ZMP
zgc:103601
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC449801 [Source:RefSeq peptide;Acc:NP_001005974]
Human Orthologues:
NAT1, NAT2
Human Descriptions:
N-acetyltransferase 1 (arylamine N-acetyltransferase) [Source:HGNC Symbol;Acc:7645]
N-acetyltransferase 2 (arylamine N-acetyltransferase) [Source:HGNC Symbol;Acc:7646]
N-acetyltransferase 2 (arylamine N-acetyltransferase) [Source:HGNC Symbol;Acc:7646]
Mouse Orthologues:
Nat1, Nat2, Nat3
Mouse Descriptions:
N-acetyl transferase 1 Gene [Source:MGI Symbol;Acc:MGI:97279]
N-acetyltransferase 2 (arylamine N-acetyltransferase) Gene [Source:MGI Symbol;Acc:MGI:109201]
N-acetyltransferase 3 Gene [Source:MGI Symbol;Acc:MGI:102537]
N-acetyltransferase 2 (arylamine N-acetyltransferase) Gene [Source:MGI Symbol;Acc:MGI:109201]
N-acetyltransferase 3 Gene [Source:MGI Symbol;Acc:MGI:102537]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9183
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 |
---|---|---|---|---|---|
ENSDART00000052357 | Nonsense | 220 | 288 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 7 (position 39586604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37923244 |
GRCz11 | 7 | 38194502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAGATGTCGGTTATGCTGCAGACTAAWCCAGACTCTCTYTTCCTGCTC[A/T]AGACCATTTGCTCCCTTCAGACGGTCACTGGCTACAGAGCTCTGCTCGGC
Long Flanking Sequence:
ATGTTATCTATAACAAAATAGTCAAGAGCAATCGAGGAGGCTGGTGTTGTGAAAACAACCTCTTGTTCTCATGGGCCCTGAAGGAGATGGGATACAAATCTACCATATTGGGTGGCAGGGTGTTCAACTCTCTGGAACAGGACTTCCTTCCTAGTGACTCTCATCTCATCAATCTGGTGGAGATTGATGGAAAGCAGTACATCGCTGACGTGAGTTTTGGTATGTCATATCAGATCTGGTATCCCTTAGAGTTGATCTCAGGTAAAGACCAGCCACAGCCTCCAGGAGTGTTTCGCCTCACAAACAACGGTGAGAAGTGGATTCTGCAGAAGACCGGAAGGAAGCAAATAATTGTAGATAACGGCTTTGTGGATTCTACCCTTGTTGACAAACGGCTCACCAAGACATTATACTCTCTCACATTAACACCACGTGATGCAGATCATTTCCTGGAGATGTCGGTTATGCTGCAGACTAATCCAGACTCTCTCTTCCTGCTC[A/T]AGACCATTTGCTCCCTTCAGACGGTCACTGGCTACAGAGCTCTGCTCGGCTCGACATACAGTGAAGTCACTTTCAAAGAGGACTCAGATTCAGTGGAAATGAAGAAAATCCTAGATGATGAGATTGAGGATGTGCTGAAAGAAAAGTTTAACATGGTGTTGGTTAATAAGTTCACACCTAAAAACCAGAAAGCTGATTACCGCATGTAGTACTCAGCTACTCTCGACTCATCTACTCACAATTTAGAAGGCTCCCTCTGTGTGTGTTTAATTGTACCTGAAAGCTCTTAGTCATTCATGTTGTTTGATATTTGCTTCATTATAGAAGAGAGCTGCATTATTATGAGACAATCATTGCTCTTGATATTTTAACATTGTTTACTAATTAATACACGTGTCTGTTGCCTCATTACAAACATATGCAGCAAATTTCACAATATATACAATAAATTAACAAAACGTACTTTTCAACAGACCTTATGCCTCTTTGGGGTGACATTC
Associated Phenotype:
Not determined