ZMP
si:dkey-12o15.1
Ensembl ID:
ZFIN ID:
Description:
RAS guanyl-releasing protein 1 [Source:RefSeq peptide;Acc:NP_001038327]
Human Orthologue:
RASGRP4
Human Description:
RAS guanyl releasing protein 4 [Source:HGNC Symbol;Acc:18958]
Mouse Orthologue:
Rasgrp4
Mouse Description:
RAS guanyl releasing protein 4 Gene [Source:MGI Symbol;Acc:MGI:2386851]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23342 | Essential Splice Site, Missense, Splice Site | Available for shipment | Available now |
sa23343 | Essential Splice Site | Available for shipment | Available now |
sa15171 | Essential Splice Site | Available for shipment | Available now |
sa45644 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23342
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:
A > T
Consequence:
Essential Splice Site, Missense, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088504 | Missense, Splice Site | 107 | 687 | 4 | 16 |
ENSDART00000140386 | Essential Splice Site | 108 | 687 | None | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 34100203)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35779359 |
GRCz11 | 18 | 35760367 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCTGTAGTCACACTGTTGTGTGCTTTCTCCTTGACTTGTGATCACAT[A/T]TAAGGATTGTCCTGCAGAGAAAAGGGGACAAAGGCGTCCACAAATCTGTC
Long Flanking Sequence:
TAGATGACTAGCTTTTATACAGCATATAGCCAGTCATAAGATTAATTTAACTAGAAACTAAAGATTTAACCTAGAAAGCACCCAGTACAACTGCATAACTCATATAATTGTGTTGAATTGAATTCTAAACTTTCTCTTTTTTTTTTTTTTTTTTTTTGCAGACTCCGATGGGAAGCTAAACAGAGGGACGCAGCTTGTCAGCATGACCCTCATGATGCACAACTGGGTCGTACCATCACACATCTTCGCCCATAAGCTACTTTCTCTATATCCTTTATGCATCTGATCCCAGAGCAGCTGAGTCCATCATTCATTGAGCAGTCTTAGATTCAGTCACAGCAACACGCAGCCTCACATGGCTCTTAATCCCACTGACAAAGAAACAAGAGCTGCCCTGTTTTTGTTTAGCCTATTAATTGAGGCTGGATTATTTTCTCTTTTAGATTAAGAGAGTCTGTAGTCACACTGTTGTGTGCTTTCTCCTTGACTTGTGATCACAT[A/T]TAAGGATTGTCCTGCAGAGAAAAGGGGACAAAGGCGTCCACAAATCTGTCACTTTATCAGGTTGGTGGATCTGCAGCATCCACACGTGCACCTAAAGACTGCAGAATGAATGGAGGGATTCACGCCTGCCCTCTACTTCTTCTGTGTCTGTTTCAGGCAGTGGATTAGCCAGTTCAGACTGATGTTTGAGATGGACCCTCTGTTAGAAAAAGCCATGGGAGATCTCTGGGCTCTGGTCAGTGCTGAGGGAACCAATTCGCACCATCAGCTCATCAACACACCTTATATGTGAGTGATTTTACCGTTGAAATTCAAGTATTGGCATAGAAAAGCATTGGTAAAGGCAGCGTTCACACTGCAGCTGAATTCAATTCACTTTATGGAGTTTTTGTAGACACTAGGACTGCAAGATATTAGGAAAAAAACTGGCATTGCAATATTTAGATTTTCTGTGATGTATATTGAGATATTTATATAAATTAAAAAGATAAAGCACATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23343
