ZMP
asap2a
Ensembl ID:
ZFIN ID:
Description:
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 [Source:RefSeq peptide;Acc:N
Human Orthologue:
ASAP2
Human Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:2721]
Mouse Orthologue:
6530401G17Rik
Mouse Description:
RIKEN cDNA 6530401G17 gene Gene [Source:MGI Symbol;Acc:MGI:1923478]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11846 | Nonsense | Available for shipment | Available now |
sa39170 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23132 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11846
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026152 | Nonsense | 52 | 991 | 2 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 35310033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 35194957 |
GRCz11 | 17 | 35142903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTYTCTGTGTGTGTGTTTAGGCCCTGGATGTGGACCGCAGTGTCCTTTA[C/A]AAGATGAAGAAGTCAGTTAAGGCTATTTACGCCTCGGGTCTGGGTAAGTG
Long Flanking Sequence:
TAGTTCTCCTTATAGTAAACGTTAGTTAATTCGTTAAAATCAAATCAGTGATTACTTTATTAATTACATTTAATGAATTATGCCTTTTTTTCATTAATGGGCATTTACTAAGACATTGACATCACCTTAGATTCATTATTGCCTATTTATTAACTTTTTTTCCTTTAAGTGCCTTAGACTTTGATTATTATTATTATTTTTGTTAACAGTGAATAACTAAAACTTTTAAAGTGCCTTAGACTTCTGTTGTTTATCTTCATGAATCTCTTATCCAAAGAGCACTGACACATTAATTACCCCTGGAGCACTTTTAGTTTGAGTCTGGAGTTAATTATTAGCTGTATTTTGAAGTAACCATGATATTAATATTGTGCACATTTATTATCATTATATAATGAATTTCTGAATATCTGCATTTGTATCTCATATGTATATATCTCTCCTTCTTTTTCTCTCTGTGTGTGTGTTTAGGCCCTGGATGTGGACCGCAGTGTCCTTTA[C/A]AAGATGAAGAAGTCAGTTAAGGCTATTTACGCCTCGGGTCTGGGTAAGTGATCATTCATCATCTCAGCGCCTCTCATGATGTGGCTGTCTGTCGTCTGATTAGATTACAGTCAGGAAATCTCTGCAGCACATCTGCACATTCATCTGACACTAGGAATGTGCTCCGCTTTATCTAAAGGTGACATTTTTGATACATGATATGATGATCGTGCTGAAAAGTTTGGAAGAGGTGGTGGTGGTGTGTTTGGTTTTGATTTTCAGAGATGTTCGGTGTCTCTCTGGGTTTTTACAGTGCTGAATCAATCAGGATTTTACACTTGGTTGTATAGTCCTAGAGAATGTGACTGCTTTTCTGTTGGTTATCTCAATAAATCTGAATTTGTTCATAGTTATTATGGTTGTTGGTGTTGTTTAGCTGCTTTATATGTATTTAATAATACAAACAGTGAAAAGTTTTGAAAGTAGTGCATTACAATATTGAGTTACTCCTCAAAAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39170
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 |
---|---|---|---|---|---|
ENSDART00000026152 | Nonsense | 663 | 991 | 20 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 35375225)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 35260149 |
GRCz11 | 17 | 35208095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTTTAAGCTAATGAAGCTGGAGAGACCCCGTTGGACATCGCCAGG[C/T]GACTCAAACATCTGCAGTGTGAGGAACTGGTGAGCCCTTTTGCTCTTGTA
Long Flanking Sequence:
