Busch Lab

ZMP

asap3

Ensembl ID:
ENSDARG00000021896
ZFIN ID:
ZDB-GENE-050913-39
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.
Availability:
Order Allele From ZIRC
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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