ZMP
zgc:174895
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC100126024 [Source:RefSeq peptide;Acc:NP_001099174]
Human Orthologue:
APRT
Human Description:
adenine phosphoribosyltransferase [Source:HGNC Symbol;Acc:626]
Mouse Orthologue:
Aprt
Mouse Description:
adenine phosphoribosyl transferase Gene [Source:MGI Symbol;Acc:MGI:88061]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35831 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42509 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35831
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109004 | Essential Splice Site | 73 | 200 | 3 | 5 |
ENSDART00000128081 | Essential Splice Site | 73 | 200 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 14476560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15521523 |
GRCz11 | 15 | 15457545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAATTCACTAAAAATCATATTTATTTAAAACTTCCTCCTGCAATTTC[A/T]GGGTCAGCTGTAGCCACAACATTGGGAAAAGGATTTCTGGCTATTCGTAA
Long Flanking Sequence:
TATTGCAATTCCCAGGTAAATAACTATACTTGTCGGAATCAAAACTTTCTCTAGTAAACCATATACGTTAATCAACAATCTAGCTCCAACTTCATGAAGCATGGAAAGTGTTAAGCTACGCTACAATGTGCTTTAAAGTTTTGACAGCGTTTTCTCCTGACTGATCCAGGCACTGTCAGATTGTGTAAAAGATCTTCTCAAACCATTCCAGAATGAGACCATTGACCTGGTGGCTGGAATAGATGCCATGGGCTTCATCCTCGGTATAAAACTTTGCTCTTTGTGTAGCTGGTGAGAACGTCTGTACTAAAGAGACTGTATTTTTAGCACAGTTCACATGTTGCAGGAAAAGTAAATATAACTCTTGGCAAATAGTCTAAATATAGAGTGGGATATACTTTAAGAGTCCATCTCTAATGAAAGTAGCCTATATATATTCACTTACTGAAATTGAAATTCACTAAAAATCATATTTATTTAAAACTTCCTCCTGCAATTTC[A/T]GGGTCAGCTGTAGCCACAACATTGGGAAAAGGATTTCTGGCTATTCGTAAAGCAGGACACTTATGTGTTGAAACTCACACTCAGGACTACAGTGACTATTCTGGACGAGAGAAAGTCATGGAAGTGCGTGTTGATGTGTTAAAGCCAGGTACTGATGTATCTGAAGTCACTATAATGGCCAATAACGCTGTAAAAGTCACATGGGGATAAAAACAAGGCATTATTCACCACAAAATGACATTTTACTAACCATTTATGACCTTTAGCCCTTTAACTGCCTGCTCTACCAAATGAATGACCATATTTTAGCTGTTTTAAATAAGTATTTACACTACACACCATTGTTGTTTACAAAAAAAAAAAAAAATCAAATGACATAAACATACACAACATAATGACATACACAACATAAACATACACTTGATTTTGGTTTTATTGTAAAAAAAAAAAAAAAAAACATGTTTAATGACAATTTGAAATATTTTATGGCACACTTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42509
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 |
---|---|---|---|---|---|
ENSDART00000109004 | Nonsense | 174 | 200 | 5 | 5 |
ENSDART00000128081 | Nonsense | 174 | 200 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 14478219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15523182 |
GRCz11 | 15 | 15459204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGGCCATTGAAAACAGTGAAGGAGGAAAATGGCTGAAGGAAAACTAT[A/T]AATATTCCCACTGCATTCCGAAAGAGCTGCAATCTCAAATAGACAGTCAA
Long Flanking Sequence:
ATTACCAAAAAGTTTTGTACAGCTGCTTTTTGTAAGGCTGACAGCTGCCTTTTGCTTGAATGAAAAGCTTACAGGTCACCAGTCAATTAACTCCCCAAAATGACAGCTATTATTTAATTAACTTTACTTTGAAGGTTTGTTTTGAACATTTAGTTGACACTTAAAATAACTTTGCACCTACATGTAAACTTGCTGTCGTTGAACTATCAGTAGATTGTCAGTTTAATATCTGCTCTCTTATTATGTTCTTGTACTACAAGTAAATTTGCCAGTACAGGTCAACCTATTAGAACCCGAACCCTACCAATCTACTATTACTGTATATTACTGTAACTTATGAGAGTTATTAGATATGTAAACAAGACATTACTTATGCATTACTTACAAAATGCGTTAAAGGGACCATTAAAATAAATTGAAGCCATTATTTCTGCCTTTTAGGTATTGCTGCTGTGGCCATTGAAAACAGTGAAGGAGGAAAATGGCTGAAGGAAAACTAT[A/T]AATATTCCCACTGCATTCCGAAAGAGCTGCAATCTCAAATAGACAGTCAATATCTGGAGTTCTTCAAGAACTTCAGTGTTTAAAGGCATGACAATCAGGTACATATTCAAGTGGAATGTAATATTTGATTTACATTTCGCTTTGACAGGATTTAAACATTGCCAATAAATCCTCACTGTAAAACATGTATACAGCACTGATTTTATATTGCTGGTATTAAATGTAGAAAGTGCCATATAAATCGAAATATAATATTTTAATACACATCTATGTTTTGTTTCTATTTCTATAATTATAATAATGATAATATAGATGGGTTTTACATTTACATGACATGTCCAGATGTGTTACATATACACATTCATATGAGATAGACAAAATCTAAAATTGAGATTTAAGGTTACCCCAATTAAAAATAGTTTTCAAATGTTTTTACTTCACATGACAGTATATTTCACTTAAGAATTTAATAACTGTACATGTAATATTGCTGCAAATGA
Associated Phenotype:
Not determined