ZMP
si:dkey-1h24.3
Ensembl ID:
ZFIN ID:
Description:
si:dkey-1h24.3 [Source:RefSeq peptide;Acc:NP_001121716]
Human Orthologue:
RAPH1
Human Description:
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 [Source:HGNC Symbol;Acc:14436]
Mouse Orthologue:
Raph1
Mouse Description:
Ras association (RalGDS/AF-6) and pleckstrin homology domains 1 Gene [Source:MGI Symbol;Acc:MGI:1924
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16153 | Essential Splice Site | Available for shipment | Available now |
sa39627 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16153
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 |
---|---|---|---|---|---|
ENSDART00000088290 | Essential Splice Site | 403 | 1511 | 9 | 15 |
ENSDART00000125402 | None | None | 108 | None | 3 |
ENSDART00000136066 | None | None | 161 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 28679553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28930382 |
GRCz11 | 1 | 29734313 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGGAGACTTCTGAGATGGCAGACAGAAACAAGGAGGCACTGCTAGAGG[T/C]AAAGCATGTTATAAAACTAATTATATTGTCAAATCATAGTACTATGACAA
Long Flanking Sequence:
CTGTTTAACTGTTTTCTCGCTAGTGAAGTGTTCAGTTTTTCAACTTACAATTGCTACATGTAAATAGCAAATGTGCCTTGGCGTGACACAACTGACTCTTAAAGGGAATGGAAGATGATATTTTCAAAACACACCCGTAACCCTTCAGGAGAACAAACTCCACCCTGTTAGACCAAGCGACACGGCGTAAACCATATTTTTCTGCCGTTAAAATTGCAAAAGGGGATTCAGACATGTCCTTATTGCTTTTGCGTTGTGTTCTTTAGACTTTGCGCCTAGATCTGTAAAATAGCGACCTTAGTGTAAATGTAACCATTCTTGACACCTAAGTTTAGCTTAATGTTAGTCATAAGTTTATGATTCTTGGTGTGTAAAGCAGTTTATATTTTGTCGCACTGACTCACTTGTTACCTGTTGTTTGTGTGCTTCTAAGAACTATTTACTTGGGAGGAAGGAGACTTCTGAGATGGCAGACAGAAACAAGGAGGCACTGCTAGAGG[T/C]AAAGCATGTTATAAAACTAATTATATTGTCAAATCATAGTACTATGACAATGCTACAATTAGAGCACATTGAATTTCAAGTAAAACTTGAAAGGCACATTAAACAGAAAAATACTGAAGACTAACTAGCCTAACTTCTCTTTAGCCAACTTTGCTTAAACTAAAATGGTATTACTTCATAGCAGGTGTTCTTAAACTCAGTCCTGGAGGGCCAGTGTGCTGCAGATTTTTGCTCCAACTATACTCAACACACCTGCAAGGATGTTTCTAGTAAGAGCTTGATTAGCTAGCGCGGATTGGGGTTAGAACCAAGCTTTGCAGGACACGGGCCCTCCAGGACTGAATTTCAGAACCCCTGCTTTATAGCTAAAGATTTAAGTTCATTTCAAGTCTAATGCAGTTGCTTGGTAAAATACTTTTATATTACTTTTACTTGCGTGTATATTTGCAATAATGCACAATGCATATAGATGTTTAGTGAGGGTGGGGAAATACTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39627
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088290 | Nonsense | 925 | 1511 | 15 | 15 |
ENSDART00000125402 | None | None | 108 | None | 3 |
ENSDART00000136066 | None | None | 161 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 28685804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 28936633 |
GRCz11 | 1 | 29740564 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTCCACCAATAATGCCCATGCAGTCAGAGCCTCTACCGCCGCCTGCA[C/T]AAATCATGCCCATGCAATCACATCCTCTTCCACCACCTCCACCTTTAGTG
Long Flanking Sequence:
CACCTCCACCTGCCTCAATGCCTCCACCTGGTTCAGCCATGGCTGTTTTGAAGCTCGGCCCTCCAGCTGCAGCAGTAATTCCACAGATCTCCCCTTCCCCCCCCTCACCTCCTCCACCACCACCTCCTCCTCCCATAATGCCAGTGCAGTCACAGCCTCAACCACCTCCTCCACCCATAATGCCCATGCAGTCACAGCCTCTACCGCCTCCTCCACCAATAACACCCATGCAGTCACACAATCTACCACCTCCTCCACCCATGCAGTCACACGCTCTACCACCTCCTCCACCCATAACACCCATGCAGTCACATGCTCTACCACCTCCTCCACCCATAACACCCATGCAGTCACATGCTCTACCACCTCCTCCACCCATAACACCCATGCAGTCACATGCTCTACCACCTCCTCCACCCATAACACCCATGCAGTCACATGCTCTACCACCTCCTCCACCAATAATGCCCATGCAGTCAGAGCCTCTACCGCCGCCTGCA[C/T]AAATCATGCCCATGCAATCACATCCTCTTCCACCACCTCCACCTTTAGTGCAAATGCAGTCACAGCCCATGCCACCACCTCCTCCCACAGTGTCATTCCAATCACAGCCTTTACCACCTCCTCCACCCCCTCTCCAGGCTAATGGCCTTCCCCCTCCTCCACCTTTAATCACTAATGGGCTTAAGCAGGCTTTTGCCCATAAATTTCCCAGCACACCACAGGATGTATTACCCCCAGCTAATCAAAACAATTTTCCTCCACCTCCCCCACCACCACCACCTCCACCACTTGCACCTACGCTCCCTCCTTACCAGCATGTTACTTCAACTTCAAATCCACCACCACCCCCACCACCACCACCTCCTCCCCCACCAGCCCCCATACATCTAGCAAATCAACCTGCGGTTTTACCCAAATTTTTCACTGGTGGATTTCCACCTCAGAAAGCACCCAAACCTTCATGTGGCATTCTTCCAGTATCCCCAGTAGCTCCAGCACTT
Associated Phenotype:
Not determined