ZMP
pnp4b
Ensembl ID:
ZFIN ID:
Description:
purine nucleoside phosphorylase 4b [Source:RefSeq peptide;Acc:NP_991206]
Human Orthologue:
PNP
Human Description:
purine nucleoside phosphorylase [Source:HGNC Symbol;Acc:7892]
Mouse Orthologues:
Pnp, Pnp2
Mouse Descriptions:
purine-nucleoside phosphorylase 2 Gene [Source:MGI Symbol;Acc:MGI:3712328]
purine-nucleoside phosphorylase Gene [Source:MGI Symbol;Acc:MGI:97365]
purine-nucleoside phosphorylase Gene [Source:MGI Symbol;Acc:MGI:97365]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22903 | Nonsense | Available for shipment | Available now |
sa22902 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22903
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041993 | Nonsense | 16 | 304 | 2 | 6 |
ENSDART00000139588 | Nonsense | 16 | 210 | 2 | 5 |
ENSDART00000141275 | Nonsense | 16 | 225 | 2 | 5 |
The following transcripts of ENSDARG00000029230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 38237971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36878454 |
GRCz11 | 16 | 36832338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTATGATGGTTTATTTCTTTAAATTAGCTGCTGCTCGTTTGATGACTGC[A/T]AACTGACCACAGAATGGCTGCTGAGCAGGACAAGACACAGGCCGAAGATC
Long Flanking Sequence:
AAAATAGAACCAGCAATCTTCTTGCTGTGAGGCGACAGTGCTAACCACCGTGCCAAGCAAGACATTTAATTACTCTAAATAACATTCTTAAAGTAAGATGCTAAATTGGCTCACAAACTTGTTTATTGTTATTTAACGCATACTTAAAATAGGAAAAAATTAGCAAATAGTATGACACATAAACCTTATTTATAATATGTTGTGCATATTCTCTCATATATTCCTCAAGCTAAACTATAATTTTCCAAAAAATATTTCTATAGATAAATTAAACACCACCAATATTTAAAAGTTAATTAAATAACTAAAATATCACACAGAAACACAATTTCTTACATTTAAAATACCCTTTAAGAATTTATATTAATACTTTGAAATTGTTAAATTAGCAGAAAAATGGGTTGATGATCATTAAAACATCAACTATTTGAGCTGTTATCAGTGTGGTAATGTATGATGGTTTATTTCTTTAAATTAGCTGCTGCTCGTTTGATGACTGC[A/T]AACTGACCACAGAATGGCTGCTGAGCAGGACAAGACACAGGCCGAAGATCGCCGTTGTGTGTGGATCTGGACTGGGTCTCCTGGCTGACAATGTACCCAACAAACAGAGCTTCCGCTACGAAGACATTCCCAACTTCCCAGTCAGCACAGGTACAGAATACTGCATATATATATATATATATATATATATATATACATACAGTATATATATATATATATATATATATTTTTTTTTTTTTTTATTTACTTATTTACATAATAGAATATTTAACACAAATGAAAGAAACCGTTCACTTTAAATTCTTTCTTTTGGCCTTTCTTTTATCTTAACGTCTTACTTCTGGCCTCTATTTTCTATTTTCATCCTTCTTATCTTTGCTTTCATTCTGTGTCATTTATTTTTGTGTCTTCATCTTTATCATTCTATCCTTGTCACTTCTTTTGTCTTCTTTCATTTGCTTTCATTCGTCCTTTCTTTCTTTTCATCTTTCCCTCTTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22902
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041993 | Nonsense | 197 | 304 | 5 | 6 |
ENSDART00000139588 | Nonsense | 103 | 210 | 4 | 5 |
ENSDART00000141275 | Nonsense | 197 | 225 | 5 | 5 |
The following transcripts of ENSDARG00000029230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 38219927)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36860410 |
GRCz11 | 16 | 36814294 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACATCACTGCAGAGCTGGGCTACTCCAACTTTGTGCATGAGGGCGTTTA[C/A]TGTATGGTCAGTGGACCCAACTTTGAAACCATTGCTGAGGCACGCATGCT
Long Flanking Sequence:
GTGTCCTTTTGTTCTGTGTTCATTTAGAAAATGGAAAATAACGCATAAAATAATCCTTTAGTTTAATGATTTAAAAGTGATAATCCCTGTTTGTGTGAATTTTTCCAGGTCACGTTCCCAGTGCGGATCTTCAAATTAATGGGTGTGGAGACCATTATCGTAACAAACGCCTCTGGAGGACTTTGTCAGGATTTCAAAGTGGGAGACATCATGGTCATTAAGGACCATATTAACTTGCCGGGCTTTGCTGGACAGCACCCGCTGTGTGGTCCAAATGATGAACGGTACAGACAAGACAGAGAAAAAAATAAAAAGCAGAATAATGTGACAAAGTTTGAGGGAGGTTTTCACTGTCTTTTTACAGCTTATTTCATGTCTTTCTTCAGGTTTGGCATCCGGTTTCCTTGCATGTCTGATGCTTACAGCAAAGACCTCAGGAAACTAGTTATGGACATCACTGCAGAGCTGGGCTACTCCAACTTTGTGCATGAGGGCGTTTA[C/A]TGTATGGTCAGTGGACCCAACTTTGAAACCATTGCTGAGGCACGCATGCTGCACATCTTGGGGAGCGACTCTGTTGGTATGGATTGAACAAATGCTTACAAAAAGAAAAATGACGAAGGCTACAGAGCTACTGCTGTGAAAGTGTATGACCCAAATTGTTAAAACAGACCATCACTTTATATACAAGTAAACTCTTAAAACATAGTTATACTGATCAAATACTGTTACACATAATCATATAGTTTTTTTTCAGCTTTTCTTCTTAGACTTTTTGTTCCAAAATTTTAATGATGCACTGCTAATTTCATTATCCTAAAATATTAGTTGTAGTTCTGATAATTCTTTAAGAATTAATTAATCATGTTTTGCATTTCTTTAAGGTAAATGTTAGTTAATACAGCAAATGGTTTAAAACAAATTAGAATTAATTATTGAAGAGCCCCTATTGTGGGTTTTTGAAAATGACCTTCTGTGCAGTGTAACACAGCTCTGAAGTGAAG
Associated Phenotype:
Not determined