ZMP
zgc:136551
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC557983 [Source:RefSeq peptide;Acc:NP_001038313]
Human Orthologue:
ARHGEF1
Human Description:
Rho guanine nucleotide exchange factor (GEF) 1 [Source:HGNC Symbol;Acc:681]
Mouse Orthologue:
Arhgef1
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 1 Gene [Source:MGI Symbol;Acc:MGI:1353510]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36146 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36145 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44852 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa22852 | Nonsense | Available for shipment | Available now |
| sa22851 | Nonsense | Available for shipment | Available now |
| sa9929 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36146
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000087624 | Nonsense | 139 | 433 | 7 | 20 |
| ENSDART00000124618 | Nonsense | 139 | 1005 | 6 | 30 |
| ENSDART00000139355 | Nonsense | 139 | 1005 | 7 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 28430588)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 26306362 |
| GRCz11 | 16 | 26179804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGATCGCTTGCGTCCAGAACTGATCAATGAAGAGCAGCAAAAACGTTA[C/A]GCTAATGAAATACAGTTTGCGCAGAGTCCAGAGATACTGCGACAGCTGGA
Long Flanking Sequence:
TTTTTACAGGACTATAAATATGAGGAAACATATGTGGTAAAAACAAAAAAACAGATTGTGTGATTGAAAAAAGGTTATTGGACTTCATAAAATGAGAAGTTGCAATAAGAAAATAAAACACAAAAAATATTTATATAATTAAATAAAGACATTTATTCACAGCTGTCTTTGCTCATATTGAAAAGTTGCCAATATTAGTGAAGGGCTCTGTATTTATGTAAAATACTCGAAGAAAAACATTCAGATGAGAAGATTTTCTCTTTTTTCTAATCTTTCTCATCCAGATTCTCAAAGTATCTGTACCAAGTAACATCGCCCCTGAAATAGGTAAGACTTTTACCAGTTAGAATTCATTCAAATAAAAAGAACTCTGGGCCTGGTGTTGACATTGTGTTAATGCTGTAATTTTATTATATTCATTCACTTCCCCATCTCTCTCGATCTGGTCTTTAAGATCGCTTGCGTCCAGAACTGATCAATGAAGAGCAGCAAAAACGTTA[C/A]GCTAATGAAATACAGTTTGCGCAGAGTCCAGAGATACTGCGACAGCTGGAAGACTTCAGGTGAGAGTTTTCTATTGATAAGTCTTGGAAATTCTAAATCATCAGTGCCATAGTGTCAAGTGCCATACTTCTTTTTTCCATGTTAGGCAAAAGAGGATGATGGGAATGACACCTAATGAGCGGGAATTAAATGATGTGGAATCCCATCGACCCACTGATCGCATCCCTATGGACATGAAGGAGAAGGCTGTCGCTGAATCCCTGCTGGAAAAGATGGTTGAGGCCAAGTAAGAGCTATAAAATAATAATATCTTTTAATTTAATAGCAATTTAAATTATTTTGATTACGGCTGCATGATATTGGAAAAATCTGATATTGCGAGATTTTATTTTTCTGCAATAAATATTGCAATATAAATACAGTTTTAAAGGATGGTTTGAGTTTGAGCTCTATTAGATGGCTTTATGGGGAGTCTTAACAGTATACAGGTAAAAATCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36145
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 |
|---|---|---|---|---|---|
| ENSDART00000087624 | Nonsense | 147 | 433 | 7 | 20 |
| ENSDART00000124618 | Nonsense | 147 | 1005 | 6 | 30 |
