ZMP
arhgef19
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARHGEF19
Human Description:
Rho guanine nucleotide exchange factor (GEF) 19 [Source:HGNC Symbol;Acc:26604]
Mouse Orthologue:
Arhgef19
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 19 Gene [Source:MGI Symbol;Acc:MGI:1925912]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29923 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45800 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9879 | Essential Splice Site | Available for shipment | Available now |
sa9613 | Essential Splice Site | Available for shipment | Available now |
sa24325 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29923
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 |
---|---|---|---|---|---|
ENSDART00000113598 | Nonsense | 59 | 958 | 1 | 15 |
ENSDART00000133269 | None | None | 499 | None | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 24435353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24221919 |
GRCz11 | 23 | 24148470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCGGGAAGGAAGGCCTCTCCTGCGGCAGCACCAACACATTGCTGTGTG[T/A]CAGCAAGAGACATTGGCCTTCATTGACCTTCAAGAGCAAAGTGTTAATGG
Long Flanking Sequence:
TGTGCTCTTTAATTAGAACAGGAAGACGCAGCGGCAGCGACTAAGCCAAGTCTGTCATGGGGGAAGAGCAGAGCCTGTTCAGTCAGACTTAACTTTACCCAGTGGAGGACCAAAACCAAAGAACTGCGCCAAGATGAGCCAAGCTTTACTGTACATATATATGTGCTGGCACAATATTAATAAAAATGAGACAGTGGAATCCACTCCTTTGTGCTCAATTTATTTTCCTTTGTACTCAAAATAAAGATGCGCTATAATATCTAATATTGTTTCTGGTTTCTTTGTTTCTCAATTGTTTTGCAGTACCCATGTGCCATCTGAGACATGCTTCCTGGCTATGGAATCTCTCCTCTTCTTGATTTCCAGCCTCACCTCCAAGCGTTCCATTGCAGAGGCGAGAGCTCTGACATGTGGTTCCCAGGCTCAGTTGAGACCCAGGCACTGAGCGATTCTCGGGAAGGAAGGCCTCTCCTGCGGCAGCACCAACACATTGCTGTGTG[T/A]CAGCAAGAGACATTGGCCTTCATTGACCTTCAAGAGCAAAGTGTTAATGGTTTCCAATCATGCACATCAGAAAACTGTAGTTCCTCTCTTTGCTCCAAGCCTCTCAGATGCAATGGAAGGAGTCCATCTGACTTTGCCAAGACTGAGAGTACAGACAGAGCACTAGACGATTATTTGACAGAGGATATCAATAATGTGGAAGTGGTTCAGGAACAGTCATGGACATACATTACTGGCTTACCTGAGACAGTTCATGAAAATCCTGATTCAGGAGTTAAGGGTCTCAATCCTCGGAATTTATTTCTGCCTTTGTCCCCTATATATGCACCTGGAGACAGGAACTCTTTGGAGTCTCAGCAGCTAAGCTCCCCCTCTTCCCCTTTAGAGGGTCCAGACCCATTTCGCCCTCAAAGACGCACCTCTTTGGGATCAATAAAAGAGAAGTCTATAAGTAAGTGCCTTCACGTTTAACTAAGTCTTAGCATACTGGTCCTAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45800
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113598 | Essential Splice Site | 428 | 958 | 4 | 15 |
ENSDART00000133269 | None | None | 499 | None | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 24433665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24220231 |
GRCz11 | 23 | 24146782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGTAATTAGAATATGATGTGTTAAAATGTATTCTACGGTTTCTTCTC[A/T]GAATGAGAAAAGTTTCTGTTGATGAGGATGGAGGCAGCCCTCCCAGTAAC
Long Flanking Sequence:
CGGCGCTTCTCTGCTTCTGAGCTCATCTCTCGCCTTCAACTCTCTCAGAGGAAAAACTCCTTTACACTTAAGCTGGGCAAGTCTCTCTCTGCTCGCGTGGCCTCCCGGGAACGCCACCTGTCTGGAAACCTCAGCTCAGACTGTAAGTGACTCATCAGGACTGATTAACCTAATGAAAGCCTTTATTGTGAAAGTCTTGTGCAGTGATGTCATTTTCACACTTTGGTGCAGTATTTTCAGATAAGTTCCTTTTGTATACCTTCTTCCTCCCTTGTCTGTTTGTAGACAAACCCAACTCCAGACATCGCTTCTCAGGGGGATCAAGTGACAGTGGACCACATAGTCCGGTGGGGTCTGCACCACCACTGCCCTCTGCTGACAGTAATCAGCCACTGCACCGAAGGAGCTCTAAGCAAAGGTGGCCCTAAAACTCAGCAAGCACCAACAGAAACCAGTAATTAGAATATGATGTGTTAAAATGTATTCTACGGTTTCTTCTC[A/T]GAATGAGAAAAGTTTCTGTTGATGAGGATGGAGGCAGCCCTCCCAGTAACTCTAAACGTCTTTCGCGTTTCTTGCCAAGCTGTAAGTCATAAACACACTTATTTAATACTACTACTACTACTAATTACTATTATTGTATTTGTGTATCAATTATCAGTTTTCTCTTTCCCTCTCAGTGATTTTGTATCAGGAATACAGTGACGTTGCCATCAACAGGGAGATACAGAGGCAACAAGGGGCAGAGCCAGGAACCGATGAAGAAAGAGGGGAGTCTGTGTCTCCTGGAAACCTCTCCCCATCCAGCTCATTCCGCTCATCACGAGGCTCGGCCTTTTCCTTATGGCAAGATATTCCTGATGTTCGATCAAGTGGACAACTTGACAATTTCAGCAATGAAGAGCGTAAACTACAGGAGGTGAGTCCACACTCAGAAATTTGATTTGATTTAGAGTTTCATCAACCAGCACATTTTGCTAAAAAGTTACATCTTGACTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9879
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113598 | Essential Splice Site | 535 | 958 | 6 | 15 |
ENSDART00000133269 | Essential Splice Site | 76 | 499 | 2 | 11 |
ENSDART00000113598 | Essential Splice Site | 535 | 958 | 6 | 15 |
ENSDART00000133269 | Essential Splice Site | 76 | 499 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 24433157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24219723 |
GRCz11 | 23 | 24146274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACCAGCACATTTTGCTAAAAAGTTACATCTTGACTTTTTTTCCCNTTTC[A/G]GGCAAAGTTTGAGTTGRTGACATCAGAGGCCTCATACATACGGAGCTTGT
Long Flanking Sequence:
AAAAGTTTCTGTTGATGAGGATGGAGGCAGCCCTCCCAGTAACTCTAAACGTCTTTCGCGTTTCTTGCCAAGCTGTAAGTCATAAACACACTTATTTAATACTACTACTACTACTAATTACTATTATTGTATTTGTGTATCAATTATCAGTTTTCTCTTTCCCTCTCAGTGATTTTGTATCAGGAATACAGTGACGTTGCCATCAACAGGGAGATACAGAGGCAACAAGGGGCAGAGCCAGGAACCGATGAAGAAAGAGGGGAGTCTGTGTCTCCTGGAAACCTCTCCCCATCCAGCTCATTCCGCTCATCACGAGGCTCGGCCTTTTCCTTATGGCAAGATATTCCTGATGTTCGATCAAGTGGACAACTTGACAATTTCAGCAATGAAGAGCGTAAACTACAGGAGGTGAGTCCACACTCAGAAATTTGATTTGATTTAGAGTTTCATCAACCAGCACATTTTGCTAAAAAGTTACATCTTGACTTTTTTTCCCTTTC[A/G]GGCAAAGTTTGAGTTGGTGACATCAGAGGCCTCATACATACGGAGCTTGTCTATTGCAGTTGACCATTTTATGATGTCTTCTGAGCTATGCGAGTGTCTTGGGACACAGGAGAGGCAGTGGCTCTTCTCCAAACTGCCTGACGTGAAAGAAGTCAGTGAGAGGTGAATATATATGAAAAGTAATTACAATTGTTGATATTTTTGAAAGTGTATGCTAACTTCTGAGATGTGCTTCATTGCAATGCCTGTTTCTTTCTGTCTCTTGTTAAATTTACTTTATGTTTTTAGGTTCCTTCAAGATTTGGAGCGTAGGTTAGAAGGAGACATTTTACGGTTCGACGTGTGTGACATTGTCCTTGACCACTGTCCTGCACTGAGGAGGGTTTATCTGCCTTATGTCACCAATCAGGCCTACCAGGAACAGACCTATCAGCGACTACTGTAAACCATTTCTGACTGTACAACAGTGCTCTAACAAGCATAACAATGTGCATATTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9613
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113598 | Essential Splice Site | 535 | 958 | 6 | 15 |
ENSDART00000133269 | Essential Splice Site | 76 | 499 | 2 | 11 |
ENSDART00000113598 | Essential Splice Site | 535 | 958 | 6 | 15 |
ENSDART00000133269 | Essential Splice Site | 76 | 499 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 24433157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24219723 |