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 |
---|---|---|---|---|---|
ENSDART00000088504 | Essential Splice Site | 506 | 687 | 12 | 16 |
ENSDART00000140386 | Essential Splice Site | 506 | 687 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 34131192)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35810348 |
GRCz11 | 18 | 35791356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATTGCTGCCAATTTCCCCTTCTCTTTCTGCACACATGAGAGTGATAG[G/A]TAAGGGAAGAACTGTTACACTAATGATTTAGTTTAGGTTTTGTAAGATTT
Long Flanking Sequence:
TTCATCATTATAATAATCTCAAAATGTAGCCTGAGGCGTACATATAAATGAGCATTATTATTTAAATAATGTTTTGTTAATTAATTTTTATTGTTTTGTTTTTTGTAGCCTGTAGCTCCTGTTAAGCCCCCAGTGGTTGCAGAGTGGGGATCTGGAGTGACTCCGCGTCTGGATCCTGCCACCATCTCAAAACACGTCAAGCAAATGGTGGATGTAAGTGAGAAAAACATGCAGATTCCCACTGTTAGAGCCAGTTCCAGTTAGATTGAGACGTAGACGGCCAGTTCCTGGCTGTCCACTCTCACTTCCTTAAAATTGTGAAAGGCCTTTAAAGCAAATGTCATAAGTGTCTCACATCGAAGCTGACAGTGATTCTGTTGCCCTCTGCAGTCCATCATGAAGAACTATGATTTGAACATGGACGGCTACATTTCTTTGGAGGAATTTGAGAAGATTGCTGCCAATTTCCCCTTCTCTTTCTGCACACATGAGAGTGATAG[G/A]TAAGGGAAGAACTGTTACACTAATGATTTAGTTTAGGTTTTGTAAGATTTGTGTTTGATTTTGAAACAGTATTAAGTTATTACAGAGACAATATCAATTTAATCAATAATACAGTAAAACAATATTATTGTAAAAAAAAAAAAAAGCTATAAATTTTCTAATTTTGAATGTGGCGTGGTGGCACAATGGGTAGCATGATCGGCTCACAGCAAGACGGTACCAGGCTCGAGCCCCAGCAGGGTCAGTTAATATTTCTGTGTGATGTTTGCATGTTTACCCCATGTTTGCGTGGGTTTCCTCCGGGACCTCCAGTTTCCCCCACAAGTCCAAAGACATTTGCTATAGGTAAATTGAATAAGCTACGGCCACAGTGTATATGTGTGAATGCAAGAGTGTTTGGGTGTTTCCCAGTGTTGGGTGGCGGCTAGAAAGCCATCCGCTGCGTAAAACATGCTGGATAAGTTGTCGGTTCATTCTGCTGTGACGGCCCCTGATAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15171
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 |
---|---|---|---|---|---|
ENSDART00000088504 | Essential Splice Site | 568 | 687 | 14 | 16 |
ENSDART00000140386 | Essential Splice Site | 568 | 687 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 34134603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35813759 |
GRCz11 | 18 | 35794767 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTTTCCATTAGTTATGGGGAGTCATAAAACAAGGCTATCACTGCAAAG[G/A]TTACAAKATCTCAATCAAYCAGTCTTAATACTGTATATAATTACACCTCA
Long Flanking Sequence:
