ZMP
LOC100332050
Ensembl ID:
Human Orthologue:
LRRK1
Human Description:
leucine-rich repeat kinase 1 [Source:HGNC Symbol;Acc:18608]
Mouse Orthologue:
Lrrk1
Mouse Description:
leucine-rich repeat kinase 1 Gene [Source:MGI Symbol;Acc:MGI:2142227]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30882 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13125 | Essential Splice Site | Available for shipment | Available now |
sa13011 | Nonsense | Available for shipment | Available now |
sa12644 | Nonsense | Available for shipment | Available now |
sa40838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30882
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029668 | Nonsense | 82 | 1389 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 10495426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 9428489 |
GRCz11 | 7 | 9673653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGTTCCCTTGAGTCATTCGCCCACGCTGAAGAACATCCAAGAGGCCTA[T/A]ACGGATGGCGAGGACCAGAGGGCACGGCAGCTAATCCGCCTGTCCTGCGA
Long Flanking Sequence:
CAGTATTGCGTGTGACTGCGGTTGACAAATTGCAGTATTGTGCGTGCAGAAACGCGCATTCTCAGTAACCATGTCTGTATCATGAGTTTGTTTTTGCGCATCATGAGTACCTCCATCAACTCAATATATTCAGATCTTTCCTGTCTCACTCCCACCCTCGAGTAGGTGCTCTTTACATCAAAGTTAAATGTGTAAAAGCGCAGCTCCACAAACACACACACGCACCAGTCCAGAGGGAAAGGCATGTGAATTCTTTATGAGGCTGACCTGATTCCCGGCTGCTCCTGCTCCTCCAGTATCTGGGGCTCATTTCCCATCGTGGCGTCTATGCTTTAGCATGAGCGTGCGCTGAGATTCTCGCTCTTATACTGAGGGTTTTGTTTGTTTGTGGTGGGCTATGCCCCATTCGCAGGCGTTTCGGAGATGGGAGCCAAGCAGTCGGCGGTTGGCAGCGTTCCCTTGAGTCATTCGCCCACGCTGAAGAACATCCAAGAGGCCTA[T/A]ACGGATGGCGAGGACCAGAGGGCACGGCAGCTAATCCGCCTGTCCTGCGAAAATAGCGGTGGAGTGGCACCAGATGGGGTGAGTTTAACCATTTTCTTATTTCAATTTACAGCAAAAGGAAGCTGGTGGATCGTGCAGTTTACCTGTGAGTGTTTTTTTAATGCTACTGTGGTGGTCTGGCACCAGATGGCCTTTATGTGACATCATCATAACAGTGTTGTTTAATAATGTCCAGATATGTTTGAACATAATGCCGAGTGGCTGAATCATGCCAACTTGGGCATTGGAGTATGCAGGCAGCATTGTAACATGCAGGGTTGTGTTCTGTTCTGTTTTATTTGATATGTATATTTTTTAATGCATTCAATCTGTTCTGTTTTTGTATATATCATTATTTTAATTATTTATTTACTTCCATTTATTCACTGACTTGTTTATTTAGTTTCATATTTACTTCATGTTTATTTACCTACTTGTTTATTTTATTTACTTATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13125
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029668 | Essential Splice Site | 226 | 1389 | 4 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 10474921)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 9407984 |
GRCz11 | 7 | 9653148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTTTGCCATCATCACCGGTTTGCCTCTGTATGCTGCGGCTCAGGGAGG[T/C]ACTGAACATKAWGAACGGAAATTTGAAATTTGTGTTGCCTGTTCATTTAC
Long Flanking Sequence:
TATAATATATGGTATATATTATAAAAATATTTATAAACTGATGTTTATGAAAAGTTCTTGACAATTAATGCAGCATTTGAACTTATTTATGGATCTGTTATGACTTTTATTTTGAAAATGAGCTGTTTAGGCCATCAGGATGCAGATCTGTTAACTAATTATTTTTTGCCAAATGATGCTGATATGTAAAGCAAAATTAAAGGACCCGCCCCTTTTTGATGTCTTTGCTTAAGTTGTTAGACATGCCCCTTTCTGCTGATTGGCTGAGAGAGTTATTTGTGAAAATATGAGTTCTTCTTGTGCTGCGTTTTTTCTTCAGGTCCGTGTGTGCGTAAGGATCTGCTGAACTGGATGTTGGCTACGGCGTCTCAGCAGGGTCATTTAGACGTGGTGAAGCTCCTGGTTCAGACGTATAATGCAGACGCAGACGGCTGTGCTGTTCATTCAGGAGAGTTTGCCATCATCACCGGTTTGCCTCTGTATGCTGCGGCTCAGGGAGG[T/C]ACTGAACATTAAGAACGGAAATTTGAAATTTGTGTTGCCTGTTCATTTACTAAATTTTTAAACTTTTGAAACTTAAAAAAATAGTCAAATTGACATGAAAAGTTAAAGAAAAAAAAAAAAAACATTCATTCAGATCATTTGATCCCTGATTCATATTGACTAACACATTGAACATTACATAAAAATTGTAGCACTTATTGTTTTATTAACTTAACAGTAATGGAAGTTTATAATTTAAATATAATGATCGTTTTAACCATGTTTTGCATGTTCAAGATTCTCTTGTGTTAGCTAGTGTTTGCGTGATGTACTGATAAAGATATAATGATAATGTTACTGATATTATACTGTTTGATTTTGGGGTTAAATTCATTGAAACCTTTTATAGTAATGTTCAGTATGTATATATATGTATGTATGTATGTATGTATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13011
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029668 | Nonsense | 293 | 1389 | 6 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 10465178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 9398241 |
GRCz11 | 7 | 9643405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGCATGTTGACTGGTCTGGACTGAAGCTGTCCTGGTTGGATCTGGACT[G/A]GTTTATGGACGWRTCGTCTCGCATCACCGTTCTGGATCTCTCTCGTAACT
Long Flanking Sequence:
GCTTCACATAATAGGTCATAGTTATGGCTTAAAGTATATCTAAAGTGCTATTCCATCATATGTAATGAGCAGTGGTTAATGCGTGTGGCTGCAGTTGTTGCAGCCTCTGCTTTAGGACACGGCAAACACTTGAACTCCGGTGTAGAAAAAAATGAGTTATGTCACACTCCCCCTTCCCAAACGAGTGACGCGCAACTACAGCCTGTCAGGTGTGTGGAAAGCACATGATGTGCGGTTCAAATCCAATCCCATCTCTAATCTTCAGTGCTAAATTCAACCTTGCGCTCATCATAACATCACAATTCACGAGACAACTTTTCACCTCGACGAGATATCTCGTTGCGATTTACTCTCGCTAGAGCTTGTAGCCCGACATCTCATCCCATCCCTACTCAGCACTAATTATTATAATTAGTTAATAAAATGTTTTGTCTGCCCTCATCCACAGGCTGTGCATGTTGACTGGTCTGGACTGAAGCTGTCCTGGTTGGATCTGGACT[G/A]GTTTATGGACGTGTCGTCTCGCATCACCGTTCTGGATCTCTCTCGTAACTGTCTGAGTTCACTGCCGTCTGTGGTGCCGTGGGGTTTGATTAATCTGCGCTCGCTCGATTTGTCCCAGAACCAGCTGAAAGAGCTTCCCACGCCAGCGTCCTCACAGCAGATCATCTGCAGCAGGTCAGTACAAGAATCGTTCACCAGACAAGCTTTTAAAGGGAACCTATTATGCAAAAATCACTTTTATAAAGAGTTTAAACACAGTTTTGTGGCAACAGTCTGTGGATATAACCATCTTCTAATGGTAAAAATATTCCTTTTTTATTATCACACTTGATAAAAACAGTCTACTGCAGTGGTAGGGAACATATGACTATCGAGCCACATGTGGCTCTTTGACTAAAAATACATGGCTCTCCAGCTGCCTTCCTTCAATAATATTTTACCATTTAAAATATTATAACGTCACTAAAAAATTAGTTTCCTATCGAAAATGCAATTACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12644
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029668 | Nonsense | 740 | 1389 | 15 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 10436167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 9369230 |
