Incidental Mutation 'IGL00827:Lrrk2'
ID |
11850 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Lrrk2
|
Ensembl Gene |
ENSMUSG00000036273 |
Gene Name |
leucine-rich repeat kinase 2 |
Synonyms |
9330188B09Rik, 4921513O20Rik, LOC381026, cI-46, D630001M17Rik |
Accession Numbers |
Genbank: NM_025730; MGI: 1913975 |
Essential gene? |
Possibly essential
(E-score: 0.533)
|
Stock # |
IGL00827
|
Quality Score |
|
Status
|
|
Chromosome |
15 |
Chromosomal Location |
91673175-91816120 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 91755790 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 1513
(I1513F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000052584
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000060642]
|
AlphaFold |
Q5S006 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000060642
AA Change: I1513F
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000052584 Gene: ENSMUSG00000036273 AA Change: I1513F
Domain | Start | End | E-Value | Type |
low complexity region
|
138 |
156 |
N/A |
INTRINSIC |
low complexity region
|
332 |
347 |
N/A |
INTRINSIC |
ANK
|
708 |
737 |
3.95e1 |
SMART |
ANK
|
770 |
800 |
4.58e2 |
SMART |
low complexity region
|
890 |
901 |
N/A |
INTRINSIC |
low complexity region
|
953 |
966 |
N/A |
INTRINSIC |
low complexity region
|
971 |
979 |
N/A |
INTRINSIC |
LRR
|
1010 |
1033 |
9.96e-1 |
SMART |
LRR
|
1034 |
1057 |
8.01e0 |
SMART |
LRR
|
1082 |
1105 |
2.45e0 |
SMART |
LRR
|
1128 |
1151 |
9.3e-1 |
SMART |
LRR
|
1195 |
1219 |
3.24e0 |
SMART |
LRR
|
1244 |
1266 |
3.87e1 |
SMART |
LRR
|
1267 |
1291 |
4.98e1 |
SMART |
Pfam:Roc
|
1336 |
1456 |
4.9e-32 |
PFAM |
Pfam:Ras
|
1336 |
1489 |
3.3e-17 |
PFAM |
Pfam:COR
|
1524 |
1740 |
4e-28 |
PFAM |
Pfam:Pkinase
|
1881 |
2132 |
4.7e-40 |
PFAM |
Pfam:Pkinase_Tyr
|
1882 |
2132 |
6.8e-39 |
PFAM |
WD40
|
2231 |
2276 |
3.09e-1 |
SMART |
WD40
|
2401 |
2438 |
1.37e2 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140734
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a RAS domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a knock-in allele exhibit impaired response to dopamine, amphetamine, and quinpirole. Mice homozygous for one knock-out allele exhibit increased neurite growth. Mice homozygous for different knock-out alleles exhibit alopecia due to excessive grooming or kdiney atrophy. [provided by MGI curators]
|
Allele List at MGI |
All alleles(7) : Targeted, knock-out(6) Targeted, other(1) |
Other mutations in this stock |
Total: 16 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
A |
G |
13: 59,689,476 |
V265A |
probably benign |
Het |
Ap3d1 |
A |
T |
10: 80,713,559 |
D803E |
possibly damaging |
Het |
Camk1d |
G |
A |
2: 5,311,073 |
|
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,448,457 |
