ZMP
asap3
Ensembl ID:
ZFIN ID:
Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:RefSeq peptide;Acc:NP_001035081]
Human Orthologue:
ASAP3
Human Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:14987]
Mouse Orthologue:
Asap3
Mouse Description:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 Gene [Source:MGI Symbol;Acc:MGI:2684986]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23092 | Nonsense | Available for shipment | Available now |
sa45611 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25041 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10680 | Essential Splice Site | Available for shipment | Available now |
sa36428 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23092
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036622 | Nonsense | 55 | 184 | 4 | 8 |
ENSDART00000130080 | Nonsense | 189 | 991 | 6 | 26 |
The following transcripts of ENSDARG00000021896 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 27050035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 27189954 |
GRCz11 | 17 | 27208345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGATCCGATTGGACATGACAGACACAGCGGAGGACATGGAAAGAGAA[C/T]GAAGGAACTTCCAGCTGCAGATGTGTGAGGTATTTGGAGGCACTCGCTTA
Long Flanking Sequence:
TGATTAGAAATTTGCATTAATAAGCAGTTGGACAGGTGTACCTAATAAAATGGCCGGTGAGTGTATATTTGTAATTTACATTAAATTACTTTTTATGTCCAAATCTGATTACTTATTTGGTGTCAAAAGATACAGTAGACTGCTTTTGTACATTTCATTTATGTATATCTGCATTGTATTAACCCTTCTGCTTAATATTTATCTTCTATCAGGAGCTGAAAAAACAGATGGAGAAAAGTTGGAAGGATTATGATGCTAAAATGTGAGTTTCTGAGTCAAATCTGTCCTTTCAAATTTGATAAAAACCCACCACTTACTTTGTCTGAAAGACAAGTCCGCCAGCTATACTACTGTTTCATTATGATCTTTTCCCTGTTTGCCCATTAATTTTCACTCTGCTTTTCAGAGGGAAGCTGGAGAAAGAAAGGAGGGAGAAACAGAAACAGCATGGGCTGATCCGATTGGACATGACAGACACAGCGGAGGACATGGAAAGAGAA[C/T]GAAGGAACTTCCAGCTGCAGATGTGTGAGGTATTTGGAGGCACTCGCTTAACAGACTATGAAACATCTGCAAAATTAACCTGACCAAGACCACGTTGTTTTGCGTCTCAGGAAGAATAAGTGCGGTTAGTACAGCTGTATGTGTGTGCTTCAGCGGGTCGTTTATGGGTTACCTCAGCTTGTTAAACTCTCTTTTGTGATGAAAACACTCTTTGTAAATTCAATAAGTGTGTGGTGTTGTCTGAAGTTACCTAAAACCGAGAAGCTGTGGGGAGTGTTTAAGAGACAGCTCTATTTGAGACCACATTGTGTTCATGTGTGTGTGTGGTTAATGATGATGACCTCACACCACATGTCTAAATGGCAACATGTTCAAGTTCTATATATTACGTGCATGTGTATGTGTCAGTTAGCAGGACTGGGGAAATTTGGACTACGCTGCTTGAACTTAGCTGTGGTAATAGAAAGAATACGGAAAAAAGTGAAGTGGAGCAATAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45611
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 |
---|---|---|---|---|---|
ENSDART00000036622 | Nonsense | 63 | 184 | 4 | 8 |
ENSDART00000130080 | Nonsense | 197 | 991 | 6 | 26 |
The following transcripts of ENSDARG00000021896 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 27050009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 27189928 |
GRCz11 | 17 | 27208319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCGGAGGACATGGAAAGAGAACGAAGGAACTTCCAGCTGCAGATGTG[T/A]GAGGTATTTGGAGGCACTCGCTTAACAGACTATGAAACATCTGCAAAATT
Long Flanking Sequence:
GTTGGACAGGTGTACCTAATAAAATGGCCGGTGAGTGTATATTTGTAATTTACATTAAATTACTTTTTATGTCCAAATCTGATTACTTATTTGGTGTCAAAAGATACAGTAGACTGCTTTTGTACATTTCATTTATGTATATCTGCATTGTATTAACCCTTCTGCTTAATATTTATCTTCTATCAGGAGCTGAAAAAACAGATGGAGAAAAGTTGGAAGGATTATGATGCTAAAATGTGAGTTTCTGAGTCAAATCTGTCCTTTCAAATTTGATAAAAACCCACCACTTACTTTGTCTGAAAGACAAGTCCGCCAGCTATACTACTGTTTCATTATGATCTTTTCCCTGTTTGCCCATTAATTTTCACTCTGCTTTTCAGAGGGAAGCTGGAGAAAGAAAGGAGGGAGAAACAGAAACAGCATGGGCTGATCCGATTGGACATGACAGACACAGCGGAGGACATGGAAAGAGAACGAAGGAACTTCCAGCTGCAGATGTG[T/A]GAGGTATTTGGAGGCACTCGCTTAACAGACTATGAAACATCTGCAAAATTAACCTGACCAAGACCACGTTGTTTTGCGTCTCAGGAAGAATAAGTGCGGTTAGTACAGCTGTATGTGTGTGCTTCAGCGGGTCGTTTATGGGTTACCTCAGCTTGTTAAACTCTCTTTTGTGATGAAAACACTCTTTGTAAATTCAATAAGTGTGTGGTGTTGTCTGAAGTTACCTAAAACCGAGAAGCTGTGGGGAGTGTTTAAGAGACAGCTCTATTTGAGACCACATTGTGTTCATGTGTGTGTGTGGTTAATGATGATGACCTCACACCACATGTCTAAATGGCAACATGTTCAAGTTCTATATATTACGTGCATGTGTATGTGTCAGTTAGCAGGACTGGGGAAATTTGGACTACGCTGCTTGAACTTAGCTGTGGTAATAGAAAGAATACGGAAAAAAGTGAAGTGGAGCAATAAAGAAATAAAGGGGGATTTTCAGTGTCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25041
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 |
---|---|---|---|---|---|
ENSDART00000036622 | None | None | 184 | None | 8 |
ENSDART00000130080 | Nonsense | 472 | 991 | 15 | 26 |
The following transcripts of ENSDARG00000021896 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 27040052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 27179971 |
GRCz11 | 17 | 27198362 |
KASP Assay ID:
554-7512.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTATCGAGTGTTCAGGAATCCATCGTGAGCTCGGAGTACATCAGTCA[C/T]GAATTCAGTCTTTAACTCTCGATGTGCTGAGCACCTCTGAGCTTCTGGTA
Long Flanking Sequence:
ACATAGCACCAAGTTGCTTACAGCGACCTGAGTTCGATTCCCAGCTCAAGGTCCTTTGCCAATCCTTTCCTTATTTCTGCTCCCCTCACTTTCCTGTATGTAAATCTCCACTGTCCTATCAGTGAAGATGAAAACCACTAAAAAATGTTTACATCATGATGACAGTTTATTTATTTATATATTTTTGAGTGAGCTATTCCTTTTAAATCATATTAAAATAATTGTTTTATTTATTTTCCACATTAATTTCATTGGCATAAACATCATAATTTTAAAGGGGTCCTATTATGCATTATACTTACATTGGTTTGTTTGTGTAAGACGATTAATGGCATTTGTATGCAAATCAGTTTCTCTGAGTTACTGAACAACACTATATTGGTCACCAACATATGTTTTACTTTTGCTCTTTAGATCCCACATGGCTCTCCACTAACCTGGGCATTCTCACCTGTATCGAGTGTTCAGGAATCCATCGTGAGCTCGGAGTACATCAGTCA[C/T]GAATTCAGTCTTTAACTCTCGATGTGCTGAGCACCTCTGAGCTTCTGGTAAACACACACACACTTCTCTTTTATTCTGAGAGTATGGGTGGTTTCCATGTTTTCTATGTTGAGGCCCACTAAACACACACACACACACCATTAATTTTCTAATTGCACATATCGTATTTCCTTTTTTTCTTTTTGCCCATAATCCACTGGGACTGAGTCAGCAGTTACTCACGAGTGACTCTTTCTCATCTGTACATGTTTATGTGAACTTTTTACCTCTTACAGTAAGGAGAAATCTTCCCAAGTGTTAGTGTCCTTTATTATTTTACTGCTTAGTTGGATATATAGGCAAACATGGATGCACAAAGCTGGATGCATGAATGAAGTGTACAGATGTGTTCATTAGATATGTTTTGATTCACAGTTGGCAGTGAGCATTGGAAATGCCAGGTTTAATGACATCATGGAGGTCAACTTACCCAATGATGCAGTCAAGCCACTTCCAAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10680
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036622 | None | None | 184 | None | 8 |
ENSDART00000130080 | Essential Splice Site | 488 | 991 | 16 | 26 |
The following transcripts of ENSDARG00000021896 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 27039638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 27179557 |
