ZMP
lrig1
Ensembl ID:
ZFIN ID:
Human Orthologue:
LRIG1
Human Description:
leucine-rich repeats and immunoglobulin-like domains 1 [Source:HGNC Symbol;Acc:17360]
Mouse Orthologue:
Lrig1
Mouse Description:
leucine-rich repeats and immunoglobulin-like domains 1 Gene [Source:MGI Symbol;Acc:MGI:107935]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu2115 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa21876 | Nonsense | Available for shipment | Available now |
sa21875 | Nonsense | Available for shipment | Available now |
sa21874 | Essential Splice Site | Available for shipment | Available now |
sa17507 | Essential Splice Site | Available for shipment | Available now |
sa35054 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21873 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu2115
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000115085 | Nonsense | 209 | 1022 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16743620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16224320 |
GRCz11 | 11 | 16358955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTGTTTTGCTCATTTTATTTACTTTATTTCTGTGTTTTGTAGGGAGT[T/A]GAGTAGGAACAGGTTGCGGTTGATCGAGGGACTCACCTTCCAAGGTTTGA
Long Flanking Sequence:
ACCCACCACATCCTGAAAAACCTACCACTTCTTCCGTCATCATTATATTTTACAGGAAAGCCTAAATGCTTTCATACATGTGATTCAAATGACGCAAGAGGCGATCTCTCTGTGATCCTTAAAAAATTATAATTAATCTACCAGAAAAAATATTATTAATTCTTGGGCCACGTGTGTTCCGAATCTTGATCCATTACAGCCCTAATTTAAGTTTATGAGTATGTTGTCAATTAGCATTGTGCAATACACAAAATATGTTTTTGAAAATTTGTAAAAAGAAAAACTGACTTTAACATGTGTAACATGTAACCTGCTCAGTATTGCCTATTTGTTGAAATTGTACAAAAATAATGTCATGTTCATTCATTCAATAATAACTTCATACAGGGTTTTATACAGTTTTTCGTTCTCATTTCTTGATTTATAAAGTCATTTTAATTGCATTCGTCTCAGCTGTTTTGCTCATTTTATTTACTTTATTTCTGTGTTTTGTAGGGAGT[T/A]GAGTAGGAACAGGTTGCGGTTGATCGAGGGACTCACCTTCCAAGGTTTGAGCAGTTTAGAAGTTCTCAAGCTTCAGAGAAACAACATCAGCAAACTAACAGATGGGGCATTCTGGGGTCTGGCCCGGATGAGGGTTCTGTGAGTCCAAACTTTCATGTTTCTACAACTTAAAAAGTGTTATACAAGTATTCATATACATTTAAATAACATGTAATAAAGTGATATGATCATTTGCATTGCTCATTGTAAAGTTTTTCACATTTTTTTGTAGGCACCTGGACTATAACAGTCTACGAGAAGTGAACAGTGGCTCTCTGTATGGTCTGGAGTCTCTGCTGCAGCTCTACCTCGCCAACAATTCCATCTCAAACTTTAACCCTGAGGGTTGGGGCTTTTGTGAGAGACTTCGAGAACTGTGAGACATCACTTTTCCTTCTCTTCTCATCCTTACAGATCCAGGATTTACTGTTTTGCTGATATAAGATCCAGTCATGATGATT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa21876
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115085 | Nonsense | 259 | 1022 | 7 | 18 |
ENSDART00000115085 | Nonsense | 259 | 1022 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16743336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16224036 |
GRCz11 | 11 | 16358671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTGCTCATTGTAAAGTTTTTCACATTTTTTTGTAGGCACCTGGACTA[T/G]AACAGTCTACGAGAAGTGAACAGTGGCTCTCTGTATGGTCTGGAGTCTCT
Long Flanking Sequence:
