ZMP
ndst2a
Ensembl ID:
ZFIN ID:
Human Orthologue:
NDST2
Human Description:
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 [Source:HGNC Symbol;Acc:7681]
Mouse Orthologue:
Ndst2
Mouse Description:
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 Gene [Source:MGI Symbol;Acc:MGI:97040]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18319 | Nonsense | Available for shipment | Available now |
sa31923 | Nonsense | Available for shipment | Available now |
sa9909 | Essential Splice Site | Available for shipment | Available now |
sa17386 | Splice Site, Nonsense | Available for shipment | Available now |
sa35466 | Nonsense | Available for shipment | Available now |
sa24930 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18319
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125149 | Nonsense | 293 | 894 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 22206299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21935637 |
GRCz11 | 13 | 22066087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCAYGATGGCATTCAAAGGGTGCTTTTYGGCAACAATCTKTCATTTTG[G/A]CTGCACAAGTTGATTTTTGTGGATGCCATAGCCTATCTGACAGGAAAAAG
Long Flanking Sequence:
AGTAAGGGTGACATGCCTACGTTGATGGAGCGGGATATTGGCCGATATGCCTTAGTCATTTATGAGAACATTCTGAAGTATGTCAACTTGGATGCTTGGAACCGTGACCTGTTGGATAAATACTGCTCAGAATTTGGCGTAGGCATTATCGGCTTCTTCAAAGCTAATGAGAACTCTCTGCTCAGTGCCCAGCTGAAGGGCTTCCCATTGTTCCTGCACTCTAATCTGGGTCTACGGGACTACCACATAAACCCTGCGGCCCCATTACTGTATATCACCAAGCCCAATGAAGTAGAGCAAGGCCTACTCCCCGGTGATGATTGGACAGTCTTTCAGTCTAACCACAGTACCTACGAACCGGTGCTCCTGGCCGTCACAAAGTCCTCTGAAGCGCTGGCCCACCTAGGCCCCCACAGAGCCCTTCATGCCACTGTAGTCCAAGACCTTGGGCTTCATGATGGCATTCAAAGGGTGCTTTTCGGCAACAATCTTTCATTTTG[G/A]CTGCACAAGTTGATTTTTGTGGATGCCATAGCCTATCTGACAGGAAAAAGACTCTGCTTGTCCTTGGAGAGATATATGCTGGTTGACGTGGATGATATATTTGTGGGAAAGGAGGGTACACGGATGAAGGTGACAGATGTGAAGGTAAGCGTCTAATCTAAATTTTTTAAAGGGATAGGCTACTAAGATATGAAAATTATGTGATGTGTAGGCATGGCCCTGATCTATAAGGCCCCACTTACACTGCCCAATTCCGATTTGTTGCCTATATCTGATTTGTTTGCCTGTCTGTTTAAACATTGTTTTAATTGTGACCCATATCCAATTCATAAGTTTAAACATGCCATACCATTTACGATGTCGCGCATGCATAAAGGCGGGTTCTACAATCTGTGCCAAACTAGCCACGATGGAAGAAATTGCCTTGTTTTTAGCTCTGCGAATATGCGAAGTGTAGTATAAGCAGTGAATGGTTTAGTCCAGATTTACCCCCACGCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31923
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125149 | Nonsense | 391 | 894 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 22218754)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21948092 |
