ZMP
LRRC7
Ensembl ID:
Description:
leucine rich repeat containing 7 [Source:HGNC Symbol;Acc:18531]
Human Orthologue:
LRRC7
Human Description:
leucine rich repeat containing 7 [Source:HGNC Symbol;Acc:18531]
Mouse Orthologue:
Lrrc7
Mouse Description:
leucine rich repeat containing 7 Gene [Source:MGI Symbol;Acc:MGI:2676665]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16585 | Nonsense | Available for shipment | Available now |
sa33883 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40711 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10855 | Essential Splice Site | Available for shipment | Available now |
sa20720 | Nonsense | Available for shipment | Available now |
sa20719 | Nonsense | Available for shipment | Available now |
sa17609 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16585
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Nonsense | 15 | 1547 | 1 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29924132)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30219775 |
GRCz11 | 6 | 30210336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTGGAGATGACGACTAAGAGGAAGATCATCGGCCGCCTGGTGCCCTGT[C/T]GATGTTTCCGGGGGGAGGAGGAGGTCATCTCAGTTCTGGATTATTCCCAC
Long Flanking Sequence:
GGCCGTGGTGTATGTGTGTGAATGCAGGAGTGCATGGGTGTTTCCCGGTGTTGTGTTGCAGCTGGAAGGACATTTGCTGCATAAAAGGTCCTGGATAAGTTGGCAGTTCATTCTGCTGTGGAAACCCCTGATTAATAAAGGGACTAAGCTGAAAAGAAAATGAATGAATGAAATTACTCTTAAGTAACTGAAGTAATTAATTTTTCAGACAAATAATACAAGAATGGATTTAAATAAAACTATAATTAGTAAATATTAATGATTTTCTTTTTGGAAGAAACACCCCACTCTGGTCTTACTGATGGTAGGAAGTAAGACACTCTTTTTGACACACACACATTATGTGTTGTATATCAGGATAGTGACAAACGATCATATGAGTCTGAAGACATGTTGGTTTTTCTGTAATAAACTGACCTGCGCTTGTCCTCTGTTCTCCTCCAGTGCAGTGTCTGGAGATGACGACTAAGAGGAAGATCATCGGCCGCCTGGTGCCCTGT[C/T]GATGTTTCCGGGGGGAGGAGGAGGTCATCTCAGTTCTGGATTATTCCCACTGTAGCCTGCAGCAGGTCCCCAAGGAGATCTTCAGCTTCGAGCGCACGCTGGAGGAGCTTTACCTGGACGCCAACCAGATTGAGGAGCTGCCTAAGGTGAGATGTCAAGTGTCAGTTTAAACATGCATACTATCTGCCTATAACATCACTGCTCTATAACATTACTGCAAACAAATTGTGCAAGAAATTATGATTATTAATGCGCATGCTTTCTTATTAAACTATAAAAGTGTTCCATATATTAAGGATGAACAGGCTTTGTTTTTAATGTATTAATCAGCAAGATTATATAAGCACCATGGACAGCTCCAATAATGTGTGCAAAGCACTGTAAAGGCCAATGGCTAGCGTCAGACTAATATGTAAGTCTGAGCTGCTTCACTGCAAAGAAACTTGCACTGATCTTAAAATATTTCAGTGCCTTGGTTTTGTTTTAAGAGGGACACCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33883
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Essential Splice Site | 64 | 1547 | 2 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29915763)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30211406 |
GRCz11 | 6 | 30201967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGAACACATTTTAACCAAATCTTTGTATTTCTGTTTTCTTTTTTTCA[G/T]CAACTCTTCAACTGTCAAGCGCTCAAGAAGCTGAGCATGCCTGACAATGA
Long Flanking Sequence:
ATACACACCCACATTCATACATTACAGACAATTCAGTTTACTTATAGCATGTCTTTGAATTGTGATGGAAAACAAAGGACCTGGAGGAAACCCTCGCTAAAATAGGGAGAACATGCAAACTCCACACAGAAATGCTGGCCTAGTCAGGACTCGAACCAGCAACTTGCTGTGAGGTGACAGTGCTAACCAATGAGCCATTGTGCCAAAATGTCACCATTCTGCTATAAAACTTTCAAATTTATAGACTTGAAATGCAGACTTTTCTCTTAATCTAAAGTCTAAAATGTGTTAAATATCGCTTGGTAGTGTGAAAAGCAAACAGCGGGACATCATACTGTACTGTGGGTGATTAAGAAGACTGTTACTTATTGTAGATTAGTGTAGATTGATCTGCCAAGGGGTAACATTTTTACAGGTGCCTTGATGGCTCTGCATATAAGTTTCTCTAAAGAAAGAACACATTTTAACCAAATCTTTGTATTTCTGTTTTCTTTTTTTCA[G/T]CAACTCTTCAACTGTCAAGCGCTCAAGAAGCTGAGCATGCCTGACAATGACCTCTCCAACCTGCCAACCACCATTGCCAGCCTTGTGAATCTGAAAGAGTTAGATATTAGTAAAAATGGTATAAGCCTAAATCAGTTTATTCTATATTTACTTTTTTAAATAGCATCTTGCACTAAATGCATTGGCAAGATTTTATATGATTGTACCTTAAAACCAATGTATCAAAATGGCTTTATTTCAGGTATTCAAGAGTTTCCAGACAACATCAAATGCTGTAAATGTCTATCAGTTGTGGAGGCCAGTGTAAATCCTATAGCCAAGTAAGTTAATCTTCTCACATTTATTAAATCAGAAACACAGAAAACTTCAATTAAAAGATTTTGGAAATGAAATATGAGTAAGGTTAAGGACATGCTTGGTGGTAGGGGTAGTTTTAAGGATGGGTTAGGGTGTAAGGCATAACTGTGAAATTATAAATTAATTTACATCAATTAATTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40711
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Essential Splice Site | 159 | 1547 | 4 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29911915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30207558 |
GRCz11 | 6 | 30198119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTTAAATGATGCCTTCCTTGAATACCTGCCTGCCAATTTTGGGAGG[T/C]AAGAGCTTCATCTTGGGGCTCTCTGTTCTTGCGCTGCCGGGGGATTGTGA
Long Flanking Sequence:
CCATAGAAGGAAAAATAAATACTATGTCAATAGCTACAGGTTTCCTGCTTTCTTTACACTTTTCCTCTTTGTGAGAAGTAAGAAACTCAAACAGTAAATAGTGAGTAAATATTGACAGAATTTTCACTTTTGGGTGAACTATGCCTTTAAGATCTTTGATTCACAAATTCATGATAAAAGATCAAACATTTCAGATCCACTGCATGGTCTCTACAGAGAGTCTCTTTTTCATAACATGATTAAATCAGCCCTCAAGTGACTGTTTTTACAGGGATGCTAACAGAGTCACTAAAAGGGGAAGAGTAGAGGGATTACAGACGGCTCTCGCTGCTCTTGAAGTACTTAACGCTTATCAAATCTTAAGGGCACTGGCCTTTGAGAGGGTCTGATCAGCTCTCTGTTCCTACAGGCTCCCGGAAGGCTTCACCCAGCTTCTAAACCTGACACAGCTCTTCTTAAATGATGCCTTCCTTGAATACCTGCCTGCCAATTTTGGGAGG[T/C]AAGAGCTTCATCTTGGGGCTCTCTGTTCTTGCGCTGCCGGGGGATTGTGAAATAGCTGTTTAACACATACACAGCAGGTAAAACAAGTAACAAACGCTTCATGATTTTTTTTCCAAAGGTGCTGCTGACTTGAAATTGTAGCAGATTTTAGTAAAAAAAAAAAAACAATTTGTTTATACAAATAAAAAAACAAAAACTAATTGAGGAATTCTTTTTTGTGTAATGACAAAACAATGGAATGACACATGGATAAATTACTGAACTACAAAAATGCATTAAGTACTTTGTATAAAAGGTTTTTTAATCATGAAAGCTTCAAGATGCCTTTTGGGAGGAGAATGGAGCTAAATGCATTGCTCAGGTGTGACCCCCCCCACAAACCCCAACATCAACAGAGTCTAAAAATCTTGATTGTTTGTAGGTCTCAAGACTATTCAGATCAGGTGATTGGCCGGGCCATTCTATTCTATCAGTTGTTAGAGTTTCCTTGTCTGTGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10855
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Essential Splice Site | 199 | 1547 | 6 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29903793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30199436 |
GRCz11 | 6 | 30189997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCGCAACTGGAGCGGTTAGACTTGGGAAGCAATGAATTCTCTGAACTGG[T/A]RAGAAAGATGCTCTCCTGTTGAAGGCTTTTTATCAATGGGACAGCTGTTA
Long Flanking Sequence:
ATTTTCAGAATGAGGCTGCATGGTGCAGTTTAAAGGCTTAACTTGGTTAATTAAACTAGGCAAGTTAAGGTAATTACTTAATTATCAATAATGTAAAACTAAAATAAATATTTTTTGCATTTTTGTCTTTAAAGAAACAAATGAAATATTTTGAAAATGTCCTAACTCTGTTAAACATAATTTAGGAAATGTTTGAAAAAAAAAAAAAGTTCACAGGAGCACTGCTAGTTTTGCCTTCAACTGTATATATTGTCTGTGTACATGTATATATTATATGGCAAATTATAGATGTGTATCACTACACCTGTGGCATATTTAAAAAAAGATGTTGAAGATATCTTATTTAATATGATATCATGGGAATTCAAGTAAATTGTTTATGTTTGCATGAACAATCCACAATTAATTTTGATTTCTTCTCTTGTCATGTTGTAGGTCAATTCATAGGCTGTCGCAACTGGAGCGGTTAGACTTGGGAAGCAATGAATTCTCTGAACTGG[T/A]AAGAAAGATGCTCTCCTGTTGAAGGCTTTTTATCAATGGGACAGCTGTTAGCGCACTCAGCATGGATTTTGGCTTTAGCAGGGAAGCTGAGAGTCTCTTGTTAGATTTCTGCTGCTGCACTGCGTTGGTTGCATCATGCGTTGATCCATTATTCATGAGTTGGTTCAAACACGCAGTGCTTGCCGCAAACGTTCACCACTGAGCTGCATTTAATTGGCTCACCCAAGCTGGAGTAAACAATGGCAGGGGATTTATCATATGTATTCCAGTTATCTGCACTCACAGCCTGCCTATAGCCGTTTCTTGCAGAGCCTGAAGCTGGCAGCACCGCATTCATTTATTTGAGTATAAATCAATGGACAAGGTACTGTGTCTGGAGGAACTGTGGCAGCTGAACACCAGAATAGCTATTAATAGCAGATTTCTTCCAATAATGGCTATGCTGTGTGATCGTTCGATTGGGAGCTGTTGGGTTTTTTAAAAAGCGCTACATGTTGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20720
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Nonsense | 629 | 1547 | 19 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29865862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30161505 |
GRCz11 | 6 | 30152066 |
KASP Assay ID:
2259-7660.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGACACTTATGTTTCCAGGACTCCATGGGAGGCTCCCCAAATGATATC[C/T]GAATCTCTGACATGAGACCAACTTTGGTAGAGCCACCAATGTACAAACCA
Long Flanking Sequence:
AATACGGGAAGTGTTTAAGCTTATTCCAATAAATTAATCACTTCATACAACCTAAATATGCATAGCTATGTTAATATGCTTTAAGCAAAATAATTTTACATGTTAACTTTTTTTTAAACTGCAATCTCTTAACTTAATGCTGTCATTATGTATTGTTTTAGCTCTAATAGAGTTTTATGTAATATGCAATTCAGCAAACAGATTTTTATACAGCCAAAATTTTCCTGTTAGTAAAGCAAAAGTTCATGTAATTTGATATGTTGACTTTTGAGAATGCATTTATTGACATTGTGACCCTAAATTGGATTAGAAATGTCAACTAATGTGTTTGAGTATAAGTTATTTATTTGCTTGGTATTTAAGTGAAAGATTAAAATTTGATTGCAGGAAAAGCTCACCCCACTCCCCTTGTTTTTCAATCCTTTTGTCTAGTGTTTAATTCACTGCGAATTTGACACTTATGTTTCCAGGACTCCATGGGAGGCTCCCCAAATGATATC[C/T]GAATCTCTGACATGAGACCAACTTTGGTAGAGCCACCAATGTACAAACCAAAAGTTGTGTTACTGGGCAAGGAAAAGAAAGGTTAGTAAGATTAAGAAAGCAAGTGAAAGTCCATTTCTTAGATACATTACAATTTGCTAAGGTTTTGGTGTCATGTTTTCTTTAACTTTTTTTTTCTTTTAACCTTATGCTAGTTCTATTTTTTTTCCAACAACCCCCTCATTATTTTTTTTATTTATTAATAAAGCTATATCTTTGACATATAATAAAGTTTTATATATAGCATAATTGCACTGGGGAACACTGTAAATATAGTTAGGGGAAACGCAATAATTTCTTTTTTATTATTATTATTATTGTTCTTGCATATACATAACTTCTTTGTATTATCTTCACCTTCATTTCAACATGCATTTTAGAGTCAACAGATGAGTCTGAACCAGACAAAATGCATTGTTTGAACAACAGCGGATCATCTGCCACTTATTCAGACTACTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20719
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Nonsense | 822 | 1547 | 21 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29862388)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30158031 |