TGACTTTAACATGTGTAACATGTAACCTGCTCAGTATTGCCTATTTGTTGAAATTGTACAAAAATAATGTCATGTTCATTCATTCAATAATAACTTCATACAGGGTTTTATACAGTTTTTCGTTCTCATTTCTTGATTTATAAAGTCATTTTAATTGCATTCGTCTCAGCTGTTTTGCTCATTTTATTTACTTTATTTCTGTGTTTTGTAGGGAGTTGAGTAGGAACAGGTTGCGGTTGATCGAGGGACTCACCTTCCAAGGTTTGAGCAGTTTAGAAGTTCTCAAGCTTCAGAGAAACAACATCAGCAAACTAACAGATGGGGCATTCTGGGGTCTGGCCCGGATGAGGGTTCTGTGAGTCCAAACTTTCATGTTTCTACAACTTAAAAAGTGTTATACAAGTATTCATATACATTTAAATAACATGTAATAAAGTGATATGATCATTTGCATTGCTCATTGTAAAGTTTTTCACATTTTTTTGTAGGCACCTGGACTA[T/G]AACAGTCTACGAGAAGTGAACAGTGGCTCTCTGTATGGTCTGGAGTCTCTGCTGCAGCTCTACCTCGCCAACAATTCCATCTCAAACTTTAACCCTGAGGGTTGGGGCTTTTGTGAGAGACTTCGAGAACTGTGAGACATCACTTTTCCTTCTCTTCTCATCCTTACAGATCCAGGATTTACTGTTTTGCTGATATAAGATCCAGTCATGATGATTGTTAACACATTAGAGCGCACTTATGTCAGTGAGATAGGAAGATTCGTAAGAATTGAATAAAAAGTACACACAAAGCTGCTGTAAAAATTGCAGAAATCTTCCAAAATAATCTTCAAATATGTGGAGTTGAAGCAATATTGGAAAATGCTTTTGACCACAGTGCCAAAACACACATGCAGCCAATCAGCAGTAAGGGGCGTGTCTAGTAATGATAATGGAGATTAGGGCTGTTTCTCAATACCAAGGATTTACATTCTTGTGGCGGCCAGTCTTGCCAAGTTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21875
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 |
---|---|---|---|---|---|
ENSDART00000115085 | Nonsense | 259 | 1022 | 7 | 18 |
ENSDART00000115085 | Nonsense | 259 | 1022 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16743336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16224036 |
GRCz11 | 11 | 16358671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTGCTCATTGTAAAGTTTTTCACATTTTTTTGTAGGCACCTGGACTA[T/G]AACAGTCTACGAGAAGTGAACAGTGGCTCTCTGTATGGTCTGGAGTCTCT
Long Flanking Sequence:
TGACTTTAACATGTGTAACATGTAACCTGCTCAGTATTGCCTATTTGTTGAAATTGTACAAAAATAATGTCATGTTCATTCATTCAATAATAACTTCATACAGGGTTTTATACAGTTTTTCGTTCTCATTTCTTGATTTATAAAGTCATTTTAATTGCATTCGTCTCAGCTGTTTTGCTCATTTTATTTACTTTATTTCTGTGTTTTGTAGGGAGTTGAGTAGGAACAGGTTGCGGTTGATCGAGGGACTCACCTTCCAAGGTTTGAGCAGTTTAGAAGTTCTCAAGCTTCAGAGAAACAACATCAGCAAACTAACAGATGGGGCATTCTGGGGTCTGGCCCGGATGAGGGTTCTGTGAGTCCAAACTTTCATGTTTCTACAACTTAAAAAGTGTTATACAAGTATTCATATACATTTAAATAACATGTAATAAAGTGATATGATCATTTGCATTGCTCATTGTAAAGTTTTTCACATTTTTTTGTAGGCACCTGGACTA[T/A]AACAGTCTACGAGAAGTGAACAGTGGCTCTCTGTATGGTCTGGAGTCTCTGCTGCAGCTCTACCTCGCCAACAATTCCATCTCAAACTTTAACCCTGAGGGTTGGGGCTTTTGTGAGAGACTTCGAGAACTGTGAGACATCACTTTTCCTTCTCTTCTCATCCTTACAGATCCAGGATTTACTGTTTTGCTGATATAAGATCCAGTCATGATGATTGTTAACACATTAGAGCGCACTTATGTCAGTGAGATAGGAAGATTCGTAAGAATTGAATAAAAAGTACACACAAAGCTGCTGTAAAAATTGCAGAAATCTTCCAAAATAATCTTCAAATATGTGGAGTTGAAGCAATATTGGAAAATGCTTTTGACCACAGTGCCAAAACACACATGCAGCCAATCAGCAGTAAGGGGCGTGTCTAGTAATGATAATGGAGATTAGGGCTGTTTCTCAATACCAAGGATTTACATTCTTGTGGCGGCCAGTCTTGCCAAGTTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21874
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 |
---|---|---|---|---|---|
ENSDART00000115085 | Essential Splice Site | 426 | 1022 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16731071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16211771 |
