ZMP
zgc:86773
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC415219 [Source:RefSeq peptide;Acc:NP_001002129]
Human Orthologue:
RAB1A
Human Description:
RAB1A, member RAS oncogene family [Source:HGNC Symbol;Acc:9758]
Mouse Orthologue:
Rab1
Mouse Description:
RAB1, member RAS oncogene family Gene [Source:MGI Symbol;Acc:MGI:97842]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24876 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa27623 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16382 | Essential Splice Site | Available for shipment | Available now |
| sa991 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24876
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078980 | Essential Splice Site | 137 | 201 | 5 | 6 |
| ENSDART00000100289 | Essential Splice Site | 99 | 163 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 27565561)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 26968355 |
| GRCz11 | 10 | 26930068 |
KASP Assay ID:
554-7365.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAGTGTGACCTGACTACAAAAAAGGTTGTGGACTACACTACCGCTAAG[G/A]TTGGTTGGTAGGGAAATAGACTGGTTAATTGCTTGGTTATTCCAAATTCT
Long Flanking Sequence:
TGGGACACGGCTGGACAGGAGAGATTCCGCACTATTACATCCAGCTACTACAGGGGCGCTCATGGGATCATCGTTGTATATGATGTTACAGATCAGGTTTGTGAGAGTTTTGAGTCATTTCTTTTTTTTTATGTATATTTGAGTGAAACTGCCTCTTGAACAAAAGACACTTGGGTGGGGTTTTTGTTAGTTCAATGGGAAGTGATTGGAATGTTGTCATTTGCTATTGGCTGATCTCATATCAGTGATGGGTTGCCCCGCCATCACAGCAGTGAACGTCATTAGAAATTATTGATAATCATCATTAGATTTTGATTACAACATTTCTGAATATTGTCAGAGAACTTTTGTTCTGGTTTTTCTTTCAGGAATCCTACAACAATGTGAAACAGTGGCTAAAGGAAATCGATCGCTATGCGAGTGAAAATGTCAACAAACTGCTTGTTGGAAATAAGTGTGACCTGACTACAAAAAAGGTTGTGGACTACACTACCGCTAAG[G/A]TTGGTTGGTAGGGAAATAGACTGGTTAATTGCTTGGTTATTCCAAATTCTGTCATCATTTACTTATCCTCATTTTATTCCAAACCCATTGGACTTTTGTTCATCAAAAACCAAACAAAGACCTTTCTGTTTTTTAAACTATGTGAATTGAGTTTTTAATTAATCTGTTCTTCAGATAAAGCGATGTTTCTCTTTAGAAGTGTGGAAATAATCACTCGATCCATGTAGATATGTATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTACATATTAGTTTTAAAGGAGCGCTCTACTTTTTTTTTTTTTTATTAAATAGGCTCACTTTCCAAGTCTCCAGCGCCCAGTTTTCAAAAAATTTAATGAGGGTCAAACTGGTCCATATTTGGAAATCCCATGTTTTGCTATTCATGATTAACTGATCTATCTTACTCTTATGATGTTTTAAAAGGAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27623
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078980 | Essential Splice Site | 137 | 201 | 5 | 6 |
| ENSDART00000100289 | Essential Splice Site | 99 | 163 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 27565562)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 26968356 |
| GRCz11 | 10 | 26930069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGTGTGACCTGACTACAAAAAAGGTTGTGGACTACACTACCGCTAAGG[T/G]TGGTTGGTAGGGAAATAGACTGGTTAATTGCTTGGTTATTCCAAATTCTG
Long Flanking Sequence:
GGGACACGGCTGGACAGGAGAGATTCCGCACTATTACATCCAGCTACTACAGGGGCGCTCATGGGATCATCGTTGTATATGATGTTACAGATCAGGTTTGTGAGAGTTTTGAGTCATTTCTTTTTTTTTATGTATATTTGAGTGAAACTGCCTCTTGAACAAAAGACACTTGGGTGGGGTTTTTGTTAGTTCAATGGGAAGTGATTGGAATGTTGTCATTTGCTATTGGCTGATCTCATATCAGTGATGGGTTGCCCCGCCATCACAGCAGTGAACGTCATTAGAAATTATTGATAATCATCATTAGATTTTGATTACAACATTTCTGAATATTGTCAGAGAACTTTTGTTCTGGTTTTTCTTTCAGGAATCCTACAACAATGTGAAACAGTGGCTAAAGGAAATCGATCGCTATGCGAGTGAAAATGTCAACAAACTGCTTGTTGGAAATAAGTGTGACCTGACTACAAAAAAGGTTGTGGACTACACTACCGCTAAGG[T/G]TGGTTGGTAGGGAAATAGACTGGTTAATTGCTTGGTTATTCCAAATTCTGTCATCATTTACTTATCCTCATTTTATTCCAAACCCATTGGACTTTTGTTCATCAAAAACCAAACAAAGACCTTTCTGTTTTTTAAACTATGTGAATTGAGTTTTTAATTAATCTGTTCTTCAGATAAAGCGATGTTTCTCTTTAGAAGTGTGGAAATAATCACTCGATCCATGTAGATATGTATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTACATATTAGTTTTAAAGGAGCGCTCTACTTTTTTTTTTTTTTATTAAATAGGCTCACTTTCCAAGTCTCCAGCGCCCAGTTTTCAAAAAATTTAATGAGGGTCAAACTGGTCCATATTTGGAAATCCCATGTTTTGCTATTCATGATTAACTGATCTATCTTACTCTTATGATGTTTTAAAAGGAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16382
