ZMP
zgc:175145
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100170821 [Source:RefSeq peptide;Acc:NP_001124128]
Human Orthologue:
RAP1GAP2
Human Description:
RAP1 GTPase activating protein 2 [Source:HGNC Symbol;Acc:29176]
Mouse Orthologue:
Rap1gap2
Mouse Description:
RAP1 GTPase activating protein 2 Gene [Source:MGI Symbol;Acc:MGI:3028623]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23979 | Essential Splice Site | Available for shipment | Available now |
| sa10392 | Essential Splice Site | Available for shipment | Available now |
| sa10469 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23979
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 |
|---|---|---|---|---|---|
| ENSDART00000111571 | Essential Splice Site | 244 | 696 | 9 | 23 |
| ENSDART00000127181 | Essential Splice Site | 270 | 722 | 11 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 29813735)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 31013986 |
| GRCz11 | 21 | 31050681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTAAACAACACCTTCAAGTTTGGTGTCATTTACCAAAAGTTTGGGCAG[G/A]TGAGGACATTAATGCTGAATGTGTGTAGTTTTTGTACCATTATAAATACT
Long Flanking Sequence:
TTAACTGTTATGTTTCCTCAGTCATTTCAATAATGCTTTTCAGGCACACACTGGATTCAAAGAAATTCGTTAAATTGTATAAATGTTTGTTTGTTTGTATTTTAAGAAAATACAACTCTTTTTAAGCAAACATTTCGTTAAAAAGTGACAGTTAAGCAATATAAACACATTGGAAAGACTTTTTGGGATACCAATGTTTCATTTTAAAATATTAGATTCATTTTTAATAGTTATAATTACGTGTGTGATTATCCTTCAGATTTGTTTTTATGAGCAAGTCTGTAGGGGCATTGCAAATGTCATTAACACTGTATTGCCTCTCACAGAGATATTAATTCCTCATTTAAAAAACTTGTTACGTGCTTTAAAATAGCCAGAGTGTTATCTTTATATATTCTTGTTCTTGTTTTTTGCAGGGCTCTCAATTAATAGTGAATTATGATGAGCATGAGTTAAACAACACCTTCAAGTTTGGTGTCATTTACCAAAAGTTTGGGCAG[G/A]TGAGGACATTAATGCTGAATGTGTGTAGTTTTTGTACCATTATAAATACTAAAACCTGGCTGAAGTACTAAAGGACACTTTCAGCTTTCTTATAAGGCTTTCCTCTCTAATCTTATCTGAATCACCAAAGCAATGCATCAATAAGTAGCTGCTGTATGTGTGTTATTTTATACTTTTACTTTATCTTATCACACTCCCTTGCCTTCCTGCTGTTTCACCTGTTGTTTACTAGTCTGTGATGTTTTCTGATACTCTGTGCTGTCCACAGACTTCAGAGGAGGAGTTGTTTGGGAACAGCGAGGAGACGCCGGCCTTCACAGAGTTTCTCCGAGTGCTGGGAGACTGTGTCCAACTGCAAGACTTTAAAGGGTATATAAAAAAAAGAGTTGATAAATAAAATATGAATGTGATTTGTTGGGATGTGTGCAAAACAGCACATTAACTGGCCACTTTAAGAGGTGCACTCTGCATGATAGGACTAGGTGTTATAATCTAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10392
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111571 | Essential Splice Site | 322 | 696 | 12 | 23 |
| ENSDART00000127181 | Essential Splice Site | 348 | 722 | 14 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 29804546)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 31004797 |
| GRCz11 | 21 | 31041492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAAYWTTAGAGATAAAACGTGACTCTATTCTTTATCCTGTAAATGCTCT[A/C]GCTCCAAAGGAAGCGTCACATTGGGAATGACATTGTGGCTGCAGTTTTTC
