ZMP
nrxn1a
Ensembl ID:
ZFIN ID:
Description:
neurexin 1a [Source:RefSeq peptide;Acc:NP_001073490]
Human Orthologue:
NRXN1
Human Description:
neurexin 1 [Source:HGNC Symbol;Acc:8008]
Mouse Orthologue:
Nrxn1
Mouse Description:
neurexin I Gene [Source:MGI Symbol;Acc:MGI:1096391]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15915 | Nonsense | Available for shipment | Available now |
sa35299 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa4466 | Essential Splice Site | F2 line generated | Not yet available |
sa641 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa15915
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 |
---|---|---|---|---|---|
ENSDART00000056256 | None | None | 419 | None | 6 |
ENSDART00000088159 | None | None | 449 | None | 7 |
ENSDART00000088178 | Nonsense | 172 | 1484 | 1 | 23 |
ENSDART00000093094 | Nonsense | 172 | 1491 | 1 | 22 |
ENSDART00000111239 | Nonsense | 172 | 1488 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 25856160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24224836 |
GRCz11 | 12 | 24346055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAACTGCGATCTGTAGCATTACGCCTCACATCTTCAGCCATAAAAGAT[G/T]AGGTTCCCTACAAAGGATGGAYAACCAACCTGAGAGTGAACGGCTCGGAG
Long Flanking Sequence:
TGCGGAACGGTGCACATCTAATCTGGATAGGCCTACTGGTTTGTTGCCTTGTCGACATGGGGGCCAGCATGGAGTTCACTGGTGCAGAAGGCCAGTGGGCAAGGTTTCCCATGTGGAACGCCTGCTGCGAAAGCGAAATGAGTTTCAACATGAAGACCAAAAGCGCTCATGGACTTTTAGTGTACTTTGACGACGAGGGATTCTGTGACTTCTTGGAACTGCTCATCCACAATGGTAGACTCAGTTTGCGGTTCTCCATCTTCTGCGCCGAGCCAGCGACCGTGTTCTCAGACACAGCCGTCAATGACAGCCGCTGGCACGCCGTGACCTTGCGCAGGAATTTCAAAAACACTACTTTAGTTGTGGACGAAGAAATCAAGTGGGTGGAGGTAAAGTCGAAACGGAGGGACATGACGGTCTTCAGCCATTTATTCTTAGGGGGGATACCTCCTGAACTGCGATCTGTAGCATTACGCCTCACATCTTCAGCCATAAAAGAT[G/T]AGGTTCCCTACAAAGGATGGATAACCAACCTGAGAGTGAACGGCTCGGAGCCGGTGCTTATCGGTAGCGATGGAGTCAACAGCGACATTTGCGAAGCCGACCACATTTGCCTGAATGGAGGAGTCTGCAGCATTGTCAACGATGAGCCCATTTGCGACTGCTCTGAAACGGGATTCCAGGGAAAAGACTGCAGTGAAGGTAAGAGGCCTGGATTCGTCGTCTCCGTTGAGGTGTTGAAATGTCTTTTCAAACACAGCCCTTTCACTTCTTTTTTTTTTCAGTTTTCAACATTGCACTAGTTCCTCAGAGGCAGTGCATGCTACATCATGTCTTTTCCCGGCCTCCACATACAGGCCCAATACATTACATGATTAGATTACAGTCAGAGAGTGCCTATTTCAGAGCATCCACAAACACCCTGTGTTTTTGCTAACAATGACGTCAGAGAAGCCAAATTAACTTAATATACTCTTGACACTGCACTGGCATTACAATTAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35299
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 |
---|---|---|---|---|---|
ENSDART00000056256 | None | None | 419 | None | 6 |
ENSDART00000088159 | None | None | 449 | None | 7 |