K3075E |
probably damaging |
Het |
Dnmt3l |
T |
C |
10: 78,053,996 |
L229P |
probably damaging |
Het |
Dntt |
G |
A |
19: 41,039,823 |
G186D |
probably benign |
Het |
Epdr1 |
A |
G |
13: 19,594,509 |
I139T |
possibly damaging |
Het |
Fam20a |
A |
T |
11: 109,677,762 |
|
probably benign |
Het |
Hcar2 |
T |
C |
5: 123,864,502 |
K313E |
probably benign |
Het |
Hdac2 |
T |
A |
10: 36,997,114 |
C323S |
probably benign |
Het |
Hsd3b5 |
G |
A |
3: 98,630,098 |
A34V |
probably benign |
Het |
Parp3 |
T |
A |
9: 106,474,406 |
M208L |
probably benign |
Het |
Ppp4r4 |
A |
G |
12: 103,579,076 |
T203A |
probably benign |
Het |
Rims2 |
G |
A |
15: 39,472,359 |
G788D |
probably damaging |
Het |
Slc4a4 |
T |
G |
5: 89,179,686 |
S626A |
probably benign |
Het |
Steap4 |
A |
G |
5: 7,976,712 |
Y225C |
probably damaging |
Het |
|
Other mutations in Lrrk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Lrrk2
|
APN |
15 |
91747799 |
missense |
possibly damaging |
0.90 |
IGL00542:Lrrk2
|
APN |
15 |
91699943 |
missense |
probably benign |
|
IGL00770:Lrrk2
|
APN |
15 |
91801833 |
splice site |
probably benign |
|
IGL00774:Lrrk2
|
APN |
15 |
91801833 |
splice site |
probably benign |
|
IGL00791:Lrrk2
|
APN |
15 |
91779841 |
missense |
probably damaging |
1.00 |
IGL00843:Lrrk2
|
APN |
15 |
91757058 |
missense |
possibly damaging |
0.58 |
IGL01109:Lrrk2
|
APN |
15 |
91738832 |
missense |
probably damaging |
1.00 |
IGL01293:Lrrk2
|
APN |
15 |
91726137 |
missense |
probably benign |
0.21 |
IGL01296:Lrrk2
|
APN |
15 |
91683142 |
missense |
probably benign |
|
IGL01301:Lrrk2
|
APN |
15 |
91767339 |
missense |
probably damaging |
1.00 |
IGL01360:Lrrk2
|
APN |
15 |
91700569 |
splice site |
probably null |
|
IGL01465:Lrrk2
|
APN |
15 |
91728925 |
missense |
probably benign |
0.21 |
IGL01529:Lrrk2
|
APN |
15 |
91812313 |
missense |
possibly damaging |
0.92 |
IGL01557:Lrrk2
|
APN |
15 |
91699989 |
missense |
probably damaging |
1.00 |
IGL01560:Lrrk2
|
APN |
15 |
91774988 |
missense |
probably benign |
0.33 |
IGL01991:Lrrk2
|
APN |
15 |
91779946 |
missense |
probably damaging |
0.99 |
IGL02003:Lrrk2
|
APN |
15 |
91731491 |
missense |
probably damaging |
0.99 |
IGL02325:Lrrk2
|
APN |
15 |
91726308 |
critical splice donor site |
probably null |
|
IGL02711:Lrrk2
|
APN |
15 |
91685822 |
missense |
possibly damaging |
0.71 |
IGL02869:Lrrk2
|
APN |
15 |
91750277 |
missense |
probably damaging |
1.00 |
IGL03104:Lrrk2
|
APN |
15 |
91747755 |
missense |
possibly damaging |
0.68 |
IGL03179:Lrrk2
|
APN |
15 |
91700578 |
missense |
probably damaging |
1.00 |
IGL03395:Lrrk2
|
APN |
15 |
91797414 |
splice site |
probably null |
|
horned
|
UTSW |
15 |
91772858 |
missense |
probably damaging |
