ZMP
si:ch211-65i12.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARHGAP24
Human Description:
Rho GTPase activating protein 24 [Source:HGNC Symbol;Acc:25361]
Mouse Orthologue:
Arhgap24
Mouse Description:
Rho GTPase activating protein 24 Gene [Source:MGI Symbol;Acc:MGI:1922647]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13603 | Nonsense | Available for shipment | Available now |
sa17867 | Essential Splice Site | Available for shipment | Available now |
sa9726 | Nonsense | Available for shipment | Available now |
sa15362 | Nonsense | Available for shipment | Available now |
sa23858 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13603
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084495 | Nonsense | 106 | 752 | 3 | 9 |
ENSDART00000137809 | Nonsense | 17 | 663 | 2 | 8 |
ENSDART00000140795 | Nonsense | 17 | 48 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 8528596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9675563 |
GRCz11 | 21 | 9768296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCCATAGGGGGCGACAGGGAGCGAATGACAWCCAATCATGAGACATA[T/A]CTGCTTATGGCCAGCACACARAATGACATGGAGGATTGGGTGAAGAGCAT
Long Flanking Sequence:
TGATTACAAAAAAAGAAAGCGGGATGGATGGATGGATGGATGGAAGAAAAGAAAGAGGGAGGGATGAATGGAAGGAAATAAAGAGGAAGTAGGGAGGGAAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAAAAGAAAAAAAGAAAGAAATGAAGGGGGAAAGAAAGAGAAAAAGTTTTAACTTGACTTTATCGAATGTTCAGATTATTGTATGCAAATAATGAAATAATGCCTGATTTGCACATTTAAGCTAATGTAAAATCATTTTTAATACCAAACACACTTGCAGTTCCTAATGTAATAGATCAGCTGCGGAAGTGTGAGGATAATTAGTTTTTGTAGATAATTGGTTTTTGATTAGTTTTTTTTTTTACCCTAGATATATATATTGACCACCTTATTTCAATCTTCTCTCCATAGGGGGCGACAGGGAGCGAATGACATCCAATCATGAGACATA[T/A]CTGCTTATGGCCAGCACACAAAATGACATGGAGGATTGGGTGAAGAGCATCCGCAGGGTGATATGGGCTCCGTTTGGAGGAGGTGAGCTGCTGCAACCAGTCTGTCAGAATTATTCAGCGTTGGTTAATGGATATAAGTTTTAAAACTGTACTTCTGCTAACAAACCTTGCATGAGTACTCATCGCTGCATGAGAACTCATCGCTGTAAAGTTTCCATTACAAAGTGTCAAGTATATCATGTGAAAAACAGCAGCCCCAGTAATTTAACCATATTTATTTGTTTTCCCCCTTTCTGCAAATATTTACAAAAATATTGAAATACTGAAATATTCATATCCTAATTATATCATTTATTTTCTGATATTCAGATTGATATGTATCTGCAACAACTTGTATTTCATCATTTAAACAGCTTAAAAATGATGATAATATCTATGATAATATGATACGATATAGGATATCAAATATGATGGGTGCTGCCGTGTTAGTCTGCACTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17867
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084495 | Essential Splice Site | 203 | 752 | None | 9 |
ENSDART00000137809 | Essential Splice Site | 114 | 663 | None | 8 |
ENSDART00000140795 | None | None | 48 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 8547115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9657044 |
GRCz11 | 21 | 9749777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGCTCCAGGACGCTTTCGACTGYGGAGAGWAGCYATCTTTTGACTGG[T/C]ACTTGCTCTTAATGCACTATATTTACAGTGTCTGTTGTGACNTTTTTTAA
Long Flanking Sequence:
TTTAATTATGTTCAACTTAATTAGTTTGTTTAAATTCAACAAAAATAAATTGTTTACAACCATTTAACGAAAAAAATTGAGTAAATCCAAGGAATCATCTTTGAATAATGTTTTTCAGTGTACTGTGATGAAAGCTTCAGTAATGAATCGCAGCAAGAAAACTTTATACTGAAAGTATGAATCAGCTGAATTCTGAATTAATTTTCAGCCAAGTGCTTCAAAGTTCTAGCATAATATCAGCAGGGTTTTCTTTATCATTATCTTATCTGGTCCTGTGTGCTTGTGTTTCAGGGATCTTTGGACAGAAGTTAGAAGAGACAGTTCGATATGAGCGTCGTTATGGCAACAAGATGGCACCCATGCTGGTGGAGCAGTGTGTGGACTTCATCCGCAACTGGGGTTTACGTGAAGAAGGCCTGTTTCGTCTGCCAGGACAAGCCAACCTTGTCAAAGAGCTCCAGGACGCTTTCGACTGTGGAGAGAAGCCATCTTTTGACTGG[T/C]ACTTGCTCTTAATGCACTATATTTACAGTGTCTGTTGTGACTTTTTTTAAGACAATCTTCCATATTATTTAGATTGATCCAGATTTACTCAACATAGGCTCATTCTAAAAAAAAACAAAGCCCTATATACATTTTTTGGAAATTGCTAATTATGTAGCCAGAAGAACGTATGGCAGCATTTCGCCTTTAAAACAAACGCTGGTTTGAAAGGGTTCAAGCCCGGCGAAGAACAATTCTAGAAATGAGGTAAAACATAAAACAAAATCCAAAAAAATAAAAAATAAACAAGTAAATAACATGATAAAAGTCAGAGGAGGGCTTTTGTTTTTCTGGATTGCTTTTTAGAACTGTCGGTTGGGTTTAGGGAAGTGGGTGGGCAGGTCAATCAGTGATTTTGAAAACACTATTGGTTGGGTTTAGGGAAGGAGGATGGTGGGTCAGTCAATCATTCAGTCATTCAGTCAGTCAACAGCAGTCTGGTGGATTTATTTGAGAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9726
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 |
---|---|---|---|---|---|
ENSDART00000084495 | Nonsense | 373 | 752 | 8 | 9 |
ENSDART00000137809 | Nonsense | 284 | 663 | 7 | 8 |
ENSDART00000140795 | None | None | 48 | None | 4 |
ENSDART00000084495 | Nonsense | 373 | 752 | 8 | 9 |
ENSDART00000137809 | Nonsense | 284 | 663 | 7 | 8 |
ENSDART00000140795 | None | None | 48 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 8560746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9643413 |
GRCz11 | 21 | 9736146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAYCAATGGSCAGCTTCAAAACAAAGAGAACAATAACACCACCGGGGCA[C/T]GACAGTGCAYTTGGGATGCCCCCGAATCACCCAACYGYACTCCTCTGGAC
Long Flanking Sequence:
ATAAACAAATTAAAAATAAAGTAAAAATGTCCCAATTTGCTTCTCAATCAAATGGGTACATACAGTGTCAGAAATCAGCTACAATGTAATTTTTTTTTCTCTTATCCAGGTTTTTGGATGAAGTTCAATCCTACTCAGGTGTGAATAAAATGAGTGTACAGAATCTGGCTACAGTCTTTGGGCCTAATATTCTGAGGCCAAAGGTTGAGGACCCAGTGACTATAATGGAAGGTAGGATTTCAACCAACCTCTCTCATTTCAGACATCTCTGAATCATAATTATTTTCTGACGTTTGATCGATGTGTTTGTTTCGTCAACAGGAACAGTGCTGGTCCAGCAGCTGATGGCTGTTCTGATTGGTCAACATGACGTTCTTTTCCCTGCCGAAGAGGAGCACTCTAGCACCCTGGAATTGGTCAATAATAACAATAATGAGACCCAGAAACAGCCTACCAATGGCCAGCTTCAAAACAAAGAGAACAATAACACCACCGGGGCA[C/T]GACAGTGCACTTGGGATGCCCCCGAATCACCCAACCGCACTCCTCTGGACAATGGCTCACCCCGTTCGGGAAGCCCACGTAATGGTTTTACAGGACAGAAATTCGAGGTGACCCGCAGTCCACCATTAGCGGTAAAAAAGAATCCAGCTTTCAGCAAAGGTAGCGGGATTGTCACCAATGGATCATTCAGCTCCTCTTCATCATCCTCCGGTGACGCCAGTCAAGACAAAACCCAGACTCTACCCAATATGGGAACGCTCCATGCCCGTCGTACTGGTGCGATAAAGGGCTCAGGCACCAAAATGGGCGTTCAAAATGGTGTGGTCAGGATGGGTGTATCCAGCACGGATGTAACTAATGGGACTATAAATGCGAGAAATGGACTCTGGGTTCCTAATGGTCACGTCACAATGCGCGATGGGAAAAGTCGAGAACCTGAGCACCAGCAAAACCGCCTGTCCACTTACGACAACGTACAAATCCACCAACAACAGATGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15362
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 |
---|---|---|---|---|---|
ENSDART00000084495 | Nonsense | 373 | 752 | 8 | 9 |
ENSDART00000137809 | Nonsense | 284 | 663 | 7 | 8 |
ENSDART00000140795 | None | None | 48 | None | 4 |
ENSDART00000084495 | Nonsense | 373 | 752 | 8 | 9 |
ENSDART00000137809 | Nonsense | 284 | 663 | 7 | 8 |
