ZMP
ap4e1
Ensembl ID:
ZFIN ID:
Human Orthologue:
AP4E1
Human Description:
adaptor-related protein complex 4, epsilon 1 subunit [Source:HGNC Symbol;Acc:573]
Mouse Orthologue:
Ap4e1
Mouse Description:
adaptor-related protein complex AP-4, epsilon 1 Gene [Source:MGI Symbol;Acc:MGI:1336993]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32509 | Essential Splice Site | Available for shipment | Available now |
sa19357 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11955 | Nonsense | Available for shipment | Available now |
sa8426 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32509
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109284 | Essential Splice Site | 432 | 1121 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 4883640)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4744882 |
GRCz11 | 25 | 4871310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATAACTACATCCTATTGTTGCACGTGAGTTTTTCTATCAAAACCCTTA[C/T]GTTTGCTCCAGACAACTCCTGGTTTATTCAGACCATGAATGATGTTTTTT
Long Flanking Sequence:
TCAACTGTATAAAATCTATCATATATTCAGCATGGATTTCAGATATTGCAAACAAAGGCTGTTACATTTTTTTTTCTGACAAATAATAAAATTTAATATCCAAATATATTATACGCATATAGAGAGAAGAGTGTTTCTACAGGTGGTTTGTCAAGCCCACTGTGTGTAGCCCATGTTTTTTTTTTATGTAGATATAGAGTGATTGTAAGAAAGGGTATGGTAAAAAGCTGGTGCAAATGTCTGGTATAGTGTAAGATTGTGTTTTCTACAGGTGGTTGTGTTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAGACACTCAGAGTTGCATACTTTTTTGAGGTTGTCGTGATGGGGTCCCATATGTTTTCAAATATATGTTGCATATATTTTATATATGTTAAATCTAAATATTAACTTGTATGTCATACATGTCATTTGCATATATAACTACATCCTATTGTTGCACGTGAGTTTTTCTATCAAAACCCTTA[C/T]GTTTGCTCCAGACAACTCCTGGTTTATTCAGACCATGAATGATGTTTTTTCTATCGGCGGAGATTTGCTGCAGCAGGACATCTCCAATAATTTTCTGCGACTGCTGGCGGAGGGTAAACGAGATTAATAGTTGGTGTGGGAGATGTTTTTTGTGTGTTGTTTTTTTTAATTTCGTGATGTTTTGCTTTGTTACAGGATCAGAGTCTAAAGAGGAGGATGATCAGCTACGGCTGTACGCTGTCGACTCGTATCTGACATTATTGAACGGAGACGCTTCTCATCTGCCGCAACGCTTCATTCAGGTCATGAGCTGGGTGTGTATGCTGTTTAATATCAGTGTATGTCCAAAGTAGTGCCTGTGGGCTAAAGTTGGCCCATGGTAACCTTTGATTTGGCCTGCCATCCCTCTGAGAAGAGAGGAGGAATAATGGGGATGGTTTTTAAGATTGTCAATTCAAATTCAATGTATCCCTTTGTTTGTTTTATTGCTAAAAGTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19357
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109284 | Nonsense | 766 | 1121 | 17 | 21 |
ENSDART00000109284 | Nonsense | 766 | 1121 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 4890209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4751451 |
GRCz11 | 25 | 4877879 |
KASP Assay ID:
554-6224.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGCAAACCAACGACAAACAGCAGCTGGCTTCCTCTTTGTTTGTTGGTT[T/A]GAGTACGCAGAGTTCCACATCTTTGGTGAGAAAATTGTTTTATGAACAAA
Long Flanking Sequence:
GGGCAAAAACAGCCCCCAACATAATGAATGTGTAGTAAACTTGACCAATACACAAGGGTTAATGCTCATGAAAAAATCCAAAAAGAACAAATTATACCTTCAAATATATTAAAGTAGAAAATTGTAGTTATAAATTGTAACATTATTATTATAATATTTTTAATGCATTTGTGATCGAATTTGGCCTTAGTGAAGCATCTTTTAAAACATTAAAACCTCATTCTTTTGTAAAATATATTGTGTAATTGTTTTGTATTTTAACATTGTGCATTGCTTCAGTGCCAGCACTCTAATCCTCGAGGGTGTAAAGAGAGTTTGGGGTAAAGATGGGTACCTTCCACAAAAAGAAACAGCAGTAACAGCCTCTCCGGTGGATGAGCCCAGTGCTGCAGTTCAGCCCGTCGGCCAGCAGGAAGCAGCAGAGAGATTAGAGCCACAGCCGGAGCCTTCAACGCAAACCAACGACAAACAGCAGCTGGCTTCCTCTTTGTTTGTTGGTT[T/A]GAGTACGCAGAGTTCCACATCTTTGGTGAGAAAATTGTTTTATGAACAAACTGAAAATTATTTTATGACGTTCGAAAGCTCAGCCAGCTGCCCTGTAGCATATGCTCACCTCATAAAACTAATTTCAAACTGACTTCAGAGAGGTTAGTAAGTTTAATGATTTACCACAAAACCGTTTGATTTACAGAAGTAAGCACTAAATGTAGAATTAGGAATTAATAGTTATAAGGGACACCGGTGGACATTAAGTGAACTGCAGCCCTATTGCTCGCACTTGTGCACACGAAACATACAGAATATGATTCAACAGCAAGGGAAATTCTCAGAGAAGTTCATTTTCATGCTGAACAAATGTTGGAAAAGCTGGAAGGTCTTTTGTAATGTATTCTGTTAACGAATATCCATGCGCCTTTCACACTGCTGAGGGTGACATGTAGATGAATATATGAGTATGTGCTGCGCTCTTTCCTTGCAATGATGAAAAAAGTGAAGACAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11955