GRCz11 | 11 | 16346406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCATCCAACCCGAGGCATTCAGCAAGATGAAGAACCTGCGCTACCTG[T/C]GAGTCTCAGTAAACCTTTTCACATGCACACACTCGTCATCCGATCATGTT
Long Flanking Sequence:
TTATTTATATTTTTTGCTAAAGAAATCAAATCTTAATAGGCAAAAATGGATGAAACAAATCAAAAGTGAAGAGTAAAAACATTTACAAATCCTTAAAATTGTTTTTATTTCTTCATAAATTGTTTTCATTTGAACTTTCTCTTCAAAAAAAAAAAAATTAAACACAATTTACAAGATAAATATTAACAGTAACCAATGCTATTGAATTATGGGCCATATGGTCAGTTTCATAAAAAAGATAATTGACTTTAAGCACTTCTCCAGACTCTGTAACTCTGTCCGATATTTGGATCTTTCCACCTTGTTGGAAGTTATCCTGTATAAAAATAGGCTACGATATCTGCACACTAGAGCACTGCAGCTGTATGTGAACATTCGCATGTCCTCTTTCTGTCACGCCTGAGGGCCCTGTTTAATCTCTCAACAGGAATTTAGGGGAAAATGCCATCCGCTCCATCCAACCCGAGGCATTCAGCAAGATGAAGAACCTGCGCTACCTG[T/C]GAGTCTCAGTAAACCTTTTCACATGCACACACTCGTCATCCGATCATGTTTCTTGACATGACAAATGTTTTGGCTGATAGTAGAAGTTATTGTGAATTATTATACATGTTTAGACATGAAGTAATTTATTTACTTATTCATTTCAATATTTTTTTATTTTTTTGTTATTATTGTTATTTGTTTTTTTATTATGCATTTGTTTTTGTTCAAATTAAATTATTTTAGAAACATTTTGAACAGTAATCAGTGTTACTTATTAATAAAATAATATATTCTTAAATATATTAAATTTATATATTTCTTACTAAAATGCTTGCCAACATTTTCCATAAAAATGACATTGTGCTAATATTAAATTATTGTAAAAACAGAGCATTATACATCCACAGTGTATGTTAAAGTCATGTTTGTCATTTTCCTGTGTGAATAAAATGTGCACATTAATCAAATAATTTGCATTAGGTTGAAGTTTTTACTGATTTCTCTGCAGTCATATTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17507
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115085 | Essential Splice Site | 426 | 1022 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16730581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16211281 |
GRCz11 | 11 | 16345916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAATCAAATAATTTGCATTAGGTTGAAGTTTTTACTGATTTCTCTGCA[G/A]TCATATTCAGAGCGACAGTTTTCTGTGTGACTGTCAGCTGCACTGGTTTC
Long Flanking Sequence:
GCGCTACCTGTGAGTCTCAGTAAACCTTTTCACATGCACACACTCGTCATCCGATCATGTTTCTTGACATGACAAATGTTTTGGCTGATAGTAGAAGTTATTGTGAATTATTATACATGTTTAGACATGAAGTAATTTATTTACTTATTCATTTCAATATTTTTTTATTTTTTTGTTATTATTGTTATTTGTTTTTTTATTATGCATTTGTTTTTGTTCAAATTAAATTATTTTAGAAACATTTTGAACAGTAATCAGTGTTACTTATTAATAAAATAATATATTCTTAAATATATTAAATTTATATATTTCTTACTAAAATGCTTGCCAACATTTTCCATAAAAATGACATTGTGCTAATATTAAATTATTGTAAAAACAGAGCATTATACATCCACAGTGTATGTTAAAGTCATGTTTGTCATTTTCCTGTGTGAATAAAATGTGCACATTAATCAAATAATTTGCATTAGGTTGAAGTTTTTACTGATTTCTCTGCA[G/A]TCATATTCAGAGCGACAGTTTTCTGTGTGACTGTCAGCTGCACTGGTTTCCAGATTGGCTCCTCACTCGAGGGCTGAACCCTGGTGTTCAGGCCACATGTGCCCATCCAGAGAGCCTAAAGGGCACCAGCATCTACCAAGCCCCACCACAGAGCTTTGTTTGTGGTATGTAGAGTTATATATCACACATGCATATTTCATAACCAACAAGTCACAATAAGGAAGAACTAACTTTATTTTCACTGCAGGTGAAAACAAAATGTATTAATACACTTCCTCAGTTGATACGTTTTTTTTCTATTACAAGATTTATAAAATGGTCGAATATGCAAACATTATGCAATATTTAATTAAATGTGCTAATTTAAGTACTTTTAAGTACATCAAAATGCCTGCTTCAACTTACTAATTTCAATTTTTGACATAGAGCCAAAGGTTTTTGCAGAGGGTTTTTTGAAATGTCTTTTTATCAACCTATAATTTCAAAAACGGATAGCTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35054
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 |
---|---|---|---|---|---|
ENSDART00000115085 | Nonsense | 476 | 1022 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16730432)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16211132 |
