ZMP
si:dkey-14o18.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate neuronal pentraxin I (NPTX1) [Source:UniProtKB/TrEMBL;Acc:Q1LUT9
Human Orthologue:
NPTX1
Human Description:
neuronal pentraxin I [Source:HGNC Symbol;Acc:7952]
Mouse Orthologue:
Nptx1
Mouse Description:
neuronal pentraxin 1 Gene [Source:MGI Symbol;Acc:MGI:107811]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45661 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11823 | Nonsense | Available for shipment | Available now |
sa23450 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5918
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 |
---|---|---|---|---|---|
ENSDART00000091661 | Nonsense | 334 | 722 | 2 | 5 |
ENSDART00000139727 | Nonsense | 155 | 416 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 10364123)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9822662 |
GRCz11 | 19 | 9741587 |
KASP Assay ID:
554-3835.1 (used for ordering genotyping assays)
KASP Sequence:
CGAGTTCATTGCGAGACCTCCTGCAACGCAAAATCAACACACTGGAAGAA[C/T]AGCTTCATCATCATTACGACAGTCACTACGGTCACTATGATCACCACGAC
Long Flanking Sequence:
AACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCTATTTATTTATTTTATTCTATTTTTATTTATTTTTCATTAAATTTTTTACCTATAAGTAAATGAATTTTTTTTTAAAAGTTAATTACTTATTTAATTTTTTATTTTTATTTACTTTTTTATTTTTTATTTGTTATTTTATTTTATTTTATTTTATTTTATTTTATATTTTATTTTATTATTATTTAATTTATTTATATTATTTTATGTTATTTTATTATTTTATTTTATTTACTTATAATTATTTATTTTTATTTACTTATTTTTAAGTTTTTTATTTACTTATTTATTTAATATCTTTTTATTTATTTGCTTTTTTTTTTATGCTAAACTAAACAAACCATACTATTTGTTTACTGTCTTTGTTTTTTGTAGGCTAGAAATTCCTCCAGTTCCTATTCGAGTTCATTGCGAGACCTCCTGCAACGCAAAATCAACACACTGGAAGAA[C/T]AGCTTCATCATCATTACGACAGTCACTACGGTCACTATGATCACCACGACCACGATTACCACCATACTGACCACCCCAGTAACCACCATGATGACAATCACGATAACCACGACAATCATCACGACGACCATCACTCCAACCGCCATCGTAACCACCATTACAGTTATCACTATGACCATCACGGCGACCACCATGATGATCACCACGACGATCATCATGACGACCACCATGACGATCACCATGACGATCACCACGACAATCATCACAACGGCCATGACAATCATCAAGACAGCCACCCTAACAACCACCATGATGATCATCATGATGATGGCCATTATAGCAATGGTCATCGTGACGATGGCCTTCATGGCAATGGCCACCATGATGATGGACACCATGGAAATGACGATGATGCCCACCATCCACCAACCTCTTTTAAGCCACCAGGGTCAAGATCTCCTGTCCGCGGAGCCATCAGTAAACTAGATGCAGTGCTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45661
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 |
---|---|---|---|---|---|
ENSDART00000091661 | Nonsense | 346 | 722 | 2 | 5 |
ENSDART00000139727 | Nonsense | 167 | 416 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 10364085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9822624 |
GRCz11 | 19 | 9741549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTGGAAGAACAGCTTCATCATCATTACGACAGTCACTACGGTCACTA[T/A]GATCACCACGACCACGATTACCACCATACTGACCACCCCAGTAACCACCA
Long Flanking Sequence:
TACTGCGCCACTGCTATTTATTTATTTTATTCTATTTTTATTTATTTTTCATTAAATTTTTTACCTATAAGTAAATGAATTTTTTTTTAAAAGTTAATTACTTATTTAATTTTTTATTTTTATTTACTTTTTTATTTTTTATTTGTTATTTTATTTTATTTTATTTTATTTTATTTTATATTTTATTTTATTATTATTTAATTTATTTATATTATTTTATGTTATTTTATTATTTTATTTTATTTACTTATAATTATTTATTTTTATTTACTTATTTTTAAGTTTTTTATTTACTTATTTATTTAATATCTTTTTATTTATTTGCTTTTTTTTTTATGCTAAACTAAACAAACCATACTATTTGTTTACTGTCTTTGTTTTTTGTAGGCTAGAAATTCCTCCAGTTCCTATTCGAGTTCATTGCGAGACCTCCTGCAACGCAAAATCAACACACTGGAAGAACAGCTTCATCATCATTACGACAGTCACTACGGTCACTA[T/A]GATCACCACGACCACGATTACCACCATACTGACCACCCCAGTAACCACCATGATGACAATCACGATAACCACGACAATCATCACGACGACCATCACTCCAACCGCCATCGTAACCACCATTACAGTTATCACTATGACCATCACGGCGACCACCATGATGATCACCACGACGATCATCATGACGACCACCATGACGATCACCATGACGATCACCACGACAATCATCACAACGGCCATGACAATCATCAAGACAGCCACCCTAACAACCACCATGATGATCATCATGATGATGGCCATTATAGCAATGGTCATCGTGACGATGGCCTTCATGGCAATGGCCACCATGATGATGGACACCATGGAAATGACGATGATGCCCACCATCCACCAACCTCTTTTAAGCCACCAGGGTCAAGATCTCCTGTCCGCGGAGCCATCAGTAAACTAGATGCAGTGCTGAGCAACATTCACCACAAACCTACTGAAGCAGGTGACGTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11823
