ZMP
nt5c3
Ensembl ID:
ZFIN ID:
Description:
Cytosolic 5'-nucleotidase 3 [Source:UniProtKB/Swiss-Prot;Acc:Q7SYN4]
Human Orthologue:
NT5C3
Human Description:
5'-nucleotidase, cytosolic III [Source:HGNC Symbol;Acc:17820]
Mouse Orthologue:
Nt5c3
Mouse Description:
5'-nucleotidase, cytosolic III Gene [Source:MGI Symbol;Acc:MGI:1927186]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39078 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42657 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36036 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12040 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39078
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081484 | Essential Splice Site | 92 | 320 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 8386615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 7306206 |
GRCz11 | 16 | 7223552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTTAAGCAGATTTGCCGTCAATGGAAAACGTTGTCCATCATGTCATAG[T/C]GAGTATGCCAAAAAAAGAGTGTATTTGCAACAAAGAATTATGCTCATATA
Long Flanking Sequence:
ATTAAAGATGAATTCAAAGAATCTTGATGAACTTTAAGAGTCCTGCAAGAACACTTTCTTTGCCACTCCAGATGACTTTATTAATAAGTTATAAGTTGTACAATACTGTACATTATTTCTGTTAAGTGACAAGACTTTTCTCTAAGCAAAGTCAGACCTTACTGTCCTAATTAAATCATTAAAAATTAAGGTATGATCATATTTTATTTTGGTCAAATAAGCGGGATCTAGAAGCCTTTGCCTTTTATATTAACCACTTCATATACCAAATGATCAGCTAGAAGTCAAGTTATTATTTGTTGTTTCTAAAACTTGGATAGGCATCAGGAAAGTTGTCAAGTAAGTATATACCAGTCTGACTACATCTAATGACCCTAAATGTGCAACTTGACTATTCTTACTGTGTTTTTTTTTTTGTACTATTTTTAGATCATCACAGATTTCGATATGACGTTAAGCAGATTTGCCGTCAATGGAAAACGTTGTCCATCATGTCATAG[T/C]GAGTATGCCAAAAAAAGAGTGTATTTGCAACAAAGAATTATGCTCATATAACACTTGCTGACATTCGTTAATCGTATTCCCTTATTCATCAGTGGAATGAACCACCTACGCAAATTTATGCATATAACAAAATATTGACTACACACAAGTATGAAATTAACTAAAGTGCATCACACAATAACAAGCACATTGTCTGTACAGATTGAATTTTAAAGCTGTGTAATCATCCTTTGCAATATTCTGAAAGAAATAGTTATAAATTAATAAATAAAGTGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAATTGGAGTAAGTTACTTAAAATAGTTTTGTTAAACTTTGCAGGTTAGTATTATTAATATTTTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42657
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081484 | Nonsense | 144 | 320 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 8384708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 7304299 |
GRCz11 | 16 | 7221645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAATTTTTTTCTTCTTCTTCTTCAGGTATTTTAAGTCTCACACATTAT[T/A]GGTTGAACAGAGATTGGAAAAAGACAAACTTCCAGAGGCCGTCAGAGAGT
Long Flanking Sequence:
TTGTGAAATATTTGAAAAAGAAAAGGAAAAAAAATCACAGGAGGGCGAATAATGTCCACTTTAACTGTATATATGTGTCCAATAAAAACTTGGGGGTTCAGTGATCACTACGTTTTGCTTTCACAGATATCATTGACAACTCAAAACTGGTGACAGACGATTGTAGGAAGAAGGTATCTGATTTTCTTGATTTCCTTAAATCTGTTGTGAGCTTTTACAAATATATAATAAAAATTTGATTTCAAATAAAAATATTTAAATAGTAATTTTTTTTTTCAGCTGGTCCACCTAAAGGAAACGTATTATCCCATAGAGATAGACCCTCATCTGACAATGGAGGAGAAATATCCATTTATGGTGGAGTGGTGAGTGTCCATGTGCACAAACTCTCATAATATGAATTGATCTTTCAAAATATGTTAAATAAATATATTATATAATAATATATAAATAAATTTTTTTCTTCTTCTTCTTCAGGTATTTTAAGTCTCACACATTAT[T/A]GGTTGAACAGAGATTGGAAAAAGACAAACTTCCAGAGGCCGTCAGAGAGTCGGACGTCAGTCTAAAGTACAAACATTTTACCTTTTTATCCAACCTTTTACTGTGAACACTAAATCAAGGGCATTATAAAGATAAATGTAGTTAATCGGCTGGTAGTTACACATCTTTGATGACAAATTGATAATATAATTTAGTTTAAACCTTAATTTCTCTTTGTTTTTATAACATGGTACAAGTTTCAAACTCTAAAAGCCTTCATGCTTGTGGTTGCCAGATGTCAAGAGATTCCCCACACTTTTCTTATTCTGCAGTGTGGAAGTCTACTTGTTCTTGCGATTTGTTTTAAAACTTCAGATTTAAAATTACCTGCTCTTCAGTTTGTATCCATACATATAAAGTAGTACTTAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTATATGTATGTGTATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36036
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081484 | Essential Splice Site | 220 | 320 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 8383173)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 7302764 |
GRCz11 | 16 | 7220110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCCCAACGTCAAAGTTGTGTCCAACTTCATGGACTTTGATGACAATG[T/C]GAGCCTCAACCCCTTTATAAATGCCATTGGTTCTCGTTATTCTCAAACAC
Long Flanking Sequence:
ATATGTGTATATATATATGTGTATATATATATGTGTATATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATGTATATATATATATATATATATATGTGTGTATGTATGTATGTATATGTATGTATGTATGTATGTATGTATGTATGTATGTATATGTATGTATGTATATGTATGTATATAAGAGTAAAAGTCCCAGACATCATTATACCTGACACAGCTAAAACATGTTGTTTTTCCCAGATATGTAATACCAGATCTGATTTTTAGCGTGTGTTTGTTTGTGACAGGGAAGGTTACGAGCAGTTCTTTGACCGGCTGCATCAGCACAGCGTTCCCGTGTTCATCTTTTCGGCGGGTCTGGGGGATGTGCTGGAGGAGATCATCAGACAAGCTGGCGTCTACCACCCCAACGTCAAAGTTGTGTCCAACTTCATGGACTTTGATGACAATG[T/C]GAGCCTCAACCCCTTTATAAATGCCATTGGTTCTCGTTATTCTCAAACACTGCTTCAGTTTTGCATCTGGTGTTCAGGATTGTGTGTATGGTCTTGCAGGGGGTTCTGAAAGGCTTTAAAGGAGAGCTGATCCATGTTTACAACAAGCATGACGGTGCTTTGAGGAACACGGAGTACTTCAAACAGCTGAAGGACAATGGAAACATTATTCTGCTAGGAGACTCGCTCGGGGATCTCACCATGGCAGATGGTGTCCCCAACGTGGAGAACATCCTCAAGATCGGCTATCTCAATGATAAGGTACTTTTTTTTTTTCTTACCACTACCCAAAATAGGACCGTTTGTTTGTAGAGCTTTAGTGAAAACTTTTTCCATAAATCGATTTTCAATTGAGTCTGTTATTAGTTTTCAACAGCAGATGGCACTATAGGCTATTGTATAAGAGCAGATGACGCTCTAGGCTAGTGTTGATGGCACTCTAGGGTGTTTTTTCAGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12040
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 |
---|---|---|---|---|---|
ENSDART00000081484 | Nonsense | 241 | 320 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 8383012)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 7302603 |
GRCz11 | 16 | 7219949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCTTTAAAGGAGAGCTGATCCATGTTTACAACAAGCATGACGGTGCTT[T/A]GAGGAACACGGAGYACTTCAAACAGCTGAAGGACAATGGAAACATTATTC
Long Flanking Sequence:
TATATGTATGTATGTATGTATGTATGTATGTATGTATGTATATGTATGTATGTATATGTATGTATATAAGAGTAAAAGTCCCAGACATCATTATACCTGACACAGCTAAAACATGTTGTTTTTCCCAGATATGTAATACCAGATCTGATTTTTAGCGTGTGTTTGTTTGTGACAGGGAAGGTTACGAGCAGTTCTTTGACCGGCTGCATCAGCACAGCGTTCCCGTGTTCATCTTTTCGGCGGGTCTGGGGGATGTGCTGGAGGAGATCATCAGACAAGCTGGCGTCTACCACCCCAACGTCAAAGTTGTGTCCAACTTCATGGACTTTGATGACAATGTGAGCCTCAACCCCTTTATAAATGCCATTGGTTCTCGTTATTCTCAAACACTGCTTCAGTTTTGCATCTGGTGTTCAGGATTGTGTGTATGGTCTTGCAGGGGGTTCTGAAAGGCTTTAAAGGAGAGCTGATCCATGTTTACAACAAGCATGACGGTGCTT[T/A]GAGGAACACGGAGTACTTCAAACAGCTGAAGGACAATGGAAACATTATTCTGCTAGGAGACTCGCTCGGGGATCTCACCATGGCAGATGGTGTCCCCAACGTGGAGAACATCCTCAAGATCGGCTATCTCAATGATAAGGTACTTTTTTTTTTTCTTACCACTACCCAAAATAGGACCGTTTGTTTGTAGAGCTTTAGTGAAAACTTTTTCCATAAATCGATTTTCAATTGAGTCTGTTATTAGTTTTCAACAGCAGATGGCACTATAGGCTATTGTATAAGAGCAGATGACGCTCTAGGCTAGTGTTGATGGCACTCTAGGGTGTTTTTTCAGCAGTGGAGGGCACTCTAGGCTTGTTTTTAAAAGCAGACAGTGCTCTGACAGTTTTTTCACATAATATGGTGCTCTAGGCTAGTTTTAAACAGCAGACAGTGCAGACACACTCTAGGCTAGTTTTTTAACAGCCAATGGCACTCAAGATGCCGCGGCCGGCTAGTTT
Associated Phenotype:
Not determined