Busch Lab

ZMP

nlgn2a

Ensembl ID:
ENSDARG00000077329
ZFIN IDs:
ZDB-GENE-090918-2, ZDB-GENE-090918-2
Description:
neuroligin 2b [Source:RefSeq peptide;Acc:NP_001159801]
Human Orthologue:
NLGN2
Human Description:
neuroligin 2 [Source:HGNC Symbol;Acc:14290]
Mouse Orthologue:
Nlgn2
Mouse Description:
neuroligin 2 Gene [Source:MGI Symbol;Acc:MGI:2681835]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa40875 Nonsense Mutation detected in F1 DNA Not yet available
sa16117 Nonsense Available for shipment Available now
sa26941 Nonsense Mutation detected in F1 DNA Not yet available
sa40874 Nonsense Mutation detected in F1 DNA Not yet available
sa30629 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40875
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112978 Nonsense 13 810 1 7
ENSDART00000125284 Nonsense 13 828 1 8
Genomic Location (Zv9):
Chromosome 7 (position 23300704)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21865889
GRCz11 7 22132227
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGGACAGTCATGTATTTGCCTCATGCCTGTAAACGGGATTTGGGCTA[T/A]GCCCACAATTCAGAGGTCACTCACACAATAGCTCTCTTCTGGTTGGCACT
Long Flanking Sequence:
AGTCAGATTTAGAACACCATGACACTGACCAAATGTAAAGATTTCTATTTCAACATGTTTGAAGTTCACATGCTTGACTTAGAAAGGGTAGCAACTTGTAAATGACCCCCTGATCACTAACCCATTCCTTTCTTGTTGTTCTTTACAGGATCAGCTGTCATCTGTGTGCTCTCTTCAACTGACCCCATGAGGACGGCTCAGGGAGATGGAACGTAACAGACTTCTCACCTTTACTCTCTATAGCATTTCCACAAAAACTCACCAGGGCTGAGCACAACCTCAGCTCCCCGTCCACCCCAACCCTTCCACAGCCCCCCATTCCTGTCCTCCCTATTCTTGCTCCTCAAACAACCAAAATAGAACAGACAGGGTCACATTTCTTACTCTAGCAGTCCTTTTTACTTCACCCTTACCAATTAAATCAGAGGCCAATAAAACAGCGAAAAACAAAACAGGACAGTCATGTATTTGCCTCATGCCTGTAAACGGGATTTGGGCTA[T/A]GCCCACAATTCAGAGGTCACTCACACAATAGCTCTCTTCTGGTTGGCACTGTGGATCACTTTGGCATCATGTCAACGCATCGATCCTGGCACTAAATATCCTACAGTCACCACAAACTACGGCAAATTGCGTGGGATTAAAAAAGAGCTTAACAATGAGATTCTGGGTCCCGTGGAACAATATCTGGGCGTTCCTTATGCCACAGCGCCAATCGGAGACCGTCGCTTTCAGCCACCAGAAGCTCCAGGGTCTTGGCAAGAAGTGCGCAATGCCACGCAGTTTGCCCCGGTTTGCCCGCAGAATGTTCATGGTGTTTTGCCCGAGATCATGCTGCCGGTGTGGTTCACCGACAGCTTGGACGTGGCTGCCACCTACATTCAGAACCAGAGTGAAGACTGTCTCTACCTCAACGTCTATGTGCCCACAGAAGATGGTGAGTGTCTGACACTACACAGCAAAGCATTGTGGTTATATCTAATAGAGTGCAACAGTGCCGTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16117
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
ENSDART00000112978 Nonsense 56 810 1 7
ENSDART00000125284 Nonsense 56 828 1 8
Genomic Location (Zv9):
Chromosome 7 (position 23300576)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21865761
GRCz11 7 22132099
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCGATCCTGGCACYAAATATCCTACAGTCACCACAAACTACGGMAAAT[T/A]GYGTGGGATTAAAAAAGAGCTKAACAATGAGATTCTGGGTCCCGTGGAAC
Long Flanking Sequence:
TTTCTTGTTGTTCTTTACAGGATCAGCTGTCATCTGTGTGCTCTCTTCAACTGACCCCATGAGGACGGCTCAGGGAGATGGAACGTAACAGACTTCTCACCTTTACTCTCTATAGCATTTCCACAAAAACTCACCAGGGCTGAGCACAACCTCAGCTCCCCGTCCACCCCAACCCTTCCACAGCCCCCCATTCCTGTCCTCCCTATTCTTGCTCCTCAAACAACCAAAATAGAACAGACAGGGTCACATTTCTTACTCTAGCAGTCCTTTTTACTTCACCCTTACCAATTAAATCAGAGGCCAATAAAACAGCGAAAAACAAAACAGGACAGTCATGTATTTGCCTCATGCCTGTAAACGGGATTTGGGCTATGCCCACAATTCAGAGGTCACTCACACAATAGCTCTCTTCTGGTTGGCACTGTGGATCACTTTGGCATCATGTCAACGCATCGATCCTGGCACTAAATATCCTACAGTCACCACAAACTACGGCAAAT[T/A]GCGTGGGATTAAAAAAGAGCTTAACAATGAGATTCTGGGTCCCGTGGAACAATATCTGGGCGTTCCTTATGCCACAGCGCCAATCGGAGACCGTCGCTTTCAGCCACCAGAAGCTCCAGGGTCTTGGCAAGAAGTGCGCAATGCCACGCAGTTTGCCCCGGTTTGCCCGCAGAATGTTCATGGTGTTTTGCCCGAGATCATGCTGCCGGTGTGGTTCACCGACAGCTTGGACGTGGCTGCCACCTACATTCAGAACCAGAGTGAAGACTGTCTCTACCTCAACGTCTATGTGCCCACAGAAGATGGTGAGTGTCTGACACTACACAGCAAAGCATTGTGGTTATATCTAATAGAGTGCAACAGTGCCGTACTCTTTTTCAGCTGCCATGTTTCTGGAAGTATTTTTTTTTTCATAGCGATTGAAAAGCCTTTTTAAATCAATCAATCCTGAACAAAACCAATCATATACGAGGTCAATCACATGTGTTTAAAAACAAGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26941
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112978 Nonsense 74 810 1 7
ENSDART00000125284 Nonsense 74 828 1 8
Genomic Location (Zv9):
Chromosome 7 (position 23300521)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21865706
GRCz11 7 22132044
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGATTAAAAAAGAGCTTAACAATGAGATTCTGGGTCCCGTGGAACAATA[T/A]CTGGGCGTTCCTTATGCCACAGCGCCAATCGGAGACCGTCGCTTTCAGCC
Long Flanking Sequence:
CCCATGAGGACGGCTCAGGGAGATGGAACGTAACAGACTTCTCACCTTTACTCTCTATAGCATTTCCACAAAAACTCACCAGGGCTGAGCACAACCTCAGCTCCCCGTCCACCCCAACCCTTCCACAGCCCCCCATTCCTGTCCTCCCTATTCTTGCTCCTCAAACAACCAAAATAGAACAGACAGGGTCACATTTCTTACTCTAGCAGTCCTTTTTACTTCACCCTTACCAATTAAATCAGAGGCCAATAAAACAGCGAAAAACAAAACAGGACAGTCATGTATTTGCCTCATGCCTGTAAACGGGATTTGGGCTATGCCCACAATTCAGAGGTCACTCACACAATAGCTCTCTTCTGGTTGGCACTGTGGATCACTTTGGCATCATGTCAACGCATCGATCCTGGCACTAAATATCCTACAGTCACCACAAACTACGGCAAATTGCGTGGGATTAAAAAAGAGCTTAACAATGAGATTCTGGGTCCCGTGGAACAATA[T/A]CTGGGCGTTCCTTATGCCACAGCGCCAATCGGAGACCGTCGCTTTCAGCCACCAGAAGCTCCAGGGTCTTGGCAAGAAGTGCGCAATGCCACGCAGTTTGCCCCGGTTTGCCCGCAGAATGTTCATGGTGTTTTGCCCGAGATCATGCTGCCGGTGTGGTTCACCGACAGCTTGGACGTGGCTGCCACCTACATTCAGAACCAGAGTGAAGACTGTCTCTACCTCAACGTCTATGTGCCCACAGAAGATGGTGAGTGTCTGACACTACACAGCAAAGCATTGTGGTTATATCTAATAGAGTGCAACAGTGCCGTACTCTTTTTCAGCTGCCATGTTTCTGGAAGTATTTTTTTTTTCATAGCGATTGAAAAGCCTTTTTAAATCAATCAATCCTGAACAAAACCAATCATATACGAGGTCAATCACATGTGTTTAAAAACAAGACTTTGATTAACACTTTTAATCGGGGAAAAGGGAAAGGTGGATTTGATTTAATTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40874
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112978 Nonsense 316 810 4 7
ENSDART00000125284 Nonsense 334 828 5 8
Genomic Location (Zv9):
Chromosome 7 (position 23119884)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21685069
