Busch Lab

ZMP

sc:d0348

Ensembl ID:
ENSDARG00000074535
ZFIN ID:
ZDB-GENE-080327-19
Description:
cDNA, clone cssl:d0348 [Source:UniProtKB/TrEMBL;Acc:A8BB68]
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 2 alleles of this gene:

Allele Name Consequence Status Availability
sa14641 Nonsense Available for shipment Available now
sa6352 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14641
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114026 Nonsense 133 628 2 2
Genomic Location (Zv9):
Chromosome 14 (position 46810284)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 44127411
GRCz11 14 44588723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTGAGCCTGGAGCCTTCRAYTCGCTCTACAGCCTCCACTCGTTGAGCT[T/A]AAAGAGCAACCGCATCAAGCTCCTCTCTCTAGGCGTCTTCACCGGCCTCT
Long Flanking Sequence:
CCTTTGTTTTACATTTAAAGATACCAACTACTAATGGTGAATCTTTCATTGATAATGTAACCTGATGAGATGTGTTAAATCAAGATGTCTCTGTTCATATTCTAACCTTTGGTCTTTCTGTTTCTTTCAGAGCCATGACAGTATGGTGGACTGTTTGAGTCGAGTCATGCTGCACACAGCCGTGTCTTGCTGGCAGCCTTTGCTGGGGCTGGCCCTGGTGGCCGTGTTCGTGGGCTCCACCCTGGCCTGCCCCTCCCGCTGCGAGTGCTCCGCCCAGAGCCGATCTGTCATCTGCCACCGCAAGCGCTACACCGCCATTCCCGATGGAGTCCCACTCGAGACGAGGATCCTTGATCTCAGCAAGAATCGCATTCAGGCTGTCAACCCTGATGACTTTGCTGCCTATCCACACATAGAAGAACTGGACCTGAGTGGAAACATTATTGCCTATGTTGAGCCTGGAGCCTTCAACTCGCTCTACAGCCTCCACTCGTTGAGCT[T/A]AAAGAGCAACCGCATCAAGCTCCTCTCTCTAGGCGTCTTCACCGGCCTCTCCAATCTAACAAACCTGGATATCAGCGACAATAAGGTTGTCATTCTGGTGGACTATATGTTCCAGGACCTGCGCAACCTCAGGTCATTGGATGTTGGAGACAACGAGCTGGTTTACATCTCCCATCGGGCTTTCAGTGGACTGTTGTCTCTGGAGAGCCTGACACTGGAGCGCTGTAACTTAACGGTGGTGCCCACAGATGCCCTGTCCCACCTGCACAACCTGGTGAGCCTGCATATGCGCTACCTCACTATCAGCACTCTCCACCCCTACTCCTTCAAAAAGCTATTCCACCTCCGTCACCTAGAGATCGACAACTGGCCATCTCTAGATGTGTTCCCCGCCAATTCTCTGCATGGCCTCAATCTCACCACGCTTTCTGTCACCAACACCAACTTGTCCACTTTCCCCTATCAGGCTCTCCACCACCTGCCTTACCTCACGCACCTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6352
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114026 Nonsense 386 628 2 2
Genomic Location (Zv9):
Chromosome 14 (position 46811044)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 44128171
GRCz11 14 44589483
KASP Assay ID:
554-5314.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCTGTTGATCAACAACAACCCTCTGGTGTGTGACTGTCGACTCATGTG[G/A]TTGCTCCAGAGGCACCATTCCATCTCCTTTGGTGACACCCAGCCTGAGTG
Long Flanking Sequence:
CACCTGCACAACCTGGTGAGCCTGCATATGCGCTACCTCACTATCAGCACTCTCCACCCCTACTCCTTCAAAAAGCTATTCCACCTCCGTCACCTAGAGATCGACAACTGGCCATCTCTAGATGTGTTCCCCGCCAATTCTCTGCATGGCCTCAATCTCACCACGCTTTCTGTCACCAACACCAACTTGTCCACTTTCCCCTATCAGGCTCTCCACCACCTGCCTTACCTCACGCACCTTAACCTCTCCTACAGTCGCATCCGAACAGTGGAAGGTGGCCTGCTTCAGAACCTGGTGCGACTGCGTGAATTGAGGTTAGCTGGATCTCATCTGGTGTCCATCGAACCCTACGCTTTCCAGGGCATCCGCTGGCTCCGCTTGCTAAACATCTCCCACAACCGCCTTGACACCCTGGAGAAGGGGGCATTTCATGCTCCGGAGGCACTACAGGTGCTGTTGATCAACAACAACCCTCTGGTGTGTGACTGTCGACTCATGTG[G/A]TTGCTCCAGAGGCACCATTCCATCTCCTTTGGTGACACCCAGCCTGAGTGCAGCAGTCCGGAGGGCAGCCAAAGACGGCAATCCAAGGAGTTCAAAGAAGCTCTTCTGTCCAACTATGTGACCTGCACCAAGCCCAAGATCCGTCGAAATCGGACTCAGTCTGTGTCTGTGGAGGAGGGACAGTCTGCCCATTTGAACTGCACTGCGGAGGGAACCCCACGGCCCACTATTTCTTGGGTCTCCCCACGTAAGGTACAGCTGAACAACAGGAACCACGGCAGAGTGATGGTCCACAACAACGGCTCATTGGATATTAAGGCGGTGGAAGTTCAGGATGGCGGTGTGTATGTATGCACGGCCTCCAACAGTGCAGGTAATGACACACTTATGGTATCACTGTCAGTGAAAAGTCTGGGCTCGCTGTATGCCAACAGGACCCAGCATTACACGGATACAAGCAATGCCACTGCCAACGGCACCAACCTCCCTAATGTGACCTT
Associated Phenotype:
Not determined