ZMP
zgc:153779
Ensembl ID:
ZFIN IDs:
Description:
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_00
Human Orthologue:
AGAP2
Human Description:
ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 [Source:HGNC Symbol;Acc:16921]
Mouse Orthologue:
Agap2
Mouse Description:
ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 Gene [Source:MGI Symbol;Acc:MGI:3580016]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44036 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37768 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12289 | Nonsense | Available for shipment | Available now |
sa44035 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32463 | Nonsense | Available for shipment | Available now |
sa8589 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44036
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086813 | Nonsense | 286 | 827 | 8 | 18 |
ENSDART00000125104 | Nonsense | 286 | 827 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 23 (position 36743334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36574811 |
GRCz11 | 23 | 36697272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTAGCGACTACCCCTCGTCTCTGCCTTCTACCCCTGTGATTAGTCAC[A/T]AAGACATACGGGGTGGAGCGAGTGGAGACGGGGTCACACAGCGAAACCCG
Long Flanking Sequence:
AATGTTTGTGTTTGAGCTTTCAAGCAAGCATAATTCCTGTCGGGTTCTTCTATATCTTCCTGCATATCTGTTTTTTTTATGTTTACAAATTTTTGTGGAGGGCATTGTGGCGTTTTGCTTTCCATCAGGATGCTAGTGTTGACTTGACATACTTGTTTTGTTCATAGTGACTCAAAAGATTGTGGCTGCCAAGAAACAAGCGGCTCTTCTGGCTTCCTGTAAATCTCTGCCCAACTCTCCAAGTCATTCAGGGGCCTCCACTCCGGTTTCAGGGCCCGGACAGGTACATAGGGGCTCATCGGGGGAAATTTTTATCTCCCTGTTGTGAAGTATTTGATTATTTTCAGTAATTGTGAAAGCTGTTGGTCTTCATTAGTCTGTCTTCATCATTCATCATCTCATCTCATTGTTTTCTCCATCCTATCATCTTGTAGGCCAGTAACGGGGCTCAGAGTAGCGACTACCCCTCGTCTCTGCCTTCTACCCCTGTGATTAGTCAC[A/T]AAGACATACGGGGTGGAGCGAGTGGAGACGGGGTCACACAGCGAAACCCGCCCCGCAGACGAACATCTTTATTTGCGGTTAGTTCTTTGAACTCATCACGAAAAAGAGTCATATTTCTGTGACGCTTTGGTAAACTGATATGAATACAATTAGACTTTTTTGGCATTACATTATGACCACCTCCAGCCTAAAGCAATGAGTGCACCTGGTAACTGAACACAGATGCAGTTTAGAGAGCAGTATATATAGCCATCCCAGGACTTCGGTCTCTGCTATCAGGATGGGAAAAGCTGCTGATTCATTGGAGTTTGCATTTGACAAATTTAAAAAGTGCTTTTCTTACTTAAAGTTTCTGGGCTCTATCCACTTTTGCTATTTTAAGGATGGAAAAAAACACTCTGCGCCCCGGCGCAAAACAGGATTGTGCTTATTCTCTTAATGAGTTCTGGGTGTATTTTGAGAATAAACCAATCAGAGTCTCATCTCCCATTCCCTTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37768
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086813 | Essential Splice Site | 312 | 827 | 9 | 18 |
