ZMP
im:7158374
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARHGEF15
Human Description:
Rho guanine nucleotide exchange factor (GEF) 15 [Source:HGNC Symbol;Acc:15590]
Mouse Orthologue:
Arhgef15
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 15 Gene [Source:MGI Symbol;Acc:MGI:3045246]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35285 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6251 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22088 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35285
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 |
---|---|---|---|---|---|
ENSDART00000088470 | Essential Splice Site | 766 | 937 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 23722629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22245791 |
GRCz11 | 12 | 22367010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTACCTCTTTCTTTTCAATGACCTACTTGTCATTGCCATCAAGAAAAG[G/A]TAAAATGCTGGAAAAACCTGTCTGTGTTATGCTTCACTTTGTTTCTTTCA
Long Flanking Sequence:
TATTTTTTATGAATTTTCGTTTTTGGGTGAACTATCCCTTAAAATGATATGCAATTGACGTAGTAAATTCTACAGGGAGTTATTTAATTGTCTTGTTGCACTTTTTAAAAGTGTTACTTTTGACAAATTCATCTTGATAAATAAAATGTGTTTTATTTAAAAAAAAAAAATTTTGAAAGCTTTTGAATGTTGACATACATATAACTATTTTATTAAAAAACCCAAATCCACAAAAAAAATCAAACAAACATTTTGGAGATTTGATTGTATTACAAATGCATTATATGTTTATGTGTATTAGTTGAAATATTGTCTCATCATTGATATATATCATATATTCAGGCAGTGCCAATTATATCTCAAACACGTTATTTGGAGAAACAAGGAGAGGTGCTGGAAGTAAATAAAGGAGGAACGTTCTTGGGCAACCTGCGCCCCAAATTTACCCCCGTCTACCTCTTTCTTTTCAATGACCTACTTGTCATTGCCATCAAGAAAAG[G/A]TAAAATGCTGGAAAAACCTGTCTGTGTTATGCTTCACTTTGTTTCTTTCATCTTGGTCTAAGCAAATTCTTGAGCATACATCAAGTTTATGTGTGCAGTGCACTCCACTAATATTTTGGTAAATATTTGTAATACAAAATGCCTTTAATTAACTTTTGCAGAAAATATAAACAAAATAGCTCTACTTTCATCAAGAGTAAACAAATGGCAGCACAGCGCACTATCAAAAAGAAAGGTCACACTTTATTTTGATGGTCCGTTTGTTGAATGAAGTTACATTGCATCTACATGCCAACTATGTAGACTGTTAGGTTGTGGTTAGGGTTGGGGTCAGGGTTAGGGTTAGTGTAAGTTGACATGTACTTGCAACGTTTTTATAGTCGGTTAAATGTCTGTTGAAGGAGCAGTATCAATAAATATTAAGCAGACAGTCTACTAATACTCAACTGGACCATCAAAATAAAGTGTTAACAAAAGAAAACATCTTTGTTAAAAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6251
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 |
---|---|---|---|---|---|
ENSDART00000088470 | Nonsense | 809 | 937 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 23721475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22244637 |
GRCz11 | 12 | 22365856 |
KASP Assay ID:
554-4547.1 (used for ordering genotyping assays)
KASP Sequence:
CCAACATAGAGCACTGCTTCTGTCTGACGCTGCTGGAGAATCACCAGGGA[C/T]GACAGATGGAGAGAATCATGAAGGCTCCCTCACAGTGCGTGAAGTTATAA
Long Flanking Sequence:
GGAAATATATAGGCAAAACTCCCTCAGGCATTCATCACACATGAGTAAGAGCACAAAAAAAATCATGTAGAGCTTCACAAAAACCAAAGGGGTTATTAGAAAAAAGGCTAAAACACTGAAAATGTTTCTAAAACTTCTGAAATCTTCCGTCATCAATCATCATCAGTTTTATTAAATTCATATTTTGAGCAAAAGATTAAAAGGTTAACCAATAAAGACCAAGTCGAGGTCCAATATTAGCGGAGGGCACTGTAATACTTTATTTATTGTCTATTTCTATAAAAAGTAACACACCTGATTTCATTTAATGGACATTTGGTTTCTGAATGGGACTGTACTAATGTACTTGTGTCTCTGTTTCTGTGTGCTGCAGTGCTGAGCGGTATGTGGTGCTGGATCATGCCCATCGTTCGCTGGTCCAGGTGCAGTCATATGAGAACTCAGCTGTGCCCAACATAGAGCACTGCTTCTGTCTGACGCTGCTGGAGAATCACCAGGGA[C/T]GACAGATGGAGAGAATCATGAAGGCTCCCTCACAGTGCGTGAAGTTATAAATAAACCTACAGTATACTATTCATTTGATTCATCCACTATACATTTTTAGTCTGATAATTTAAGCATGTTTCAAATTTAAATACACTTGTCATTTTATATACAGTGTATTCGGAAAGTACTCATAGCGCTTCACTTTTTCCACCTTTTTTTTGTTACAGCCTTATTCCAAAATTGATTAAAGTGAAAAAAGATTGTTTGTACATAAATATTCACAGCCTTTGTTGTGAAGCTCTAAAATGAGCTCATGTACCTTCTGTTTCCGCTGATCATTCTTGAGATGTTTCAGCAACTTAATTGAAGTTCACCTGTGGTAAATTCAGTTGATTGGACATGATTTGAAAAGGCATACACCTGTCTATATAAGGTCCCAGGGTTGACAGTGCATGTCAAAGCACAAATCAAGCATGAAGACAATGGAATTGTCTGTAGACAATGTGGAAAATGTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22088
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088470 | Nonsense | 854 | 937 | 14 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 23719633)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22242795 |
GRCz11 | 12 | 22364014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTGCTCTTGAATCACATGTGGTTTTGTATGTCAGATTGTCCTCAGGTG[C/T]AGTGTGTGGAGCAGTATGTGGCAAAACAATCGGATGAATTAAATCTGGAG
Long Flanking Sequence:
AGTATTCTTTTACGACATAGCGCATATGAGATAAATGACATCAGTACGTTATAACAGTTGATGATCTATTAATGAACCGATAGGATTGTCCATGTTTGCATTGCAATGCATTGAAGAAACAATTAATTTAGGATATACATTTTAGGATAAATGGATATGGTAGCTTTATAGAATACATAGGGCCAGGAATATTATACTCAGTCAGGCTGTAAAGATATATGCTGCTTTTAATGATACATAAGTCATGTATCTTTTATCTCACCAATTAGATCTGACTCACAAAGATGGTTGGCAGTGTTTCCAAATCCTGACGACCCCAAAAATGATCAAGAAGAAGTCATATATGAAGACTGGGGTAAGTTTTTGTCCCAGTTGCTGAGGATTTCACTCATGTCCGACATGCTAGTGCTTGACATTGATTTCCATCACATTCTGTTCTCTCTTCCGAAACGTTGCTCTTGAATCACATGTGGTTTTGTATGTCAGATTGTCCTCAGGTG[C/T]AGTGTGTGGAGCAGTATGTGGCAAAACAATCGGATGAATTAAATCTGGAGCGCACAGAGATCATCAATGTTATACGCAAAACCAATGAAGGTGTGTAACGATTCACATTCCCTTCATAAGAAGCACACTGTCAGTTTTGAGATTTAGTGATTTAGTTTTTTCTCTCTAAAGGAAAAAGATACTTTCATACATCATTTGCTTGAATATATTTTATTCTACCAAAAACTGTGGAAAATTTCAGTCATATACAGGGTTCACACAGGTCATGGAATTTCTGCAATAACATGGCGTTTCAAAGTTTCTATTCTAAACACTGAAATTGAGAGAATTATATATATTTTATGTCATGAAAGACGTTGAATTTCAGGAATTTTTTCTGTCATTTCAAGTTTAACTTTTCCATTTATTTATTTATTTTTTTACCAGTTTTGTATTGCGTTGTAATAAAAAACACATAAAGTGTAGTCTATATTAGCTACCATAAATGGTCGCTGACAGAA
Associated Phenotype:
Not determined