GRCz11 | 13 | 22078542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGATGAAGGAGATGACATGCTGCTGCAGCACCGGCATGAGTTCTGGTG[G/A]TTTCCACACATGTGGAGTCACATGCAGCCTCACCTCTTTCACAATGTCAG
Long Flanking Sequence:
TTATAGCATATTAATAATGAAATCCAAAAATGATAGTATAATATTGAGAGTTTATTTTAAAATCTCGGGCCCACCTGCAGGATCCCTGAGGCCTACTAGTTGAGAATCACTGCTCTAATGAATAGAAAGTAAAAAAAAAAAAAATACAAAATTAGCATTATTTTTTTGGTTGAACTCTAAGTCATTTACTTTCTACTCTTTAATTTAATAAGTCATCTTTTAGTGAAACTTTGATTAGAATAAAAATCTACTGACCCCAGATGTTTCAATGGTATTGTTTTAGACTTTTATACATTTTCTAATCAGCAAAATTTAACCCATCTAAAATGCATTGACAAAACCAAATAGTCTTTTATGAAGCTTTTTTTCATATTTTTTTTATATATATATATTTATATTTACTGTTAAACTTCAACAAAATGCACCTGTGTATTTGCAGGTACAGAAGAGGAGGATGAAGGAGATGACATGCTGCTGCAGCACCGGCATGAGTTCTGGTG[G/A]TTTCCACACATGTGGAGTCACATGCAGCCTCACCTCTTTCACAATGTCAGCGTGTTGGCAGAGCAAATGAGACTCAACATGCAGTTTGCACAGGTTAGTTGCTACTATTGATTGAAATGCCACTAACAGTGCCGAATAAAATTACAATCCTAATGTTAACAAAAAGGTATGCCAAACACTTGCATTATTTGGTCAAACAGTTGATTCAGTTTCAAATGGCGCTCTTTTAATTCCATATCTTGAAAGGATATGCCCTTTTAATCTACAAAAGATTAAAATATTAAGCTTAGAGAGACAAAGAAATGAGTTTCTTCAATTATTTTGGTATTAGTTCATTTTCTCATTTATTTTCTTCCTACACGGAAGCACACTTTGTTCCTTCATCATTGTGTTACTATTTACAGCCATTATTGCTGCTGTCGCAGAGGTGTGGGTATCGATCCCCTGCCCCGCCAGCTTTATCTCATGTTGGTATTTCATTATAGATCTGTATTAGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9909
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125149 | Essential Splice Site | 621 | 894 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 22227088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21956426 |
GRCz11 | 13 | 22086876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGTGATCGGCTGCCCAAATTTCTGGTTGTTGGCCCACAGAAAACAGG[T/A]CAGTCTTACYATTTCCAGAYTCAAAGAMTAAAATYATTATGGATTTAAAC
Long Flanking Sequence:
ATTGTAAACATAAAGTTGGAATATTCTGAATTGATTTTGAATTTGCTTGTAGCATTTTTTTTTAAATGTGAAATCCTTTGAGCAAAAAAGCTTCTAAAACTTTTGCATCCATTATGTTATTATTATTATTTTTTTTCTGGATAATAAAATATGCTGATCTGTGTCTTTTTTTTCTTTCCATGTGATGCTGGCTTTAGTGTGTGCCCTGACAAATGTTTAAAGATTATTATATTTCTATCTTGCAAAACGTGAACTATCCCTTTAAGATATTTAAACAATTCAAAACACAACATATATTCCAGAAAATATGGTAATAATCATTTAAAAACATAATAATAAATAAATCTAAATGTACTGATTAAACAGTGGGTAAATGTTTTCTTCATCTTTCCATCCATTCAGAACCCCTGTCATGACAAGAGACATAAAGACATCTGGTCCAAAGAGAAGACCTGTGATCGGCTGCCCAAATTTCTGGTTGTTGGCCCACAGAAAACAGG[T/A]CAGTCTTACCATTTCCAGACTCAAAGAATAAAATCATTATGGATTTAAACATGAGAAGAAGTTGCTTGGTCCGAAATACCAACCATAAAGCTTTATTTCTCCCACACAGGTACCACAGCTTTGCACTCCTTCCTAACCCTTCACCCCGCCATCACCAGCAACTTCCCCAGTCCAGTCACCTTTGAGGAGATCCAGTTCTTCAACGGGCCCAATTACCACAACGGCATTGACTGGTAATACAGAGCGCACAGCTTTTTCTCTCCCAGACGATGAAGCAGACACAAACCATTACTCATAATAAATTTGTTTCACCACTCCACTTTATTATATCTTTAACACTGTCTAAGTTCCATATCGAAATCCTAATAGATCTATTACTTACAAGAGCTACAGGACATTTTAATAGCAAGACATCATTTATAGCATCTTGTAATGGAAAACTAATCCCAGTTTATTTGAAAGTAAAACCGATCTGACTGTTGCCTCTTAAAGCATATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17386
