ZMP
arhgef11
Ensembl ID:
ZFIN ID:
Description:
rho guanine nucleotide exchange factor 11 [Source:RefSeq peptide;Acc:NP_001027010]
Human Orthologue:
ARHGEF11
Human Description:
Rho guanine nucleotide exchange factor (GEF) 11 [Source:HGNC Symbol;Acc:14580]
Mouse Orthologue:
Arhgef11
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 11 Gene [Source:MGI Symbol;Acc:MGI:2441869]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26876 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20855 | Nonsense | Available for shipment | Available now |
sa15205 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26876
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017140 | Essential Splice Site | 32 | 1406 | None | 40 |
ENSDART00000136594 | Essential Splice Site | 43 | 524 | None | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 6314828)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 5349166 |
GRCz11 | 7 | 5470813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGGCCAGCAGAGGGAAACACTGCCTGATCTCTCTTCAGACAACACCGG[T/C]AATGCAGATTTCTGTTACAAGCACATTTACACTGGGCATGCGCCAGTATG
Long Flanking Sequence:
GTTGAAATATTCACAGCTTAAAAAAACAGATATGTTAAATTTCAGCACAATTCAAGTCATTAAATGCAAGAACTTGTTAATTCTGTGTATTATTCCTTACAGTTTGTGCTATTCAACAAGATTTTTAATTCAAGACTTTTGGCATTGATTTTGGCCCATAATAAAGTTTGTTAATTAACTTAAAAGATACTTATTTGATCCTGTTACATGGCGAGGAAACACTACAAAAACATGATATCCTTTCACAGTCAGTCTTGTGGCTGTTTTAAACATGCAATAGAGATAAAGTAAACTTCTCTTTATTTCCTTGTTCTCAATCTCTCTGTTTGTGTCTCCTGCTCCTCTAGTCATCCATTTCTCCTCTTCCGTCTATTGATTTTAATGTCTGCTTGTTTGTCTTCTGTTAGGTTGAGCAGTCTGACATTAGGAGACTCTGAGCGCAGGTCTTCTCCTGGCCAGCAGAGGGAAACACTGCCTGATCTCTCTTCAGACAACACCGG[T/C]AATGCAGATTTCTGTTACAAGCACATTTACACTGGGCATGCGCCAGTATGAGATTCTGACTCCGTGATAAACCTTGGAATTAAAAATATTGTGGTTACTGCTCTAAAATAAGTCCCTTTTTAGATGTCCTGGCAAAAAAACAACAACTTTTTTCCCCCATTGAACACAGTATATTTTATTCTAAGAAACATTTAAAGTATTTTGGTGCATGCAAAGTAAATCATTGAGTTCTGCCGTCTTCATTAGTTTGCACAGATTTCTATCTCTTGTAAAGGCATCTTTGGATGTCTTTTCTGTGGATATAAAGTAAAGCAGCTTCTCTGTTCAGGCCCATAGCATGCTGGGATGTTGGTGTATAAGTGTTTTGTTTTGTCAAATGTTTCCTGAATCGTGAGCTGAACAGTAGCTTTTGATGTAGATGGTCGTCACGATTATAAAGATGGTAAGTCAAGGCGAAAGGGAGTAACATTAATTTTGGGTGAAACACACAAGCAAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20855
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017140 | Nonsense | 35 | 1406 | 2 | 40 |
ENSDART00000136594 | Nonsense | 46 | 524 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 6311663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 5346001 |
GRCz11 | 7 | 5467648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACTCATCTTTATATTTTCTGTTCCTCCTGATTTGACAGGAACGGGTT[T/A]GGTCCAAAGATGCGTGGTCGTGCAGAGGGACAATCTGGGGTTTGGCTTCA
Long Flanking Sequence:
TAGGACTCACACAGACCACAGGTTGAGCGCCCCCTGCTGGCCTCACTAACACCACTTCCAACAGCAACCTATTGTTCCCTAGTGGTCTCCCATCCAGGTACTGACCAGGCTCAGCCCTGCTTAGCTTCAGTGAGTAACCGGTCTTGGGCTGTAGGGTGATATGTCTGTGATTGAAAAAAAGTGTATGGATACAGCTAGAGCTTGCTTGTTTTTACACAAATATCTAAAACATAATTTTTTTTATTATTTATTTATTGCTGTGTTATTAAATGTATTTAAATTATAATCATTTTTTGATAGGGCAAATAAAAATCTTTTTACATTTGTGCCATTCTTTAGCATTTAGCCCTTCATGAGTCTAAAATTTCATTCGTAATTGTCTTAAAATGTCATTTAAAAGTCTTAAATTTAACTCAGTGAAACCCTGTTATATTTATCTGTTTATATTCATCTACTCATCTTTATATTTTCTGTTCCTCCTGATTTGACAGGAACGGGTT[T/A]GGTCCAAAGATGCGTGGTCGTGCAGAGGGACAATCTGGGGTTTGGCTTCACGGTGTGCGGAGAGAGAATCAAACTGGTGCAGAACGTCCGGCCGGGTAACAAACACTCTTTGTTTTGGGTCAATAAGATTTTATTTGAAGTTACATTAACACTTTAATTTAATGTGAGTTTGTTAAATTGATCAAAAGTTATAGAGTGCAGATTTTTAAGATTTCAGATAAATGCTGATTTTCATCCAGAAATCTTGAAATACATATATCACAGTTACCACAAAGGTTTACTAATAATTGTTTTGTACATTGATATTAATGAGACATGTGCAGCCAGTCATTATATTAGAAAGATTTCTGAAGAACAGTGTGATATTACAACATGATCTCACGGCAATTCGTAATTTTTTATGGAGACAGATAAGACTCATAAGTAATTCACGCAAAAGACACGATATACACATGCGTAGCCAAATTCACGTGCGTAAAATATTTATTTATATTCACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15205
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 |
---|---|---|---|---|---|
ENSDART00000017140 | Essential Splice Site | 801 | 1406 | 26 | 40 |
ENSDART00000136594 | None | None | 524 | None | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 6256699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 5291127 |
GRCz11 | 7 | 5412843 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGAATCAGTGATMGTTCAGGGCATTGGAGACATCATGCTGGCCAGAG[T/C]GAGTCTCATTTCTCTGTCTTCATCTCWGGATTTCKGTCTGTGTTGGTGAA
Long Flanking Sequence:
CTTGATAATTTTATTCATGTCTATATTCTAAAGGTTTTTACTGAAGGGTTTGTTCATATATAATTTGAGTCATTTTAGGGAACATTTTATACATCATAACCTGATCAAAATGTGTTTAATTCTGGCTTTAATATTTTATTTTTCTAAAACTTTCAACACTATTTAAAATTCATTCTATTAAAACCTTTATTGCTAATATATCAACAAAATTACTTACTACAATGACTTAATTCATTGTTATGCATTATTTTGTGTACATTTTCTCAAAATATTCTGATTTAACTTTACAGCATATGTAATCATGCAAAAAATGCCATCATCAATGTAATAAATCAGTTAAATTAACCATATTCTTGTCTGAAGTCCTGCGCCAATACTAATGTTGATTTTGGTATTTAAATCTTAATTTTTTTGTCTTTCAGCAAGTTTATGTGAGTCCATGAAGAAGTGCAGAGAATCAGTGATAGTTCAGGGCATTGGAGACATCATGCTGGCCAGAG[T/C]GAGTCTCATTTCTCTGTCTTCATCTCTGGATTTCTGTCTGTGTTGGTGAAGTGTGTGTTTTTACCAGTGTTTGTGTGTGTTAGTTTGAGGGAGAGGCTGGAGATCAGTTTGAGGAGCAGGTTTCGCATCTGTGCAGTCAACAGAGTCCAGCGCTGGAGCTCATCAAGAACAAACAGCGAAAAGACCCTCGATTCGCCCACCTCATACAGGTAATTCAACGGCACAGTTTATTTGCACTGATTATCTGAAGTAATTTAATCTGATGGCAGATCTGTTTACATGGACTCTAAACATTGTAATCTCATTCAAGCATCCATCTATGATATATATTCTGATTAAAACTTTAGCATTTAATAATGTTTAAGTTCAACGCAGGGGTAAGCAGAATGATCTTGTTTTGCTTTGACATAGCATTTGGTCACACTTTATTCTGATGGCCTGTTTGTTGAATTTATTTTTCTGTGTTTCTGTGGTGTTTTTCAGGAGTGTGAGGCCAGTCC
Associated Phenotype:
Not determined