GRCz11 | 7 | 9614394 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAGCATGTCGACGGTCAACCAGTGTTTCTTCACTGATAAAGCTCTGTA[T/A]ATGGTGATCTGGAATCTGGCTTTAGGAGAAGAAGCCGTGGCAAACCTGCA
Long Flanking Sequence:
GTTTAAAATGATTATAAATATGACTAAATTATACAAAATCTAAAAGTAAGCATATAATAAGGCATAAGTCTCAGAATCTTTTCTTCTATCATTGGCAATAATCTTAAAATCAATATTATATGAGAAAGTGTGACACACTCAAGCAAAACACAGCAAAGTGAGTATTTCTTGATTCATTTAGTTTTCCCACTGCACTTCATTTAAATACAACTTGTATTTACTAATAGAGATAGCTGATAAATGTACTTTTGTTTTATTAAACTAGATATGCCTGTCAAGTTGCTTTGAGAGTTTATTTTCTTGTAGTTGCATTGGTGATTAATAAAACACTATTAATATCTTCACTTCTTTACCTGATTCAGTTTAGAGGAGGAATGAATATGTTTGTTTGTGTTTTGGTCCACACAGGTAGATTCAGTCTCCTTTAATGTGTGGGACATCGGTGGTCCGGCCAGCATGTCGACGGTCAACCAGTGTTTCTTCACTGATAAAGCTCTGTA[T/A]ATGGTGATCTGGAATCTGGCTTTAGGAGAAGAAGCCGTGGCAAACCTGCAGTCCTGGCTGCTCAACATCGAGGTGAGAGAAAAGAGAGAACAAACTAGACAAACATCATTACAAACCATCTGAATAAATGTACAGTTGTGTATTGTATATTATTTTCCTTTATTTTAATACTAATATATTTTTAATCTTTTAATTTCTTAAAAGTTTGAATTAATAATAACTTCTCTTTTAATCCATATGTTGGTATTTGTTTCTTATTTCTGTATGTGTTTATCAAAATTCTAAATGTATTTATGCAGTTTATCATTTTAACTTTATTACTTCATTTTTAAAGGTTTCATTAAAATGCTATGAAGCTCTTTTGAATTGAATTGAAAAGAGAATTTCTGTATACTTCTGAGTGAAATGTATGGCTTAAAGTGACCGCTTGCTTTTTTAAATATGAAAACAGGTATATTTTATATACTTTATGTTGCATATATTAGTATTTTAGCAACTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40838
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029668 | Nonsense | 1300 | 1389 | 24 | 25 |
Genomic Location (Zv9):
Chromosome 7 (position 10404553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 9337616 |
GRCz11 | 7 | 9582780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAGCTAAATACAGAGGCCATCCGGTGGCCATTAAACGCTTCCACTTC[A/T]AGAAATGCAAGCAGCAGTCACTCAACAGCAGCACAGGTATGTTTCACTCC
Long Flanking Sequence:
TTAACAGCAGATGGTGCTCTACTCTAGTTTTTAACAGCAAACTAGATTGATTTTTAACTCCAGCTGGCGCACTAAGCTAGTTTTTAACAGCAGATGGCTCTCTACGCTAGTTTTTAACAGCAGATGGTGCTTTTGGCTAGTTTTTAACAGCAGATGGTGCTCTAGGCTAGTTTTTCTGGGCTAAGCAAAATTGAAAAGCTTGCTTTAGGACATGAATAAGTGTTGTTCAATAGTTTTAGGGCAACTTGATGAAAGCTTATGAACTACTTCATATGTTGACTACTGTACGCTTAAAGGCGAAAGCATACATTGTAAATTAAATGCACACACAATATGTTATCAGCACCTCTGTCTGTGTGTATTTTAGGTTGTTTCTGCTGAAGAGTGACCTTGAGTGGACTGAAGATGAAGCTGATATCCTTGGTCAGGGCGGCAGTGGCACCATCATCTACAGAGCTAAATACAGAGGCCATCCGGTGGCCATTAAACGCTTCCACTTC[A/T]AGAAATGCAAGCAGCAGTCACTCAACAGCAGCACAGGTATGTTTCACTCCTCCACTGACCCTGAACTTCCTCCGGAATAAGCTGTTATTATCTTTAGACCTTTCCTCTGGGTCGCTCGAAGGCCCTGCATTGCAAACACGAATGGCAAAGTATTTCAAAGTAGAGCTTTTTTTTTTTTTTTTTTTTAATAATGCATTATGATTCAGATTTTAACAGCAGACACTGTTCTAGGCTAGTTTTTAAACCACAGATGCTGCTCCAGGCTAGTTTTTAACAGCAGACTACACTCTAGGCTAGTTTTTAATTTTTTTCTAGTCTCGTTTTTAACAGCAGATGAAACTTTTGATGAAACAGGCTAGTTTTTAACCACAGATGGCACTCTAGGCTAGTTTTTAACAGCAGACGACACTCTGGCTTAGTTTTTACAGCAGATGGCACTCTAGGGGTAGTCTTTAATGCAGCTCTAGGTTAGTTTTTAAACCACAGATGCTGCTCTTGGC
Associated Phenotype:
Not determined