ZMP
ARHGEF40
Ensembl ID:
Description:
Rho guanine nucleotide exchange factor (GEF) 40 [Source:HGNC Symbol;Acc:25516]
Human Orthologue:
ARHGEF40
Human Description:
Rho guanine nucleotide exchange factor (GEF) 40 [Source:HGNC Symbol;Acc:25516]
Mouse Orthologue:
E130112L23Rik
Mouse Description:
RIKEN cDNA E130112L23 gene Gene [Source:MGI Symbol;Acc:MGI:2685515]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21160 | Nonsense | Available for shipment | Available now |
sa34259 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21160
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 |
---|---|---|---|---|---|
ENSDART00000110330 | Nonsense | 1377 | 1752 | 19 | 26 |
Genomic Location (Zv9):
Chromosome 7 (position 76556378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73332273 |
GRCz11 | 7 | 73554386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCTCATCATCTCTCCATATCTGTGTCCGCCGCAGTAAGCTGTATCTG[C/T]AGTGGTGTCGGCTGGTCAGCACAGAGAGGCAGTACGTGGCTGTTCTTAAA
Long Flanking Sequence:
TGTCCGCACTCCTTGCTTATGGTGACTTGCGCTCTGCGCCTCTGCAGCTCATACTGAATTGAACAGACGCACGTCACTTCATAGCTATAGCGGCCGTTTTTCGACTGAACTAAATTTATTTTTATGTCTTGGTCACACTATTTGGAGGGCCAGAACAAATTGCCTCGGGGGCCGGGTTCGACCCGTGGGCCGCCAATTGAATAGCCCTGATATATGTCATCTTGTGCAGCATTTAATAATCATTCTTTAATATTAACTGATGCATTATGAAAATCCAAAGTTGCATGAGTTAATATGAACTAACGTTATTTAACCTAAATAATATTAGCTAACTTTAATAAAGATGAATAAACACAGAAATAAATAGTAAATACACTAACATTAACTAATAGATCATTATTTTAAGGGGTTACCACAAACTCTTCTTGCGCATGTTTTGAGTTCAGGAGCACATCTCATCATCTCTCCATATCTGTGTCCGCCGCAGTAAGCTGTATCTG[C/T]AGTGGTGTCGGCTGGTCAGCACAGAGAGGCAGTACGTGGCTGTTCTTAAAGGTGTGGAGGAAAACTACCTGCCCCTGCTGGAGTCTCCTGACGTCCCGTCCGCTCTGAGAGGAAAAGCAGAGTCGCTATTCTGTAACTGGAAAAGCCTTTCTGCTTTCCACTCGCAGTTACTCCTGCCGGCCATGGAGGGCGCTCTCTCGCAGACACTGCAGCAGACCGACTGCTTCACCAAATATGTGAGTAGCACCTCATGATCTTAACTCTTTAGATTGACTCCCCTTTGCTTATGTTGGGGGCTGTTTTTGACCCATTGGCTTTCATTATAAGCAACTGCAAATGGCTGGCTCATTGTTCCTCTTCCCGACAGGGAAAACCAGCAACAATCAAGAATGCATGAGTACATGCTATCATGTCTTTGCAGTCAATAAAGTCATTATAATGGAAGTCAATGGGGTGAAAACAGCACCAACATAAGCAAAGGGGCGTCAATTTATCAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34259
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 |
---|---|---|---|---|---|
ENSDART00000110330 | Nonsense | 1490 | 1752 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 7 (position 76561624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 73337519 |
GRCz11 | 7 | 73559632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTTATATTGAGTGTTTCTCCCTCTGTGTGTGCAGATGAAGCTGTGTT[C/A]GTCTCTGGTTCCTGCTCCTCCATTCCCGCAGTGTCTTTCGGCTCCTCTTC
Long Flanking Sequence:
TTCCCTCAGCTTCGAATGTTATCACTGGATTGAATGGCCATTATCAGTGGTCATCAGCTAGTATTAGATGTGGGCCAGTAGGGGTAGGCTCAGAAGGCTGTTATCATCCATCCACATGGTTATTCAGCTATACTAAGAGAGAAGACTCCTAATCAAGATCTGCTTTTGGATTACTGTGAGGGTTGGGTTTAGGGTCGGGGGTAGACATTGATAAAATACTATTAATGGGAAATTTAAGAAATTATATGAATAATTCCTGTTAGCTTCTGCCCACAGGCTTATGTGATATCTGGTTAACCATTTGGATGGATGATAACAGCCTTCTGAGCCTACTAGCAGCCCATATCTATCAGCTGGTAACCACTGATAATGCTTATTCAGTCAATCGAGCGATAACATTCAAAGCGGGTGATTTTTCAGGGGTCACCACAGTGCAATGAACCGCCTAGCAGTGTTATATTGAGTGTTTCTCCCTCTGTGTGTGCAGATGAAGCTGTGTT[C/A]GTCTCTGGTTCCTGCTCCTCCATTCCCGCAGTGTCTTTCGGCTCCTCTTCAGCGACTCCAGCAGTACACACAGGCTCTGGAGGAACTGGCCGGACTTAACCCCGGCTCTGACTCCGCCCTCTCCATCATCAAACACGCCCATCGGCACGGAGAAGACCTGAGGGCCAGTGAGCTCATCAGCGGCTGTCCGGTAACAACAGCATATATCATTTAACTGATGATGTATTTATAAATTATTCATTATTTTTTAATCATTCAATTTAAATTATTTATTTATCATATATTATCTATACATATTACAATGATGTATTTTTTATTTTAAGTTAAATTTAGTTATTAATTTAATATAATTATTTAATTAATTAATATATTTATTTAATTAAAAAATTTATTTCTTGCACTGAAACCGCACCTGCTGAAATCCACAATTTTTTCCCCCATTAATAAATATTTTTATTTAAAGGGACAGTACACATAAAAATGAGACTTTCTTTCTTCTG
Associated Phenotype:
Not determined