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125149 | Splice Site, Nonsense | 662 | 894 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 22227618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21956956 |
GRCz11 | 13 | 22087406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCCTCTTRAAGCATATYTGCAGTTACCGAGKGTCTTGATYTCTCGCAG[G/A]TACATGGACTTCTTTCCCTTCCCCTCAAATGTCAGCACAGACTTCATGTT
Long Flanking Sequence:
AAAATCATTATGGATTTAAACATGAGAAGAAGTTGCTTGGTCCGAAATACCAACCATAAAGCTTTATTTCTCCCACACAGGTACCACAGCTTTGCACTCCTTCCTAACCCTTCACCCCGCCATCACCAGCAACTTCCCCAGTCCAGTCACCTTTGAGGAGATCCAGTTCTTCAACGGGCCCAATTACCACAACGGCATTGACTGGTAATACAGAGCGCACAGCTTTTTCTCTCCCAGACGATGAAGCAGACACAAACCATTACTCATAATAAATTTGTTTCACCACTCCACTTTATTATATCTTTAACACTGTCTAAGTTCCATATCGAAATCCTAATAGATCTATTACTTACAAGAGCTACAGGACATTTTAATAGCAAGACATCATTTATAGCATCTTGTAATGGAAAACTAATCCCAGTTTATTTGAAAGTAAAACCGATCTGACTGTTGCCTCTTAAAGCATATCTGCAGTTACCGAGTGTCTTGATCTCTCGCAG[G/A]TACATGGACTTCTTTCCCTTCCCCTCAAATGTCAGCACAGACTTCATGTTTGAGAAAAGTGCCAACTACTTTGACTCAGAGGTGGCTCCAAATAGAGCTGCCGCCTTACTGCCCAGAGCCAAGATCATAGCAGTGCTCATCAACCCAGCTGACAGAGCTTACTCGTGGTATCAGGTACTCCACAACAGCTTTCTCTCACTTTGAGTCGTGATTGGTGTAATAGTCTAGCATTGCAATCATTTAAAGGTCCAGTTGTTAGCTATTTTTTTTTTTGAATGAAGTGGCACTCAGAAAATATCCCCATTATCTGACACAAAGCACTGAATTACATGTCTTTGTGGCAGCCGTAGATTTTTGCCTCACTTCCTTTCTGTCAGTTATTTTGTGCATGAATGCCGTAACTATAAAAGTACAGAAGGAAGTCGTTTTTTTATTTTATTGCAAGCTTTCCAGAGTTTATCGTGACTGTGAATCTGCCTTCACCCTTCTCTTTCACCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35466
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 |
---|---|---|---|---|---|
ENSDART00000125149 | Nonsense | 816 | 894 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 22231065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21960403 |
GRCz11 | 13 | 22090853 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACGGCATCCAGCGCTTTTTGGGGATCACCCCAATATTCAACTACACC[C/T]AAGCTCTTGTGTGAGTCCTGCTGTTGCTCTCATCTCCTTGCTCTATATTT
Long Flanking Sequence:
AGTGCTTTAATTACTCGCAGTCGCCTCCCTTGCCATAGTGAGCTACCGCCAAATAAGGCATATGAGATTAATGATGTCAGTACATAATAACCGGTTATTATTGTTACTGAACTGATACCCAATTGTTCGCATCTGCATTGTGGTGCAGAGGTGCGGGGTGACACCCCTATCGTCAACTCTAATCAAACACAACTGATCCAACTAATCAAGGTGTTCAATCAAGTCTACTAGACACTATTAAACAGGTGTGACTTGGAGGTGGTTGGAGATAAACTATGCAGAGCTGCGGCCCTCTAGGAATTGAGTTTGAGACCATTGCTTTAAAATAAAGTGGTATTGTTTTGCTTTTGTTATTTTAACAAAAATAAAATTGTAATTCTTGTTTGTTTTACGTACATCAGCTTCATATAGTGGATGGCACCCTGCTCCGCTCCAACCCAGTTTTGGTGATGGACGGCATCCAGCGCTTTTTGGGGATCACCCCAATATTCAACTACACC[C/T]AAGCTCTTGTGTGAGTCCTGCTGTTGCTCTCATCTCCTTGCTCTATATTTGAACACTCATTAATCTATGTAGATTTGAAAATCATCTGAACACGTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCATATAAACCTGTGTTGCAGCTTTGATGAGGGTAAAGGATTCTGGTGTCAGAGGCTGGAAGGTGGACGTCCGAAGTGTCTGGGGAAGAGTAAAGGCAGAAAATATCCTGAAATGGCCCCTGAGGTAGATGATAGGCTCATCTTGTCTCTCCTCTCTCATAAAGCATGCTCTCTCTGTCGTTCTGAGCTATGCCAGTGGCAAGGACATGCCGTTATAGATGTGTGAGAAGTGATAGGCTCGACCTCACACTGATCAGATCACCATGTGTGCTGTACATCACTGGATAGCTTTCAACTAGTGGAATATAACAATCATTATTTTTGTTGCCGACAGATTGTAACGACACAGGGTCAGCCATGACGTTTACAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24930
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 |
---|---|---|---|---|---|
ENSDART00000125149 | Nonsense | 875 | 894 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 22235009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21964347 |
GRCz11 | 13 | 22094797 |
KASP Assay ID:
554-7734.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGGAGTATTACCGGGAGCACAACCTGGAACTGCTGCGGCTGCTGAAT[C/T]GATTGGGACAGGCGTTACCCTCCTGGCTCAGAGAAGAGCTCCAGAGCACC
Long Flanking Sequence:
TGAAAGCACAAACATTCAGTACAAATAAGTAGTCTTAAATAAATAAATAAAGCAGTCCTTTAGCCTAAATATAGAGAGATGTTCAGTGTTTGCTATTTTGATAGGACTAAGACAAGACTTTTTCATTTATGTTTTTATTTATGTTTTTATTTACATTTTCGTTGTTGATTATATTTTACTATCTTATTTTATGTCTGAATTATTGTAAATGTCCAGTAGGTGGTGGGTTAAACCACAAGTGGCTATATAAATATTTGGAGGGGTTGAATTGTTTTATTTTTGGCATCAGTTGTGGCCCAGAGGAGCAGTTTGAGGAGCAGATTAAAGCAAAGGCATTACTTCATTAAAGCAAAGGCACTCAGAAATGTTCTCTGATTTGCAGGCTTTCTTAAACAGCTTTTTGTGTGTGTGTTTCTCTCTCGCTCTCTCTCTTCCAGACTCGTGCCTTCCTGACGGAGTATTACCGGGAGCACAACCTGGAACTGCTGCGGCTGCTGAAT[C/T]GATTGGGACAGGCGTTACCCTCCTGGCTCAGAGAAGAGCTCCAGAGCACCAGCTGGAGCTGAGAGGACGTCCATTATCTGAACGCCTGAAAAACACTGTCCGCTCACTACAGAGGTACCAAAACCACTCTTCAAAACCATAGTAGCAGACGAAATGACTGACGGCACAGAGTGGACTGCAAACCTCAGCCTCTCGCTGCTGCCGAGGTGCTCACATGACACGATGAAGACGAGGGAAAGCTGAGAAACGTAGTCCCTCCTCTTCTCTTAATGACAAGACCTGCGAATCAGGACCAGAATGCACTAGCGGTGTGGACAAGCATGAATTTACTGGTGACTTAAAACTAAAACACACAAAGTCTAGCCTTGCTCATCTCGTCTGAGGAATGATTGTAAAACATTGTACATTTAAAAGCGTTGTATATTTTGGGTCCGCTCGGGTGGGATTGTCGACAATAGACAGCGTTTGTGTACAGCCAGAGCTCTGTTTGAGTAGGACGT
Associated Phenotype:
Not determined