1.00 |
R1312_Lrrk2_980
|
UTSW |
15 |
91699895 |
missense |
probably damaging |
1.00 |
R4710_lrrk2_232
|
UTSW |
15 |
91699927 |
missense |
possibly damaging |
0.88 |
R5245_Lrrk2_127
|
UTSW |
15 |
91796089 |
missense |
probably damaging |
1.00 |
spree
|
UTSW |
15 |
91702247 |
missense |
probably benign |
0.00 |
Spur
|
UTSW |
15 |
91774995 |
nonsense |
probably null |
|
3-1:Lrrk2
|
UTSW |
15 |
91801934 |
missense |
probably benign |
0.01 |
ANU18:Lrrk2
|
UTSW |
15 |
91767339 |
missense |
probably damaging |
1.00 |
H8562:Lrrk2
|
UTSW |
15 |
91673358 |
missense |
probably benign |
|
H8786:Lrrk2
|
UTSW |
15 |
91673358 |
missense |
probably benign |
|
IGL02835:Lrrk2
|
UTSW |
15 |
91814660 |
critical splice acceptor site |
probably null |
|
R0014:Lrrk2
|
UTSW |
15 |
91802045 |
splice site |
probably benign |
|
R0014:Lrrk2
|
UTSW |
15 |
91802045 |
splice site |
probably benign |
|
R0078:Lrrk2
|
UTSW |
15 |
91734009 |
missense |
probably benign |
0.01 |
R0100:Lrrk2
|
UTSW |
15 |
91745796 |
missense |
probably damaging |
1.00 |
R0282:Lrrk2
|
UTSW |
15 |
91778414 |
splice site |
probably benign |
|
R0448:Lrrk2
|
UTSW |
15 |
91709305 |
missense |
probably damaging |
0.99 |
R0449:Lrrk2
|
UTSW |
15 |
91750275 |
missense |
probably damaging |
1.00 |
R0610:Lrrk2
|
UTSW |
15 |
91815416 |
missense |
probably benign |
|
R0617:Lrrk2
|
UTSW |
15 |
91752278 |
missense |
probably benign |
0.00 |
R0632:Lrrk2
|
UTSW |
15 |
91796028 |
missense |
probably damaging |
0.98 |
R0639:Lrrk2
|
UTSW |
15 |
91772996 |
missense |
probably benign |
0.03 |
R0661:Lrrk2
|
UTSW |
15 |
91787016 |
missense |
probably damaging |
1.00 |
R0666:Lrrk2
|
UTSW |
15 |
91757070 |
critical splice donor site |
probably null |
|
R0764:Lrrk2
|
UTSW |
15 |
91775046 |
splice site |
probably null |
|
R0766:Lrrk2
|
UTSW |
15 |
91699895 |
missense |
probably damaging |
1.00 |
R0845:Lrrk2
|
UTSW |
15 |
91755962 |
missense |
probably benign |
0.22 |
R0940:Lrrk2
|
UTSW |
15 |
91729081 |
missense |
possibly damaging |
0.83 |
R0970:Lrrk2
|
UTSW |
15 |
91729169 |
missense |
probably benign |
0.22 |
R1080:Lrrk2
|
UTSW |
15 |
91673689 |
missense |
probably benign |
0.01 |
R1114:Lrrk2
|
UTSW |
15 |
91700468 |
nonsense |
probably null |
|
R1223:Lrrk2
|
UTSW |
15 |
91673635 |
missense |
probably benign |
0.00 |
R1289:Lrrk2
|
UTSW |
15 |
91812360 |
missense |
probably benign |
0.00 |
R1296:Lrrk2
|
UTSW |
15 |
91728920 |
missense |
probably damaging |
1.00 |
R1312:Lrrk2
|
UTSW |
15 |
91699895 |
missense |
probably damaging |
1.00 |
R1637:Lrrk2
|
UTSW |
15 |
91734058 |
missense |
probably benign |
|
R1773:Lrrk2
|
UTSW |
15 |
91779981 |
missense |
possibly damaging |
0.96 |
R1809:Lrrk2
|
UTSW |
15 |
91699892 |
missense |
possibly damaging |
0.86 |
