ZMP
si:dkey-233k19.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
RAPGEF5
Human Description:
Rap guanine nucleotide exchange factor (GEF) 5 [Source:HGNC Symbol;Acc:16862]
Mouse Orthologue:
Rapgef5
Mouse Description:
Rap guanine nucleotide exchange factor (GEF) 5 Gene [Source:MGI Symbol;Acc:MGI:2444365]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39094 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16233 | Essential Splice Site | Available for shipment | Available now |
sa2850 | Nonsense | Available for shipment | Available now |
sa32084 | Essential Splice Site | Available for shipment | Available now |
sa22805 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39094
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 |
---|---|---|---|---|---|
ENSDART00000114954 | Nonsense | 104 | 860 | 4 | 26 |
ENSDART00000138126 | None | None | 364 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21000411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19237166 |
GRCz11 | 16 | 19042805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATCTTTAACACTTTCCTGTGTTTGCTTTATATTATCAGGAGGACGTA[T/A]ATTGGTATAGAGCTGGTGGAATGGCTGATGGACCATTGCGAATTCATCCA
Long Flanking Sequence:
CACCATGCCACCCTTCTAGGAAAGGAGGAGGAGTAGGAGTGGAAGGGGAATTCTTCAAAAGGAAAGATGGCTATTATATGGAACTTAGGGTATTTATAGTGGCGTAGGAATTGTCTGATTGGTGAATCATAATTTATATAATGCGGGGCCAACTGCTAGCTAACATAAGCACGTGATCCTCTCAAATTAGTTCATAAATAAACTACACTTATCATCATTTGAAAAACATTGGTGGAATAAAGTGAAATTTATATTTTTAAGTTGAGAACTTTTATTTAGTTAAATAAATAATAATTATACATTACATTTGTAATGTATCAAATCACATACGTCACATTAGCAATCATTTAACACCACATTTTGCATTCACATTTAAAATGAATTGGAAAAAAAACTGTTTTATAAATAGTAATATTTCATATTAGTTTTATTTTAGTTAATACAGTCTATAACATCTTTAACACTTTCCTGTGTTTGCTTTATATTATCAGGAGGACGTA[T/A]ATTGGTATAGAGCTGGTGGAATGGCTGATGGACCATTGCGAATTCATCCAAAACAGGGAAATAGCTTCCAAAATCTGGAATGTTCTCCTAGATTTGGGCATTCTGCTTTCAGGTACACAACCAATGCTGGGGAAGAACAAAGCAGACACACAAGTTTGGATGATTTATATAAAATGTTTGATTAATATTTTTATTATTATTATGTTATAAGGTACTATATACATTTGCAGTTTGCATAACAGCCGATTTCATCCAATGTGGTGCCTAAACAGAACATACATTTACATAAGCTTTGTCTAGATATAGCTTTATGTTGGATGTTTAACCCCAATGTGCTTCTGTTGTGTCCAGTGGAGCAGAACAATATATTTGAGGACTCCAGGTCTTTATACCAGTTCACCTTTAAGGAATGTGAGGCCCAGAGCTGTGATTTCAGAAATCAGGTCAACTGGCGGAGTGCAGTGCATCTGCTCCTTCAGCTGGTCCCACACGAGCAGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16233
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114954 | Essential Splice Site | 198 | 860 | None | 26 |
ENSDART00000138126 | None | None | 364 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21000933)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19237688 |
GRCz11 | 16 | 19043327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTTCAGCTGGTCCCACAYGAGCAGCTCTGTRGTGGAACCCAGAGGCGG[T/C]GAGCACATGGTTACACATAAAGCTTAATAATGGTGTTTTTTYCAAGGTCC
Long Flanking Sequence:
