ZMP
aspg
Ensembl ID:
ZFIN ID:
Description:
asparaginase homolog [Source:RefSeq peptide;Acc:NP_001096091]
Human Orthologue:
ASPG
Human Description:
asparaginase homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:20123]
Mouse Orthologue:
Aspg
Mouse Description:
asparaginase homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2144822]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17418 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17418
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 |
---|---|---|---|---|---|
ENSDART00000074875 | Nonsense | 181 | 626 | 4 | 16 |
ENSDART00000109525 | Nonsense | 203 | 665 | 4 | 18 |
ENSDART00000135073 | Nonsense | 203 | 648 | 4 | 16 |
ENSDART00000143525 | Nonsense | 215 | 289 | 5 | 7 |
ENSDART00000145882 | None | None | 74 | None | 4 |
The following transcripts of ENSDARG00000052942 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 45916187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 45765419 |
GRCz11 | 17 | 45748671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAYGGTACAGACACTATGGCTTACACCGCATCTGCCTTATCCTTCATGTG[T/A]GARARCCTKGGGAAGCCRGTCATCCTCACWGGATCACAGGTAAMCTAYAA
Long Flanking Sequence:
TGTTTGGGAAATTATTTATGAGCTTTAAATCACAAAAATTGCACAAAAACATTAGTCATTATAAGAACTGATCTTGATTTAAATGATTGAAAATTATACAAATTTTCAGATTGATTAATAAAATCATATATTTTGGTAAGAGTTTACGATACAGGACACAATTAATGTTAATGTATTTTCTAACATAAACAAATAAACGTATTCATGTTTTTTAAAGTTAGTGAAAATAAAGTTGTTCATTGTTCATGTTAACCCACGTTGCATTAACTTACAACAAGCTCAGCTTTGGATTTTAACAATGTGTTAGTAAATGTTTAGCCATAATTAATAAATACTGTACAACAATTGTTCATTGTTTGTTCATGTTAGTAAATAGGTTACCTACATGTCTCTTTTTCTTCCTTGTGTTCACAGAAACACTATGAGCAATATGATGGTTTCGTCATCCTGCACGGTACAGACACTATGGCTTACACCGCATCTGCCTTATCCTTCATGTG[T/A]GAAAACCTGGGGAAGCCAGTCATCCTCACTGGATCACAGGTAAACTATAAATCATTGACTCGCCCTTGTGTTAAAAATAAAAACCCCTATGACTTTCTTTTCATGAGCACAAATTGAGTAGACCTAAGGCATGGTTACACATAATTCGCTCTTTTGGTTTGTTCGCTTAGCATTTTTACTGTCATTTTAAAAGTAGAACCAAATGAAACCAAAAAATAAAACAACAACAACAACAACAACAACAACAACAACAACAACAACAACAACAACAAAATAACTTGTTTTATTATGCAGATACAGTTACAAAATAATTAGCTTTCTTGTGAAATTTTGCATTATTTTTCAAGCTTATCTCACGAAACTATTTACACAAATTTTCAAACCTAGTAGTTTTAAAAACTATTTTCTAATAAATAATTTCAATATGCTATTATTCAGCTTAAAGTGTAATGGGGTATATGCTGAAGCATGCTAATAGGACTTTTAATTTGCCAGTAACC
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa28926
Status:
Less stringent filtering
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:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074875 | Nonsense | 597 | 626 | 15 | 16 |
ENSDART00000109525 | Nonsense | 619 | 665 | 15 | 18 |
ENSDART00000135073 | Nonsense | 619 | 648 | 15 | 16 |
ENSDART00000143525 | None | None | 289 | None | 7 |
ENSDART00000145882 | Nonsense | 36 | 74 | 2 | 4 |
The following transcripts of ENSDARG00000052942 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 45933653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 45782885 |
GRCz11 | 17 | 45766137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGTTGAATGAATGTACTTCTGTCTCCTTTAGGCAAGAGCCACTGGATG[T/A]GTGGAGTCTGTTGAGTTCTTAAAACAGGCAGCTCTGTACCAAACTCAGGT
Long Flanking Sequence:
AAAATAATATTAACCAAAACCAATAACATTACACATAAAACAATTGCACATAAAATATTTCAAGTAATAAAGTGATACAACACTCATTTAAAAAACAATGATATTGCACTAAAAATATACAGTGCAAATCTACACGCTAAAACCCGTAATAAGTAAATATACTGCACGAGCAGCAAGGCATTGCATAGATTACTGTAAGGGTAAGTGACTGAGGGAGACGTTATGAAGTCTGATAGCAGTGGGAAGGAAGGATTTTCTGTGGCGTTCAGTGGAACACTTTAAGCTGGTAAGTCTGTGACTAAAGGTACTTCTCAGCTCGTCAACCACATTATGAAGAGGATGATCTACATTGTACATAATTGACCGAAGTCTGCACAATGTTCTCCTTTCAGCCACTTCATCAAAGTTGTCCGAAAACTATTAAACAGAACCTTGCAAAAGTATTCCTGTAAAGTTGAATGAATGTACTTCTGTCTCCTTTAGGCAAGAGCCACTGGATG[T/A]GTGGAGTCTGTTGAGTTCTTAAAACAGGCAGCTCTGTACCAAACTCAGGTATGGAACATATCACTCGTTTCTATATATCAATTTATTTAAAAATAGTAAATTGCCTATATTTGCATAAGGCCCATTCACACTGAGCATGTTTTTTTTTTTGTGATGAGAGGTGGCTATTTTGAATGGTTTTGGCCCTGCGCACCTCACGTTTTAACCGTCTACTGTTTCTAGTGTTTTTGCCAATACGCTCTGTGCGCCTGCTGTGGAAAAAAACGTCAGTTGAGTCTTTTTCAATCCTAAACAAAATGAAAGCAAAGTTTTCATCGAGGTTTACTGTAGGGGTTGTGTTGACGCTATTTGACTTTCGATCTGGAGCTGACAAATTGTGAATATTATATAAATAAAATGAATAAAAAATTGAACAATATTACTAAAAAGCAGCAGGCCTGGAAACTAGTGATTCTGGCATTGGAGATGACAGGTAAGCATCACATCATAAAGTTCCTCTC
Associated Phenotype:
Not determined