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 |
---|---|---|---|---|---|
ENSDART00000091661 | Nonsense | 572 | 722 | 3 | 5 |
ENSDART00000139727 | Nonsense | 266 | 416 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 10360726)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9819265 |
GRCz11 | 19 | 9738190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGCTCGGGTCCTGGCCTCGGAACCCCGTTCTCCTACTCTGTCCCTGGA[C/T]AAGCCAACGAGCTCGTCCTCAYTGAGTGGGGCAACAAWCCCATKGAGCTG
Long Flanking Sequence:
GTCAGTTGAACACAAAAGAAAATGTTTAGAAAAATAATTGAAATGGTAAGCATTTACTTTCATAATAAATGTTTTTCCTACTATGAATGTCAATCGATTACCAGCTTTCTTCAAAATGAATTTGACTTGAGGGTGGGTAAATAGTGATTGTTATTTTTAGGTGAATTTTCCTTTAAGTCCAAGCACTGCAAAATTTAGTTAAACAGTCTGCTTACAGTAGATCTGAGTCTTTTTTATTTTTAAAAGTAGCTTTTTGTGAAATGCAGAAGAGAAATAATATCCCATTTCACGCTTCCTCATTTCCACATCTCACAGGATCAAATAAGAAGCCCAAGAATCCTGACGCGTTTCAGATTGGCTTCCCGATGCGCACCAACTACATGTACGGGCGAATCAAGCGCACCCTTCTGAGCGAGATCTTCGCCCTTACCGTCTGTCTTTGGTTAAAAGGAGGCTCGGGTCCTGGCCTCGGAACCCCGTTCTCCTACTCTGTCCCTGGA[C/T]AAGCCAACGAGCTCGTCCTCATTGAGTGGGGCAACAATCCCATGGAGCTGCTGGTAAACGACAAGGTAAAGAATCAGTGATTACATAATGAAAGATCTATGGCCTAGATTCAGTATACCGGGGTCGTATACAGTAGCTTAGAAGTGGATTTAATAGGATACAATGAAGCATGTCACAACACCAGACGAAATAACTGTGATATGTTAATTAATAGTGAAATGTTGGGTCTCTTCGTTAGGATAGGGTCAACAGATTTACTTACCCTGCTGATGCCCTTGTCCTGTCCTTGCAACAGTCTGCAAAGCCGTCTCTTCCTCTCGGCTTCCCAGCCAATTGCATCATCCTGTCTAATTAGTTAATGGCTTATCTGTGGCTGACGTGTGAATACATTCTACTGTTTTTTTTTTGTTTTTTTTTACTGAAATAAGACAGACCTCTTCTCTGATAGACTGTTTACATGCTGTCAGATAAAGTGGTGTTGAGATACTGAAGCCTATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23450
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 |
---|---|---|---|---|---|
ENSDART00000091661 | Nonsense | 653 | 722 | 4 | 5 |
ENSDART00000139727 | Nonsense | 347 | 416 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 10357852)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9816391 |
GRCz11 | 19 | 9735316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCCTGGCATCCCATTAAACCAGGAGGAGTCTTCATTCTTGGCCAAGAG[C/T]AGGTATGGTCTTACTGAATCAAACTTAAAGCTTATACTTTTTAAGCATAT
Long Flanking Sequence:
TTCCAGTATCGTGCAACCCTATATCCCTTCCAGTTTAAATGTTACTACCCTAAACATAAAAGCAAATTTGGATAAGGGGTGGTGCTAAAGAGAGTTAGAGACTCCATATTTGCAGTGGCTAATGTCCTCTATTTAAGTTCACAACATATCTGCAAGTGTTTCTGTGGGTTGCCATTCCTTGGTGCTTGGACCCTAATTAACTTTTAAAATATATGCAAAACAGATATTTTGACGCAAAGTGTGTATGACAAAATTCCATTGACTATGATTACCAAGCAGTGACTGTAATGTTTAAAGATGTACTGTTTTTTGCCCTCTTGCAGGCAGTCACTCTTCCTCTTTCTCTGACGGACGGGAAGTGGCACCATCTCTGTGTAACATGGTCCACACGTGATGGCATGTGGGAGGCTTATCAAGATGGTGTGAAAAGGGGCACTGGAGAGAATCTGTCGCCCTGGCATCCCATTAAACCAGGAGGAGTCTTCATTCTTGGCCAAGAG[C/T]AGGTATGGTCTTACTGAATCAAACTTAAAGCTTATACTTTTTAAGCATATATTCAATTCAATTCAATTCAATTCAGTTCAATTCAATTCAATTCAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTCAATTCAATGACTCTTTATTTCTGTAGAGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATACAGTCGGAGATTATAGTAAATTGAAACCGCTTTAGTGAACTTTTCAGACTTGAAGTTCAGTTTATTGTAGTTTAGATTTCATTGCTGAAAGTCCAAACACTTAAGAGCAAATTCATCGATGCACAGCTCCACAAGTCCCAATTCAAATAAGCCTGTGGCGACAGTGGCGAGGAACAAAACTTCACAAACTGACCAAAGTGAAGGAAAAAACCTCGAGAAAAAAACAGGCTCAGTATATTG
Associated Phenotype:
Not determined