ZMP
arsa
Ensembl ID:
ZFIN ID:
Description:
arylsulfatase A [Source:RefSeq peptide;Acc:NP_001013561]
Human Orthologue:
ARSA
Human Description:
arylsulfatase A [Source:HGNC Symbol;Acc:713]
Mouse Orthologue:
Arsa
Mouse Description:
arylsulfatase A Gene [Source:MGI Symbol;Acc:MGI:88077]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14243 | Nonsense | Available for shipment | Available now |
| sa6501 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32188 | Nonsense | Available for shipment | Available now |
| sa43044 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43045 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36571 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14243
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:
Founder:
SL4_06_H10
KASP Assay Location:
Project idt6, Plate 1, Well E12
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061989 | Nonsense | 108 | 499 | 2 | 8 |
| ENSDART00000140193 | Nonsense | 112 | 503 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 7699518)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 8276896 |
| GRCz11 | 18 | 8234915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATCCGGGCTCAAGAGGCGGTCTCCCTCTCAACGAGACCACCATAGCC[G/T]AGGTGCTGAAGACTCAGGGTTACTCCACAGCAATAGTCGGAAAGTGGCAT
Long Flanking Sequence:
ACATTAACTAATGCATTATTAATATCCAAAGTTGTACTTGTTAACAAAGCACCATGAGTTACTATGTTATTTAACTTAACATTAACTAACAAAGATAAATAAATAATGTATTAACCCTTTAACAAGCATCATAACCACCTGGTTAATCTTTCATTGGGGATTATTATTATTATTATTTTAATTGCTTATTACTATTTATCAGAGTTGTGTCAGTGTATTTTTCAATAGAAGATGTGGGCCAAAAAAGATTGTTTTCAAAGAGTGCACCTTAAAGGGTTAAATGTATCACTAATAGTTTGTTCATGTTAGTAAATGCATGTAGTAACATTAACTAATGGACCATTTTTTTCCAATCTAACATACAGTATTCTGTTTTACATACTTTTTGCTCCAGGGCTGCATTGCTGACGGGCCGCTATCAGACTCGCTCTGGGATTTATCCAGGTGTGCTGTATCCGGGCTCAAGAGGCGGTCTCCCTCTCAACGAGACCACCATAGCC[G/T]AGGTGCTGAAGACTCAGGGTTACTCCACAGCAATAGTCGGAAAGTGGCATCTGGGAGTAGGGCTGAACGGCACCTACCTGCCCACCCGGCACGGCTTTGACAGTTATCTCGGTATCCCATACTCACATGATCAGGTACCTATATTTTCTTTTGTCATACAGAATCTGATCTGCAAATCAACAAGGAAATTGCATAGCCTTCTTTTTATTTTATTTATACAAATGTTTTACACAATAATTACATTGAAACAAATGATTAATTTCAGTGCAAGTACATATTAGTTAAGACCACCTAATGTAAAGTGGCACAAACAAAGTCTCATTTAATATTCTTTGCTCATATTGTCTTTGCACAATGTTTAAGGCATGATTTCTCTATTATAGGGTCCCTGTCAGAATCTGAGCTGCTTCCCTCCGGATGTGAAGTGTTTTGGCCTGTGTGATCAGGGTGTTGTGACTGTACCTCTCCTGTTTAATGAGATTATCAAGCAGCAGCCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6501
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
Founder:
SL4-107
KASP Assay Location:
Project 554.35, Plate 6, Well A12
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061989 | Nonsense | 155 | 499 | 3 | 8 |
| ENSDART00000140193 | Nonsense | 159 | 503 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 7699910)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 8277288 |
| GRCz11 | 18 | 8235307 |
KASP Assay ID:
554-4556.1 (used for ordering genotyping assays)
KASP Sequence:
TTKTCWTTGCACAATKTTTAAGGYATGATTTCTCTATTATAGGGTCCCTG[T/A]CAGAATCTGAGCTGCTTCCCTCCGGATGTGAAGTGTTTTGGCCTGTGTGA
Long Flanking Sequence:
AGGGCTGCATTGCTGACGGGCCGCTATCAGACTCGCTCTGGGATTTATCCAGGTGTGCTGTATCCGGGCTCAAGAGGCGGTCTCCCTCTCAACGAGACCACCATAGCCGAGGTGCTGAAGACTCAGGGTTACTCCACAGCAATAGTCGGAAAGTGGCATCTGGGAGTAGGGCTGAACGGCACCTACCTGCCCACCCGGCACGGCTTTGACAGTTATCTCGGTATCCCATACTCACATGATCAGGTACCTATATTTTCTTTTGTCATACAGAATCTGATCTGCAAATCAACAAGGAAATTGCATAGCCTTCTTTTTATTTTATTTATACAAATGTTTTACACAATAATTACATTGAAACAAATGATTAATTTCAGTGCAAGTACATATTAGTTAAGACCACCTAATGTAAAGTGGCACAAACAAAGTCTCATTTAATATTCTTTGCTCATATTGTCTTTGCACAATGTTTAAGGCATGATTTCTCTATTATAGGGTCCCTG[T/A]CAGAATCTGAGCTGCTTCCCTCCGGATGTGAAGTGTTTTGGCCTGTGTGATCAGGGTGTTGTGACTGTACCTCTCCTGTTTAATGAGATTATCAAGCAGCAGCCTGCAGATTTCCTCCAGCTGGAGAAAGCCTATGGTGAATTCGCCTCTCAGTTCATCAGTGACTCTGTCAAGGACAATCGCCCATTCTTCTTGTACTATCCTTCACATGTGAGTCAAGAACAGTTACCTTTATCAGAATACATCTCTACACTCGTATGCAACATCTCAAAATATACTCACTCAGTTTAGCAGTTAAGTGATATACACTACCTGACAAAAGTCTTGTCGTGGATCCCAGTTGTAAAAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTCTAAAAGTGGCAGAAGGTAGATTTTTCTGATGAATCATCTATTGAACTGCATCCCAATCATCACAAATACTGCAGAAGACCTACTGGAGCCCGAATGAACCCAAGATTCTCATAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32188
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:
Founder:
SL6_01_E9
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061989 | Nonsense | 188 | 499 | 3 | 8 |
| ENSDART00000140193 | Nonsense | 192 | 503 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 7700007)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 8277385 |
| GRCz11 | 18 | 8235404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATCAGGGTGTTGTGACTGTACCTCTCCTGTTTAATGAGATTATCAAG[C/T]AGCAGCCTGCAGATTTCCTCCAGCTGGAGAAAGCCTATGGTGAATTCGCC
Long Flanking Sequence:
CCACCATAGCCGAGGTGCTGAAGACTCAGGGTTACTCCACAGCAATAGTCGGAAAGTGGCATCTGGGAGTAGGGCTGAACGGCACCTACCTGCCCACCCGGCACGGCTTTGACAGTTATCTCGGTATCCCATACTCACATGATCAGGTACCTATATTTTCTTTTGTCATACAGAATCTGATCTGCAAATCAACAAGGAAATTGCATAGCCTTCTTTTTATTTTATTTATACAAATGTTTTACACAATAATTACATTGAAACAAATGATTAATTTCAGTGCAAGTACATATTAGTTAAGACCACCTAATGTAAAGTGGCACAAACAAAGTCTCATTTAATATTCTTTGCTCATATTGTCTTTGCACAATGTTTAAGGCATGATTTCTCTATTATAGGGTCCCTGTCAGAATCTGAGCTGCTTCCCTCCGGATGTGAAGTGTTTTGGCCTGTGTGATCAGGGTGTTGTGACTGTACCTCTCCTGTTTAATGAGATTATCAAG[C/T]AGCAGCCTGCAGATTTCCTCCAGCTGGAGAAAGCCTATGGTGAATTCGCCTCTCAGTTCATCAGTGACTCTGTCAAGGACAATCGCCCATTCTTCTTGTACTATCCTTCACATGTGAGTCAAGAACAGTTACCTTTATCAGAATACATCTCTACACTCGTATGCAACATCTCAAAATATACTCACTCAGTTTAGCAGTTAAGTGATATACACTACCTGACAAAAGTCTTGTCGTGGATCCCAGTTGTAAAAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTCTAAAAGTGGCAGAAGGTAGATTTTTCTGATGAATCATCTATTGAACTGCATCCCAATCATCACAAATACTGCAGAAGACCTACTGGAGCCCGAATGAACCCAAGATTCTCATAGAAAACAGTCAAGTTTGGTGAAGGAAAAATCTTGGTTTGGGGTTATATTCAGTATGGGGGTGTGCGAGAGATCTGCAGAGTGGATCTCAACATCAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43044
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
Founder:
SL7_05_C6
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061989 | Nonsense | 206 | 499 | 3 | 8 |
| ENSDART00000140193 | Nonsense | 210 | 503 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 7700061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 8277439 |
| GRCz11 | 18 | 8235458 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCTGCAGATTTCCTCCAGCTGGAGAAAGCCTATGGTGAATTCGCCTCT[C/T]AGTTCATCAGTGACTCTGTCAAGGACAATCGCCCATTCTTCTTGTACTAT
Long Flanking Sequence:
AGTGGCATCTGGGAGTAGGGCTGAACGGCACCTACCTGCCCACCCGGCACGGCTTTGACAGTTATCTCGGTATCCCATACTCACATGATCAGGTACCTATATTTTCTTTTGTCATACAGAATCTGATCTGCAAATCAACAAGGAAATTGCATAGCCTTCTTTTTATTTTATTTATACAAATGTTTTACACAATAATTACATTGAAACAAATGATTAATTTCAGTGCAAGTACATATTAGTTAAGACCACCTAATGTAAAGTGGCACAAACAAAGTCTCATTTAATATTCTTTGCTCATATTGTCTTTGCACAATGTTTAAGGCATGATTTCTCTATTATAGGGTCCCTGTCAGAATCTGAGCTGCTTCCCTCCGGATGTGAAGTGTTTTGGCCTGTGTGATCAGGGTGTTGTGACTGTACCTCTCCTGTTTAATGAGATTATCAAGCAGCAGCCTGCAGATTTCCTCCAGCTGGAGAAAGCCTATGGTGAATTCGCCTCT[C/T]AGTTCATCAGTGACTCTGTCAAGGACAATCGCCCATTCTTCTTGTACTATCCTTCACATGTGAGTCAAGAACAGTTACCTTTATCAGAATACATCTCTACACTCGTATGCAACATCTCAAAATATACTCACTCAGTTTAGCAGTTAAGTGATATACACTACCTGACAAAAGTCTTGTCGTGGATCCCAGTTGTAAAAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTCTAAAAGTGGCAGAAGGTAGATTTTTCTGATGAATCATCTATTGAACTGCATCCCAATCATCACAAATACTGCAGAAGACCTACTGGAGCCCGAATGAACCCAAGATTCTCATAGAAAACAGTCAAGTTTGGTGAAGGAAAAATCTTGGTTTGGGGTTATATTCAGTATGGGGGTGTGCGAGAGATCTGCAGAGTGGATCTCAACATCAACAGCCTGAGACATTTTGTGCTGCTCATTACATTATAAACCAACAGGAGAGGGCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43045
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
Founder:
SL7_04_E11
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061989 | Nonsense | 222 | 499 | 3 | 8 |
| ENSDART00000140193 | Nonsense | 226 | 503 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 7700111)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 8277489 |
| GRCz11 | 18 | 8235508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTCATCAGTGACTCTGTCAAGGACAATCGCCCATTCTTCTTGTACTA[T/A]CCTTCACATGTGAGTCAAGAACAGTTACCTTTATCAGAATACATCTCTAC
Long Flanking Sequence:
GGCTTTGACAGTTATCTCGGTATCCCATACTCACATGATCAGGTACCTATATTTTCTTTTGTCATACAGAATCTGATCTGCAAATCAACAAGGAAATTGCATAGCCTTCTTTTTATTTTATTTATACAAATGTTTTACACAATAATTACATTGAAACAAATGATTAATTTCAGTGCAAGTACATATTAGTTAAGACCACCTAATGTAAAGTGGCACAAACAAAGTCTCATTTAATATTCTTTGCTCATATTGTCTTTGCACAATGTTTAAGGCATGATTTCTCTATTATAGGGTCCCTGTCAGAATCTGAGCTGCTTCCCTCCGGATGTGAAGTGTTTTGGCCTGTGTGATCAGGGTGTTGTGACTGTACCTCTCCTGTTTAATGAGATTATCAAGCAGCAGCCTGCAGATTTCCTCCAGCTGGAGAAAGCCTATGGTGAATTCGCCTCTCAGTTCATCAGTGACTCTGTCAAGGACAATCGCCCATTCTTCTTGTACTA[T/A]CCTTCACATGTGAGTCAAGAACAGTTACCTTTATCAGAATACATCTCTACACTCGTATGCAACATCTCAAAATATACTCACTCAGTTTAGCAGTTAAGTGATATACACTACCTGACAAAAGTCTTGTCGTGGATCCCAGTTGTAAAAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTCTAAAAGTGGCAGAAGGTAGATTTTTCTGATGAATCATCTATTGAACTGCATCCCAATCATCACAAATACTGCAGAAGACCTACTGGAGCCCGAATGAACCCAAGATTCTCATAGAAAACAGTCAAGTTTGGTGAAGGAAAAATCTTGGTTTGGGGTTATATTCAGTATGGGGGTGTGCGAGAGATCTGCAGAGTGGATCTCAACATCAACAGCCTGAGACATTTTGTGCTGCTCATTACATTATAAACCAACAGGAGAGGGCAAATTTTTCAGCAGGATAGCGCTCCTTCTCATATTTCAGCCTCCACATCAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36571
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
Founder:
SL6_08_D12
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061989 | Nonsense | 262 | 499 | 4 | 8 |
| ENSDART00000140193 | Nonsense | 266 | 503 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 18 (position 7702525)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 8279903 |
| GRCz11 | 18 | 8237922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTCGGTGATGCTCTGATGGAGTTTGATGGCACTGTAGGGAAGATTCTG[C/T]AGACTCTGGAAGAAACGGGTGTCATCAACAACACTCTCATCTTCTTCACT
Long Flanking Sequence:
TATTCTAAATTTAATAAATTAAGAAAAAAAGATGATTAAGTAATGCATTTATTTTCCCTGGTAACAGTGACTTTTCTGATTGGACAATTGACAGAGGATTGTGGGTAGTGTAGTTTTTCATTCATAATTCTACAATTAAACCAGTTTCAGTTAATAATTTAAACTAATGAATAATACATAATGGTTAAATGCAGGTTTTTTTATGGTAACAGTGATTTTTCTGTCTTCATGGTCTAAGCAGTATTGTAGGCAGTGTGGTGTTGTTTTTCTGAAGGTTTCACGCAATCTTAGACCTCATAATAGGTCCTTCTGAAAAGATTTGAATAATATATATTTAAATAGGACTTTTACTTCAACTTTTACCTTGACCCATATTTGTCTGTCTCCTCCAGCACACACACTACCCTCAGTATGCGGGTGCAGATTACGCAGGCAAGTCTCCGCGTGGGCCGTTCGGTGATGCTCTGATGGAGTTTGATGGCACTGTAGGGAAGATTCTG[C/T]AGACTCTGGAAGAAACGGGTGTCATCAACAACACTCTCATCTTCTTCACTGGTGACAACGGGTCAGTGTCGCTTGAGTCTTTCTTTTTGACTGTTTATATTTTCTTGACATCTACTGCTAAAAGCAAAAACATCAGCCCTTCTCTGAAATTTGTATTCTTTTTCAAAATGTGCTCCAATTCAAAGGGCTCTTTTATGAAGAGAAGAAAATAACTAAATACTCATTTCTCTAGTTTTTTCTATGATGACAGTACATAATATTTCACTAGCTATTTTGCAAGAATCTAGTATTCAGCTTTAAGTGCAATTTTAAGGCATAATTGGGTTCATTTGGCTTTACTTGGGGAGTTAGATTAATTATGAAAGTCATTAGATAACAGTGCTGGCCAATAATTGGATAAGGGGGCTGAAATATTTGATTCCTTAATATTCATAAACTCCACAAAAGAAAAATACATAATAGGAAACACTGTGAAATATAGTTAGGCTAAGTTAAATGGT
Associated Phenotype:
Not determined