ZMP
arhgap10
Ensembl ID:
ZFIN ID:
Description:
rho GTPase-activating protein 10 [Source:RefSeq peptide;Acc:NP_001038715]
Human Orthologue:
ARHGAP10
Human Description:
Rho GTPase activating protein 10 [Source:HGNC Symbol;Acc:26099]
Mouse Orthologue:
Arhgap10
Mouse Description:
Rho GTPase activating protein 10 Gene [Source:MGI Symbol;Acc:MGI:1925764]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39645 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32716 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24852 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6595 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25621 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14465 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39645
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109314 | Nonsense | 12 | 764 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 36480498)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36040356 |
| GRCz11 | 1 | 36772383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGTCCAGTAAAAATGGGTTTACACCCGTTGGAGTTCAGTGAATGTTA[C/A]CTGGACAGTCCTGCTTTCAGGGACAAAATCAAAGCTCATGAAGCAGAGCT
Long Flanking Sequence:
CTCCGTTGTTCCCCCTCAAAAAAATCCCGATTTTCCAGAGAGCCAAGCGTGATGACGTGATGGCAGAAAAAGCCCCGGAGTCCTGCACGCGGGAGGAGACTCGCGCTCGACTGTCATTCGCGGACCAAAAACCACACTGGATATTATTACCTCTATTTCAAGCGATATCGGTGTAGCCCAGAGCTGTTTTATCTTATCATACACGAGTTTAAACCCGGGATTTACTTAATCCAGCCAGGACTAAGTTTACTCGTGCGCCTTTGGAAAGAGTTCCATTCCCAAGAGGAGTCCCGACGCGTTTAGTCTTCCTAAAATACACGAGCACGCGTTAGAAACGACTTTTTAACAACAGCCTTTTTATTCAGCTTCTTGATTTGACCATTTTTTGTATTTATTCATTCGCTGGTCGCTTTGTAACGGGATTTAAACGCTAGCTAGTCTTTAAACTAGCTGAGTCCAGTAAAAATGGGTTTACACCCGTTGGAGTTCAGTGAATGTTA[C/A]CTGGACAGTCCTGCTTTCAGGGACAAAATCAAAGCTCATGAAGCAGAGCTGGAAAAAACAGGCAGATTCATCAAAGAGTTGTACAAAGATGGAAAGAATCTCATCAATGCCACCAAACGTAAGTGTCCTGTCATTTTGGCTCTGCTTTAAAACCCATAAAGAATTGTGTATCAAATGAAGAGACAATTTTCCATTTAGTCAATGTTTTATTCATGTTATACAAGTGTAATTTAATATCAACAACTCCAATCAGGCAGTTTTTGTGTGTTTGGTCAAGGTCATCACCATGTCATTACTGTTTCCACTACTCGAGAGGTTAAAAAACTGCTAGGTTAAAAAAGCACACCGTTCATTTGGTGTATATAAAATGAGCTTGCGTGGCATAACACTTGCTGACCTCACCCGTTTTTTTGTGTGTGTTATGATTCACACTAATTATGTGCAAATCGTCAGGTGTTTCAAGTTTGCATTTTGATCAGGTTGCATTAAGGATCTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32716
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109314 | Essential Splice Site | 128 | 764 | 4 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 36538286)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36098144 |
