ZMP
zgc:91931
Ensembl ID:
ZFIN ID:
Description:
AP-4 complex subunit mu-1 [Source:RefSeq peptide;Acc:NP_001002672]
Human Orthologue:
AP4M1
Human Description:
adaptor-related protein complex 4, mu 1 subunit [Source:HGNC Symbol;Acc:574]
Mouse Orthologue:
Ap4m1
Mouse Description:
adaptor-related protein complex AP-4, mu 1 Gene [Source:MGI Symbol;Acc:MGI:1337063]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41654 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1209 | Nonsense | F2 line generated | Not yet available |
| sa41655 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21726 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41654
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079437 | Essential Splice Site | 20 | 442 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 23055309)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22885647 |
| GRCz11 | 10 | 22855099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATTTTCATCTTGTCATCAAAAGGAGATCATCTCATATATAAAGACTG[T/A]ATCCTTCCCACGGGCTTGTGTGATGTGATGTGTTTATAACTGTCTGATAT
Long Flanking Sequence:
CCTCACAAACGGCTTCATCCATCTATTTCGCGCCGTCTGCCATCCTGTTACTTCCTCTCTTGAATAAAAACGTACATAAATGCAGAGTAATAAAGATACAAGTTTGCTTCGCTCATGTTCATGATGCCAAGAAGCAGCTCTTATTCCAGCTCAATAGATGGCAGTAAGCGGTACTGTTAACTCACGTATGACCTCACGAAGAAGAAAAACCCGGCTGTTTACAGTCATGACGGCATAGTCCTGCACTATTTGAGACCTAAACGGGTTTATTTTGTCCCTTTAAGAATTCAAATAACAGTGAATGAGGAAACTTGTTGAAGAAATGAATGAATGAGGACATTTGTTTAGACATATTTCTGAATGTAAGTGACGGCAGAAGAAGAGCGGGGTGATTTTTAACAAACATCCTTTTAATAAAGGTAATCCCGTGTGCTGGAGAAAATGATCAGTCAAATTTTCATCTTGTCATCAAAAGGAGATCATCTCATATATAAAGACTG[T/A]ATCCTTCCCACGGGCTTGTGTGATGTGATGTGTTTATAACTGTCTGATATCGAATCTTGTGTTTATATGCACGGATCTTCATGTAATCAGAGCTATCTCTATTAGATCAGTGGTCATATGACATTAAATGTATGCTTCCTGCTTATGATTTTCTTAATTCTGCATATCAGTCCGAGGAGAGGCCAGTAAAGACTCAATAAATGTCTTCTATGAGATGGTCACAGCTCTCAGTGGAGATCAGCCTCCTGTTGTCATGGTAGGCTACAGTTATGTTTTTTTGATATACACAACAACATTGTGATTGTTTAGTGTATTACATGAACTAACACTGACTGTTTATCTTGCTGTAGACACACAAAGATCTTCATTTTATCCATGTAAGGCAGGGTGGACTGTACTGGGTGGCATCAACCAAAACAAACCCTTCCCCTTTCACCATAATTGAGTTCCTTAACAGGTTAACAAATATAATTTTTGGATCAGTAATGTGATAATATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1209
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079437 | Nonsense | 33 | 442 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 23055520)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22885858 |
| GRCz11 | 10 | 22855310 |
KASP Assay ID:
554-1118.1 (used for ordering genotyping assays)
KASP Sequence:
TGCATATCAGTCCGAGGAGAGGCCAGTAAAGACTCAATAAATGTCTTCTA[T/A]GAGATGGTCACAGCTCTCAGTGGAGATCAGCCTCCTGTTGTCATGGTAGG
Long Flanking Sequence:
CGGCTGTTTACAGTCATGACGGCATAGTCCTGCACTATTTGAGACCTAAACGGGTTTATTTTGTCCCTTTAAGAATTCAAATAACAGTGAATGAGGAAACTTGTTGAAGAAATGAATGAATGAGGACATTTGTTTAGACATATTTCTGAATGTAAGTGACGGCAGAAGAAGAGCGGGGTGATTTTTAACAAACATCCTTTTAATAAAGGTAATCCCGTGTGCTGGAGAAAATGATCAGTCAAATTTTCATCTTGTCATCAAAAGGAGATCATCTCATATATAAAGACTGTATCCTTCCCACGGGCTTGTGTGATGTGATGTGTTTATAACTGTCTGATATCGAATCTTGTGTTTATATGCACGGATCTTCATGTAATCAGAGCTATCTCTATTAGATCAGTGGTCATATGACATTAAATGTATGCTTCCTGCTTATGATTTTCTTAATTCTGCATATCAGTCCGAGGAGAGGCCAGTAAAGACTCAATAAATGTCTTCTA[T/A]GAGATGGTCACAGCTCTCAGTGGAGATCAGCCTCCTGTTGTCATGGTAGGCTACAGTTATGTTTTTTTGATATACACAACAACATTGTGATTGTTTAGTGTATTACATGAACTAACACTGACTGTTTATCTTGCTGTAGACACACAAAGATCTTCATTTTATCCATGTAAGGCAGGGTGGACTGTACTGGGTGGCATCAACCAAAACAAACCCTTCCCCTTTCACCATAATTGAGTTCCTTAACAGGTTAACAAATATAATTTTTGGATCAGTAATGTGATAATATGATTTTCTTTAGGTGTGCAGATTGCATGATGATAAGTGACTGTTTTGTGTCTCCCAGATTAGCAGCTCTTACAAAGGACTACTGTGGCAGTTTGTCAGAAAAATCAGTGAGGATGAATTTCGCACTAATTTATGAGCTGCTGGATGAGATGGTGGTAAATGTTCTCTCTGTTTGCATATTTATTTTTCTCAGACCAAATGAATTAGACTTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41655
