ZMP
sulf2
Ensembl ID:
ZFIN ID:
Description:
sulfatase 2 [Source:RefSeq peptide;Acc:NP_957230]
Human Orthologue:
SULF2
Human Description:
sulfatase 2 [Source:HGNC Symbol;Acc:20392]
Mouse Orthologue:
Sulf2
Mouse Description:
sulfatase 2 Gene [Source:MGI Symbol;Acc:MGI:1919293]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35085 | Nonsense | Available for shipment | Available now |
sa13794 | Nonsense | Available for shipment | Available now |
sa17565 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35085
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 |
---|---|---|---|---|---|
ENSDART00000008038 | Nonsense | 342 | 873 | 7 | 21 |
ENSDART00000131431 | None | None | 191 | None | 4 |
ENSDART00000145647 | None | None | 60 | None | 2 |
The following transcripts of ENSDARG00000018423 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25909265)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24738090 |
GRCz11 | 11 | 24975706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTTTGGGTTGGTCAAAGGCAAATCAATGCCATATGAGTTTGACATT[C/T]GAATCCCCTTCTACGTGCGAGGGCCCAACGTGGAAGCTGGTGCCATGTGA
Long Flanking Sequence:
AAGTAAACTAAGCCTGTTGTTGAGACACATTAAATGGATAACAAATTCTGTCATTATTTTTTCACCCTGTACTAGTTACAGACCTGTCCGAATTTCATTCTTCTGTTGAACAAAGAAAAATATATTCTGAAGAATGTTCAAAACTTTTAGACACTGACTTCCCTACTATTTTTCCTACTATGGAAGTCAATGGTTGTTAGTTACCAAAATATCTACTTCTGTGTTCAACAGAATAAAAAGAAACTTATAAAATGTTTTAAACCATTTATGGGTGAGTAAATATTGAGTAAATGTTCCTTTTTGTGTGAAGTGTCCCTTTAAAATAAAACAGCTTAAATTGACGTGCTTAATTATTATCTTTTTCCTGACAGGTCTACAATATGTTGGTGGAAACTGGGGAGCTGGACAACACCTACATCATTTACATGTCTGATCATGGCTATCACATTGGTCAGTTTGGGTTGGTCAAAGGCAAATCAATGCCATATGAGTTTGACATT[C/T]GAATCCCCTTCTACGTGCGAGGGCCCAACGTGGAAGCTGGTGCCATGTGAGTCCGAGATAATAACTAAACTTTACAGTGAAGTACAAAAAAAAAAAACACAGAGTTGACTGTACGTTTGTGTTCCTGCTCCAGTAATCCTCACATAGTCCTGAACACTGACCTTGCTCCTACCTTGCTGGATATGGCTGGGATTGACATTCCACAGGACATGGATGGCAAGTCCATTCTCAAGCTGTTAGAAACAGAAAGACCAGTTAACAGGTACTAAAGCACGCAAACATACACATTTAATGCTGAAAATGTGTAATTTTATCTGTCTGACTACACTGAACTGATTTTAATAACTACAATATTGCCTTCTGTACAAATACTGTATACCTATATGTTATATAAATATTAACGAATATTGCATTGCAGTTTTATGATTTTTTCTTTTTATATGAACTAACTCAAGCAAATTGATGACCCAGCAAGCAGTTTTTGTTTTTAAAATATGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13794
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 |
---|---|---|---|---|---|
ENSDART00000008038 | Nonsense | 631 | 873 | 13 | 21 |
ENSDART00000131431 | None | None | 191 | None | 4 |
ENSDART00000145647 | None | None | 60 | None | 2 |
The following transcripts of ENSDARG00000018423 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25914536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24743361 |
GRCz11 | 11 | 24980977 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTAATGAAYGACACAGTTAAATGYGATGGTGGATTATATAAATCTCTA[C/T]AAGCATGGAAAGATCACAAACTACACATTGAGCATGAGGTGAGTTCACAA