ENSDART00000088178 | Nonsense | 425 | 1484 | 7 | 23 |
ENSDART00000093094 | Nonsense | 425 | 1491 | 7 | 22 |
ENSDART00000111239 | Nonsense | 422 | 1488 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 25956139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24328601 |
GRCz11 | 12 | 24449820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGCCGATCTTCCTGGATCACCTGTCAGCAACAACTTTATGGGCTGCT[T/A]GAAAGAGGTAAGAGATTTGAACAATTGCTCCTCGGAAAAAATCAAATCGT
Long Flanking Sequence:
TGTGTCTGCTGATTCACTTTTGTGTGCTCGATTTAAGTGGCACCGCTAACTTTGAGCCTGGGCTAATGTGCCGCAGACTTCCTCAGATGACTTTACTAGAAGTTAAACACATCAATCTAGAAAGTTAAACCAGTAACAAGTAAGATTTTCTGAAACAGACATGAAAATGGGTTCACATTTGAAATCAATAAAAAGAGAAAAGCAAATAAATAAATAAGAACAAAAGGAAAAAGAAATCTAAACAAATCCAAGCATTCAAATCCTTACGAGGGGGACCAAAGCCCTGTAACAGTATTGAAGTTATATGTGAGTATAGCGTGTCCTTTCCCTGTGCTTTGTTGTCTAGGTTACAATATCCGTGGATGGGATTCTGACCACCACTGGATATACGCAAGAGGACTACACCATGCTAGGCTCGGATGACTTTTTCTATGTCGGCGGTAGTCCCAGCACTGCCGATCTTCCTGGATCACCTGTCAGCAACAACTTTATGGGCTGCT[T/A]GAAAGAGGTAAGAGATTTGAACAATTGCTCCTCGGAAAAAATCAAATCGTTCCATCCAGAATTATGCCTGTAATTTAATCGCTGTCTGGTTACGCTGTGTTCTGTGTATTCGTTGACTTTTGGGATGATGGAAAGATATGACCTTGCAGTTAATCCTCTGAATGTATTCACTATGATTTCAGGTATATCTAACAAGTTTATTTTTGTATAAATAAATATTTACGGCATATTAATGGCTGCCCAAGTGTATTTAGTGACATTTTTATTTACTATTATTATCATTCTTTTAAACTTTCTTCTATCTGCCAAAATATAACCAAACATCCAAGATCGATTAAGTAGTGGAACATCTTCTTTTATTTACCCATTTCATCTCACATGCTTTGCATACCTAGAGAGATGTACCTTTTTGGGGCTTAAAAAAAATAGTCTGCATGGCTAGGTTTCTAAATATCCTAAAATGTCTGGGATTTTGCTTTGCTTTCACTTTCTAAAGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4466
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056256 | None | None | 419 | None | 6 |
ENSDART00000088159 | None | None | 449 | None | 7 |
ENSDART00000088178 | Essential Splice Site | 771 | 1484 | 10 | 23 |
ENSDART00000093094 | Essential Splice Site | 771 | 1491 | 10 | 22 |
ENSDART00000111239 | Essential Splice Site | 768 | 1488 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 26015096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24387537 |
GRCz11 | 12 | 24508756 |
KASP Assay ID:
554-3590.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGAGGCTGGAGCTGGACGGAGGGCGGGTCCGACTCACTGTCAATCTAG[G/A]TACATCTGCCAATAAGAGCGCTCGTATTGATGGTTNNNACCACCACACAGTAG
Long Flanking Sequence:
ATAACAAGCAAAAATACATGTCACAGTTTCTTCATAAACACAGCCTCCCCATAAAAAGAAACATGTTGCATAATAAACATTTTTATGTTATTAATTTGAGCAGTTCTGTTGCTACTGTTGTGCAGTGCTGTAGAAGATTTCAGTGTCTTTCAGTGGTTTTAAAGCATTTTAGTAAACAGTCTTTCATCTGTTGATTTCAACACTGGAGTTTATGATCACAGTCACTGGCCACAATTCTCCTCCTTTAATGTTTGCTAAATTCTTTTTGGTCTCCTTCCTTTCTTGCTGTCTCTCAGATGCCACGATCCTCAGTTACGATGGTAGTAAGTTCATGAAGATCCAGCTGCCGGTGGTGATGCACACAGAAGCGGAGGACGTGTCCCTGCGCTTTCGTTCTCAACGGGCCTACGGTGTTCTAATGGCGACCACATCGCAAAACTCTGCTGATACTCTGAGGCTGGAGCTGGACGGAGGGCGGGTCCGACTCACTGTCAATCTAG[G/A]TACATCTGCCAATAAGAGCGCTCGTATTGATGGTTACCACCACACAGTAGACGTGAAGCATAACATGTTAACACAGCATGGAATTTTTTGTTTTTAATTATTATTATATTTTTTCTCAAATGTGATTTTATATCTATTGTATGGTAATGAATTTTACAATGTAAGATTAGTTTTTGCCAATTTCTGACAAATATTTAGTTGACTACGGGAATATAGACATGTATATAATAAATACTTGACTTTCTATTGTTTTTACATACAGCTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTTTACATACAATTTTATGTAAATATAAGTTATATATTATTAGAAGTAGTCTGCTAATTTGTTCTACGCTGTAAAAATATACTGACAATAAGTAAAGATCAGGTTTCAACTAAATATTATAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa641
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056256 | None | None | 419 | None | 6 |
ENSDART00000088159 | None | None | 449 | None | 7 |
ENSDART00000088178 | Nonsense | 1022 | 1484 | 15 | 23 |
ENSDART00000093094 | Nonsense | 1022 | 1491 | 15 | 22 |
ENSDART00000111239 | Nonsense | 1019 | 1488 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 12 (position 26044040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24416481 |
GRCz11 | 12 | 24537700 |
KASP Assay ID:
554-0550.1 (used for ordering genotyping assays)
KASP Sequence:
GCATGAATTTTGCTGCCTTTACAGGTGATCTGTATGTTGGAGGTGTGGCT[A/T]AAGATATGTATAAGGACTTGCCAAAGCTGGTGCATTCAAAAGAGGGCTTC
Long Flanking Sequence:
TTAAAAAGTCCTCTTATGCCTACCAAGGCTGAATTTAATTAATACATGGTTTAAATAAGTAAAAAAGTAATTAATTTAAAGGTATTTAAAAATGTAATTTATTACTACTGTAGTGTTTGGAAGTTATTATGTGTTTTGTTTTTCAAATGATATTATTTTTCAAAAGAAATACACATATCATTGCTTGATTAATACGATCAGAAGAAAAATTGTAAGATGATTATTTTTTTTACTGCCAATTTAATGTATATTTGATCAATAAAATAATACCAATTTAAAAAAAATAATAGCTATCCTGAACAAAAACTTGAATTTGTGCAAGATGTTGTGCATGATGTTGTAAACTGTAATAAACAAACGCACCACCAGGGGTCAGTGGTGCACCTTTCTTCCTGTATTTACATAACATGCCCCCTTGGTGGTTAAATTGAAAAGGCACTGTCAGTCAGAGCATGAATTTTGCTGCCTTTACAGGTGATCTGTATGTTGGAGGTGTGGCT[A/T]AAGATATGTATAAGGACTTGCCAAAGCTGGTGCATTCAAAAGAGGGCTTCCAGGGCTGCCTGGCATCTGTGGACCTGAACGGCCGCTTGCCAGACCTGCAGTCAGACGCACTGTCCACCGCCGGCCAGGTGGAGAGAGGCTGCGAAGGTGAGGAAAACGGTATGAATGGCGCATATATACACCGGGTCGGCTTAGCGCGGTCCTTCAGTCTCCAAAGCCCCGTCTCATCTCATGCACACCTGCTCATCCTTTCTGCTTCCTGTTCTCTTCACTATCTGTTTTGTGTTTTCTTCATGCTGGGCCAATTTTAAGCAGTTTTCAGGCTTCTGTCAAGTGTTCTTTTGCCTCTGCTGGAAATAAATATTAGGGATGAATGGGGGTCAAAAAATCTTACGTTTTTTTAAAGATGTAACTTTGAGGAAGCTGAAAATATGAGAGAAAGGAGATTTGTTACTGCCAGTTTGTTAATGCAGTGTAGTGTTTAGTGATTATATTAATTA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |