ZMP
si:dkey-287f10.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8DZ82]
Human Orthologue:
ARHGAP32
Human Description:
Rho GTPase activating protein 32 [Source:HGNC Symbol;Acc:17399]
Mouse Orthologue:
Arhgap32
Mouse Description:
Rho GTPase activating protein 32 Gene [Source:MGI Symbol;Acc:MGI:2450166]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35857 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32026 | Essential Splice Site | Available for shipment | Available now |
| sa35856 | Nonsense | Available for shipment | Available now |
| sa12990 | Essential Splice Site | Available for shipment | Available now |
| sa28431 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17301 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35857
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108818 | Essential Splice Site | 30 | 1676 | None | 21 |
| ENSDART00000136263 | Essential Splice Site | 30 | 119 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 18022140)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 19185954 |
| GRCz11 | 15 | 19121686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTTCAACACCTCCGACAGACGCAAGCACTCATGATCCCAGTGAAGGG[T/C]AAGAAACAGCCTGCACACTTCACCTTCTCCGTGGGCTTTTGCCTGCAGCT
Long Flanking Sequence:
TAAAATGATTTTGGTTAATATACAATAAAATAAATCATCTTTGAACTATTTTATTTTTAATTTAATTAATTATTATTCAATATAATTTAATTTATTTCATTTCACTTTCCTTTGGGCTTATTCCCTGCTTTTTCCAGGGGTCAAAACGGAATGAACTGCTTATTTCATGTGATCAAAACTATGTACAGTATGTAGAAATGAATGAATTTATTCAATATTATGTCAAAATAAACTAAATATATAAACTTATACAGGCTTGCTACACACTCCTGCACCCCACAGGGCCTCCTCCAGTGTCTGTATTGTAGGTGTAGACACTAAAGTGAAGTCCGGTCTCTCTCACACTCCCACTCTCTCTCTCTCTCTCCTCCTCCCTCACAGACGGGCAGCTGTAGCAGTGACTCAGTATCATGGAGGCGAGCAGCAGGACTGCAGCAGCGACAAACGCCAGAGCTTCAACACCTCCGACAGACGCAAGCACTCATGATCCCAGTGAAGGG[T/C]AAGAAACAGCCTGCACACTTCACCTTCTCCGTGGGCTTTTGCCTGCAGCTAGTTATGCATTATAGCGTGCGTTTTGTCTTGCAAGGTTAGATGAGGCATTTTCTTCACAATTGGCTGAATGTCTGCATAATCAGGTGCAGTGTGCATGTAGTGTTGGTTTTTGCACTCGCAGGCGTTTCCAGTGTCATGTGACTGGTCACCTTATTTTAATTCTGAGACAGCAGATTTAGCCAGCGCTGCATGCAGCAGATGTGAATTTGTCCCCTGAGGATGAAATTACAGGGGTGATTTGTGTGCAACTGGTGCCCAGCGGAGATGATAACAAGGATGGTAGAGGCATCAATGAATGAACGTGCTGGACCACATTACGGAAGCAGGCTTGCTGTAATGTGATAGTTAATGACATTCTTTTACTAGCTGTTAATTAAAATCATAAAAACTGTAATTCATACAAATATTAGGGTAATAACTGTTTTGATATAGTTAAATTGGCATTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32026
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108818 | Essential Splice Site | 320 | 1676 | 11 | 21 |
| ENSDART00000136263 | None | None | 119 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 17951652)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 19115466 |