R1839:Lrrk2
|
UTSW |
15 |
91683134 |
missense |
probably benign |
0.00 |
R1946:Lrrk2
|
UTSW |
15 |
91736661 |
splice site |
probably null |
|
R2160:Lrrk2
|
UTSW |
15 |
91796060 |
missense |
probably damaging |
1.00 |
R2232:Lrrk2
|
UTSW |
15 |
91764716 |
missense |
probably benign |
0.05 |
R2419:Lrrk2
|
UTSW |
15 |
91797526 |
splice site |
probably benign |
|
R2516:Lrrk2
|
UTSW |
15 |
91755927 |
missense |
probably benign |
|
R3110:Lrrk2
|
UTSW |
15 |
91814695 |
missense |
probably benign |
0.02 |
R3112:Lrrk2
|
UTSW |
15 |
91814695 |
missense |
probably benign |
0.02 |
R3801:Lrrk2
|
UTSW |
15 |
91737111 |
missense |
probably benign |
|
R3842:Lrrk2
|
UTSW |
15 |
91755916 |
missense |
probably benign |
0.01 |
R3903:Lrrk2
|
UTSW |
15 |
91747700 |
missense |
probably damaging |
1.00 |
R3903:Lrrk2
|
UTSW |
15 |
91747701 |
missense |
probably damaging |
1.00 |
R3930:Lrrk2
|
UTSW |
15 |
91767461 |
critical splice donor site |
probably null |
|
R3937:Lrrk2
|
UTSW |
15 |
91778504 |
missense |
probably damaging |
0.98 |
R3938:Lrrk2
|
UTSW |
15 |
91712780 |
missense |
possibly damaging |
0.69 |
R3938:Lrrk2
|
UTSW |
15 |
91778504 |
missense |
probably damaging |
0.98 |
R3982:Lrrk2
|
UTSW |
15 |
91709284 |
missense |
probably benign |
0.22 |
R4125:Lrrk2
|
UTSW |
15 |
91815483 |
missense |
probably benign |
0.01 |
R4130:Lrrk2
|
UTSW |
15 |
91755794 |
missense |
probably benign |
0.19 |
R4296:Lrrk2
|
UTSW |
15 |
91699895 |
missense |
probably damaging |
1.00 |
R4465:Lrrk2
|
UTSW |
15 |
91747820 |
missense |
probably damaging |
0.96 |
R4478:Lrrk2
|
UTSW |
15 |
91723188 |
missense |
probably damaging |
1.00 |
R4517:Lrrk2
|
UTSW |
15 |
91705120 |
missense |
probably benign |
|
R4539:Lrrk2
|
UTSW |
15 |
91729142 |
missense |
possibly damaging |
0.86 |
R4654:Lrrk2
|
UTSW |
15 |
91765681 |
missense |
probably damaging |
0.96 |
R4710:Lrrk2
|
UTSW |
15 |
91699927 |
missense |
possibly damaging |
0.88 |
R4722:Lrrk2
|
UTSW |
15 |
91688901 |
missense |
probably damaging |
1.00 |
R4723:Lrrk2
|
UTSW |
15 |
91764759 |
missense |
probably damaging |
1.00 |
R4732:Lrrk2
|
UTSW |
15 |
91688849 |
missense |
probably damaging |
1.00 |
R4732:Lrrk2
|
UTSW |
15 |
91765747 |
missense |
probably damaging |
1.00 |
R4733:Lrrk2
|
UTSW |
15 |
91688849 |
missense |
probably damaging |
1.00 |
R4733:Lrrk2
|
UTSW |
15 |
91765747 |
missense |
probably damaging |
1.00 |
R4787:Lrrk2
|
UTSW |
15 |
91712828 |
missense |
probably benign |
|
R4945:Lrrk2
|
UTSW |
15 |
91804920 |
missense |
probably benign |
0.02 |
R4948:Lrrk2
|
UTSW |
15 |
91803389 |
missense |
probably benign |
0.20 |
R5000:Lrrk2
|
UTSW |
15 |
91749878 |
missense |
probably damaging |
1.00 |
R5031:Lrrk2
|
UTSW |
15 |
91700619 |
missense |
possibly damaging |
