ZMP
npas2
Ensembl ID:
ZFIN ID:
Description:
neuronal PAS domain protein 2 [Source:RefSeq peptide;Acc:NP_840084]
Human Orthologue:
NPAS2
Human Description:
neuronal PAS domain protein 2 [Source:HGNC Symbol;Acc:7895]
Mouse Orthologue:
Npas2
Mouse Description:
neuronal PAS domain protein 2 Gene [Source:MGI Symbol;Acc:MGI:109232]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38465 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa26455 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33580 | Nonsense | Available for shipment | Available now |
sa20391 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38465
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014806 | Essential Splice Site | 197 | 845 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 24584412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22297284 |
GRCz11 | 5 | 22801084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACACATGCTTCTGACTGAGTCTTCTACTGTAGACCTGCTCAACAGCA[G/A]TGAGTAAACTGCGCATAAACACACACACATGCACAAACACACAGACACAC
Long Flanking Sequence:
TTTAAAAGACTTCTTTAATAATTACAAATTATAACATTAATAATAATAATAATAATAAAAATAATACTTAAAACTACTGATAATAGTAATAATATTAACCATTATGATGACATCTACAATATTAAAAAATTTATAATATATATTATATAATATAATATTATTTATAATATAATAATAACTATAATAATAATAAATAATAATTCATAATAATAATTATAATATTAAAATTTATCTACTAAGCAATTGTTATTTCATTTTTGTGATTGTGGTTATATATATATATATACTGTAAGTGCTATGTATTGTGGGAAATGTATTGCACAGTGTAGTCCTTCTGAAAGAGAGTAACTTTGTCATATACATTGCTGTGTCTTAGTCAGATATGGTGGACCAGAACATCCTGAACTTCCTGCCAGAGCGAGAGCACGCAGATGTGTATAAACTCCTGTCTTCACACATGCTTCTGACTGAGTCTTCTACTGTAGACCTGCTCAACAGCA[G/A]TGAGTAAACTGCGCATAAACACACACACATGCACAAACACACAGACACACACACACACACACACTAAAAAAGAATATGTCGTTGTATTTGTCGGCTGTGTTGTGCTCCATGATTACACTCCAGGCTAATTATAGAGGCTCCGTGTGTGCAGTGTAACACAGATTATCTGTTACCACACTCTAATAATCCCACATACAGCTCTTACCCTGACCTCAATCCCTGAAACACACACACACACTAATACTGGGATATACTGGTTGAAAAAAAATGGACAGAGCTGACTTATTGATCTCAGTCAATCACAACAAGCACCTACTTCACTGGTCAAACACAACCACATGCAAACACACAAACACAATATGTACACATAAGGACACACTTTCTGCTGCATGGCTCACTACTGCACTTCAGAATCATGAAAGTCACACTGAGGCCACAGCCATAGCAGACCATTAAAGCTGTAGTGTGTAAACTTTTTGGTATAAAATTATTCAAAACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26455
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014806 | Essential Splice Site | 198 | 845 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 24584413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22297285 |
GRCz11 | 5 | 22801085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACACATGCTTCTGACTGAGTCTTCTACTGTAGACCTGCTCAACAGCAG[T/A]GAGTAAACTGCGCATAAACACACACACATGCACAAACACACAGACACACA
Long Flanking Sequence:
TTAAAAGACTTCTTTAATAATTACAAATTATAACATTAATAATAATAATAATAATAAAAATAATACTTAAAACTACTGATAATAGTAATAATATTAACCATTATGATGACATCTACAATATTAAAAAATTTATAATATATATTATATAATATAATATTATTTATAATATAATAATAACTATAATAATAATAAATAATAATTCATAATAATAATTATAATATTAAAATTTATCTACTAAGCAATTGTTATTTCATTTTTGTGATTGTGGTTATATATATATATATACTGTAAGTGCTATGTATTGTGGGAAATGTATTGCACAGTGTAGTCCTTCTGAAAGAGAGTAACTTTGTCATATACATTGCTGTGTCTTAGTCAGATATGGTGGACCAGAACATCCTGAACTTCCTGCCAGAGCGAGAGCACGCAGATGTGTATAAACTCCTGTCTTCACACATGCTTCTGACTGAGTCTTCTACTGTAGACCTGCTCAACAGCAG[T/A]GAGTAAACTGCGCATAAACACACACACATGCACAAACACACAGACACACACACACACACACACTAAAAAAGAATATGTCGTTGTATTTGTCGGCTGTGTTGTGCTCCATGATTACACTCCAGGCTAATTATAGAGGCTCCGTGTGTGCAGTGTAACACAGATTATCTGTTACCACACTCTAATAATCCCACATACAGCTCTTACCCTGACCTCAATCCCTGAAACACACACACACACTAATACTGGGATATACTGGTTGAAAAAAAATGGACAGAGCTGACTTATTGATCTCAGTCAATCACAACAAGCACCTACTTCACTGGTCAAACACAACCACATGCAAACACACAAACACAATATGTACACATAAGGACACACTTTCTGCTGCATGGCTCACTACTGCACTTCAGAATCATGAAAGTCACACTGAGGCCACAGCCATAGCAGACCATTAAAGCTGTAGTGTGTAAACTTTTTGGTATAAAATTATTCAAAACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33580
