ZMP
ENSDARG00000091607
Ensembl ID:
Human Orthologue:
RP11-428C6.1
Human Description:
Rho-guanine nucleotide exchange factor [Source:UniProtKB/Swiss-Prot;Acc:Q8N1W1]
Mouse Orthologue:
Rgnef
Mouse Description:
Rho-guanine nucleotide exchange factor Gene [Source:MGI Symbol;Acc:MGI:1346016]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15457 | Nonsense | Available for shipment | Available now |
sa12818 | Nonsense | Available for shipment | Available now |
sa6388 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15457
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 |
---|---|---|---|---|---|
ENSDART00000128436 | Nonsense | 142 | 315 | 4 | 8 |
ENSDART00000128436 | Nonsense | 142 | 315 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 34306583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 35152359 |
GRCz11 | 15 | 35010328 |
KASP Assay ID:
2260-8821.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTGAASCCAACTMTCTTTYATTCCCAGTGGTGAAGCTGGCTGTCACCT[T/A]GCTGTCTTGGCTTTTCCCGTGCATATTGTCACCAAGTACCCCTGACAGCT
Long Flanking Sequence:
GTGGCGACCCCTGATTAATAAAGGCACTAAGCTGAAAGGAAAATGAATGAATGAATTGAACTCTTCATATATCTGTGTGTATTTTAGTCTTCCAGATGACCAAACCAAGAAGAATGAGGGGGAAATTAAAGTCAAGAAGATACAGAAACTGCAAGGTATACATCCATACATCACTTTGTCCGTGGCTTTATCATTCCTTGTGTCTGATTTCTTGGTTGTGTCTGCATTTAGAGGCGCTGTTTTCACTGGACCTGCAGGTGTGCTCAGTCATCGAGGAGAAGTTAAGGATCTGCAGAGGCACTGGTGGTAGATGGAATCTGGCTAGCTGTCGCCTTCTCGTTCAACCCCATCCTGAAAACACCCCTCAGTGTGTCACATTACTGTCTGACGCACAGGAAGAGGGTAAAAACAATCTCCTTTCACCTCTGCAGACACATATTAATGCTGTTTGTCTGAAGCCAACTCTCTTTCATTCCCAGTGGTGAAGCTGGCTGTCACCT[T/A]GCTGTCTTGGCTTTTCCCGTGCATATTGTCACCAAGTACCCCTGACAGCTTTAGAGAGGAAAGAGGAAACTGTGAGTAATACCTTTACACCCAGATTCATATATGAGCAATATCACACTCGTAGCAGTGTGATATGGCTGAATATTGGCACTGTTGGGAGGTGTTTGTTGGCTAGAGACTGCAGGCAGAGTGCCTTAGTGCCCCCCACCAGTGCCAATATAAGTCATATCGCACTGCTACGAGTGTGATAGTGCATTTACACAACAGTTCAACAGCATAATTGTGTGTATGAAAAAGAAAATCAAACGCGGAGAGTCTCAGAAACCCTTTTGTATGAGGAACTACTTTCTTCTGCCATTCATTCACATCTGAAGTTGACGTCAGAATAGCAGAAACCTACGTGTCTATGTGATGACAAATAAGATGATTTTGCTCAAATTTTAAGAGTATAAGGCTGAATGGCATTAATTGCCATCAATCTACAGAGATCTCCCAGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12818
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 |
---|---|---|---|---|---|
ENSDART00000128436 | Nonsense | 142 | 315 | 4 | 8 |
ENSDART00000128436 | Nonsense | 142 | 315 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 34306583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 35152359 |
GRCz11 | 15 | 35010328 |
KASP Assay ID:
2260-8821.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTGAASCYAACTMTCTTTYATTCCCAGTGGTGAAGCTGGCTGTCACCT[T/A]GCTGTCTTGGCTTTTCCCGTGCATATTGTCACCAAGTACCCCTGACAGCT
