ZMP
si:ch73-92i20.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARHGEF9
Human Description:
Cdc42 guanine nucleotide exchange factor (GEF) 9 [Source:HGNC Symbol;Acc:14561]
Mouse Orthologue:
Arhgef9
Mouse Description:
CDC42 guanine nucleotide exchange factor (GEF) 9 Gene [Source:MGI Symbol;Acc:MGI:2442233]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5740 | Nonsense | F2 line generated | Not yet available |
sa2229 | Nonsense | F2 line generated | Not yet available |
sa9176 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17928 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5740
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000088408 | Nonsense | 149 | 521 | 3 | 10 |
ENSDART00000134393 | Nonsense | 152 | 251 | 4 | 5 |
ENSDART00000143878 | Nonsense | 180 | 549 | 5 | 11 |
ENSDART00000088408 | Nonsense | 149 | 521 | 3 | 10 |
ENSDART00000134393 | Nonsense | 152 | 251 | 4 | 5 |
ENSDART00000143878 | Nonsense | 180 | 549 | 5 | 11 |
The following transcripts of ENSDARG00000061746 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 23735602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 21448474 |
GRCz11 | 5 | 21952274 |
KASP Assay ID:
554-2900.1 (used for ordering genotyping assays)
KASP Sequence:
AGGGGTATCTTCGCCAGTGTAAAAAGCGAAGAGACATGTTCAACGACGAT[C/T]AGCTGAAAGTGATCTTCGGAAATATAGAAGACATTTACAGATTCCARCTA
Long Flanking Sequence:
CACATCTTGTCTAAAATCTTATGTTGCATGGGTTTATTTTTGGAAATAGCCAAAAATACATTGTGTGGGTCAGAATTATAGATTTTTTCTTGATGCCAAAAATCAAATGAATATTAAGTGATGTTTATATGAAGATATTTTGCACATTTCCAACTGTAAATGTATTTTGGACTATTAATATGTATTGCTAAGCACTTCATTTAGACATTTTAAAGATGATTTTCTTAATATTAGAATTTTTTTGAACACTCATATTCGAATAGTCTCAGCAAAATATCGTCCTGTCATATCAAAGCAAGCATCAACGGCAAGTTATTCAGCTTTCAGATTATGTATGAATCTCAATCTTATAACTGATTTTGTGGCCCAAGTTCACATATTGTCAATTTACTGTGGTAAATGTAGCTTTAAGCACACAACATTTTTAGTTTAAATCTGTGTTTATGTTTCAGGGGTATCTTCGCCAGTGTAAAAAGCGAAGAGACATGTTCAACGACGAT[C/T]AGCTGAAAGTGATCTTCGGAAATATAGAAGACATTTACAGATTCCAGCTAAGCTTTGTCAGAGACCTGGAGAAACAGTTCAACACAGAAGAACCTCATCTCAGTGAGATCGGACCCTGCTTTCTGGAACACGTCTGTATTTAAACACAAGACGAATCACACATTAAATCACTCTGTAGATATGTTGAGGAACTAATTGTTCCATCTCCTATGTTTTTTACGTGCAGCAAGATGGATTCTGGATCTACTCTGAATACTGTAACAATCACGTTGACGCCTGCATGGAGCTCACACGTCTGATGCGAGACGCACGATACCAGCACTTCTTTGAAGCGTGTCGATTGGTTCAGCAGATGATCGACATCGCCATCGACGGCTACTTGCTCACACCGGTTCAGAAAATCTGCAAATACCCTCTACAGCTGGCAGAGTTACTGAAATACACGGTACAAGAACACAGGTACGCTAACTCCTGGTGCTCCCACAAAATATATGACTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2229
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000088408 | Nonsense | 149 | 521 | 3 | 10 |
