ZMP
si:dkey-38o13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to rho/rac guanine nucleotide exchange factor (GEF) 18 (Arhgef18) [Source:UniP
Human Orthologue:
ARHGEF18
Human Description:
Rho/Rac guanine nucleotide exchange factor (GEF) 18 [Source:HGNC Symbol;Acc:17090]
Mouse Orthologue:
Arhgef18
Mouse Description:
rho/rac guanine nucleotide exchange factor (GEF) 18 Gene [Source:MGI Symbol;Acc:MGI:2142567]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24090 | Nonsense | Available for shipment | Available now |
sa24089 | Nonsense | Available for shipment | Available now |
sa10836 | Essential Splice Site | Available for shipment | Available now |
sa13725 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24090
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 |
---|---|---|---|---|---|
ENSDART00000010991 | Nonsense | 534 | 1150 | 13 | 23 |
ENSDART00000141572 | None | None | 280 | None | 4 |
ENSDART00000145229 | Nonsense | 458 | 692 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 10957347)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10817515 |
GRCz11 | 22 | 10847197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGTGTTCGTTTTTTCCACAGGACAACAAGCCGTCGGTCATTTCTTTG[C/T]AGAAGTTGATTGTGCGTGAGGTGGCGCACGAAGAGCGGGCAATGTTCCTC
Long Flanking Sequence:
AAAAATTAATAAAAATATTCAAAAAGGTGTGTACTCAGTTTTGTTACGCACTGTTGATTTAATAATCACTCAAGTAATTAATAAGTCCACTCAAATAACCGCCATCAGGACATCATTCAATATACTTGTTCCTGCTGCTTGCAGTAGCGGTACTGTGTTGTCATGGCAATTGAATTTTTTATTATTAGCTTGTATGTTTTTTTTTTTTGTAAATTTTTAATATCTTACAAATCACATTATATAATCAAATAAAATAATAAATAATCATTACAAAACCAAGTTTTCAGCCAAGTGTGTCCACATTGTTGTTATTATTATTATTATTATTATATATTTATTATTATTATTATTATTATTATATATTTATTATTATTATTATTATTATTGGTTTCAGCCCGGAATTTTCATTTCAGTGCATTCCTTTAAGAAATAGATCCTCTTAATGCATCCATCTGTGTTCGTTTTTTCCACAGGACAACAAGCCGTCGGTCATTTCTTTG[C/T]AGAAGTTGATTGTGCGTGAGGTGGCGCACGAAGAGCGGGCAATGTTCCTCATCTGCGCTTCCTCAAATGAACCCGAGATGTACGAAATCCACACCGCCTCAAAAGAAGACCGCAACACGTGGATCACCCATATCCGTCAGGCGGTGGAGAGGTCTGTGTGCGTCCGGAACAGTAATGATGATATCTGCTGTCTGCAGATCTGTAATGTTCCTTTGTTTCTTTCTGCCAGCTGTCCGCATACTGAAGAGAGATTGTTCAGTGAGGAAGAGGAGGCCAGAGTTGCCCGCGTCCGGGAGTACCAAGGTTAATCACCACATCTAGCTTGTCTGTTTATGTTTTGCTTCTCATTTTTGGTTTGTATGACGGTTGTTTTAGGTGCTTTAAAGAAAACACAAGAGGGCGCAATTGGTTTTCATAAATAATGTTTGTAACTTCAGTTATCAACTTATATATTTATATATATATATTTTTTTCTTTCATTTAACATTTTTTTCAAGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24089
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010991 | Nonsense | 540 | 1150 | 13 | 23 |
ENSDART00000141572 | None | None | 280 | None | 4 |
ENSDART00000145229 | Nonsense | 464 | 692 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 10957329)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10817497 |
GRCz11 | 22 | 10847179 |
KASP Assay ID:
2261-6482.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGGACAACAAGCCGTCGGTCATTTCTTTGCAGAAGTTGATTGTGCGT[G/T]AGGTGGCGCACGAAGAGCGGGCAATGTTCCTCATCTGCGCTTCCTCAAAT
Long Flanking Sequence:
TCAAAAAGGTGTGTACTCAGTTTTGTTACGCACTGTTGATTTAATAATCACTCAAGTAATTAATAAGTCCACTCAAATAACCGCCATCAGGACATCATTCAATATACTTGTTCCTGCTGCTTGCAGTAGCGGTACTGTGTTGTCATGGCAATTGAATTTTTTATTATTAGCTTGTATGTTTTTTTTTTTTGTAAATTTTTAATATCTTACAAATCACATTATATAATCAAATAAAATAATAAATAATCATTACAAAACCAAGTTTTCAGCCAAGTGTGTCCACATTGTTGTTATTATTATTATTATTATTATATATTTATTATTATTATTATTATTATTATATATTTATTATTATTATTATTATTATTGGTTTCAGCCCGGAATTTTCATTTCAGTGCATTCCTTTAAGAAATAGATCCTCTTAATGCATCCATCTGTGTTCGTTTTTTCCACAGGACAACAAGCCGTCGGTCATTTCTTTGCAGAAGTTGATTGTGCGT[G/T]AGGTGGCGCACGAAGAGCGGGCAATGTTCCTCATCTGCGCTTCCTCAAATGAACCCGAGATGTACGAAATCCACACCGCCTCAAAAGAAGACCGCAACACGTGGATCACCCATATCCGTCAGGCGGTGGAGAGGTCTGTGTGCGTCCGGAACAGTAATGATGATATCTGCTGTCTGCAGATCTGTAATGTTCCTTTGTTTCTTTCTGCCAGCTGTCCGCATACTGAAGAGAGATTGTTCAGTGAGGAAGAGGAGGCCAGAGTTGCCCGCGTCCGGGAGTACCAAGGTTAATCACCACATCTAGCTTGTCTGTTTATGTTTTGCTTCTCATTTTTGGTTTGTATGACGGTTGTTTTAGGTGCTTTAAAGAAAACACAAGAGGGCGCAATTGGTTTTCATAAATAATGTTTGTAACTTCAGTTATCAACTTATATATTTATATATATATATTTTTTTCTTTCATTTAACATTTTTTTCAAGTAACAAAACAGTTTGTTAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10836
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010991 | Essential Splice Site | 720 | 1150 | 16 | 23 |
ENSDART00000141572 | None | None | 280 | None | 4 |
ENSDART00000145229 | Essential Splice Site | 644 | 692 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 10954689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10814857 |
GRCz11 | 22 | 10844539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCGACACATTCGGCGGATACGATAGCAATTCTAGYGCACTGCCTAAGAG[T/A]AAGAGTCAYACCAATAAACATGTTTTACGTTAGGAATGCATCGATTTAAA
Long Flanking Sequence:
TAAAGCTTTAATTTGTTTAAAAATAAAAACTACCACCCCCACTGTTTACAATACGTCTGGTTTTCCTCAGAGCGTCTGGCGCTGAAGGATGCTCAGATCACTCAGAGTCTGGCAGAGAAGCTGCAGCTGTTTGCGGAGCTGTCTGAATGTGTGGCCGGTCTGGAGGACTCGGGCTCCCGTTCTCGTCTGCTCCTCCGCGGAGACACGTCTGACCTCCAGCAGGGGGAGACTCTGCTCAAAGCAGCCATCACTGAAGGTATCAGCAGCACATCTCACACACAAACCAGCTTGTCTCATATACATAATGCAGCTAAATGCAGTGAGCGAGTCATATCTCTGTGCCTTTCAATAGTGGAGAACCTGCAGAACCTCCTGACGTCTCGAGTTCGAGGAACATCGGCACAGACTGAAGGAAACCAGAGTCCGTCCTTGAGCTTGCTTCCACGCCGAGCCGACACATTCGGCGGATACGATAGCAATTCTAGTGCACTGCCTAAGAG[T/A]AAGAGTCACACCAATAAACATGTTTTACGTTAGGAATGCATCGATTTAAAGGCCACATGAAATTAAAATAATGTTTTTTTAGATGTTAGTATTAGTGTGTTAGTCTAAAGGATATCTAGAAGCTAGTGTGCTCCAAAACGGTGACAAAATTCAAGTTTAGAAGATATAAACATGCAAATATTGCAGTTTGTCACTTTCGCCTAAATGTGTCAATGATTTTTGTGACATCATACTTCAGTCTTCTGACCAATCAAATGCTCACTAGTATCTGACATGCCATGCCCCCTTAAAGATGCATCTTATTTTGATGTGTTTGAGCTCAACCACGCTCACTGGCAGAGCTATGATAAAAACGGAACTCTATTGGCTGTTTTTTGAAAAAGGGGAGGAGCTCTGATATTTCCCGCCCTGTCTTTGTGTTTCAGTTGAGATAATGACAGATGTCTAATTTAAAAAATACACGTCGTCATTATTATTTATTTATTATTATTTTATATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13725
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010991 | Essential Splice Site | 780 | 1150 | 18 | 23 |
ENSDART00000141572 | None | None | 280 | None | 4 |
ENSDART00000145229 | None | None | 692 | None | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 10950330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10810498 |
GRCz11 | 22 | 10840180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGCCAGCAYCAACATGTGGTCCTCRTGTAAACTTCCTGAATCAGAGG[T/G]GAGAGCGAGCGTTCATCATCATGCAGAAATTAAGACGATTATGCCTCTCT
Long Flanking Sequence:
ACATTAGAAGTTTGATTGAGTCATTTGAATAAAATATTAAATATAATAATGATTAACACTACAATATTGTAATGCACTCCTGGTCTGAAATAATGTCTAAGAATCATCATTTAATTAAGTTTTTTTCTTAAAACAAGCTAAATAATCTGCCAACAGGGTAAGCAAAATAATCCTGTTTTCCTTTTGACCTGAGATTATTTTGCTTACCCCATTGGCACATTATGTAGCTTGTTTTACGGAAAAACCCACTTAATTTTGGCATATTACTTCTTTAAAAAAAAAAGATATTATTTTAATTGTCTAGAAAATGCTTCTTGATTTAAGTATTTTTTTTAGAAATTTTGATAAGACAAAAAATCCAAGTAAGAAAAGCATTTTTTGAAGTTTATACACAATAATATGTTTTTCTTTTATTTTATGGTGTCTGTCTCTTCAGGACGAGGCTTCCTCACCTGCCAGCACCAACATGTGGTCCTCGTGTAAACTTCCTGAATCAGAGG[T/G]GAGAGCGAGCGTTCATCATCATGCAGAAATTAAGACGATTATGCCTCTCTCTGTTTCTCATGAGAGATCAAAGACACATATTCTTTCTCACACGCCTCCCCATAAGTATTTGAGAAGCTGACCTTTGCATTCACCGCACCTAATCGCCAGCTAAGGCGAGACTCCACAGGCTGAAACTGTTTATTTTTTTCATTTACCTGTCGATTTTGAGATTTCAGGCTTTTTGGCTTCTCATGAAGTGTTTTTTTTTTTTTCAAGTCTAATGGAAGGAAAACATACCAAATACACTATTAAGTGTTTATTTTGTTGGACTTTATTTATTAGCGTCTGTAGATTTTAATTACAACACACATTTTTAAAGGTTGCTTTCTCAAGATGTGTTTTTTTTTTCCTCCTTCACTGAGCCATAAATCTCCACTTCAGCATCAATTATATAAATCAAACTTTACCGTTTTATTCATATCTGTATTTGGAAAGTTCTTACAGAGGGATTTGATTGT
Associated Phenotype:
Not determined