ZMP
si:ch211-214j8.1
Ensembl ID:
ZFIN ID:
Description:
N-acetylated-alpha-linked acidic dipeptidase-like protein [Source:RefSeq peptide;Acc:NP_001091660]
Human Orthologue:
NAALADL1
Human Description:
N-acetylated alpha-linked acidic dipeptidase-like 1 [Source:HGNC Symbol;Acc:23536]
Mouse Orthologue:
Naaladl1
Mouse Description:
N-acetylated alpha-linked acidic dipeptidase-like 1 Gene [Source:MGI Symbol;Acc:MGI:2685810]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33603 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7565 | Missense | Mutation detected in F1 DNA | Not yet available |
sa14612 | Nonsense | Available for shipment | Available now |
sa33604 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33603
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079049 | Nonsense | 109 | 740 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 27893488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 25648786 |
GRCz11 | 5 | 26248939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCCAAAACAGGCTTGGACAGTGCATGGAGGGAGGACTACAAGGTGTA[T/G]CTGTCATTTCCAAACAAGGATAATCCTAACAAAGTCTCTGTTGGTAAGAA
Long Flanking Sequence:
TTAAGAGCTCTGACATCTTAACGTTATGCTTAAGGAGGTGCTATTGGGTGTTCTAGGAGGAGCAGCAGCTCTTACTGTAGGAATTCTACTGGGACACTTCGCCATTGAAAAGGGCAGTTCAGCACCAGAGTGGGTCCGGGATGCATCTCAAGATGTGGATGAAAGTATCATTAAGAAATTCCTTGCAGAACTGGACACCAATGAAATTAAAGAGAACCTCAGGTGAAGTATTAATACTGAGGCACATGACAGAATGATTAAATGAGCTTTGCAAGACCATTTCAGTAAATGGCGAACATTTCTATGTGATCTGTTTGTGGCTGTTTAATTTCCAGCTGAATTGAAAATTTACTTTTGTCTTTTGTGCAAAGGGAGCTGACTAAGGTTCCCCACATGGCCACCACCCCTGGAGATGAAGCAACTGTTGCGTTTATGCTGAAAAGGTGGCAAGACCCCAAAACAGGCTTGGACAGTGCATGGAGGGAGGACTACAAGGTGTA[T/G]CTGTCATTTCCAAACAAGGATAATCCTAACAAAGTCTCTGTTGGTAAGAAATTGGTTAGAGAGTGGTGCAGTGGGTAGTGCTGTCTCCTCACAGCAAGAAGGTCGCTGGTTCAAGCTTCGGCTGGGTCAGTTGGCATTTCTGTATGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCTGGTGGCTCTGGTTGGGCTAAATTGTCCGTAGTGTATGTGTGTGAATGAGTGTGTATGGATGTATCCCAGAGATGGGTTGAAGCTGGAAGGGCATCCACTGCGTAAAACATGTGCTGAATAAGTTGGCGGTTTATTCCGCTGTGGCGACCCCAGATTAATAAAGGAACTAAGCTGAAAACAAAATGAATGAATTAATGAATGAATGATGGATGATGGAATTTAAATGACATATTATCCCAGAAATATGTTAAATGATGCATTAAAATATATTTTTTATTTAGTTGATCCAGAAAACCAGGTCCTATTTACAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7565
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:
T > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079049 | Missense | 457 | 740 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 27899731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 25655029 |
GRCz11 | 5 | 26255182 |
KASP Assay ID:
554-4347.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGTTYGCACTGCTGAAATGTTCTTTGTCCACAACAGCTAATGCCACTC[T/C]CAGAGCCTCAGCTTCTCCAGCAGCACAGAGTGTGCTTTTTACCGCCTCCA
Long Flanking Sequence:
TTTAGTTTTATGTTTGAAAATATTTACATTTACAAAAAGCTCTATTTTATATGGCCAACGAAATTAATTCTGCAATTGCAATAAAGAGGAAAGATTTAGCAATGCTTATAGTGTGATGAAGCAAAAAAAAAAAAAGAATCCAACACTAATTCTCTACCTGAAAGGGAAATGGCGACCTCGGCGGTCCATTATCTTTGGCAGTTGGGGAGCTGAAGAATTTGGCCTTATCGGATCTGCAGAATACACAGAGGTTTGTTAATAATCACACCAACTGATGTGCTACAAATTGGAATTAGAGTTAAGAAAAGATTGTACTGTATATGTGTTGAAAGTATTCTTCATTCGCAGGAGTACTTCAGTAAGCTGAGTGAGCGCACCGTGGCCTACATCAACGTGGACATCTCAGTGTTTGGTATGACTCTTTTCGTCAGATTATAACTTTGATCCTGATGTGTTCGCACTGCTGAAATGTTCTTTGTCCACAACAGCTAATGCCACTC[T/C]CAGAGCCTCAGCTTCTCCAGCAGCACAGAGTGTGCTTTTTACCGCCTCCAAACAGGTGAGGAACAAACCCCCAATCTGTTCTCTTAGCTGAAATGTGATTTTAACATCCTTCATGAGGCTTTGACCAGTCCTGTGCTTTCAGGTTGATGCTCCCGGGACAACCATGTCAGTCTATGACAACTGGATACGGTATTACAACAGAACCAGTCCAAATTATGGGATTATACCTAAGTATGCTCTTAATTTTATTCAGTACCACCTCATAGTTCAGCTTTTAATACACCAGTTAACCACAGGTCATTTTATACTGTTAATTCACATTGTATTTAATTAATATTTGAACAATATTAATATTTATATTATTAATATTATATATTAATATAATATTAATATATATTGTCACGTTATAATTAAAAGGTTCTCTGACATTTTTGTCAAAATTGAGTTATTGACATATTCTTATTAAATGACAACATATTTACATTATGTGATGTGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14612