TGGCTGATGGACCATTGCGAATTCATCCAAAACAGGGAAATAGCTTCCAAAATCTGGAATGTTCTCCTAGATTTGGGCATTCTGCTTTCAGGTACACAACCAATGCTGGGGAAGAACAAAGCAGACACACAAGTTTGGATGATTTATATAAAATGTTTGATTAATATTTTTATTATTATTATGTTATAAGGTACTATATACATTTGCAGTTTGCATAACAGCCGATTTCATCCAATGTGGTGCCTAAACAGAACATACATTTACATAAGCTTTGTCTAGATATAGCTTTATGTTGGATGTTTAACCCCAATGTGCTTCTGTTGTGTCCAGTGGAGCAGAACAATATATTTGAGGACTCCAGGTCTTTATACCAGTTCACCTTTAAGGAATGTGAGGCCCAGAGCTGTGATTTCAGAAATCAGGTCAACTGGCGGAGTGCAGTGCATCTGCTCCTTCAGCTGGTCCCACACGAGCAGCTCTGTGGTGGAACCCAGAGGCGG[T/C]GAGCACATGGTTACACATAAAGCTTAATAATGGTGTTTTTTTCAAGGTCCAAGGTCTTTAAACATCTTGTCCTACAAGGGTGTAAAACTTAATAGCTTTTTATTTACCATCCATTGCTAACAGAACGTGCCCATACGCATCAACAGTCTTTACTGATTACCTAAGTAGAGCTAAACGTATTTAAAATGGGTATTAATTACCCTGTAAGTAGAGCGACAGGTAGAGTAAGTTGTTAGCATTTACTACTTGAAGTTTTTTCTGGCTTGCATCCCAAAGGAGGCTAAAGATTTACTTTCATTCTATAATCAGCGTTGATCCAGTTAACCCAGAATGTTTTGTTTGTATTTTTTTCATTTTATATATATATATATATATATATATTGTTTTACATTTTACTTAGTTTCCTGTGTCCCCATAATTGGAGTTTTAAGATTAAATTTTATCTCAAATTACAACATTGTTTAATTATATAGTGTTGGGCAACGATGTTTCTGTGACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2850
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 |
---|---|---|---|---|---|
ENSDART00000114954 | Nonsense | 210 | 860 | 6 | 26 |
ENSDART00000138126 | None | None | 364 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21006327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19243082 |
GRCz11 | 16 | 19048721 |
KASP Assay ID:
554-2883.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTGCTTTGTAGCTGTAAAGAAGATAAACAGAAAACACCTGATGCTTG[T/A]AATCCAGTTCTTCAAATGAGGGCATTGGAGCATTTCACCTCAACAGTAAG
Long Flanking Sequence:
GTATCTATATATTACGATTTTCGTGAGTTTTGTAATTATTATAGACCTTACAATCAGTGTCGTGCAGAATATTTTATTATATTAAGTTAATGTTTATGAATTTTGGACGGTTTTATTTTAGGGGTTCTCTTTATGATGTTTTTTCCTCTGTGCATGTTATTTACATCAATAAACTTCAATACATCAATAAGTTTTGTACACATATATTTTTGATATATATTGACGTATAAAATGGCATTTTTTAATTTCTTTAAGAAAAGAGTTATCCCCTTAATATTACATTATTATTACTGTAATATTACCTTTTATTCTCAGTACAGTTTTGATATTTCTAAATGAATGTCTCCTAAAAATATTAAAATACATTTAAAAACTATTTTATCATAGAATTATATTATTTGTGTTATTGTCAATGTGGAAATGTAAATGTAGTAAACAAAACAACATTATTTTTTGCTTTGTAGCTGTAAAGAAGATAAACAGAAAACACCTGATGCTTG[T/A]AATCCAGTTCTTCAAATGAGGGCATTGGAGCATTTCACCTCAACAGTAAGTCAATTACATTGCATTTTTTGCATCTTCTATCATTTCCCTCAATTTTAAATGGATTCACACAAAACAATAATCATGTCAGTAACTAAGCCTCCACTTGCTCCAAACACTAAAGAAGATATTTTGAAGAATGTTGCCAACCAGTAATCATTGACGTCCGTAGTATTTGTTTTCCTGCTATAAATGTCAGTGGCTACAAGTAATCAACACAAAATAAATAATATTTGTATTTTAGTTTATTTTAGAATGCTTTAACACCTGTAGATCGATTGTTTTGTTCCGAAACAGGGATTAAAATTCTAACAATGTTGGACTTTGTTCTTGTTGCGGGTCACTTTTAAAGTTTCTAAACGGACCAAAATGGCTACAATAAGTTGCATGCCAGTAAACTCTTCCCACATTGCACAGATTGAGTTCCATGGTTTATTTGTTTTATACATCCTGCCATAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32084
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114954 | Essential Splice Site | 380 | 860 | 12 | 26 |
ENSDART00000138126 | None | None | 364 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 21081987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19318742 |
