ZMP
phpt1
Ensembl ID:
ZFIN ID:
Description:
14 kDa phosphohistidine phosphatase [Source:RefSeq peptide;Acc:NP_001003566]
Human Orthologue:
PHPT1
Human Description:
phosphohistidine phosphatase 1 [Source:HGNC Symbol;Acc:30033]
Mouse Orthologue:
Phpt1
Mouse Description:
phosphohistidine phosphatase 1 Gene [Source:MGI Symbol;Acc:MGI:1922704]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23890 | Essential Splice Site | Available for shipment | Available now |
sa13227 | Missense, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23890
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067004 | Essential Splice Site | 49 | 121 | 1 | 3 |
ENSDART00000130436 | None | None | 108 | None | 2 |
ENSDART00000134278 | Essential Splice Site | 49 | 146 | 1 | 4 |
ENSDART00000143100 | None | None | 96 | None | 4 |
ENSDART00000067004 | Essential Splice Site | 49 | 121 | None | 3 |
ENSDART00000130436 | None | None | 108 | None | 2 |
ENSDART00000134278 | Essential Splice Site | 49 | 146 | None | 4 |
ENSDART00000143100 | None | None | 96 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 13017838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 14719012 |
GRCz11 | 21 | 14815741 |
KASP Assay ID:
2261-5395.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTCATATGTTGATATAGTGAGAGGATACGCGTGGGCCGAATATCACGG[T/C]AAGATCCATTCATGTGTATGAGCCATGAATTACAGCTGATAGATAACCGT
Long Flanking Sequence:
GTAAGTGATAATATTTCAGGGGAAGTTTCTGGTCTTCGGTTTTAACTTACCATTTCACAATTTAAGGTCCTAATAAGTACTTAAATCCGAGCAGAAAGTCTTAAATTCATAACTTCGTGACTTAAATGTTGCTTAAACTGCAATTTTCATAAGAATAGTTTAGCAAACAAACAAAAATAAACGTACCAGTTTGGAGAGAAGTTTTGAGTATGCCGTACTTGCTCCAAACCGGAGGGTGTCGCTAATGTGAACACGTGTGTTCAATTCAACACGGTAAATGAAGCTCTTTTCTTCTGGCGCTGGATTGAACTTCGCTGTTGTGTTTGGGGTTTTTTTACGGTCGCTTTTGCAATAATGTCAGCGGAACGTCTCGCTAAAATTCCAGAGGTGGATTTAGACCCCAACGGCGTCTTTAAATACGTCCTCATTCGCGTTCATAGCAAAGACGACGATTCATATGTTGATATAGTGAGAGGATACGCGTGGGCCGAATATCACGG[T/C]AAGATCCATTCATGTGTATGAGCCATGAATTACAGCTGATAGATAACCGTGAGCACTGAAATTAACACTTGTGGCATTAACAGTAGTTAAATATGTCAGAAAATGCCCCCAAAAATTATTATGGCTATATCTTAATTACAGCTGTCTTGTTTTTGGGCTTATTTTTTCTGCCATAAATTCAGTACAAGCGTCTCGTGAAAATTAACCACCGTTTTACTGCAAAGAGAACCCAAACTTCAACGTAAAATTCATAACCACACATTTATTAAAGTTTAACTATTATGTTTTTTAGTAAACCCGCAGTAAGCTACAACTCGTGATCCATACTCTCCACTAAAAGCATGTTTGATGTTACTTCAGTTTTCTGCGATAAAAAAAAACATAAATTTTAAGTGTTGTGTGTTACTTGAAAGTTTTTTTTTTGCCCTTCAAAAACATAATTTTTAGGCAAAAACTGAACTCCAATCTTTCACAAACTGACTGAGAAATGTCAGATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13227
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067004 | None | None | 121 | None | 3 |
ENSDART00000130436 | Nonsense | 4 | 108 | 1 | 2 |
ENSDART00000134278 | None | None | 146 | None | 4 |
ENSDART00000143100 | Missense | 39 | 96 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 13009262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 14710436 |
GRCz11 | 21 | 14807165 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCCTGACACATTTTNCCWGTTGTCTTTTGGGGGTTGAATGGAAGGTTA[T/A]YTTGGGCCAAASTTTGTGTGTGATTTTGAGCATGAGGGCAAATGTGGATG
Long Flanking Sequence:
TTTTTTGTTTGTCTAAAAAATGTTTCTTGATTTAGGGTTTTTGAGATATTTGGGCTATAGAAACAGGTAAACACAATATAGAAACACTGTAAAAGGCCAGTCCTGTGTGTTGATCACTGTTCATATTCAGCAGCTGTGGCTCTGGATGGAAAGGATTGCAGCAGTTCTCCAGAAAACAGATGTGACTTCATTTGTGACTGCAAAGACTGCAGTGATGAGCAAGACTGTGGTAAGATACTCACCTTTTATTTATTTTGACCTTTTCGCATCTGATATTATTAACTGCACAATTCTGGATAAACTCCCTGTTGAAATAACAATAATAGAAAGCATAGATTTTTGCAATAGTTTCTATGATTATAGTGTAAATTAGAAGTCGACTATATGTTGTCCATTGGTAATTGGAATCAAAACAATATTCCTGTCGATATGTTATGAGATATGCTTGTCTCTCCTGACACATTTTTCCTGTTGTCTTTTGGGGGTTGAATGGAAGGTTA[T/A]CTTGGGCCAAAGTTTGTGTGTGATTTTGAGCATGAGGGCAAATGTGGATGGACTGCAAAGCCAGCTGAAGGTGCGTACATGTGGCAGAGACAGAGGAGAGGAAAAACACTGCCGGACAGCGGCCCGTCCTCAGACTACACCACTGGAACCTCAACAGGTACATGTCCATTCAACTTAATCCATTCACAAATTTACTGGGGCAAATAAATAAATAAATAAATCTTAATTAAGATGGAAATTAGTTTTCGGTTTAGCAGATTTAGCTCCATACAAAAATGTGAATATATTAAGTGGAAAAAAGCTAGTTGAAGATTTTCAGTTTTTTATTTTTATTTTTTATAAAATTATGAAGGCAAATCTACAGTTGAGAATTGTTCTGAAGTTTGGGATCAGTAAGATTTTGTTAAAGAAATTATTGCTTTATTTGGGCAATGGTCAATTTAATTAATAAACTGTGACAGTAAAAACATTACAGTTTTACAAATAATTCTTTTTACAAA
Associated Phenotype:
Not determined