ZMP
si:ch211-223a10.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARHGAP22
Human Description:
Rho GTPase activating protein 22 [Source:HGNC Symbol;Acc:30320]
Mouse Orthologue:
Arhgap22
Mouse Description:
Rho GTPase activating protein 22 Gene [Source:MGI Symbol;Acc:MGI:2443418]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42227 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42228 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22334 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42227
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014922 | Nonsense | 57 | 698 | 2 | 10 |
ENSDART00000142245 | Nonsense | 42 | 317 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 31332061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30978009 |
GRCz11 | 13 | 31108459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGTGAAGGCCGGCTGGCTGAAGAAACAGCGCAGCATCATGAAGAACTG[G/A]CAACTGCGCTGGTTTGTGCTCCGAACTGACCACCTCTACTTCTACAAGGA
Long Flanking Sequence:
TTTGCATGTTCTCCATGTTGGCGTCAGTTTCCTCCAGGTGTTACGATAAATTGGTAAATTGGATTAACTAAATTGGCCATAGTGTTTAAATGTGAGCATGAATGGTTGTTTCCCCGGACTGGGTTGTGGCTGGAAGGGCATCCGTTGCGTAAAACATATGTTGGATAAGTTGGTGGTTCATTCCACTGTGGCGACCTCTGATAAATAAGGGTCAAAGCCAAAGGAAAATGAACGACTGATGAATATTAATGGACGGCACTATGCATGTCCAAACTCACAGAGGCTGATACACTTAGTTTGGATGAACTGTATGTGAACATACTGTAACTGTGTGACGAAGTCTTAACATGTTTGTGTGTGTTTACTGTTTCAGCGAGGTCTAAGAGCATGGTCATGGGGGAACTGTCCCGTGGGTCCAGCAGGCCATCGTCCCCCAGCCTTCAAGAGCAGGTAGTGAAGGCCGGCTGGCTGAAGAAACAGCGCAGCATCATGAAGAACTG[G/A]CAACTGCGCTGGTTTGTGCTCCGAACTGACCACCTCTACTTCTACAAGGATGAGGAGGAAACCAAACCACAGGTACAGCGGAAAGAGGACAGAGCAACCTGGAAATAAAAATAAAGACAGGCAGATGATTTATTACTAATATATTTTTGCTCTTCAGTGTTTGAACTCTCAGTAATGATTAAATCACACTGAACTGAGCTAAACTGAACTGAACTGAAGAACTGAACTTAAACACTAAAACCTGAACCACACTGTTCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTGAATTGAATTGCATTTTTCCTGAAATATAAGGTTGTCTTTTTTTAAAGCATTAATCAAAAAAAAAAGAAAAAAAAGAAAAACAAACTGATCCCATTGTGTCTAAACAAGGTGACGGTTATTGTTGAAAAAATAAAATAAAATAAGACCATGACCTTTTATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42228
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 |
---|---|---|---|---|---|
ENSDART00000014922 | Essential Splice Site | 153 | 698 | 4 | 10 |
ENSDART00000142245 | Essential Splice Site | 138 | 317 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 31352253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30998201 |
GRCz11 | 13 | 31128651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATTGGGTCAAAGCCATCAGACGTGTCATCTGGGCTCCCTTTGGAGGAG[G/A]TAACTCATATTTATGGACCACACAAGCACAGAGACACAGGCAAAAATGAA
Long Flanking Sequence:
AGTATTAATTTATTAAATGCATGGTATACATATATTAGTGTTACAACTAAATGGTATTTTTCATGTTGATGATAATAATATAAAACCGACTAACAAAATAGCTGGTTATTCTGGCCACTAACAGGTATTGATTATACTACTCCACAGAACTGCTATTATGTGATTTTAATGATTCAAAAAATATAACGAATAAATGTATTTAAAGTGTTCTTTGTACAAACAGTGGGGGCAATCGCAATGAATAAAGAAAATTATTCATGTTTTGATATTTATCTGTCATTCAAAGCATCAGGGGACTCAGGCAGACTAAATGTTATCAGTGTCAATCAAATGATTTACTCGAAATTTTTATCCCCTCTCTGCCTCCATAGGCTGTACAGGAGAGAAGGACAGATCGGCTCTCAGCCATGAGGCTTTCCTGCTTATGGCAAACTCCCAGAATGACATGGAGGATTGGGTCAAAGCCATCAGACGTGTCATCTGGGCTCCCTTTGGAGGAG[G/A]TAACTCATATTTATGGACCACACAAGCACAGAGACACAGGCAAAAATGAATCATTAGTTTCACTGAGGCTCTGCAGATTTCAAGAAAACAATATAAAAAACTAGCAGCAAGCATGTGTCTGTTTTTGTACTCTCGTCTTATTTGAGTAGAGTGATCTATATCTGGTTTATGCTGCGTGGCTAATATACAGGCTAACTAAAATAACAACAGCACTAGCGGCCTGTAAGTGTCTGAATCTTTAGGCATTATGTTACAGTTCTTTAATAAAATGGGTTTTTGGGGGGTCTGAATATAAAGGAAAATATTTAAATATACATTTAATGATTTTGAAAATCCACCACACAGTTTTTATTTCCTATGATATACAGTGCTAGCTTAGCTCATAGACACAACACGTTCCTCAGAGACCTACAGGTGAAGTGAAAAGGCCAACTTGGTAAGAAAATAAGCTTGCAGATAAAAGTTAGCCCAGTAGCGATCCTGAAAAACATTACTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22334
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 |
---|---|---|---|---|---|
ENSDART00000014922 | Nonsense | 697 | 698 | 10 | 10 |
ENSDART00000142245 | None | None | 317 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 31363360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31009308 |
GRCz11 | 13 | 31139758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTTCTTCTCCACTCTGGGGGATCTTACACTGGGAACAAGAACAAGC[A/T]AAATTTGACCGGCAGCCATGCTTATTTAACTCGGAGAGACTTCTGTGTTT
Long Flanking Sequence:
CCAGCATAGTTTAGCTTCAAATTTCTTTAACACGTCTGCCTGGAAAATTCTAGTATACCTAGATAGAGCTTGATCAGCTGGTTCAGGTGTGACTAATTGGGGTTGGAACTAAACTCTCTATGACACCGGTCCTCTAGGACAGAGTTTGGGCACTCCTGATCTAAACTCTTCAATTGTAAAACAAAATTTCTCCTTAATAATGGAGAAAATGAATAGCGTAATATACAATAGCACAACATATTTGGCAATACTTTTAAAATGGATCTGATATAATTTCTTTTTTAAGGCTAGAGGAATCAAGTGCCGCTTTGCACAAGCAAATGGAAAGGCTGGAGGAGGAGATGGACCAGGAGAAGAAGAAGTATCGCATGTTGGAAATTAAACTGCGAAATTCTGAACGTGCTCGTGAGGACGCAGAGACCCGCAACCGCTTGCTCCAGAACGAGATGGAGGAGTTCTTCTCCACTCTGGGGGATCTTACACTGGGAACAAGAACAAGC[A/T]AAATTTGACCGGCAGCCATGCTTATTTAACTCGGAGAGACTTCTGTGTTTGTTGTAGATAGAATTTCAAAATCTCGTTGCTCATGCATCATGGGTACTCAGAGGTCATTTTGTGCTGTTTTGTTTTATTTTTTAACGGCAATTTGATTATGTGTAGCATTTTTCACCTTTCTCTCTGATCCTCAGACTTACAGTTTTAAAGGGATAGTTCACGCAAAAATACAAATCCTCTGATTATTTATACTTAGCTTTGTTCTCAAGCTATAAACTGTTTTGTCTGCAAAAAAAACAAACAGCAAAAAATATTTTGTGTGAAAAACCAATGTTAACAAAATCTGAAAACTTGCCCCTGTTGTTTGTAAATAATGACAAGTTATTTTGGGGTGAACTATGCCTTTAAGGTTCAGTCCAGTTATTACACTGAATAAATTTTCATTGGATTTACTCAATTTTTTAGGGTAAGTGGTTGCAAACAATTTATACTGATTGAAAGCTTCACAA
Associated Phenotype:
Not determined