ZMP
zgc:101668
Ensembl ID:
ZFIN ID:
Description:
rho GTPase-activating protein 28 [Source:RefSeq peptide;Acc:NP_001007436]
Human Orthologue:
ARHGAP28
Human Description:
Rho GTPase activating protein 28 [Source:HGNC Symbol;Acc:25509]
Mouse Orthologue:
Arhgap28
Mouse Description:
Rho GTPase activating protein 28 Gene [Source:MGI Symbol;Acc:MGI:2147003]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9396 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32504 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9396
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 |
---|---|---|---|---|---|
ENSDART00000125591 | Nonsense | 162 | 619 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 43572212)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41907950 |
GRCz11 | 24 | 41872320 |
KASP Assay ID:
2261-9174.1 (used for ordering genotyping assays)
KASP Sequence:
TACAGTCTGARCTGACGYCTCCTGTTTCCCCGAATRGAGAGATCTCCCCC[A/T]AACCCCCGCAGTCGAATCCTCCTAAAGGTCAGACAACATCAGATTTTTTT
Long Flanking Sequence:
CGCGGTGGCAACCCCTGATCAATAAAGGGACTAAGCTGAAAAGGAAATGAATGTATGAATGAATGAATTAATGCCTTAAAAACATGATTTGGGCTTTTTAAAAAAGATTTTGAATATCCCAAAATGCTAAAATAATAATAATAATAATAATATTGTCATAATGTCAAGGAGTAAAGATTAAGAGTTTCCTTAAAAACTTTAAAAGTGTTTTTTTATATAATTATATTTTGTGTGTTTAATCAGACTGTATTATATAATATTATAAATAATAATATAAACAAAAATAATTGAAGAAAACCATGTGGACTTATTTTTAAAATATGTATTAGGCTTTCTTTGTAAATAACAATTAATAGTCATCTTGTTTTATAACAATAAATCCTGATGTATTACTGATGTCTGACGGCAAACCCACCATTTACCTTATGTGTGTGTGTGTGTGTGTTCTCTTACAGTCTGAACTGACGTCTCCTGTTTCCCCGAATGGAGAGATCTCCCCC[A/T]AACCCCCGCAGTCGAATCCTCCTAAAGGTCAGACAACATCAGATTTTTTTTAGATCAGATGTGTACATTATCAGCATGTGCTCATTCAGCAGACGCATTCAGGACACAGTCCTTTACAACATCACGAGAGACACAATATTACCAGCACATGATGGCAAACACACACCATTATCATTTATTATTGCATTACCTTTCTTTCTTGAAAGTGCGTTTATGTTTGAGCTAAGATGGAAATATCATTATCACTGAAGACTGAAAGTGCTTGTAGTTTTCTGTTTGGTTATTACACACACACACACACACACATACTTGCACACACATACAAGCAGACACACCCATATATGCACAAACAGCACAAATGCACACACACACACACACACAGACCTACACATGCGCAGCAAACCACACACATTTAGTGCTGTCAAACAATTAATCGCGATTAATCTTATCCAAAGTTTGTATTTACATAATGTGTGTAAATATATATGACATACGAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32504
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125591 | Essential Splice Site | 529 | 619 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 24 (position 43557755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41891598 |
GRCz11 | 24 | 41791651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGCAAACGTGGACTTTTGAGTCGGTGGAAGGACCGCGAGCGCAGTGAA[G/A]TGAGTGATCGTAGGATTTAATCGTCAGATGAGGGGGCTAATACTTAATCA
Long Flanking Sequence:
TTTCTAAGTAAAGAATGAGCTGATGCGTTACCTTTAGTTGAGTTAATTAGCTTTTAAAAATGAAATAGCTGATCTACAATGAACATCGTCATGTTGAATCCGGCACTGGATGAGAGAATACAGAAACAGAAAGCAGGACGGCTCTGGCTTACATTTCTGCCATGATGGAGGTATTCTCATTATTCTGAACACATGAAGAAAAGGAAAAGAGGACTGCAGTGTCAGTGCACACTGATTATACCGCACTAATAAGACAAAAACAGCAAACAAACTGCTTTAAACTGTCATTAATGAGGCGTTTCAGCTGACTCGTGTAAGCGGTTTGCTCTTGATCATCATGTTTATTGTCGTTTTCTGTGTTTTTGCATGCACAGGTTCCGTGTTTTCTCATCAATCAAGTGAGAAAAATGAACGATGCTGCGATGGCCAAGAAATCTCTGAGCTTCGAGAGGAGCAAACGTGGACTTTTGAGTCGGTGGAAGGACCGCGAGCGCAGTGAA[G/A]TGAGTGATCGTAGGATTTAATCGTCAGATGAGGGGGCTAATACTTAATCACAATGATACAACTATTGCACACAAAATGAAATCTGTATTTGCATAATATCTGTGCGTGTACAATTATTACGTATAATGCACAAAAAACTGTGATTTTCAATTATTAATCAAGAATAATCGCATACAAAATAAGTTTGTATTTACATATGTGTATGTACATTATATATATATATATATATATATATATATATATATATATATATGCATATGTATTTCACCAAAATACAGAACCTATTTCTAAGTTTTTTGGGTAAGCAAGTATTTTTCAGTGCTTTAGAAATACTCAAAAATGCATCTGTCAGTGTTGTCTAACTATTCTATTTGATTTACCAAAGTCACACCAGTGGCCATTTCACATTGGTCACATCCATAACGAAGAGATGTCACATCCATAATGACACTTTTTCCTCATAAATGTGAAAATATTCAATAAAAATCAACCAGTTTTGT
Associated Phenotype:
Not determined