Incidental Mutation 'R1843:Lrriq1'
| ID |
207450 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Lrriq1
|
| Ensembl Gene |
ENSMUSG00000019892 |
| Gene Name |
leucine-rich repeats and IQ motif containing 1 |
| Synonyms |
Gm1557, LOC380658, 4930503E15Rik |
| MMRRC Submission |
039868-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.079)
|
| Stock # |
R1843 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
10 |
| Chromosomal Location |
102881892-103072183 bp(-) (GRCm39) |
| Type of Mutation |
splice site (3 bp from exon) |
| DNA Base Change (assembly) |
T to A
at 103063034 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000131419
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020043]
[ENSMUST00000123364]
[ENSMUST00000166240]
|
| AlphaFold |
Q0P5X1 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000020043
|
| SMART Domains |
Protein: ENSMUSP00000020043
Gene: ENSMUSG00000019892
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
11 |
31 |
N/A |
INTRINSIC |
|
low complexity region
|
35 |
48 |
N/A |
INTRINSIC |
|
coiled coil region
|
183 |
286 |
N/A |
INTRINSIC |
|
Blast:IQ
|
290 |
312 |
1e-6 |
BLAST |
|
coiled coil region
|
314 |
390 |
N/A |
INTRINSIC |
|
low complexity region
|
550 |
559 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000123364
|
| SMART Domains |
Protein: ENSMUSP00000119783
Gene: ENSMUSG00000019892
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
11 |
31 |
N/A |
INTRINSIC |
|
low complexity region
|
35 |
48 |
N/A |
INTRINSIC |
|
coiled coil region
|
183 |
286 |
N/A |
INTRINSIC |
|
Blast:IQ
|
290 |
312 |
6e-6 |
BLAST |
|
coiled coil region
|
314 |
390 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000166240
|
| SMART Domains |
Protein: ENSMUSP00000131419
Gene: ENSMUSG00000019892
| Domain | Start | End | E-Value | Type |
|---|
|
coiled coil region
|
11 |
31 |
N/A |
INTRINSIC |
|
low complexity region
|
35 |
48 |
N/A |
INTRINSIC |
|
coiled coil region
|
183 |
286 |
N/A |
INTRINSIC |
|
IQ
|
290 |
312 |
9.78e1 |
SMART |
|
coiled coil region
|
314 |
390 |
N/A |
INTRINSIC |
|
low complexity region
|
550 |
559 |
N/A |
INTRINSIC |
|
LRR
|
873 |
894 |
2.14e1 |
SMART |
|
LRR
|
895 |
917 |
4.45e1 |
SMART |
|
LRR
|
984 |
1005 |
2.03e2 |
SMART |
|
LRR
|
1029 |
1052 |
3.65e0 |
SMART |
|
low complexity region
|
1244 |
1258 |
N/A |
INTRINSIC |
|
IQ
|
1279 |
1301 |
5.61e1 |
SMART |
|
IQ
|
1339 |
1361 |
6.7e-3 |
SMART |
|
low complexity region
|
1369 |
1394 |
N/A |
INTRINSIC |
|
low complexity region
|
1502 |
1518 |
N/A |
INTRINSIC |
|
low complexity region
|
1528 |
1543 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.4%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 102 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933405L10Rik |
C |
T |
8: 106,435,606 (GRCm39) |
T88M |
probably damaging |
Het |
| 9430038I01Rik |
A |
G |
7: 136,978,795 (GRCm39) |
|
probably benign |
Het |
| Adgra3 |
A |
C |
5: 50,118,834 (GRCm39) |
S905A |
probably damaging |
Het |
| Adgrv1 |
A |
G |
13: 81,692,652 (GRCm39) |
Y1618H |
probably damaging |
Het |
| Anapc15-ps |
T |
C |
10: 95,509,176 (GRCm39) |
T26A |
probably benign |
Het |
| Ankrd13d |
T |
C |
19: 4,321,623 (GRCm39) |
K360E |
probably damaging |
Het |
| Anks1b |
T |
A |
10: 90,348,751 (GRCm39) |
|
probably null |
Het |
| Apob |
T |
C |
12: 8,057,602 (GRCm39) |
F2028S |
possibly damaging |
Het |
| Arap3 |
G |
A |
18: 38,108,636 (GRCm39) |
R1265W |
probably damaging |
Het |
| Arhgef37 |
A |
G |
18: 61,651,121 (GRCm39) |
Y135H |
probably damaging |
Het |
| Armh3 |
A |
C |
19: 45,963,691 (GRCm39) |
S42R |
probably benign |
Het |
| Atp1a1 |
T |
C |
3: 101,489,333 (GRCm39) |
T760A |
probably benign |
Het |
| Cdc42bpb |
T |
A |
12: 111,289,255 (GRCm39) |
M497L |
probably benign |
Het |
| Ces5a |
C |
T |
8: 94,240,859 (GRCm39) |
V413M |
probably damaging |
Het |
| Chd5 |
A |
T |
4: 152,470,263 (GRCm39) |
Y1903F |
probably damaging |
Het |
| Chd9 |
T |
A |
8: 91,737,422 (GRCm39) |
N1500K |
probably benign |
Het |
| Chmp7 |
G |
T |
14: 69,957,248 (GRCm39) |
D303E |
probably benign |
Het |
| Chrnb4 |
A |
T |
9: 54,942,102 (GRCm39) |
Y391N |
possibly damaging |
Het |
| Crtc1 |
T |
C |
8: 70,840,802 (GRCm39) |
T475A |
probably benign |
Het |
| Cyp2c69 |
A |
G |
19: 39,865,972 (GRCm39) |
I207T |
probably benign |
Het |
| Dcp1a |
A |
G |
14: 30,240,940 (GRCm39) |
E250G |
probably damaging |
Het |
| Ddx20 |
T |
C |
3: 105,586,398 (GRCm39) |
Q649R |
probably benign |
Het |
| Defb12 |
T |
A |
8: 19,162,754 (GRCm39) |
K59N |
probably damaging |
Het |
| Dpy19l3 |
A |
T |
7: 35,429,185 (GRCm39) |
I85N |
probably damaging |
Het |
| Duox2 |
C |
T |
2: 122,122,739 (GRCm39) |
|
probably null |
Het |
| Ebi3 |
T |
A |
17: 56,263,679 (GRCm39) |
Y197N |
probably damaging |
Het |
| Emc1 |
G |
A |
4: 139,102,823 (GRCm39) |
R994Q |
probably benign |
Het |
| Ercc6 |
G |
T |
14: 32,268,777 (GRCm39) |
M530I |
probably damaging |
Het |
| Evl |
T |
A |
12: 108,619,255 (GRCm39) |
D70E |
probably damaging |
Het |
| Fbln2 |
A |
G |
6: 91,242,757 (GRCm39) |
N819S |
probably damaging |
Het |
| Foxk2 |
A |
G |
11: 121,176,363 (GRCm39) |
I170V |
probably benign |
Het |
| Gfm1 |
T |
C |
3: 67,342,943 (GRCm39) |
V159A |
probably damaging |
Het |
| Gm10837 |
A |
G |
14: 122,728,177 (GRCm39) |
T18A |
unknown |
Het |
| Gm12887 |
A |
T |
4: 121,479,227 (GRCm39) |
V25E |
probably damaging |
Het |
| Hectd4 |
A |
G |
5: 121,435,243 (GRCm39) |
H985R |
possibly damaging |
Het |
| Hsfy2 |
A |
G |
1: 56,675,791 (GRCm39) |
Y249H |
possibly damaging |
Het |
| Hspg2 |
T |
C |
4: 137,272,878 (GRCm39) |
V2639A |
probably damaging |
Het |
| Igf2r |
A |
G |
17: 12,923,157 (GRCm39) |
|
probably null |
Het |
| Invs |
T |
A |
4: 48,422,035 (GRCm39) |
I889N |
probably damaging |
Het |
| Kcnq1 |
A |
T |
7: 142,736,857 (GRCm39) |
M209L |
probably benign |
Het |
| Klra7 |
A |
G |
6: 130,206,957 (GRCm39) |
I48T |
possibly damaging |
Het |
| Krt26 |
CTAGTA |
CTA |
11: 99,224,352 (GRCm39) |
|
probably benign |
Het |
| Lrif1 |
T |
A |
3: 106,640,127 (GRCm39) |
V404D |
probably damaging |
Het |
| Lypd6 |
T |
A |
2: 50,078,774 (GRCm39) |
I90N |
possibly damaging |
Het |
| Mbp |
A |
G |
18: 82,602,247 (GRCm39) |
D174G |
probably damaging |
Het |
| Megf9 |
G |
T |
4: 70,453,022 (GRCm39) |
P13Q |
probably damaging |
Het |
| Myo15b |
A |
T |
11: 115,760,412 (GRCm39) |
T1155S |
probably benign |
Het |
| Nherf2 |
C |
T |
17: 24,860,693 (GRCm39) |
S150N |
possibly damaging |
Het |
| Nlrp6 |
T |
A |
7: 140,503,006 (GRCm39) |
C371S |
probably damaging |
Het |
| Nosip |
T |
A |
7: 44,726,733 (GRCm39) |
|
probably null |
Het |
| Nox3 |
G |
T |
17: 3,720,153 (GRCm39) |
P344H |
probably damaging |
Het |
| Nup210l |
T |
C |
3: 90,079,393 (GRCm39) |
V959A |
probably damaging |
Het |
| Or10d1 |
A |
G |
9: 39,484,031 (GRCm39) |
Y175H |
possibly damaging |
Het |
| Or2b2b |
C |
A |
13: 21,858,842 (GRCm39) |
V91L |
probably benign |
Het |
| Or2k2 |
T |
C |
4: 58,785,384 (GRCm39) |
I113V |
probably benign |
Het |
| Or5b119 |
A |
G |
19: 13,457,295 (GRCm39) |
I89T |
probably benign |
Het |
| Or5k8 |
T |
A |
16: 58,644,440 (GRCm39) |
