Busch Lab

ZMP

asap1

Ensembl ID:
ENSDARG00000002607
Human Orthologues:
ASAP1, ASAP2, ASAP3
Human Descriptions:
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 [Source:HGNC Symbol;Acc:2720]
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:2721]
ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 [Source:HGNC Symbol;Acc:14987]
Mouse Orthologues:
6530401G17Rik, Asap1, Asap3
Mouse Descriptions:
ArfGAP with SH# domain, ankyrin repeat and PH domain1 Gene [Source:MGI Symbol;Acc:MGI:1342335]
ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 Gene [Source:MGI Symbol;Acc:MGI:2684986]
RIKEN cDNA 6530401G17 gene Gene [Source:MGI Symbol;Acc:MGI:1923478]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa6210 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6211 Nonsense Mutation detected in F1 DNA Not yet available
sa38846 Nonsense Mutation detected in F1 DNA Not yet available
sa7350 Missense Mutation detected in F1 DNA Not yet available
sa21921 Essential Splice Site Available for shipment Available now
sa1614 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa6210
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103507 Essential Splice Site 254 1018 8 28
Genomic Location (Zv9):
Chromosome 11 (position 27442752)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 26271578
GRCz11 11 26509194
KASP Assay ID:
554-5111.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGAAGCTGAAGCAGTACATTGATGCCCTCRCAGGACAGCTGAGCGCAG[T/C]GAGTGATTCTTGCATGCCAAYGATTGTACAAATGTATTCTGTGAATCGAA
Long Flanking Sequence:
TGTTACTTTAAATACTGTTATGACTGTTTTAGAAAACTGTTCTTCGGATCTGACCTAGAATGCAAAAATGATTTATAACTTCATCCTGCATTTCTATGGCTATATATCAGACCCGCAGACAAGAAAAAGCCATCATAAATCAAGAATATCAGTCTTTCACAACAGAGCAGTCCAGTGACATGAACTGTAGCACGACGAAATGAATAAAGTGATCCGTGTGCAGAGAAATCTCACAGCTGGGCTTGCTGGCAGCTTCAGAATCATGTGTGGCTTGGCTGATTGCATTGCTTTATAGTCGCGTCCCTCCACGCTCGAGTCTGTCACGCTTTTTTGAGTCTGACTGGAATTTAAGAGTGAGGAAAAGCGTTGAAAGAAGAGCGGTTTGTTATGGGACCTGTAATAAATAAGGCTTTCTTGTGTCAGTTTCTTTCAGGAGTGTCTGGCTGCTACAGAGAAGCTGAAGCAGTACATTGATGCCCTCACAGGACAGCTGAGCGCAG[T/C]GAGTGATTCTTGCATGCCAATGATTGTACAAATGTATTCTGTGAATCGAATCGTAATTTAATCTCAATAATTAGCCACAATCATACTTGGAAAAGAAAAGCTTAATTTGATTTATTCTTTTGGTTTGTTTAGGCTTTTGATTTTATTTATTTAAGGTTTGATATAAAAATATCCTAACCTTAGGTGGTGGCAGGTTTCAACAAACCACACAGTGAAATAGATATAAAAAAACCAAAGTAAATAATAATAATAATAATAATAATGGTAATACTACTACTACTACTACTACTATTACTACTACTAATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATAATTATTATATTAATGTTATACTTCTTTTTCTTCTTCTTCTTATCATTATTACTATTATTATTATTATTATTATTATTATTATTATTATTATTGCTATTATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6211
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
ENSDART00000103507 Nonsense 303 1018 10 28
Genomic Location (Zv9):
Chromosome 11 (position 27454476)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 26283302
GRCz11 11 26520918
KASP Assay ID:
554-5112.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGACAGACYGTATACAGCAWGCATCAGCTTCAAGGCAACAAGCAATA[T/A]GGTACAGAGAAATCCGGCTACCTCTACAAGAGGAGTGATGGGTAAATGCA
Long Flanking Sequence:
AAGGTTTTAGTTTTTTACTCAGACATTTAAAAAGAATATATTTTAGAACAGAAATCACAATACCGTAAAACCGTGATTTTTTTCCCCCCAAGGTTATCATAACATCAGAATCTTATACCAGCCCATGCCTAGCTGAAGTCCTTCCAAAGGATCTGTTATGAGCAATGTGAAACATGAAGCAGAACAAAAAAAGAAACTGTTTTAAAAGCAAAAGTTCTATTTTATCTGTTTTAGACTTCTCATCCTCTTTTATTGTATGAAAAAGAGCAACGAGAACATTCTGTTAAACTTCTCCTTATTTTTGTTCCCACAAAAGAAAGAAAATGATACAGGAACTACCTATTGTATGCAATTTTTCATACAAACAAGCATTTAAATTCCGTTGGGCATCATACAGTAAACAAACCATGAATTCCCCTTTTTCATCTTTCTGTTGTGCAGGATTCTCTAAGCAGACAGACCGTATACAGCATGCATCAGCTTCAAGGCAACAAGCAATA[T/A]GGTACAGAGAAATCCGGCTACCTCTACAAGAGGAGTGATGGGTAAATGCATTTATGTTGTAGTTAATGGCCAAGATATCATCAACTTTGTGTTCCCAGATACAGCATTCTTCAGACATGACATACAATCCACACATTCATTTAGATTTTCTCTGATAAATCCCTTTAGAAATGCTCTGTTAGGCCTTCGTTTCACATTATTTATGTTTGGTGGGACAAATAGTCCTGGTATTCTCTGTATAGCATTGTGCTGATTGAGGAGAATGTGATGTGGATGCTCATTTGTCTGCTAGGTTGAGGAAGATGTGGCAGAAGAGGAAGTGTACTGTGCAGAACTGCTATCTCACCATCGCTCATGGAACTGTGAGTGCTCACATCACCCTATAGCGCAGTTTCTTTCCTCTGCTTCTTTCTGTGATAGAATGGGGATACATCCGAGATATGAATTCTGTTCCTTGCTCTATAACAGGCTATTATGGACTGCAGCAACTTATTTTTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38846
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103507 Nonsense 356 1018 12 28
Genomic Location (Zv9):
Chromosome 11 (position 27457366)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 26286192
GRCz11 11 26523808
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGCCCAATAAATCACCAGCTAAACTCAACCTACTCACCTGCCAAGTC[A/T]AGCCCAGTCTAGAAGACAAGAAATGCTTTGACCTCATCTCACGTGAGTAA
Long Flanking Sequence:
ATATATTTTAATATTTTAATTCAAGCATTTTAAAATCATTTGTTTAGTTAGAGTCTAAGCTGAAGGAAAATGAATGAATGAATTTATGTATTTATTTTATTTAATTTTTAATTTTTATTTTTTTAGTTATTTGTTTTAATCACCTTTCACTTACTCATTTACGTATTTTATTTTATTTTATTTATTTTAATTTTTTTAGTTATTTGTCACCTTTTCACCTTTTCATGTATGCATTTATTTATTCTACATTTTTTGTATTTTTGCTTATATATCTATTCATATTCCCATAATTATTCATATTTATTTTAATATTTTGATTTTACCTATTTGCATTATGACTGACCATAACCAAGACTGTTATTCACACAACAAAAACGAACGAGACATACACAAAGCTGGCAGACAGGCCTTTAGTCATACCATGTAAGTAATTATATTCTTCCCCTTCACTGCAGCCCAATAAATCACCAGCTAAACTCAACCTACTCACCTGCCAAGTC[A/T]AGCCCAGTCTAGAAGACAAGAAATGCTTTGACCTCATCTCACGTGAGTAAACCACACACTCGCATCCATCCCACTCTTTTAAGTTATATAATGGACAAAAAAACCATCAGAGGTAGATTTTGGGAGCTTCATGCAGAGCTGAAGCGTAAAAACCCCAGGCTATTGGGGAGTGCATTGCTTAATTGTATCTTCATGCATCCATGCATTATTCAGGCCTCAGGTCTCCAGCGTCGTTATGACATCATACAAAAATCCAGACATATTTTGGGACACAATACCGAGGTCCTTGAACTCAGAGCAGGTTGTTCCTAAACACTATTTAAAGATTTGGTATTTGCACTTGAGCACAAATGATTTGTTCTTTCCTCCCACTTGTGTTTTAACAAAGGACCTCAAACCTGTTTTTATCTCCTGATTGTTTGCTGATTACACGTTAGCTGGTGCCAGCTGAGGATGAATTGTAAATTTGCAAGGAATAATGAGGGTTGTTTTATTTTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7350
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103507 Missense 454 1018 15 28
Genomic Location (Zv9):
Chromosome 11 (position 27465945)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 26294771
GRCz11 11 26532387
KASP Assay ID:
554-4115.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTTCTTTCAGATCCGAGTTGGATCTCTATAAACCTGGGAATCCTGACA[T/A]GCATTGAGTGCTCAGGGATCCATCGGGAGATGGGTGTACATTATTCACGG
Long Flanking Sequence:
GTCAAATTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATTGACTTTCATCATGGCAAAGATAAAATAAAAAACTATTATGTTTATTAATGTGTTGAAAAAATCTTCTCCCTGTTAAACAGAAACTGGGGAAAAATAAACAGGGGGCTAATAATTCAGGGGGCTATTAATTCTGAATTCAACTGTATATTTATATACACTATATACACCATACATTTCTATATATTATATTTGTATATTTGGAAATAGTAAAAATTTAGCAATTTTTAAAATTTCTGTTTAATTTTAAATTTTTTAACATGGGTGCATTTCTAAAAAAAAATTACAGTGCATTTAGTTTTACTTAACAATATGAAAACTACACAGGGGTAATATTGATAAGGCTTTTTTTTTCTCAATTTCGGATGTCTGGCAGCTGTTCATGAATTTTCTTTACACTCTTTTCTTTCAGATCCGAGTTGGATCTCTATAAACCTGGGAATCCTGACA[T/A]GCATTGAGTGCTCAGGGATCCATCGGGAGATGGGTGTACATTATTCACGGATTCAGTCACTTTCGCTGGATAAACTAGGCACTTCCGAATTGCTGGTAAGGTTTTACAGTGATCGACAGATGAGGAAAAATCTATTTAGTTTTATTGTTTACTGTCACAGGGTGTCATCATTTTTACGTTCATGTGTAGAGTTTTTCACAGTTTGACAAAATTGACAAGGCGAGATGTTGTACTGTAGGATAGAAAAAAATTCTGTAAAGCTTTTCAAATGCTTTTCAGTAAAATACAAATATTAATTAAAACACCCAAGATACACTTTGGAGGTTTTCTTTTCTTTTCTCTTTTTCAGTTTATCAACGTGTTTCTGTAGATTCAGTTACAGTGCAAATTTGTAAAGGCTGTTTTCTCAAAATGTTTATTTCTCTTGTCCTGTATCATAAGTCTGCACTTACTGTACACTAAACATCACATTTATATAAGGTATATGTTCATATATTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21921
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103507 Essential Splice Site 516 1018 17 28
Genomic Location (Zv9):
Chromosome 11 (position 27469010)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 26297836
GRCz11 11 26535452
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGACTCAATAAAACAGAGAGTGTACTTAAATATGTGGTGTTATTCGC[A/C]GGGCTGTACGCAAGGACTTTATACTCTCGAAATACATGGAGTGGCAGTTT
Long Flanking Sequence:
ATCAGTAATTATAAACAATCCTTTGCATAGTGGTTAGTCTTAAAGGTACAGTAGCAAAATAGTGGCTCAGATTTTATCACTCAAAAAAAAGGTGTGGATAGTAAGCTAAAACTATCTTGAGTTGACTTCAGGACGACAAATAAACAATGAAATGTATGCGTGGCCCCTTTAAGGGCTCGGTCAGCTGTTGTCTGCTGGTGTCTGACATGGAGGCTTAGAGTTGGATTTTTCCAAATGTCAGTTGTCAACCCACATCTGTCCAACACACTACAAGAAACGAGATGAGAATTGCACTAATGAGAGCTCCGGAAATGTTGTCTGTTACAATCTGTAGCATGTAATGAGCTAGTAAGCATTACCGAGATGTTGCTTTTTACAATTTCACTGGACGAAAACCAGAATAATTTTATTGCAAATATTTCTTGCACATGTTTAATTTGACTACCACTTTTAGGACTCAATAAAACAGAGAGTGTACTTAAATATGTGGTGTTATTCGC[A/C]GGGCTGTACGCAAGGACTTTATACTCTCGAAATACATGGAGTGGCAGTTTGCACAGCGCAGCGGCGGCTCACTGGAAACAAAGCGCAAATATCTGCAGGACGCTGTTCGCAGTCGGGACGTTTTCAGCCTGTTACAGCTTTACACCGAGAGAACAGATTTCAGCCTGTCACTGCCATGCCCTCTACAGGTCAGCTGTCTTATCTTAAATGAACAACTCAGCAAAAAATTAATATTAACTTTGGTGTTGTTCCAGTGCCATATGCCATTCTTTCATGTTTTGGACCACAAAGAGAGAAATTTAATTAAATTTCCTGTCCATAAAGTAGCAGTGAATCATGAACGGTCCCATCTGACGTGTCTTTTTATTAGAAGTGCTTTAGGAATAAATGAATAGTGATTTGAGAAAAGGAAAGCCAATTATAATGTAACATATAGCAAAAATTATTAACTTGATTGTCTGTGAATAAATATGGCTCGCTAAGAATAATCACACAATTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1614
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
ENSDART00000103507 Nonsense 534 1018 17 28
Genomic Location (Zv9):
Chromosome 11 (position 27469064)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 26297890
GRCz11 11 26535506
KASP Assay ID:
554-1555.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTACGCAAGGACTTTATACTCTCGAAATACATGGAGTGGCAGTTTGCA[C/T]AGCGCAGCGGCGGCTCACTGGAAACAAAGCGCAAATATCTGCAGGACGCT
Long Flanking Sequence:
CAAAATAGTGGCTCAGATTTTATCACTCAAAAAAAAGGTGTGGATAGTAAGCTAAAACTATCTTGAGTTGACTTCAGGACGACAAATAAACAATGAAATGTATGCGTGGCCCCTTTAAGGGCTCGGTCAGCTGTTGTCTGCTGGTGTCTGACATGGAGGCTTAGAGTTGGATTTTTCCAAATGTCAGTTGTCAACCCACATCTGTCCAACACACTACAAGAAACGAGATGAGAATTGCACTAATGAGAGCTCCGGAAATGTTGTCTGTTACAATCTGTAGCATGTAATGAGCTAGTAAGCATTACCGAGATGTTGCTTTTTACAATTTCACTGGACGAAAACCAGAATAATTTTATTGCAAATATTTCTTGCACATGTTTAATTTGACTACCACTTTTAGGACTCAATAAAACAGAGAGTGTACTTAAATATGTGGTGTTATTCGCAGGGCTGTACGCAAGGACTTTATACTCTCGAAATACATGGAGTGGCAGTTTGCA[C/T]AGCGCAGCGGCGGCTCACTGGAAACAAAGCGCAAATATCTGCAGGACGCTGTTCGCAGTCGGGACGTTTTCAGCCTGTTACAGCTTTACACCGAGAGAACAGATTTCAGCCTGTCACTGCCATGCCCTCTACAGGTCAGCTGTCTTATCTTAAATGAACAACTCAGCAAAAAATTAATATTAACTTTGGTGTTGTTCCAGTGCCATATGCCATTCTTTCATGTTTTGGACCACAAAGAGAGAAATTTAATTAAATTTCCTGTCCATAAAGTAGCAGTGAATCATGAACGGTCCCATCTGACGTGTCTTTTTATTAGAAGTGCTTTAGGAATAAATGAATAGTGATTTGAGAAAAGGAAAGCCAATTATAATGTAACATATAGCAAAAATTATTAACTTGATTGTCTGTGAATAAATATGGCTCGCTAAGAATAATCACACAATTCCACTGGTTTATTAAGCCAAAGTTGACTCAAAAATCTTTGTAAATACTCCATAAAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461