ZMP
si:ch211-200o3.4
Ensembl ID:
ZFIN ID:
Description:
membrane alanine aminiopeptidase [Source:RefSeq peptide;Acc:NP_001038326]
Human Orthologue:
ANPEP
Human Description:
alanyl (membrane) aminopeptidase [Source:HGNC Symbol;Acc:500]
Mouse Orthologue:
Anpep
Mouse Description:
alanyl (membrane) aminopeptidase Gene [Source:MGI Symbol;Acc:MGI:96749]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12011 | Nonsense | Available for shipment | Available now |
| sa23292 | Essential Splice Site | Available for shipment | Available now |
| sa43096 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12973 | Nonsense | Available for shipment | Available now |
| sa23291 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12011
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060196 | Nonsense | 142 | 946 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 20877951)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 21108174 |
| GRCz11 | 18 | 21097240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAGTGAGAAAATCGGATACCAATGAGAAATTGCCATTGAAGGGATAT[C/T]AAATYTTCAAGAACGAAACTAATTTCCTTGACATCCATCTTGAGGTTGCG
Long Flanking Sequence:
CAGAGTCTAAAACCTGCCAGCAAGTGCTCCAGTAGCTCACTTCATACTTGAGGGGAGCTTCTCGGGAAGGATCAGAAATGGCCAAATCAACTGGCATGTCCAAAGCCTTGGCTATTGGCATTGGGGTGATCACAGTTTGTTCTGTTGGTTGTTTAGTGGTGATGGCTGTTTTTTTCCAAATTCAGGTAGGCAACAACAAGCCAACGCCTCCACCAAGGCCAATATTACCTACGCCTCTCCCAACAGATCTTCCAGAGTCTCTTAGACTTCCAGACAGCTTGATTCCTGAGAGCTACAACGTTTTCCTACAACCGTACCTTTACGCGGCGATAACCAACAACTATACCGAACAATCTTACCTCTTCACCGGGAACTCAACTGTAAGGGTGAACTGTACGAAAACCTCCAGCAGGGTCTTTCTTCATGTTCACAATATTAATGTGACGGCGGTGGAAGTGAGAAAATCGGATACCAATGAGAAATTGCCATTGAAGGGATAT[C/T]AAATTTTCAAGAACGAAACTAATTTCCTTGACATCCATCTTGAGGTTGCGATAAAAGAAAATGGGACCTATGATATTTTTACTGAATTTGAAGGGGAGCTTCTTGAGGACTTGACTGGGTTTTATGCGAGCCGGTACACAGGGAAGGGAACTGATGACGAGGACGAAGAGAGGTAAAGATTTACCATACATTATAGGCTAATAGATTCTTAAAACTAAAAAATAGCAAAACATTTAAATAGGTTGTAGTGGAATGAAAACTTTAATTAGTTAAATGAAATGGATATAGATTTTCACTGTTTATATATTTTTGTGTTCAAATATATTTACTGTTCAGTTAAAAACACCCCAAAAGTCCTTATGTTAATGTAATGTGCATGTCCAATGCAATCTCACAGCAGTTTTTAACTTTTTTCTTTAGTGGCTAATTCTTATGAATTCGTACGATCTAATTTGCACAATTTAGTACGATTTGCTCATCACCCAATGACGGTTGGGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23292
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060196 | Essential Splice Site | 295 | 946 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 20875995)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 21106218 |
| GRCz11 | 18 | 21095284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACATACATTCTCATATGTATCTAAAGGAACCCGGACAAAAATACATG[T/A]AGGTTGAGTGCCTGCTTATTTATTACAATTTTAATCATTTCACATCTAAT
Long Flanking Sequence:
TTGCTTAAAGGGGCTGATATTTTTGGGGCTGCTTTTATTCTAGCCGAAATAAAACAAATAAGATTTTCTTTACAGGAAATAATATTATCAGACATACTTTGAAAATTTCTCTGCTCTGTTACATAATTTGGGAAATATTTAAAAATAGAAAAATAATTTAAATGGGAGCTAATAATTCTGACTTCAACTGTATATTTACTCCTCATGTATCTAATACAGATATAAATATCAAAACAGGAAGCATGTTCAAATTAAGACTTTGCCTATTTGCAAACCACTTACAAATGAACAAATGAAATCAATGTTTTTATGTCCAGTGGATAACTTTTGCTTTTTTGCTTTATCATCAGATCCACGTACAATACAAATTAACGGAACGGACTGGATTAGAACCACATTCAAGCCCACCAAAAAAATGTCATCTTATCTCCTGGGCTTCATTATATATGATACACATACATTCTCATATGTATCTAAAGGAACCCGGACAAAAATACATG[T/A]AGGTTGAGTGCCTGCTTATTTATTACAATTTTAATCATTTCACATCTAATCATTATTATGTGTTTCTAAGGTACATGGTCGATCAGAGGCTATTGATGCTGGCCATGCTGACTACGCACTGGAAACAACTGAAACCATTCTAAGCCACTATGAGAATATATTTGGACTTCGATACCCAATGTCAAAAATAGGCAAGTCCATTAAAAAAAGAACAATTGAGGGAGAATAAAATTCACACAAGGTGGATAAAGCACTGAGAAACTGAACAATCAAGGAAAATATTGGTGTAATTGGTGTCATTTCAGCTCAATTTAAATTGGCAGAACAAACAGCAAATGTCATTTTTGAGTGGAGGAAGCCACCAATGCACGTCTGAATCAAAATTCTACCTCACTTCCTGTCTTGGGAGATACCTTTTTCTGATTGAATTTCAAACGAAGCATAAATCTATCTATGCCTCCAGAGTCACTGCCTAATTGGGCATAAAACTTTTGGGTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43096
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060196 | Nonsense | 299 | 946 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 20875915)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 21106138 |
| GRCz11 | 18 | 21095204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAATCATTTCACATCTAATCATTATTATGTGTTTCTAAGGTACATGGT[C/T]GATCAGAGGCTATTGATGCTGGCCATGCTGACTACGCACTGGAAACAACT
Long Flanking Sequence:
AATATTATCAGACATACTTTGAAAATTTCTCTGCTCTGTTACATAATTTGGGAAATATTTAAAAATAGAAAAATAATTTAAATGGGAGCTAATAATTCTGACTTCAACTGTATATTTACTCCTCATGTATCTAATACAGATATAAATATCAAAACAGGAAGCATGTTCAAATTAAGACTTTGCCTATTTGCAAACCACTTACAAATGAACAAATGAAATCAATGTTTTTATGTCCAGTGGATAACTTTTGCTTTTTTGCTTTATCATCAGATCCACGTACAATACAAATTAACGGAACGGACTGGATTAGAACCACATTCAAGCCCACCAAAAAAATGTCATCTTATCTCCTGGGCTTCATTATATATGATACACATACATTCTCATATGTATCTAAAGGAACCCGGACAAAAATACATGTAGGTTGAGTGCCTGCTTATTTATTACAATTTTAATCATTTCACATCTAATCATTATTATGTGTTTCTAAGGTACATGGT[C/T]GATCAGAGGCTATTGATGCTGGCCATGCTGACTACGCACTGGAAACAACTGAAACCATTCTAAGCCACTATGAGAATATATTTGGACTTCGATACCCAATGTCAAAAATAGGCAAGTCCATTAAAAAAAGAACAATTGAGGGAGAATAAAATTCACACAAGGTGGATAAAGCACTGAGAAACTGAACAATCAAGGAAAATATTGGTGTAATTGGTGTCATTTCAGCTCAATTTAAATTGGCAGAACAAACAGCAAATGTCATTTTTGAGTGGAGGAAGCCACCAATGCACGTCTGAATCAAAATTCTACCTCACTTCCTGTCTTGGGAGATACCTTTTTCTGATTGAATTTCAAACGAAGCATAAATCTATCTATGCCTCCAGAGTCACTGCCTAATTGGGCATAAAACTTTTGGGTCACACTTTATTTTGATGGTCCATTTGTTGAATTTAAGTTGGTTTGCATCTACATGCCAGCTAATTCTCATTAGATAAAGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12973
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 |
|---|---|---|---|---|---|
| ENSDART00000060196 | Nonsense | 595 | 946 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 20868603)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 21098826 |