TGGAACAAATTAGTTTAAAAACTGAATATAAATGTACACTCACTTACACAAGTAAATAAAAAGACTTAATGGGCTAAAAGTCTGCGGATTTCTGTGGGCACAGATTCCGTACTGATCTATGACTATATGCTAGCCATCATGGTTTCAGCAAAAATCTTATTTTAAAAATCCGTCTTATACGGGTGAAGGCCGATTAAATAGACCCCATATTTTCACTTTCACTTCAGCAGTGTTCCCCAAACAATGGCAAGAGCAGATAAGAGCTGCATGTGTCTGAGTGTGTGTGTGTGTGAATCTGTGCCAGGGAGTCTCCTCTCCATTATTTCTGCCAGAGTCTTCTGTGAGCAAGCTGTCTGGATCTTTGTTCAACTCATTGCACAAAGCCAAGAGTACTAAATGTCATGGGACATCCTCCTTCTTTATTAAATGCATCATAGCTGTGTTTGTTTGTGTGTGTTTAAGCTAATGAAGCTGGAGAGACCCCGTTGGACATCGCCAGG[C/T]GACTCAAACATCTGCAGTGTGAGGAACTGGTGAGCCCTTTTGCTCTTGTAGTTTAATATGAGATGAAAGCGCGCTGGGTTTATGGTGTCTCTGTGTGTGTGTTTTAGCTGAACCAGGCTCTTGCAGGGAAGTTCAATGCTCATGTGCATGTGGAGTATGAGTGGAGACTTCAGCATGAAGACCTGGACGAGAGTGATGAAGATCTGGATGAGAAGGTGAAAAACGACTCGATGCTTGTATTCGATTTTGACTTATGACTAGGCCAGATTTCCACAGATTTTAAGCCCATCAAATATATTTCTTTACTTGTGTAAATCTATATTTACTCCGTTTTTACATTTATTTCAGTAATATTATTAACTAACATGAGAGTGTTCACATGATTTATTTACAGTAAAGTTTGTGCAGTAATATTTTGTCCTTTAGTAGATGTATTATGTGAGAGACTTGCTTTGTTTATCAAATAAGCGGATCTAGATGGATTTGCATTGTAAACATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23132
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026152 | Essential Splice Site | 874 | 991 | 24 | 28 |
Genomic Location (Zv9):
Chromosome 17 (position 35382928)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 35267852 |
GRCz11 | 17 | 35215798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAACCCGGACAGGGGCCTCCTGGACAGAACATCAACCGGGCTACAAGG[T/C]CAGATTAACAAATAACCCATTACCACAAGCACACACTCTAATATACTCAT
Long Flanking Sequence:
TCAAATAATCATTGTGAACGTTCTTACTGTAGTATTTCTAATAAAGGTTACGAGACATCTGCTTCCTCCATGATTGTCACTGTGCTGTTTATCTGACGCAGCCATGGTGGAGATCGAGGCACACTCTGAGAGGCATATGGGAATGGTGGGCGGGGAGGACTAGCATTAAAGGCACAGGCCACAAAAACAGCTACATTGTGTTTAGAGCAGAAAACCCCAATATTTTAAAAGGTATAATAAATAATCTGATGTGTGTTTTGAGGTGAAACTGTCCAGACACATTCTTGAGACACAAAAGACCTCTCTTAAATCTTGAAAAAGGGGTCAAATTGGTGCCCTTTAGTGTAATGATGTTTGTTGTTGATGCTCTATTTGCAGTTCTAATGCCCAGCGGTGCTGCTCCTCCTCTGGCTAAAGCTACTGGTATGATGGAGACCATGAATATGCAACCCAAACCCGGACAGGGGCCTCCTGGACAGAACATCAACCGGGCTACAAGG[T/C]CAGATTAACAAATAACCCATTACCACAAGCACACACTCTAATATACTCATGTCCTCTGACAGTCCTGCCCTACAGGACAACTCCATTAAACTCATTATATCTCCAAATAGCCGCTGGTGAAAATGTTTGTTGAGTCTGACTCCAGTAAAAGGTGAACACAAAGGTGGAAATGGCCTGTTGGGAACTGCAGATTCACCAGCTCATTAATTCCTATTCAAGGCCTCATTCACGCACACAGTGCCAGAGGACCAGACAAGTAGGCCACTCGGATTACTAATGGGGTTACCTTGAATGACCCGAGCACAAGACCCTGTTTCCACGTGATATTAACATGCAGTCTCATGGCCACTTGTGTTTAGATTTCATCGAGACCCTCTTATTTCAGCATGCTCTAGAGTACTTTTGCCGGAGCTCTCAGTGTAAAACTAATAAAAGATGTGGATGTTAACTTTAGTTTAACGGTTATTTGTGTGCTTGTGTACAGTGCAGCCAAGTATGAA
Associated Phenotype:
Not determined