ZMP
zgc:136763
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC559813 [Source:RefSeq peptide;Acc:NP_001038371]
Human Orthologue:
ARHGAP6
Human Description:
Rho GTPase activating protein 6 [Source:HGNC Symbol;Acc:676]
Mouse Orthologue:
Arhgap6
Mouse Description:
Rho GTPase activating protein 6 Gene [Source:MGI Symbol;Acc:MGI:1196332]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21070 | Nonsense | Available for shipment | Available now |
| sa31595 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21070
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000083189 | Nonsense | 180 | 630 | 5 | 13 |
| ENSDART00000130906 | Nonsense | 218 | 668 | 5 | 13 |
The following transcripts of ENSDARG00000059672 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 52842947)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 51112697 |
| GRCz11 | 7 | 51387767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGATGTCGGTGGACTCCATCTCTGATATGGTGGAGAGTCAGTCCAGAT[T/G]ACTAGAAGCTCTGCAGCTCTCTCACCCCAATGAGCTGGAGATGAAGAAGG
Long Flanking Sequence:
ATAAAGATGTTCGCTCAACTGGCTCAGTTGGCAGTGGCATCAGTCAGCATGGCTCAGGTTGTTGTTTTGATGGCGTGCGGGTGCTTTCCATTCCTCTCTCAGCATGACTGAGACATCATCTCTCTATGGGTGGCTCCATATCAGCAGGAGGGAGTGCGATTTTTAGTCCGTGCCTCTGCCAAATCAAACTCTCCATTCTGTCCGCCCAAACATGGAGAGAGAAAGGAAAAAGAACAGATAACAGGGATATTCACTCATCTCTGTGATGACTTTCGAAAAAACTTTTATGAAAATCTGCTTACATTTCTTCTTGATTTACTGATTTTTCTTCACACACCAGTGTGACAGACTTACATAATTATTTGTAAATGGAAGAGGCTTTTACTCAAATCTATGTTGACCTTTCATTTTGACCATTATAAATGTTTTATTTCTCTCTCTTTCTCAGGGAGGGATGTCGGTGGACTCCATCTCTGATATGGTGGAGAGTCAGTCCAGAT[T/G]ACTAGAAGCTCTGCAGCTCTCTCACCCCAATGAGCTGGAGATGAAGAAGGCGGCGGGTCGCACACAGGCCAAACTCAGTCTCAACCCAATCTACAGGCAGGTTCCCCGCGTGGTGGAGCGTTGCTGTAACCACATACAGACCTACGGTGAGCAGCAAACAGCATTACAGTACAACACACCACTGGATTTGATTTGGCACAGGAAGCTTAATTCATAGCTTACATTATTCAGTTAGTTATGTCTATTCTTACACACTGTATGTCAAGTTTTACAAACACATTTTGAGATGAGTATGTGAAATGATTGAGCACGGCTGGCCTCTCATCCGTAATCAGCAATGATCTAATCAGATTGATTCAAGCTTACATTATAGAGACCAAGACTGTGTCCGAAACGGCATACTTCCATACTATATAGTATGCTAAAATCAGTATGCGAGCCGGAAGACTTACTACTTCCGGCGAGATTCTGGAGTGCGCATCCCATGCACGCTGCGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31595
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 |
|---|---|---|---|---|---|
| ENSDART00000083189 | Essential Splice Site | 297 | 630 | 7 | 13 |
| ENSDART00000130906 | Essential Splice Site | 335 | 668 | 7 | 13 |
The following transcripts of ENSDARG00000059672 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 52833806)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 51103556 |
| GRCz11 | 7 | 51378626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACCCCCTCCTGCCACGAGAACTGTACCGGGCCTTCCTGCACGCTAACC[G/A]TACGAGCATATGATCATAAAGAAAAGCTCAATAAGTTCGAAGAGATCATA
Long Flanking Sequence:
ATCAATTGGTCCAGCTGGGACTCAAACCAGCAACCTTCTTGCTGTGAGGCGACAGTGTTAACCTCTAAGCCACCTTGCTGCCTTCATTGCCATCCTAATAAGTATAATCAGAGTATAAATGTGCATGTAAACTCAATCAGACTCTAACCTGTACAGCGAATGTCTCAGATACTCTTCATAGCATGTGCAGCGTCTTGCTTTAATAGCTGACCTCAAACTGCCTGTGATTTGTGTGTGTTTATTGTACTGTGTTTAGACAGGAACAGGAAACCTGGGGTACTTGAGTCTCGTGTGTGGTGGCAGTATGTTTGATTGTGTTTCATCCCCCCGTGTCCGTGTGTGTTTTCAGCTGCGCGAGGACTTCGACAATGGGATAGACGTGGTGTTAGACGAGGAGCACAGTGTTCATGACGTGGCTGCATTACTGAAGGAGTTCCTGCGGGACATGCCGGACCCCCTCCTGCCACGAGAACTGTACCGGGCCTTCCTGCACGCTAACC[G/A]TACGAGCATATGATCATAAAGAAAAGCTCAATAAGTTCGAAGAGATCATAAACTGATTTTTGTTTTATGCTCTGAGGTCCACATTTAATAAGATTTGTACATAATAAACATTATAATTTAGAAATAAGGCTTTATTCTATAGAAGACTTGGAAATACACTCACTGGCCATTTTTTTAGGTACAACTGTCCAACTGCTCGTTAACACAAATTTTAATCAGCCAATCACATGGCAGCAAACTGAGCATCAGAATGGGAAAAAAGGTGATTTAAGTGAACATGGCATGGTTGTTGGTTGAAGACGGGCTGGTCTGAGTATTTCAGAAACTGAGACTACAATTCACACTGGCTCACCAAAACTGGACAAAAGAAGATTGGAAAATTGTTGCCTGGTCTGATGAGTCTCGATTTCTGCTGCAACATTTTTATGGTACGGTCAAAATTTGCCGTCAGCAAGATGAAAGCATGGATTCAGTGTTGTTGCTGATCATGTACATCCCTT
Associated Phenotype:
Not determined