| GRCz11 | 1 | 36830171 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGAAGCCCTTAGAAAACTTTCGAAAAGAGCATCTTGGCTCAGCAAAG[G/A]TAAATTCGGTTTCAGATCATCTCTCATTATTTATTAAATATAGGATGTTT
Long Flanking Sequence:
ACAGTTGTTAATCGCTCCCTGCCTTCTCCCCTGCTCTGCTGGCCACGCACACTCCTCCCTCTGAACGCGGAGCTCCGTGCCCATTATGATGCATTTTTTGAAAAAAATTCTCTATGCTCTTTGAGTTAATTGAAAGCCTTGTTGTGTTATCCAACTCATGCAGTGGGGAAGTTCTTACTGCATCAATGGTTGAATGCTGTCATATGAACAATATTAATGCAGTTTTGAAGAAATTTGTGGAGCTTTCGGCATTTACAGTTTCATTGCAGCTTTACTTATCATTGTGAATTCTCTTTTTACAGTATCAAATGACTAGAGGTAACCATATTGCTGGTGGATGACATTGTTTCAAACTGGAATTTACTATTTGTGCAAGTTATGAAAAAGAAATAATGAATTAATAATTATTACCAAATTGTGTTTCACAGATGAGAAACATCACAGAGACACTGATGAAGCCCTTAGAAAACTTTCGAAAAGAGCATCTTGGCTCAGCAAAG[G/A]TAAATTCGGTTTCAGATCATCTCTCATTATTTATTAAATATAGGATGTTTGCACTAGAGGAAGTGAAAACATATGTTTATATATGAAGAGTTCAGATGCAAAAACCTCTAAGTGTCATCTGAATTTTTTTTTCTAATATTAGCATATTTCTCAGGATCCTTTGTCTTGATTTAGTAATTTTACTTTTATGGTAAAGAATAGGTTATTTTCATCACTTTTAACATGAAATAACTGAACATAAACATAAGAGGCTGAATAAAATGCTCATTCTAGAAGAGAATTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAGTTCAGATGCAAAAACCTCTAAGTGTCATCTGAATTTTTTTTTCTAATATTAGCATATTTCTCAGGATCCTTTGTCTTGATTTAGTAATTTTACTTTTATGGTAAAGAATAGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24852
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 |
|---|---|---|---|---|---|
| ENSDART00000109314 | Nonsense | 375 | 764 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 36553120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36112683 |
| GRCz11 | 1 | 36844710 |
KASP Assay ID:
554-7825.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTCTGGTTTGTGTTTTCTGATGTTTATCTCTCTCATGCAGATGCAGTG[T/A]CTCAACCGGACACATTCAAGAGAAAGAGGAAGTAAGAGACCAAATTAACA
Long Flanking Sequence:
TTTATTTATTTATTATTATTTTTATTTTTTTTACTTAACATATGCTTATTTAAAACAGTTTCCTGGCCTGACTAATAGTTAACACCACAAATCTTTACATTGTTACAAAATACTCTTCTATGCATTAATTAATTAAAAACCTCAAAAGCTGCAGTTTTTATTTATTTTTTACTTTTTACATTTTTATAAAGTATTCTTTTCTATTCATCAAATTATAAATAAATAAATACACATTAATTAATTACATTTAATTTTTTATTTTTTTCAGAATTACATTTTATTATTTTACAGTATGTTTGATGAATGCAGCCTGGTGAGCATTAAAGACTTAAAAAGACACACATAGTCCCTAGCATTTTCAACAGTAGTTAACTGTAACATGTTTAATGTTAAATAGTAGTCTCTTGTTTGGTTTATAAATTGTGCTCCGTTTGCTGTGGTGTTTCATGTGGGTCTGGTTTGTGTTTTCTGATGTTTATCTCTCTCATGCAGATGCAGTG[T/A]CTCAACCGGACACATTCAAGAGAAAGAGGAAGTAAGAGACCAAATTAACATCAAACTTCATAGTTTATGAGTAATGCTTATACGCATTCTAATGAAATATGTGTGTATTTCCGTAGTTGACGCACAGTTGGATGACGTGGGAATAAGCTTTGTGAAAAACTCAATAAATGCCATTGAAGCCAGAGGTAAGTCTTTGCTGTGAATATTAAATGTGAAAATAATATTTCAATTAAAGATAATAAACAGAAGCAAAATGTATCAGGCAGGATGTGTATTTTCTGTCAGCAAAGGAAGTCCCATTTGCACATGGTTTATTTAATGTAGTAACACCATGTTAACACTAGAGGGCAGAATTATCTAGCAGATTTTCTCAGCTAACGCTAAAAACATGTTGGGATTTGTTCAGGAGATATGTTGGTGCACTTCTGATTAGTTTGGTGCTTCAGCTGGAATGTGTGTGTGTATGTATTGCCAATCTAACACGGCAAAATAATGTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6595
