ZMP
A4QP97_DANRE
Ensembl ID:
Description:
Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:A4QP97]
Human Orthologue:
ASPH
Human Description:
aspartate beta-hydroxylase [Source:HGNC Symbol;Acc:757]
Mouse Orthologue:
Asph
Mouse Description:
aspartate-beta-hydroxylase Gene [Source:MGI Symbol;Acc:MGI:1914186]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17803 | Essential Splice Site | Available for shipment | Available now |
hu7910 | Essential Splice Site | Available for shipment | Available now |
sa2365 | Essential Splice Site | Available for shipment | Available now |
sa13653 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17803
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114008 | Essential Splice Site | 61 | 436 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 59450373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57902982 |
GRCz11 | 7 | 58205422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGCAGAAATWTCCACATAGTCCGAGGTGCAGATACGGTAAAGCACAG[G/A]YAACACATTATCATAAMAGGTTGCAATGCTGATGTGTCTATGKTATATTA
Long Flanking Sequence:
GATTTTTAATCAGACTTTATAAATTCGACCTATAATTTTACCTAAGTAGGACACCAGACAACTTAAAATATCGTAATAGCACCACAAAACCACAGTTGTCAAGTTTGTAAGAACAATTCAACCTACATTTGTCTCTGCTCAAGCATTTTTAAGATGATTTGTATGGAATTGATATTGTGTGAAAAGCACAACACTTCAAGAAAGACTTATGCTGTGGTGAATTCTCTTACAGCCAAAGCGAAGAAACCGAAGCTCCTTAATAAATTTGACAAAACAATCAAATCGGAAATCAACTCTGCAAAGAAACTACGGAAGAAGGTAAAATGTATACAAAAATGATGCTCTGTTACAGCACAAATAAAATATGATTAGTAAAAATTTGCAGACAGAATTAATAGTCTTTTTGTCTTCAGGGAAAGGTTGAGGAGTCTCTGCAGGCTTTTGAAGATCTTGTGCAGAAATTTCCACATAGTCCGAGGTGCAGATACGGTAAAGCACAG[G/A]TAACACATTATCATAAAAGGTTGCAATGCTGATGTGTCTATGTTATATTATGAGCACTCATAAACATGTGTTCAGGCTGAAGATGATTTGGCAGAGAAAAAGCGCAGTAATGAGATGCTGCTGAAGGCGGTGAACACATACAGAGAAGTAGCCGAGCTCCCAGATGTTCCACCAGACCTCATCAAAGCCACACTGAAGAGACGGGCAGACAGGCAGCAGTTTCTAGGTACATATTTTAAACATTAATGTGCCATCTAGCTATGGTGAAATCCAATTGTTAAAGGTCCTGTGAAATAATAAGATTGTTTAGATGTTAGAAAGATGCTAGTTTTAGATGCTAGTTTTAAGGATATCTATTGACCTTATTCTGTGATGTGGAAGTGCACTAGTTTTTGCGATTTGTTTTAGAACTTCCAAATCAGTTGCCCTATGGGAGAAATGACTAGAAATAATAAATGGCAGAATAAGGTCAAGCTACTTGCGCTACAAACAGGTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7910
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114008 | Essential Splice Site | 61 | 436 | 3 | 13 |
ENSDART00000114008 | Essential Splice Site | 61 | 436 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 59450372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57902981 |
GRCz11 | 7 | 58205421 |
KASP Assay ID:
554-2396.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGCAGAAATWTCCACATAGTCCGAGGTGCAGATACGGTAAAGCACAGG[T/C]AACACATTATCATAAMAGGTTGCAATGCTGATGTGTCTATGTTATRTTAT
Long Flanking Sequence:
ATTTTTAATCAGACTTTATAAATTCGACCTATAATTTTACCTAAGTAGGACACCAGACAACTTAAAATATCGTAATAGCACCACAAAACCACAGTTGTCAAGTTTGTAAGAACAATTCAACCTACATTTGTCTCTGCTCAAGCATTTTTAAGATGATTTGTATGGAATTGATATTGTGTGAAAAGCACAACACTTCAAGAAAGACTTATGCTGTGGTGAATTCTCTTACAGCCAAAGCGAAGAAACCGAAGCTCCTTAATAAATTTGACAAAACAATCAAATCGGAAATCAACTCTGCAAAGAAACTACGGAAGAAGGTAAAATGTATACAAAAATGATGCTCTGTTACAGCACAAATAAAATATGATTAGTAAAAATTTGCAGACAGAATTAATAGTCTTTTTGTCTTCAGGGAAAGGTTGAGGAGTCTCTGCAGGCTTTTGAAGATCTTGTGCAGAAATTTCCACATAGTCCGAGGTGCAGATACGGTAAAGCACAGG[T/C]AACACATTATCATAAAAGGTTGCAATGCTGATGTGTCTATGTTATATTATGAGCACTCATAAACATGTGTTCAGGCTGAAGATGATTTGGCAGAGAAAAAGCGCAGTAATGAGATGCTGCTGAAGGCGGTGAACACATACAGAGAAGTAGCCGAGCTCCCAGATGTTCCACCAGACCTCATCAAAGCCACACTGAAGAGACGGGCAGACAGGCAGCAGTTTCTAGGTACATATTTTAAACATTAATGTGCCATCTAGCTATGGTGAAATCCAATTGTTAAAGGTCCTGTGAAATAATAAGATTGTTTAGATGTTAGAAAGATGCTAGTTTTAGATGCTAGTTTTAAGGATATCTATTGACCTTATTCTGTGATGTGGAAGTGCACTAGTTTTTGCGATTTGTTTTAGAACTTCCAAATCAGTTGCCCTATGGGAGAAATGACTAGAAATAATAAATGGCAGAATAAGGTCAAGCTACTTGCGCTACAAACAGGTGTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2365
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114008 | Essential Splice Site | 61 | 436 | 3 | 13 |
ENSDART00000114008 | Essential Splice Site | 61 | 436 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 59450372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57902981 |
GRCz11 | 7 | 58205421 |
KASP Assay ID:
554-2396.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGCAGAAATTTCCACATAGTCCGAGGTGCAGATACGGTAAAGCACAGG[T/C]AACACATTATCATAAAAGGTTGCAATGCTGATGTGTCTATGTTATATTAT
Long Flanking Sequence:
ATTTTTAATCAGACTTTATAAATTCGACCTATAATTTTACCTAAGTAGGACACCAGACAACTTAAAATATCGTAATAGCACCACAAAACCACAGTTGTCAAGTTTGTAAGAACAATTCAACCTACATTTGTCTCTGCTCAAGCATTTTTAAGATGATTTGTATGGAATTGATATTGTGTGAAAAGCACAACACTTCAAGAAAGACTTATGCTGTGGTGAATTCTCTTACAGCCAAAGCGAAGAAACCGAAGCTCCTTAATAAATTTGACAAAACAATCAAATCGGAAATCAACTCTGCAAAGAAACTACGGAAGAAGGTAAAATGTATACAAAAATGATGCTCTGTTACAGCACAAATAAAATATGATTAGTAAAAATTTGCAGACAGAATTAATAGTCTTTTTGTCTTCAGGGAAAGGTTGAGGAGTCTCTGCAGGCTTTTGAAGATCTTGTGCAGAAATTTCCACATAGTCCGAGGTGCAGATACGGTAAAGCACAGG[T/C]AACACATTATCATAAAAGGTTGCAATGCTGATGTGTCTATGTTATATTATGAGCACTCATAAACATGTGTTCAGGCTGAAGATGATTTGGCAGAGAAAAAGCGCAGTAATGAGATGCTGCTGAAGGCGGTGAACACATACAGAGAAGTAGCCGAGCTCCCAGATGTTCCACCAGACCTCATCAAAGCCACACTGAAGAGACGGGCAGACAGGCAGCAGTTTCTAGGTACATATTTTAAACATTAATGTGCCATCTAGCTATGGTGAAATCCAATTGTTAAAGGTCCTGTGAAATAATAAGATTGTTTAGATGTTAGAAAGATGCTAGTTTTAGATGCTAGTTTTAAGGATATCTATTGACCTTATTCTGTGATGTGGAAGTGCACTAGTTTTTGCGATTTGTTTTAGAACTTCCAAATCAGTTGCCCTATGGGAGAAATGACTAGAAATAATAAATGGCAGAATAAGGTCAAGCTACTTGCGCTACAAACAGGTGTATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13653
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 |
---|---|---|---|---|---|
ENSDART00000114008 | Nonsense | 121 | 436 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 59445167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57897776 |
GRCz11 | 7 | 58200216 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AARATTCCAAAWTTACCATGCAGGTCGTACGAGGGGATCTTTAGCWACTT[T/A]GGAGAAGCTAGTCCAGATTTYTCCCGAAGACATCAGCCTTAAGAATGATT
Long Flanking Sequence:
ATAAAAGCAAACAGTGGGATTCTGCCAGAATAGAATAGAAAAAGAAAAGAAACTCTGTGTGTTACTTGCTTTATGGTCATAAAAAATGTATCTATAAAGAGCAAAATGTCCTTTTTTTAACCTATAAAGTTCGTTTAAACATTTGTTTGCTGATCAGTGATTATATGCAAGTAAAAGCCAACAATTTCAACAAATAAAGAGGTCATGTCTCTTCAAAAGGCTTGGATTAAACTACCAAACTCATATGGATATAACTGTTTTGAAACATCAAAGATTGTTTGAATATAATGGAGGAACAGAAATTTGCTATGTTGGATTAAAAATATATTTAATTGTGAACACATTTCTTAAGGGTCTTGATATTATACGAGTAAATGATGGAGATTTATATTTTGGTGTGAACTAACTCTTAACCCCTGAAACAGACACACATGTCAATGACATTCTAAGAAGATTCCAAAATTACCATGCAGGTCGTACGAGGGGATCTTTAGCTACTT[T/A]GGAGAAGCTAGTCCAGATTTTTCCCGAAGACATCAGCCTTAAGAATGATTTGGGAGTAGCACATCTGCTTCTGGGTGACAACAAGAGTGCGAAACAAATATATGAAGAGGTAAGCGATATTATGATGATGATGCTGTTGTTGTAATTACATTTGATGCATTGATGTTAAGGAAATCTAATGATTTAATGATTTCCCCTCTTTCTGATTTCCTCTTCAGGTTTTAGCCAGTGCCCCAAGGGATGGATTTGCTAAAGTGCATTACGGGTTCATACTTAAATCTGAAAACAAGATTGCAGAGAGCATACCGTACCTGAGGGTAATTGTGATTTAAATGTTGGCTTCATAAATTTTTTTTATTTATTTGATAAGAAACCGTAATGAGATTAACATTGTTAAATATATTGAAAAGTTAAAAATTATTATGTATTAGTTAAATCGTATTTCTATAATGGCAAAGCTTAATACAGTGTCCACAGCTTCGTAAAAAGGTTTTAAAAAA
Associated Phenotype:
Not determined