ZMP
si:ch73-389o21.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARHGAP19
Human Description:
Rho GTPase activating protein 19 [Source:HGNC Symbol;Acc:23724]
Mouse Orthologue:
Arhgap19
Mouse Description:
Rho GTPase activating protein 19 Gene [Source:MGI Symbol;Acc:MGI:1918335]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37564 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30733 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37564
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 |
|---|---|---|---|---|---|
| ENSDART00000116455 | Essential Splice Site | 130 | 454 | 3 | 12 |
| ENSDART00000133537 | Essential Splice Site | 130 | 454 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 37809541)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 34994421 |
| GRCz11 | 22 | 34970170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGAAGGAATAGCCCAGATATATCAGCTCATCGCTTACCTCAGCAAAA[G/A]TAAGTGCATGATATTAATAAAGTTGATGGCTTTATTATACAGTTCACCCA
Long Flanking Sequence:
TTGCACATTTATTTACTTGTTTGTCCTACTCTGCTGAGCTTCTCTAATTGTGCTTAAGACAAAACTTGTTTAAACTACTTAAAAAAATGTTTCTATTCTAGTAAGTTCAAGGTGTTTTTCTTCACACCAATTGTGATGAGTTTTTGCACCTGAATAGAAACATTCTGATGTCAAATTTGGTGTGTGTTTAGCCAAAATAAAAACAGAGGATTTTATACAGCAAATATTGCCTTCCGGTTTCCTGTTCAAGGTTAAAATGTAGAACAATAGTATATGTGCCCATTTAAAACAAATCTATCCCTATTAAATGATTCTTTGGCAAGCAGAATTAAATATAAGCATCAAATTCATTTCATGTATTAGAGAAAAGATGCATTCTTTTGGAAGAGGCGTTGACTGATTGTCGTATTTATTTTCAGACAAAGGTGTTGTGTTCGGCATGCCCCTCACAGAAGAAGGAATAGCCCAGATATATCAGCTCATCGCTTACCTCAGCAAAA[G/A]TAAGTGCATGATATTAATAAAGTTGATGGCTTTATTATACAGTTCACCCAAAAAATGTACATTCTGTCCTCATTTACTCCTCCATTCGTTCAAAACTCCTTTGAGTTTTCTTATGTTGAACACAAAAGATGTAAAAAAAATTGTGGGTTGCTGTTTCCCCTACTATATGAGTTGTTGAACTCTTCCAAATATCTTCTTCTGTGTTTAATAGAAGAAAGAAAATTCAAACAGGTTTAAAATTAGTCAAGAATAAGTAAATGAATGGGTGAACTATTGCTTAAAATACACTAAAACATTGGAAGATTGACAAGTATTTGAATCTTTATGGTAAGGACACTGTTAAGAGGTGCTTGAACAGGTTGTTTTCCTGTAGATCTCCATGTGCAGGGTCTGTTTCGAGTTCCTGGGAACAGTCTGAGGCAGCAGACGCTGAGAGAGCAGCTCAACAGTGGAGCCGATATTGACTTCGCCGCTGGTGACTTTCATCCCAATGACGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30733
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000116455 | Nonsense | 301 | 454 | 6 | 12 |
| ENSDART00000133537 | Nonsense | 301 | 454 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 37805680)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 34990560 |
| GRCz11 | 22 | 34966309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACCTGAAGAAGCTCAACAGCGGGATGGCGTTTCTCATCAAACACTCA[C/T]AGAAGATCTTTAGGGTATCTTTTCAGATCAAACCTTTTCTCACTGCAGCT
Long Flanking Sequence:
TTGTTTACATCCCTCAAAAAAGTGTAAAAATCCCTTTTTTACACAAAGTGTAACCCCCAATAATACCCCCCTCAATCTGGAATAAAATCGGAAACGGGTCTTTATTAACTCTCCACAGAACTGACCACGTTTGACGATGAAGGCAACAAGACGAGTTTTCCGGATAAGGAGCGTCAGATCGAGGCTCTGCAGCTCCTCCTCCTGCTTCTTCCCACCGCCAACCGAACACTCCTCAAGCTGCTGCTGGACCTGCTCTACCACACCGCCAAACAGCAGGACAAAAACAAGATGTCTGCTCACAACCTGGCGCTCATGTTCGGCCCGCACGTCATCTGGCCCAAGAATGTACGCCGCCGGCTTTCTTTTGAAGTCATTCATGCTCAAGCATGTTTTTTTTTTTTCATGTTGTTCTCTGTGTCTTTCTTCAGATGAATGCCAGTGACCTTCAGGAGAACCTGAAGAAGCTCAACAGCGGGATGGCGTTTCTCATCAAACACTCA[C/T]AGAAGATCTTTAGGGTATCTTTTCAGATCAAACCTTTTCTCACTGCAGCTTATTAATGTGCATATAATGATGAGATGGAAAGCAATTGAAATTTTACAGAAAGCTACAGTTTTTATTTCTATATGTGTTTATTTATTTGTAAATTTATAAGCGCCTTGTCACCCTGCGAAGCAAACTCATTTCGCCCACTTATAAGATCTTTTCTTTTTGGTCATGACTAGGGCCAGACGGAATCTGCGGACGTTTTTTGCTATTTCTGCGAATAATTTAGGTAAAAATCTGCGCATTTCTGCGGAATTATTTTTGGAGTATCATAACTAAAAACTTAATATATGAAATAAAAATAATATCTTTTTAAATGTACTATAATATTTAAAACGCAATTAGATTCACTTTATTTGGTAAATAAAGCAAGTTTGTCATATAATATCTCTATTAAAAGACAGAAAATATTAATGTACAAACTGCATTGTACATAAATCAGATGAACACAATAGTCA
Associated Phenotype:
Not determined