ZMP
ndst2
Ensembl 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 |
---|---|---|---|
sa13344 | Nonsense | Available for shipment | Available now |
sa31891 | Nonsense | Available for shipment | Available now |
sa35347 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9179 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27994 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9867 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13344
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085743 | Nonsense | 124 | 894 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 36005693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35216202 |
GRCz11 | 12 | 35317265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAAGARATTGTTGCCATTTTAGAGTCAAGCCGATTTCATTATCGCACT[G/T]AAATTGCACCGGGTAAAGGAGACATGCCRCCTCTGGCTTGGCGAGGCCGT
Long Flanking Sequence:
GATTCAGTGATCGTTTCCTGGCAGGGCAACTCCATTCCCATCTAATCCCTGCTCTCTTTTATTTCTACCTCCCTTCCAGAGTGAGGCGCCACCCTCTCTCTGTCCCTACCACCTGCTTTGCCAAGACAGCTATGGCTGGAGTAAGAAAGTTGGCGCGAGTCATCAGGCACCAAGGTCTCCATCGCCTGATCCTTGCACTCATCCTCTTCTGTCTGCTTTCTATGGCCTACCTAGCTTATCATGTCAGTGCTGGACACAAGATCAAGGAAGCCCCTCTGCCGCTGCCCCTAGGAGACTGTGTAGCTTCATCAGTCATTGGTGGTGGGCAAAGGACTCCACTGTTCCTGCCATCACAGATCAGCCAGCGCCGACACTCAGCAAAGACGGTGGACACCTCTCGGACAGAGCCTGTGGTCTTACTCTTTGTGGAAAGCATCTACTCACAACTCGGACAAGAAATTGTTGCCATTTTAGAGTCAAGCCGATTTCATTATCGCACT[G/T]AAATTGCACCGGGTAAAGGAGACATGCCACCTCTGGCTTGGCGAGGCCGTGGCCGATACTCACTCATCATCTATGAGAACCTGCTCAAGTATGTCAACTTGGACTCGTGGAACCGCCAGTTGCTGGATAAATACTGCCAAGACTATGGAGTGGGAATCATTGGCTTTTATAGGGCGAATGAAAACTCTCCATCCAGTGCTCAGCTCCGAGGCTTCCCCCTGTTCTTGCGTTCAAACTTGCCACTTTGGGATTACCGAGTCAGCCCTGCCGCACCGCTGCTCTACATCACCAAACCTAATGAGCTGGAGCCGGGCCCTCTACCTGCAGATAACTGGACCACCTTCCTCTCCAACCACAGCACGTATGAGCCTGTGCTGCTAGCGAGCCCCAAGCCTGCAGAAGCCAATCAGCTCCCAACACACTCACACCAACAGAGAGCACTGCTGGCTACGGTTGTGCAGGATTTAGGTCTTCACGATGGGATCCAGCGGGTGTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31891
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 |
---|---|---|---|---|---|
ENSDART00000085743 | Nonsense | 142 | 894 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 36005639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35216256 |
GRCz11 | 12 | 35317319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCACCGGGTAAAGGAGACATGCCACCTCTGGCTTGGCGAGGCCGTGGC[C/T]GATACTCACTCATCATCTATGAGAACCTGCTCAAGTATGTCAACTTGGAC
