ZMP
nlgn2a
Ensembl ID:
ZFIN IDs:
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.
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.
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 |
---|---|---|---|---|---|
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.
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.
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.
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