ZMP
sulf1
Ensembl ID:
ZFIN ID:
Description:
extracellular sulfatase Sulf-1 [Source:RefSeq peptide;Acc:NP_001003846]
Human Orthologue:
SULF1
Human Description:
sulfatase 1 [Source:HGNC Symbol;Acc:20391]
Mouse Orthologue:
Sulf1
Mouse Description:
sulfatase 1 Gene [Source:MGI Symbol;Acc:MGI:2138563]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37866 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9192 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa199 | Nonsense | Available for shipment | Available now |
sa37867 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11702 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37866
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027022 | Nonsense | 116 | 874 | 3 | 20 |
ENSDART00000056080 | Nonsense | 116 | 892 | 3 | 21 |
ENSDART00000056081 | Nonsense | 116 | 1099 | 3 | 19 |
ENSDART00000137175 | None | None | 118 | None | 4 |
ENSDART00000140379 | Nonsense | 116 | 874 | 2 | 19 |
ENSDART00000142830 | Nonsense | 116 | 892 | 2 | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20093964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19400118 |
GRCz11 | 24 | 19544537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAATCACAACACCTACACCAACAATGAGAACTGCTCGTCACCTTCAT[G/A]GCAAGCTCAGCATGAGCCACGATCTTTTGCAGTTTATCTTAACAACACTG
Long Flanking Sequence:
TATGTACTTCCAACTGAAACAGAATATTGAGTAGGGGGTGAGAATTTTTTGCTCATCAATCTCGCATAGCAAACTAATGGTAAGAGGTGCATGGTTAAGAATATTGTGTTTAAAGCCCTTAAACTGAGATCAACGAAGAAGTTCAAATGTGGAAGTAAATGGTCAGACTTTCTTTAAAGAATACTAAAACTCTTTTTTTTCAGTGGATTTACTTTCATGAATTAATTGTACACCTAAAGAATCTGCACTAGCAAAATAAACTACTGTTTGATTTCACACTAAGTTTAAGTTCTTCTCTTTGTGTTGTCTGTCTTGTGTGTCAGGATCTTTGCAGGTGATGAACAAAACCCGCAAGATCATGGAGGATGGTGGCACATCATTCACGAATGCATTTGTTACTACACCCATGTGCTGTCCTTCACGATCCTCTATGCTGACGGGGAAGTACGTCCACAATCACAACACCTACACCAACAATGAGAACTGCTCGTCACCTTCAT[G/A]GCAAGCTCAGCATGAGCCACGATCTTTTGCAGTTTATCTTAACAACACTGGATATCGAACAGGTAAGAAAAACAATGAGTGTTTTATAACCTTTCTAGGCTCTAAATTAATTCAGTACAATACTGTATATATATATATATATATATAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAATTATGATTCCTAATTTAGCCAAAACTTTTTCTGTTTCAGTTGGCAGTATGAATTTTAGATGTGTCAACGTATTTTGACACATATTTTGAGACAATGCTTACAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTATTTTTATTTTTTTTTTACGTTTTTTTTAACGTTGGAATTTTATTAATATATATATATATATATATATATATATATATATATATATATATATATATATTAATAAAATAAAAAAACTCAATGATACATTGTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9192