Long Flanking Sequence:
TCTTTTATTTCTACCTCCCTTCCAGAGTGAGGCGCCACCCTCTCTCTGTCCCTACCACCTGCTTTGCCAAGACAGCTATGGCTGGAGTAAGAAAGTTGGCGCGAGTCATCAGGCACCAAGGTCTCCATCGCCTGATCCTTGCACTCATCCTCTTCTGTCTGCTTTCTATGGCCTACCTAGCTTATCATGTCAGTGCTGGACACAAGATCAAGGAAGCCCCTCTGCCGCTGCCCCTAGGAGACTGTGTAGCTTCATCAGTCATTGGTGGTGGGCAAAGGACTCCACTGTTCCTGCCATCACAGATCAGCCAGCGCCGACACTCAGCAAAGACGGTGGACACCTCTCGGACAGAGCCTGTGGTCTTACTCTTTGTGGAAAGCATCTACTCACAACTCGGACAAGAAATTGTTGCCATTTTAGAGTCAAGCCGATTTCATTATCGCACTGAAATTGCACCGGGTAAAGGAGACATGCCACCTCTGGCTTGGCGAGGCCGTGGC[C/T]GATACTCACTCATCATCTATGAGAACCTGCTCAAGTATGTCAACTTGGACTCGTGGAACCGCCAGTTGCTGGATAAATACTGCCAAGACTATGGAGTGGGAATCATTGGCTTTTATAGGGCGAATGAAAACTCTCCATCCAGTGCTCAGCTCCGAGGCTTCCCCCTGTTCTTGCGTTCAAACTTGCCACTTTGGGATTACCGAGTCAGCCCTGCCGCACCGCTGCTCTACATCACCAAACCTAATGAGCTGGAGCCGGGCCCTCTACCTGCAGATAACTGGACCACCTTCCTCTCCAACCACAGCACGTATGAGCCTGTGCTGCTAGCGAGCCCCAAGCCTGCAGAAGCCAATCAGCTCCCAACACACTCACACCAACAGAGAGCACTGCTGGCTACGGTTGTGCAGGATTTAGGTCTTCACGATGGGATCCAGCGGGTGTTCTTTGGTGGTAGCTTGTCTTTTTGGCTGCACAAACTGCTCTTTGTGGATGCTGTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35347
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 |
---|---|---|---|---|---|
ENSDART00000085743 | Nonsense | 394 | 894 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 36001156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35220739 |
GRCz11 | 12 | 35321802 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAAGACGAGGGTGACGACACGCTGCTACGTCACCGGCAGGAGTTTT[G/A]GTGGTTTCCGCACATGTGGAGTCACATGCAGCCTCATCTCTTCCACAACG
Long Flanking Sequence:
AGAGAGATTTTTACAAGAAGACTCAATCAAAAGAAATGAAACCTTTGTGCTCACTCCTGACACATGAAACAACAATGTTCAAGATAATCCCAAAAGAGCTATTTTGTACTGCAATGCTGGGCACATTACAAAATAACTGTTTAGCAAGATATCACTGTTACTAGCTGTGTTTTAAGTTTAAATTTCACTCACCCTTAGCTGTAGCCTAAGCTGAAATGTTCACAGTCTTTTTCCTTCTTCATCTTCCTCAAAGGCTCTGCTTCACACACAGAATAAACTTCGTTCTCTGGTTCCCAATTTCACCTTCAACTTGGGATTCTCTGGCAAGTTTTTTCATACAGGTATGATGGAGCTAACGTTGTTTGAGTTACACACATAAAAAGAGCCCATCACCTCTGCTCATTGGTGGTTGTTTTTTTCTCATTCATGTTTCTTCTCTACAGGTACAGATGAAGAAGACGAGGGTGACGACACGCTGCTACGTCACCGGCAGGAGTTTT[G/A]GTGGTTTCCGCACATGTGGAGTCACATGCAGCCTCATCTCTTCCACAACGTCAGCGTGCTGGCAGAACAAATGAGACTTAATAGACAGTTTGCACAGGTCTGCCCTGATCAAGATCACTGTCCCTGCTGCACAAATGCATCAAGAATATTTAGTTACAACTTCTTGCTTATCAAATATATTTGATTCAAATACAAACGCTAGACAAAGAGGTGTATTTTGTTAAACTAGTCATTTGAAAATACAAAACTTACAAGCAATCATTTAAGATGCAGAACAGTTGCTTTATTCTTTTTTTGTATTTAAAACTAAAAACAAACGCAGAACAAAGTAATACTGATGCATGGATCAAACATACATGGGGCTTTTAACTATTTATTTTTACTCAAAGTTGCAATAGGTGATTGTCTTTAGAAACTATTTTTGTTATGCTGGTTGTGAGTCTCTTCACATCCTGATAGCAATTATTAAGTTAAGGTTCAAATGTATTTATATGTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9179
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085743 | Nonsense | 587 | 894 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 35996993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35224902 |
GRCz11 | 12 | 35325965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTCCTGTCAGACTCGCTCAYAAATACTTCCAGATTTTCCCTGATGAG[A/T]GAGACCCCTTGTGGCAGGTTTGTGCAAGTACATTTTTGTGATTTATTATT
Long Flanking Sequence:
ACATAATCCTAAATTAGCATGAACTACTCAAATGCTGTAGAATCAAGTTCTCTTTCAAGTTACCAAAACTGTTAAGATTTCTGACCAATATGTTGTTTATGTTTTTGTACATCAGGTTCTCCCCCGGCAGACCTGTGGGCTTTTCACACACACCATCTTCTATAAGGATTATCCTGGTGGCCCTCAGGAGCTGGACAAAAGCATTCGTGGAGGGGAGCTGTTTCTCACAGTGCTGCTCAATCCGGTTAGTCTCACACCCACAGAAAACTCCTAACTCAAATGCAGTCGACGCCTACAGTAATTCTGCAATATGACAAATGTCTCTTTTTGAGTAGGTTAGTATATTCATGACTCACCTGTCTAACTATGGCAATGACCGGCTGGGTCTGTACACCTTCGAGTCGCTGGTGAGGTTTGTGCAGTGCTGGACTCACCTGCGCCTGCAGACGCTTCCTCCTGTCAGACTCGCTCACAAATACTTCCAGATTTTCCCTGATGAG[A/T]GAGACCCCTTGTGGCAGGTTTGTGCAAGTACATTTTTGTGATTTATTATTGCTGGAGCTTTTGTTATAGGGTGAATCTCGCAAATGTACTCATAAATATGGGACAAAGATGCATTTTGTTTTTATGAAAGATGAATTTTATTTTTTAAAATTAGGATGTGTCCAGTTAAATGGTCTTAATCATACAGTTTTACGTGATTTAGTCAACCATTAAAATGTATTTCTTGTTGCAATATTTATTCTATACTTTGACACTATTATTTATTATTTGTTAGCAAGAAAATAGTAAATATTATAATAGACATTATTTAAAATGTATTCAAATTTAGTTTAATCAGTCATTGTTTTATATATGTTAATAATCACAACTCATCACAACAATAAGTATGTGTGTTTGTAGTTTTTGTCAGCCCTCCCCTTTGTCTACATTTGGTACTAATACTAACATAAAAGTAAAGTCCTATACTTTAATACATTATAAATAATTATTGTTGAATTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27994
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 |
---|---|---|---|---|---|
ENSDART00000085743 | Nonsense | 726 | 894 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 35990764)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35231131 |
GRCz11 | 12 | 35332194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGAGCTGAAAATAGTTTAATCCGTCTGCCGTCTCTCTGTCTCCAGCAT[C/T]AGAGGGCTCATCAGGACCCTGTGGCGCTGAACCACACATTTGATGAGGTG
Long Flanking Sequence:
AAAGTTAGAATACATCATAATTCCTTCACCCACTTAAGCAATGTTTGTTTTTGATTTCTACAGAACAAAGTGAAAAAAAAAAAGTTTTGCATTGTGATTATTTAATCTCTGTATCTAAATACCCCAGAAAACCTCAAATAGTGCTATTCAAACCATCTTGTGAAGCTGTAGTCATATTGCAATATTTAACGCAGAAAAATAAAGTATCATAACAGATTTTTTTTCCAAAATTGTGCAGCCGTTCTCCCATTGGCAATGATATAATGTACATTTAAACTCATTGCATCTTATACAGATGTCCGTCCAGAATGTTTTTATTATATGTATACAATACCACTGAACACATGCATTTTCTGTGATATAAAATGACAAATTTCAGAATCTTGACTACTAGTGAATGTACGCTAAACAACTTCCACTGAGACGTACAGGACTTATTAAGTAGCAGCACGTGAGCTGAAAATAGTTTAATCCGTCTGCCGTCTCTCTGTCTCCAGCAT[C/T]AGAGGGCTCATCAGGACCCTGTGGCGCTGAACCACACATTTGATGAGGTGGTTTCTGCTGCTCCGTCATCTCCTGCAAGCCTGCTGTCTCTGCACCGTCGCTGCCTGCAGCCTGGAGCCTACAGCAGCCATCTGGAGCGCTGGCTACACCACTACCAGCCCAGCCAGGTGTGTTTGTACGCCACTTTAATAGCTATTACTCCACTGTTATGCATACAATAGATCTGTGTGTCTTAAAAGAGTTTTTGATTGATGCAGAGACTTTGAAACATGCCAAAACAGACTATATATGAGCAGCACACACAAAGCACAAATAAAAGCTGACTTTTTGTGTTTACCCTAATTTTACATCTATTTCCTAAAGCAGAAAGCAGGCAAAATAATGTTAAAATGTAACTTTTTCCTATAACTGCAGTGCTGAATTTTCAGCAGGAATTACTTTAATGTCTTTTAATAATCTTTCATGATGAAAAGGGAAGAGCTGCTTATTTTTTTTAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9867
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 |
---|---|---|---|---|---|
ENSDART00000085743 | Nonsense | 847 | 894 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 35985226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 35236669 |
GRCz11 | 12 | 35337732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAGAGGCAGGACGCTCTCGCTGTCTGGGAAAAAGCAAAGGAAGGAAATA[T/A]CCCGACATGAGCCTTGAGGTACAWCTCACTTCTCAGCATCAGATCTCCAG
Long Flanking Sequence:
AACATTATTTAACATGCAAATGGTTCTGAACATGCTTATGATGACTGAAGAACTTCCAGTCACACAATGTATATCAGACATTGAGTCTGTAAAAAGTTTCTTTCACACACTGATCTTTTTGCTTCATATTACTTCAAGGTATTATCAGTAATTTAGTTTTCCCTGTGCATGTTTGTTTGACTCTCAAGCTGACTTTTAGCAGCAATTAGTGAAGTATTAAGCTAATGTTCTACTGAAGAAAAAGTCAATCACATCTTGACCTCAGAGTCAGTGTGCAATTATTTTACAACCACTTGTTGTTTTGTTATATAATGTCGTTAAATGAATGCAACTTTATTCTTTTAATGCAGAAATGTTATTCCTTAAAAAAATGCATTATTACTATTATAGAAGTAACCTCTGCTCTCTATTTAAAGGTTTGATGAGAGTAAAGGTTTCTGGTGTCAGAAACTAGAGGCAGGACGCTCTCGCTGTCTGGGAAAAAGCAAAGGAAGGAAATA[T/A]CCCGACATGAGCCTTGAGGTACATCTCACTTCTCAGCATCAGATCTCCAGATATGAATAGCATTTCAGATATAGCAAGTGAAATTTGAGTAATCTTTTCCTCTCTGTAATTGATTGCACATTTGAGAAAGCTGTTTTAATCTCTATGTTGTGTTTGAAATCAAGTGAGAATAGAGAAAAATAGATTAAAGTGCAGTTAAAACTGTTCACTGATCAGTTAGTTGCAGCATTAGGTCACATCATGACCAGTCTAATAAACACTAAAACAAGTTTTTCCTGGGTGATTAGAATTTTCTTTTTAATTTTTAATTGTTTTTATTTATACGCTTTTTCAATATAATTGAATAATAGCCGTCTCTGACACTTTAGAGAAATATAAATCCTCAGAAACTTTTTTTTTTTTCTTGTTTTTGGTAAAATGGTTGAAATTGCGATAATAATTGTACAAAATGTAAAACGTGTTGTTGGTATCCACATTTCATCTTTTGTTATTTCTTTTTG
Associated Phenotype:
Not determined