ZMP
nrxn2a
Ensembl ID:
ZFIN ID:
Description:
neurexin 2a [Source:RefSeq peptide;Acc:NP_001073439]
Human Orthologue:
NRXN2
Human Description:
neurexin 2 [Source:HGNC Symbol;Acc:8009]
Mouse Orthologue:
Nrxn2
Mouse Description:
neurexin II Gene [Source:MGI Symbol;Acc:MGI:1096362]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32351 | Nonsense | Available for shipment | Available now |
sa45740 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16817 | Essential Splice Site | Available for shipment | Available now |
sa18390 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32351
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087657 | Nonsense | 455 | 1670 | 9 | 24 |
ENSDART00000087660 | None | None | 642 | None | 7 |
ENSDART00000132583 | None | None | 648 | None | 7 |
ENSDART00000141629 | Nonsense | 455 | 1670 | 10 | 24 |
The following transcripts of ENSDARG00000061454 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 27473300)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 28042211 |
GRCz11 | 21 | 28078906 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCTCTCCCTGTCCCAGGTGGTCTACACCAATAATGAGTTCAGACTA[G/T]AGCTCTCCCATCTGGCGGAATTGCGTGACCCTAAGGTTACCCTCCATGGC
Long Flanking Sequence:
CACATGTGACAGAAACAAAAAACCAACCTTAAGGGGACACAGTCAGCATGCAGGAATGTTATTTTAGGAGCAGTTTTGTCATACGGTGGCACGTGTGGGCTAGACATCATATCATACATTGAGATTTTTCAGTTGACGTCACTTAATGAATGCGCTGTTTATGCGCGCGATTCAGAAAAGCACTTAGCCGCGGCATCGTCAGAGCTAATGTTAGCGTAGGATGATTCATCATATTAATGAAACAGAATATCGATTAGCCGAGGGTTGCTGTAGTGCTCTGGATGATGTCTCTCGGTTTATGTGATCCACTCATGCTTTTGAGTATTTAAAGAGACTGCCGTGTTTACTGACTTGAAAACCGTGCCCTCTAGGTACACACATCAGCTGGGGTTTGTTTGTACCAGTGGGCAGCATACTACTCCATTCCCTCCTGTTAGCATTTAAGCTTTTTTTCTCTCTCCCTGTCCCAGGTGGTCTACACCAATAATGAGTTCAGACTA[G/T]AGCTCTCCCATCTGGCGGAATTGCGTGACCCTAAGGTTACCCTCCATGGCGATTTGACCTTCCGCTGCGAGGACGTCGCTGCATTGGACCCAGTCAGTTTCGACGCGCCCACTGCTTATGTAACCCTCCCGCGCTGGAATGGCAAGAAAGCTGGCTCTGTGTCCTTCGATTTTCGAACCACCGAGCCCAACGGACTGCTGTTGTTCAGTCACGGGCGGCCGCAGGGTTCAAAAGATCACAGACCAAGGGTGGACTTCTTCGCCATGGAACTGCTGGATGGATTCCTCCACCTGCTCATGGACATGGGCTCCGGGAGCATCAAGATTAAAGTGGGGAACAAGAAGGTCAATGATGGAGAATGGTGCCACGTAGACTTCCAGAGAGAGGGCAGGAAAGGTCAGGATATTGCAAGATCAGCACACACATTATTGCTAAACCTGCTCTCGCTTTGATTCCTACTCTGACGCTTTCCTCTTAATCTCTGCCGTTAAAGCACTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45740
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087657 | Essential Splice Site | 783 | 1670 | 11 | 24 |
ENSDART00000087660 | None | None | 642 | None | 7 |
