ZMP
zgc:92107
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC492329 [Source:RefSeq peptide;Acc:NP_001007296]
Human Orthologue:
ARHGAP39
Human Description:
Rho GTPase activating protein 39 [Source:HGNC Symbol;Acc:29351]
Mouse Orthologue:
Arhgap39
Mouse Description:
Rho GTPase activating protein 39 Gene [Source:MGI Symbol;Acc:MGI:107858]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10787 | Essential Splice Site | Available for shipment | Available now |
sa18288 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10787
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 |
---|---|---|---|---|---|
ENSDART00000065955 | Essential Splice Site | 585 | 1067 | 3 | 10 |
ENSDART00000129211 | Essential Splice Site | 585 | 1067 | 3 | 10 |
The following transcripts of ENSDARG00000044874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25960213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24789038 |
GRCz11 | 11 | 25026654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGAGAGTTATTTGTCTTTGCCDGAGACTTCTGGACCCCCCTCACAGG[T/C]ACTGCATAGATTMWCTGTTTGAYTCCTTATAAYCAGGTTGAATAATTTGA
Long Flanking Sequence:
GGAAGTGCACCACAGCCGACAGGGCAGCCAGGGATCTCAGGACTATTCAACACCACCTCCTCCTGCTGTTAGCTACCAGGACTCTGGTTACTCAACTGGTCCATCTCCCAGCATTCGGAGAAAAAGCAGGAGGAGAATAGCCCAGGGTCGCCCAGGCTCTGTGGGCAGCACTGGGGAGCTCACTGCTTTAAATGAGCGTCTCATGGAAGAGATGAGGGAGGTGGTCAGTCGCTCAAACACAATGCGGGAGACCAAAACCAGTCTGGACTCTGAGATGTCAGAAAGCTCTTCCTCTCAGCGCACACACAGCGTGGGACAGTGCTCCTCCAGGGAGGATGTTGCATCTTGCAGCAAGTCACTAAACAGGACAAATAACAATCCTAGTATGGCCTTCACACCTCTGGATATTCCAGGAAGACAGAAGCGGACTTATGAAAAAGTGGACACGCTTGAAGAGAGTTATTTGTCTTTGCCAGAGACTTCTGGACCCCCCTCACAGG[T/C]ACTGCATAGATTCACTGTTTGACTCCTTATAATCAGGTTGAATAATTTGACATATCATGAAATAAAAATTAACAATACGTTTGTTTAAAAAAAAAGTAAATGCCTTTATATTTTACACAAATGACTGCAAGTTATTAGGGCCATAAAAAGCATTCAAACCCATTTATAATGGGTTTTTTAGCTCAGTTTAGCATAGATTGTTGAATGGGATTAGACCATTATCATCTCACTCAGAAAATACCAAAAAGTTTCAATAATTTTTCTAGAGAAAACAGAATGACAGAATGAAAGTTGATATTTTCTAGGCAGACATGGTTAAGAATTATTCTCCCATTCCAGCATAATAATCAAGGGACTTTGCTCCCGTATCATGGCTACAGCATGCCCAATGATAATCTTGCAACCTTGGAGACATTTGTGAGAGACTCTTTTTTTTTTCAGGTGCTGCATAATATCATTGAGCCTCCAATTATTTATTTTTCGTTAGTAGTACAAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18288
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 |
---|---|---|---|---|---|
ENSDART00000065955 | Nonsense | 655 | 1067 | 4 | 10 |
ENSDART00000129211 | Nonsense | 655 | 1067 | 4 | 10 |
The following transcripts of ENSDARG00000044874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25964851)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24793676 |
GRCz11 | 11 | 25031292 |
KASP Assay ID:
2260-4296.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGCCTCCACCCCCAGACACCAGCATGACMGACKGGGCCAGCAAACACT[T/A]GAACAYGCACACCCAGGGCCTTTTCCGGCGCAAAGTCTCTATTGCCAACA
Long Flanking Sequence:
AAAATGAGGCCATTGCTGGATATGCACTATTTTTTAGAGACATGGAAGGAGAAATGACTTGCTGTAGAAGTTTTCATGTCAGTGATTGGTCACACTTCATCTATAGTGAATTGGAATTCTTTATCTGTGGAGTTGAAACATTTTAGGGGACAGATCCTGCAGTTATAGCAGAGCAGAACATAGGGATGGAGACAGTTAAGTTCATTGAAAAGCAGTTTAAGAATCTCACGGTGTGTTGAAACAAGCTATTTTATGAATATTACCCTTTCATCTTGTTTCTCCTTATTTGCAGGCTGGAACTGTAGAGCCAAAGGCTCAGTTGGACAGCAGAAAGAAAGGTATAGTAGACAACAGAACGGGTTCCCTTGGCCCTCATCGTCACATAGCCAGCGAGACCAATTTACAGGGAGGTGATGGTGCTACCTACCAGCTTTCCTACGCCACCCTCCGTCAGCCTCCACCCCCAGACACCAGCATGACAGACTGGGCCAGCAAACACT[T/A]GAACATGCACACCCAGGGCCTTTTCCGGCGCAAAGTCTCTATTGCCAACATGCTGTCCTGGAATCGCGGCTCCATCAAGAAGCCCATGCTGATGACCAATGACCGCACTGTCCGCAAAGAAGCCTGCGAAATGTTTAAGTTGGTCCAGGCTTACATGGGGGACCGACCTTCACGTCTAGACCGCCGCCATGCAGCTCTCCTCATAGTCACTAAGTGCTGGGGCATGCAGGGCCTGAGGGACGAGCTCTACGTCCAGCTGGTAAGGCAGACCACAGGAAACACCAGCCCGCGAAGCCTGGCTGCAGGCTGGGAGCTCATGGCTGTGTGTCTGGCCTTCTTCGCTCCTTCACCCAAGTTCTGCTGCTACCTGGAAGGATACATTCAGCGGCACATAGAGCCAACCAATGACAAGAAAAGTGAGTTTGATTTTTTTATTTAAACCATATAGAAAATATTAATCATGCTAGTTGGTGTGTCTGCTAGGCTACAGAGAAAAAGTC
Associated Phenotype:
Not determined