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109284 | Nonsense | 766 | 1121 | 17 | 21 |
ENSDART00000109284 | Nonsense | 766 | 1121 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 4890209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4751451 |
GRCz11 | 25 | 4877879 |
KASP Assay ID:
554-6224.1 (used for ordering genotyping assays)
KASP Sequence:
AACGCAAAYCAACGACAAACAGCAGCTGGCTTCCTCTTTGTTTGTTGGYT[T/A]GAGTACGCAGAGTTCCACATCTTTGGTGAGAAAWTTGTTTTATGAACAAA
Long Flanking Sequence:
GGGCAAAAACAGCCCCCAACATAATGAATGTGTAGTAAACTTGACCAATACACAAGGGTTAATGCTCATGAAAAAATCCAAAAAGAACAAATTATACCTTCAAATATATTAAAGTAGAAAATTGTAGTTATAAATTGTAACATTATTATTATAATATTTTTAATGCATTTGTGATCGAATTTGGCCTTAGTGAAGCATCTTTTAAAACATTAAAACCTCATTCTTTTGTAAAATATATTGTGTAATTGTTTTGTATTTTAACATTGTGCATTGCTTCAGTGCCAGCACTCTAATCCTCGAGGGTGTAAAGAGAGTTTGGGGTAAAGATGGGTACCTTCCACAAAAAGAAACAGCAGTAACAGCCTCTCCGGTGGATGAGCCCAGTGCTGCAGTTCAGCCCGTCGGCCAGCAGGAAGCAGCAGAGAGATTAGAGCCACAGCCGGAGCCTTCAACGCAAACCAACGACAAACAGCAGCTGGCTTCCTCTTTGTTTGTTGGTT[T/A]GAGTACGCAGAGTTCCACATCTTTGGTGAGAAAATTGTTTTATGAACAAACTGAAAATTATTTTATGACGTTCGAAAGCTCAGCCAGCTGCCCTGTAGCATATGCTCACCTCATAAAACTAATTTCAAACTGACTTCAGAGAGGTTAGTAAGTTTAATGATTTACCACAAAACCGTTTGATTTACAGAAGTAAGCACTAAATGTAGAATTAGGAATTAATAGTTATAAGGGACACCGGTGGACATTAAGTGAACTGCAGCCCTATTGCTCGCACTTGTGCACACGAAACATACAGAATATGATTCAACAGCAAGGGAAATTCTCAGAGAAGTTCATTTTCATGCTGAACAAATGTTGGAAAAGCTGGAAGGTCTTTTGTAATGTATTCTGTTAACGAATATCCATGCGCCTTTCACACTGCTGAGGGTGACATGTAGATGAATATATGAGTATGTGCTGCGCTCTTTCCTTGCAATGATGAAAAAAGTGAAGACAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8426
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 |
---|---|---|---|---|---|
ENSDART00000109284 | Nonsense | 877 | 1121 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 25 (position 4892523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 4753765 |
GRCz11 | 25 | 4880193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CRTCTCAGATACTGGGCAGTGATATGGTGATAGTGCGGCCCAACACAATA[C/T]AACACAAKCCGTCCACGTCTTCAGACCTGACCACTCTCTTACCTGCAGAC
Long Flanking Sequence:
AGAAGCCCTGCACAATAATTCAGAATAAGCCAGAAAAGTCCCGTCCAAAAATAAGCCAGAAAGAAGCTCTGCCCCTCAATTCAGAATAAGCCAGAAAGAAGCTCCGCCTCTTTAATTCAGAAATAAGCCCTGCCCAATACTTCACAATCAGCCAGAAATCTGTTTGTAATTTGCTACTTTTCTGTTTCCTTAAGCTGGGAAAATCTGAAGCTCCGCCTCCTCGGTTCAGAAAGAAGCCCCGCCCTCATGGATCATCATTATCATCCTCATCCTCATCAGGAACAAGTGAAAAGTCTTCCTCCTCCCGGACCTCACATAACACAACTGACAGCTTCCTGTATGGCAGTTTGCTAGAGGAGGAGCCAGCCGGTTTTGACCACACCCCCAAATCCATCACAGCCAATGGTCTTGGCCAAAATAAAGACGTTAAAGAAGACAGACGTACAAACACATCTCAGATACTGGGCAGTGATATGGTGATAGTGCGGCCCAACACAATA[C/T]AACACAATCCGTCCACGTCTTCAGACCTGACCACTCTCTTACCTGCAGACCTTAAAGACCTACCTCACTCTGATGTCATCAGCCTGACCTCTGACCCCAGCCTGAGTGTGTCATCCTGCCGCGTGTTCAGAGATGAAGCTCTGCTGCTCGTCATCTTCATTTCTAACAGCACAGAGACTGATATAAGAGATGTTGCAGTGCAGCTCAACTGTGACCAGCTGGAGGTGTGTATATATTATTCATAAATTAAAAATAATTATTATTAATATCAGTGATGAAAACTGTTTGGCTGCTTCATATTTTTGTCAAAACTGTGATACACTAAAGTTCTAAATTAACATTAAAATGTGTTTTTATTCACTAAATTTATCATTTTTTATTTGGAAGGTGTAAAAGCAGATTTAATTTCAAGTAGATGTTATCTAGACTTTTCTTTTCATCATTTACTGTATAATAATAATGTAATTAGGGATGCTCCGATCAGCATTTTTGCAGCTGAT
Associated Phenotype:
Not determined