Long Flanking Sequence:
TCTGTTTTAATCATTATTTTAGTGTAAAATATGGCATTTCTAATTTGCTTTATTCGTTTTTTTAACTATAGTTTTTTTTTTTTTAGTGTGTGATTTCTCCACAAAGAATCATTAAATTAGTTGTTTCATCAGCTTACTCTTGTATATTTCATACCTCATTTTCCCACTCCTGATCTTCTATTCAGGTTTCGAGGGGGGTTGGATGTGTCTCACGGTCAGACGGGTTCTCAGTCGGTCTACACTGTGTTTAAAGGACAGGAACTAATGTTTCACATCTCCACCAAGCTACCATATATTGAGGGAGACACGCAGCAGGTGCTCACTGAAATTGACATTTTCATAAGTAAATCCACCATAGGGCTGTAAAACATTATTTTTCGAAGTCATAAATAAAACTTTAAGTCTTTATTACATTTTTCTGTGTGAAAATAGATTTTATATCAATTTTTTCTAACATTAGAGATAAAACGTGACTCTATTCTTTATCCTGTAAATGCTCT[A/C]GCTCCAAAGGAAGCGTCACATTGGGAATGACATTGTGGCTGCAGTTTTTCAGGAGGAGGCCACACCTTTTGTGCCTGACATGATCGCTTCCAATTTCCTCCACGCTTACATTCTCGTTCAGGTGGAGAACTCTGGAACAGATGAAGCCACATACAAGGTAAATCATCAAAATTTATTTTGTAAAATATCTGGGTAAAAGGTTTTAATAAATACAAGATTGTATAATTTGTTTATTTTTTCAATGGGGAGTGTAATTTTTACTTTTTGATTTTATTAGACCAACTTGTCATTTTAATTAAAGAATCTAATCATGTCACTCTTTTCATTGTAATTGGAAGTTGTGATCATATGATGCAGGTGTCTGTCACAGCACGTGAAGATGTGCCGCAGTTTGGCCCTCCGCTTCCTAATCCGCCTATTTTCAAAAAGGTAAACAAGACAGTGTCCCACTACTGCTGCTAAAATCTAATCATGCTTCAGATTATCATTAAAATTATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10469
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 |
|---|---|---|---|---|---|
| ENSDART00000111571 | Essential Splice Site | 523 | 696 | 16 | 23 |
| ENSDART00000127181 | Essential Splice Site | 549 | 722 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 21 (position 29796133)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 30996384 |
| GRCz11 | 21 | 31033079 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCGGAGTCAGTCTGACGCACAGCAGCTCTGAGGCCGCAAAAAACTCAG[T/C]GAGCATCTWATTACATTCACACAGATAAACCACATCTGAACAGCTAAATT
Long Flanking Sequence:
ATTATTAATTTAACCTAATTGTCTCATGTTCAGTCTACCTTAATGTGTAAAAATGATTAAGTTAGCTTGATCAATTTGTGTTGGGAAAACACAAAGCAATTGTGTGGAACCCAGCATTTTTTACATTGTAGTGTGAAATCATTCAATTTTGGGGGAGAACTGTCCCTTCCCTGTTGTATGCTGTGGCAATATTTACAAGCGGTATCCAAAATGGTATCGTCATACATCAATACTTTTTAAGGTATCATATGGAAGTTAGGAATTCCAGTATCGTGACAACACTAATCTAAAATAACATGTCATTTCAATTCTTCTAAATGTGTGTGTGTGTTTTTTATTTGTGTGTCAGCGGGCGATGCGTGTGCGCAGTCACTCAATGGAGACGATGGTGGGCACCCACAAACATGGCCGCTGTTCTCCAGCAGCAGGAGCAGGAGTTCCTACAAGCCTGAGCGGAGTCAGTCTGACGCACAGCAGCTCTGAGGCCGCAAAAAACTCAG[T/C]GAGCATCTAATTACATTCACACAGATAAACCACATCTGAACAGCTAAATTAATATGGGAACGGGCAGCCTCAGTGTAATAACATTGGGGTTCGCTTTAATTATCTGGTTATGCTTTATTTTGATGGTTTCCCAACAGACTTTCTACTGACTTTGCAACTATGTCAACTTACTCTAGCTAACAATTACTCTAATGACTGAAAGCAGACATGTTCAGTGCTTTCACTAATATTGGTGCCCTTAGTATATGAGCAAATAAGGTTGGGGAAGGCGAGGCAGTGGCGTAGTAGGTAATGCTGTCGCCTCACAGCAAGAAGGTCGCTGGGTTGCTGGTTCGAACCTCGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTCCTCCGGGTGCTCCAGTTTCCCCCAAAGACATGCAGTACAGGTGAATTGGGTTGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGTGGATGATTCCCAGAGATGGGTTGCGGCT
Associated Phenotype:
Not determined