| ENSDART00000139355 | Nonsense | 147 | 1005 | 7 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 28430566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 26306340 |
| GRCz11 | 16 | 26179782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCAATGAAGAGCAGCAAAAACGTTACGCTAATGAAATACAGTTTGCG[C/T]AGAGTCCAGAGATACTGCGACAGCTGGAAGACTTCAGGTGAGAGTTTTCT
Long Flanking Sequence:
AGGAAACATATGTGGTAAAAACAAAAAAACAGATTGTGTGATTGAAAAAAGGTTATTGGACTTCATAAAATGAGAAGTTGCAATAAGAAAATAAAACACAAAAAATATTTATATAATTAAATAAAGACATTTATTCACAGCTGTCTTTGCTCATATTGAAAAGTTGCCAATATTAGTGAAGGGCTCTGTATTTATGTAAAATACTCGAAGAAAAACATTCAGATGAGAAGATTTTCTCTTTTTTCTAATCTTTCTCATCCAGATTCTCAAAGTATCTGTACCAAGTAACATCGCCCCTGAAATAGGTAAGACTTTTACCAGTTAGAATTCATTCAAATAAAAAGAACTCTGGGCCTGGTGTTGACATTGTGTTAATGCTGTAATTTTATTATATTCATTCACTTCCCCATCTCTCTCGATCTGGTCTTTAAGATCGCTTGCGTCCAGAACTGATCAATGAAGAGCAGCAAAAACGTTACGCTAATGAAATACAGTTTGCG[C/T]AGAGTCCAGAGATACTGCGACAGCTGGAAGACTTCAGGTGAGAGTTTTCTATTGATAAGTCTTGGAAATTCTAAATCATCAGTGCCATAGTGTCAAGTGCCATACTTCTTTTTTCCATGTTAGGCAAAAGAGGATGATGGGAATGACACCTAATGAGCGGGAATTAAATGATGTGGAATCCCATCGACCCACTGATCGCATCCCTATGGACATGAAGGAGAAGGCTGTCGCTGAATCCCTGCTGGAAAAGATGGTTGAGGCCAAGTAAGAGCTATAAAATAATAATATCTTTTAATTTAATAGCAATTTAAATTATTTTGATTACGGCTGCATGATATTGGAAAAATCTGATATTGCGAGATTTTATTTTTCTGCAATAAATATTGCAATATAAATACAGTTTTAAAGGATGGTTTGAGTTTGAGCTCTATTAGATGGCTTTATGGGGAGTCTTAACAGTATACAGGTAAAAATCACAATGGAAAAAAAATGCTTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44852
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 |
|---|---|---|---|---|---|
| ENSDART00000087624 | Nonsense | 180 | 433 | 8 | 20 |
| ENSDART00000124618 | Nonsense | 180 | 1005 | 7 | 30 |
| ENSDART00000139355 | Nonsense | 180 | 1005 | 8 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 28430381)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 26306155 |
| GRCz11 | 16 | 26179597 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGGGAATGACACCTAATGAGCGGGAATTAAATGATGTGGAATCCCAT[C/T]GACCCACTGATCGCATCCCTATGGACATGAAGGAGAAGGCTGTCGCTGAA
Long Flanking Sequence:
CTGTATTTATGTAAAATACTCGAAGAAAAACATTCAGATGAGAAGATTTTCTCTTTTTTCTAATCTTTCTCATCCAGATTCTCAAAGTATCTGTACCAAGTAACATCGCCCCTGAAATAGGTAAGACTTTTACCAGTTAGAATTCATTCAAATAAAAAGAACTCTGGGCCTGGTGTTGACATTGTGTTAATGCTGTAATTTTATTATATTCATTCACTTCCCCATCTCTCTCGATCTGGTCTTTAAGATCGCTTGCGTCCAGAACTGATCAATGAAGAGCAGCAAAAACGTTACGCTAATGAAATACAGTTTGCGCAGAGTCCAGAGATACTGCGACAGCTGGAAGACTTCAGGTGAGAGTTTTCTATTGATAAGTCTTGGAAATTCTAAATCATCAGTGCCATAGTGTCAAGTGCCATACTTCTTTTTTCCATGTTAGGCAAAAGAGGATGATGGGAATGACACCTAATGAGCGGGAATTAAATGATGTGGAATCCCAT[C/T]GACCCACTGATCGCATCCCTATGGACATGAAGGAGAAGGCTGTCGCTGAATCCCTGCTGGAAAAGATGGTTGAGGCCAAGTAAGAGCTATAAAATAATAATATCTTTTAATTTAATAGCAATTTAAATTATTTTGATTACGGCTGCATGATATTGGAAAAATCTGATATTGCGAGATTTTATTTTTCTGCAATAAATATTGCAATATAAATACAGTTTTAAAGGATGGTTTGAGTTTGAGCTCTATTAGATGGCTTTATGGGGAGTCTTAACAGTATACAGGTAAAAATCACAATGGAAAAAAAATGCTTTTCTTCTTTTTTGTCTTGTTTCTAATCCAAATATCAAAACAATTTTTAGACCAAGTCAAAATATTGTTTAATTTTCACCGTCAGAAGGAATAAGTGAAAATTAATAGATTTAGCTTGTTTTAAGGAAATTATCTGCCTGTGGGGTATGTGAAATAATCTTTGGCCCAAAAACAAGACAAAAATTCTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22852
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 |
|---|---|---|---|---|---|
| ENSDART00000087624 | None | None | 433 | 17 | 20 |
| ENSDART00000124618 | Nonsense | 459 | 1005 | 15 | 30 |
| ENSDART00000139355 | Nonsense | 459 | 1005 | 16 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 28407891)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 26283665 |
| GRCz11 | 16 | 26157107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGAAATAATTGTTTCCTGTCGTTCTCCCAGAGCTGTTTGTGACAGAA[C/T]AAGCACACGTCCGTATGCTGAGTGTATTGCAGACAGTGTTTTCTCGTCCA
Long Flanking Sequence:
GTTTACTTGCATTAGATCCTGGATTGTTTTTCTTGTAAACCTACATTTCTTTCTGCATTTCACCTTTGTTCTTGGAAGAATAAACAATAAGGAAATATATTTTGGGTGAACTATTCCTAATTGTATCTACTTTTACCATGCTTAAATATGTATGGAACCCTTTTAATTGTGCTCCTCTATTTGTCTCTCTCAGCGTGGAAGGTGACAAAACACCGGAAATCGCTCTCCTCACTCCCACTTTTGTCCCGGCCCCTCAGCAAGAAGAGATAGAGCCCCGTCTCCTGGAGCTCGAGCAGGACCCACTCAACTGGAGAGAACTTGCTTCCAGTGAAAGCCTGCATAAGCTGAGCAAGAAGGAAGCCAAAAGACAAGAAGTCATAAATGGTAATAAAAGCAATGGGAAAGAAATTGTTTAAAACGGACTTAATATTTTGAATCAGCCATGTAGAAAGGTGAAATAATTGTTTCCTGTCGTTCTCCCAGAGCTGTTTGTGACAGAA[C/T]AAGCACACGTCCGTATGCTGAGTGTATTGCAGACAGTGTTTTCTCGTCCACTTGAGAAGCAAGAGTATATGACTGCAAATGAGGTGGCCACCATCTTCTCCAGCCTGGATGACATCATAGAGATGCACTGTAAGTAATTGCCTCAAGCGTTAACGCATTACATTCTGCTTCATTTTAAAGTATTTTGATTGCCTCTTATCTCTTGTGTACAGAAATAGCATATTTTCTATTTCTAATTTGTCAGTTGCATTTATTAAGATTTCTGAAAGCCCAGATTAGTCATGTTGGTGGGAAAGTCATGTTTTATATTTTCATTCAGGAATAAAGTTAAATAGGTCACTAGCGTGTATATTAGTTTTCCTTTCCACAACAAACATTAAAATTGAGCAATATTCAATAGAGTGCAAAATAAACGATGCAAGTATGTAAAGAGTAACAATCACTATAAAAAAATTTATTATAAAATTCAAACCCAAATAAATTAATTTAATGGTGCAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22851
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 |
|---|---|---|---|---|---|
| ENSDART00000087624 | None | None | 433 | 20 | 20 |
| ENSDART00000124618 | Nonsense | 583 | 1005 | 18 | 30 |
| ENSDART00000139355 | Nonsense | 583 | 1005 | 19 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 28404394)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 26280168 |
| GRCz11 | 16 | 26153610 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGTTTGTTTTTAGGAAGCAGAGAGTAAGCCACAGTGTCGGAGGCTA[C/T]AGCTAAAGGATATCATACCCATAGAGATGCAGAGACTAACAAAATACCCT
Long Flanking Sequence:
AGACTTATCATTTCTAAAATTCATTCTTCCACTTTGTAGATGTTTTCTATGAGAACCTGAAGAAACTGCGTGAAGAAGATGAATACATTGTCAAAACTATCAGCACACCACTTCTCAACAGAGTAAGTGACTTCGAGTGCATTAACCGCTACTTTTCTGTTCTTTTTAAATTCTCTTTAATTGTTTTGCTGTGTTATACATGAAGACATGTCTTGATTTTTGTAGTTCAGTGGATCTGAAGGAGAATGGTTTCAAAAGCTCACAGCACGCTTCTGTAGCTACCAGTCCTGGGCTCTGGAGCAGATCAAGAGCAGGCAGAAGAAGGACCCCCGATTCAATGCTTTTATACTGGTGAACCATTTAAAACACTGCTCAGTCACATAAATGTACTGTTGCACATTGGAACATGATACATTTTTTTTGGGAATTAGCTTGGCATCAGTTGGTTTTTCTGTGTTTGTTTTTAGGAAGCAGAGAGTAAGCCACAGTGTCGGAGGCTA[C/T]AGCTAAAGGATATCATACCCATAGAGATGCAGAGACTAACAAAATACCCTCTTCTGCTGGAAAACATTGCTAAGAACACAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGCGTGCTGCATGCTTATCTGTTTTTTTGACACATAAGGACAGAAATTTATATAATGACATTATGACACAGGTATTACAAGGAGAAGGTGACTTTTGAGGACATTGCCCCATGTGCCCATTTTTCAAAAGGCTCATAAATCAAACAAAATTAGTTTTATTTTTTTTATTTTTTTAAGTAAAAATACACAGTTTTCCTTTTGGGTTGGGTTTAGGCATAGGGTTGTGGTAGGACAATATAAAATACAGTTTGGACTAGGGCTTCACAATATATGGTTTAAGCATCAATATCGAAATGTGTGCTTCCGCTTTAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9929
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 |
|---|---|---|---|---|---|
| ENSDART00000087624 | None | None | 433 | None | 20 |
| ENSDART00000124618 | Nonsense | 842 | 1005 | 26 | 30 |
| ENSDART00000139355 | Nonsense | 842 | 1005 | 27 | 31 |
Genomic Location (Zv9):
Chromosome 16 (position 28397596)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 26273370 |
| GRCz11 | 16 | 26146812 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTCGGTGTTGTGTTTTTATTCTGAATTGTGGTTTACTTCACCCCAGGG[C/T]GATTTAGTGAGAAGATTCGRGAAAGTGATCCTCCACTCATCGACTATCTA
Long Flanking Sequence:
TTAATTGTCCTATGTCTATGTAAAGCTAATCAATCCATAAAAATACATTTAACTAAAGTTTTATTAAATAACTCTGTTTACCAATGTGGTTTAATTATCTTACTTACAAAACATTACTTTAAACGATACATTTATTTATAGATCTGGACCGACTGTTGTGAATATATTTAGTTTGCTTTAGTTTGAAATTTCATTTATAATGGTTACTGTATATTGGACTTGATGAAACCTGCAGAAACCCTGATACTAAAGAACCCTCTTGAGTGTCAAAAAATCAAGGGAATTTAGATTTGTCAGTTCATGTCCTCCTGTTAGCCAACTTCTGTCAAAACTCTTTCCCTTTTGCTTCTCCAGAGCTCATCCTCCTCTTAGCCCCACTGAAAATGGAGGTGAACTGCTGAAAAATCGCGTCGGTGAGACATTTGCCTCTTGGAAACTGATCTATAAGTTGCTTCGGTGTTGTGTTTTTATTCTGAATTGTGGTTTACTTCACCCCAGGG[C/T]GATTTAGTGAGAAGATTCGAGAAAGTGATCCTCCACTCATCGACTATCTAGCAGCCAACGGCTTTGACCTGCTCACCCACAGCCACACACCTCCGGAGAAATCTGCTACTGTTGCTTTGGATGAAGGTCAGCATTTATGAAATGTCATTTCATATAAACATTTTATTGAACAATTAGAATTTTAATTTAATGAAACATTTTTGCTTGTATTTTTTTTCAGTCATGTGTTTGAAGAGGCTATTGGTTGGGAGTATTAGCCTGTCAGATGATGCTCAGACTCTTGGGGAAAACGGTGGGATGGCACCTGAAAGTCAGGATGCAGATGGAACTCAACTGTCAGGTACTGTGCACATTTTGCATCAGGTTTTAAACTCGGGATATTCAGGCTCACATTTTAAGAGATACTTCACTCAAAAATGTAAACTTGCTCACTATTACTCACCCTATATGTAATACAATGTATTACTTACCTATATCATTGTAGGTTGACCTTGTTGTTT
Associated Phenotype:
Not determined