I211F |
probably damaging |
Het |
| Osbpl3 |
A |
C |
6: 50,347,123 (GRCm39) |
S25A |
probably damaging |
Het |
| Otog |
G |
A |
7: 45,895,707 (GRCm39) |
C107Y |
probably damaging |
Het |
| Pax7 |
G |
A |
4: 139,511,802 (GRCm39) |
R260C |
probably damaging |
Het |
| Pbrm1 |
A |
T |
14: 30,760,914 (GRCm39) |
I224F |
probably damaging |
Het |
| Pcdh1 |
T |
A |
18: 38,325,278 (GRCm39) |
|
probably null |
Het |
| Pcnx1 |
T |
C |
12: 82,027,709 (GRCm39) |
L1585P |
probably damaging |
Het |
| Pde4c |
C |
T |
8: 71,200,599 (GRCm39) |
H362Y |
probably damaging |
Het |
| Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
| Pgm1 |
A |
T |
4: 99,818,675 (GRCm39) |
Q90L |
probably damaging |
Het |
| Phlpp1 |
A |
G |
1: 106,271,235 (GRCm39) |
H814R |
probably benign |
Het |
| Pknox2 |
A |
T |
9: 36,866,127 (GRCm39) |
M5K |
possibly damaging |
Het |
| Pole |
G |
A |
5: 110,478,701 (GRCm39) |
|
probably null |
Het |
| Polr1b |
A |
G |
2: 128,944,886 (GRCm39) |
I61V |
probably benign |
Het |
| Prelp |
T |
C |
1: 133,842,495 (GRCm39) |
K217E |
probably damaging |
Het |
| Prkce |
C |
T |
17: 86,782,974 (GRCm39) |
Q202* |
probably null |
Het |
| Psmd2 |
T |
G |
16: 20,475,332 (GRCm39) |
M370R |
probably benign |
Het |
| Rimklb |
A |
T |
6: 122,440,968 (GRCm39) |
H68Q |
probably damaging |
Het |
| Rnasel |
A |
G |
1: 153,630,420 (GRCm39) |
D312G |
possibly damaging |
Het |
| Rxrg |
A |
T |
1: 167,426,321 (GRCm39) |
M1L |
probably benign |
Het |
| Scrn1 |
A |
G |
6: 54,499,826 (GRCm39) |
F220L |
possibly damaging |
Het |
| Scyl3 |
A |
G |
1: 163,778,244 (GRCm39) |
S461G |
probably benign |
Het |
| Serpina1c |
T |
A |
12: 103,861,282 (GRCm39) |
T411S |
probably benign |
Het |
| Serpinb6d |
C |
T |
13: 33,855,364 (GRCm39) |
P346L |
probably benign |
Het |
| Shld2 |
A |
G |
14: 33,989,760 (GRCm39) |
I382T |
probably benign |
Het |
| Spg21 |
G |
T |
9: 65,372,618 (GRCm39) |
V17F |
probably damaging |
Het |
| Spink5 |
A |
T |
18: 44,132,958 (GRCm39) |
M525L |
probably benign |
Het |
| Sun2 |
T |
C |
15: 79,621,764 (GRCm39) |
T155A |
probably benign |
Het |
| Tchh |
T |
A |
3: 93,354,087 (GRCm39) |
F1176I |
unknown |
Het |
| Tex15 |
T |
A |
8: 34,066,682 (GRCm39) |
D2037E |
probably benign |
Het |
| Tfdp2 |
T |
C |
9: 96,199,857 (GRCm39) |
C392R |
possibly damaging |
Het |
| Tmem30c |
T |
C |
16: 57,097,143 (GRCm39) |
N139S |
probably benign |
Het |
| Tns2 |
C |
T |
15: 102,021,568 (GRCm39) |
|
probably null |
Het |
| Trim66 |
T |
C |
7: 109,075,046 (GRCm39) |
E405G |
probably damaging |
Het |
| Trpc4 |
T |
A |
3: 54,187,415 (GRCm39) |
F456I |
probably benign |
Het |
| Tspo2 |
T |
C |
17: 48,755,818 (GRCm39) |
D108G |
possibly damaging |
Het |
| Tyk2 |
A |
T |
9: 21,032,850 (GRCm39) |
C304* |
probably null |
Het |
| Vgll4 |
A |
T |
6: 114,839,756 (GRCm39) |
S185T |
probably benign |
Het |
| Vmn2r94 |
A |
C |
17: 18,464,732 (GRCm39) |
S519R |
probably benign |
Het |
| Vmn2r96 |
T |
G |
17: 18,818,183 (GRCm39) |
S587A |
probably benign |
Het |
| Vps4b |
C |
A |
1: 106,706,712 (GRCm39) |
A287S |
possibly damaging |
Het |
| Yeats2 |
C |
T |
16: 20,048,314 (GRCm39) |
P1332S |
probably benign |
Het |
| Zfp462 |
T |
G |
4: 55,010,010 (GRCm39) |
S659A |
possibly damaging |
Het |
| Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
| Zfp764l1 |
A |
C |
7: 126,990,660 (GRCm39) |
D442E |
probably benign |
Het |
| Zswim5 |
G |
T |
4: 116,734,896 (GRCm39) |
E80D |
unknown |
Het |
|
| Other mutations in Lrriq1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00988:Lrriq1
|
APN |
10 |
