Busch Lab

ZMP

lnx2a

Ensembl ID:
ENSDARG00000029177
ZFIN ID:
ZDB-GENE-060228-2
Description:
ligand of numb-protein X 2a [Source:RefSeq peptide;Acc:NP_001106696]
Human Orthologue:
LNX2
Human Description:
ligand of numb-protein X 2 [Source:HGNC Symbol;Acc:20421]
Mouse Orthologue:
Lnx2
Mouse Description:
ligand of numb-protein X 2 Gene [Source:MGI Symbol;Acc:MGI:2155959]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa24497 Nonsense Available for shipment Available now
sa24496 Essential Splice Site Available for shipment Available now
sa37882 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24497
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
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046211 Nonsense 113 737 2 11
ENSDART00000123216 Nonsense 113 705 2 11
Genomic Location (Zv9):
Chromosome 24 (position 22279101)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 21525979
GRCz11 24 21671153
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTCCAGCATTCTGGTGCACAAGCTGCTGGACAAGTTGTCGGTCACCTG[T/A]CCGCTCACGCCCTCCTGCTCGCTCAGCATGCCTCGCTGCGACCTGGAGGC
Long Flanking Sequence:
ACAAACACTGTCTCTCATTCACAATAGTTACCTCACTGTTTCTCTGCCACCCTTCAGAGTGATGTCACTGTGCCTGCCAGGGGGTGGTCGTCCCCTGCCGGAGTCGCACAGCCTCTGACGCCCGCGGGATGGACTGAGTGAGTGTAGCCAAAGCCGAGAGCAATGGGCAGTCTGGGAGAGGGAGTGGACCCGGGCATGGTGAGCGAAGCTCTTCTGGAGGCCCTTTGCTCTGAATGTGGACAGATTCACCGCACCTGGGAGAACCACCTTTATAACTATCGTTTGGAAGTGGATGATGATTTGGTGTGCCACATCTGCCTTCAGCCGTTAGTTCAGCCCCTGGATACACCATGTGGCCACACCTTCTGTGCCCGCTGTCTGCGCAGCTTCCTGCAGGAACGGGACTTCTGTCCACTGGACCGTGCGCATCTGCAGCTGCAGGTCTGCCGGCGCTCCAGCATTCTGGTGCACAAGCTGCTGGACAAGTTGTCGGTCACCTG[T/A]CCGCTCACGCCCTCCTGCTCGCTCAGCATGCCTCGCTGCGACCTGGAGGCACATCTCAAACACAGGTAAAGTTCTCAAGACAAATATTCAGACTCAAATAAGCACTATTTGATGTCAATGTTTTGGTACTCGAGCATTAGGTTATTTTTATCTGATGCCATTGATGTTGCATGAAATTCAGATAGAGGGCAGGAAGTGGTTCTTTTACATAGGAACTGCAATCAGAACATCAAAATGTGTATATTTTATGTTGTTTATAATTGTTTAGATTGGCCAAAATAAGAAATGGCGAACAGCTTTTTATAGACTGCCAAAATTTTTTGCTCAAAAAGTCAAAAAGGGGGGAAAGTTTATGAAAATGTCTGAAAAGCAGAAGAAAAGGAGGCATGTTATCAACATTTAATCAATACATCCATGTGTACAAACTTTTTTTTTTGAACGTGATAATTAATTTAACAGCACCAATAAACCTTATATACAGGCCTAGCTATGTGTATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24496
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046211 Essential Splice Site 256 737 None 11
ENSDART00000123216 Essential Splice Site 224 705 None 11
Genomic Location (Zv9):
Chromosome 24 (position 22267686)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 21514564
GRCz11 24 21659738
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCAGGATGGGACTTTGTTGAAACTCTTCCTCTTTCTGCTGAAGAAGG[T/C]ATCATTTCATCCTGCTCTACACTACACCTCTTTCTATAGGATGAAATGCC
