ZMP
nprl2
Ensembl ID:
ZFIN ID:
Description:
tumor suppressor candidate 4 [Source:RefSeq peptide;Acc:NP_001039312]
Human Orthologue:
NPRL2
Human Description:
nitrogen permease regulator-like 2 (S. cerevisiae) [Source:HGNC Symbol;Acc:24969]
Mouse Orthologue:
Nprl2
Mouse Description:
nitrogen permease regulator-like 2 (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1914482]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18351 | Nonsense | Available for shipment | Available now |
sa25337 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18351
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 |
---|---|---|---|---|---|
ENSDART00000083038 | Nonsense | 26 | 379 | 1 | 11 |
The following transcripts of ENSDARG00000059613 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 24053321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20308767 |
GRCz11 | 6 | 22368989 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTATATTTTTYAGTGAATTTCATCCAACGTTAGGACCAAAGATCACATAT[C/T]AGGTAACATCACAGAAACCWGTATTTGGGAACARATGWATGTTTGGCWGC
Long Flanking Sequence:
ATTCAGGGAGAAAATATATAGGTAACTATAGGATTCATTAAGAATAGTGGATTATAAAATAGAATTTAGAAATCCAGTGTCATGACGCTACATCACAGTAAGTGGCCATATGCACCTCAAAAGTTGGTTCGCAACTCGCCATAGAACCAAGAAGAAGAACAGTAATGCTTGTTTTAGCTATGTTTATAACTTAACGAAAGACGCATGGTTAAGTCACAGAATTTAGTAGTTATATAAAAGAAAAAAATAATAATTTACTTATTTTTTGATCACAATAAGAAAATATGGGTTAGATTACTCCTGATCTGCACTCCAATCCAGATGGTGGCGGTAATTCTCAAAAAAGCTGGTTGCCAACCGCCATAAAAATTACAACAAGAAGAACAGTATTGTTTTTACATCAACAGAAAACTTTACTTAAAGAAATGGGTACTTACAGACGAATAGACTGTATATTTTTTAGTGAATTTCATCCAACGTTAGGACCAAAGATCACATAT[C/T]AGGTAACATCACAGAAACCTGTATTTGGGAACAGATGTATGTTTGGCTGCATGGCTTGCAAAAGAGCACAGTACGCTCAGCAAGATAATGTTTATCTAGTTAACTGGCTTATCACAGCAAAGTTACGTACATGACGTTTTACTGTGATCATACTTATAAATTGACAAGTCGTAATAAGTTACGACGTCGGGTGTGTTCAGGTTCCTTTTGTCGGCAAAAAATAGTGTTATGCCTACTTTTTATAGATTACAAGAAAATATAGCAGGGTTTGTTAACTTTGCTTATCGAAAAACGAAAAGCCAAGAATTCGCATCAATTGTGTTTTGTCAATGAAAATCCACAAGTGTTTACTTAATATATAGCATTATATTTCTCACTGACACGCCCCCAACTCGGAAACCGTCCATTTAATTTCACTAGTGTCATGGGCAGATGCTATGTTATATAGCATTTATATACTATGTACCAGGGATCTGGAACCTTTTTTCAGCAAAGAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25337
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 |
---|---|---|---|---|---|
ENSDART00000083038 | Essential Splice Site | 240 | 379 | 7 | 11 |
The following transcripts of ENSDARG00000059613 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 24039458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20294904 |
GRCz11 | 6 | 22355126 |
KASP Assay ID:
554-7420.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTTTTACAGGTATTATGACGTGGTAACTCTGGTATCCATATTTCAGG[T/C]ATGTTTTTTTGTTGATGTTGTTTATTCTCATTCTTGTAATGGGTTCTTTT
Long Flanking Sequence:
AAATCTTTAGGAAATATTTTTGGTACATCAAAGGGTATGGATATGATCAACAAAAAAAGCTAATCCAGCTAAAAGTAGTGCTTAAAATGTCACTAAAATGCAGAATTATACTTATCATTAAATAGAAAATCAGGCAAATAACTGCAAAAGCTCCACTTTTTGTACCACCACTTTTACCAGGCTGGCTATGGGCCTGTAATAGGGCAGAAAATATTGATAATGACTTGAAAATTTGTATTAGCTCAGTAAAGGCATGAAAAGCAGCATGAATCAGTGTTCAAAATAGACAAACATTTAAGGAATACAGTACAGAAATTTATGAATTACATGGCATGTTGCCACAATTGATTATGTGAAGCTGTTTAAAATCTTACCTATTTGATATCTCGTTATATATTAAATAGTGTAAACAATCATTCTACAGTTAAGACTTCACACTGAAGCAGTGGATCTGTTTTACAGGTATTATGACGTGGTAACTCTGGTATCCATATTTCAGG[T/C]ATGTTTTTTTGTTGATGTTGTTTATTCTCATTCTTGTAATGGGTTCTTTTTCTTACATTTTTGGTTGTCGTACTTTACAGTACTCAAATGTGTACTGCACAACACCTAAAGTGCAAAACCTAATAGATAAGAAGTGCCTTCAGGAAGAGTGTCTACATTATGTCAGTAAGCCAGGTGAGCAAGTACAAAGAGATAGTAAATGTATTTTTCTGCATCATGAGTGTATGAAAGTGAGATGTTTCTATTCACAGTGCTTATTTTGCTGTGTGTTATGTCACCAGGGCAGAGGACAAGTCTCAGGGATGTGTTCCAGTTGTACTGTGGTTTGACCCCAGGTACGACTGTACGTGACCTCTGTTCCCGCTATTCTCACCAGCTACAAAAAGTGGACGACAGGCAAGTTTGTCTCAGTCTGATTGCTGCTTTAAGATGATTGATAATCATTATTCCAAGCATTGGGCTGAGGTTCATTTTTAATTAGTTTTACAACTCGTCAATGG
Associated Phenotype:
Not determined