ZMP
nt5c2a
Ensembl ID:
ZFIN ID:
Description:
5'-nucleotidase, cytosolic IIa [Source:RefSeq peptide;Acc:NP_958830]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35506 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5861 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17723 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35506
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 |
---|---|---|---|---|---|
ENSDART00000057574 | Nonsense | 225 | 403 | 9 | 18 |
ENSDART00000122754 | Nonsense | 225 | 551 | 9 | 18 |
ENSDART00000128370 | Nonsense | 227 | 563 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 28886822)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28532770 |
GRCz11 | 13 | 28663220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTCAGGGCTCACTAAAGGAGAAAACGGTTGAAAACCTAGAGAAATA[T/A]GTGGTGAAAGATGTAAGCCAACCAGATTGTTGTGTAGACGTGAGCTGTAT
Long Flanking Sequence:
CCCTAATATATATATATATATATATATATATATATATATATATATATATAAAGATAATATCTGTAGTTTATGTATGAGCTCACATTATATGTGTTTGTGTTTTTTTAGAGACATATCTATTTGCCTGCCTGGTGGACTTCTTCACTAGTTGCTCAAGATACACCAGGTCTTTTTTCTGCTCTCATTTTATCTCCTATGTAACTATTCTGATATATAATTATAGTAAAAGTGGTGTTTTGTGTCTTTTTATTTTCATTCCAACAGTTGTGAGATGGGCTTTAAAGATGGAGATCTTTTCATGTCTTTTAAGAGCATGTTTCAGGATGTCAGAGATGCTGTGGATTGGGTCCATTTTAAGGTAAAGGCCATTTTTACATGTTAACATACTTGATTCTTATAAAGAACTGCACTTTGTGTAAATCTTAAACTGTGGATAACCTCTTCTGTGTAATATTTCAGGGCTCACTAAAGGAGAAAACGGTTGAAAACCTAGAGAAATA[T/A]GTGGTGAAAGATGTAAGCCAACCAGATTGTTGTGTAGACGTGAGCTGTATTCCAGAAAGCAATCAAATATACATCAAATATACATTTCCAAACAATTTAGCCTAAATAAGTTTCTGGGAATAAGTTTAGTTATCTCAAAGTATGATTGCTCTGAATATACAAGACATTTTCAACAAAATACAATGTCCTAATATCCCCTAGCTGGTCATGCTTAAGTTGCAATGATTACTTGCATACCTTGAAAGTTACCCCATCCTTTAGAGCCGAATGTTTAGGTTATCTATTTAACATAACCTCTTATATCACATAACCTGCTTTCAAGAATACACTCCAAGAATTATTATGTTGCAATTTTACGTTTATTAATAATTAATTACAATGAATAGTTTACCGACATAAGTATTTTATGTTTCCATATCTTTTGTCTTTTCTTAATCTAGGCTAAATTACCATTGCTTCTAAGCCGAATGAATGAAGTTGCCAAAGTGTTTCTTGTTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5861
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 |
---|---|---|---|---|---|
ENSDART00000057574 | Nonsense | 272 | 403 | 12 | 18 |
ENSDART00000122754 | Nonsense | 272 | 551 | 12 | 18 |
ENSDART00000128370 | Nonsense | 274 | 563 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 28884953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28530901 |
GRCz11 | 13 | 28661351 |
KASP Assay ID:
554-3789.1 (used for ordering genotyping assays)
KASP Sequence:
TCACATTCACAGACATTGAAAGACTAAATCTAATATTTCTTTATTACAGT[T/A]GGGTTCTCCTCATCGACCCTGGCAGTCCTACTTTGATCTTATTCTGGTGG
Long Flanking Sequence:
TTTACATAAAGACATAAAAAAAAAAAAAAAAAAGTGTTCTAATCATTTCCTCTCTCTTTTTCAGAAAATTATGACATACTTGTTTGATTTTCCACATGGTCCAAAAGTAAGTAACCATTCTTCAGTAACATTGTTATTTTGTGTATATATATGTAAACAATTATACTGGTAGTGCCTGCATTTTTATTCGTCCCAGAACACCATTACAAATGTCAAATGAGAAAGGACAGCACACATTTTACATCAAATTTGTGTTGAAAACTTGAACCAGAAAACAAAGACAAACACCATTGTTAAGAGAAAGACCCTGAGGAATAATTTGTCATTTATGATGTATCTGTAACACCATCAGCTTTTTTTTATTTAGGAGCAAATATTTGGAAAAGAGATTAAAAAGAAAGATGAGGATTATCAGGGGCCATATAAGATCTTTTATATGTTGCAGGTTTATCACATTCACAGACATTGAAAGACTAAATCTAATATTTCTTTATTACAGT[T/A]GGGTTCTCCTCATCGACCCTGGCAGTCCTACTTTGATCTTATTCTGGTGGACGCCAGGAAGCCAATGTTTTTTGGGGAGGGCACAGTCTTGAGACAAGTGGACACGGTAAGATCTGCTTAGACTCACAAGAGTAACTTTCAGAAAAAAAAAAAATTTTATTGATTCACATTCAGCAATTTGTCTGTTCTGTAGACCACTGGGAGACTGAAGATTGGGACATATACAGGTCCCTTGCAGCATGGCATAGTATATTCTGGTGGTACGTGGTATATGCAGGTTTTTATTTATTTAATAATTGGTTACAATTCATACTGTTGACTACTGGCTTATTACCTGCCTATAATAAGATATTAACTGTTCTTTAACAGTTGCAAACCATGATCTTATTCTGCATTCCTAATCCTACCTTAACCCAACTTCTACCTTACTTACTATTAATAAACAGTTAGTTAGTAATTTATTAAGCTAGTAGTGTTAGTTAATGGTTTGTTAATACCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17723
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 |
---|---|---|---|---|---|
ENSDART00000057574 | Nonsense | 374 | 403 | 14 | 18 |
ENSDART00000122754 | Nonsense | 374 | 551 | 14 | 18 |
ENSDART00000128370 | Nonsense | 376 | 563 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 28884248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28530196 |
GRCz11 | 13 | 28660646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTGAAGTCTAAGAAGCGTCAGGGTTGGAGAACGTTCCTGGTGAKTCCT[G/T]AGCTGGCTCAGGAGCTTCACGTTTGGACTGACAAGAGCAGTAAGTATKGA
Long Flanking Sequence:
ACTGAAGATTGGGACATATACAGGTCCCTTGCAGCATGGCATAGTATATTCTGGTGGTACGTGGTATATGCAGGTTTTTATTTATTTAATAATTGGTTACAATTCATACTGTTGACTACTGGCTTATTACCTGCCTATAATAAGATATTAACTGTTCTTTAACAGTTGCAAACCATGATCTTATTCTGCATTCCTAATCCTACCTTAACCCAACTTCTACCTTACTTACTATTAATAAACAGTTAGTTAGTAATTTATTAAGCTAGTAGTGTTAGTTAATGGTTTGTTAATACCGTAAGTTGTGACCTTAATTAAAGTGTTACCAATAATTGTCTGATCTGGCTGATAGAATTTGTTTTTCCACCTCAGGTTCATCAGACATAGTTTGTGATCTGCTGGGAGCAAAAGGAAAGGACATTCTGTACATTGGTGACCACATCTTTGGAGATATCCTGAAGTCTAAGAAGCGTCAGGGTTGGAGAACGTTCCTGGTGATTCCT[G/T]AGCTGGCTCAGGAGCTTCACGTTTGGACTGACAAGAGCAGTAAGTATTGAAAGTGTTGTGTCTTGGCAAACTTGGTAGACTGTCACTGATCAAAAGGCAAAATCTTCAAAAATGTTTTTTTATAAAGATTTTTTTGTGTGCAAAGAATGGGTCAGACATTGTGACAAAGACTGTAAAACTAGCTTCCCATTATATCTGTTTTCTCCAATCCTCAAGGTTACAGGCTAATCTTCTACATATCCCAAGATTGTAAATAGCATTTCATTGCTTCCTCACCCTTGAGCTTTGTGTACTTGGGTTGATTATTATGGTGACCCTCACAACATTCCTGAACCTGATGGCTTGACCTAAGAATATTGTTCACTAATCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGGTATTGAAACAATGG
Associated Phenotype:
Not determined