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 |
---|---|---|---|---|---|
ENSDART00000014806 | Nonsense | 241 | 845 | 8 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 24589131)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22302003 |
GRCz11 | 5 | 22805803 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACAGAATGTGTTGTTTTTGTGTGTGTTCCAGTGCCTCTGTCTTCATG[T/A]AATGGTTATGATCTGGCGTTTCCTCGCACGCTGCAGTCCTCAATAGAGGA
Long Flanking Sequence:
CACAAGAATATTGTTTAGTTGCAGCTGTTTTGCTGACAATGATTTAATAACCAAGACGAATTAAAGCACAATTAATAGTGAAATCATTAATCGTTGCATCCTATGTCCAACAGGGAAAACCGCCAACGATAAAGAATGCATGATCATATGGTGTCATGGCTTTAGTTTGCAAACAAAGTAATTATAATTGAAGTCAATTGGGCAAAAACAGGCATGAACATAACAAATGGTGGTAAATTTGCCCATAGCTTATTGTTGAGTTTCAAGTTCCAAAGCATTTTCCCAAAAATTGTGTCCAAATACAATTTGTCACCAAAAAATAATTTCATTTGCTGAAATACAGAGTAAGATGTGGCTAAATTAAGACTTAAAATCACCCCAAGTGGATGAAAACATCCCCAACATCACCCAAGGGTTAATATTTATCTGTCCACTGTGGGTGTTTTCCTTTAAACAGAATGTGTTGTTTTTGTGTGTGTTCCAGTGCCTCTGTCTTCATG[T/A]AATGGTTATGATCTGGCGTTTCCTCGCACGCTGCAGTCCTCAATAGAGGAGCAGGTCTGCCTCGTGGCCACAGTCAGACTCGCAACCCCTCAGTTCCTCAAGGTATACACACTCATTCACATACACACAAAATCAATATCACACACACTGCTCACTTTCACCATAACTTCAAAGAACACGCAGCCTTATTCTGTGTATGTGCATGTGTTTATTAAAGGATCTTTGCAACGTGGAGGATGTGTGTGATGAATTCACATCAAGACACAGTCTGGAATGGAAATTTCTCTTCTTAGATCACAGGTGAGTCAAATGCTGCTCCATTATGCAAACGACTCCTCTGCTGTTATGATTCTGCACGAAGCTCCTTTGGTTCATTCGATCAGAGGCTCTTCCTGATTATGTCATGCTTTTGATTCATTCATCAGCCGCTGACCCACTTACATTTGCACATTCAGGCTTTCCGCTGTCCCACGCATGGCTAGGGGTGTCATCAGTTCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20391
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014806 | Nonsense | 349 | 845 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 5 (position 24597503)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22310375 |
GRCz11 | 5 | 22814175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTTTGTGTGTATTGCAGTGATGCAGTGTGGGAAAGGAAAGTCTTGTTA[C/A]TATCGGTTCCTGACTAAAGGACAGCAGTGGATCTGGCTGCAGACGCACTA
Long Flanking Sequence:
TTTCTCAGCCCCTCTACTCTCAAAATTGTTCCATAACAATCTGCAGATTTTTTTTACAAATCAGAAATTCCACAGTTGCCCTACCGTTTTGTGCATGTTTTTAATGGGTACAGAGAGTATGTAATAACTGTGTGTGTGTGTGTGTTTACAGGGCCTCTCCTATCATCGGGTACCTGCCGTTTGAGGTTTTGGGGACCTCGGGTTATGATTACTACCATGTGGACGACCTGGAGCTGATTGCTCAATGTCATAAACAATGTGAGTGTTATCTCTGCTGCTCTCGCTCTCTCTTCGTTCTCAAACTAGGTCAATGTACTGTCTTGGAAATTTTCTCCTGTTTGTGCGAATCACAGAGGAGCTGAAAATGGCCCCGCCAGGAAAGATGAAAGACCTTGTAAGAAGCTCTCAAGCCTTTTGTAGAGAGTGCTGATCTTGTGTGTTTGTGTGCATGCGTTTGTGTGTATTGCAGTGATGCAGTGTGGGAAAGGAAAGTCTTGTTA[C/A]TATCGGTTCCTGACTAAAGGACAGCAGTGGATCTGGCTGCAGACGCACTATTACATCACGTACCACCAGTGGAACTCCAAACCTGAGTTCATCGTCTGCACACACAGCGTGGTCAGGTAAAACAAACACTAGCGGCATTTATATGTGTGTATGGAAAGTGTGGGCATGGCAAGCACACTGGAAAGTACTTGAACTTATTTATAAGCATATAAACAAAAACGCTTTGCTTCGCACAGTAATTTGAATTAGAGTTAATTTCATCTTTGCTTTAATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGAAGAGATCAGATGCAAAGCCCTCTAAATCCATCAGACCTCTTTTCTTGTGAATAAGCATTTTCTATCAGGCTCATATAATAAGGTTCAGATGTTTCATTTCATAGATAATGAAAAGGTTATT
Associated Phenotype:
Not determined