ENSDART00000125104 | Essential Splice Site | 312 | 827 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 23 (position 36741252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36572729 |
GRCz11 | 23 | 36695190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCCACTTTTGTTTTATTCGTACTTTATTTAACATGTCTGCTATTGT[A/G]GAATCGGCGTGGCAGTGACTCTGAGAAAAGATCTTCAGATAGCAGAAGTG
Long Flanking Sequence:
ATGTAATTCGACAGTGCCTGAAAATAGTGCACAGCTGGGTCTGACTTTTGATAGTTTTCCACCACTGTATGTAAACACTCATTATGTTACCAGACATTACAGAAGACCTATCTCTACCTCACTAAATCAGTGCATCAAACTTTAAAGTAGGTCCTACAGGTTATTAAGTGGGCGGTCATAAAGTAATGGCTCATCTGTGTATATATTAATGATCAGGTCAGAGGTAATTTTTTTTTTTTTAACTCAGAGGTTTTTTTTTTTTTTTTTTTTTTTGATCTATCCGAACAAACTTATTCTGTAAGTCTGATGGGGAAACCTGTTCGGGCACAGTCAACATTTTCACAAAAAAAGCAGAAGCATGACAGTCTCTTTAGTATTTCTTTGTTCGTGAACTCTCTGTCATCTCTAACCATCTCATGTCATGACTCACTTCTGTTTTCTTTCTTTATGTGTTTCCACTTTTGTTTTATTCGTACTTTATTTAACATGTCTGCTATTGT[A/G]GAATCGGCGTGGCAGTGACTCTGAGAAAAGATCTTCAGATAGCAGAAGTGACACGAGCCGGTCAGTCCCTATCAAACAGGTATGCACTAAACCTCTGTGAAATCAACTGTGAAATGCAGTAGCCTACTATATGTATTTCATTAAACGCAAGAAAACTATAGGAATAAATTGGATGAAGCCACATCGTCCAACAATAATCAGTGGATAGAAATTCTAATTAAAATCAATTGCACATTTTTATGCAAAGGTGGGCACCTGTTTTTATGTATTGATATTGTTATTTATTTTATTATTTGAACTTCTGCTGCTGTCACTGAATGTCTAGTTATTTGTTTGTAAATTGCTTGTACAAGTGTTGGACAATGAAACACTGGCCAATTTAGAGTTTGAGGTTTCATGGCTAAATTTGACCAGCCTGGTGGTCAGCCTTCATTGACTGCATTTTCCACCAGTAAGAGCAGAGAAGGTTTAATAAGCAGAGTAATAGTATAGATAGATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12289
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086813 | Nonsense | 320 | 827 | 9 | 18 |
ENSDART00000125104 | Nonsense | 320 | 827 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 23 (position 36741226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36572703 |
GRCz11 | 23 | 36695164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTRTTTAACATGTCTGCTATTGTAGAATCGGCGTGGCAGTGACTCTGAG[A/T]AAAGATCTTCAGATAGCAGAAGTGACACGAGCCGGTCAGTCCCTATCAAA
Long Flanking Sequence:
GTGCACAGCTGGGTCTGACTTTTGATAGTTTTCCACCACTGTATGTAAACACTCATTATGTTACCAGACATTACAGAAGACCTATCTCTACCTCACTAAATCAGTGCATCAAACTTTAAAGTAGGTCCTACAGGTTATTAAGTGGGCGGTCATAAAGTAATGGCTCATCTGTGTATATATTAATGATCAGGTCAGAGGTAATTTTTTTTTTTTTAACTCAGAGGTTTTTTTTTTTTTTTTTTTTTTTGATCTATCCGAACAAACTTATTCTGTAAGTCTGATGGGGAAACCTGTTCGGGCACAGTCAACATTTTCACAAAAAAAGCAGAAGCATGACAGTCTCTTTAGTATTTCTTTGTTCGTGAACTCTCTGTCATCTCTAACCATCTCATGTCATGACTCACTTCTGTTTTCTTTCTTTATGTGTTTCCACTTTTGTTTTATTCGTACTTTATTTAACATGTCTGCTATTGTAGAATCGGCGTGGCAGTGACTCTGAG[A/T]AAAGATCTTCAGATAGCAGAAGTGACACGAGCCGGTCAGTCCCTATCAAACAGGTATGCACTAAACCTCTGTGAAATCAACTGTGAAATGCAGTAGCCTACTATATGTATTTCATTAAACGCAAGAAAACTATAGGAATAAATTGGATGAAGCCACATCGTCCAACAATAATCAGTGGATAGAAATTCTAATTAAAATCAATTGCACATTTTTATGCAAAGGTGGGCACCTGTTTTTATGTATTGATATTGTTATTTATTTTATTATTTGAACTTCTGCTGCTGTCACTGAATGTCTAGTTATTTGTTTGTAAATTGCTTGTACAAGTGTTGGACAATGAAACACTGGCCAATTTAGAGTTTGAGGTTTCATGGCTAAATTTGACCAGCCTGGTGGTCAGCCTTCATTGACTGCATTTTCCACCAGTAAGAGCAGAGAAGGTTTAATAAGCAGAGTAATAGTATAGATAGATCCTGCTGGCGCATCTGTGACCAGAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44035
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086813 | Essential Splice Site | 515 | 827 | 13 | 18 |
ENSDART00000125104 | Essential Splice Site | 515 | 827 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 23 (position 36734221)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36565698 |
GRCz11 | 23 | 36688159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCGAAGTATTAATCTGAAAGGAGATGCAGCGGCCGGTCAGGCTGAAG[G/T]TAGCAGACCGTACCATTGATCTACTATCACTGATAATAAAGCCATCTGAT
Long Flanking Sequence:
GGTTTGACAAATATAGCGAGATTAGATCTAGCGGTAGATCCTTGATGAACAGTCCGACGTGCACAGCCCTCATTGCTGCAGTACATGTGTGTGTGTGTGGTCACATGATGTGCATTTTCAGTGGTATAATGTGCACGGAGAGCTGTTCTGAAACGCTAGTGTGGACGCGGATTGTTTTCATTCTAAAACGCCATTTTAAAACTAAAACATACTAGTGTAAACGGGGCCTAAAGTACTGTTTTGTTAATTTTGTAATAGTTTAATTAATCTTTCTATATTTAATAAAAAATACAGTAAATGACACAACTGGAGCATGAAACATTATGATAAAAACACTATGATTTTTTTTTTTTTTGTAATAGACTCAAGCATCGAGGGAGCCACAAGTCCTCCTTTAGGAAAAGAGCACATGCCGTCTTCTCCAATGACTGACCGGAAGAAGAAGAAGCGAAACCGAAGTATTAATCTGAAAGGAGATGCAGCGGCCGGTCAGGCTGAAG[G/T]TAGCAGACCGTACCATTGATCTACTATCACTGATAATAAAGCCATCTGATGTTTTATTGAGAAGAGTTTGCAGATTTGCTTTCCTCTGCTTTTCTTTATGATTGCAGTGTGGACCTGATTAATTATTGCTTTCTCTAAGGTCCAATCTCTTTTACTTCTTTCTTCTCTTCACTTTTTTTCCTCTTATCCTCTGCTGCCGTGGACTAATTTCTTGCACCGCAAGCCAAGCGCAAAATGTGGAAATTAAAAAGCTTTGGTAGCTTGAGAAACATTAACAAAACAGGTAACTTGAATGTATGAAGCGTGTAAACGGTGTAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTCTCTGACTAAAATATATTTTAAATATATTGTGTAAATGTAAACGTATTCAATTTCAGCCTTAATAAACCTAAATGTATTTCATGGTCAGGGAAATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32463
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086813 | Nonsense | 584 | 827 | 15 | 18 |
ENSDART00000125104 | Nonsense | 584 | 827 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 23 (position 36727940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36559417 |
GRCz11 | 23 | 36681878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGAACAGCCAAAGTGAAGCTGTTGCCCTGCAGGCCATTCGAAACGCC[A/T]AAGGGAACGACCTCTGTGTGGACTGTGCAGCACCAAGTAAGCCTGTCCTA
Long Flanking Sequence:
AACCATTCTCAAAAACCAAAATCATTCTGTTGAACACAGAATAAGATATTCTGAAGAATGTTGGAAATGTGGTATAAAATTACTACAAATATCAATGGCTGCTGCTTTTTTCCAACATTTTTTTTTAAATAGCTTCCTTTGTGTTCAACAAAAGCAAGAATAGAGTTTTCCATTTTGGTTGAACTATACTTTTAACAATAATTTAAAAAAACTCCTTGTTTTTGGTAGCACCAAAAACACATTTACTTGTGCGTCTCTTTAAATGCAAATGAGCTTCTTCTTCCCGCCCCATTTCCAGAAGAGGGAGGAGCCTTTACAGCTCTTGCCTCAGTTAACAACAAACAAACAAAACATGCATGCCTGCTTAATCCTACATACAAAACACATATTAGGAAGCAACACACTGGAGATATTACAAATTAATAGACTTCATTTTCATCTCTCAGGCTCGAAGGAACAGCCAAAGTGAAGCTGTTGCCCTGCAGGCCATTCGAAACGCC[A/T]AAGGGAACGACCTCTGTGTGGACTGTGCAGCACCAAGTAAGCCTGTCCTATATTATAATGAGAACGAAATCAATAAAAAGCCAATGTCAAATTTTTTGTCATTGATATTGTGGTCTCCTTGCAGATCCAACATGGGCAAGTCTTAATCTGGGCGCTCTAATCTGCATTGAGTGTTCAGGGATACATCGAAATCTGGGCACGCACCTGTCCCGCGTGCGCTCGCTAGACCTGGACGTCTGGCCCAGTGAGCTCACTAAAGTTCTTTCGGCTATAGGAAACCACATGGCCAACCATATTTGGGAGACTTGTACACAGGGGTGTCAGAAATTGACGCCTGAAGCAACAAGGTGAGGTTGTCAATAAAATCAGTGGAAAAAAAACTAAACATTTTTTAAACAAATATTGCAGAAACTTTATGTAAAATAAAATATATATTTTGCAAGGTATGTACAGTTAAGTGTAAGAAAATATGCCTAAAGCAATATTATATTTTATTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8589
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086813 | Nonsense | 680 | 827 | 17 | 18 |
ENSDART00000125104 | Nonsense | 680 | 827 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 23 (position 36725953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 36557430 |
GRCz11 | 23 | 36679891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTATTTTGTGTTGGTCTCAGAGAGCAGAGGGAGTCGTGGATCCGTGCC[A/T]AATACGAACAGCGAGCRTTTGTGTCGCCCTTGCCTGCTCAGTGTTCAGAG
Long Flanking Sequence:
ATGATTTATTATTATTATTAATTTTTCTTTATTTATTTGTTTATTTGGCAGGAACAGTGTACATTAATTAGCATTTCTGCAAATGCACCAGAAAATCCTAAATCTGTTTAATCATTAAATAATTAATTCATGTGATGGCAAAACCGGCTTTTCTCTCTCACACGATCTTTTAGAAATAAATATGTTAATATGCAAATCAATTTGCTGCACAAGTTCTGCTTGATACACTTGATAGAAATTGTGATAAAATAATTCAACATTTGTTGATAAATAGAATATTTAAAATATTATAATAAATAACAGAAATCAAAAACAAAATTTGTTAGATTCATTTCATTTAAAATATTTTACTGACCTCATTATATTTAAAGAATTATAAGATTAAATTAAATAAAATAAATAAATAAATAAAAAAGCTAATGTGGTTCGCCACTCAATTAATTATTTGGCCTTTATTTTGTGTTGGTCTCAGAGAGCAGAGGGAGTCGTGGATCCGTGCC[A/T]AATACGAACAGCGAGCATTTGTGTCGCCCTTGCCTGCTCAGTGTTCAGAGGACACGATGTCCACTTGGTTGCTTAAAGCAGTCATCAACAGGGATCTTCCCAATCTTCTACTGCTCCTTGCTCACAGCACCAAGGAGCTGATCAACATCCCGCCGGAAGGAGCAGGACAGCAGCATCACAGCGCCTTACACGCGGCCTGCCAGCTGGGAGACGTGGTCATGACACAGCTGTTGGTCTGGGTAATTCACCGTTTACAGCTTCTGTTTACACATACTTTTCTTTTTCAGTCCAATCACAAAAGGAGGATATTAAATACAAGGATCTGAAATGTTTTGAGCTTGTGCACTTTCGACCACTGCCAGAGGAATTTTTAAAAATGTAATATATCAAAGTTTTCACCAATCATGTCATATACAGTTGAAGTGAAGATTATTAGCTCTCCTGTGATTTTATTTTATTTTTTCCAAATATTTCCCAAATGACATTTAACAGAGCAAAGA
Associated Phenotype:
Not determined