ZMP
galns
Ensembl ID:
ZFIN IDs:
Description:
N-acetylgalactosamine-6-sulfatase [Source:RefSeq peptide;Acc:NP_001074110]
Human Orthologue:
GALNS
Human Description:
galactosamine (N-acetyl)-6-sulfate sulfatase [Source:HGNC Symbol;Acc:4122]
Mouse Orthologue:
Galns
Mouse Description:
galactosamine (N-acetyl)-6-sulfate sulfatase Gene [Source:MGI Symbol;Acc:MGI:1355303]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31602 | Essential Splice Site | Available for shipment | Available now |
sa21091 | Nonsense | Available for shipment | Available now |
sa41037 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31601 | Essential Splice Site | Available for shipment | Available now |
sa41036 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31602
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 |
---|---|---|---|---|---|
ENSDART00000073556 | Essential Splice Site | 154 | 488 | 5 | 14 |
ENSDART00000098468 | Essential Splice Site | 31 | 365 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 56882266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55317592 |
GRCz11 | 7 | 55619003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCCCGTCCCAATATACCTGTCTACAACAACTCTGAAATGAAGGGAAG[G/A]TGAGGTACAAACATAAAGCGTTTTGGGTTCTTGCCGATAACACCTTAAAG
Long Flanking Sequence:
CCTCAAGTGGTTTCAAACTTTTATGATTTTCTTAATTTTTGTGAACACAAACCAGGATTTTAAAGAAAGCTGAAAACTGGTAGCCATTGACATCCATGGTTTGTTTAATACTGCATTTTTTATCTCTCCATAGTTTTGACTGAACAGATTTCAAATGAAAGAAGATAAATTTGAAATATTTGATTGCGAATTTGTTCATTTGTGTTCTGAAGTTTAATAAGTTTCTTATGGGTTTGGAACAAAATTAAGATGAGTCAATGTGACAGAACTTTGGAGTAAAACATACCATACAGTACATGCTGCATACTGTCTTACTTGGTGACTCTTTGTTCTTCATCTCCTATACTGTATCTCAGGCACCTTGGGCACAGAACTCAATACCTACCTCTGAAACATGGCTTTGATGAATGGTTTGGTGCACCCAACTGCCATTTTGGCCCCTACAACGACAGCTCCCGTCCCAATATACCTGTCTACAACAACTCTGAAATGAAGGGAAG[G/A]TGAGGTACAAACATAAAGCGTTTTGGGTTCTTGCCGATAACACCTTAAAGGTTTTAAATGTCATCATATTTTTTAAGAGACATGCTAAGTTAACATACTTGTTTATCTTAAAAGCAATGATGCAGTTGGTTATTCTGCTTTGAAAATGTGCTTTCCGTGTCTGAATGTCTGACATTGTTTTAGTCTGTATAACCCATTTACTACAAGTTTAATATATTTCAGCACCCCAGCTTGCCTTGATGGAAAACATAGCATATTTAATTATTTTAGCTTTTATTAAGTTAGCTGAGCCTATTAAAAATCATTGGATGCAGCTCAGATTGATCTCATCTATCTGGCAACCTGTGTGGGCATTGAGTTGCAAGGAAGGGGTCAGATGAAAAAAAAACCCTCTCCAATATTAGAAATTTGGACTGCAATACCTAATCCAACCACTAGGTATCAATCTGCACCATTAAAATCTGCATTAAACAGAGGTTGCTGAGATTTATTACAGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21091
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073556 | Nonsense | 155 | 488 | 6 | 14 |
ENSDART00000098468 | Nonsense | 32 | 365 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 56879664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55314990 |
GRCz11 | 7 | 55616401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTCATTAGATCTGCGGAAAGCTGAGATGGTCTGTGTGTTTTGCAGGTA[T/G]TACGAGGAGTTTGAGATTAATGTGAAAACGGGTGAATCCAACCTCACCCA
Long Flanking Sequence:
GTTTTACGAAGTAATTTTCCTTCTTTTTTCGCACCAGCTGCAATGTAGCATCTAATTTTCTGCCCATTTGTTCCTTCCAAAACATTCATATGTGCATTCTGGGTCATTGGCTTTGGCGATAGGGCTAGTTTTGTGCTTAGCAGTGAGTTTAATCAGCATGGCGTGTTTGAGGCTGGCCAGATAAACACACACACACATACACTGACACCCCAGAGATGGCAGGTTGTGTTAGCGCTATGTTTGGACACCTGGAACAGCCGGAGCATAAGAGAGTTGCCTTTACCACTCCACGCCTCAGCACCTTCTCACAACACATGTGTGTCTTCTGAGACCCAATCTCACAATTTACCTCTTCAAATTCACTTCCAAATCACACCCTGGTGCAGCTCTTGGTTTAGGAAGCTTGTCATTTGGAACAGGAGCTCATATGGTGTTGAGTTTGTAGGGATTGTCTCATTAGATCTGCGGAAAGCTGAGATGGTCTGTGTGTTTTGCAGGTA[T/G]TACGAGGAGTTTGAGATTAATGTGAAAACGGGTGAATCCAACCTCACCCAACTCTATTTGAAGGTGAGTTTTCCTGCTCGTTGGCTTGATTAATGTTTATTTGTGTGGATCAGACATGGACAGATGCACTGCAGGATTTGCCTGATATAGGTTTTGATCCTATCTGTCTATAGGAAGGCTTGGACTTTATCTCTCAGCAAGCCATGGCCCAGAGGCCCTTCTTTCTCTACTGGGCTCCAGATGCAACCCATGCACCTGTCTACGCCTCAAAACCCTTCTTGGGAAAGAGTCAGAGGGGACGGTAGGCCAGAATTACAGTATTAAAAAGTATAAAACTGCACAGTGTAACTTTATTAGTATGTTGGAGTGGAATATTTATTGATAAATTATGATTAGCAGAATATCTATCAGTTTTGCAAAGTGGGTGCAATAAGTCATATTTTTGTGTGCCTAAATCGAATGCATAGGATGTTTATCCAACTGTAACCAATCAGATTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41037
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073556 | Essential Splice Site | 219 | 488 | 7 | 14 |
ENSDART00000098468 | Essential Splice Site | 96 | 365 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 56879362)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55314688 |
GRCz11 | 7 | 55616099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACCTGTCTACGCCTCAAAACCCTTCTTGGGAAAGAGTCAGAGGGGACG[G/A]TAGGCCAGAATTACAGTATTAAAAAGTATAAAACTGCACAGTGTAACTTT
Long Flanking Sequence:
TTCTCACAACACATGTGTGTCTTCTGAGACCCAATCTCACAATTTACCTCTTCAAATTCACTTCCAAATCACACCCTGGTGCAGCTCTTGGTTTAGGAAGCTTGTCATTTGGAACAGGAGCTCATATGGTGTTGAGTTTGTAGGGATTGTCTCATTAGATCTGCGGAAAGCTGAGATGGTCTGTGTGTTTTGCAGGTATTACGAGGAGTTTGAGATTAATGTGAAAACGGGTGAATCCAACCTCACCCAACTCTATTTGAAGGTGAGTTTTCCTGCTCGTTGGCTTGATTAATGTTTATTTGTGTGGATCAGACATGGACAGATGCACTGCAGGATTTGCCTGATATAGGTTTTGATCCTATCTGTCTATAGGAAGGCTTGGACTTTATCTCTCAGCAAGCCATGGCCCAGAGGCCCTTCTTTCTCTACTGGGCTCCAGATGCAACCCATGCACCTGTCTACGCCTCAAAACCCTTCTTGGGAAAGAGTCAGAGGGGACG[G/A]TAGGCCAGAATTACAGTATTAAAAAGTATAAAACTGCACAGTGTAACTTTATTAGTATGTTGGAGTGGAATATTTATTGATAAATTATGATTAGCAGAATATCTATCAGTTTTGCAAAGTGGGTGCAATAAGTCATATTTTTGTGTGCCTAAATCGAATGCATAGGATGTTTATCCAACTGTAACCAATCAGATTGTCGCTCACAGTCTTTTTACCCACCTCCCCAGTATAGGTGCGGTTCTGCTATTGGCTAGACTGGGTCCAGAGAGCTGAAAATAAATATTAATGGCAGGAGTAAAAAAAATCAAGTCAAGTAGAAAAATCAAGTCAAGTTTTCAGTCATTTGTCTTCTTTAAAAGTCTAAATGTTTGCACCTTGACATGTTTTTTGTTTGTTTGTTTGTTTGCTTATTTGTTTTTTGCTGGAATTAGATTTAATTTGGTCATAAAAATATTAATTATTTGTTTATTTTAGTGTTATAATTACATTTAAAAAGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31601
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 |
---|---|---|---|---|---|
ENSDART00000073556 | Essential Splice Site | 265 | 488 | 8 | 14 |
ENSDART00000098468 | Essential Splice Site | 142 | 365 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 56873343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55308669 |