CAGTGTGCGCCAAACTCGGCTTTAACCTCCACAACCTTCACAACTTTCACGAGACTACGTACAAAAGGCCCACATTCTGCGACACCTGTGGAGGATTTGTACGTATTTAAACCAACACTACACTTTTCTTAAGCCTTTTTCACAAGTCGCCTAGAGTTAAACAATTGACTTGAAACATTTTTGAATCCATTCAGCCGATTTCTTGTTCTGGCAGAGTCACTTTTAGCTTAGCTTAGCATAATTAATTGAATCTGATTAGACCATTAGCATTTCAATCAAAAGAAAATTTATAATATTCTCAATTAAAAGTATATATATTTCTTTTTTAAAAACTGTTTAACTCTAGGAGACTTGTAAAAAACTTTTTAAAAGTATTATGTTCTTTTAAACTTATAGCCAATATATTTTAGCAGATTTGACTAAATGTAACATCTAACTTTTCCCCCCTCTGCTTTTCCATTAGTTATGGGGAGTCATAAAACAAGGCTATCACTGCAAAG[G/A]TTACAATATCTCAATCAATCAGTCTTAATACTGTATATAATTACACCTCAGCACCACAATAACTTTGCTGCTTCTTTCTGGCTCTCTCTTTCAGACTGCGGAGTGAACTGTCATAAGCACTGTAAGGATGTGGTAGGAATGGAGTGTCTGAAGAGGCTTCAGGTCAACAGTAGCTCTTGTCCCTGTACACCAGGACCAGTTTCAGGCCTTCACACTAAAGGCAACAGCTGGAGTGAGTTTTCTCAATGTATGTGAGCTGCTCATTAATGCTAAATAGATCAATATCCTTCAGTGATCATTATAATATTATATACTTATATAGCTCTAAAAAAAATTGCTCTTCGAGATATGAGGAACTTTTTACAGTATTTATTTTTTTGTCTTATTTCTTTTAGTTTGGCAGGAATACAAACATTTACATTTGAAAATTATTAGTGGTAATATTATTAGCTCCCTTAAGAGTTTATGACTACAGAATAAAGCTCTGTTATCCAACGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45644
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088504 | Nonsense | 686 | 687 | 16 | 16 |
ENSDART00000140386 | Nonsense | 686 | 687 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 18 (position 34141158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 35820314 |
GRCz11 | 18 | 35801322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGATCGTCTTCATTCCCAGAAACAGCATCCACCTCTTGAAAAGGTAT[T/A]GCCATGAAGCATTGTGTTTCTTTTCATAAGCTTTTCCACAGCGTGTTTTA
Long Flanking Sequence:
GCTAATCACGTTAATCACCGGCTGCATCCATGCTTCATGTCGAATGCACCTAATGTTCTCGAGTCATACAAGAGATTTGGTTCAAAATGAATGAGTCGTTTAAGAACGATCCATTACTACTGGTAAAGCCCCCCAAAAGTGAGCCATACTGAATCAAATTGTTTCATACCATTGCTGTGGAAAAGTGCCTTTACTAGCTGAACACCATCACACACATTGAGGAAATGTGCATAATATGGGCACTTTAAACTGGCAGGTGATTTACTAACCGTTCTCCTGTGTTGCAGCCTTTCAATCAGGTTCCGAAGAGGAAGCGTTCGTCTTTCCAAATGGAAATGAATCTGAACACTCCAAGGGCCAAACTTCATCAGACAGCGACGCAGAAGCGGCCACACTATCCGACAGGTCAACTCAAACAGAGCCAGGAGTTTGGACACCGGTGGCCAAACGGAAAGATCGTCTTCATTCCCAGAAACAGCATCCACCTCTTGAAAAGGTAT[T/A]GCCATGAAGCATTGTGTTTCTTTTCATAAGCTTTTCCACAGCGTGTTTTAAAATACATTACATAGAAGCTAATGTAATGAGCGAGTGGGTAACCAAAACGTCTTGAGACTAACGTCACCTACCTGCCTTATATCATCCCAGAGCGCAACTCTTCCGGCAAGGGTGCGAGGTTCATCTGCCCCTAGCTCTCTCCTACAGGAGAAAATGGATGAACTGAAGCTGAACAAAGATAAACGAAAGGAACCAGACTGAAGTAGTTTTTGTGCATGTGGCCGTCTGGTTGTGTGTGTGTGTGTGGGGGGGAACTGTTAAATACACTGGACAGAACACTTTGAAGAACGTGTCCTCGTCTTTCTCGCCAACTGTCTTCTTCTATTGTCTTCAACAGATTGTTCATGACGTTCATTAACTATGATGAAATTCTACCCAGAAGGGATTTTATTTAAGGAATTGCTGATGATCTGTATTTTGATGAGCCTATTGGTGGATCCGTACGGTTA
Associated Phenotype:
Not determined