102,997,757 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01523:Lrriq1
|
APN |
10 |
103,053,977 (GRCm39) |
nonsense |
probably null |
|
|
IGL01637:Lrriq1
|
APN |
10 |
103,051,489 (GRCm39) |
missense |
probably benign |
|
|
IGL02019:Lrriq1
|
APN |
10 |
103,014,661 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02153:Lrriq1
|
APN |
10 |
103,006,340 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02341:Lrriq1
|
APN |
10 |
103,060,802 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02343:Lrriq1
|
APN |
10 |
103,070,024 (GRCm39) |
splice site |
probably benign |
|
|
IGL02408:Lrriq1
|
APN |
10 |
102,982,142 (GRCm39) |
missense |
probably benign |
0.17 |
|
IGL02431:Lrriq1
|
APN |
10 |
103,036,500 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02540:Lrriq1
|
APN |
10 |
103,050,880 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02558:Lrriq1
|
APN |
10 |
102,982,144 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02613:Lrriq1
|
APN |
10 |
102,980,409 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02642:Lrriq1
|
APN |
10 |
103,057,322 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL03027:Lrriq1
|
APN |
10 |
103,063,057 (GRCm39) |
missense |
probably benign |
0.35 |
|
PIT4362001:Lrriq1
|
UTSW |
10 |
102,907,055 (GRCm39) |
missense |
probably benign |
0.26 |
|
R0050:Lrriq1
|
UTSW |
10 |
102,904,792 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0050:Lrriq1
|
UTSW |
10 |
102,904,792 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0068:Lrriq1
|
UTSW |
10 |
102,899,279 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0068:Lrriq1
|
UTSW |
10 |
102,899,279 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0124:Lrriq1
|
UTSW |
10 |
103,006,281 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0244:Lrriq1
|
UTSW |
10 |
103,051,634 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0323:Lrriq1
|
UTSW |
10 |
103,057,150 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R0515:Lrriq1
|
UTSW |
10 |
102,904,829 (GRCm39) |
splice site |
probably null |
|
|
R0522:Lrriq1
|
UTSW |
10 |
102,997,638 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0701:Lrriq1
|
UTSW |
10 |
103,069,905 (GRCm39) |
missense |
probably benign |
|
|
R1220:Lrriq1
|
UTSW |
10 |
102,906,990 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1261:Lrriq1
|
UTSW |
10 |
103,069,998 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R1262:Lrriq1
|
UTSW |
10 |
103,069,998 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R1451:Lrriq1
|
UTSW |
10 |
103,038,376 (GRCm39) |
splice site |
probably benign |
|
|
R1642:Lrriq1
|
UTSW |
10 |
103,050,317 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1643:Lrriq1
|
UTSW |
10 |
103,050,685 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1647:Lrriq1
|
UTSW |
10 |
103,006,509 (GRCm39) |
nonsense |
probably null |
|
|
R1830:Lrriq1
|
UTSW |
10 |
102,997,620 (GRCm39) |
missense |
probably benign |
|
|
R2128:Lrriq1
|
UTSW |
10 |
103,050,718 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2129:Lrriq1
|
UTSW |
10 |
103,050,718 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2199:Lrriq1
|
UTSW |
10 |
102,904,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2354:Lrriq1
|
UTSW |
10 |
103,025,848 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2495:Lrriq1
|
UTSW |
10 |
103,038,242 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R2897:Lrriq1
|
UTSW |
10 |
103,063,111 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2898:Lrriq1
|
UTSW |
10 |
103,063,111 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2922:Lrriq1
|
UTSW |
10 |
103,050,536 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2939:Lrriq1
|
UTSW |
10 |
102,980,750 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2965:Lrriq1
|
UTSW |
10 |
103,050,761 (GRCm39) |
missense |
probably benign |
0.07 |
|
R2966:Lrriq1
|
UTSW |
10 |
103,050,761 (GRCm39) |
missense |
probably benign |
0.07 |
|
R3081:Lrriq1
|
UTSW |
10 |
102,980,750 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3115:Lrriq1
|
UTSW |
10 |
103,006,294 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3745:Lrriq1
|
UTSW |
10 |
103,006,717 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3813:Lrriq1
|
UTSW |
10 |
103,051,972 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3814:Lrriq1
|
UTSW |
10 |
103,051,972 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3885:Lrriq1
|
UTSW |
10 |
103,051,967 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4378:Lrriq1
|
UTSW |
10 |
103,038,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4632:Lrriq1
|
UTSW |
10 |
103,057,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4633:Lrriq1
|
UTSW |
10 |
103,036,424 (GRCm39) |
nonsense |
probably null |
|
|
R4663:Lrriq1
|
UTSW |
10 |
102,899,273 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4702:Lrriq1
|
UTSW |
10 |
103,051,610 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R4793:Lrriq1
|
UTSW |
10 |
103,006,327 (GRCm39) |
missense |
probably benign |
0.25 |
|
R4801:Lrriq1
|
UTSW |
10 |
103,057,179 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4802:Lrriq1
|
UTSW |
10 |
103,057,179 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4815:Lrriq1
|
UTSW |
10 |
102,980,739 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4872:Lrriq1
|
UTSW |
10 |
103,014,649 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R4877:Lrriq1
|
UTSW |
10 |
103,069,899 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4894:Lrriq1
|
UTSW |
10 |
102,997,613 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4990:Lrriq1
|
UTSW |
10 |
103,036,420 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4991:Lrriq1
|
UTSW |
10 |
103,036,420 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5011:Lrriq1
|
UTSW |
10 |
103,025,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5013:Lrriq1
|
UTSW |
10 |
103,025,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5122:Lrriq1
|
UTSW |
10 |
103,023,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5282:Lrriq1
|
UTSW |
10 |
103,051,206 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5311:Lrriq1
|
UTSW |
10 |
103,050,448 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5567:Lrriq1
|
UTSW |
10 |
103,006,457 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R5643:Lrriq1
|
UTSW |
10 |
103,051,301 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5683:Lrriq1
|
UTSW |
10 |
103,009,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5916:Lrriq1
|
UTSW |
10 |
103,057,243 (GRCm39) |
nonsense |
probably null |
|
|
R6008:Lrriq1
|
UTSW |
10 |
103,006,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6022:Lrriq1
|
UTSW |
10 |
103,051,395 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6224:Lrriq1
|
UTSW |
10 |
103,051,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6254:Lrriq1
|
UTSW |
10 |
103,051,312 (GRCm39) |
missense |
probably benign |
0.15 |
|
R6311:Lrriq1
|
UTSW |
10 |
103,009,254 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6460:Lrriq1
|
UTSW |
10 |
103,036,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6502:Lrriq1
