ZMP
si:ch211-168b3.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate centaurin, beta 2 (CENTB2) [Source:UniProtKB/TrEMBL;Acc:B8JLA1]
Human Orthologue:
ACAP2
Human Description:
ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 [Source:HGNC Symbol;Acc:16469]
Mouse Orthologue:
Acap2
Mouse Description:
ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 Gene [Source:MGI Symbol;Acc:MGI:1925868]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2032 | Essential Splice Site | Available for shipment | Available now |
sa39760 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2032
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 |
---|---|---|---|---|---|
ENSDART00000092525 | Essential Splice Site | 37 | 735 | 2 | 22 |
ENSDART00000131688 | None | None | 129 | None | 4 |
ENSDART00000147831 | Essential Splice Site | 37 | 499 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 5533190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5978918 |
GRCz11 | 2 | 5890800 |
KASP Assay ID:
554-2588.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGGATGTGGAGGAAGACTTTGGAGAACTGGAGTCAAAACTTGACAAGG[T/A]ATGATTTTCTCATTGACATACTGGCTTTAAAGTTTGCTTATGTGNNTTTT
Long Flanking Sequence:
TAAATTGGATAATGCAGGACCGGCTGTAAGCAATCAAAAGCACGTGATCCTCTTGAAATTAGTTTATAAATAAACTTCTCTTATTGCTTCACTCAGTGAACTGCTAATAATGGAAATTCTGTGATAATTGCTTTTTCTTTGTATATGTCTACATGTTACATATAAAAACATTATTAAAGTAGTTTGAATGAATAATAAACAGAGCCTTCTGTTTGAATTTAAAGAATGAAGCGATTAAATGGCGAAACAAGAGTAAACTGTGTTCAAGTTATATTCAGATGACGGGATTTGATTTCATCGGTTCCAAAGGAATTTAATCTTTGGTTCCATTTGCCTACAATTAAGTTGAAATAGCATCCTTCAATTATGTGTCAAATGTCTGTCTGTATTCATAAGTTCACAGATGATGCTTCAGATAATTTGTGCAATGATATTTTGTAGGGCCACAATAGAGGATGTGGAGGAAGACTTTGGAGAACTGGAGTCAAAACTTGACAAGG[T/A]ATGATTTTCTCATTGACATACTGGCTTTAAAGTTTGCTTATGTGTTTTTTTTTTACTTTATATATTAGAATTGTTTGCCATAATAGAATAATGGAGGTCACACTTAAAGAAAAAACACAACAGTTTTATTCTTGGGTCTGAACAACAAACAACTAGCACCAACGAAACTCAACTGTGTTGCACCCTCAAGTTGGATTGCATCTAGACCCAAAATCTGTGCGTGAACACACCGAATGGACGAAAGGCGGCTGGAACAAGAGCCACGTTCTAAACGTCTGCAAGATTACGTGTCTTTCCACGGGGGAGCGTATCTGTTTACTTCCAAACTTCTTCCAAACAAAGCAGCATTCAGTACCGTTATCACAGTAATTGTCACTCACCATGGAGGGATTTTCTCATGCAAATAAGTCTGATAATCCAATAATCCATATGGTTTGCAAATATTTGAGAAATATAGCAAAATTATCGTGTTTTGATTTGTTGCAGAATAACCAGTCAGA
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:
sa39760
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, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092525 | Essential Splice Site | 436 | 735 | 15 | 22 |
ENSDART00000131688 | None | None | 129 | None | 4 |
ENSDART00000147831 | Splice Site | None | 499 | None | 17 |
Genomic Location (Zv9):
Chromosome 2 (position 5553070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5998798 |
GRCz11 | 2 | 5910680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGGCATAATGAAATTGACATAAATATTGATAATTATTTTTTTTCTTT[T/C]CAGGAGTTTAGGAGTTCACAATTCAAAGGTGCGATCTCTCACACTCGACA
Long Flanking Sequence:
ACCTCAAGGGTAGTTCATGTGTTGGTGCTCTTTGAATAAGGGATTCGTAAAGATAGATGACAAAATCAACGACCTTTATTGTTTTAACACCTCTAGTTTGGAAAAAGTCAGGAAAGTGTCCAGCTCTGTTTAGGTGGCAAGGTGCATAAAAAATTTGCACAAAAATGGGAGTTTTCGGTTCGTGCACACAGAGGCAATACAAACACACAGATGCAGAGGAGATGTCAAAAACCAGGGGTGTCCAAACTCGGTCCTGGAGGGCCGGTGTCCTGCATAGTTTAGCTCTAACTTTGTTTAACACATCTGCCTGGAGCTTTCTAGTATGCCTAGAAAGAGCTTGATTAGCTGGTTCAGGAGTGTTTAATTGTGGTTGGAACTAAAATATGCAGGACAGCAGCCCTCCAGGACCAAGTTTGGGCAGCCCTTGTGTAAACCAATTAGAGGACCCAGAATTGGCATAATGAAATTGACATAAATATTGATAATTATTTTTTTTCTTT[T/C]CAGGAGTTTAGGAGTTCACAATTCAAAGGTGCGATCTCTCACACTCGACACATGGGAGCCAGAACTGCTGAAGGTAAAAGTGCATTGTTAGGGGGTTTAATTTGTGTGTTTTGGTGTTGTGGTGTATTAATTCACTCATATGTGCCGTATGTTTAGCAGTTGTCTCACTGTGTGTTTTATTTGCAGTTGATGTGTGAGCTGGGAAATGATGTTATTAATCAGATCTATGAAGCGCACAGAGAAGAGAATGGTGGCAAGAAGCCTCAGCCTGGAGATCCCAGGTATCCTGAACACTGTTTGTCTACACTACCTGACCAAAGTCTTATCGCTAATCCCAGTTGTAAGAGCAACAAATAATAACTTCACTTCTAGTTGATCATTTGGAAAATTGGCAGAAGGTCGACTTCTTTAGATGAATCATCTGTTGAGCTGCATCCTAAACTTCAGAAATACTGCAGTAGACCTACCTGAACATACATGGTACATACATAGGGGCCTGT
Associated Phenotype:
Not determined