GRCz11 | 17 | 27197948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNTGAATGAAGTGTACAGATGTRTTCATTAGATATGTTTTGATTCACA[G/A]TTGGCAGTGAGCATTGGAAATGCCAGGTTTAATGACATCATGGAGGTCAA
Long Flanking Sequence:
ATCCCACATGGCTCTCCACTAACCTGGGCATTCTCACCTGTATCGAGTGTTCAGGAATCCATCGTGAGCTCGGAGTACATCAGTCACGAATTCAGTCTTTAACTCTCGATGTGCTGAGCACCTCTGAGCTTCTGGTAAACACACACACACTTCTCTTTTATTCTGAGAGTATGGGTGGTTTCCATGTTTTCTATGTTGAGGCCCACTAAACACACACACACACACCATTAATTTTCTAATTGCACATATCGTATTTCCTTTTTTTCTTTTTGCCCATAATCCACTGGGACTGAGTCAGCAGTTACTCACGAGTGACTCTTTCTCATCTGTACATGTTTATGTGAACTTTTTACCTCTTACAGTAAGGAGAAATCTTCCCAAGTGTTAGTGTCCTTTATTATTTTACTGCTTAGTTGGATATATAGGCAAACATGGATGCACAAAGCTGGATGCATGAATGAAGTGTACAGATGTGTTCATTAGATATGTTTTGATTCACA[G/A]TTGGCAGTGAGCATTGGAAATGCCAGGTTTAATGACATCATGGAGGTCAACTTACCCAATGATGCAGTCAAGCCACTTCCAAAGAGTGACATGTGAGTCAAATTGTGTAGTTTACAAACACAGCGTCTTGATAACAGCAACATGTATTTGCTGATAGTAGCTGTGCTTTAGAATTTTTTCTGATTCATTTTGTTTTTGTGCATCTCAGGACAGCGAGGAAGGAATACATTGTAGCGAAGTATGCAGAGCGGCGCTATGTTCTCCCTAAAGAGCACTCTGAAGCATACCGCGTGTTTGACACTGTGAGGAGCAAAGACCTCGTGTCACTGCTGCAGCACTATGCAGAGGGAGAGGACCTGTCTAAACCAGTCGCCATTCCCGATGGACAGGTGAGACAGCTCAGCCCCACCACTATGATAACATAAACATTCCATTGCTCCATTTCTGACTTCAGACATTTCCTGAGATGTTCAATTCCATATGAGATTTCCTGCGGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36428
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036622 | None | None | 184 | None | 8 |
ENSDART00000130080 | Nonsense | 730 | 991 | 22 | 26 |
The following transcripts of ENSDARG00000021896 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 27036298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 27176217 |
GRCz11 | 17 | 27194608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACTTCCCCCTACTGGTGTGAACGGGCACTGCTCTTCTGCGTGGAATT[T/G]AAATAAAAGCTGTCCAGCCAGAACCTATGAGAACATTGACTTCCTATATC
Long Flanking Sequence:
TATCATCACATAAAGCAAGCATACAATAATGATGCAGTTTAATATCATTTCTGCCAAATTAAAGGCCGGGGTCATGCAGTCCCCGATGGTTGATTATAAAGTTTTTGTTTTGCTGTATCTTATTTATATCAGTCTTGTCAAAACTGTAACCATGTGAGCCGGCTATGATATTTCTTATCTTTTTTGTGTATGTTCAGTTGGAATTGGCACACAGTGGGAAGTTTAACTCTCAGATCCATGTTGAATACACATGGGAGATGCCACAGGACATGTATGACAGTGAAGACGATCTGGATGAAAGGGTCTGTTATGACTTCATACTATATGAATTTTTGTATTAGCAAAGTAGTCCTCAGGAAAACAGATTTCTCTTTTTTTTTTATTCCAAATCTAAATACAAATGCTCAATGTCATTGTTTAGGCAAGTCCTCATCCTAAAGTATCACGGTCTCCACTTCCCCCTACTGGTGTGAACGGGCACTGCTCTTCTGCGTGGAATT[T/G]AAATAAAAGCTGTCCAGCCAGAACCTATGAGAACATTGACTTCCTATATCGAAATCCACCCAACAACAGCGCCCCCACTGGTGGTCACATGCCACCTCCACTACCAGCTAAAGCAATACAGAGAGGTAAGATGCTGTTTATCAGCCTTTAATTGCTGAAGTCTGGAATTAAGCATCGACAAAAGAGCTGAATGTTGAGCTGATCAAAATTGAATAGACAAACAAAAATTATTTTATTTTATTTGAAAAGATGAAGTGAGCTGGTTGCATATGTAGATTTCTATAGAAACCCTGCAGGTTTATTCCAGACAAACCACAGCACGGTCATAGGTAATATGTGTCCCCACAGGACGTTCAGATCCTCAGATTTCGGGTTCCATTCCAGAGACTCACACTCCGTACCGCCAGAGTTCTCATCCCACGGGTTGCTTTCAGAAAATTAGCACCACACCTCCAGAGCCCTGTGGACCCACACCTGCACGCTCTCACAGCACCGGGCCA
Associated Phenotype:
Not determined