ZMP
lingo2
Ensembl ID:
ZFIN ID:
Description:
leucine rich repeat and Ig domain containing 2-like [Source:RefSeq peptide;Acc:NP_001139054]
Human Orthologue:
LINGO2
Human Description:
leucine rich repeat and Ig domain containing 2 [Source:HGNC Symbol;Acc:21207]
Mouse Orthologue:
Lingo2
Mouse Description:
leucine rich repeat and Ig domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2442298]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9260 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9317 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35437 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9260
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102279 | Nonsense | 508 | 607 | 1 | 1 |
ENSDART00000102279 | Nonsense | 508 | 607 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 13 (position 12609987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 12608355 |
GRCz11 | 13 | 12740830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCYGTAACACTCGCRGTTAAAACCTCTGGAATCAGGGACAGGGCCCTTTA[C/A]GCGAACCGCAGCTTTCTTTTTGACCCCGACTACAATAGTTCCCTGATAAA
Long Flanking Sequence:
GAGGCCCTGCAGACTCTTTTGATTGGCCAGAATCCGTTAGTTTGCGACTGCCGTCTACGCTGGCTCCTGGAAAGGACTCCACCTTTGCTGTATGGAGATGTTCAACCTGAATGTAGTGCTCCTGCCCCCTTGGCTGGAAAGCCTCTTCGAGATCTTGTGGAAGCTCAAATCTCTCGCTATGTAATTTGCACCAAACCCAGGGTCATCTCCATGGCGTCTTACCCGGCACAGGCAGAAGAAGGACAGAGAGCTTGGCTGTATTGCAGTGCCGATGGAGCGCCGCCTCCATCAGTGTCATGGCTAACACCACTTAGACGACACATTACCACAAAGAGTACTGGAAGGGTGGTGGTCCACACTAATGGCTCGCTTGAGTTTCGCATGGCAGAGCCTCAGGATAGTGGCATGTACGTCTGCGTAGCATCAAACCCCGCAGGTAATGCTACTCTGTCCGTAACACTCGCGGTTAAAACCTCTGGAATCAGGGACAGGGCCCTTTA[C/A]GCGAACCGCAGCTTTCTTTTTGACCCCGACTACAATAGTTCCCTGATAAACGGCACAGAGGAGTACACCATCAGGGTGGTCCTGGACTTCACCACCATCCTGGTCTCTACAGCAATGGGCTGCCTCAGCTTTCTGGGTGTTGTTTTGTTTTGTTTCTTGTTGTTGTTTGCATGGAGTCGTGGCAAAGGGAAGCACAGAGGAAGCGTGGACATTCAATACGTTCCACGGAAGAGGAAAGGCGCAAACTCAGAACTTACAGAAACAAGCGGGCCAAGACGAGTCAACATGAAGATGATCTGAACTTTGTGAATGACAGAGGATTTCACAGGTTGCATGGTTGCGTATGCGTATCTGTTGGACTTTGTGAGTCTTTGGGTAAATGTGCTGCACAGGATGTGTTTAGTCATGAAAGTTTACATGTGGTATCCCAATGAAAAAAAAAGAGAGCAAAAGAACTACGCCAAACCATATAACGCGCGTCGTCTGCGATGCTTTGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9317
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102279 | Nonsense | 508 | 607 | 1 | 1 |
ENSDART00000102279 | Nonsense | 508 | 607 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 13 (position 12609987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 12608355 |
GRCz11 | 13 | 12740830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCYGTAACACTCGCRGTTAAAACCTCTGGAATCAGGGACAGGGCCCTTTA[C/A]GCGAACCGCAGCTTTCTTTTTGACCCCGACTACAATAGTTCCCTGATAAA