GRCz11 | 16 | 19124381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCATTGGATCGTCTAATGTGTGTGTTACATGTTATGTTTATTTTCA[G/T]ATAGTCTGCTGGATGATTTTCTTCTGACGTACCCAGTGTTCATGTCTACT
Long Flanking Sequence:
TGAGCCACTTGTACATCCAGGAAGTGTTCAGGAAAAGCAAAACAGCAGCGAAGAAACTTGACACAGAGGAACATTTACACCTCATTGCCAACTAGCGTTTCGGAAGTGTTATTGCAAACCAACAGAGACAGCGCACAGAAGTATAAATGCATAGCTACGTGCGTTGCATGTGCCGTGGGTTACGCCGGTCACTTGACGCAGAAGTATAAACCAGGCTTAACCCATTGTCATCAGAAAAGTTTGTTTACATAATGAACCAAGAAAACACGGTTATTCTTTCTGCACATTAAGAGCCACCAATTGGAACCAATTAGCATTTTTATTTAGCATACACTACTTTGTATTACTTTGTTTTGTACTTGTGTTTTTATATATACACAGCAATTTAAAAATGAAAACAATAGATGTAATTCTAGTTGAAAACTTCAGACTTTTCCATTTCCAGTCAGTTTTCTCATTGGATCGTCTAATGTGTGTGTTACATGTTATGTTTATTTTCA[G/T]ATAGTCTGCTGGATGATTTTCTTCTGACGTACCCAGTGTTCATGTCTACTAGTGACCTGTGTCAAGCTCTACTTGGTCAATATCCTTCAGAACACAAACACGCACTGTCTAAAAATATGTTTTAAACCCATTTACAAATTATTAATTTGTCACTATGTAAATATACAAGAAACATTATAAACCTAATTGACATTTTAAGATTGATATTTCTCACAGAAGTTTGATCATATTTGATGGGCCATGACACCTAAACGATTGAAAACCCTTGCATTAAAGGATAAGTTCACCAAAAATGAATATTCCATTGTTAATTACTCACCTTCATGTCACTTCAAACCCCTAAGGACTTCGTTTATCTTCTGGATGCTAAGTAAAAAATTGTTCATGAAATCTAAGAGCTCTCTTATTCATAGACAGCAACAGCCAGTCATTCAACTCTAATTATATGAAGTTTTAAGAGCACTTTTGTATTTCAAAATTAGATTTTCTACATGGAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22805
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 |
---|---|---|---|---|---|
ENSDART00000114954 | Essential Splice Site | 524 | 860 | 16 | 26 |
ENSDART00000138126 | Essential Splice Site | 28 | 364 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 16 (position 21093778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 19330533 |
GRCz11 | 16 | 19136172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGAGAGCTGGCATCCCATGAGGGGACCAGAGAGAGAGAGGAAAGAAGG[T/G]AAGCTCATAAAATATTCCTCTCATTTTTCTCTCATCACTCTCCGACTGCC
Long Flanking Sequence:
CCATTTTCAAATATAGAATAAAATGTACAGTATATTTCCCATAGAATTAAATGTATATTTCTCTTAACTATGGAGTTTGTGGGAGGCTGATTTTTTTTGTTTTGTTTTTTTCCAAATTGAAGGTTACTAAATCAAAAATAAAAAAAAGTAAAAATTTAGTAATAACATTCTGCAATGTTTTTAATTTCTGTCTACTGTCTGAACATGTACATCATGACAAGTTTGACTGTAATTTATTTTTCTGTCAAAATAAACCCTGTGCAGTACAAAAAGGTTGACAACAACATTTTAATATCCAAGAGTGAGATAAAGTCTCCTTCAAATTACTATCTTTACAGTGTCCAGCTTTCACTGTCACTTCAGGCTGTGTGTTAGTTTGTGTGTATCATTAGCAACAATATTCTGCTTGCTGTCATCCAGAATAAAGCTCTGTTCCACCAGCTCAGTCTGAAGGAGAGCTGGCATCCCATGAGGGGACCAGAGAGAGAGAGGAAAGAAGG[T/G]AAGCTCATAAAATATTCCTCTCATTTTTCTCTCATCACTCTCCGACTGCCTGCAGAGCTGCTGGAGATATTGGCAGATTCTTCATTAATAACAGCATGAGAAATCTTGTTTTATGTGTGTGTTTCAGTGCTGTGTCGTGTGTACGTGACCGTCGACTCGTATGTTAGCGTGAGGACACACAGCGAGGTGTGTGTCCAGGAACTTCTGAGGGCTGTGGCTGAAAGACTGGACTGTGCTGAAGATGACATGGTGCTGATGGCCCTCACATATCCTGGAGGTCTGAAAGAGTTCATATTGGCTGACATTTGCTGCTGTGTGTTTGTTTATAAGACAGCTTTGTCTGCAGGGGGAACATTAGGCTTTCAAATTAGTCATTAGGTAACAACAGGGTTAAATGTCCCATTTTCTGATAGTTAAGTGTTAATGAAGAGTGCACTTATTTTATGTTAGTGACAGAGTATGACAATCTTGTCCTTCAGGCAGTAAAAATAAGTCCAAGA
Associated Phenotype:
Not determined