0.50 |
R5067:Lrrk2
|
UTSW |
15 |
91765790 |
missense |
probably benign |
0.01 |
R5245:Lrrk2
|
UTSW |
15 |
91796089 |
missense |
probably damaging |
1.00 |
R5341:Lrrk2
|
UTSW |
15 |
91772858 |
missense |
probably damaging |
1.00 |
R5460:Lrrk2
|
UTSW |
15 |
91814644 |
splice site |
probably null |
|
R5551:Lrrk2
|
UTSW |
15 |
91812350 |
missense |
probably benign |
|
R5574:Lrrk2
|
UTSW |
15 |
91787016 |
missense |
probably damaging |
1.00 |
R5577:Lrrk2
|
UTSW |
15 |
91765745 |
missense |
probably damaging |
1.00 |
R5685:Lrrk2
|
UTSW |
15 |
91803301 |
nonsense |
probably null |
|
R5712:Lrrk2
|
UTSW |
15 |
91702222 |
nonsense |
probably null |
|
R5728:Lrrk2
|
UTSW |
15 |
91774974 |
missense |
probably benign |
0.36 |
R5782:Lrrk2
|
UTSW |
15 |
91702183 |
missense |
probably damaging |
1.00 |
R5788:Lrrk2
|
UTSW |
15 |
91764648 |
missense |
possibly damaging |
0.55 |
R5821:Lrrk2
|
UTSW |
15 |
91709390 |
critical splice donor site |
probably null |
|
R5852:Lrrk2
|
UTSW |
15 |
91755949 |
missense |
probably damaging |
1.00 |
R5934:Lrrk2
|
UTSW |
15 |
91734046 |
missense |
probably benign |
0.00 |
R5935:Lrrk2
|
UTSW |
15 |
91745831 |
missense |
probably benign |
0.14 |
R5979:Lrrk2
|
UTSW |
15 |
91772945 |
missense |
possibly damaging |
0.47 |
R6101:Lrrk2
|
UTSW |
15 |
91723135 |
missense |
probably benign |
0.10 |
R6114:Lrrk2
|
UTSW |
15 |
91747826 |
missense |
probably benign |
0.33 |
R6259:Lrrk2
|
UTSW |
15 |
91702247 |
missense |
probably benign |
0.00 |
R6376:Lrrk2
|
UTSW |
15 |
91742266 |
missense |
possibly damaging |
0.89 |
R6417:Lrrk2
|
UTSW |
15 |
91812346 |
missense |
probably benign |
0.03 |
R6420:Lrrk2
|
UTSW |
15 |
91812346 |
missense |
probably benign |
0.03 |
R6737:Lrrk2
|
UTSW |
15 |
91723218 |
missense |
possibly damaging |
0.50 |
R7056:Lrrk2
|
UTSW |
15 |
91774995 |
nonsense |
probably null |
|
R7072:Lrrk2
|
UTSW |
15 |
91801920 |
missense |
probably benign |
0.03 |
R7109:Lrrk2
|
UTSW |
15 |
91764782 |
missense |
probably damaging |
1.00 |
R7128:Lrrk2
|
UTSW |
15 |
91801885 |
missense |
probably benign |
|
R7144:Lrrk2
|
UTSW |
15 |
91734055 |
missense |
possibly damaging |
0.54 |
R7187:Lrrk2
|
UTSW |
15 |
91757001 |
missense |
possibly damaging |
0.92 |
R7270:Lrrk2
|
UTSW |
15 |
91700441 |
missense |
probably benign |
0.01 |
R7356:Lrrk2
|
UTSW |
15 |
91738744 |
missense |
probably benign |
0.07 |
R7360:Lrrk2
|
UTSW |
15 |
91731655 |
critical splice donor site |
probably null |
|
R7373:Lrrk2
|
UTSW |
15 |
91700004 |
critical splice donor site |
probably null |
|
R7465:Lrrk2
|
UTSW |
15 |
91767340 |
missense |
probably damaging |
1.00 |
R7477:Lrrk2
|
UTSW |
15 |
91812325 |
missense |
probably damaging |
0.98 |
R7614:Lrrk2
|
UTSW |
15 |
91772858 |
missense |