ENSDART00000140795 | None | None | 48 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 8560746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9643413 |
GRCz11 | 21 | 9736146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAYCAATGGSCAGCTTCAAAACAAAGAGAACAATAACACCACCGGGGCA[C/T]GACAGTGCAYTTGGGATGCCCCCGAATCACCCAACYGYACTCCTCTGGAC
Long Flanking Sequence:
ATAAACAAATTAAAAATAAAGTAAAAATGTCCCAATTTGCTTCTCAATCAAATGGGTACATACAGTGTCAGAAATCAGCTACAATGTAATTTTTTTTTCTCTTATCCAGGTTTTTGGATGAAGTTCAATCCTACTCAGGTGTGAATAAAATGAGTGTACAGAATCTGGCTACAGTCTTTGGGCCTAATATTCTGAGGCCAAAGGTTGAGGACCCAGTGACTATAATGGAAGGTAGGATTTCAACCAACCTCTCTCATTTCAGACATCTCTGAATCATAATTATTTTCTGACGTTTGATCGATGTGTTTGTTTCGTCAACAGGAACAGTGCTGGTCCAGCAGCTGATGGCTGTTCTGATTGGTCAACATGACGTTCTTTTCCCTGCCGAAGAGGAGCACTCTAGCACCCTGGAATTGGTCAATAATAACAATAATGAGACCCAGAAACAGCCTACCAATGGCCAGCTTCAAAACAAAGAGAACAATAACACCACCGGGGCA[C/T]GACAGTGCACTTGGGATGCCCCCGAATCACCCAACCGCACTCCTCTGGACAATGGCTCACCCCGTTCGGGAAGCCCACGTAATGGTTTTACAGGACAGAAATTCGAGGTGACCCGCAGTCCACCATTAGCGGTAAAAAAGAATCCAGCTTTCAGCAAAGGTAGCGGGATTGTCACCAATGGATCATTCAGCTCCTCTTCATCATCCTCCGGTGACGCCAGTCAAGACAAAACCCAGACTCTACCCAATATGGGAACGCTCCATGCCCGTCGTACTGGTGCGATAAAGGGCTCAGGCACCAAAATGGGCGTTCAAAATGGTGTGGTCAGGATGGGTGTATCCAGCACGGATGTAACTAATGGGACTATAAATGCGAGAAATGGACTCTGGGTTCCTAATGGTCACGTCACAATGCGCGATGGGAAAAGTCGAGAACCTGAGCACCAGCAAAACCGCCTGTCCACTTACGACAACGTACAAATCCACCAACAACAGATGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23858
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084495 | Nonsense | 631 | 752 | 8 | 9 |
ENSDART00000137809 | Nonsense | 542 | 663 | 7 | 8 |
ENSDART00000140795 | None | None | 48 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 8561520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9642639 |
GRCz11 | 21 | 9735372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACCAGTAATGGAGGAGGCAGGGGAAGCAGAGGAACCAGCAACAGCAGC[G/T]AGAACAGCGATACGTTTCCTGTCACCAATGGACCGACCAATCACAGCGCA
Long Flanking Sequence:
CTGGTGCGATAAAGGGCTCAGGCACCAAAATGGGCGTTCAAAATGGTGTGGTCAGGATGGGTGTATCCAGCACGGATGTAACTAATGGGACTATAAATGCGAGAAATGGACTCTGGGTTCCTAATGGTCACGTCACAATGCGCGATGGGAAAAGTCGAGAACCTGAGCACCAGCAAAACCGCCTGTCCACTTACGACAACGTACAAATCCACCAACAACAGATGACGCAGCCTAGCCTGAGCAGCAGCTGTGAGGACAAGCAAAGCGTTGATAGCGCCACATGGTCCACTTCCTCTTGCGAAATTTCCCTGCCAGAAAACTCAACCTCATGTCGCTCCTCTACGACCACATGCCCGGAGCAGGACTTCTTCGGCAGCAACTTTGAGGACCCTTTGCTGGACGGGCCGGTGCAGGAGGAGAACAGACTGGCGCTGGAGGACAGGGAGCAGCGGACCAGTAATGGAGGAGGCAGGGGAAGCAGAGGAACCAGCAACAGCAGC[G/T]AGAACAGCGATACGTTTCCTGTCACCAATGGACCGACCAATCACAGCGCACTGCACAGCCTGGTTTCCAGTCTTAAACAGGAAATGCTCAAGCAGAAGAATGAATATGAGGCCAGGATCAAGAGGTAAGAATCATGAACGTTTAAAGCTAATGGTATCAAGTTAGTGCTTGTCTTTGGCTCTGTCTGTTTAAACTTGGTCTTAACGAAATTATTTAGCAAGTGGTGGAAACCGTTTAAAAAGGTTTTCCTCTTTGAGCAGTTGAGAATGCATAGGTACTGTACTTGGCAACACATTTGATTGGATTACTTGTATTGTGTAGATGCTCATGTGGTTGTTTTTATTATTTTGTTTCCCTGTTGTTGTTGTTGTTTTGGATAAATGTATCTGTCACGTTAGCGAGAACATAACAGGAACAAAAACAGGTGTAGAATCCAAGTGCAGAATTGAATGACGATTGTGCAGTGAAAGTGACAAAAAAATACAAAAAAAATCCAAAGT
Associated Phenotype:
Not determined