ZMP
zgc:165534
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC569719 [Source:RefSeq peptide;Acc:NP_001103185]
Human Orthologue:
NAGPA
Human Description:
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase [Source:HGNC Symbol;Acc:17378]
Mouse Orthologue:
Nagpa
Mouse Description:
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36220 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36221 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36220
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126129 | Essential Splice Site | 190 | 586 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 43184267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40567717 |
GRCz11 | 16 | 40517749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAAAACGCTCAGTTTGGCATCAGAAAAGATGGGACACTGGTGTTTGG[G/A]TAAGCACGCAGCCCACAGTCTCTCTCTCTCTGCAGTCTTTCCCTCAGGCC
Long Flanking Sequence:
CCTCATTTTCTTGGCAGACATTCCTCGGATGACGACCTCTTGTTACCCTACACCAAATCCCACGGTCCATCTCATTCCCACCGCTACGTGAGGGACTGCCAGCCTGTCGCCCACGGCACTGTAACCCATGAAACCCAGGCAGCAAGCAAACACTCCAACTCGCCAGTGTTGGAGTCGAATATATTCATCTCGGACATCACAGACGACTCTGGCACTCACAGATGGGTGAGCGGGCACATCACAGAGGTGCACGACCCACTAAGATCAGTGTCGGTTCTTGAACCAGGAGGCCCTGGAGGATGCGCGCACAATCACAGAGAGCTGGTGGAGGTCACTGCCAAAACTAGAAAGTGCCTGGTTGCCCAGAACGGAGGTTACTTTGACACTCATACCGGACAGTGTTTAGGGAATATCATAAGTGATGGGAAACTGGTGAGGAACAGCGGAGGAATTCAAAACGCTCAGTTTGGCATCAGAAAAGATGGGACACTGGTGTTTGG[G/A]TAAGCACGCAGCCCACAGTCTCTCTCTCTCTGCAGTCTTTCCCTCAGGCCCTCGTGATGTTTTGCATTACCACAGGGTTTGTTTTTGTGTGGAGAGCCAATAACAATACAAAATTGAGCTAGTCTTTCCTGGTCGGGAGCTGGTGTACTTTTGACCTCCCTAAAATGAGTTGAGCTTTTCTATCTGTAGTGCACACTTAAAAGGATAATTTAACCAAAAATTAATACATTTAAATGAATTTACTCACCACCCTGACATGAGTTTGCTTCATCAGTAGAATATTAAGCAAGGCAAGTTTATTTATATAGCACATTTCATATACAATGATAATTCAAAGTGCTTTACATAAACAAGAATAAAAGAAACGAGTATAAAACAATAATAAAACAACAGTAGAGATAAAAAAAAATATTAAAAAGTGTTAAAACATGTTTTAAAGGAACGAAAAAGTAAAGAAAGACACTATAGTGCGATCTGTCGGATGTAGCACAGTGCTCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36221
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 |
---|---|---|---|---|---|
ENSDART00000126129 | Essential Splice Site | 399 | 586 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 43196523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 40579973 |
GRCz11 | 16 | 40530005 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGAAGTGCCGTCAGACTTCTACGTTGAACTGTCTGTGTGTATGTTTGC[A/T]GTATGCACAGCAGGTTTGTATGGCGATGGCTGCAATCAGACATGCACATG
Long Flanking Sequence:
TAATATAGGGACTAAGCTGAAAAGAAATGAATGAATGAATAAATGGCTTGTGGTCAGTTATTCCTTATAAATGTAATGTTTTGACCATGAAATTGCCAGCTATTTTCAGAGAAATAATCAGAAATATAATGTGAGCTAACACTGCTTCTGTTAAAGTGAATAAAAGCAGATTGTTGTACTGTTTGTTGTTTTGTAACTCTCCTATCTCTCTATCTTTCTCTCCTATACTTGATTTCTTGAACAGACGGGTGTGTTTGCGATGCTGGATGGATGGGTTTATACTGCAGCCAAGGTAAAGACTACATCAGCTTGGCTGTCATACTGGTTCAGACTATCAAATAAAGCTGACCGGCTATTTGCTGTTAGACTCTTATATAAGAGTTCTGTTGGTTGCAACATATCTGCTACAGTCAGCAATGGTCGTATATTGATTTTGGACCAGTAAGTTCATCTGAAGTGCCGTCAGACTTCTACGTTGAACTGTCTGTGTGTATGTTTGC[A/T]GTATGCACAGCAGGTTTGTATGGCGATGGCTGCAATCAGACATGCACATGCGCAAATGGAGGCTCATGTGATCCTGTCCACGGCCGTTGCACCTGTCCTGCTGGCTTCCATGGAGACTCCTGTGAGCAGGGTGTGCAGTCTAATCTCTAATGTACTAAATTGGTGTAAATGGAGTCAAAACTTTGCAGACTTGACCTGAGAGTTATCTTACATGTTATAACAAACCATAAAAAGATGTTTTCAATTTTGCAGTAGATAATCTCACTATGCTCTCTTTGTGTTTCCAGAATGCCCCATTGGTTTCTATGGGCTGAATTGTAAGCAGCTTTGCCAGTGCCAGGACATGTGCCCATGTGACGCCGCCACTGGAAGCTGCAACACCACATACCAGGGAGAGAGAAACATCAGCCTTCACAGAGGTATGATCCAGCTCCTATTAGCACTCACACGACATGCAAACAACACATTCCTGGTGTGACGTCTCTATAGATCAGTGGTAA
Associated Phenotype:
Not determined