probably damaging |
1.00 |
R7622:Lrrk2
|
UTSW |
15 |
91812323 |
missense |
probably damaging |
1.00 |
R7658:Lrrk2
|
UTSW |
15 |
91700358 |
missense |
possibly damaging |
0.91 |
R7679:Lrrk2
|
UTSW |
15 |
91726186 |
missense |
possibly damaging |
0.58 |
R7737:Lrrk2
|
UTSW |
15 |
91815446 |
missense |
probably damaging |
0.98 |
R7739:Lrrk2
|
UTSW |
15 |
91700613 |
missense |
probably damaging |
1.00 |
R7740:Lrrk2
|
UTSW |
15 |
91767324 |
missense |
probably damaging |
1.00 |
R7908:Lrrk2
|
UTSW |
15 |
91726152 |
missense |
probably damaging |
1.00 |
R8299:Lrrk2
|
UTSW |
15 |
91673240 |
start gained |
probably benign |
|
R8389:Lrrk2
|
UTSW |
15 |
91699991 |
missense |
probably damaging |
1.00 |
R8462:Lrrk2
|
UTSW |
15 |
91731477 |
missense |
probably benign |
|
R8698:Lrrk2
|
UTSW |
15 |
91752197 |
missense |
probably benign |
0.38 |
R8947:Lrrk2
|
UTSW |
15 |
91702270 |
nonsense |
probably null |
|
R9084:Lrrk2
|
UTSW |
15 |
91750266 |
missense |
|
|
R9086:Lrrk2
|
UTSW |
15 |
91755848 |
missense |
probably benign |
0.01 |
R9096:Lrrk2
|
UTSW |
15 |
91673256 |
start gained |
probably benign |
|
R9097:Lrrk2
|
UTSW |
15 |
91673256 |
start gained |
probably benign |
|
R9267:Lrrk2
|
UTSW |
15 |
91700426 |
missense |
probably damaging |
0.99 |
R9285:Lrrk2
|
UTSW |
15 |
91778483 |
missense |
probably damaging |
1.00 |
R9341:Lrrk2
|
UTSW |
15 |
91700415 |
missense |
probably benign |
0.18 |
R9343:Lrrk2
|
UTSW |
15 |
91700415 |
missense |
probably benign |
0.18 |
R9371:Lrrk2
|
UTSW |
15 |
91723204 |
missense |
probably damaging |
1.00 |
R9424:Lrrk2
|
UTSW |
15 |
91752185 |
nonsense |
probably null |
|
R9489:Lrrk2
|
UTSW |
15 |
91737217 |
missense |
probably benign |
0.37 |
R9502:Lrrk2
|
UTSW |
15 |
91723162 |
missense |
probably damaging |
0.98 |
R9563:Lrrk2
|
UTSW |
15 |
91749840 |
missense |
possibly damaging |
0.90 |
R9576:Lrrk2
|
UTSW |
15 |
91752185 |
nonsense |
probably null |
|
R9605:Lrrk2
|
UTSW |
15 |
91737217 |
missense |
probably benign |
0.37 |
R9635:Lrrk2
|
UTSW |
15 |
91812324 |
missense |
probably benign |
0.21 |
R9641:Lrrk2
|
UTSW |
15 |
91787048 |
missense |
possibly damaging |
0.94 |
R9660:Lrrk2
|
UTSW |
15 |
91734025 |
missense |
probably benign |
0.00 |
R9673:Lrrk2
|
UTSW |
15 |
91765681 |
missense |
probably damaging |
1.00 |
R9708:Lrrk2
|
UTSW |
15 |
91750279 |
nonsense |
probably null |
|
R9728:Lrrk2
|
UTSW |
15 |
91734025 |
missense |
probably benign |
0.00 |
R9757:Lrrk2
|
UTSW |
15 |
91811026 |
missense |
probably benign |
0.03 |
RF001:Lrrk2
|
UTSW |
15 |
91736633 |
missense |
probably benign |
0.11 |
X0028:Lrrk2
|
UTSW |
15 |
91738851 |
missense |
probably benign |
0.00 |
Z1088:Lrrk2
|
UTSW |
15 |
91726240 |
missense |
probably benign |
0.12 |
|
Posted On |
2012-12-06 |