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 |
---|---|---|---|---|---|
ENSDART00000079049 | Nonsense | 495 | 740 | 13 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 27899931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 25655229 |
GRCz11 | 5 | 26255382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCCGGGACAACCATGTCAGTCTATGACAACTGGATACGGTATTACAAC[A/T]GAACCAGTCCAAATTATGGGATTATACCWAAGTATGCTCWTAAWTTTATY
Long Flanking Sequence:
GTTGGGGAGCTGAAGAATTTGGCCTTATCGGATCTGCAGAATACACAGAGGTTTGTTAATAATCACACCAACTGATGTGCTACAAATTGGAATTAGAGTTAAGAAAAGATTGTACTGTATATGTGTTGAAAGTATTCTTCATTCGCAGGAGTACTTCAGTAAGCTGAGTGAGCGCACCGTGGCCTACATCAACGTGGACATCTCAGTGTTTGGTATGACTCTTTTCGTCAGATTATAACTTTGATCCTGATGTGTTCGCACTGCTGAAATGTTCTTTGTCCACAACAGCTAATGCCACTCTCAGAGCCTCAGCTTCTCCAGCAGCACAGAGTGTGCTTTTTACCGCCTCCAAACAGGTGAGGAACAAACCCCCAATCTGTTCTCTTAGCTGAAATGTGATTTTAACATCCTTCATGAGGCTTTGACCAGTCCTGTGCTTTCAGGTTGATGCTCCCGGGACAACCATGTCAGTCTATGACAACTGGATACGGTATTACAAC[A/T]GAACCAGTCCAAATTATGGGATTATACCTAAGTATGCTCTTAATTTTATTCAGTACCACCTCATAGTTCAGCTTTTAATACACCAGTTAACCACAGGTCATTTTATACTGTTAATTCACATTGTATTTAATTAATATTTGAACAATATTAATATTTATATTATTAATATTATATATTAATATAATATTAATATATATTGTCACGTTATAATTAAAAGGTTCTCTGACATTTTTGTCAAAATTGAGTTATTGACATATTCTTATTAAATGACAACATATTTACATTATGTGATGTGTTTTATAATTTGTTTACATTTTAAGACTTTTTATTTAAAAAACAAATATTACACACATTGTTTGCAATAAAATGCAAAAACTTTGAAGCTCAATATCTCAAAATCAGTCAGAATAGAACCTTATAATTCCAAGGTGATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33604
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079049 | Essential Splice Site | 505 | 740 | 13 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 27899964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 25655262 |
GRCz11 | 5 | 26255415 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATACGGTATTACAACAGAACCAGTCCAAATTATGGGATTATACCTAAG[T/C]ATGCTCTTAATTTTATTCAGTACCACCTCATAGTTCAGCTTTTAATACAC
Long Flanking Sequence:
CTGCAGAATACACAGAGGTTTGTTAATAATCACACCAACTGATGTGCTACAAATTGGAATTAGAGTTAAGAAAAGATTGTACTGTATATGTGTTGAAAGTATTCTTCATTCGCAGGAGTACTTCAGTAAGCTGAGTGAGCGCACCGTGGCCTACATCAACGTGGACATCTCAGTGTTTGGTATGACTCTTTTCGTCAGATTATAACTTTGATCCTGATGTGTTCGCACTGCTGAAATGTTCTTTGTCCACAACAGCTAATGCCACTCTCAGAGCCTCAGCTTCTCCAGCAGCACAGAGTGTGCTTTTTACCGCCTCCAAACAGGTGAGGAACAAACCCCCAATCTGTTCTCTTAGCTGAAATGTGATTTTAACATCCTTCATGAGGCTTTGACCAGTCCTGTGCTTTCAGGTTGATGCTCCCGGGACAACCATGTCAGTCTATGACAACTGGATACGGTATTACAACAGAACCAGTCCAAATTATGGGATTATACCTAAG[T/C]ATGCTCTTAATTTTATTCAGTACCACCTCATAGTTCAGCTTTTAATACACCAGTTAACCACAGGTCATTTTATACTGTTAATTCACATTGTATTTAATTAATATTTGAACAATATTAATATTTATATTATTAATATTATATATTAATATAATATTAATATATATTGTCACGTTATAATTAAAAGGTTCTCTGACATTTTTGTCAAAATTGAGTTATTGACATATTCTTATTAAATGACAACATATTTACATTATGTGATGTGTTTTATAATTTGTTTACATTTTAAGACTTTTTATTTAAAAAACAAATATTACACACATTGTTTGCAATAAAATGCAAAAACTTTGAAGCTCAATATCTCAAAATCAGTCAGAATAGAACCTTATAATTCCAAGGTGATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTATATTGTTATTCAC
Associated Phenotype:
Not determined