Long Flanking Sequence:
TTGATTAAATACGTATGTAATGTTAAGTTATGACACCGGTTTAATTAATCGATATACCTGTTACTGCACCTGTACTAATTCCATGTACTATTTTCCAGAACTGAAGAACAAAAAGAGTGTACCACGGAATCGCTGGGCCCGCTCTGTCCCCTATCATTTGGACTCAAATGTGTACACTTTGGACCTGGAGAAGGGCTACCGTCCCCTCAACCTCAACACCAGCCTCATGCTAGGCAGAAAGCAGGCGGTGTATGGACAGAATGAAGAATATAGCGGCATGGGGCCCACAGAAGACAACTTCAACTCCCTCACGCCACCTGCTGCTCTTAAAGTCACCTACAGGTATGGCATACATAGTCCAGTTATGCTGGATAACAATAACAATACATGCCAGTGATGGAACAGTAATTAAAACACAAAACCTCTCTGTATTTTTGTTCAGATGCTCAATACTAATGAATGACACAGTTAAATGTGATGGTGGATTATATAAATCTCTA[C/T]AAGCATGGAAAGATCACAAACTACACATTGAGCATGAGGTGAGTTCACAAAGTAAATAGCTCTCTAAGGCAACAACAATAAAAGAAACACATAATATTTTACTTTTAACTACTTTTGTTGCTGTTTAAATAGATTGAGACACTGCAAACCAAAATAAAGAACCTCAGAGAGGTTAAAGGACATCTAAAGGAGGTTCGACCAAAAGAGTGTGAATGCAACAAAAACATGTAAGTCTTTTCAAACAAAAATGAATGTATACATTCACCAAATAGTTTACCAAAAAATAAACTAGCTGTTAATTTACTCATGCTCAGGCCTTCAGTTGTGGCTTTTTTTTCTTTAGTAGAAAATTAAACACATTTTTAGCTCAAATCGTAGTCCTTGGACAATGGCTTTAGTTACTTTTAGTATCCAATAACATACAAAGGCAAAATAAAATTAATTCCTGTCACTACTGATGATACATTGAAGTCTTATTCAAAAACTGAACTATTGATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17565
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 |
---|---|---|---|---|---|
ENSDART00000008038 | Nonsense | 744 | 873 | 16 | 21 |
ENSDART00000131431 | None | None | 191 | None | 4 |
ENSDART00000145647 | None | None | 60 | None | 2 |
The following transcripts of ENSDARG00000018423 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25916876)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24745701 |
GRCz11 | 11 | 24983317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGCAGCATGCCTGGSCTCACCTGCTTCACTCAMGACAACCAGCACTGG[C/T]AGACCGCCCCCTTCTGGACAAGTACTGCATTACATGCCACAGCTCTTCTT
Long Flanking Sequence:
CCAAGGACCAGAATCTTTGTAGCTTGTTACATGACCACATACAATGTGTTAAAGTACCTACATCAATTTTACATTTCAAACACATAGGTGAATTAGAAGGATTAAATAGATGTCTGCGGTTAGGGGAGATACTTTATAAGTGTTTGCTTGATTTTTTTTCTTATATCTGACATAATTATGTTTAATTTTTTTTAAAGGTATCAGTACAGCAGCAGAGCACTGTTTAAACTCAAATCAGCCCAGACACATTCTGTCAAGTACGTCTTCGTTCATCATCTGTACATAAAGGTACATTGCTGCAATCTAACATACACACAGTTGATATTAGTGATGTGTGTTCTTTTAATCTAAGTAGAATGACCTCCAAAGATAAGAAACAGTGGCTGATGAAAGAGCAGAAGCGCAGGAAGAAGCTGAGGAAACTCCTGAAGCGTCTGCGTAATAATGACACTTGCAGCATGCCTGGGCTCACCTGCTTCACTCACGACAACCAGCACTGG[C/T]AGACCGCCCCCTTCTGGACAAGTACTGCATTACATGCCACAGCTCTTCTTTCAGATATCACATAAAAAACTATTTAAATGAGACATGACTTTTGAAATTAAAGTTGCCTTGATCTTTTTACATATAAGAGGTTTCCACTAAAACATCCTAAAAAACGTTTTAAAAGAACTTTCGCTTTGACACATCTGGTTTAAACAGGTGGTTTCCGTCACTGTACACTGAATTCAAAAGGATCTTAGTACCAGGAACAAGGAACAAATTAAGTTAAAGTCACCCTGATCTTTTGACATATACAAGTTTTTTCCATTAAAGCATTTTGGCAGTTACAAATAAAATCTTTCGCTTTGACACATCTGGTTTAAACAGGTTGTTTCTGTCACTGTACAGACTTTAGCAGGATCCCAGTATCAGGAACTAGAAACAATTTAATTAATTCATTATTTTTTAACAATGGCACATGTGCATTATTAGGACATATTACTCCAGATTGTTTTTACTCC
Associated Phenotype:
Not determined