GRCz11 | 23 | 24146274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACCAGCACATTTTGCTAAAAAGTTACATCTTGACTTTTTTTCCCNTTTC[A/G]GGCAAAGTTTGAGTTGRTGACATCAGAGGCCTCATACATACGGAGCTTGT
Long Flanking Sequence:
AAAAGTTTCTGTTGATGAGGATGGAGGCAGCCCTCCCAGTAACTCTAAACGTCTTTCGCGTTTCTTGCCAAGCTGTAAGTCATAAACACACTTATTTAATACTACTACTACTACTAATTACTATTATTGTATTTGTGTATCAATTATCAGTTTTCTCTTTCCCTCTCAGTGATTTTGTATCAGGAATACAGTGACGTTGCCATCAACAGGGAGATACAGAGGCAACAAGGGGCAGAGCCAGGAACCGATGAAGAAAGAGGGGAGTCTGTGTCTCCTGGAAACCTCTCCCCATCCAGCTCATTCCGCTCATCACGAGGCTCGGCCTTTTCCTTATGGCAAGATATTCCTGATGTTCGATCAAGTGGACAACTTGACAATTTCAGCAATGAAGAGCGTAAACTACAGGAGGTGAGTCCACACTCAGAAATTTGATTTGATTTAGAGTTTCATCAACCAGCACATTTTGCTAAAAAGTTACATCTTGACTTTTTTTCCCTTTC[A/G]GGCAAAGTTTGAGTTGGTGACATCAGAGGCCTCATACATACGGAGCTTGTCTATTGCAGTTGACCATTTTATGATGTCTTCTGAGCTATGCGAGTGTCTTGGGACACAGGAGAGGCAGTGGCTCTTCTCCAAACTGCCTGACGTGAAAGAAGTCAGTGAGAGGTGAATATATATGAAAAGTAATTACAATTGTTGATATTTTTGAAAGTGTATGCTAACTTCTGAGATGTGCTTCATTGCAATGCCTGTTTCTTTCTGTCTCTTGTTAAATTTACTTTATGTTTTTAGGTTCCTTCAAGATTTGGAGCGTAGGTTAGAAGGAGACATTTTACGGTTCGACGTGTGTGACATTGTCCTTGACCACTGTCCTGCACTGAGGAGGGTTTATCTGCCTTATGTCACCAATCAGGCCTACCAGGAACAGACCTATCAGCGACTACTGTAAACCATTTCTGACTGTACAACAGTGCTCTAACAAGCATAACAATGTGCATATTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24325
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 |
---|---|---|---|---|---|
ENSDART00000113598 | Essential Splice Site | 682 | 958 | 8 | 15 |
ENSDART00000133269 | Essential Splice Site | 223 | 499 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 24432473)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24219039 |
GRCz11 | 23 | 24145590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCATTCTTCCTTTTCAAAGAATCACACGCCTCAAAATGCTAGTGGAGG[T/C]ATTTCATCATGCATGTCCAATGCGATAGTGACAGTTATCTGTATCCCTTG
Long Flanking Sequence:
TTACAATTGTTGATATTTTTGAAAGTGTATGCTAACTTCTGAGATGTGCTTCATTGCAATGCCTGTTTCTTTCTGTCTCTTGTTAAATTTACTTTATGTTTTTAGGTTCCTTCAAGATTTGGAGCGTAGGTTAGAAGGAGACATTTTACGGTTCGACGTGTGTGACATTGTCCTTGACCACTGTCCTGCACTGAGGAGGGTTTATCTGCCTTATGTCACCAATCAGGCCTACCAGGAACAGACCTATCAGCGACTACTGTAAACCATTTCTGACTGTACAACAGTGCTCTAACAAGCATAACAATGTGCATATTGCAAATGTTGCCATGTTTAAGCAGTTCTTAAATTTTCTTTGTGGTGTTTTCTTAGGCAAGAGAATGCCCGGTTCCCTGGGATCCTTGCCCGCCTGGAAGAGGACCCAATATGCCAGAGGCTGCCTCTTACATCATTTCTCATTCTTCCTTTTCAAAGAATCACACGCCTCAAAATGCTAGTGGAGG[T/C]ATTTCATCATGCATGTCCAATGCGATAGTGACAGTTATCTGTATCCCTTGTTATTTTCCTGTGCTAATGAGCTGTGTTTCCTTAAATAGAATATCTTAAAGAGAACAACGCCTGGGTCACGAGATGAGGACACTGCCACCAAAGCACTTAATGAGCTCAAAAAGGTCTGAAAAGCAGTTGAAGAAAGAAAGAAACGGTCACAAACATTGTTTTAAATTACCATAAAAAAATGAAAATGTGTTCTGCTGCACTAGATTATAAAGGAATGTAACTCCAGTGTCCAGTCCATGAAGAGAATGGAAGAACTAATTCACCTAAACAAGAAAATTCACTTTGAGGGCAAGGTATAATATCAAACATTGCTTAACCTACTGTGTATCATGCAAGGGTGACATGCACCAGTTATAAATTTATTTGCTGACAAGCCAGTGAAAGTCCTGCCTCACTTTGTACCTTTCAGAAAGTTCTTTTTGGCCACTCAATTCCTTTGAAAACTGAAG
Associated Phenotype:
Not determined