GRCz11 | 6 | 30148592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGACAAGACCGCATCGTTGGAGTTCCCCTAGAGCTCGATCAGACACAA[C/T]AAACTTTCCACACAGTTCGCAACACCCCTGACACTGAAGTGCCTGCTCCT
Long Flanking Sequence:
ACTAAAATGTATTAGTGTAAACGAGGCAAATGCTTGCAGTTAGTGTTGTGTACTGAAAAGCATTGTCTTCTGAGTAAATTTTTTTTGTTGTTGTTTTGATGTCATGTTTAGTCCATGGCAATGTGTACAGAATTTTTTCTATGTAGTGCACTGATCAAATGTATTTGTCTAAATACATCAACAGGCTGGCTCAGTCTTTCCCAAAGCCCATTGAAACCAAGCCTCTTCTAAGCCAGAGGGAAACACCTCCTTCCAGCACGCTGCAGCAGCGAGGTGAGAGGCGGCCACTCAGCGACACCTTCGACAGCTGGAACGATGCCCCCCACTATGATAACACAGGTTTTGTTGCCGAGGAGATGCCTCTTGACACTCCGAGCAGCAGTGCTGGAAACCCCATGCTAGGCTCAAAGCCCCGGAGTGCATCGACAGCACATGGGCGACGGCCTCTCATGAGACAAGACCGCATCGTTGGAGTTCCCCTAGAGCTCGATCAGACACAA[C/T]AAACTTTCCACACAGTTCGCAACACCCCTGACACTGAAGTGCCTGCTCCTTCAAACCCCTGGCAAAACTGGACAAGGACTCCCAGTCCTTTTGAGGACAGGACAGCTTTCCCTTCCAAGTTGGAAATTACCCCAGCCAACAGCCCTAATCCTGACCGTAAGGACTTTGAGCAGGAGATGGGAGAAATACCCGGCACTTTCCCCTCAACTGGAGCCTGGGGGTTTCTGGACTCTACAGACTCAGGGACGGGACGAGGTCATCCCAACGTTTATACGCACATCCAGGTTGGGAAAGAACCAAATAAGGGAAACACTATGGTTCTTAGCAAAAGTTCTGAAAGACTTTCACCAATGATGAAGGAGGTAAAAGCAAAATTTAAGAAATCCCAGAGCATAGATGAAATCGATACCGGGTCATACAAGGTCTATAGCATCCCTATGGACAGCTACAGTTCTAGCATAGAAAATCAGGGAAGTGTTGATCGAGCAGACTTTCCTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17609
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113924 | Essential Splice Site | 1287 | 1547 | 21 | 27 |
Genomic Location (Zv9):
Chromosome 6 (position 29860990)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 30156633 |
GRCz11 | 6 | 30147194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGGAGACAGCAGCTGCTTAGACAYATAGAAGCGAAGAGACTAGACCGG[G/T]TGAGTAAGRAAGTTTTGCTTTATTTTTTNATACAACRRAGTTTGTTAGCT
Long Flanking Sequence:
TAAGTTCGACGGAGATGGCGCTGTTCCGCAGAGTGGCTGAGAACCATGAACTCCAGCTGGCAGAGCACTACAGCAGACCTCAACAAATAAAGAGCATGCTGGAGCAACAGAACAGCTTGTCTACCATGGCTGACACTCAGTTCCACAAGAGGAATGGTAGGTATGATGAAGATTACTCATCTTATCAAGAACCCAAAAAGCCCATCATGGGTTATCCCACCAAGAGTCTGACACAACGTCGCCCCCTGTCTGCACGGAGCTACAGCACAGAGACATACGGGGCATCTCAGGCAAGGCCAGTGTCTGCCCGGCCCACAATGGCTGCTCTTCTAGAGAAATTGCCTTCAGATTACAATCTTAGTACATGCACTGAGAAAAGCCCTGAAGCCGACATGAACCTGAGACCTGTCCCTCAGAAACAAGAGGACCTGACCTCCAAAATGCCAGTAGACTGGAGACAGCAGCTGCTTAGACACATAGAAGCGAAGAGACTAGACCGG[G/T]TGAGTAAGAAAGTTTTGCTTTATTTTTTTATACAACGAAGTTTGTTAGCTTGAACTTTATATAGCCTTAGTATTTAAAGGGATAGTTCACCCAAAAATGAACTATATCTACTCACCCTCAAGTGGTTCCAAAACTTTATGACTTTCTTTCTTCACAAAAGGAAAGCTAAAAATCTGCAACCATTGACTTCCATATTTGGAAAAGCAAATACTAAGGAAATCAATGGTTGCAATTATTAAAATATATATATTTTTTTGTGTTTCACAGAAGAAAGAAACTTATAAAGTTTGAAACAAAAAAGGGGGAGTAAACGATGACAGAAATTTTATTTTTGGGTGAACTATCCTTTTAAGGTATAGGTCTCAAACTCAATTCCTGGAGGGCTGCTGGGTCTGCACAGTTTTGCTTCAACCCTGATCAAATATAGCTGATCCAAATAATCGAGGTGCTCAAAAGTCAAAAGTCATGAACACTTTCACTGTTTGGATCAGCTGTTTCTG
Associated Phenotype:
Not determined