GRCz11 7 21951407
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCGTAAAGTGGGATGCACATATGGAGAGACCGCAGACCTGGTGGATTG[T/A]CTCCGCAGGAAAAATTTCAGAGAGCTGGTAGATCAGGACATCCAGCCGGC
Long Flanking Sequence:
ACTATCAAAGTCAGTGGCAGCCAGTCTTTATCTTCCTTATACTTAGACTTTTCATTTTGGAGTATCATGCATCAACTTCCCGTATGAGCATGTATGTTATTTCTATTGAACACTAAATAAGTTAGAAGAATGTTGTAAGCTGATAGTCATTGAAATCCATAGTAGGAAAAAATAAAATTAAAGTAAATGGCTGCTCGTCTCCAACTCTAACAGGATTGAAACAAGTGGAGCTTCAGCAAATGATGACAGATTTTCAGTTTTGGGGTTTCATGCATCACCTTCCTGCACAAGCATGGGTATTATGAGTCCAGGCTTTTTTGTATGTAGGTAACAGCTTGTTTTTGCTTCCTCCCCACTACAGGTCTGTTTCAGAGAGCCATCGCTCAGAGTGGATCAGCCATCTCCAGCTGGTCCATTAGCTACCAGCCCTTGAAGTACACTAAGATCCTGGCTCGTAAAGTGGGATGCACATATGGAGAGACCGCAGACCTGGTGGATTG[T/A]CTCCGCAGGAAAAATTTCAGAGAGCTGGTAGATCAGGACATCCAGCCGGCCCGCTACCACATTGCATTTGGGCCGGTGATGGACGGAGACGTGGTGCCAGATGACCCGGAGATTCTGATGCAGCAGGTGATCTTGACTACTAGGTGGTTTCTAGGTCTTAAATTATGCATGTTCTACCAAAGATTTTACATGGTGAACTGACGCTTCCCAAGCCAAGGATTAGGTTGTAAAGTAAGACATTCAATGGACACTTGAAGGTCCTATGGAGAAGAAATATATGGGGGATTCATTAATTAAGTCCACTGGAGTCTGAAATCATTTTTGTAACAGAACAAATTTTGCTAACCCAAGTATTTCAGGTTAAATTGAGCTGTTTTGATTCGCTAGTTAAAGGGATAGTTCACTCAAAAACTAAGATTTTCTCACTATTTATTGACATATCAAGTGATTCCAAACCTTTAGTGTCTTTACTATGTTGAACACTAAAGAAGATTTTTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30629
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112978 Nonsense 328 810 4 7
ENSDART00000125284 Nonsense 346 828 5 8
Genomic Location (Zv9):
Chromosome 7 (position 23119850)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21685035
GRCz11 7 21951373
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACCTGGTGGATTGTCTCCGCAGGAAAAATTTCAGAGAGCTGGTAGAT[C/T]AGGACATCCAGCCGGCCCGCTACCACATTGCATTTGGGCCGGTGATGGAC
Long Flanking Sequence:
CCTTATACTTAGACTTTTCATTTTGGAGTATCATGCATCAACTTCCCGTATGAGCATGTATGTTATTTCTATTGAACACTAAATAAGTTAGAAGAATGTTGTAAGCTGATAGTCATTGAAATCCATAGTAGGAAAAAATAAAATTAAAGTAAATGGCTGCTCGTCTCCAACTCTAACAGGATTGAAACAAGTGGAGCTTCAGCAAATGATGACAGATTTTCAGTTTTGGGGTTTCATGCATCACCTTCCTGCACAAGCATGGGTATTATGAGTCCAGGCTTTTTTGTATGTAGGTAACAGCTTGTTTTTGCTTCCTCCCCACTACAGGTCTGTTTCAGAGAGCCATCGCTCAGAGTGGATCAGCCATCTCCAGCTGGTCCATTAGCTACCAGCCCTTGAAGTACACTAAGATCCTGGCTCGTAAAGTGGGATGCACATATGGAGAGACCGCAGACCTGGTGGATTGTCTCCGCAGGAAAAATTTCAGAGAGCTGGTAGAT[C/T]AGGACATCCAGCCGGCCCGCTACCACATTGCATTTGGGCCGGTGATGGACGGAGACGTGGTGCCAGATGACCCGGAGATTCTGATGCAGCAGGTGATCTTGACTACTAGGTGGTTTCTAGGTCTTAAATTATGCATGTTCTACCAAAGATTTTACATGGTGAACTGACGCTTCCCAAGCCAAGGATTAGGTTGTAAAGTAAGACATTCAATGGACACTTGAAGGTCCTATGGAGAAGAAATATATGGGGGATTCATTAATTAAGTCCACTGGAGTCTGAAATCATTTTTGTAACAGAACAAATTTTGCTAACCCAAGTATTTCAGGTTAAATTGAGCTGTTTTGATTCGCTAGTTAAAGGGATAGTTCACTCAAAAACTAAGATTTTCTCACTATTTATTGACATATCAAGTGATTCCAAACCTTTAGTGTCTTTACTATGTTGAACACTAAAGAAGATTTTTTTAAGAAAGCTGAAAAAGTGTAACCATTGACTTCCAT
Associated Phenotype:
Not determined