| GRCz11 | 15 | 19051198 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTACATCTTGCATTGAGATTTTGAAGTCTGTTATTGTAATTTTCTGC[A/T]GTGTCTAAGAAGCATGGCAAGCTGATCACTTTTCTGCGCACGTTCATGAA
Long Flanking Sequence:
GGGAGGAATCTTAGTGGTGATAAAACATGTTGTAAAGTAATTGCTACTGATTCTCAGGGCTACAAATAATGAATTCGTATTGTGCAACAGCTAGATTGTACATTTTATATATACTGAGGGATTCGCAGACTTATTCACTGACGTACCTTTAAGAGATTTCAGACTGTTTAAAGAGAGCAATTATGATAATTGTGCCCTTGTTGAAATGAAGTGAGATAAGAAGCGTTTCAATAAATTTTGGGGTTCTCAGGTGTTTTATCTTTTCCTTCACAGGTGGGATTTTTTCCGTCTGAATGTGTGGAATTAATTAGTGAGAAAATCCCCTCCAACGTGACCAGCTCATTGGCCAAACCAGGTAGACACTTTTGCACAAATTATCAGTATCTTTAGGTTTTTATGGTTTAAAGGTCCTTAAATTTGAGATCCTAAAAAAAACCTGCAAATTAAAGTGTTTTACATCTTGCATTGAGATTTTGAAGTCTGTTATTGTAATTTTCTGC[A/T]GTGTCTAAGAAGCATGGCAAGCTGATCACTTTTCTGCGCACGTTCATGAAGTCCCGTCCCACCAAGCAGAAGCTAAAACAGAGAGGGATCCTGAAGGAAAGAGTTTTCGGCTGTGACCTTGGAGAACATTTGCTGAACTCAGGCCATGATGGTGAGGGGAATCTGAGGATGTTTAATGTGTCTAAATCTTTCATTGAAATAGTATAATTGTGTGTAATTTGTATTTGTGATGTGTGTTGCTCTTACAGTTCCTCAGGTCATCAGAAGCTGCACTGAGTTCATTGAGAGACATGGAGTTGTGGATGGGATTTACCGCTTGTCTGGAATCTCCTCTAACATTCAGAAACTGAGGTCTGGAATTTAAATAATAATAATAATAATAATAATAATTATTGTTATTATTATTAATGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAGATAATAACCACTTAATACATTTTACTTTATTATTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35856
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 |
|---|---|---|---|---|---|
| ENSDART00000108818 | Nonsense | 383 | 1676 | 12 | 21 |
| ENSDART00000136263 | None | None | 119 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 17951365)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 19115179 |
| GRCz11 | 15 | 19050911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTCTTACAGTTCCTCAGGTCATCAGAAGCTGCACTGAGTTCATTGAG[A/T]GACATGGAGTTGTGGATGGGATTTACCGCTTGTCTGGAATCTCCTCTAAC
Long Flanking Sequence:
GTCTGAATGTGTGGAATTAATTAGTGAGAAAATCCCCTCCAACGTGACCAGCTCATTGGCCAAACCAGGTAGACACTTTTGCACAAATTATCAGTATCTTTAGGTTTTTATGGTTTAAAGGTCCTTAAATTTGAGATCCTAAAAAAAACCTGCAAATTAAAGTGTTTTACATCTTGCATTGAGATTTTGAAGTCTGTTATTGTAATTTTCTGCAGTGTCTAAGAAGCATGGCAAGCTGATCACTTTTCTGCGCACGTTCATGAAGTCCCGTCCCACCAAGCAGAAGCTAAAACAGAGAGGGATCCTGAAGGAAAGAGTTTTCGGCTGTGACCTTGGAGAACATTTGCTGAACTCAGGCCATGATGGTGAGGGGAATCTGAGGATGTTTAATGTGTCTAAATCTTTCATTGAAATAGTATAATTGTGTGTAATTTGTATTTGTGATGTGTGTTGCTCTTACAGTTCCTCAGGTCATCAGAAGCTGCACTGAGTTCATTGAG[A/T]GACATGGAGTTGTGGATGGGATTTACCGCTTGTCTGGAATCTCCTCTAACATTCAGAAACTGAGGTCTGGAATTTAAATAATAATAATAATAATAATAATAATTATTGTTATTATTATTAATGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAGATAATAACCACTTAATACATTTTACTTTATTATTAAATAAAGTATTTCACTGCATGATATTGGAAAATTGGACATTACAATATTGGACATTGCGATATTTTGTTTTGTTGCGATATATAAATATATATAAATATAAATATAAATATATGTATTATTGTGATATGAATATACATTCACTAAATGATTTAAATAGCTCTATTGGGAAAAATCAATCATTTTTTAAAGCTAAATTACCAACAATAAAAGTTAAATAAATGGTGCTTTATGGTTTTCTGTGGAGACTAACAGTATCCAATTGCAGAAATTCAAATGCAATTAAATGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12990
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 |
|---|---|---|---|---|---|
| ENSDART00000108818 | Essential Splice Site | 919 | 1676 | 20 | 21 |
| ENSDART00000136263 | None | None | 119 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 17942410)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 19106224 |
| GRCz11 | 15 | 19041956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGAAAGTAAATCTGCAGATGTAAAGCAGCACAGAAGAGCAGACTCAGG[T/C]CAGCAACCTTGCACAACCTTTCATTYATCTAAATAATCGAATGATACAGA
Long Flanking Sequence:
TCTTCTTCTTGTGTGCCAGCTCTTATATCTCCACCCCATCCTTCAGCAGACGCTGAGTTTATAGGTATATCCTCCTTAGACATAGACCCATTGGCATTTCAGTCAGCACGGTTGGTTGAGCAGGAAAATAAGAAAAAAGGCAGTCGCAAGAAGGCAGGAGGCAAAAACCATGAGTTAGAGCCTTCCAACAAAGTCACAAGTCCTTCACAACCTCCTGATCTCATTCCACTGCGTGCAGAAGATTCAAAACACAGACCCTCTGAACTGCCACTCTCCTCAACTAATCTAGATGTAGGCTTCTCTAAGACCGGCCAAATGGGCACCTCAAGGAGTTCAGTACCAAAAAGCAGTACTGTGTCCTGTCCTTCTGACATTGTGTCCCTCATGAAAAAGCCCAGCGTGTCTATGAAAGCTGGAGAAGGCCATCAGCGATCTGCGAGCTTCTGCAAAACTGAAAGTAAATCTGCAGATGTAAAGCAGCACAGAAGAGCAGACTCAGG[T/C]CAGCAACCTTGCACAACCTTTCATTTATCTAAATAATCGAATGATACAGATATTTATATAAAGGAACCTATGCTCAGCTACTAGTGTCATGCATATAAATTTCTCAACATAACACTTACACTAATTATTTTGTTTACTTTCTTCAAAACTTAACTGAATGTGCTAAGCAGATAACTGCAAAAGAAAATCAGACAATTATTAGTTATATACCTTTTTATAGTTCTGAAGTTGTACTTTGTTTAATTGGATTCACAAAGTAAAATTAAATTAAAAACAGCGCTGTCAAGAAATGTTCAACAAAGTTAGTGAGGCTAACTTTTAACCCGAAGGAATAAAATAATAGAGATATGCTATATTCACACTTTATTTTAATGTACAATTCACACTATTAAAAAAACAGTAACTAAGACCCTAACTAAGCTCATTAACACCCATTTCCACTGAGTGGTATGGTATTGTTTGGTACATTTTTATGGCCATTTTCACTGTCAAAAGGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28431
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108818 | Nonsense | 1248 | 1676 | 21 | 21 |
| ENSDART00000136263 | None | None | 119 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 17939854)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 19103668 |
| GRCz11 | 15 | 19039400 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGAAGACTACTCCTCAGTTGGTGTCTATAGACATGGAGGACCAAGGTA[T/A]CCACCGTTGGATGGAGCCTCCGTCTACCCAACTATCCGCAGGGTGCGCTC
Long Flanking Sequence:
GATAATATCCGTCATGTTGGAGTTGGTACAGATGGAGGTGGATCAAGCCTTGATGCTGAGATGGAGGTACGTGGAAGTTTACAGACGACACTCTCTGAAAGATACTCTTCCTTGGATAGTCCTTCAGCCATTGATGCACTCCACAACAAGCAGGCTGCTAATGCTGCTAACTTCCGAGCCATATTGGCGGAAACAGCCATGCCTGCTTCAGTACAAGAAGTTCTTCCACAAGCATCAAGTACTCCACCGAGTGTGTTGTATCAGTACAAACCCAGAGAGCAAAGGTCTGCTTACTCCCAACACTCCCAACAATGGTCAAGTTCGGATGGGCAAAGCACATCTTATTATCAGGTTGACGATGGGCGTCCACATCCTAGAGTTCTCTCAAGAAGCTACTGCAATACCCTTGCTCCACGATCCCTACATCAGTCTATTAAGTATAAAGGTCAACGGGAAGACTACTCCTCAGTTGGTGTCTATAGACATGGAGGACCAAGGTA[T/A]CCACCGTTGGATGGAGCCTCCGTCTACCCAACTATCCGCAGGGTGCGCTCTATGCACACTCCACCTGAGGACAAATTTTTCTTCCTTCAACGGCAAGGAAGCCAAAGCAAACCTTACCAAAATCCACCACCATCAGACATCCAGCATGTGCGGCCTTACTTTGAAGATGGGAAAGTTCGGTATAGGTACAGCCCCTATTCAGAGGCTCGCTACAATCAATACCGAGAGAACAGTGGGTACACTCTGTCTTACACACTCAACAAACTGCCTTCTCGCTCATCAAAGGTGATGGCCACTTCCGAAAACTACCACAAGCCTCTACGCAACCTCCCTTTGAACAATGAGTCTGACTTCATGACCAGAGATGCTGGTTTTCTGCCAAGAAAGAAGAACCCTTCTTTCTATGAGGCTTTTAATTCTGGTTTATCTGATCGACATTTCAGTCAGTCCATTAGGCAGGAAAATGCAGCCAAGGAAAGGCCGTTGGGTCCGGTTGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17301
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108818 | Nonsense | 1445 | 1676 | 21 | 21 |
| ENSDART00000136263 | None | None | 119 | None | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 17939264)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 19103078 |
| GRCz11 | 15 | 19038810 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAATGCACACCAGGAGCAGGTCAAACTCTGGGAAGGAGATGCTGATTT[C/A]AACTGAAGGGGCTGATGGGAAATACAGGGTCACKATGGTATCCCATTACT
Long Flanking Sequence:
ACGGCAAGGAAGCCAAAGCAAACCTTACCAAAATCCACCACCATCAGACATCCAGCATGTGCGGCCTTACTTTGAAGATGGGAAAGTTCGGTATAGGTACAGCCCCTATTCAGAGGCTCGCTACAATCAATACCGAGAGAACAGTGGGTACACTCTGTCTTACACACTCAACAAACTGCCTTCTCGCTCATCAAAGGTGATGGCCACTTCCGAAAACTACCACAAGCCTCTACGCAACCTCCCTTTGAACAATGAGTCTGACTTCATGACCAGAGATGCTGGTTTTCTGCCAAGAAAGAAGAACCCTTCTTTCTATGAGGCTTTTAATTCTGGTTTATCTGATCGACATTTCAGTCAGTCCATTAGGCAGGAAAATGCAGCCAAGGAAAGGCCGTTGGGTCCGGTTGTGGCCCAGCCCCATCTTGTAAGATGCGATCGTCAATGCCAAGAAACAATGCACACCAGGAGCAGGTCAAACTCTGGGAAGGAGATGCTGATTT[C/A]AACTGAAGGGGCTGATGGGAAATACAGGGTCACGATGGTATCCCATTACTCCCCAGAGCACCCACTTTCTGAGCCTGATATGCCTGTGCCCTCAAAGTCAGACAGGCATGACAGCGGGCAGGGAGCCAAATCGGCTCTTATAATGAAGCAGAGTCGGTCCATGCACAACTATCCTCAACACAGGCTTGAGTCCACAGCACTGCCACACAATCTGACCCTGCATAAGGAATACAGCTGCCCTGACTTCAAACACACCGGGTCCAGCGATAGCTTCGGTGTCACACACCGCAACCAGGACAGGCTTATATATAAGACTCTCAGCAATCCTAAAGAGGACTACCAGTACATTCAGGCAATGAGCAGAGAACCGCAGAGGTCTAAGAGATCGCAGAGTGTAAAAAATCGCAATCCACCTGGTCAAGCCAAAATGACTCTGGAGCGGGATCACAGACTGCCTTTCTCCTCCCATAGCAGGACAAGAACTCGTAGTATGTATGTGC
Associated Phenotype:
Not determined