| GRCz11 | 18 | 21087892 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATGAGTAACCCAGCAACTGYTTTCTTACAGATCCAATTCCAGATTTC[A/T]AAATTGGCAAAGATAACTGGCTTCTTGCCAACWTCAACTGCACAGGCTTT
Long Flanking Sequence:
TCAAGAAAAAAGACCACAGAAAGCCTAAAACATGATTTCTTGCTCCAGGCTGAGACACATCTTCTAATACAGAGTACTTCTACACACAATATCTAGAATGTTTGTAAATGTTACCTGCATTTTTTTAAAAGTTAATTTGTTGGTTAATTGAATTTGCCACTGTAAATTACTGAACTGTTAAGCCGTAATTGACAACAGAATTTAGCTGCAGTTGCACATGTCACTAGTCTTCTTTAGTCAAGCTGATTCTTAATGATTCATTCAACTCTTTATTTTGCTCCTAACAGCTCTTTATGGCATATACCAATCAAATACATGACACTTAAGGCGGGGGTGAAAGAGTTTCCCAATTTTTTTACAGATAAAGGTCCAGGTAAGAAACAAACTTTAATGATTCATTTAAAAATATAAGAAAATACCTGACAAAACAACAATCGCCTCTCGTTGTTTTTTATGAGTAACCCAGCAACTGCTTTCTTACAGATCCAATTCCAGATTTC[A/T]AAATTGGCAAAGATAACTGGCTTCTTGCCAACATCAACTGCACAGGCTTTTATCGTGTGAACTACGATGAAGAAAACTGGAACAGGCTTACTGCACAACTTCAAAAAAATCATCGCGTAAGCATCTTTTTTTTATTTTTTTATCTGTTATTAGTCTCATTTCAAATCATTCTATACAATCGAGGGCAGCAACATAACATTGAGCTAGTACACAAATGCAGACTCACTTATCGTGTTCATGTGGTTTGACTGGAAATACCTTTTTAAGGTGCTTTTTTATTCTTACGCTTTAAAACGAAAGTCAAAGAGGCAACATTCTAAAAAGCATGTTATTCCATGCATGTTGTTACTCAAGCAAGTTGTAATAAAAATGCTAGACACCTTCCAATTCGAAGCTTGCATGCTGTGAAGGTACAAACCCAAATGGTACACTAAACCCTTGCAGTCCTACACAAAATTTGTACTTTCATGAAGTAGTGGTAATGTATGATATATACATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23291
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060196 | Essential Splice Site | 702 | 946 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 20865449)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 21095672 |
| GRCz11 | 18 | 21084738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACACACCAAAAACACCATAAAAGCTTTAACTTTACATTTCTATGTTT[A/T]GAAATACCTACGAAACTTGGTCACACCATTATATGAGGAATATGAGGAGT
Long Flanking Sequence:
ATGCCTCCTCGTTTATAAGTCACTTTGGATGAAAGCATATAAAACGTTCATGAAGTAAAATTACAACAAATTATTTAGAGCTCCAATACAATGCCAGTAATGTTGAATGTTTTGAATCTATCTTTAGATCATTCCACTCATTAACCGAGGGCAACTCATTGATGACGCTTTCAATCTTGCAAGGTACTTTTTTCATTTTGCAAATATACTAAAGAAATATATTGTTAACTGATTTGTTGCTGCACATTAATCGCTAATATTTCTTTGAAGGGCTCATCGTCTCAACGTCACTATTGCGTTAAATCTAACCAAATACCTGATAAATGATTTGGAGTATATCCCATGGGAATCAGCACTGAAAAACCTGGACTTCTTTACCCTTATGTTTGATCGCTCCGAGGTCTACGGTCCAATAATGGTGAGCCTAAGGAAAGGAGACTAAACTTAATATGTACACACCAAAAACACCATAAAAGCTTTAACTTTACATTTCTATGTTT[A/T]GAAATACCTACGAAACTTGGTCACACCATTATATGAGGAATATGAGGAGTACACAATTAACGGAACCATTCCAATAGAGAAGTACACTGACCAGTAAGCATTGTTTTTGGTTTTGCTGTAAATACATTTAAAGACAAAAGTATTTGAATTCTTTTTTTTAAACACAGTGGGGGAAATCAGTATTGAACACGTCTTGTTTTTATTTCCTGGGAATAATATTGCTAAAGGAGCTGTTGACATGGAATTGAACCACATTTTGCAAAAAACCCAAACTATGCAAACATTAGAATAGAACAAAACAAAGAAAATCAGAAAAATTAGTTACAGTATAATAACAATGAAATGACACAACGAGAAAGTACTGAACTACTGAAACGTGTTGTAAACTGTAAATGTTTTTTGGTAATGGCAGCTTAAAGACGCCTCTCATATGGAGAATGAAGTCACGTAAATTTCTCAGGTGTGATTTTGTTCACAGACTTCAACAGCGTGTAAAAATC
Associated Phenotype:
Not determined