ZMP
LRIG3
Ensembl ID:
Description:
leucine-rich repeats and immunoglobulin-like domains 3 [Source:HGNC Symbol;Acc:30991]
Human Orthologue:
LRIG3
Human Description:
leucine-rich repeats and immunoglobulin-like domains 3 [Source:HGNC Symbol;Acc:30991]
Mouse Orthologue:
Lrig3
Mouse Description:
leucine-rich repeats and immunoglobulin-like domains 3 Gene [Source:MGI Symbol;Acc:MGI:2443955]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39025 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7233 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12526 | Nonsense | Available for shipment | Available now |
sa7234 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39025
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110613 | Essential Splice Site | 264 | 913 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 15 (position 3027575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3002582 |
GRCz11 | KZ115982.1 | 13761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGAGGACATGAACGGCCCCTTCTCTGCTCTGGACAACCTGCGCAAACT[G/A]TACGCTTCCACAAACTCCATTAGTTTTTAATCTGAATTGTTGTAAATGTG
Long Flanking Sequence:
CTTAACTACACCATACATGTGAGACATCAACTAAGGACTAGCATAAAAGTAATCTAAATGTAATCCAAAAGTACTCAGAGTACACTAACATGAATATAAAATCTAAGAGATTATATTACTGTCTACATTACATTATTTTTTGTAATCTGTAATCAGTAGCTGATAATAATTCATAAGTAATCTAGCCAGCACAGCATTATTATGACATAAACAAGCTGTTATTGTAGTTTATATTCAGTAAACAGGCCTGTTTGATTGAGAGGTTGTGTGTGTTTGCTTGTTTTAAAGTGTCAGTATCAGGGTTGTGTTGTCTGTTTTTCAGCTCATTTTTAGCAGTACACATGAACACACTGCAGCTTTACGACTGCCGCTCTCTGGGTGTGGATTTTAACAGTGTGGTTTTTCTCTCTCTCTCTCAGAGATCTGAAGTTTAATGAGATTTCGTGGACCATCGAGGACATGAACGGCCCCTTCTCTGCTCTGGACAACCTGCGCAAACT[G/A]TACGCTTCCACAAACTCCATTAGTTTTTAATCTGAATTGTTGTAAATGTGTCAGAAAATACTGTTTATTTTTTAAACACATTTTATTTTGATAGTTTTTTTTATTAAATAACACAAAACAAACAATCACCATTCTCAAATATCTGGGGGAAAAGAAAAATAAGTAAATAAAATCAAGCAAATATATATATATAATAAATACATTTCAGTTGTAGATCCAAAACACACAGCAAAAGTTGTGAAGACGTGGTTAGCAGACAAAAATATTAACGTTTTGCAGTGGCCCAGCCAGAGTCCTGACTTAAACCTAATTGAGAATCTGTGTAGGCAGCTGAAGTGTTTCTGTTATTTAATGTATAAGTGATTTCATATTTTCAGCATTATCATTAATTCAGATGTTCTGCATAGCTTTGCTAACCATTTCGCATTGTCTCCCTTTATTTTAAGGTTTCTCCAAGGGAATCGCATCCGATCAGTCACCAGAAAGTCCTTCACTGGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7233
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110613 | Nonsense | 801 | 913 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 15 (position 3035384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3010391 |
KASP Assay ID:
554-5045.1 (used for ordering genotyping assays)
KASP Sequence:
RATCRCTGATTGGCTCCTATGCCAGAAGGYGGGCTTTAKTTGCCATATAT[C/T]GATCGCTGATTRGCTCCTATGCCAGAAGGYGGGCTTTATTTGCCATATAK
Long Flanking Sequence:
TAGTTTCATTTCTGAATGTTCGTATCACACAAAATCTGCAGAAACTCTCATCTGGTCCGAGCCCCTCCCTCTGAGAATTGTCATTCTATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTACCATATAGCGATCACTGGATTGGCTCCTATGCCAGAAGGTGGGCTTTATTTGCCATATAGCGATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATAGCGATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTAGTTGCCATATAGCAATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTAGTTGCCATATAGCAATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATAT[C/T]GATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTGTACTACAAGGGCGGGGCTTTTCAATTGTTTTTGTATTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATGTTATTGTGTGTGTGTGTGTGTGTGTGATGTAACAGTAGTCCTATATGAGTTACTCTTTTGTTACTTGTAATGCGCTACAGCTAACACTGATAATGCTAGCATGAATGAAAGTGGCTTTATTGTGTGTACAGCTATACACATGATGCATTAATTACGCTTCTTACATCATATTATATTATTATTATATTAATTGTATTTATTATATACTCACCGGCCACTTTATTAGGTACACCATGCCGCGCTCGAAGTCACTTAAATAAGTTCCGATGCTCAGTCTGACCTGCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12526
