ZMP
nt5c2b
Ensembl ID:
ZFIN IDs:
Description:
cytosolic purine 5'-nucleotidase [Source:RefSeq peptide;Acc:NP_001073435]
Human Orthologue:
NT5C2
Human Description:
5'-nucleotidase, cytosolic II [Source:HGNC Symbol;Acc:8022]
Mouse Orthologue:
Nt5c2
Mouse Description:
5'-nucleotidase, cytosolic II Gene [Source:MGI Symbol;Acc:MGI:2178563]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12322 | Essential Splice Site | Available for shipment | Available now |
sa25609 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12322
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065125 | Essential Splice Site | 35 | 562 | 3 | 18 |
ENSDART00000126286 | Essential Splice Site | 35 | 562 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 31300956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31114416 |
GRCz11 | 1 | 31846984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGAAAATTGTTGCAGAAACATCTTTAACTGTTTTACTTTCTTCCCCA[G/T]AGTGTTTGTGAACAGAAGTCTGGCCATGKAAAAGATKAAATGCTTTGGCT
Long Flanking Sequence:
AATCGTAATGTGTAATAGTAAAATTTTATTATTTGTGTTTTTAAGGCCAGTGACTGATCAAGTAAGAGTTTAAATCATTCAGGCGCAAGAAATTGTATCCTTTGTAACTTTTGATAAAGATGAATTTTATTGAATTATTCATACAATCAAGACTATACACACAGTGTTATTTTGCTTTAGATTTTTACATGTCTGTGCCTGAATACTGTCTTTGCTCTGTTGTATTGATTTTTGCTTAGAATTTGTTTATTAAATTCTGTGCATGGTTCATTCCTCTACAAAATTACCCCAGTCAATCTGAAATGATTATTTCCAAATAGAGCTATTGAAATCATTTGGTGAAATTACATTTATATCGCAATATATTGCAGAAATTAATGTTAGAATTTTACAATGCCATGTAGCCCATATTTTTAAAAACAGTGTTCCTTTAAGTGTTCCTTTAAGCCTAGCAGAAAATTGTTGCAGAAACATCTTTAACTGTTTTACTTTCTTCCCCA[G/T]AGTGTTTGTGAACAGAAGTCTGGCCATGGAAAAGATTAAATGCTTTGGCTTTGACATGGATTACACTTTAGCAGGTAAGGTGTTTCTAATTTCACTGTAGATACACACTTAACTAATTACAGTTGGATGTACTCTTTGCTCCTGCAGCACAAAAACACAAAATTGCACCAATGTCTTATGTTGAGGCACCGCAAATGGAGCCAGTAACACTCTTGCTTAGAATCTCTGGGTAAACATACAGTAAGAGTCTTGGGTATATTTAGCCACGTTTTGTCTGGTTTTAGAGTTTGGAAAACTGAGGTGATGTCTGGCAAACACAGAGTGCTCCTTTATGCGATCTACACCTTAGAATTGATCTACATAAACAAGCCACCTTATTTACAGCATAATATATTTATGTCATGTAGGTCAGCCAAGAACCTGAAATAAGAGAGGGTTTGGTTCTTATGGCGCAACAGTTTAACATGGATCAGATGCATTGGGTTTCTCAAATCCCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25609
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 |
---|---|---|---|---|---|
ENSDART00000065125 | Nonsense | 532 | 562 | 18 | 18 |
ENSDART00000126286 | Nonsense | 532 | 562 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 31263401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31076861 |
GRCz11 | 1 | 31809429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACATCGACTGCAAAAGAAACCAGCTCACACGCTCCATCAGCGAAATC[A/T]AACCACCGCATCTGTTCGCTCAACCACCACAGGAAATCACACACTGCCAC
Long Flanking Sequence:
ACGTTTTAACTTTTGTAAGTTTTACAACAGAGTTGTGTGTGGGCGCATATTCCGTGTGGGCCTTCCCAGGGTTAAGCACAGTATGAAAAGCCCTTATATGTACTTATAAACCGGCCAATATCTTAATAACAGGCAGGTAATCCGCAGGTAGTTTATATTGGAAATTGTTACTCAAAATAAAGTGTAACCAAAATGTCTTGAATGTTGAATAAGGTCTTTAAAAATGTTGCTAATAAGCATGAGCGACAAACATCCCAGTCTGCGCAATGCTTTCAAAAAAACATATACTCTTGTGCTCAGTGCCTAGACCAGTTGAACGTAATTTTTACTGTCGCTGTCTCCTCTTTTCTCTTTTCCAGATGCCCCATGAGTCCACAGTAGAACACGCTCATGTAGAGACCGACACAGAGTCTCCTCTGGCCACACGTAACCGCCACTGTGTGGACTGCAAAGACATCGACTGCAAAAGAAACCAGCTCACACGCTCCATCAGCGAAATC[A/T]AACCACCGCATCTGTTCGCTCAACCACCACAGGAAATCACACACTGCCACGATGAAGACGATGATGAAGAAGAAGAGGAAGAGGAGGAGGAGTAGACGGTTTTGACCATTTGAAGGGTAAAACACGCTGGATGATAAGGAGGAGGAAATGGATGAGTTGATGTATGAAGCTGAAAACAAGTGCAGTTCACCCTAACTGACGGTTTCCTGTTAAAGATGACTAAAGAAATGAACAAAGGTTTGTTTAAAAAAAAACATTGGATGGCAATCATTTATCGCTCACTATATATTGTCATGTGATATTCATCCAGTGGAAGGGACACTTACTTTACTGTGAACTGATGGTAAAACTTGCGAGTTTACATTAGACATTCATGTATGATCATACATGCAGCATATTGGTGAAACCTTGCGTTATTTTTTTATACAACGACTCGAAAAATCAGAGTCTTGATAGGTGTTAAAGTGCGATACACATGTTTTTAAGGATGTTAGAGAAAT
Associated Phenotype:
Not determined