Long Flanking Sequence:
GAGGCCCTGCAGACTCTTTTGATTGGCCAGAATCCGTTAGTTTGCGACTGCCGTCTACGCTGGCTCCTGGAAAGGACTCCACCTTTGCTGTATGGAGATGTTCAACCTGAATGTAGTGCTCCTGCCCCCTTGGCTGGAAAGCCTCTTCGAGATCTTGTGGAAGCTCAAATCTCTCGCTATGTAATTTGCACCAAACCCAGGGTCATCTCCATGGCGTCTTACCCGGCACAGGCAGAAGAAGGACAGAGAGCTTGGCTGTATTGCAGTGCCGATGGAGCGCCGCCTCCATCAGTGTCATGGCTAACACCACTTAGACGACACATTACCACAAAGAGTACTGGAAGGGTGGTGGTCCACACTAATGGCTCGCTTGAGTTTCGCATGGCAGAGCCTCAGGATAGTGGCATGTACGTCTGCGTAGCATCAAACCCCGCAGGTAATGCTACTCTGTCCGTAACACTCGCGGTTAAAACCTCTGGAATCAGGGACAGGGCCCTTTA[C/A]GCGAACCGCAGCTTTCTTTTTGACCCCGACTACAATAGTTCCCTGATAAACGGCACAGAGGAGTACACCATCAGGGTGGTCCTGGACTTCACCACCATCCTGGTCTCTACAGCAATGGGCTGCCTCAGCTTTCTGGGTGTTGTTTTGTTTTGTTTCTTGTTGTTGTTTGCATGGAGTCGTGGCAAAGGGAAGCACAGAGGAAGCGTGGACATTCAATACGTTCCACGGAAGAGGAAAGGCGCAAACTCAGAACTTACAGAAACAAGCGGGCCAAGACGAGTCAACATGAAGATGATCTGAACTTTGTGAATGACAGAGGATTTCACAGGTTGCATGGTTGCGTATGCGTATCTGTTGGACTTTGTGAGTCTTTGGGTAAATGTGCTGCACAGGATGTGTTTAGTCATGAAAGTTTACATGTGGTATCCCAATGAAAAAAAAAGAGAGCAAAAGAACTACGCCAAACCATATAACGCGCGTCGTCTGCGATGCTTTGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35437
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 |
---|---|---|---|---|---|
ENSDART00000102279 | Nonsense | 601 | 607 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 13 (position 12610264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 12608632 |
GRCz11 | 13 | 12741107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAGAGGAAAGGCGCAAACTCAGAACTTACAGAAACAAGCGGGCCAAGA[C/T]GAGTCAACATGAAGATGATCTGAACTTTGTGAATGACAGAGGATTTCACA
Long Flanking Sequence:
CGCCGCCTCCATCAGTGTCATGGCTAACACCACTTAGACGACACATTACCACAAAGAGTACTGGAAGGGTGGTGGTCCACACTAATGGCTCGCTTGAGTTTCGCATGGCAGAGCCTCAGGATAGTGGCATGTACGTCTGCGTAGCATCAAACCCCGCAGGTAATGCTACTCTGTCCGTAACACTCGCGGTTAAAACCTCTGGAATCAGGGACAGGGCCCTTTACGCGAACCGCAGCTTTCTTTTTGACCCCGACTACAATAGTTCCCTGATAAACGGCACAGAGGAGTACACCATCAGGGTGGTCCTGGACTTCACCACCATCCTGGTCTCTACAGCAATGGGCTGCCTCAGCTTTCTGGGTGTTGTTTTGTTTTGTTTCTTGTTGTTGTTTGCATGGAGTCGTGGCAAAGGGAAGCACAGAGGAAGCGTGGACATTCAATACGTTCCACGGAAGAGGAAAGGCGCAAACTCAGAACTTACAGAAACAAGCGGGCCAAGA[C/T]GAGTCAACATGAAGATGATCTGAACTTTGTGAATGACAGAGGATTTCACAGGTTGCATGGTTGCGTATGCGTATCTGTTGGACTTTGTGAGTCTTTGGGTAAATGTGCTGCACAGGATGTGTTTAGTCATGAAAGTTTACATGTGGTATCCCAATGAAAAAAAAAGAGAGCAAAAGAACTACGCCAAACCATATAACGCGCGTCGTCTGCGATGCTTTGTCTGTGGAAAGCATTATTTGGACATTGCAGACGTGATTTAGTTAAAGTTGTTGTATATATTTCATATTTGTGGGAAAGAATGGTATATTTCTATATATAAATATATACACACACACATGAATATATATCTATTTACAGATACATTACAATTACTTTTCAAAACGCTGCAAAAACTCAAAAGTTGTCTTCCCCAATAAGCAAAGTATCTACTGGAAAAAGCCTCGGCTGTGCTGTGTTGTGAAGTGTTTGGTTTTGCTCAGAATTCTTGTTCTCCTGGGACA
Associated Phenotype:
Not determined