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 |
---|---|---|---|---|---|
ENSDART00000027022 | Nonsense | 518 | 874 | 11 | 20 |
ENSDART00000056080 | Nonsense | 518 | 892 | 11 | 21 |
ENSDART00000056081 | Nonsense | 518 | 1099 | 11 | 19 |
ENSDART00000137175 | None | None | 118 | None | 4 |
ENSDART00000140379 | Nonsense | 518 | 874 | 10 | 19 |
ENSDART00000142830 | Nonsense | 518 | 892 | 10 | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20120670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19426824 |
GRCz11 | 24 | 19571243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAAGACTGCCATTGTGGTGAACGGCCTTACAAAGCAGCCAAAGCAGCA[C/T]RACGGGCACACAGAMAATTCGGACAGAGCAGTAACCCACGTAAGTATGGT
Long Flanking Sequence:
AGCTGTCTGTGCACATGTCTGAGCCGTGGTCAGTTTACAAAGCAAACAGCTCTGAGAAATTAGGAGATTAAGTCTAAATTGTCTTCAGATTGCTTCTTTATGGGAAAGAATTGTGAGGTGGCTCTTGTGCCGTGTGATTGTGAATTAATGGGATTACTTCACAGGCGCAGATGTTTGACCGCTAAGCTCTCAGCCGCTCACAGACAGAAGATTCATTTCATTCATAAAAACATCTGTGGTTATGCAAATGAGGCGGCTCCAGCACAATAAGTGGCTCGCCACACAAAAATCTCTGTCCTGCAGCTAAATTCCTTCTGTTTTTGGTACAGAAATGGCACTGTGTAGAGGAGGTCAGCGGGAAGTGGCGTTTGCAGAAGTGTAAGGGTTCTCTGAAGGAGGGATCTAAAAAGAGGACGAGGAGTTTGCGATCACGAAGCTACGACAACCGTGAGAAAGACTGCCATTGTGGTGAACGGCCTTACAAAGCAGCCAAAGCAGCA[C/T]GACGGGCACACAGACAATTCGGACAGAGCAGTAACCCACGTAAGTATGGTTGTGTCCCAAATAACACTATATACTCTTATATGTTTATGCACTCAAACATTTTGTATAAGAGTTTAGTGTCATCTCAAATGGAACTCTAACATTTTGTTTTGCGGAAAATTTAAATGGAAATTCACAATCGATGTTTAACAGTGGCAAATTAGTTAAATAAGAGACCAAATTACCAAATACCTGTCAGGAGTATAACCACATTCATTGTTGATAGCGGCATTTTCATTTACGTAGGAGAATTTTGCTTGCACAATCCAAAATAAAGTAATCCAACCTCAGTGCTTGATAGCTCCTGCCCTTCCGCTATGTGAGCAAAGCTGCAAACATGTGCATGAAGTGTTTTTCAGTTGAATAAATTGCATGATGGGAGTATTTAAATGAGCTTGTTTCTTTTCTTTTAAAATTTTCAGTGTAAACACACTACTTATGTTATTTACACTACAAAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa199
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 |
---|---|---|---|---|---|
ENSDART00000027022 | Nonsense | 569 | 874 | 12 | 20 |
ENSDART00000056080 | Nonsense | 569 | 892 | 12 | 21 |
ENSDART00000056081 | Nonsense | 569 | 1099 | 12 | 19 |
ENSDART00000137175 | None | None | 118 | None | 4 |
ENSDART00000140379 | Nonsense | 569 | 874 | 11 | 19 |
ENSDART00000142830 | Nonsense | 569 | 892 | 11 | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20123653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19429807 |
GRCz11 | 24 | 19574226 |
KASP Assay ID:
554-0110.1 (used for ordering genotyping assays)
KASP Sequence:
AAATCTATGACGTTGATCTGCAGGCTGATGATAAAACGCCACTCGAGCCT[C/T]GACCAATCAGCAAGCGCCACTATGAGCCAGAGCCAGGTTTTGATTCGGAC
Long Flanking Sequence:
TTCTGTTGTATGTCGCTGCAAAAAAAGCTAGCGATTTGTCTATGTTTTGAATTTCTGTCCAGAAGAGGTCATGTTTTGATCCTAGATTGGTCTAACGCAGTCAAGTGATGCGATTTTACCAAGCTTGAACTTCACCATGTTTCAAGATAAATTCACCAAGCTTGAACTTTGCACTGCATCAACCTGCGAAACTTGCCACATGACCTTGCGTTTTCGGTCTGATGCGTTCGTGTGCGTATGAATGGAAGTCTATGGGGTTGTGACTGCAGCTTAAGTGTGCTGAAGCAGGGTTGAAACTAAACTGTGCAGGGCTGCGGCACCCCTGCTTTTTAGCTATGGATCATAAACATTGAAATATGTGCAGCTTACACTGATGTCCTCCCTCAGGATACAGACCTCGTTTTGTGCACACACGGCCAGCCAGATCCCTGTCAGTCGAGTTTGAGGGGGAAATCTATGACGTTGATCTGCAGGCTGATGATAAAACGCCACTCGAGCCT[C/T]GACCAATCAGCAAGCGCCACTATGAGCCAGAGCCAGGTTTTGATTCGGACTTTGGGTTGGAGTCTGATGACGGATCCGAGGAGATGCAGTCAGATGACACAAATGCTGTGGGGTACCCGAATTCTCTCAAAGTCACCCACAAGTAAGCCTCGAAGCATAATCTTTATTTTATTGTTATTAAAAAAAATGTGTTAGAACCAATATCCAAAATCCACTTGCAGCCAATCAGCAGTAGGGGTGTGTCTTGTAATTAGAGTTGAGAAATCAAAAAGGGGCGTGATTTTAAGTTATGGGCGTGTTTATTTTTGTGCCTTCCGATATCAGAAACTGTATAAAGACATAAAGAATACAATAAATGAATAAAATCGTTTTACATGATTTTCATATAGGATAAACAGGAAAAAAGAGAACTAATTTTAATATAATTAAACAAAAATAATTTAAATGAGGCTGCATGAAAAATCTCATCATATTTCTTCAAAAAAGAAACACATTTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37867
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027022 | Essential Splice Site | 853 | 874 | 19 | 20 |
ENSDART00000056080 | Essential Splice Site | 853 | 892 | 19 | 21 |
ENSDART00000056081 | None | None | 1099 | None | 19 |
ENSDART00000137175 | Essential Splice Site | 89 | 118 | 3 | 4 |
ENSDART00000140379 | Essential Splice Site | 853 | 874 | 18 | 19 |
ENSDART00000142830 | Essential Splice Site | 853 | 892 | 18 | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20132577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19438731 |
GRCz11 | 24 | 19583150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAATCGCAAAAGACATTAAACATTTGAATTGCTCTTATTTTCCTGATC[A/G]GGAAGTAAAGATGGAGGAAGCTATGATCAACACAGGTATCCATACTTTTT
Long Flanking Sequence:
CAACAAGAGTCTAATGTTGATTTTTATCCAAAATGGTTTTTATTTTCAATGAACTATTCCTTTAAAGGTGTCCACACTTGTACACATCCCTACAGTACTCATGTTTATGTTGATCGAATTAAGAAAGGCATACAAAGTAGTATTTTCCACTTAGTAATGAAACAAAACATTACAAAAAACAGATGCATGTCAATTAGTCTGCATGTTGGTGTATTTTCATGTTATTTGCAACTTCAACACTGTTAACATAATCCCATCATGTAACATTCATTCCATTTTTAACACTACACTTCTGTACCAGCTTTTTCTTCAGGAGCATCAGAGGATATTTCCTCATTCATCTTTCACGTCATCATTTCTTCATTGTTTCTTTAATCTAACAATACCTCTCTTCAGGAGTTGGGGGTTATGCATGAAGAACTGCAATGATTTTGTTTGTTTATTATTTTTTTAAATCGCAAAAGACATTAAACATTTGAATTGCTCTTATTTTCCTGATC[A/G]GGAAGTAAAGATGGAGGAAGCTATGATCAACACAGGTATCCATACTTTTTGAATCCCTCATTGGCTTTTGAAATAACTGCATGGGCAGCTTGTTTTCACTAATATGCCATGTTTCATTGAGCTAAGTTTGTGTGATTGCATGCTGGGTTAAGCTAACAATTTAAGTATGTTTAAAAATCACATTAAAAAACTAGCTATTAAAACCCCAAATTCATTCATTCATCTAATTTTAACTCCCATTTGACTGCTTGTTGTTGTTCATTAAATTAATGTATTCATTCTGTAGGTGTAACTTAAACTGGAATTATTTAGAAAAAAAAAATAAGTAAAAAAAAATTAAGGGCCAGATTTACTAAACAGGGAAAAATAGCATGAAATCCCATAAAATCACAAACGTGAGTGAAAGTTTTTTTTTTTTTTTTTTTTTTTTTTCTGATGATCAACTTATTATGTGCAAAACACAGTTCATTTTCATAATGATCAACACAAATTAGAGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11702
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 |
---|---|---|---|---|---|
ENSDART00000027022 | None | None | 874 | 20 | 20 |
ENSDART00000056080 | None | None | 892 | 21 | 21 |
ENSDART00000056081 | Nonsense | 1002 | 1099 | 19 | 19 |
ENSDART00000137175 | None | None | 118 | None | 4 |
ENSDART00000140379 | None | None | 874 | None | 19 |
ENSDART00000142830 | None | None | 892 | None | 20 |
The following transcripts of ENSDARG00000038428 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 20135720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 19441874 |
GRCz11 | 24 | 19586293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCCCCCTTCCACGCGGAGACACCTGGKTTCATCAGCTGGAAAATGAGT[T/A]GGGCGATGATGGATTGACGTTTAGTGGCAATGGCGTCACTGAACTAGAGA
Long Flanking Sequence:
GCGCAGCAGTCATCAGCCCTTACTGACTTTTCCCCGCTTCTCCCGTTTCTCAGAACACAGCCAACCTGGGACGTCCACAAAGGTTAAGCTGCCCAATTTCACAGAGGACGTCGACTGGCAAGGACTGGCAGATTTGTACAGCATGAACGAGAGTCTGTACGAACACAGACACAACTACAGTCCCGTTCTGGATGACTGGATGAACTTTTGGAAGGATGTAGATAGTATGTTTGCACTGCTGAGAAATTTAAAGACACTCAACCAAACCGATAAGCTTGATCCCCTGGTAGAGCTGGGTTCCGGGGTCCTGGAGGAAGCCAGTGGAGCTGGATCCCTCATCCTAGAGAACCTCGCAACCGCAGGTCCCTCAGTAGACCTGACCCCAAGAACATTTCAAGAAAGTCACCTCAAGTCTCTTAATGAACTCCCGGAAGGCCGCCCGACAAAAGTGAGCCCCCTTCCACGCGGAGACACCTGGGTTCATCAGCTGGAAAATGAGT[T/A]GGGCGATGATGGATTGACGTTTAGTGGCAATGGCGTCACTGAACTAGAGACCCGCCATGACTTTGTGTTGCGCAGCTCTAAAATGCTGGATCTCCACCAGCAGGAAGAAGAGGAGGACATTTTTCAGGCCCAGGGTTACCTTCCCGTATCGCCCCAACCAGAGCCTGCTGAGGAAACTCCTCCAGCCCAGAGCGACCGACCACAGGAGAGGTGGAACTTTAGCATCAAATCCTTTACCCATAAGCCCAGGGACATTCAAGACTCAGAGGGTAGTGCCTCAGGCCTGTCCCATTGAGAAAGGACTGCTGCCATGCACTGTGAAGCCAGCCAACTCAGAGACACTAACCCCACAGAGCATGGACTGCTCTCCTGTATAATCCGATGAATTATTTTATTTTTTACAGGTGCTTCCATTTATTAGAAATCAGTGTTATGTATTTTGTAAAAAAAAAAAGAAAATCTATATATAAATATAAAAATGTAGAGGTAAAGTATCGGAT
Associated Phenotype:
Not determined