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 |
|---|---|---|---|---|---|
| ENSDART00000079437 | Essential Splice Site | 84 | 442 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 23055767)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22886105 |
| GRCz11 | 10 | 22855557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACCAAAACAAACCCTTCCCCTTTCACCATAATTGAGTTCCTTAACAG[G/A]TTAACAAATATAATTTTTGGATCAGTAATGTGATAATATGATTTTCTTTA
Long Flanking Sequence:
CATCTTGTCATCAAAAGGAGATCATCTCATATATAAAGACTGTATCCTTCCCACGGGCTTGTGTGATGTGATGTGTTTATAACTGTCTGATATCGAATCTTGTGTTTATATGCACGGATCTTCATGTAATCAGAGCTATCTCTATTAGATCAGTGGTCATATGACATTAAATGTATGCTTCCTGCTTATGATTTTCTTAATTCTGCATATCAGTCCGAGGAGAGGCCAGTAAAGACTCAATAAATGTCTTCTATGAGATGGTCACAGCTCTCAGTGGAGATCAGCCTCCTGTTGTCATGGTAGGCTACAGTTATGTTTTTTTGATATACACAACAACATTGTGATTGTTTAGTGTATTACATGAACTAACACTGACTGTTTATCTTGCTGTAGACACACAAAGATCTTCATTTTATCCATGTAAGGCAGGGTGGACTGTACTGGGTGGCATCAACCAAAACAAACCCTTCCCCTTTCACCATAATTGAGTTCCTTAACAG[G/A]TTAACAAATATAATTTTTGGATCAGTAATGTGATAATATGATTTTCTTTAGGTGTGCAGATTGCATGATGATAAGTGACTGTTTTGTGTCTCCCAGATTAGCAGCTCTTACAAAGGACTACTGTGGCAGTTTGTCAGAAAAATCAGTGAGGATGAATTTCGCACTAATTTATGAGCTGCTGGATGAGATGGTGGTAAATGTTCTCTCTGTTTGCATATTTATTTTTCTCAGACCAAATGAATTAGACTTAGAAGCAACCCAATTCTATGTATAATTTCCTCTGTGTTTCTGATCAACAGGATTTTGGCTACGTACAGACAACCTCAACTGACATACTGAAAAACTTCATCCAGACAGAAGCTGTTTCATCCAAACCCTTCAGTCTCTTTGACCTCAGTAATGTTGGATTGGTAAATTGTTGCATTTCTTTTGAATATTTTGCGTCTGTTTACTCAATATTTCAAAAAACTGTGTAATGCGATTCAGGTAAATCTTGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21726
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079437 | Essential Splice Site | 201 | 442 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 10 (position 23058061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 22888399 |
| GRCz11 | 10 | 22857851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCTTTGTGGATGTGATAGAGAGGCTGTCTGTGGTTATTGGCTCCAAT[G/A]TAAGTAAAGCTCAATGAATCATGGCTTGACATTAAACTACTGATCATTTA
Long Flanking Sequence:
AATTAATGCGGGTATAGTGTAAAAACATACTAATGCATGCTAGCTCCATGTTAAAATGTTGGCCATGTGTTAAACATGATGGAAACATTCCATTAACATAAATTAGTACTAATGTAGTGTAAAAACATACTAATGTGTGCTATCATCACCATGTTAAACTTGTTAAAAAATTCATGCTAGCTCCATGTTAAAACATGTTAGCCATGTGTTGGAAACCTGCTAGCAACATATCAGTTAAAGCTAGTACAGTGTAAACATGCTAATTCATGTTAGCGCCATACTAATACATGCTAGTCATGCTTTCTAGCATGTTAATGAATGTTAGCACAGTATTACAAAATACTAATTCACGTTTTTGCCATTTAAAACAATAACAACATGCTAATCAATATTAGCATAGCATAAAAATGTACCTACGTTTGTCTTTCTGGCTGCAGGGGGGAAAGAATGAGATCTTTGTGGATGTGATAGAGAGGCTGTCTGTGGTTATTGGCTCCAAT[G/A]TAAGTAAAGCTCAATGAATCATGGCTTGACATTAAACTACTGATCATTTAGATTTTTCACACGTTTTTCTTCTTTTCAGGGAGTTTTAATGAAATCAGATATTCAGGGAGAGATTAGGATAAAATGCTTTCTTCCAACCTGTTCAGGTGAGTTTGCTACAGATTCAATTCAAGTTAATATATATAGCGATTTTACAATGTAGATTTTGTTAAAGCCGCTTGACATAGAAGTTCTAGTAAAGTCTAGATTTCATATTGCGGTCCATGCCAATGCAGATTGTAAACGGATCTTCACTTCTATGATTGTGTATCACTCTTGTAGAGATGCGGATTGGACTGAATGAAGAGCTCAATATTGGAAAGTCGCAGCTGAAAGGTTGAATATGCAAAACTGGTCAATATAATATTTGCATACACATCTCTAGAGGCTGTGTATCTTTAATTACAACTGTTTAAATCTGTTTCTTTAGGCTATAGTTCAGCTGTACGTGTGGATGAGTG
Associated Phenotype:
Not determined