|
UTSW |
10 |
103,063,045 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6637:Lrriq1
|
UTSW |
10 |
103,057,293 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6719:Lrriq1
|
UTSW |
10 |
102,906,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6736:Lrriq1
|
UTSW |
10 |
103,017,750 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R6928:Lrriq1
|
UTSW |
10 |
103,050,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6991:Lrriq1
|
UTSW |
10 |
103,023,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7174:Lrriq1
|
UTSW |
10 |
103,060,826 (GRCm39) |
missense |
probably benign |
|
|
R7241:Lrriq1
|
UTSW |
10 |
103,051,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7248:Lrriq1
|
UTSW |
10 |
103,059,611 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7287:Lrriq1
|
UTSW |
10 |
103,051,877 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7402:Lrriq1
|
UTSW |
10 |
103,057,185 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7439:Lrriq1
|
UTSW |
10 |
103,050,380 (GRCm39) |
missense |
probably benign |
0.21 |
|
R7585:Lrriq1
|
UTSW |
10 |
103,050,807 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7611:Lrriq1
|
UTSW |
10 |
103,036,432 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R7634:Lrriq1
|
UTSW |
10 |
103,036,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7767:Lrriq1
|
UTSW |
10 |
103,051,815 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7809:Lrriq1
|
UTSW |
10 |
103,051,678 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7910:Lrriq1
|
UTSW |
10 |
103,051,055 (GRCm39) |
nonsense |
probably null |
|
|
R8131:Lrriq1
|
UTSW |
10 |
103,051,572 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R8156:Lrriq1
|
UTSW |
10 |
102,992,196 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8211:Lrriq1
|
UTSW |
10 |
103,006,408 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8304:Lrriq1
|
UTSW |
10 |
103,069,929 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R8487:Lrriq1
|
UTSW |
10 |
103,050,914 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8500:Lrriq1
|
UTSW |
10 |
102,882,016 (GRCm39) |
missense |
|
|
|
R9013:Lrriq1
|
UTSW |
10 |
103,050,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9099:Lrriq1
|
UTSW |
10 |
103,051,864 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9155:Lrriq1
|
UTSW |
10 |
103,050,640 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9320:Lrriq1
|
UTSW |
10 |
103,057,144 (GRCm39) |
missense |
probably benign |
|
|
R9384:Lrriq1
|
UTSW |
10 |
103,006,458 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9469:Lrriq1
|
UTSW |
10 |
103,050,761 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9585:Lrriq1
|
UTSW |
10 |
103,051,250 (GRCm39) |
missense |
probably benign |
|
|
R9706:Lrriq1
|
UTSW |
10 |
102,881,902 (GRCm39) |
missense |
|
|
|
R9780:Lrriq1
|
UTSW |
10 |
103,025,824 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0026:Lrriq1
|
UTSW |
10 |
103,051,565 (GRCm39) |
nonsense |
probably null |
|
|
Z1088:Lrriq1
|
UTSW |
10 |
103,038,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Lrriq1
|
UTSW |
10 |
103,069,946 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1176:Lrriq1
|
UTSW |
10 |
103,038,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Lrriq1
|
UTSW |
10 |
103,038,220 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGCATACTGACACTGACTCTG -3'
(R):5'- GGGCACTTTTACCTATTTACACAG -3'
Sequencing Primer
(F):5'- ATACTGACACTGACTCTGTGTTTTC -3'
(R):5'- GACTGCAATACTTGACATATGACC -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation