Busch Lab

ZMP

arfgap2

Ensembl ID:
ENSDARG00000067601
ZFIN ID:
ZDB-GENE-051120-177
Description:
ADP-ribosylation factor GTPase-activating protein 2 [Source:RefSeq peptide;Acc:NP_001032507]
Human Orthologue:
ARFGAP2
Human Description:
ADP-ribosylation factor GTPase activating protein 2 [Source:HGNC Symbol;Acc:13504]
Mouse Orthologue:
Arfgap2
Mouse Description:
ADP-ribosylation factor GTPase activating protein 2 Gene [Source:MGI Symbol;Acc:MGI:1924288]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa43166 Nonsense Mutation detected in F1 DNA Not yet available
sa29091 Nonsense Mutation detected in F1 DNA Not yet available
sa13828 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa43166
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097328 Nonsense 83 536 3 16

The following transcripts of ENSDARG00000067601 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 43269359)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44859250
GRCz11 18 44852704
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAACTGGATTCCAACTGGAACTGGTTTCAGCTGAGATGCATGCAGGTT[G/T]GAGGAAACGCCAATGCGGTCAGTTCTCCTATAATATGCATAGAGTTGCAT
Long Flanking Sequence:
TCTTTCGGTTAATGTTAATTGGTTATTATAAGTATCCCTAATACTAACTAAAATTATTGTATAGTTTTAAATGTCAGTATCGATATTTACTGAAATTTTGATATTTTTGACAACACTAAAATACACAAACTTTTTTTTTTTTTGCAACTTATTATTATTTGTATTTATTTCTAGGCCTGTTTTGACTGTGCGGCTAAGAACCCGAGCTGGGCCAGTATTTCATATGGAGTATTTCTGTGCATCGACTGCTCTGGAATACATCGCTCTTTGGGAGTGCACTTGAGCTTTATCAGGTCAGCTCTGTTGTTTTCCTGTTTTTATATAATGTGTGCAGTCATGTGAATGTCTGCCAAGGTTTTCTTTATCTCTCCCATTACAGAATGTGACATTCATTATTAGTATGAGCTAGTAGTATGTGTTAAAGAGTGGAGCGTTGTCTTTTCAGATCCACAGAACTGGATTCCAACTGGAACTGGTTTCAGCTGAGATGCATGCAGGTT[G/T]GAGGAAACGCCAATGCGGTCAGTTCTCCTATAATATGCATAGAGTTGCATCATATTCACTGTAGACTCCATGCTTTTTGTATCACTTCCTATTTCATGTGATTTCCTTGTGCACAGATGGGTTTTTTCCGCCAGCATGGCTGTACCACCAATGACACTAATGCGAAGTATAACAGTCGTGCGGCTCAGATGTACAGAGAGAAGATTCGACAGCTTGCCAACGCTGCCCTCTCTAAGTATGGCACCGATGTGAGTATATAAATCTGATATTGTTCCAGTATTATCTCTGGCTACAATGTGAACTATGCCCTTCAGATTTGTTGTCAGCAGTTGTTATTAACAGATATCTTACTGTCATGCGGGTAACAAAAGCAGTGCCTCCCACCTGGCTTTAAAACCTGGAATTTACATGGGGTATTTTATGACAACCTAACAGTTTTAAAAGATAAATATAATAATATTATTAACAATACAGGGTGTTCACAGTGTCTTAGGGTGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29091
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097328 Nonsense 375 536 12 16

The following transcripts of ENSDARG00000067601 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 43286914)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44876805
GRCz11 18 44870259
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAGTAACTTGTAACTGTGTTTTCAGGTACAAGGACAACCCTTTCACAT[C/A]AGGAGACAGCTTTGGGTCACGGTGGGACAATGATGGCGGGTCGTCGTTCT
Long Flanking Sequence:
TCAATTCTTTTCTAAGGGTTTTCTATGAAATTAACTAACTCGAGATGTTCAGCAAAGGAATTTTTGTTAAGGCTTTTTATCACGTATTAATTGGTAAAAACCTAATTTCAGTAAAATGGTAAAAATCCTTTGTATTCATTTGTTTGTGTTTTTTTTAATTGTATATTTATATGTATAAATGTTGCTGACATGACATAATTTTAAATGTGTGTATATATATGATATGATCTTTTCTAAGGGCGCATGTCCAGTGAAGCATTTTTTTTCGGCCGGAGTTTAGTGTATTTTTCAGTTGTTATCAGTGAAAGTAAAAAAAAAAATTGAAATAGGTTTGTTTAATTTTGGCCTGACTGAGACATGAGGTTGTGACACTGGTAAATGGAGGGAAAAAAAGACATGCACAAATGTTGCAGTTTCCTTATATCATACAATTTCTAGTATCTTGACAACACTAGTAACTTGTAACTGTGTTTTCAGGTACAAGGACAACCCTTTCACAT[C/A]AGGAGACAGCTTTGGGTCACGGTGGGACAATGATGGCGGGTCGTCGTTCTCCTCCTGGGCTCTGGAGAAGGAGGAGCCTAAAGACAGCGAGGTCACCATCTCAAGCATCCAGCCAATCGGAGAAAGGTAACGTCCTCATCCGGCAGTCAGTGGGTTTGGTTTTGATTAGTGTCTGGTTTTTGTGATTCTGGACTCTCGTCTTATCTCAGGTTGCCCAGCAGACGGAAGCCGGAGGTTTCTGTGCCGGTCTCAGAGTCTAGCGAAGCGCGCCAGAAGTTTGCGAATGCTAAAGCCATCTCATCAGACATGTTCTTCGGCCGTGAGAGCAACCCAGAGGTACAAGGAGAACCACTACTTTACTTCATAACCCCCTTTTTCTGTACTTATTTACATTTGACTTCTTCCTTAACCCTTTATTATATGTTCTTTATATACAGTAGAAGTTTGTTTCTTAAAGTTATTTCGTATGCTCACCAAGGCCAAGCAAAAATGCAGATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13828
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000097328 Nonsense 415 536 12 16

The following transcripts of ENSDARG00000067601 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 43287033)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44876924
GRCz11 18 44870378
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGGAGCCTAAAGACAGCGAGGTCACCATCTCAAGCATCCAGCCAATC[G/T]GAGAAAGGTAACGTCCTCATCYGGCAGTCAGTGGGTTTGGYTTTGATTAG
Long Flanking Sequence:
TAAAAATCCTTTGTATTCATTTGTTTGTGTTTTTTTTAATTGTATATTTATATGTATAAATGTTGCTGACATGACATAATTTTAAATGTGTGTATATATATGATATGATCTTTTCTAAGGGCGCATGTCCAGTGAAGCATTTTTTTTCGGCCGGAGTTTAGTGTATTTTTCAGTTGTTATCAGTGAAAGTAAAAAAAAAAATTGAAATAGGTTTGTTTAATTTTGGCCTGACTGAGACATGAGGTTGTGACACTGGTAAATGGAGGGAAAAAAAGACATGCACAAATGTTGCAGTTTCCTTATATCATACAATTTCTAGTATCTTGACAACACTAGTAACTTGTAACTGTGTTTTCAGGTACAAGGACAACCCTTTCACATCAGGAGACAGCTTTGGGTCACGGTGGGACAATGATGGCGGGTCGTCGTTCTCCTCCTGGGCTCTGGAGAAGGAGGAGCCTAAAGACAGCGAGGTCACCATCTCAAGCATCCAGCCAATC[G/T]GAGAAAGGTAACGTCCTCATCCGGCAGTCAGTGGGTTTGGTTTTGATTAGTGTCTGGTTTTTGTGATTCTGGACTCTCGTCTTATCTCAGGTTGCCCAGCAGACGGAAGCCGGAGGTTTCTGTGCCGGTCTCAGAGTCTAGCGAAGCGCGCCAGAAGTTTGCGAATGCTAAAGCCATCTCATCAGACATGTTCTTCGGCCGTGAGAGCAACCCAGAGGTACAAGGAGAACCACTACTTTACTTCATAACCCCCTTTTTCTGTACTTATTTACATTTGACTTCTTCCTTAACCCTTTATTATATGTTCTTTATATACAGTAGAAGTTTGTTTCTTAAAGTTATTTCGTATGCTCACCAAGGCCAAGCAAAAATGCAGATAAACAGTAATATTTTAAAAAATTTCTATTTAAAATAACTGTAATTTCTCTCTTTAAGCAGCCAATAAAATGCTGTTTTTTCCCCAAATTCTTTTCTTTAAAAGTAATTTTAATATGCTGATT
Associated Phenotype:
Not determined