GRCz11 | 7 | 55610080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTTCACCTCGGATAATGGAGCAGCACTGATGTCTGGACCACTGCAAA[G/A]TAGGAGATCTGTTCACACTTTTCCAACTCAAACATTAACACATCTAATTG
Long Flanking Sequence:
CGGCCTGGTGCTTCGGAATACTGGGGCTTCAGTAAGCATACGTTTCTTCTGAATGCTAAATGAGGTTTGTGTTGACAGAGGAATGGATCAAGGCTGAGGGGTATTAGCCAGGTGCTGGCAGTAGAGGGATTCAGCCTGACACGCCACGTCTTAAAATTTTATAACCGCTGCACATCTATCTGAGCCATCTATCTTCCCCTATATATCACATCCGTCTGTCACAGGACAGGTTTTCAAACGTGGGCTAATTTGACAGAATTTGTTATGCCGTCTGAGTTAGAGCAGCTGAACAGGTTATCTAAGGGTAATTTTCAATAGTTTGATTGCTGTGGTAAGACGCAATGTAATTTTGTTTCATAGTTATGGTGATGCAGTAATGGAGCTGGATGACAGCATTGGTCAGATTTTGGCTCATCTGGTCAGTCTGGGCATCCAAAACGACACTCTGGTGTTCTTCACCTCGGATAATGGAGCAGCACTGATGTCTGGACCACTGCAAA[G/A]TAGGAGATCTGTTCACACTTTTCCAACTCAAACATTAACACATCTAATTGTCCGTTTCCACTGAGTGGTACAGTACGGTACGGTTCGATACGGGTCACCTTTATCAGGATTGTGTTTCCACTGCCAAAAGGGAAAGTTTCAGACAACGTCATTCTCACTCAAGGACATGTCAAAGTAAAGCTGTAAAGGTCTTTCCCATTTCATATGAGAAGCTCTTCTCACAAAAAAGATGCTTTATACACATAAATACTTGTGTATAAATGTTCATTGCTAACCTATCTATGAACATAATTTGATTATAACTGCAGATCAGTAGCCTACTGTAACATCTGTGATTACATAAAATAAATAAATAAATAAATAAATGCAACATATATGAACACATACAAACCCTTACAGTCTCCAATTACAGAAAATCTACACACAGCAAACACTTAGTCCTTATTTGGGTCCAAAAACAACACGCAACATAGCCCACAGTCAGTGCAAACCTCTCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41036
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 |
---|---|---|---|---|---|
ENSDART00000073556 | Nonsense | 412 | 488 | 12 | 14 |
ENSDART00000098468 | Nonsense | 289 | 365 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 56839067)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55274393 |
GRCz11 | 7 | 55575804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACACTCAACAGGAGCACACCATGCAGCCACTCATCTTCCACCTGGGA[C/T]GAGACCCTGGAGAGAGATACCCACTCAGGTAAGTGCTGAAGAGTGGACAA
Long Flanking Sequence:
AAATAAGGACTCTATAAGGAAAATATTCCTTTTATCGCATGTCGTTGCTTTTAGTTAGAAAACGGTTCAAATCAGCCTTTGCTTGAATGTCAGGCACATTCACATCAATCTGGCTACCTGCACTTTCTTTGACTCGTCAGAGGAGGATCCGAGAGAAAATGTGTTTTGATTCAGGAGTGCAATACCTAGTTTAACCACTGGGTGTCAAACTTCTATAGTGCACCTTTAAATATGATTTCTGAAAGATCATATGACACTGGAGGCTCATTCAATCAATACTACAGTGCTCAGTTTCAACATGACAGGAAGAAATAACATTCTACCTCAAGTACTCAAGTACTAAAAAAATGTCAAACGAAACATTTCCAGTTTTGAAGATGATCATTATTCTCTTGCTTTCCAAACAGGGTATAAACTTCTGCCCTGGTCAGGAGGTTCCTGGTGTCACCACACACACTCAACAGGAGCACACCATGCAGCCACTCATCTTCCACCTGGGA[C/T]GAGACCCTGGAGAGAGATACCCACTCAGGTAAGTGCTGAAGAGTGGACAACAGCTGCCAAGAAACACACTATTTATTAACTGGTTAGTTCACTCAAAAACTTAGATTATGATTTTAGACTTAAGATTATAGCTGCGTCCCAAATGGCACACTATACACTATGCACTCATGCACTATGTACCTATGCACTTACACTTACACTTACATACATAGTACATGTATGTAGTGGCATCCCAAATGGCAAACTAATGTTTTTTTACTAAGCGGAAATTCAAACCGTTTCCCTGATGACGTTTGACGGTTGCCAAATCAGTGAAATAAACGACCGAATTATCAAATAATACCTGCTGCGAGTATTGCCGCATTCACCATCGGGAGACGCTATTATCACTCTTGTGGGAGAATTTTGCTTTCACAATCCAAAATAAATAAAGTTATTCAACATGTGCGTCCGATAGCTCTGCCCCTTCCGCTACGTAAGCAAACCTGCGGCCCTTGAGT
Associated Phenotype:
Not determined