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 |
---|---|---|---|---|---|
ENSDART00000110613 | Nonsense | 801 | 913 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 15 (position 3035384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3010391 |
KASP Assay ID:
554-5045.1 (used for ordering genotyping assays)
KASP Sequence:
RATCRCTGATTGGCTCCTATGCCAGAAGGYGGGCTTTWKTTGCCATATAT[C/T]GATCGCTGATTRGCTCCTATGCCAGAAGGYGGGCTTTATTTGCCATATAK
Long Flanking Sequence:
TAGTTTCATTTCTGAATGTTCGTATCACACAAAATCTGCAGAAACTCTCATCTGGTCCGAGCCCCTCCCTCTGAGAATTGTCATTCTATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTACCATATAGCGATCACTGGATTGGCTCCTATGCCAGAAGGTGGGCTTTATTTGCCATATAGCGATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATAGCGATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTAGTTGCCATATAGCAATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTAGTTGCCATATAGCAATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATAT[C/T]GATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTGTACTACAAGGGCGGGGCTTTTCAATTGTTTTTGTATTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATGTTATTGTGTGTGTGTGTGTGTGTGTGATGTAACAGTAGTCCTATATGAGTTACTCTTTTGTTACTTGTAATGCGCTACAGCTAACACTGATAATGCTAGCATGAATGAAAGTGGCTTTATTGTGTGTACAGCTATACACATGATGCATTAATTACGCTTCTTACATCATATTATATTATTATTATATTAATTGTATTTATTATATACTCACCGGCCACTTTATTAGGTACACCATGCCGCGCTCGAAGTCACTTAAATAAGTTCCGATGCTCAGTCTGACCTGCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7234
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110613 | Nonsense | 818 | 913 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 15 (position 3035435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3010442 |
KASP Assay ID:
554-5046.1 (used for ordering genotyping assays)
KASP Sequence:
GATCGCTGATTRGCTCCTATGCCAGAAGGYGGGCTTTATTTGCCATATAK[C/T]GATCRCTGATTGGCTCCTGTACTASAANGGCGGGGCTTTTCARTTGTTTT
Long Flanking Sequence:
CTGGTCCGAGCCCCTCCCTCTGAGAATTGTCATTCTATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTACCATATAGCGATCACTGGATTGGCTCCTATGCCAGAAGGTGGGCTTTATTTGCCATATAGCGATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATAGCGATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTAGTTGCCATATAGCAATCACTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTAGTTGCCATATAGCAATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATATCGATCGCTGATTGGCTCCTATGCCAGAAGGCGGGCTTTATTTGCCATATAT[C/T]GATCGCTGATTGGCTCCTGTACTACAAGGGCGGGGCTTTTCAATTGTTTTTGTATTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATGTTATTGTGTGTGTGTGTGTGTGTGTGATGTAACAGTAGTCCTATATGAGTTACTCTTTTGTTACTTGTAATGCGCTACAGCTAACACTGATAATGCTAGCATGAATGAAAGTGGCTTTATTGTGTGTACAGCTATACACATGATGCATTAATTACGCTTCTTACATCATATTATATTATTATTATATTAATTGTATTTATTATATACTCACCGGCCACTTTATTAGGTACACCATGCCGCGCTCGAAGTCACTTAAATAAGTTCCGATGCTCAGTCTGACCTGCAGCAGATGGTCTTGACCATGTCTACATGCCTAAATGCAGTGAGCTGCTGCTGCCG
Associated Phenotype:
Not determined