ZMP
zgc:153898
Ensembl ID:
ZFIN ID:
Description:
zgc:153898 (zgc:153898), mRNA [Source:RefSeq DNA;Acc:NM_001077555]
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39055 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32040 | Nonsense | Available for shipment | Available now |
sa22667 | Nonsense | Available for shipment | Available now |
sa35910 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2799 | Essential Splice Site | F2 line generated | Not yet available |
sa18310 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39055
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 |
---|---|---|---|---|---|
ENSDART00000099895 | None | None | 472 | None | 15 |
ENSDART00000126559 | Nonsense | 32 | 700 | 3 | 23 |
ENSDART00000137817 | None | None | 629 | None | 19 |
The following transcripts of ENSDARG00000061551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 28619129)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29337159 |
GRCz11 | 15 | 29270035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGGAAACAAGAGTTGCTGACCATCTCCAGTGTGCCTCTGGGAGAATG[T/A]CCACCTTCACCTCCCCGCACTGCACCCCCCACCATGAAGGTGAGTGTTCA
Long Flanking Sequence:
CCTAAACAAAGAAAAAGCACAGAACAGACTCACGTTTAAGAGCGAGGGGAGGCCCCTGGTAGTTCGGCGGTAAGGGATGCGTATAGGGAGGCTCGGCTCTTTAATGTTTATTTGCCACCCTTCAGAGAAAGACTGAAAGTATGGAAGAAATACGGGAAAAAACCTTTACGGAATGATAGCTTGATAGAACTGTAAAATATGGGAGAAAAACGGGAGGGTTGACAGGTATGACTTGTTGTAAACTATATTTTTACTTATTCTTCCACTTGTTTACTTGATATGCAAAGCTAAAAACCATACACAAAATACAGACGCATCAGTCAAGATAGGTAGTTTATTTGCTTCTGCGAATGAGAGCTAGTCTTCAGTGCAAAAAACAACTTTAGATCAGGTTAGTCTTCCTCATAAAGTGCTTACCATTTGCCTGACTGACCCTATATGTGTGTTTTTTTCAGGAAACAAGAGTTGCTGACCATCTCCAGTGTGCCTCTGGGAGAATG[T/A]CCACCTTCACCTCCCCGCACTGCACCCCCCACCATGAAGGTGAGTGTTCATATGCACACTCATACACACTGGGTTTTCATGATTGATAGGGACTTCCCAGTGAAATAATGGTTTTTATACTGTACAGACTGTATAAGTTGTCCTCTTATCCCGACCCTAACCCTAAATTCAACTCTCACAGAAAATAATCTGCAGTTTTATTTTTTAAAAATGCTTCATTGTGTGTAATTAATCTGCTGGTTTCATCATGGGGACCAAAATAAAATTTCCCCACAAGGGTAAAACTTACTGGTATGACTGGTATATTTGTGGGGACATTTGGTCACACACATATACACACACACACATACACACTCTCACCGCTCCATTAGCTGTGGTTAGCCCAGATTTGCTGCATTCACCTCTGGACCAAATTAACCTCTATTAGCACTGATAGCGCGTGAAAGTGCGATTGCCCTTTGTAGCACACCATATAAAATGACCCTAGTTTGGCTACAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32040
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099895 | Nonsense | 71 | 472 | 4 | 15 |
ENSDART00000126559 | Nonsense | 122 | 700 | 6 | 23 |
ENSDART00000137817 | Nonsense | 65 | 629 | 2 | 19 |
The following transcripts of ENSDARG00000061551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 28643594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29361624 |
