ZMP
zgc:86896
Ensembl ID:
ZFIN ID:
Description:
actin-related protein 2/3 complex subunit 1A [Source:RefSeq peptide;Acc:NP_001002100]
Human Orthologues:
ARPC1A, ARPC1B
Human Descriptions:
actin related protein 2/3 complex, subunit 1A, 41kDa [Source:HGNC Symbol;Acc:703]
actin related protein 2/3 complex, subunit 1B, 41kDa [Source:HGNC Symbol;Acc:704]
actin related protein 2/3 complex, subunit 1B, 41kDa [Source:HGNC Symbol;Acc:704]
Mouse Orthologues:
Arpc1a, Arpc1b
Mouse Descriptions:
actin related protein 2/3 complex, subunit 1A Gene [Source:MGI Symbol;Acc:MGI:1928896]
actin related protein 2/3 complex, subunit 1B Gene [Source:MGI Symbol;Acc:MGI:1343142]
actin related protein 2/3 complex, subunit 1B Gene [Source:MGI Symbol;Acc:MGI:1343142]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9106 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1729 | Nonsense | Available for shipment | Available now |
sa16742 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9106
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102883 | Nonsense | 150 | 357 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 36279807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36151091 |
GRCz11 | 3 | 36280689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTAAGCATATCAAGAAACCCATTAACTCCACRGTTCTAAGTCTWGACTG[G/A]CATCCCAACAACATGCTGCTGGCTGCCGGCTCTGCTGATCTCCACTGCAG
Long Flanking Sequence:
TCCAACATAATCTATTGCACTTGACAGAAATCTGCCATTATTTGTATTCAAATGATTAATAAACTTAACTAACAACTGATTTGCTTTCAGGGATTGACTGGGCCCCAGAGTCTAATCGAATAGTGACTTGTGCCTCGGACAGGAATGCCTATGTATGGACACTCAAGGATGGGGTCTGGAAGCCGACACTGGTGCTGGTTCGCATCAATCGAGCTGCCACATGTGTCAAGTGGTCGCCTCTTGAGAACAAGTTTGCTCTTGGAAGCGGGGCCAAACTTATTTCCATCTGCTACTTCGAAAAAGAAAACGACTGGTGAGACTTGCTTGCATAATGTCTTGTAATGTAATTTTGCAAAGTTGATTCGTCTGGTGACTGAGAGACACATTACAGTATCTCCAGTGTAGCTGTGCCACAGTTCTTATGTGCTTGATTGATCCCATAGGTGGCTGAGTAAGCATATCAAGAAACCCATTAACTCCACGGTTCTAAGTCTAGACTG[G/A]CATCCCAACAACATGCTGCTGGCTGCCGGCTCTGCTGATCTCCACTGCAGGTTTCAATATTCAGATGCTGCACAATATTCCAACATTCATAATATTTTAGGGTAACTTCACTTTTTATTGTTGTTGTTTTCAGAATATTTTCAGCATATATCAAGGACATCGAGGACAGGCCTGGACCAACACCATGGGGTTCCAAAATGCCCTTTGGGGAGTTGCTTCTGGAGTATAAGGAGTGTGGTGGCTGGGTGCACAGTGTCTGTTTCTCTCCATCTGGTGATTCTCTGGCCTGGGTTAGCCATAACAGCGCCATCAATGTAGCAGATGCTTCACAGGGGAAAGAGTAATAACAGCATTTACAATAACAAAATGTCTTCATTTTTGTCTAGAGTGACAGAAAATCTGTTATTAAATATTCTTGAATTCGATGCATCTATAGAAAACTCTACCTGACGGCAATAATATGCGCAGTTCAACCTTTTCCTGTCATGTTTAGATACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1729
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 |
---|---|---|---|---|---|
ENSDART00000102883 | Nonsense | 199 | 357 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 36280035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36151319 |
GRCz11 | 3 | 36280917 |
KASP Assay ID:
554-1674.1 (used for ordering genotyping assays)
KASP Sequence:
CAACACCATGGGGTTCCAAAATGCCCTTTGGGGAGTTGCTTCTGGAGTAT[A/T]AGGAGTGTGGTGGCTGGGTGCACAGTGTCTGTTTCTCTCCATCTGGTGAT
Long Flanking Sequence:
AGTGGTCGCCTCTTGAGAACAAGTTTGCTCTTGGAAGCGGGGCCAAACTTATTTCCATCTGCTACTTCGAAAAAGAAAACGACTGGTGAGACTTGCTTGCATAATGTCTTGTAATGTAATTTTGCAAAGTTGATTCGTCTGGTGACTGAGAGACACATTACAGTATCTCCAGTGTAGCTGTGCCACAGTTCTTATGTGCTTGATTGATCCCATAGGTGGCTGAGTAAGCATATCAAGAAACCCATTAACTCCACGGTTCTAAGTCTAGACTGGCATCCCAACAACATGCTGCTGGCTGCCGGCTCTGCTGATCTCCACTGCAGGTTTCAATATTCAGATGCTGCACAATATTCCAACATTCATAATATTTTAGGGTAACTTCACTTTTTATTGTTGTTGTTTTCAGAATATTTTCAGCATATATCAAGGACATCGAGGACAGGCCTGGACCAACACCATGGGGTTCCAAAATGCCCTTTGGGGAGTTGCTTCTGGAGTAT[A/T]AGGAGTGTGGTGGCTGGGTGCACAGTGTCTGTTTCTCTCCATCTGGTGATTCTCTGGCCTGGGTTAGCCATAACAGCGCCATCAATGTAGCAGATGCTTCACAGGGGAAAGAGTAATAACAGCATTTACAATAACAAAATGTCTTCATTTTTGTCTAGAGTGACAGAAAATCTGTTATTAAATATTCTTGAATTCGATGCATCTATAGAAAACTCTACCTGACGGCAATAATATGCGCAGTTCAACCTTTTCCTGTCATGTTTAGATACATATCAAATTGTGTGCATTGCAGGGTCACTCAGTTGACTACAAGACATCTCCCATTGCTGAGCGTGCTGTATGTCAGCGAGACTGAGATTGTAGCTGCGGTAAGGAATTGTCCATCACTTGTAGTTGTATGTAAAATGAATTGCAAATGGAAGTGAGCAACCCTAATGCCCTACTCCCTTTGAAAGGCAGATCCCTCAAAGTCTGTTCTGGCATTACTGTTAAACTTTCAT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa16742
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 |
---|---|---|---|---|---|
ENSDART00000102883 | Essential Splice Site | 356 | 357 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 3 (position 36282879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36154163 |
GRCz11 | 3 | 36283761 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTYAGTAGTGTGGGCTTGGATGGTGCCATGGTTGTCTGGGATTTTAAGG[T/A]ATTTTCANTTWTTTTANNNNNNNNNAGGGATTTTAAGTCTCAATAARCAACTCAMTATGC
Long Flanking Sequence:
TTAAAGTAGCTACATTCACAGCTTCTTAGTTGAGAGAGATGTAAAAATGCAGTCAGGTAATCGTTTTTATCTCACACATACTGTATGTATGTGTGTGTTTTAGGGCCATGACTGTTGCCCTTATCAGTTCTCATACAAGGGTCCTGGAAGCTTGGAGTTTGTGAAGAAAGTAGACATTCCTAAGCAGAGCTCCAAGGGCAACATGTCTGCCATGCAGCATTTTCGAAATCTGGACAAAAAGGCGACCACTGAGGAGGAAGACACTGGGTTGGGCAGTTTGCACCAGAACAGCATCACGTAATGAACAGCTTTACAGTCAGCCATACAATATCAAATAATTAAATCTTCTATATGCATGTTTTGCATTGTGTTAATGTTTTAACAATACTGTTAATATTTCTGCTATAGCCAGTTGTGTATTCTGGAAGGGTTGAAGGCCAAGGTGGAGAAATTCAGTAGTGTGGGCTTGGATGGTGCCATGGTTGTCTGGGATTTTAAGG[T/A]ATTTTCATTATTTTAAGGGATTTTAAGTCTCAATAAACAACTCACTATGCAGTGATGTTCCTGCGTTTTTATTAATAATGACTTATTGTTATTTTCTTCATTTTAGCACTGAAACTCCATGGGATCTGGAGCGAGCAGAAAACAATTATAATCTGGATCGACTGTATATGTTTGTTTTCCTCACATGCTTTTTTTTTTTACTAATAGCTCCCATTCAAAGCTTTTTTAATCTATGATTGCATATTCCTATATTGGAAGTATGCATTTTTCCCACTTAAAGTATTAATTAATCAAAACTGCAAAAAAAAATGAAAAAAATGCAATCCCATAATTGTCAATAACTGTGTTGTTTCAACTCATTTTAAATAAGTAGTTTGAACGAGCAACAAAAAATTATATATATATATATATATATATATATATATATATGCAAATGTATGTTCCAACTGTGCCGCTAGTGTGAAAAGCACACAGACTCAGTCTCATTTTATGCACAAATA
Associated Phenotype:
Not determined