GRCz11 | 11 | 16345767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCCATCCAGAGAGCCTAAAGGGCACCAGCATCTACCAAGCCCCACCA[C/T]AGAGCTTTGTTTGTGGTATGTAGAGTTATATATCACACATGCATATTTCA
Long Flanking Sequence:
CATTTCAATATTTTTTTATTTTTTTGTTATTATTGTTATTTGTTTTTTTATTATGCATTTGTTTTTGTTCAAATTAAATTATTTTAGAAACATTTTGAACAGTAATCAGTGTTACTTATTAATAAAATAATATATTCTTAAATATATTAAATTTATATATTTCTTACTAAAATGCTTGCCAACATTTTCCATAAAAATGACATTGTGCTAATATTAAATTATTGTAAAAACAGAGCATTATACATCCACAGTGTATGTTAAAGTCATGTTTGTCATTTTCCTGTGTGAATAAAATGTGCACATTAATCAAATAATTTGCATTAGGTTGAAGTTTTTACTGATTTCTCTGCAGTCATATTCAGAGCGACAGTTTTCTGTGTGACTGTCAGCTGCACTGGTTTCCAGATTGGCTCCTCACTCGAGGGCTGAACCCTGGTGTTCAGGCCACATGTGCCCATCCAGAGAGCCTAAAGGGCACCAGCATCTACCAAGCCCCACCA[C/T]AGAGCTTTGTTTGTGGTATGTAGAGTTATATATCACACATGCATATTTCATAACCAACAAGTCACAATAAGGAAGAACTAACTTTATTTTCACTGCAGGTGAAAACAAAATGTATTAATACACTTCCTCAGTTGATACGTTTTTTTTCTATTACAAGATTTATAAAATGGTCGAATATGCAAACATTATGCAATATTTAATTAAATGTGCTAATTTAAGTACTTTTAAGTACATCAAAATGCCTGCTTCAACTTACTAATTTCAATTTTTGACATAGAGCCAAAGGTTTTTGCAGAGGGTTTTTTGAAATGTCTTTTTATCAACCTATAATTTCAAAAACGGATAGCTTCTCTCAATTATAGCAAACAGCCAGAAAATAAATAATTTCCTAAAGTTTTTTTTTTTTTTTTTGTAAAAACTGCTGTAAATATTCAGCCAAATTATGTACAAACAAATCCTTGTTTAAAAGCCTCCAGAACATAGATGTGAATAAAAGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21873
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 |
---|---|---|---|---|---|
ENSDART00000115085 | Nonsense | 620 | 1022 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 11 (position 16726179)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16206879 |
GRCz11 | 11 | 16341514 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCACCAAAGCGCGGTTGGAGTGTGCGGCCGAAGGGCATCCGACTCCA[C/T]AGGTGGCATGGCAGAAAGATGGCGGAACAGACTTCCCTGCTGCCCGAGAG
Long Flanking Sequence:
TTTTTTTACTATTAAATAATTTCATAGCCATTTTTTTGTTATCATCACACCAGTTGCACAAAATTCCCATCATGCAACAGTTGCTCATCATTTGTCTTTTTGCACAAACGTTGCATGAACTGTTTCAGCAAAATTCAGCTTGATCGTACTACAGCTTGGGCCTTTTTTATCCTCTCCGCTGTTTGCAGTGCACTTGGATTACATGCCTTGTCAGTTCTAGCAACAGATGCAAATTGACGGTCTTGAGGCATTTTTGGTCTCATGCCCGTCCAAATCAAGCTATTTCCCATCGCCAATTGTGTTAGTCACAGCTATGAATGCTGGGCTTGTTTAGTGCTGATGTAGCAACATTACGAAAATAGTCCTTGCTAAGGCTAATTTTCCTCTGCCTCTTTATGCACACAGTCCTGCCTTCGTTCGTCAAGACCCCACGTGACATCACCATCCGCACAGGCACCAAAGCGCGGTTGGAGTGTGCGGCCGAAGGGCATCCGACTCCA[C/T]AGGTGGCATGGCAGAAAGATGGCGGAACAGACTTCCCTGCTGCCCGAGAGCGGCGCATGCGTGTGATGCCTGATGATGATGTGTTCTTTATCATGGATGTGAAGCCAGAGGATATGGGTGTTTACAGCTGCACAGCGAAAAACACAGCAGGCATGATCTCCGCCAACGTCACCTTAACAGTGCTAGGTAAGCTTAGCGTTTATAGAGCTTCTTGATCATGATTAGTGTTGCGTATAGTTAGTCAGTTATTAATTTACTTTTGAACTGAAATTGTCATTCATTTTACACTAAACATAAATTCAATGATTCCGATTCAGACTAATCAAACAAATCAGTTCAGAGAAGCAGATTATAGGGTAGTATCGATTCAAATAATTATTGAGTGCAGAGTTACCACACTTTTTGAAAGTACTTGAATTTCAGACATGGATTTAAGGCCTGGAAAGTCCTTAAACAGGGTGTCTATGTGGTTTTAAAGTCTTAATGTCCTAAATCTCAAA
Associated Phenotype:
Not determined