GRCz11 | 15 | 29294500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCTGTGAGGAGGAGAATGATGATCTGAGTCCCAGTGGAGGAGGAGGT[G/T]GAGGAGGATTCGGATACAGGATGGAGTGTAACAGCACGTCACGAGCCTAT
Long Flanking Sequence:
GTAATAACATACAGTATACAATGAAATGACGCTGACACATTTTGGTGAAAACAACTATTAGACTGAGAAGTTTAGATCAGCAAGATATATTCACTTGGAAATTTTGCTAAATGTAGGCTATCTTGATCATTTGCAAAGATGTACGTATACATTTGCAATTTGATGGAATTAATGAGAATTTCAAATCTGTTGTGAACAATTGCCAAGTGGTTTGGCGGTTTGTCCATATTGTTTTGAGAATGTAATTTCTGTTTTAAGAAATGAGCAAAAACCAATGGAGAACAACTGTAAATAGTGTTATTGAGTTGCTGATGCTTTAATTCATCATATTCACTGTCTAGGTGCTGGAGAAGGGTGGTCCATACCCTCAAGTTATTTTACCTCAGTTTGGGGGGTACTGGATTGAGGACCCAGAGGCTCCAGTTGGGACGCCTACATCCTCAGACAGCAGCTTCTGTGAGGAGGAGAATGATGATCTGAGTCCCAGTGGAGGAGGAGGT[G/T]GAGGAGGATTCGGATACAGGATGGAGTGTAACAGCACGTCACGAGCCTATCGCAAACACTTTCTTGGAAAGGTGAGGTTGCATTTGTTAGTGCTTAAAGTAGATTCATCTTCTATGATTTAAAGGAACTGTTCACTGAAAATTGAAAATTGTGTTTGTCAGTTACGCCCCCTTCAGTTATTTTAAAGCAGTTTGACTTTCTTCTGTTCAAGAAAAATGAAGTTATTTTGAAGAAAGCTGGAATACTGTAAATATTACCTTTCATTGTATTTGTTTTTCCTACTGTGGAAGTCAGTGGATACAGGGTTTCCAGCTTACTTCAAAAATATCTTCTTTTGTGTTGAAGCTCATAATAAATAGTAAGTAAATGTTCTAATCCAATCCTTCAAATGCTCTATATTACAAATTCATTTTACTTTTACTTGATAATAAATCAAGAAAACAATTTTGACATTCACTGTTTAAATGCTTATTTTTCAACAACACACTTGAATATTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22667
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 |
---|---|---|---|---|---|
ENSDART00000099895 | Nonsense | 85 | 472 | 4 | 15 |
ENSDART00000126559 | Nonsense | 136 | 700 | 6 | 23 |
ENSDART00000137817 | Nonsense | 79 | 629 | 2 | 19 |
The following transcripts of ENSDARG00000061551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 28643636)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29361666 |
GRCz11 | 15 | 29294542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGGTGGAGGAGGATTCGGATACAGGATGGAGTGTAACAGCACGTCA[C/T]GAGCCTATCGCAAACACTTTCTTGGAAAGGTGAGGTTGCATTTGTTAGTG
Long Flanking Sequence:
TGGTGAAAACAACTATTAGACTGAGAAGTTTAGATCAGCAAGATATATTCACTTGGAAATTTTGCTAAATGTAGGCTATCTTGATCATTTGCAAAGATGTACGTATACATTTGCAATTTGATGGAATTAATGAGAATTTCAAATCTGTTGTGAACAATTGCCAAGTGGTTTGGCGGTTTGTCCATATTGTTTTGAGAATGTAATTTCTGTTTTAAGAAATGAGCAAAAACCAATGGAGAACAACTGTAAATAGTGTTATTGAGTTGCTGATGCTTTAATTCATCATATTCACTGTCTAGGTGCTGGAGAAGGGTGGTCCATACCCTCAAGTTATTTTACCTCAGTTTGGGGGGTACTGGATTGAGGACCCAGAGGCTCCAGTTGGGACGCCTACATCCTCAGACAGCAGCTTCTGTGAGGAGGAGAATGATGATCTGAGTCCCAGTGGAGGAGGAGGTGGAGGAGGATTCGGATACAGGATGGAGTGTAACAGCACGTCA[C/T]GAGCCTATCGCAAACACTTTCTTGGAAAGGTGAGGTTGCATTTGTTAGTGCTTAAAGTAGATTCATCTTCTATGATTTAAAGGAACTGTTCACTGAAAATTGAAAATTGTGTTTGTCAGTTACGCCCCCTTCAGTTATTTTAAAGCAGTTTGACTTTCTTCTGTTCAAGAAAAATGAAGTTATTTTGAAGAAAGCTGGAATACTGTAAATATTACCTTTCATTGTATTTGTTTTTCCTACTGTGGAAGTCAGTGGATACAGGGTTTCCAGCTTACTTCAAAAATATCTTCTTTTGTGTTGAAGCTCATAATAAATAGTAAGTAAATGTTCTAATCCAATCCTTCAAATGCTCTATATTACAAATTCATTTTACTTTTACTTGATAATAAATCAAGAAAACAATTTTGACATTCACTGTTTAAATGCTTATTTTTCAACAACACACTTGAATATTAATAAAAAAAAAACAAAAAAATAAAAATAAATAAATAACATGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35910
