ZMP
si:ch211-160i2.3
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100170829 [Source:RefSeq peptide;Acc:NP_001124135]
Human Orthologue:
ASAP1
Human Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:2720]
Mouse Orthologue:
Asap1
Mouse Description:
ArfGAP with SH# domain, ankyrin repeat and PH domain1 Gene [Source:MGI Symbol;Acc:MGI:1342335]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19798 | Essential Splice Site | Available for shipment | Available now |
sa10661 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19798
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 |
---|---|---|---|---|---|
ENSDART00000077151 | Essential Splice Site | 386 | 1077 | 13 | 27 |
ENSDART00000144870 | Essential Splice Site | 387 | 1132 | 13 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 32011965)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32310872 |
GRCz11 | 2 | 32294090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATCGAACATATCATTTCCAGGCAGAGGACGAACAGGAGTTTGTGATG[T/A]AAGTGTGAATGTGTGAGGTCGAGATCTTCATCTGTTATTTCCCTCATGTG
Long Flanking Sequence:
GTTATATTTTTGACTTCAGTTGCGGGCCAGGAGTAAGAGACCCCTGCTATAGACCTTGCTTAGTGAATTCAGGTTTACTTTTTTGCATGTAATATTTTTGGACATGCCTTCCTTAGTTATATTTGTCCTGTCTCTTGATGTGTAGCTCACTCACTTACTAACTGTAATTACTGTACTCCCTGTCCAGTCCAACAGGCAGCCGGTGAGACTGAATCTGCTGACCTGCCAGGTTAAACCCAGTGGAGAGGATAAGAAGTGCTTTGACCTCATCTCTCGTGAGTGTCTACACAGAAACTAAACTTCAGAGTACTTTCATGCGTGCCGAGTGCTCGAAGTGTAACTCCATTACTGAGCCAGAGAGCACTCAGTGCAGTGTTGAGGGACTGAAGGCCAGTTAGCGTAATGGACTTTCTTCATCCTAATAATCTCTCTGCCTCTTTCCCTCTGCAGATAATCGAACATATCATTTCCAGGCAGAGGACGAACAGGAGTTTGTGATG[T/A]AAGTGTGAATGTGTGAGGTCGAGATCTTCATCTGTTATTTCCCTCATGTGTGTAAATGAGATGTGTGTATCTGAGCTTCTGCGTGTTAACCAGAGTAGATTGTGCCTGTGTGTAAGGCTAGAGCTTTGTAAATTTTATATACAGTCATGGCCAAAATTATTGGCACCCATGAATTTTTTTCAGTAAATCAAGTATTTCTCACAGACAAGTATTGCATTAACATGTTTTACTATACACATGTTTATTCCCTTTGAGTTTGTTGGAAAAAAAAGGGAGGAAAAAAGCTCATTTTACATAATGTCGCACAAAACTCCGAAATAGGCTGGACAAAATTATTGGCACCCTTAACTTAATATTAGGTTGCACACCCATTGCAAAAATTGCTTCCTACAACCGTCAATAAGCTTTTTACACCTCTAACCACGAATTTTCGACCACTCTTCCGTTGCAAACTGCTACAGGTCTCTTATATTGGAAGAGCACCTTTTGTCAACATCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10661
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077151 | Essential Splice Site | 1012 | 1077 | 25 | 27 |
ENSDART00000144870 | Essential Splice Site | 1067 | 1132 | 26 | 28 |
Genomic Location (Zv9):
Chromosome 2 (position 31988682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32287589 |
GRCz11 | 2 | 32270807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAGCCTTGGAAATGCCAGTCCCAATGCCACGCRAAATTAACACAGTA[G/C]TGAGTAAAAGACGTGTTTTATGGGTCAAAAATGGAACGTCATCAGTGTAA
Long Flanking Sequence:
ATGTGCTTCAGAAACCCCCACAGGCCCAGGATGCACCTCCCACCAGAGCCTCAGATACAATAACCAGACCCACTGAACCTCCACCTAAAATTCCACAGGTCGCAGAACGATCCCAGCCTGTGGATGTCCCGCAGAAACCGCACATCTCAGACCTTCCTCCCAAACCGCAACTATCAGATCTTCCCCCCAAACCCCAATTGTCGGATTTACCACCAAAACCTCAGCTTTCTGACCTGCCCCCGAAGCCTCAGCTTAAGGATCTTCCCCCTAAGCCGCAGATCAGTGATCTGCCATCCAAACCGGCCGTGTGTTCTGCATCTGAGGCCACACAAAGGCAGTCAACGCAGGAGGAAACCAGTCCGAAGCCCCAGCTGACGGAGACACAGTCATTCAGCCAGCAGGAGGAGCTCTCACCCCGACAGGCCAGCGAGGACACCAATGGAGCGCCCGCAGGAGCCTTGGAAATGCCAGTCCCAATGCCACGCAAAATTAACACAGTA[G/C]TGAGTAAAAGACGTGTTTTATGGGTCAAAAATGGAACGTCATCAGTGTAATAGATATATTTGTTGTAAGAACGAAACATTTATTTTTAACTGTATACAAAATTTAAAGCTGTTGGAAATATGCATTTTCAATGCCCTTTTCATCTTTGACCCATTTAGGTAAAATGGATGCACTTCCAAAATCTTTTTTTCAAACCACATTTTATGAATTACTATTGTTTTATGACTACCAAACCAAAAAAGGGTTTAAATTTAACATTTTAAGTTGTGGCTTAAAAGACTAATGATTTTATTTTTCCGATATTAATACTTTTTTGCACATGGAAAACATTAAATTATTCAAAAGTGAAAGTAAAATTATTCAAAAACGATCACGTTTCCACATATATTAATCAGTGAAAAGGTTTTCTGATAATAATTATGTTTTTTTTTTTCCTGAGAATCAAATCAGCAAATATAAACAGTGTTTAAAAGATTTATAATATAAAACTGAAGACTGGA
Associated Phenotype:
Not determined