ZMP
LOC100333630
Ensembl ID:
Human Orthologue:
ARHGEF17
Human Description:
Rho guanine nucleotide exchange factor (GEF) 17 [Source:HGNC Symbol;Acc:21726]
Mouse Orthologue:
Arhgef17
Mouse Description:
Rho guanine nucleotide exchange factor (GEF) 17 Gene [Source:MGI Symbol;Acc:MGI:2673002]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13368 | Nonsense | Available for shipment | Available now |
sa12689 | Nonsense | Available for shipment | Available now |
sa28957 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43025 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13368
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121713 | Nonsense | 13 | 1327 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 2726463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 6692855 |
GRCz11 | 18 | 2978449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGGCATCGCGATGGCTGAAAGGGAGACTGAGAGAAAAGCGCCTGTATA[T/G]AGAAGCGTCTCTTTTAAAAAGTTGGAGAGCTGGAGCGCCAAGAAGCGCAG
Long Flanking Sequence:
AGTCACGGAAACCCTTAATTGTGACCAAAAATAAGACCGAGCGCACTTATTATTCAAGCTGGAAATAAAGCATGCTTCAGAAGGAAGACAGTCGGAGGAGGAAATGGGATTTACTTTGGAAAACGCAAACCATTCAATCGTTTCTCTAGTGTGTTTTGGGCTGAAACACTTGGGAGTTTTCTCAAACTTTGAGCCCTTTCTGAATGCATGGATGAGGGAGGCAAACATGCGCAAAGGTCTGGATGTATAACTGTTTTACTAAACAATCATCTGTTGTTCGTGACCAATTTTTTTGTATTCCTCTGCGGGAAACACTGCCAAGCAACTTTTGTGGTTAAATGGGGGCATTGTGAGTTGTTTTCAGGGGGGGTAAAGGCGAGCACGGAAAAAGGAGGAGAAGAAAAGTTTGGACTATTTATCAATGAACTAAGAGAATAGACAAGTGGGAGGACAGGCATCGCGATGGCTGAAAGGGAGACTGAGAGAAAAGCGCCTGTATA[T/G]AGAAGCGTCTCTTTTAAAAAGTTGGAGAGCTGGAGCGCCAAGAAGCGCAGATCATTTGGAGAGGATTTGGATAGGTGCGGTGCCCTTCCCCCAGAGCACAGCGCGCAGCCATCACAGGCGACGCACGCTGTTACTGTATCCAGAAAAGTTTCCAAAATCTCAGCGGCCAGCCTCTCGACCGCAGACCTCAAGAAAGCCTCTCCTGGAATATCTCCATCGGTTCGGCAGCTCTCCGAGAAGTTTAACTCGAGCACAACCGGCACGCAGAGCTCATTAATCAACACTGGAGGCGTTAAAAACACAAAAAGCGCCGAAGATTTGTCTTTGAGCGAGAGCGGCTGCCTATCCGAGGAGTTTTCGGAGTCTGCGACCGAGAAACTCAAGGAGACTGTTAGATATAGCTCGGCTCAAGAGTCGGTGTCAGGGTCGGATTCGGACAGAGGAGATAAACACAGGCTCTGGAAGACTGTGGGAGGCACGAGCACAGGTAAGATACTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12689
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 |
---|---|---|---|---|---|
ENSDART00000121713 | Nonsense | 745 | 1327 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 2729140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 6695532 |
GRCz11 | 18 | 2981126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTCTTATGGATACGATGAGCCAATGCCRACACCTTTACAAGACCGTTA[T/A]TTGCAGGAAGCCAGACAGGTAATAAGAGACATTTGTCAAATGGGTGAAAG
Long Flanking Sequence:
GCAGACTGTAAAACGGGTAGTTCAGAAAACCGAGTTTTCAGCAACTCTTTAAATAATGAAAAAGACAGAAATAGGATTTCCCTGTCCAACCCTGACATTGCTTCGGAAACACTGTCACTTCTTAGCTACCTTAAGACTGATCTTTCAGAGTTAAGAATGAGGAAAAAGGGACAAGACGATGAGGATAGTCTGAACTCTGATCAAGGCACATCTGTGTACAGAATGGGCTCCAGGACAAATCGACTTCACCCTGGGCGTCCTTCCTTGAAGGATCTCACTGCCACTTTAAGAAGGGCAAATTCTTTTACTTACTCTGAGAAGCCAATAGTACAGCGATATTACGGTAGTGGACCAGGCTTAAGGAGTTCCTCTGAACAAAGACTCGACTCTGAAGGCAGTGGTGAGCAGGTGATAATTGCTGACAGAGAAGTGGAAAGCGATGACTGCAGAAGTTCTTATGGATACGATGAGCCAATGCCAACACCTTTACAAGACCGTTA[T/A]TTGCAGGAAGCCAGACAGGTAATAAGAGACATTTGTCAAATGGGTGAAAGTAAGGATGATGATTATGTGGAGGACAATTTTAAAACAAAACCCAGTGACGCTAAAATAAATAATGAAGAAGGCGATGAGACGAAGCAGGAGGTAAGGAGACTTGAATACCCTGTTTTTACTGGGTGCAAGGAAGAGGAGGCTGATGGAAAAAGTGGAAAATGTTTACAGAAGGGAAATTCAGAGGAGAACATGTTCTGTGATAAGTCATTGGATGAACTCTCTGGTCATGAATCTAGTCTGACAGATGAAGGAATTGTCACAGAGCCAGAGGTTGGCTCATATGGGGGGCTGTCCTGCAGTAAAGACGTGCTGGGTCAGACCCTCGCCGTTTGGAATCAGTCAGGGTTGTACGATGAGCAATTGCCTGATACAACACCAGAGGAATCTCTTTCATCTCAGATTCCGTCTGTTAGGACGGAGTGTGAGGGAGTAGCCATAGGAGGAGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28957
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 |
---|---|---|---|---|---|
ENSDART00000121713 | Nonsense | 1116 | 1327 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 2730251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 6696643 |
GRCz11 | 18 | 2982237 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCATCTTATCAGAGCAAAGAGATGAGTTGTGGGCGCTAAATAGTGAA[C/T]AACGACAGCATTACTGTTCACCCAGAAGGTCTCGTTCACAGTCTGAGCAT
Long Flanking Sequence:
GCAATGGCAGTAATGGGGAGTCGAACGGTGAATCTGCGTACCGCTCCTTGAGTGATCCCATGCCTCATAGACACCGTTCAGTCACAGAGGATGGAAAGAGCTTCTCGATGGACAGCAACCTGCTTGGCTCGCTTTCTCTAAACTCCAAGGTGGGTGGTATGGAGTCTTCTGCAGCAGATCTTTCTGAATACACAGGCAGCGCTGCCAGTGATCTTTCCGTGTGTAGCGACAGTCTGAAAGACTACAGTACTGTGATTCAGAGCATTGTATGCGAGCCTGGTGCAATGGACAATCTTATTGACGAAAAAGCGAATGGCAAGGCTGTGAAGAAGAAGAGCTTTAGTGACCCTAGCCGACGTGGAGAAGAAGTGGACACAGTCCTGGAATTTCAAAAGCATCCAAACGAGCCAATTAATGAGCAAGAACAATCCATACCACCTTCTAGCAGCGAGCCCATCTTATCAGAGCAAAGAGATGAGTTGTGGGCGCTAAATAGTGAA[C/T]AACGACAGCATTACTGTTCACCCAGAAGGTCTCGTTCACAGTCTGAGCATGTTTTGGCATCCCACCTGGGTCACAATGGAGAAACAAAAGCAGCAGGTGAGCCCTCCTTTCCTTTTGACCCTAAGCTAGCTCATGTGTTGTCTCCTCGCATCAGTCGCAGAAGCCCCAAGAAACGCACAAATCGCTTTACACATCAGGTGTCTTGTGATGATGCGGATCACTTAGATGAACAAAGTGAAGAGCAATCCAATGCATCCTCCCTCCCCCAGCTTCCATCCTCAAAACCCAAACCCAAGCATGTACGTCACGCTAGTGAACCTGCCACATTTGTGCCCATCATTCCTTCACATGGCTCACAGGACCTCCCCAGGTCATCCCATGTTACAGAGTCCTCTCCAACCAACAAAATAGCTCTAGGGGAGGACACTCCATCATTGGAGGATGTCACTGAGCAATACATCTTGGCTGTAAATTCCCCAGAGACCCCGACAGAGACCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43025
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121713 | Nonsense | 1169 | 1327 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 18 (position 2730410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 6696802 |
GRCz11 | 18 | 2982396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTTTTGACCCTAAGCTAGCTCATGTGTTGTCTCCTCGCATCAGTCGC[A/T]GAAGCCCCAAGAAACGCACAAATCGCTTTACACATCAGGTGTCTTGTGAT
Long Flanking Sequence:
TGGAGTCTTCTGCAGCAGATCTTTCTGAATACACAGGCAGCGCTGCCAGTGATCTTTCCGTGTGTAGCGACAGTCTGAAAGACTACAGTACTGTGATTCAGAGCATTGTATGCGAGCCTGGTGCAATGGACAATCTTATTGACGAAAAAGCGAATGGCAAGGCTGTGAAGAAGAAGAGCTTTAGTGACCCTAGCCGACGTGGAGAAGAAGTGGACACAGTCCTGGAATTTCAAAAGCATCCAAACGAGCCAATTAATGAGCAAGAACAATCCATACCACCTTCTAGCAGCGAGCCCATCTTATCAGAGCAAAGAGATGAGTTGTGGGCGCTAAATAGTGAACAACGACAGCATTACTGTTCACCCAGAAGGTCTCGTTCACAGTCTGAGCATGTTTTGGCATCCCACCTGGGTCACAATGGAGAAACAAAAGCAGCAGGTGAGCCCTCCTTTCCTTTTGACCCTAAGCTAGCTCATGTGTTGTCTCCTCGCATCAGTCGC[A/T]GAAGCCCCAAGAAACGCACAAATCGCTTTACACATCAGGTGTCTTGTGATGATGCGGATCACTTAGATGAACAAAGTGAAGAGCAATCCAATGCATCCTCCCTCCCCCAGCTTCCATCCTCAAAACCCAAACCCAAGCATGTACGTCACGCTAGTGAACCTGCCACATTTGTGCCCATCATTCCTTCACATGGCTCACAGGACCTCCCCAGGTCATCCCATGTTACAGAGTCCTCTCCAACCAACAAAATAGCTCTAGGGGAGGACACTCCATCATTGGAGGATGTCACTGAGCAATACATCTTGGCTGTAAATTCCCCAGAGACCCCGACAGAGACCCCTGCGGCCACTAGTGGGGTGATTGTGGAGGGAACTACTTCGACACCTTCAGCTCCAGCCACCGCTTCTGAGACGAGACTAGAGAGGAAGTCCAGCGAGGAACTTTCCACTGCCCCTCTGAAGGCCAAACCAAGAGTGGTGAGTGACGTTCTGTTCGCTAAT
Associated Phenotype:
Not determined