ZMP
RGL3 (2 of 3)
Ensembl ID:
Description:
ral guanine nucleotide dissociation stimulator-like 3 [Source:HGNC Symbol;Acc:30282]
Human Orthologue:
RGL3
Human Description:
ral guanine nucleotide dissociation stimulator-like 3 [Source:HGNC Symbol;Acc:30282]
Mouse Orthologue:
Rgl3
Mouse Description:
ral guanine nucleotide dissociation stimulator-like 3 Gene [Source:MGI Symbol;Acc:MGI:1918996]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16278 | Essential Splice Site | Available for shipment | Available now |
sa13355 | Nonsense | Available for shipment | Available now |
sa6028 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19960 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12680 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16278
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 |
---|---|---|---|---|---|
ENSDART00000001755 | Essential Splice Site | 184 | 717 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 3 (position 13793450)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 13851737 |
GRCz11 | 3 | 14001583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCGCTCGCTAAACAATATGAAGCGCTCCTTAAGAGATTCCAGACTGAAG[G/A]TYATTACAGGATTGATAYATTAYGAATTATTGCWTTTGTGTTTGATATGC
Long Flanking Sequence:
AAGGACAGCTTCATTCACTCTTCACTCGCCTCAGTGAAGTTTTTTTCCCTCTCCGCTGTGGCCATTAGCTTGCATAGTTTGGGATCAGTAGAGCTACCCATCGATAGATTTGCTCTTCAGTGTTTGGACTCTCAGTAATGATTTTAAAGCACACTGAACTGAGCTAAACTGAACTTAAACACTAAGAACTGAACTACTCTGTTCCAATTAGTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAATTAAAGCTGAATTGAATTGAATTGAATGTTTTCTCATATTGTCTCTTATTCCCCCATACAGCTGTTTGTGGACAGTGCTTCAGTTGTGGTTGGATGAGTACAGTGAGGATTTCAGGGATTCTCCTATGCACTCTTCACTGCGCCTCATGTGTTTAAAGCTGAGAGGACACCCGTCTCTCTTCCCGCTCGCTAAACAATATGAAGCGCTCCTTAAGAGATTCCAGACTGAAG[G/A]TTATTACAGGATTGATACATTACGAATTATTGCTTTTGTGTTTGATATGCACATTATTTCAAGTTTTAATAGGATAGTTTGCACAAAAACGAAAGATTCAATCGTCATTTACTCACCCTTTATTTGATACTTCTGTTGAACACAAAAAATAGGTTTTGAAGAAAGCTGGAAATCAATCAATCAATCAATCTATCTATCTATCAATCTATCAATCAATCAATCAATCAATCAATCAATCTATCAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCAATCAATCAATCAATCAATCAACCAATCAACCAATCAACCAATCAACCAATCAATCAATCAATCTATCTATCTATCTATCTATCTATCTATCTATCATCTGTCCGTCCATCCATCCATCCATTCCTGTATCTCTATTTATCTGTCCGTCCGTCTGTGCGTCCGTCCATCCATCCATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13355
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 |
---|---|---|---|---|---|
ENSDART00000001755 | Nonsense | 225 | 717 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 3 (position 13794695)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 13852982 |
GRCz11 | 3 | 14002828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGASGATTTCCTGGATTTTTCCATCATGGGTGTTGCTGAACAGCTCACA[C/T]GAATAGATGCTGTGAGCGCTCKTTTTATTGCTYGCTTYTGATTGGCTCTK
Long Flanking Sequence:
CATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCATTTTGTCATTCTATCTATCCTACCCTCCAGTTATCCAATCGTTCTATCTATCTATTTATCTATCTTATACATGCACAAATATGTAATCTATCAGCTGTATTATGTAATATGTTGATTGTAGGATTATATCATGTACTCTACATGGTCACTTTTCAATCAATGTGCATGCCCTAATTCTAATTAATAGTTGAAAAAATGTGTAATAATGTATCTCTGACTTTAATTTCCTCTGTCTTTTGCACATCTAGATGTTGTGGCAGCTGTTTCAGCCGATCTTACCGAAGAATCCAATTTGAATATGGAGATGAGAAACTTTGAATTTGACAACATGGAGGATTTCCTGGATTTTTCCATCATGGGTGTTGCTGAACAGCTCACA[C/T]GAATAGATGCTGTGAGCGCTCTTTTTATTGCTCGCTTCTGATTGGCTCTTTATGGTCATATAGACTAATAATCTGCAATGGTGCTTCATTTGATGTTGTAGGATTTATTCGTGAAGGTGGTCCCTTTCCAGTGTCTGGGATGTGTGTGGTCCCAACGAGACAAGAATGAAAACCTTTCGCCCTCTGTCTGGGCCACCATCACACAGTTCAATGCGGTCACCAATCGGGTTATCACGTCTCTGCTTAATTCCCCAACCTCCACCGCCTCACAGAGAGCCAGAGTTATTGAAAAATGGGTTCGAGTTGCTCAGGTAAACACTTCAGCTCATGGAATTCTTCGAAAATCAGCAAATTTTATATACATTTGAGGTCAAAATGATTAGCCCTTCTGTGAAATATATACTGTATATATTTCAAACATTTCTCATGTGATATTTAATGGAGCAAGGAAAACTTCATAGTATTTTCTATAATATTTTTTCTTCTTGAGAAAGTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6028
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001755 | Essential Splice Site | 335 | 717 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 3 (position 13798875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 13857162 |
GRCz11 | 3 | 14007008 |
KASP Assay ID:
554-3882.1 (used for ordering genotyping assays)
KASP Sequence:
AATAACAAAAATCATAATAAAATATAGCTTTAAAAGTAGCCAAGAACAGG[G/C]TAAATTGAAATAAACTCAGCTAAAACTGGAACTTTCTGTAATTTTAAAAG
Long Flanking Sequence:
TATTTAATTTAAAATGAGAACTAAGAAAAGTAAACGTGATTAAGTGTAATTTGAAATAAAAATTTAATATAGTATGAAAAAAATATGTATAATAAAATAAAAAAACAACTTTCACATTTAAACAAGGCATTTTTGTACTCTAAAATTGATCTAAAACAGAATTAAGTGTTTAAAGTGATTTTCAATCCCACATGAATTTAGCCTTTTAAAATAAGCCTAAAAGGTTTGATAAAATCGTATTATGTTAAGTAAGTAAAACATTAAACATTACTTTAAAATAAAATGTATTCCTTACCAAAATTAAAACTAAAAGTGAAAAGTGTCATCTCAAATGAAAATAATCTTAAATAGTACACTTAAAAATGTAAATAAAATATGCCTTAATATTAATCCTCAGTCCTAATAAATAAGTCTAAAAAGGATCAAATTATAATAAAATTAAATATTTTTAATAACAAAAATCATAATAAAATATAGCTTTAAAAGTAGCCAAGAACAGG[G/C]TAAATTGAAATAAACTCAGCTAAAACTGGAACTTTCTGTAATTTTAAAAGAGATTCACTAAATTATGGAATGACATCATATCCTTTTCCTAATGTTTGCTTCTGTTGTGTGTCCTCAGCTATGAGCTTTCCAGACAGCTGGAGTTTCCTCAAGACACTTCACCATCCAGCAGTGGCTGGAGCCACCGAATGCTCACCAAGAAACTCTCATCGTGAGTAAATCAGTCCCTAAATGTTTTCCGCACTCGTCCTATCAACTGCAAGCTTTCATTGGCATAATAGATGCTACACCAGATCTAATGCAGTCTAGTACATAACAGTATTTCATTTATATTGATTATTATATTGTATATTATAATATATAATTATTATTTATTGATTCTAGGCTTTTGTCCGGGAATGAGGGATCCAGAAAGAATGCAGATCAGATCAGCGTGTCCTCGTCAGGATCTAGCAGCTCTGAAACTGAGGACATGTCTTCTCAATCGTCAGCTTTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19960
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001755 | Essential Splice Site | 417 | 717 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 3 (position 13799813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 13858100 |
GRCz11 | 3 | 14007946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCAATTTATGCTAAGCTAAGCTAAAAGTGCTCCCACCAGACATGAAG[A/G]TCAAAGCACATTGAATGCTTTCTTCTTTCCACAAATTTTAAACAACATGC
Long Flanking Sequence:
CCTCGTCAGGATCTAGCAGCTCTGAAACTGAGGACATGTCTTCTCAATCGTCAGCTTTTATATCACCGGTACTTGTGTTCACATATACTTTCATCATTACAAATGCTTTTATTATTGTTGTTAGCATTATTAAAGGCTCATTTTACAAGTAACCTATAGTAAACAGTAGTGTTTTACCATTTTGAATCTATTTAGACGATTTCCACGTGTGGAAATCTTTTAGCACTTTTAGCTTAGCTTAGCATAGATCATTGAATCGGATTAGACCATTAGCATCTTGCTCAAAAATGACCAAAGAGTTTAGATAATTTTCCTATTAAGAAAGCTTGACACTTTTGTTGTTACATTACTGTATCAAGACTGATGGAAAAAAAGTTCTAGGCTGATAGGGCTATACTCTCAAAATTATCAAAACTCTTTAAAAAAAAATTTATGAGATGCTAATGGTCTAATCCAATTTATGCTAAGCTAAGCTAAAAGTGCTCCCACCAGACATGAAG[A/G]TCAAAGCACATTGAATGCTTTCTTCTTTCCACAAATTTTAAACAACATGCTACAAAAAAAATCCAAATATCCCTAATTCCTCAAATTCAGCGCATGAAAAGGCCTGTTGTTTTGCATGCGTTTTTATGTTCTTTAAGGGATAGTTCACCTAAAAATGAAAAATTCTTCATCATTTACTTAAACTCATGTGGTTGTAAACTTTTAGGGGTTTCTTTCTTCTGTTGAACACAAATTTCAGCTTATTTCTGCATCTGACATCCGATTCAATGACATATGCTAAGCTAAAAAGATAAGCTAAGCATATGTCATTGAATTGGATTAGATCGTTAGCATCCTGTTCAAAAATGACCAAAGAGTTTCGATAATTTTCATATTCTTAAAGCTTGACATTTTTGTAATTACATTGTGTACAAAGACTGGTGGAAAATGAGAAGTTGCTATTTTTAGGCTTATATGGCTATACCCTTAAAATTATCAAGACAATTTTTTAAAATAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12680
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 |
---|---|---|---|---|---|
ENSDART00000001755 | Nonsense | 605 | 717 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 3 (position 13803785)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 13862072 |
GRCz11 | 3 | 14011918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCGTCTCATAAAYGCTCGTTCTCCATGACCACCCTGCCTTTCTACAAC[C/T]GACAGGTGGACGACTCCTGCATCATCAGGGTCAGCGTGGAGTTCTGCAAC
Long Flanking Sequence:
AGAGATTTTAACACATTTATGAACATTATAGTTTTAATAACTCATTTCTAATAACTGACTTATTTTATCTTTGCCATGATGGCAGTAAATAATATTTGACTAGGTATTTTAGATACTAGTATTCAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGAAAGTTGGGGTAATCAGGGAAACCATTATCTAACGATAGTTTGTTCTGTAGACAATCAATAGCTTAAAGGGGCTTTTGATACTAAAATGTCTGGCTCTAAATGAGACTCTTTTTTCCACCTCTAGTCTCATTCTAGCTGCGGTCAGAGCTCGACTGAGGCTTTTCCATCATCTTACACTCCAGATTCCTCCATCATGTCCAGTTCGTCCTTCAGCTCTCAGCAGGACCTCAGTCTGAGCCAACCTTCTCCCTCATCATCTTCAGCTTCATCAGACCCTCAGCACGTCTCGTCTCATAAACGCTCGTTCTCCATGACCACCCTGCCTTTCTACAAC[C/T]GACAGGTGGACGACTCCTGCATCATCAGGGTCAGCGTGGAGTTCTGCAACAATGGCAACATGTACAAGAGCATACTGGTAAGAACTTGAATTTTGCACACATTTAAATGGGTCCCGTGAAACTAAAACAAAAAATGTGGAGGCTTATTTCAGTTTCAGATTGTTTTGAGAATATCTATAAGCTAGTGTGCTTAAAAACAGTGACAAAATTTGCATTTAGAAACTATAAACTGATATAAAGATCCAAAGCTTGCAGTTTGTCACTTCCACGTCACCTCATACTTCAGTTTCTCATCAAATCCTCTGACCAATCAAGTGCTCTCTAGTATCTGACATGCTCCACCCCTTCAAGACGCTTCACATTTGTTTTCATTTGATGCGCTTGAGCTCAACCACTCTCACTGGCAAAGCTGTGATCAAACAAAACGCTATTGGCTGTTTTTCTAAATGGGGAGGAGCTACTGTATGTCCCACCCTCTCTTTGTTTTTCAATCGAGATTA
Associated Phenotype:
Not determined