ENSDART00000132583 | None | None | 648 | None | 7 |
ENSDART00000141629 | Essential Splice Site | 783 | 1670 | 12 | 24 |
The following transcripts of ENSDARG00000061454 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 27469106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 28038017 |
GRCz11 | 21 | 28074712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCGCCTGGAGCTGGACGGGGGAAGAGTCAAGCTTACCGTCAACCTCGG[T/C]AAAACCACCAGACTCGAGGCTCTTCCCAAAACACATTTCACTCTCATTCC
Long Flanking Sequence:
GATATACTGTAGCTGTTATTACTGTTACTGTGACCATGTAACTTAAAATGAAATGTCTTAATAGCAGTAGCAATTAGTTACATTTTATTTGGATTCAAATACAATGCAAATCCCTGAGTTTATTAAAGAGTAATTAAAACTGAATAAAAATATTGATAATGTTTACATTTACTTTGCTTTTTAACATTATATAAACATAAAAAAATACTGTTTGAAAAATGCATACAAAAATATATCTTTTAATTTTGCATCCTAGTGTTTGCTGACCTGTAGTGTCTTGTTCTGCCTCTTTCAGAGTCTGCAGTGTTGAGTTACGACGGCAGCATGTTTCTGAAAGTCCTGATGCCTCACGCAGCTCACAGCGAGGCCGAGGACGTGTCTCTGCGCTTCATGTCTCAGAGGGCTTATGGTCTGCTCATGGCCACCACCTCCAAAGAGTCCGCCGATACCCTGCGCCTGGAGCTGGACGGGGGAAGAGTCAAGCTTACCGTCAACCTCGG[T/C]AAAACCACCAGACTCGAGGCTCTTCCCAAAACACATTTCACTCTCATTCCTCCATCTTTATCTCTTTCTGCTCTTCTTCTTCTTCTCTCTCTCTCTCTCTCTCTTTCTTTCTCGCTCTGTCTTTCTCTCTCCACCTGTGCAGCCTTCAATGGCTTTCACTTCTGCAGCTTTCAGAGCAGACAGCCAGAGAGACCAGATCATTTAGTGTCAAACACATTGAGTTAAACTAGGGGAGACTGAGGGGAAATTATATTGTTTTACCTTTTGAATTTTTCTATAACTTTATAATGTTTAAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAATATAAATCTCTGTATTTTAAAAGGTCAACTTCAAAGTAAGAATATGATATGAATCCTGCACAGTATTCTTAGTTTTTATTATTATTAAATTGCTTACATAATGAGGCTGAGTAGTTTTGTCTTTAGGAATAATATGCAAGCAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16817
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087657 | Essential Splice Site | 962 | 1670 | 15 | 24 |
ENSDART00000087660 | None | None | 642 | None | 7 |
ENSDART00000132583 | None | None | 648 | None | 7 |
ENSDART00000141629 | Essential Splice Site | 962 | 1670 | 15 | 24 |
The following transcripts of ENSDARG00000061454 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 27445497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 28014408 |
GRCz11 | 21 | 28051103 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACTCTGGGGATGGCAGTGACTTTATCGTGATYGAGCTTGTAAAAGGG[T/A]AAGTGTGAGTTTTAATTGAACAATTTTAACAAATAATACAGGGTTTCTGT
Long Flanking Sequence:
CTCTGAACTGAACATCAAAAGCTGTACTTGCCTTGGGATGGGCTCAGGCAGCACGCCATTCCCTCATATCATCTGCTCCCAGACCTGACTAATCGAGCGTGTTTGGTTCTGCCACAGGCCAGATGAGCGGAGCACACACGCAGCTGGAGTTCCACCACATAGAGACGGGCATCATGACTGAGCGCCGCTTTATCTCAGTCATGCCATCCAACTTCATCGGCCACCTGCAGGGCCTCTCTTTCAACGGCATGCCTTACCTAGACCAGTGCAAGAATGGTGACATCTCCTACTGTGAGCTCAACGCCCGCTTCGGCATGCGCCGCATAGTGGCCGATCCGGTCAGCTTCCGAAATCGAGCCAGTTATGTGGCGCTGTCCACCTTACAAGCCTACGCCTCCATGCACCTCTTCTTCCAGTTCAAAACAACCAGCCCTGATGGTCTGATTCTCTTCAACTCTGGGGATGGCAGTGACTTTATCGTGATTGAGCTTGTAAAAGGG[T/A]AAGTGTGAGTTTTAATTGAACAATTTTAACAAATAATACAGGGTTTCTGTGCTTCTTCAAAAAGTGAAGTTCATTTATAATTTTTTTAGAGGAGCACCTGCTTATGATTGACCACAGCTGGTCCAGCATTAGCTATTAAATGATTTACCAATCAGATGAATCCAAACGTACATAAATAACCAGATTTTCTTACCTTAGTCATCTTCATCTAGAAGAATCCCCCCCATCCACAGTTCCTCCTGCCCCTCTTACCGAGAATAATCCAGAATAGGCTAGCACATCAGCTAAGTGGTTAGCACTGTTACCTCACAGCAAGGTTTGAGTCCCGACTGGGCTGGGTGTTTCTGTGGGAAGTTTACATGTTCTCCTCATACTCACATGGGTTTCCCTCAGGTACTCAGTATAAGGGATTTAAATAAACCAAATTGGCACAGTATATTGGTGTTTTAGTACTCAGCATTCACCGCATAAACATATGCTGGTTTAGTTGGTGGTTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18390
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087657 | Nonsense | 1080 | 1670 | 17 | 24 |
ENSDART00000087660 | None | None | 642 | None | 7 |
ENSDART00000132583 | None | None | 648 | None | 7 |
ENSDART00000141629 | Nonsense | 1080 | 1670 | 17 | 24 |
The following transcripts of ENSDARG00000061454 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 27407096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 27976007 |
GRCz11 | 21 | 28012702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACTTTCAGACCTGATTGCAGATGCTCTGCACCGTGTKGGCCAAGTGGAG[C/T]GAGGATGTGAGGGTCAGTATACTGATGCTCTGAGGCAATCATGACAACAT
Long Flanking Sequence:
AGAATAGTATCCCAAAATATATTTATTGCATCATATTGAGAGATGCACAGACACTTTTTCTCTCATATTAGTTTTTCCACTGGCATTCACTCTAAAATGGCATATTAAATTTAGCAACAGAAGCCTGGAATACAGTAATGACATAAGAAATTACAAATGTTTTGAAATAAAACATGATGTGAACTTTTTATGATTTACTTATGACTTATTTTCGTGTTTTCATTTATTGACTCCAGACTGTTAAGTTATATATGAAATATGGCTTAACTTTTTTCAATTGATTTAGCTGGCTATTATTAACCATTCCTTACTGTATCTTTATTTTCTTCTGCTCTATAGGAGAGCTGTACATTGGAGGTGTGGGGAAGAGCATGTACAACAGTCTGCCAAAGCTCATTGCATCGCGGGATGGTTATCAGGGCTGCCTGGCCTCAGTTGACCTGAATGGCAGACTTTCAGACCTGATTGCAGATGCTCTGCACCGTGTGGGCCAAGTGGAG[C/T]GAGGATGTGAGGGTCAGTATACTGATGCTCTGAGGCAATCATGACAACATATGAGCCTTAAATCAAATTATATTTCTGGCATGCTCAATTAAAGACTATGCAGTACACAAGATGAACATTATTGTCTAGCAAAATGCTACCAATTTCATTGTTAGTACTTGAAATGCCCAATTTAATCGCATCAGCTTTGAGAGTGCTAAACCTAAAAAATATGTTTGCTGTTTGTTCAAACTGATTATTTAAACTGAGCTGAAACAACACAATTCTTGAGATGTTTTGGAGACAACTTACTTGTTTTATGTTCAATCAACTTAAAGTAAAAATAAAAAAAATAAGTTAACCCAGCAATTTTTACAGTGTAAGCTGTAAAACAAAATGCTGAGTTCCACACAATTCATTCAGGTTGTCCCAACATAAATCAATTAAGTTAACTTAATCTCAAGAATTAGGCTCAGGATGTATAAACTCAAGAATTGTGTTTTTACAAAGGTAACACAGTC
Associated Phenotype:
Not determined