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109314 | Essential Splice Site | 481 | 764 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 36565522)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36125085 |
| GRCz11 | 1 | 36857112 |
KASP Assay ID:
554-4100.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGCCTCTAATGACATACGAGCTGTATAAGGAGTTCATCGTCCCTGCAA[G/A]TAAGGTCTTTGTCCTTGCTTTGACAATAATCAAGYAATACCCAAAACGAA
Long Flanking Sequence:
AAAAAATGAATGAATAAATGTTAACTGTTAAATGTGTCATGGGGAAATATGCTTTTTAAATGATTTGTCAGATTCACAGTGGGACATTCCTTCCAGTGTCATGTAATTAATTAATTCAACATTCAATTAATTTTCTGATTGATGCGGTGCAATAAAGTAGCAGACGGCAGATTTTATAGGAGGGCATCACTTTTGTCTTTGTACTCCACTACAAGTATGAATGATGTTGGTTTGCTGGGCTCATTTTGGGCTAACGTTGCCGGGACGGGTGCCAGACACTGAGCGAATGTACCTTCAGATGAACTTGGTCCTGAACAGTGTGTATGTGCGTTTGTGTGCTCGTCTAATTTCTTGCCGTGATCAGCCACATTAATCATAGTGTTGTGTATATAATAATGCCCAATAAAGCCAATAAATCTCTCCCCCTCTGTTTCTCTCAAGGAGCCTTCCAGAGCCTCTAATGACATACGAGCTGTATAAGGAGTTCATCGTCCCTGCAA[G/A]TAAGGTCTTTGTCCTTGCTTTGACAATAATCAAGTAATACCCAAAACGAATCAATTATTTGACAAATGCTGTAAACCTAGAAAATGTGAATGTCTCTGGGAAAAGAGTGCATGATTTGGAGAATTCTAAATGGGGTTAATGCTTTTAGAAAAGTGTGGCTGAATTTAATTTAGTAAAGGAATTTAGAAAAATAACTTCAGCCAGAAAATATAAACTCACCGGCCACTTTATTAGGTACACATGTCCAACTGTTTGTAACGCAAATTTTGAATCAGCCGATTACACGGCAGCAACTCAATGCATTTAGGCATGTAGACATGGTTGAGAATCTTCTGCAATTTAAACCAAACATCACAATGGGGAAGCAAGGTGATTTAAGTGACTTTGAATGTGGCATGGTTGTTGGTGCCATATGGGCTGGTCTGAGTGTTTCAGAAACTGATGATCTACTACGATTTTCATGCACAACCATCTTTAGGGTTTACAGAGAATGGTCCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25621
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 |
|---|---|---|---|---|---|
| ENSDART00000109314 | Essential Splice Site | 570 | 764 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 36575648)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36135211 |
| GRCz11 | 1 | 36867238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTTCCAGAACATTGTGGTGGAAATTCTCATAGAACAGCATGAAAAGG[T/C]GAGTGACAAGTTACACATAATGAGTGAGCTTTATTTATTGATTTTCAAAC
Long Flanking Sequence:
AAAAGAAAGGAAATCTTGAGACAAATCAAGTTTTAGATTTTTCTGCCAACCTTCTCCTCCCTAATGCAAGTTATTTATGTCATAAATCAACCTCTCTCTCTCTCATTTTTTAATGTCTATAAATATTACAACTAGAGTGAATTAGGCAGTGATCATTGGCAGTGAGATTGAAGATTGTGTTTATACTTTATAATTGGAGGCAAACTGCATTTACTGTCAGAATCAAAACACCCTATCAAACTCAATTGTTTATAAAATGCGAGTCAGTTCTTTTCTTATATTTATCGTGATTATTGTTTAATTTAATTTCTGCTTTTCTTTGTGTGTTTGTGTGTGTAGTGTTGCTGCCAACAGCAAACAGAACCTGATGACGGTGGCGAATCTAGGTGTAGTGTTTGGCCCCACACTCATGAGGCCACAGGAAGAAACCGTTGCAGCCATAATGGACCTCAAGTTCCAGAACATTGTGGTGGAAATTCTCATAGAACAGCATGAAAAGG[T/C]GAGTGACAAGTTACACATAATGAGTGAGCTTTATTTATTGATTTTCAAACTCTCTAACGTTATGCTATACTAAAGTTGAAGTACTTTTATCTGCAGCCAGCAGGGGGAGCTATGTGTGTTTTGACTGGCCGCTATTTAGTTGGCTTCTCTTTCTGATGGCTCAAATACAGTTGGAGCAACATTCTCATTTGACTAAAATACAGGTTAAAACACTGACTTAATCAGCTTTAGTAACAGTAATCTGGTTAATCCTTAAATGGGGTTCATTCTGAGGGACAAAGGCAAAAAGAGTGGGATTACTTCATAATCTCTGAATTATTTAGCCTACATCTGAAACGGGGTGATGAATTGCTTTCATACTATGTGCAATGTTGTGACAGATTATCATATTTCAGTTCAGCTTTCAAAATAAACACTGGCATCTATTAGTCACTTTGGCTGATTAGATCTTTGCATATTTTTTTAGGGTTGCCTAAAGTTGTTTATTTAATAATAATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14465
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 |
|---|---|---|---|---|---|
| ENSDART00000109314 | Nonsense | 627 | 764 | 20 | 23 |
Genomic Location (Zv9):
Chromosome 1 (position 36596242)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36155805 |
| GRCz11 | 1 | 36887832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTKCTGCTTGCTGTGACAGTGTCTCCATCCYCTGAGAGTGYAGGCCTGTG[T/A]AATGATGAGACATCAGTGGGCAGTAATGAGTCAGTCTCCTCCCAGTCMTC
Long Flanking Sequence:
TGGGTGCACCCAAAGCAAACCTCCCCAAACTCTGCAATGATGTCACATTTGCCGCACGCTCTTAAGCGAAATAGGGGACGTGTCGAGTATAAACCAGGCTTACCATTTAAGTTATTGCTAGTATGAATAACGCAGCAGCCACATCGGTTGGCCTAAATCTTTTTTTTTTAAACATAATTATTACTTGAAGCCCATAAATGCATAAAAAATAAGGAAGCATAAGAGAATCTTTTTTTTTTCCTATTTGAGTAAAAAATGAGAAAATCTTTTTTGAATGTGTTTGATATTTAAAACCAACTTGAGGACAGTTAATTTACTATTTACCTTAAATTAGAAGTTTTCTAGTGGAAAATTCCTATAATGTGTTATTCGTCATGTGAATTCATTTGAACTACATTCCCATTTTTATTTTACGTTTCCATTTTCTCTTTTTTTCTTTCCATGCCATTCTTGCTGCTTGCTGTGACAGTGTCTCCATCCTCTGAGAGTGCAGGCCTGTG[T/A]AATGATGAGACATCAGTGGGCAGTAATGAGTCAGTCTCCTCCCAGTCCTCCAATGCCTCTGGAACGCCTCCTGAGAAATCCAAGAATCACCACACTACCATTAGCACATCCCTGCAAGAAGGCACTGGGTATGTAGCAAATGCTCTCTTCTGTCTCACAAAAAATAGAAATGTAGTTAATTTACTTTATATTTAAAACTAATAAGGTTTTTTATATATAAAAAAAAGAAATTAATTTTGATGTACTTTGCTTTTTAGCTTAAATGTATGTAAAGCTATAATATAATACAGCTATAAAGTTTTAATATAAATATACATAAAGAGCAAAAGCCGCTAAACGCCATTTCCACCAAAAAAGAGATAATGACATTGAGTGAATGCTTTAGGCATATAGTACACCATCAACAAATAGATTTGCTTCAAAACTGAATCACAGCATTAGCGTATTCAGAAATGACAGTTTGTTGGCAAAAGCCGCTAAACGCCACTTCCCTTTGACAG
Associated Phenotype:
Not determined