSW |
3 |
59,233,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Igsf10
|
UTSW |
3 |
59,238,964 (GRCm39) |
missense |
probably damaging |
0.96 |
R7749:Igsf10
|
UTSW |
3 |
59,236,549 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7808:Igsf10
|
UTSW |
3 |
59,235,489 (GRCm39) |
missense |
probably benign |
0.00 |
R7850:Igsf10
|
UTSW |
3 |
59,227,053 (GRCm39) |
missense |
probably benign |
0.33 |
R7879:Igsf10
|
UTSW |
3 |
59,238,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R7886:Igsf10
|
UTSW |
3 |
59,235,748 (GRCm39) |
missense |
probably benign |
0.01 |
R7891:Igsf10
|
UTSW |
3 |
59,235,832 (GRCm39) |
nonsense |
probably null |
|
R7946:Igsf10
|
UTSW |
3 |
59,227,125 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7948:Igsf10
|
UTSW |
3 |
59,239,279 (GRCm39) |
missense |
probably benign |
0.02 |
R8004:Igsf10
|
UTSW |
3 |
59,237,130 (GRCm39) |
missense |
probably benign |
0.01 |
R8096:Igsf10
|
UTSW |
3 |
59,236,380 (GRCm39) |
missense |
probably damaging |
0.98 |
R8141:Igsf10
|
UTSW |
3 |
59,237,949 (GRCm39) |
missense |
probably damaging |
0.96 |
R8183:Igsf10
|
UTSW |
3 |
59,238,036 (GRCm39) |
missense |
probably benign |
0.04 |
R8203:Igsf10
|
UTSW |
3 |
59,236,254 (GRCm39) |
missense |
probably benign |
0.11 |
R8325:Igsf10
|
UTSW |
3 |
59,225,954 (GRCm39) |
missense |
probably damaging |
0.96 |
R8350:Igsf10
|
UTSW |
3 |
59,238,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8387:Igsf10
|
UTSW |
3 |
59,236,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R8488:Igsf10
|
UTSW |
3 |
59,227,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8697:Igsf10
|
UTSW |
3 |
59,226,308 (GRCm39) |
missense |
probably benign |
0.02 |
R8786:Igsf10
|
UTSW |
3 |
59,238,063 (GRCm39) |
missense |
probably benign |
0.25 |
R8804:Igsf10
|
UTSW |
3 |
59,243,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R8886:Igsf10
|
UTSW |
3 |
59,237,410 (GRCm39) |
missense |
probably benign |
0.00 |
R8902:Igsf10
|
UTSW |
3 |
59,243,633 (GRCm39) |
missense |
probably benign |
0.00 |
R8906:Igsf10
|
UTSW |
3 |
59,233,739 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Igsf10
|
UTSW |
3 |
59,226,888 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9051:Igsf10
|
UTSW |
3 |
59,236,668 (GRCm39) |
missense |
probably benign |
0.00 |
R9178:Igsf10
|
UTSW |
3 |
59,233,480 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9228:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9230:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9417:Igsf10
|
UTSW |
3 |
59,236,526 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9609:Igsf10
|
UTSW |
3 |
59,226,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R9631:Igsf10
|
UTSW |
3 |
59,237,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Igsf10
|
UTSW |
3 |
59,233,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R9762:Igsf10
|
UTSW |
3 |
59,237,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R9770:Igsf10
|
UTSW |
3 |
59,227,199 (GRCm39) |
missense |
probably benign |
0.07 |
R9798:Igsf10
|
UTSW |
3 |
59,239,126 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Igsf10
|
UTSW |
3 |
59,237,359 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1177:Igsf10
|
UTSW |
3 |
59,237,026 (GRCm39) |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- TGACAGGCTTATTTCTGGCC -3'
(R):5'- CGCAATGAAAAGAGCCTCCG -3'
Sequencing Primer
(F):5'- CTGAGTATGACCTGAGCTGAAATTTG -3'
(R):5'- GAAAAGAGCCTCCGCCACAC -3'
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Posted On |
2016-06-06 |