ZMP
arhgef1
Ensembl ID:
ZFIN ID:
Description:
rho guanine nucleotide exchange factor (GEF) 1 [Source:RefSeq peptide;Acc:NP_001075100]
Human Orthologue:
ARHGEF2
Human Description:
Rho/Rac guanine nucleotide exchange factor (GEF) 2 [Source:HGNC Symbol;Acc:682]
Mouse Orthologue:
Arhgef2
Mouse Description:
rho/rac guanine nucleotide exchange factor (GEF) 2 Gene [Source:MGI Symbol;Acc:MGI:103264]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23467 | Essential Splice Site | Available for shipment | Available now |
sa16009 | Nonsense | Available for shipment | Available now |
sa23466 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23467
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059102 | Essential Splice Site | 98 | 935 | 3 | 22 |
ENSDART00000114710 | Essential Splice Site | 312 | 1149 | 8 | 27 |
Genomic Location (Zv9):
Chromosome 19 (position 11569518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 11161270 |
GRCz11 | 19 | 11079268 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACCGCTGCAGGGACACACTACCAAACTGTGTGAAAATGAAACAAAAG[G/A]TGGGATATTAGTGCACGCATGGGTCACGTGGAATACATGAACCACTGACA
Long Flanking Sequence:
TAGAATGCTCTAAAGAAGATTACTAATAAGAATTTTAACGCAGACATGGAGAGAGTTCAAGAGGGAGAGACAGATAGGAAAAAAACTGGTATGGTACATTTACTTCATTATTTAAAGTAATATACAATGTACAAATCTCAAAGGGAAAGTAGGAGATCTTCATATGTTTTTTTTTTTTTCATAGGAAATCAATTGTACGCTAAGCTAGTAGTTGTGATTGGCGACGTAGACTGGTTAGTTCAGACTGATAGATCCTCTTAGACCAAAACAAACCACTCATACAAGTCTATTATAGTCAAGAATGGCTTTAGTGGCATTTAATGACCAAATAGAACAAGCTGAGGTGTGTAAATGTGACCGTATGTAGATTATGCTATGTGACGACAATGTAAAATAACAAGATTGGTTCTGGTGTGTTCTTTTGTTTTTCAGCCTGTAACGTCACCATACACAACCGCTGCAGGGACACACTACCAAACTGTGTGAAAATGAAACAAAAG[G/A]TGGGATATTAGTGCACGCATGGGTCACGTGGAATACATGAACCACTGACATGCAGAAACATTTTACTTCATGGAATGATGATGGTATAGATTTAGATGTAATCTAAATATGTCATCTGTGTGTGTCACAACAGCAACAAAAAATGGCACTGATGAGGAACAATTCAGCCTATCAGAACGTAACACTGAGGAATAAAGGTGAGGATGGAGTAGAAATAAGTCAACTGTCTATTTATTTATGTCAATCCAATCAAAAGTGAGCAGTTGCGTGGGACAGATCTTATTGAGAAGACCATGTGACTTGTTCGTTGAGTGAAATAGATTTACTCTAGGTGTAAATTTAGTCCAAGTGTAAAAATGACATTGATCTCTCTTTTTCTACCTTTCTAAAGCCCATTTAAAGGAAAGGCCGAGTTCTGCCATCTACCCTTCAGACAGCCTTCGCCAGTCGCTACTCGGGTCCCGTCGTGGACGCTCTTCTCTTTTACTTTCAAAGAGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16009
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059102 | Nonsense | 557 | 935 | 13 | 22 |
ENSDART00000114710 | Nonsense | 771 | 1149 | 18 | 27 |
Genomic Location (Zv9):
Chromosome 19 (position 11545578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 11137330 |
GRCz11 | 19 | 11055328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCGAGGSTTGTTTCTGATCAGCAGTGAGTCCAGCCCACCTGAGATGTA[C/A]GAGCTCTATGCRGCRAGCAAAGATGACAGAAACACCTGGCTTCGCCTYAT
