ZMP

nlgn2b

Ensembl ID:

ENSDARG00000079251

ZFIN ID:

ZDB-GENE-090918-3

Description:

neuroligin 2a [Source:RefSeq peptide;Acc:NP_001159808]

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6171	Nonsense	Mutation detected in F1 DNA	Not yet available
sa9514	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa6171

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
ENSDART00000112484	Nonsense	132	860	1	8

Genomic Location (Zv9):

Chromosome 10 (position 22582631)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	22412969
GRCz11	10	22382421

KASP Assay ID:

554-5405.1 (used for ordering genotyping assays)

KASP Sequence:

TGCCCSCAGAACATCCATGGGGTGCTGCCAGAGATCATGCTTCCCGTATG[G/A]TTCACYGACAACCTGGATGCAGCCGCTGCTTAYGTACAGAACCAGAGCGA

Long Flanking Sequence:

CCTTTCCGCATATCCCGGAGTCAGTGGGGTGGCCAGAAAGTATTTGCTCTTGTCCATTTCATAACCGTTCCCCATCACTGGGGCAGCGTTCACCCCAGCCGAAGCATGTCATCGGTGGACGTGGCCCGATCACGGCGGGAGACGGTTCGCTCCTGTCCACGACGCATATCTGACACTTGCCTGGTGTGGCTGCTGGGCTTGGCGCTGCGCCTTGCGCTATCCTCCTGCCAACGGGCAGACCTCACCGCCGCCAAGCACCCTATGGTCACCACAGGCTACGGGAAGCTTCGGGGAGTACGCAAGGAGCTGAACAATGAGATTCTAGGCCCGGTCGAGCAGTACTTGGGTGTCCCCTACGCCACCCCGCCAGTGGGCGAGAGACGCTTCCAACCCCCGGAGGCACCCGGCTCCTGGCAGGAGATCCGTAACGCTACTCAGTTTGCACCCGTTTGCCCGCAGAACATCCATGGGGTGCTGCCAGAGATCATGCTTCCCGTATG[G/A]TTCACTGACAACCTGGATGCAGCCGCTGCTTACGTACAGAACCAGAGCGAGGACTGCCTTTACCTCAATGTCTATGTTCCCACAGAGGATGGTAAGTTTATGAAGCATATTAAATAAGTGGTACATTTATGTTTCATTCCTATTCTCATTCAGCTTATATAAATTTTCACCAATACAAATAGCATTCCCATCATTCCCACTCTAGTTTTGGGAAGCGAATCACCTACTGTATATTCATTTTGTGGCATTCAATCTTTTTTATGGGATTTACTGCAGCAATGTGTGGTATAACATGTTTCTACAACATAAAAGAAAGAATCCATATCTTAGAATAAGACACTTTCTCTATGTGACCTGCGGACAGCCTTGGGATCCTTTTCAATTTGATCTTCTTAAAAAGAAGCTTATCTGTAGCATGGGATCACATCCAGAGTTTAAGTTAGATTGCTTGCATTTAGTGGATACAAAGAGGTAGTTGCCAGCCTAGTTCTGAGAATCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9514

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112484	Nonsense	351	860	5	8

Genomic Location (Zv9):

Chromosome 10 (position 22675977)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	22506315
GRCz11	10	22475767

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGATCTGGTTGACTGTCTRCGAAGGAARAGCTACAGGGAGCTGGTGGAT[C/T]AGGATGTCCAACCTGCCCGATACCACATWGCRTTTGGACCAGTGGTGGAT

Long Flanking Sequence:

ATCTGTGTTTACAGTGTGAATCTGAAACCTATTTCCAAAGGTAAAACAATTAGATCCTAAAGTGGGAGCCAAGTTTTTGCACATTTTTTTTTTTTTTCAGTTGGAGGCATTTAGGTTTCGCTTGACTGAAACTGACTATTTAAAGTCAATGTAAAAACATTTAAAATTTCACTGACCTAGCCTTTTGGTAAAAAAAAAAGAGATCCGGTGTCTTTATTTTGCTCATGGTCATGTGTCACACACTCTCTCTCCACATTGACTCACTCACATTACAGCCAGCTCCCTGACATCTCTTACTCATTGTCTTGTAACTGATCCCGGTTTTAGGTTTGTTCCAGAGGGCCATTGCGCAGAGCGGCTCTGCCATATCCAGTTGGTCAGTGAACTACCGGCCCCTGATGTACACCAAGATCCTGGCCAAGAAGGTGGGCTGCAGTTACAGTGACACTGCAGATCTGGTTGACTGTCTGCGAAGGAAAAGCTACAGGGAGCTGGTGGAT[C/T]AGGATGTCCAACCTGCCCGATACCACATTGCGTTTGGACCAGTGGTGGATGGAGATGTGGTCCCTGATGACCCCGAGATCCTCATGCAGCAGGTGTGATGTTGAACACTGCGGGGTCCATGAGATTAGAGTTCTGCCAGAGTCTAACCATGACAGTTCCTTAGCGAAAGTGTGTACTGTGGGTGACATTTCTGTGATGTCCTCAGGGGGAGTTCCTGAACTACGACATCCTGTTGGGGGTGAACCAAGGTGAAGGGCTGAAATTTGTGGATGACAATGAGGGCGAGGAAGGAATTTCAGCTGCTTCCTTTGACTACACCATTTCCAACTTTGTAGACAACCTATATGGATACCCAGAGGGTAAGCTTCAATGATGCATGCTTACACACATATACAATATATTATCAAGTATTAGGAGTCTGATTTGCCATTGCCAACAATGAATTTACAGCCACCAATGAGCAATGCTGTTCATTTACTTGTTTGGATGTGCAATTGAAT

Associated Phenotype:

Not determined