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 |
|---|---|---|---|---|---|
| ENSDART00000078980 | Essential Splice Site | 138 | 201 | 6 | 6 |
| ENSDART00000100289 | Essential Splice Site | 100 | 163 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 27567859)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 26970653 |
| GRCz11 | 10 | 26932366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAATTTGATGTAAAGTAACTNNAAACACAAAATTCYTCTCTCTCCWCA[G/A]GAATTTGCTGACTCTCYTGGCATCCCTTTCCTTGAGACGAGTGCCAAAAA
Long Flanking Sequence:
ATTAGCATCACTCTTAATATATTAATAATTTTACCATTTAAAGCTTTACCATTAATGATCAACAGACTTTGCTGCTATACCATGGCTGCAGTGGGCACAAGGGTATTATGCACAGCCTAAAAATAGCAGTCCCCAGCTAGGGAACAGCATTGCATAATGCATTGTACAGCAGCAAAAATCCTTGATTGTTACCTTGATTTATTATCCAAGGGTCTTACAAGTTTGAGTGAGATGCTAATGGTCTAATCCAATACGGCAGTTTTAAAATGAGCCTTTTTCAAAAAAAAAAGGAAAAAATTACCCCTTTTAAAGGGTCATTTTTTTAAGTAAACAGACTTTCAATGGCAAGAATATTTCAGGTTTGTGTTTCAAATATGAACAAAAATCTGGAAGAAGGAAGCAAGTGATGACAGAACGTTCTTTTAAAGGTGAATTGTCATGTTCATGCAAAAGAATTTGATGTAAAGTAACTAAAAACACAAAATTCTTCTCTCTCCACA[G/A]GAATTTGCTGACTCTCTTGGCATCCCTTTCCTTGAGACGAGTGCCAAAAATGCCACAAACGTGGAGCAGGCCTTCATGACCATGGCAGAGGAGATAAAGAAGCGCATGAGACCAGGAGCTTCAGGGGGCTCTGAGAAACCTGACCTTAAAATCGAAAGCACCCCGGTGCAACAGTCAGGCGGCGGCTGCTGTTAGAAAACTCTTGTTTTCTCAGGGAGAGTGTGAGGAGCAGGACGGGACACCGGGGAAGATTGTGTAGAGGTGGCCAATCTGGATATCAATGAAAGACTTTCTCCTATGTGGTGCTCAATAAAGTCAGAATACATTACGGTTGTTTAACATTGATGGCTCTTCCTCCTGCATCTTTATTTTTTTGTCTTGTATTTGAAAGTAAGATTAAAGCACAGGCACACACTCGTTCAGGTACTTGCCTGAATAATGAAGGTGATAATGTCCAGACCACTGTGTTAATAGCCGCTAACATTCATCCTTCTGTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa991
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 |
|---|---|---|---|---|---|
| ENSDART00000078980 | Nonsense | 195 | 201 | 6 | 6 |
| ENSDART00000100289 | Nonsense | 157 | 163 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 10 (position 27568031)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 26970825 |
| GRCz11 | 10 | 26932538 |
KASP Assay ID:
554-0895.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGGGGCTCTGAGAAACCTGACCTTAAAATCGAAAGCACCCCGGTGCAA[C/T]AGTCAGGCGGCGGCTGCTGTTAGAAAACTCTTGTTTTCTCAGGGAGAGTG
Long Flanking Sequence:
CAAAAATCCTTGATTGTTACCTTGATTTATTATCCAAGGGTCTTACAAGTTTGAGTGAGATGCTAATGGTCTAATCCAATACGGCAGTTTTAAAATGAGCCTTTTTCAAAAAAAAAAGGAAAAAATTACCCCTTTTAAAGGGTCATTTTTTTAAGTAAACAGACTTTCAATGGCAAGAATATTTCAGGTTTGTGTTTCAAATATGAACAAAAATCTGGAAGAAGGAAGCAAGTGATGACAGAACGTTCTTTTAAAGGTGAATTGTCATGTTCATGCAAAAGAATTTGATGTAAAGTAACTAAAAACACAAAATTCTTCTCTCTCCACAGGAATTTGCTGACTCTCTTGGCATCCCTTTCCTTGAGACGAGTGCCAAAAATGCCACAAACGTGGAGCAGGCCTTCATGACCATGGCAGAGGAGATAAAGAAGCGCATGAGACCAGGAGCTTCAGGGGGCTCTGAGAAACCTGACCTTAAAATCGAAAGCACCCCGGTGCAA[C/T]AGTCAGGCGGCGGCTGCTGTTAGAAAACTCTTGTTTTCTCAGGGAGAGTGTGAGGAGCAGGACGGGACACCGGGGAAGATTGTGTAGAGGTGGCCAATCTGGATATCAATGAAAGACTTTCTCCTATGTGGTGCTCAATAAAGTCAGAATACATTACGGTTGTTTAACATTGATGGCTCTTCCTCCTGCATCTTTATTTTTTTGTCTTGTATTTGAAAGTAAGATTAAAGCACAGGCACACACTCGTTCAGGTACTTGCCTGAATAATGAAGGTGATAATGTCCAGACCACTGTGTTAATAGCCGCTAACATTCATCCTTCTGTATCAATATTCATGATTTATGAACTGGGATGCGCGACTTGCTGAAGTGGTGCCTTTTCTTGTTCAGGCTTTAATGAAGATCAAGTGGTCAGCATGTGAAGCAGTGACTCTCCAGCGTCTTCGTGTAGGGTTTGTCTGTGGTTCTGTGATATTAAACAACATTGTTTAGTGTGTGTTT
Associated Phenotype:
Not determined