ZMP
ARHGEF25 (1 of 2)
Ensembl ID:
Description:
Rho guanine nucleotide exchange factor (GEF) 25 [Source:HGNC Symbol;Acc:30275]
Human Orthologue:
ARHGEF25
Human Description:
Rho guanine nucleotide exchange factor (GEF) 25 [Source:HGNC Symbol;Acc:30275]
Mouse Orthologue:
D10Ertd610e
Mouse Description:
DNA segment, Chr 10, ERATO Doi 610, expressed Gene [Source:MGI Symbol;Acc:MGI:1277173]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39412 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37737 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12815 | Nonsense | Available for shipment | Available now |
sa15460 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39412
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 |
---|---|---|---|---|---|
ENSDART00000048694 | Nonsense | 137 | 685 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 28213549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28043735 |
GRCz11 | 23 | 27970276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTGTTTTAAAGCAGTCTTGTGTACGTGTGTTTTGTGTGTGTAGGAGTG[G/A]AAAGATGGACTGCCTGCTCTTGGTGACTGTGATCCAGGTCTCCTGCAGTC
Long Flanking Sequence:
TAATTAATCTCTCCAGCTCTGCATATGAGTATATTGATAATAAAAGAAAATTTAACTAATCAATTAACTGATTATTTGTTTCCTCAAACTGCAAGAATCTTGTTTAGAAACTAAGCAAAATAATCATGATGATCAGTTTAACCATTATCATGCAGCCGGGGTATCAACAAGCCTTCATATCCTGTTTGTTCGATCACAGAAAGTATCAGTTTACATCACACTACAGGTGTTACTCTGTTTTTCATAACGCAGTGTGAGTTGCACCACACCGTGCGGCCAACTGCTCGCTACAGCCCTGCGGTTCGCCTCTGTCCAGGTGAACTGACCTTTAATTGCAGTGACCCTCCAATACACTTCTCATCATAGTCTCACACAGAGAGGAATTATGGGTCAGCTTTATTTTGACCTGAGTATTGATGTTTGGGAAAGACAGTGAAGGTTGTGGTTCCTGCTTGTTTTAAAGCAGTCTTGTGTACGTGTGTTTTGTGTGTGTAGGAGTG[G/A]AAAGATGGACTGCCTGCTCTTGGTGACTGTGATCCAGGTCTCCTGCAGTCCTACAGCTTCCAATCGGACTCTCCACAGGGATCCACAACACTAGGACAAACACAGGTAATGCTGTGATCAGTGTTTTTCCATTTTGATAGTCATGGTGTCAGATTGTGTTAGGGCTTGGACAAGAAAGATGTTAGACTACATGTTTTGCTATCTGACCACATCTTTAAAGGAGTAGTTCACCCAAAAAGGAAAATCCTGTCATTATTTACTCATCTTCCACTGTTTCTAAATCTTCCATTGACTCTCATAGTATCTTAGTGTTCATACTATGGATGTCAATGACTATGTTTTTATTTAAAGATGCTAATTAGATTCATGAGCATATTGTATAAAGCATGGGAGAATAAAGCTATGTTTCCATCTAATGAGTCAAAAGAACAAATTCGTCACCTAAGAAATTGGAAAAATTGAACTTTGCTGCCATAATAGAAGCCACAGTGGGGCTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37736
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 |
---|---|---|---|---|---|
ENSDART00000048694 | Nonsense | 286 | 685 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 28231695)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTAGTTATTTCCTGGCCGAGCTGGAGAAATGTGTGGCCGAGCCTGAA[C/T]GACTGGCGCAACTTTTTATCAAACATGTGAGTGTGTCTCTTTTTTTCTGT
Long Flanking Sequence:
CCCTCAAGGACCAAAGATTTTAACCTGTGAATTATCATCATTTTAATATAAATTATCTCTTGTGAACTCCTTTTACACCAATTTTGAAGCAAATTTATACAATTATGGTACGAGATATCTCTCTGTTTTAGTCCACTGGCCAACAAATGCTATCATTTGCATATTTAAATAACTTAAAACCTAAATGTTCAATCTTAAGCTCATTTGTGTAAAGAGAAAAAAATAAGCGCGATAAAATGCTTCCTTGTTGATACATAGATACATAGATAGATGTGTTTACAATAATTTGTGTGTGTGTGTGTGTTTGTGTATTACAAATCTTACAGGGCTTTAAGTATGTTTCCAAAACTTCCAAAAAGTTCAGATCAAACTAATTTTACATAACACGTTTTTAGGGAAAAAGTCGATTGGCCCTGCTACTGACTAATGCTGAGTTATACGTCTGATCTCTTCCTAGTTATTTCCTGGCCGAGCTGGAGAAATGTGTGGCCGAGCCTGAA[C/T]GACTGGCGCAACTTTTTATCAAACATGTGAGTGTGTCTCTTTTTTTCTGTCTGTCTGTCTGTGCCAAGCAAACTTCCTCTCACACTTTGAGCAAGCAGATTTGAGAAAACACAGAGGTTTTTAACACGCTCACCCATTTTAACACCCCATTTATCCTCCCATCAACCCAGTCTATTTCTGTCCCCGTGTTACTGATACGGCCCATTTGAGGCTGTGCGTTTGCTTGTGTGTCCATTGGCTTATTACCACAAGGGAAAAAGAGGCGGGAAAAATAAGAGGCGGAATAACAAGCACAGCTACGTCCTTTGATAACACTCTACTTTACACTCCGAGTCTATTTCTGGAGTTCAGTCCTACACTATGGACATACACGCATAAATAACTCACCAAGAAAATAAACAACACAATTCCCAGCACCCACAGGCGTAAAATTTGCAGATTTATAGCTGTGGAAGTACTTCACAGTGGCAGTAATTTGTTGCCACATGCTGTGATACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37737
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 |
---|---|---|---|---|---|
ENSDART00000048694 | Essential Splice Site | 324 | 685 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 28239421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28069310 |
GRCz11 | 23 | 27995851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTAAATCTGAGCACATCGTGTCAGAATACATCGAGACCTACTTTGAG[G/A]TAAGTGCATGTCAAGGGCAAGCAGAAGATTATTGGAGTTCTCAAAGATCC
Long Flanking Sequence:
GAGCCACGCTGCTCCCCACCGCTTATGGCTGCCGGCTCCCATTAAAAATGAATGACTTCCAGCTACTTTGATGCTCTCGCCGCTTTCGGTGTGAATGTACAGTTAAAGGGAATGGTAGATGAGACTCTGATTGGTTGATTCTCAAAACACACCCAGAACTAATTAAGAGAATAAGCACAACCCTGTTAGACCATGCGAAAGTGCATTCGGAAATGCTCTTAATGCTTTTGCGCCCTGCGATTTATACTTTGCACCTAGATTGTTAAAAAAGAGCCCTAGGATTTAAGAAATCCAATCCAAAAACGTTTTTCTTGGTGGGTAAATTATAGGGTTAAGAGAATATTTTGTAGCTCAACTATATATCTACTAAACTGGGCTAATTCACTCTTCTCTGTTTACATAATCTGCAGGAAAGACGGCTTCACATGTATGTGGTGTATTGCCAGAACAAACCTAAATCTGAGCACATCGTGTCAGAATACATCGAGACCTACTTTGAG[G/A]TAAGTGCATGTCAAGGGCAAGCAGAAGATTATTGGAGTTCTCAAAGATCCACAGGTTACGCCTGAGGGACTGTTTTGGTCCATCTGTGTAAATATCTCAAGGCAGACTCTCTTCCTTCCCATTTGCACGGTGTGTGTGCATGTGCGATTGTGTGCGTTTGTGTGTGTGTGTCTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTAATGATCACTCAGTGGACATGAAGGCCCTGACTGACCTATCAATTCTTGGAACAGATAAATCAGGGAGATGCTTGATCGAAAAGTTTGACACCTTAATGGATTCTCAGTGCTGTACCAAAACATTTGAAGGTTTGATAGCTGGCATTACTTTAGGTTTTATTGACTGAGATTGCAGGGTACTATGGGGTAATGGATCAAGGAGAGTGTTTAGCTATGTTTGGAGTGGAAAACCAGAAGGTCAAAAGATTAATGCATATTGCCTAGTTTTTTGTGCATGTCCAGGGTTTAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12815
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 |
---|---|---|---|---|---|
ENSDART00000048694 | Nonsense | 436 | 685 | 12 | 16 |
ENSDART00000048694 | Nonsense | 436 | 685 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 28248481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28078520 |
GRCz11 | 23 | 28005061 |
KASP Assay ID:
2261-7904.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGCAGCATCCTGTCCCGCGCTAAAGAGAGACGGGTCTTCCTGTTTGAA[C/T]AACTTGTCATCTTTAGCGAGCCAATYGACAGGAAGAAAGGATTTTCTCTA
Long Flanking Sequence:
TTAAAAGTCTGTGTGCATATACGCCATTGCAGTGCTTTGTTCATGCATGTTTGGTATGTTGCATTTTTCTAGGAAATCCTTAACTTTTCTAGCTGTTTCTGCAAACATTTGAAAATGTTTTTTCTATATGCTAATATCATGTGGGCATTTAACTAATTTAGAATAAATATTTTCCAGATAATACTTTAATCATTTGTTTACTAAACTAAACTCCAAAAATGCATTTTGAAACCAATGATATGATCTTTGTGTACTAATAATGTACAAATACAGCTATCTGAGGCAAATCAAAACAGACAAATGCAAATCTGTTTAGATTTTAGAGAGCGAATCGTATTTGGATATCCCAAAGGTTTTGAAAACCCCTGCTAATTTTGTCTCTTTATCAGGGGAAGATCACGGCACAAGGAAAACTTCTCCAGCAAGACACATTCACAATCACCGAGCAGGACAGCAGCATCCTGTCCCGCGCTAAAGAGAGACGGGTCTTCCTGTTTGAA[C/T]AACTTGTCATCTTTAGCGAGCCAATTGACAGGAAGAAAGGATTTTCTCTACCTGGTTACATTTTTAAGAACAGTATTAAGGTGAGTTACCGCTTTAGAGAAAGTCATTAGGATATACAGTAAGATTTCAATGTGACGCAGTATGTTTGCATGTTTTCTTCAGATAAGTTGTTTGGGTGTGGAGGCTTGTGTAGATGGTGACCCAAATCGCTTTGCCCTGACGTCCCGGGGGGCCGATGGTAGCACAGTGCGATATGTTTTGTACTCCTCATCGCCGGATATCTGCATGGCTTGGGTCAGTGACGTGAGCCAAATACTGGAGACCCAACGCAATTTCCTTAATGGTGAGACATTCATTTAGTCTGCATCCACACCCAACAGCCTGCTGATTTCATCTCTGCCCTCAGTCAGTAGTGTAAAGCATTTTAATAAATATAATTAGTCACTGTACACAAGTATATTTTTTAGCTTACTTAGACTGAGAATCTTTTTCAACTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15460
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 |
---|---|---|---|---|---|
ENSDART00000048694 | Nonsense | 436 | 685 | 12 | 16 |
ENSDART00000048694 | Nonsense | 436 | 685 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 28248481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 28078520 |
GRCz11 | 23 | 28005061 |
KASP Assay ID:
2261-7904.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGCAGCATCCTGTCCCGCGCTAAAGAGAGACGRGTCTTCCTGTTTGAA[C/T]AACTTGTCATCTTTAGCGAGCCAATYGACAGGAAGAAAGGATTTTCTCTA
Long Flanking Sequence:
TTAAAAGTCTGTGTGCATATACGCCATTGCAGTGCTTTGTTCATGCATGTTTGGTATGTTGCATTTTTCTAGGAAATCCTTAACTTTTCTAGCTGTTTCTGCAAACATTTGAAAATGTTTTTTCTATATGCTAATATCATGTGGGCATTTAACTAATTTAGAATAAATATTTTCCAGATAATACTTTAATCATTTGTTTACTAAACTAAACTCCAAAAATGCATTTTGAAACCAATGATATGATCTTTGTGTACTAATAATGTACAAATACAGCTATCTGAGGCAAATCAAAACAGACAAATGCAAATCTGTTTAGATTTTAGAGAGCGAATCGTATTTGGATATCCCAAAGGTTTTGAAAACCCCTGCTAATTTTGTCTCTTTATCAGGGGAAGATCACGGCACAAGGAAAACTTCTCCAGCAAGACACATTCACAATCACCGAGCAGGACAGCAGCATCCTGTCCCGCGCTAAAGAGAGACGGGTCTTCCTGTTTGAA[C/T]AACTTGTCATCTTTAGCGAGCCAATTGACAGGAAGAAAGGATTTTCTCTACCTGGTTACATTTTTAAGAACAGTATTAAGGTGAGTTACCGCTTTAGAGAAAGTCATTAGGATATACAGTAAGATTTCAATGTGACGCAGTATGTTTGCATGTTTTCTTCAGATAAGTTGTTTGGGTGTGGAGGCTTGTGTAGATGGTGACCCAAATCGCTTTGCCCTGACGTCCCGGGGGGCCGATGGTAGCACAGTGCGATATGTTTTGTACTCCTCATCGCCGGATATCTGCATGGCTTGGGTCAGTGACGTGAGCCAAATACTGGAGACCCAACGCAATTTCCTTAATGGTGAGACATTCATTTAGTCTGCATCCACACCCAACAGCCTGCTGATTTCATCTCTGCCCTCAGTCAGTAGTGTAAAGCATTTTAATAAATATAATTAGTCACTGTACACAAGTATATTTTTTAGCTTACTTAGACTGAGAATCTTTTTCAACTGTGA
Associated Phenotype:
Not determined