Long Flanking Sequence:
GTGGCGACCCCTGATTAATAAAGGCACTAAGCTGAAAGGAAAATGAATGAATGAATTGAACTCTTCATATATCTGTGTGTATTTTAGTCTTCCAGATGACCAAACCAAGAAGAATGAGGGGGAAATTAAAGTCAAGAAGATACAGAAACTGCAAGGTATACATCCATACATCACTTTGTCCGTGGCTTTATCATTCCTTGTGTCTGATTTCTTGGTTGTGTCTGCATTTAGAGGCGCTGTTTTCACTGGACCTGCAGGTGTGCTCAGTCATCGAGGAGAAGTTAAGGATCTGCAGAGGCACTGGTGGTAGATGGAATCTGGCTAGCTGTCGCCTTCTCGTTCAACCCCATCCTGAAAACACCCCTCAGTGTGTCACATTACTGTCTGACGCACAGGAAGAGGGTAAAAACAATCTCCTTTCACCTCTGCAGACACATATTAATGCTGTTTGTCTGAAGCCAACTCTCTTTCATTCCCAGTGGTGAAGCTGGCTGTCACCT[T/A]GCTGTCTTGGCTTTTCCCGTGCATATTGTCACCAAGTACCCCTGACAGCTTTAGAGAGGAAAGAGGAAACTGTGAGTAATACCTTTACACCCAGATTCATATATGAGCAATATCACACTCGTAGCAGTGTGATATGGCTGAATATTGGCACTGTTGGGAGGTGTTTGTTGGCTAGAGACTGCAGGCAGAGTGCCTTAGTGCCCCCCACCAGTGCCAATATAAGTCATATCGCACTGCTACGAGTGTGATAGTGCATTTACACAACAGTTCAACAGCATAATTGTGTGTATGAAAAAGAAAATCAAACGCGGAGAGTCTCAGAAACCCTTTTGTATGAGGAACTACTTTCTTCTGCCATTCATTCACATCTGAAGTTGACGTCAGAATAGCAGAAACCTACGTGTCTATGTGATGACAAATAAGATGATTTTGCTCAAATTTTAAGAGTATAAGGCTGAATGGCATTAATTGCCATCAATCTACAGAGATCTCCCAGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6388
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 |
---|---|---|---|---|---|
ENSDART00000128436 | Essential Splice Site | 166 | 315 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 34306510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 35152286 |
GRCz11 | 15 | 35010255 |
KASP Assay ID:
554-5334.1 (used for ordering genotyping assays)
KASP Sequence:
ATATTGTCACCAAGTACCCCTGACAGCTTTAGAGAGGAAAGAGGAAACTG[T/C]GAGTAATACCTTTACACCMAGAWTCATATATGAGCAATATCACACTCGTA
Long Flanking Sequence:
TGTGTGTATTTTAGTCTTCCAGATGACCAAACCAAGAAGAATGAGGGGGAAATTAAAGTCAAGAAGATACAGAAACTGCAAGGTATACATCCATACATCACTTTGTCCGTGGCTTTATCATTCCTTGTGTCTGATTTCTTGGTTGTGTCTGCATTTAGAGGCGCTGTTTTCACTGGACCTGCAGGTGTGCTCAGTCATCGAGGAGAAGTTAAGGATCTGCAGAGGCACTGGTGGTAGATGGAATCTGGCTAGCTGTCGCCTTCTCGTTCAACCCCATCCTGAAAACACCCCTCAGTGTGTCACATTACTGTCTGACGCACAGGAAGAGGGTAAAAACAATCTCCTTTCACCTCTGCAGACACATATTAATGCTGTTTGTCTGAAGCCAACTCTCTTTCATTCCCAGTGGTGAAGCTGGCTGTCACCTTGCTGTCTTGGCTTTTCCCGTGCATATTGTCACCAAGTACCCCTGACAGCTTTAGAGAGGAAAGAGGAAACTG[T/C]GAGTAATACCTTTACACCCAGATTCATATATGAGCAATATCACACTCGTAGCAGTGTGATATGGCTGAATATTGGCACTGTTGGGAGGTGTTTGTTGGCTAGAGACTGCAGGCAGAGTGCCTTAGTGCCCCCCACCAGTGCCAATATAAGTCATATCGCACTGCTACGAGTGTGATAGTGCATTTACACAACAGTTCAACAGCATAATTGTGTGTATGAAAAAGAAAATCAAACGCGGAGAGTCTCAGAAACCCTTTTGTATGAGGAACTACTTTCTTCTGCCATTCATTCACATCTGAAGTTGACGTCAGAATAGCAGAAACCTACGTGTCTATGTGATGACAAATAAGATGATTTTGCTCAAATTTTAAGAGTATAAGGCTGAATGGCATTAATTGCCATCAATCTACAGAGATCTCCCAGTATTTCCCAGGAAAAATATAACCCTGAAAAAGCAAAGCAATCACTATTAGATATTTTTTGGCATAAATACAGCAATA
Associated Phenotype:
Not determined