Long Flanking Sequence:
TCACATCTACATGTCTAACTATTCTCTCTTTGAAAGTGTCACCCTGCCTTAGACCCCTTTTGATTTCAAAGCCCTGCAATGGTATCTTAAAAAATTTGAGTTCTGAACAAGTACCAACGGTCTACACTATCGAAATCTTTTTAGGCTCCATAAATTTGGCATATTTTAAGCTCCATAAACCTCTGGATAAGGAAGAGTCGATCAGAATAGCGTAAGAATAGATACCATTCTTCTTACAGTTTACTTTCCGGACATGTCTTCAAATTTGTTTGCCCTTAGCATTGCATCCTAACAATTCCTAAAGGGGTTTGAATTTACTGATTGCATTTGGATGTTATCAGTATGCTAATGCACACAGATGGCAAATTTGTTCTGTTTGTGTCGTGTGTGTAGGACAAGTCTGCTGTAGTGTCACTGCAGAGTCTATTGGTTCGAGATATAGCCAATCAGGAGCGAGGGTTGTTTCTGATCAGCAGTGAGTCCAGCCCACCTGAGATGTA[C/A]GAGCTCTATGCGGCAAGCAAAGATGACAGAAACACCTGGCTTCGCCTTATACAGCAGACCATCGGCAGGTACAAACACATCTTTGTCTTTGCAGTGGAATTTGAAATTGCATTTCTTTTGAATTTGGATAATAAGCGGAAATATTTTGAAGGGATTTGTCAATCTGCTGGAAGCATTACTTGCCAAGTAGCCTGTGTTTGTTTTACAACTCAGCTAAAACTAATCTGACCCTAATACCATAGACATAGTTTAGACATAGTTTAGACAAAGTTTAGTTCCAACCCCAATCAGACACACCTGAGCTAGCTAATCAAGCTCATACTAGGCTTTCTAGAAACATTTATGCTGGTATGTTGAGCCAAGTTGGAGCTAAAATCTGCAGGACACCGGCCTTCCAGGACTGAGTTTGGACACCCCTGGCTCAGACCATGCTGGCAAAAAGTTATAGATCTTTCCAGTTGCTCTGTAGCTTGTTTGCCTTTCTTGTTTATGATGTGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23466
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059102 | Essential Splice Site | 580 | 935 | 13 | 22 |
ENSDART00000114710 | Essential Splice Site | 794 | 1149 | 18 | 27 |
Genomic Location (Zv9):
Chromosome 19 (position 11545509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 11137261 |
GRCz11 | 19 | 11055259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGATGACAGAAACACCTGGCTTCGCCTTATACAGCAGACCATCGGCAG[G/A]TACAAACACATCTTTGTCTTTGCAGTGGAATTTGAAATTGCATTTCTTTT
Long Flanking Sequence:
AGCCCTGCAATGGTATCTTAAAAAATTTGAGTTCTGAACAAGTACCAACGGTCTACACTATCGAAATCTTTTTAGGCTCCATAAATTTGGCATATTTTAAGCTCCATAAACCTCTGGATAAGGAAGAGTCGATCAGAATAGCGTAAGAATAGATACCATTCTTCTTACAGTTTACTTTCCGGACATGTCTTCAAATTTGTTTGCCCTTAGCATTGCATCCTAACAATTCCTAAAGGGGTTTGAATTTACTGATTGCATTTGGATGTTATCAGTATGCTAATGCACACAGATGGCAAATTTGTTCTGTTTGTGTCGTGTGTGTAGGACAAGTCTGCTGTAGTGTCACTGCAGAGTCTATTGGTTCGAGATATAGCCAATCAGGAGCGAGGGTTGTTTCTGATCAGCAGTGAGTCCAGCCCACCTGAGATGTACGAGCTCTATGCGGCAAGCAAAGATGACAGAAACACCTGGCTTCGCCTTATACAGCAGACCATCGGCAG[G/A]TACAAACACATCTTTGTCTTTGCAGTGGAATTTGAAATTGCATTTCTTTTGAATTTGGATAATAAGCGGAAATATTTTGAAGGGATTTGTCAATCTGCTGGAAGCATTACTTGCCAAGTAGCCTGTGTTTGTTTTACAACTCAGCTAAAACTAATCTGACCCTAATACCATAGACATAGTTTAGACATAGTTTAGACAAAGTTTAGTTCCAACCCCAATCAGACACACCTGAGCTAGCTAATCAAGCTCATACTAGGCTTTCTAGAAACATTTATGCTGGTATGTTGAGCCAAGTTGGAGCTAAAATCTGCAGGACACCGGCCTTCCAGGACTGAGTTTGGACACCCCTGGCTCAGACCATGCTGGCAAAAAGTTATAGATCTTTCCAGTTGCTCTGTAGCTTGTTTGCCTTTCTTGTTTATGATGTGACCTCTGGGCTGCTTGGCCCTGATAATTGCTGCTTGCAGCTATATTTATCAGTATTATTAATACATTACAAT
Associated Phenotype:
Not determined