ENSDART00000134393 | Nonsense | 152 | 251 | 4 | 5 |
ENSDART00000143878 | Nonsense | 180 | 549 | 5 | 11 |
ENSDART00000088408 | Nonsense | 149 | 521 | 3 | 10 |
ENSDART00000134393 | Nonsense | 152 | 251 | 4 | 5 |
ENSDART00000143878 | Nonsense | 180 | 549 | 5 | 11 |
The following transcripts of ENSDARG00000061746 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 23735602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 21448474 |
GRCz11 | 5 | 21952274 |
KASP Assay ID:
554-2900.1 (used for ordering genotyping assays)
KASP Sequence:
AGGGGTATCTTCGCCAGTGTAAAAAGCGAAGAGACATGTTCAACGACGAT[C/T]AGCTGAAAGTGATCTTCGGAAATATAGAAGACATTTACAGATTCCARCTA
Long Flanking Sequence:
CACATCTTGTCTAAAATCTTATGTTGCATGGGTTTATTTTTGGAAATAGCCAAAAATACATTGTGTGGGTCAGAATTATAGATTTTTTCTTGATGCCAAAAATCAAATGAATATTAAGTGATGTTTATATGAAGATATTTTGCACATTTCCAACTGTAAATGTATTTTGGACTATTAATATGTATTGCTAAGCACTTCATTTAGACATTTTAAAGATGATTTTCTTAATATTAGAATTTTTTTGAACACTCATATTCGAATAGTCTCAGCAAAATATCGTCCTGTCATATCAAAGCAAGCATCAACGGCAAGTTATTCAGCTTTCAGATTATGTATGAATCTCAATCTTATAACTGATTTTGTGGCCCAAGTTCACATATTGTCAATTTACTGTGGTAAATGTAGCTTTAAGCACACAACATTTTTAGTTTAAATCTGTGTTTATGTTTCAGGGGTATCTTCGCCAGTGTAAAAAGCGAAGAGACATGTTCAACGACGAT[C/T]AGCTGAAAGTGATCTTCGGAAATATAGAAGACATTTACAGATTCCAGCTAAGCTTTGTCAGAGACCTGGAGAAACAGTTCAACACAGAAGAACCTCATCTCAGTGAGATCGGACCCTGCTTTCTGGAACACGTCTGTATTTAAACACAAGACGAATCACACATTAAATCACTCTGTAGATATGTTGAGGAACTAATTGTTCCATCTCCTATGTTTTTTACGTGCAGCAAGATGGATTCTGGATCTACTCTGAATACTGTAACAATCACGTTGACGCCTGCATGGAGCTCACACGTCTGATGCGAGACGCACGATACCAGCACTTCTTTGAAGCGTGTCGATTGGTTCAGCAGATGATCGACATCGCCATCGACGGCTACTTGCTCACACCGGTTCAGAAAATCTGCAAATACCCTCTACAGCTGGCAGAGTTACTGAAATACACGGTACAAGAACACAGGTACGCTAACTCCTGGTGCTCCCACAAAATATATGACTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9176
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 |
---|---|---|---|---|---|
ENSDART00000088408 | Essential Splice Site | 313 | 521 | 5 | 10 |
ENSDART00000134393 | None | None | 251 | None | 5 |
ENSDART00000143878 | Essential Splice Site | 344 | 549 | 7 | 11 |
The following transcripts of ENSDARG00000061746 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 23734862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 21447734 |
GRCz11 | 5 | 21951534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACATCGACAAAATYGCYCAAWGGCAGGCCTCTRTGCTGGACTGGGAG[G/A]TGGGTGGCTGAAGSTTTTCATGCAAAGTTYATTAGTTGGRTGGAAAAGAG
Long Flanking Sequence:
GGATCTACTCTGAATACTGTAACAATCACGTTGACGCCTGCATGGAGCTCACACGTCTGATGCGAGACGCACGATACCAGCACTTCTTTGAAGCGTGTCGATTGGTTCAGCAGATGATCGACATCGCCATCGACGGCTACTTGCTCACACCGGTTCAGAAAATCTGCAAATACCCTCTACAGCTGGCAGAGTTACTGAAATACACGGTACAAGAACACAGGTACGCTAACTCCTGGTGCTCCCACAAAATATATGACTGCGTAAACGATGAATTTTCAGCTGACATATCTGCTTTCCACTTATCATTTTGACAGGCCTCGTATTTTTTTCGCTCTTCTTCTTGGCTCATTCTTTTCCCTTTCTCTCCCAGTGATTATCGGTACGTGGCTGCTGCGCTAGCTGTAATGAGAAATGTCACTCAGCAAATCAACGAACGCAAACGAAGGCTTGAGAACATCGACAAAATTGCCCAATGGCAGGCCTCTGTGCTGGACTGGGAG[G/A]TGGGTGGCTGAAGCTTTTCATGCAAAGTTTATTAGTTGGGTGGAAAAGAGAGCAATGGAGTGGTCGAAGCTGAAAGATTGGTTATTATTATGAAAATTGAGCTGTACTGCATTCCCTAATGGTCAGTCGATTGGAATAATTACAGTTTTTGTCTTTGAAAGAAGTGTCTTGTTAAGAGGACTGATGGTCCTTTATTATTCATTATTGGGATGAGCCTTCAAAGACATTTAAAATCTTGATCATTAAAATACTTTGATTAGTAGTGTACTTATTCATTCATTCATTTTCTTTTCGGATTAGTCCCTTTAATCATCAGGGGTCACCACAGCGGAATGAACCACTAACTTAAAAAGCATTTTATGCAGTGGATGCCCTTTCAGCTGCAAGTACTGGGGAGCATCCATACACTCTCATTCACACACATACACTATGGATAATTTAGCTTATTCAATTCACCTATAGTGCAGGTCTTTGGACTGTGGGGGAAACCGGAGCACCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17928
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088408 | Nonsense | 421 | 521 | 7 | 10 |
ENSDART00000134393 | None | None | 251 | None | 5 |
ENSDART00000143878 | Nonsense | 452 | 549 | 9 | 11 |
The following transcripts of ENSDARG00000061746 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 23726615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 21439487 |
GRCz11 | 5 | 21943287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAYGAGATCCATCTGTTCCTGCCCAAAAAGCTRGAGGAGAAAATCCGTTG[G/A]CTTCGGGCATTTCAAGAGGAAAGAAAGATGGTCCAGGAAGAYGAAAAAAT
Long Flanking Sequence:
ATATAAGGTAACTACAAGGGGTAAAGGATCAGGGGTAGATTTAGGGATAAAAACTAGTTTTCACCCAGTTTATAGTGACTATTATACTACATATTATAACATGTAAAACAGGACTGGGAAATAAAGTGCTACCATTGAATTCAATGAAACTTGTTGTTGGTGGAAAAGAAAGGAGGTGAAATATAAAAGTGATATATTACAGGTTTAGTGCTTTGAGAGAATAATCAATCAGTCAGTTTCATTCTCTTAGTAATTTGTCTGGGATACCAACTACAGACATACTAATAAGGCCTCTCCACCTCTCCACAGGATCTCATTCGCAGAGATATTCTCTACTATAAGGGGCGGATTGATTTGGATCGATACGAGGTCATTGATGCAATCGATGGCCGAGATGATGATTTTAACGTTAGTGTGAAGAACGCCTTCAAACTGGCCAACCGAGACACAGACGAGATCCATCTGTTCCTGCCCAAAAAGCTGGAGGAGAAAATCCGTTG[G/A]CTTCGGGCATTTCAAGAGGAAAGAAAGATGGTCCAGGAAGACGAAAAAATTGGTGAGAAATATCACAGCACAGTTCAGTCGTCATTCATCTTTGTGTAGTTTTTATTTTGTATGTGATTTATTTTTTTGGTCACACTTTACAATAAGGTTTCATTAGTTAATGTATTTACTAACAATGACTATTAATGAACAATACTTGAACAGCATTTACTAATCATAGTTCTGCATTTACTAATGCATTATTAAAATTTGAATTTATGCCTGTTAACATTAGTTAATGCACTGTGAGTTTAACATGAACTAATAATAAACAACTGTTTTCTATTTACTAGTGTTGACTACAATCTGTAATAAATGTATTGTTCATTGTTTTTTCATGTTAGTAAAAGCATTAACTAACAGTAACTAATACAACCTTATTGTAAACTGTTACCATTTATTTTGATGTATGTTGAAGAACATTTGGACCACTATTTGTATGCAGTGAACATACAATTTCA
Associated Phenotype:
Not determined