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099895 | Essential Splice Site | 201 | 472 | 8 | 15 |
ENSDART00000126559 | Essential Splice Site | 252 | 700 | 10 | 23 |
ENSDART00000137817 | Essential Splice Site | 195 | 629 | 6 | 19 |
The following transcripts of ENSDARG00000061551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 28646376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29364406 |
GRCz11 | 15 | 29297282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGAACAACACTTTCAAGTTTGGAGTCATTTATCAGAAGTTCGGTCAG[G/T]TGAGAGTTGCTTTCTTCAGTTTCAGACTTCCTCCTTTTCTCATTTATTCT
Long Flanking Sequence:
GATGTGAGTTGTTGAAATCGAATGTGTCCCGTGTGTTTCAGCTGCTCTGCGATGATGTCACAGGCCTGAAGTTCAACCCCGTTCTCTACCCCAGGGTGAGCATCTCTCAGTTTCTCTCTCACTCCATCTGTGACTTACCTACTCCAGGCATCAGGGTGAACCGGGGCTCCGTTTGCTCCGTTTCACCCTAGTACCCGGCTCATCTGAATTAATATGTTCCTGAGCTCCAGGGGACTCACAAATCCATCTGCTTCACAGCGCCTCGGTCTGCCTTAGAGAAGCCTTGACCATCTCAAGGCTTCGCCGAGGTCTCTCAGGCATGGCGAACACAAATGCCTGAATTATGGAAAAAGCACTGACACACATATTTACCCCTGCAGGCGCTCTCGCTCACTTTCTGCTTTCTCTTGCCCAAGGCTTCGCAACTGATCGTCAGCTTTGATGAGCACGAAGTGAACAACACTTTCAAGTTTGGAGTCATTTATCAGAAGTTCGGTCAG[G/T]TGAGAGTTGCTTTCTTCAGTTTCAGACTTCCTCCTTTTCTCATTTATTCTCCTTTTTTTTTATTGTTATTGTCTCTTCACATCAGACATCAGAGGAAGAGCTGTTCGGGAACAACGAGGAGACGCCTGCATTTGCTGAATTCCTCAGTGTTTTAGGAGACAACATTGAATTGCAGGATTTTAAAGGGTGAGAGACGGAGATTGAACTCTGAAAAGTGCTGCTCAGGATCACCTGTTCACACTATAAAGGCCTACTTTAAAGTGTATTCATAGAGGCCGCTTGTGAATAATTTATTTAATTTAGCCATTGTACTTGATTTTGGCAGGATGTCTGCTTTCGGTTATCAGATTGATTTGCATGAGCTTCTGCTGAACTCTTTTGTCTGGTGTGTTATGTACAGGTTCAGAGGTGGTCTGGATGTGTCTCACGGACAGACGGGATCTGAGTCTGTATATACTACGTTTCGTCAGAGAGAAATCATGTTTCACGTTTCCACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2799
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099895 | Essential Splice Site | 330 | 472 | 11 | 15 |
ENSDART00000126559 | Essential Splice Site | 381 | 700 | 13 | 23 |
ENSDART00000137817 | Essential Splice Site | 324 | 629 | 9 | 19 |
The following transcripts of ENSDARG00000061551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 28650669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29368699 |
GRCz11 | 15 | 29301575 |
KASP Assay ID:
554-2844.1 (used for ordering genotyping assays)
KASP Sequence:
CATATTAGTGCAGGCAGAAAACCCTTGCACCGATCACACAACATACAAGG[T/A]TTGTCAACAAGCAGCTCACTTAATTACATCCAGATGGCCATCAATCCCTT
Long Flanking Sequence:
CCACAATGCAAATGTATTGTTATATACACATATATAAAAGAAATATGTATAAAAACCAATATAAAGCAATGCATAACGTTTTGGATTAAGTGGCTATATTTATTTGTACCATTTCATTTGTACATTGTATTACTATTTGCTCTTCCCCCAGTGATAGGTAAGTATAGGGGTGGGGTTTGTGGGCATGTCTCCCTTTAAAAATTGTATGTTTTCATATGCCATTTTACTAACAATACATAAAATAGTTACATTTCCTCGTGAGATCATGCTGGTATAAACATCAGTACCTGTTTGTTGAACCAAATACAATCGAAATATTTAGATGTAAATATCTCTCTCTCAGCTCCAGAGGAAGAGACATATTGGCAATGACATAGTGGCAGCCATCTTCCAGGAAGAGCCCACGCCATTTGTGCCTGATATGATCGCATCCAACTTCCTTCATGCCTACATATTAGTGCAGGCAGAAAACCCTTGCACCGATCACACAACATACAAGG[T/A]TTGTCAACAAGCAGCTCACTTAATTACATCCAGATGGCCATCAATCCCTTAACAAACACTGATCAGAGAAATTGACCGGTGTTCACAGGTGTCCGTCACGGCAAGAGAGGACGTCCCACCATTCGGCCCCCCTCTGCCAAACCCCTCAGTCTTTAAGAAGGTAATGTTAGAAGACTAGTTCTAGTGAAATGTGGCAGCAGATGATGATGATGTGTGTAGACCATTTTGAGGGATGTAAACAAAAACAATGGTCCCACCGTATTTCCTGTTTTACATTTTTAATATTTTATATATACATTTCTATAGCTTCCGAAAATCCAAAGAGAGCCACATATTGATGAATAATGTTATGATAGCTGTTTTAACATTAAGTTATGATTTAACTGCCTCTTCCTTCAGTTTTAATAACAAGCAGGAAATGTTTATGGGCAAATGACATGACTGCATTGAAATGGTCTATTATAAAATGATGGCTCAATTCTTCCGCAGGGTCCTGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18310
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 |
---|---|---|---|---|---|
ENSDART00000099895 | Essential Splice Site | 354 | 472 | 12 | 15 |
ENSDART00000126559 | Essential Splice Site | 405 | 700 | 14 | 23 |
ENSDART00000137817 | Essential Splice Site | 348 | 629 | 10 | 19 |
The following transcripts of ENSDARG00000061551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 28650830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29368860 |
GRCz11 | 15 | 29301736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACRTCCCACCATTMGRCCCCCCTCTGCCAAACCCCTCAGTCTTTAAGAAG[G/A]TAATGTTAGAAGACTAGTTCTAGTGAAATKTGGCAGCAGATGATGAWGAT
Long Flanking Sequence:
GTATAGGGGTGGGGTTTGTGGGCATGTCTCCCTTTAAAAATTGTATGTTTTCATATGCCATTTTACTAACAATACATAAAATAGTTACATTTCCTCGTGAGATCATGCTGGTATAAACATCAGTACCTGTTTGTTGAACCAAATACAATCGAAATATTTAGATGTAAATATCTCTCTCTCAGCTCCAGAGGAAGAGACATATTGGCAATGACATAGTGGCAGCCATCTTCCAGGAAGAGCCCACGCCATTTGTGCCTGATATGATCGCATCCAACTTCCTTCATGCCTACATATTAGTGCAGGCAGAAAACCCTTGCACCGATCACACAACATACAAGGTTTGTCAACAAGCAGCTCACTTAATTACATCCAGATGGCCATCAATCCCTTAACAAACACTGATCAGAGAAATTGACCGGTGTTCACAGGTGTCCGTCACGGCAAGAGAGGACGTCCCACCATTCGGCCCCCCTCTGCCAAACCCCTCAGTCTTTAAGAAG[G/A]TAATGTTAGAAGACTAGTTCTAGTGAAATGTGGCAGCAGATGATGATGATGTGTGTAGACCATTTTGAGGGATGTAAACAAAAACAATGGTCCCACCGTATTTCCTGTTTTACATTTTTAATATTTTATATATACATTTCTATAGCTTCCGAAAATCCAAAGAGAGCCACATATTGATGAATAATGTTATGATAGCTGTTTTAACATTAAGTTATGATTTAACTGCCTCTTCCTTCAGTTTTAATAACAAGCAGGAAATGTTTATGGGCAAATGACATGACTGCATTGAAATGGTCTATTATAAAATGATGGCTCAATTCTTCCGCAGGGTCCTGAATTCAGGGAATATTTCCTGACAAAACTGATCAATGCAGAGAACGCTTGCTACAAATCAGACAAGTTCGCCAAGCTGGAGGTGAGAAAAAGACATTCAGAAATCAACCTAACTGTTAGATTGTATTTTATATATAGGAAAAATATAAAGGATTCACTATCTGGTT
Associated Phenotype:
Not determined