Long Flanking Sequence:
TGGCCTCCAGAATCACTTGAACTCAATCCAACAGAATCCCACTGGGATGTTCTGGAAGATTCACAAAAGATAAAAAAAAATATATGCAAAAACCAAATAACAATATCTTTTCAATATCTTTTTAACGATTTATTAGTCAGCATAAAAAATAAGTAATCCTATGGAGAGAATAAATGGGATTTTTCTTCTGCAACAATAGTGTTAGATGTTAGAAATTACAAAAATGCCCAAAATGATTATTATTTAAAGAGTTGATTCCAGTGGAAATGTATATGATAGACATGTTGCTAAGCTAACACAATACACTAAAATTCCTTTTTTTGCGAGGGAATGAAATTGACCTATATTTTTTTCCTCAAAGGTGTTCATGGTCTTGAGTGTGCTCTTCCACGTGTGAAGCGTCCTCTCAGCAACCCATGCATTCATCTTCTTCGCACTGGCAGTTCGGCTTCTTCAGGATGGGACTTTGTTGAAACTCTTCCTCTTTCTGCTGAAGAAGG[T/C]ATCATTTCATCCTGCTCTACACTACACCTCTTTCTATAGGATGAAATGCCCTTTATATCTTTTCTATGTGCCTTTTCCTTCAGGTTGTGTAAAACTTCCTTCTCTACCTGAGGGAGAAATCACTACTATTGAGGTTCACCGTACAAACCCCTACTCGGAGATGGGCATAAGTATTGTGGGTGGAAATGAGACTCCCCTGATAAATGTGGTAATACAGGAGGTGTACCGTGACGGTGTTATAGCCCGAGACGGAAGGCTGCTGGCCGGAGACCAAATACTTCAGGTACTGCCGCTATGCTCCAAAAGAAGTGTCTGATTAAAACAGGCATTTTCACTGCTATTTACAGATCAGCCTTGATACTTTAATCAATCTCTAAAAAGCTCTAATGAATACTGATGGCAGGATCACTATCTGCATGAATAGATGCAGCTTTTTTTTTTTTTTTTACCTCAAATACAAAACAGCATTCTTTAAACTGCCATTCACTAAAATATGCGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37882
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046211 Essential Splice Site 505 737 7 11
ENSDART00000123216 Essential Splice Site 473 705 7 11
Genomic Location (Zv9):
Chromosome 24 (position 22263274)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 21510152
GRCz11 24 21655326
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAAGTCCCGTCCCCAGTCTGCACCTTGCCAGGTCTTCCACCCAGAGAG[T/A]GAGTACACACGCCTTGCGGCCAAGTCTGTTTGTGTTGCAGAATCTATTTT
Long Flanking Sequence:
CATATTTTCTTTTTAAAATGATAAATATTTCCTTCTACTAAATATTCCTCTTATAAAACAGCTGGTGTCAAATCTCAGTGCCTGTTTAGGACATTAGGACACACTCTGCTGCCCTGCTCAGAGGGTAATGTGATTGATAGTATCTTTATGTCTACGTGAGCTGCTTTTTCCCCATCTGGCTGCCCCGATCACAGAGAAAGGGCAACTAAAGTGTTATTAAGAATAGCACTGGCAGATAGCAGACCGTCTTTGTTGGATGCAGTGCCACCTCTATAAGAGTATTAGGTATTTATACGACCGCCTACTGTCATCTTTATAGGCTAGCGGAGAAAGAGTCAATCTGCTGATTAGCCGGTCCAGCAAGCAGACTATGGCGGTGCACACAGGCTCCACCTTGACCAGGGACATTTGGAGCCATGATCACATCCCGCCACTTCCCAGTACTGCGACCCCAAGTCCCGTCCCCAGTCTGCACCTTGCCAGGTCTTCCACCCAGAGAG[T/A]GAGTACACACGCCTTGCGGCCAAGTCTGTTTGTGTTGCAGAATCTATTTTAGCATTGTGGAGACGTAATTAGGGAGCCCTATTTACGAAGCATCTGGGTAGCCTCCAGTTTTCCATGAGTTCAGACCACAACCTTAATTACTCCTTGTCGGATCTATTATGAGATCAATTCGGAAGTACAGCTGATCCCGTTGGGATGACGAACAGCACTCTACAGAGAGCCGATCAGAGTGTCAGTTTAGAAACGGGCTTCCTTTTTCTTTATCCATACCTTTGAGACACGTTTAGACTTGATGCTCTGATGCTTTTCTAATATGAGTGTGTGTTGCAGGATCTCTCCCAGTGTGTGAACTGTAAAGAGAAACACATCACTGTGAAGAAGGAGCCTCATGAGTCTCTGGGAATGACTGTGGCAGGAGGACGGGGCAGCAAAAGTGGGGAACTGCCCATATTTGTGACGAGCGTCCAGCCCCATGGCTGCCTGTCACGTGACGGACGAAT
Associated Phenotype:
Not determined