ZMP
zgc:158419
Ensembl ID:
ZFIN ID:
Description:
rab GTPase-binding effector protein 2 [Source:RefSeq peptide;Acc:NP_001074094]
Human Orthologue:
RABEP2
Human Description:
rabaptin, RAB GTPase binding effector protein 2 [Source:HGNC Symbol;Acc:24817]
Mouse Orthologue:
Rabep2
Mouse Description:
rabaptin, RAB GTPase binding effector protein 2 Gene [Source:MGI Symbol;Acc:MGI:1917564]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15994 | Essential Splice Site | Available for shipment | Available now |
sa2121 | Nonsense | F2 line generated | Not yet available |
sa1964 | Nonsense | F2 line generated | Not yet available |
sa38390 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15994
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 |
---|---|---|---|---|---|
ENSDART00000087064 | Essential Splice Site | 19 | 483 | None | 14 |
ENSDART00000113890 | Essential Splice Site | 19 | 483 | None | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 26863684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26040552 |
GRCz11 | 3 | 26171423 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTCGGACACGNNNACRACAGCAGCCGCGTCGCGCAGTGACGAGCGTGACGG[T/C]ATGAACAACCGCTACATTATTACAGTCTGTCTSTGTKTGAAGTGTCGATG
Long Flanking Sequence:
ACAACATTCCCAACAATTTTAGTCGCAGTGTTTTGAAGAACAACTGCATCAAAACCATATAGCCTAGTTGTCAAATACAAATGTTTGGGATCGCATGTATCGCCCACATCCTCTCTGGGACTGTAGCAAAATCATGTCAGCTGCCTCTCTAGGCAGCATCACGAGCGCCTACACGAACAGCTCAGAGCTGCGCGCTCACTCTACTCTAGTGCCCTCGCTAGTGTTTGAGACACGTTGAGTGCCTGTGTGTGAGAGAGAGACTCTAGGGAGGATGGTTAGGTAACATCCGCAGGACTGAACCGGGGAAAGTTGTTTCCTGAACTCTTGGCGCAGTTTGCTGAAGGCCGGCCCTGCTGCACTGCACACAGGAAAAGGAAGACGGATGCGGGCGAAGGGAAGAATAACGAAACCAAAGGGAAATATCGAGACAAATGACGTGAAGCCATGGAAGTGTCGGACACGACAACAGCAGCCGCGTCGCGCAGTGACGAGCGTGACGG[T/C]ATGAACAACCGCTACATTATTACAGTCTGTCTGTGTGTGAAGTGTCGATGTAAACACATTTTGGCGATCATTCCGAGATGTGTTGCGATTATATTAGCTAGGAATGGTCAGTTGAGCTCTGAGGGCAAATGTCTGACCACGTAACGCTGGCTCTTAAAGCGCACGAGCTGCATCATAGCACATATGCATTAATAACAGTTGTGAACGCGGGTTGATTTTGGGTCACTCTTGTATTTTATTAAAGAGCAGCAACAGCTAAATAAATTGATGAAAAAATGGAGGAAAAACAGTTCTGCAGAGGTCAACAGGTGTTTTCGACTATAATCAGAATAAGACACTTGACATGGTGTGTGTAGAATTTAAACCTTAAATAGCATTAGACATATTAAACCCTGCTCTTTTATGGTTTATCTGCTTTTGGCAAATTCATCTCGTTAATAGAGCTCCATCATGAGTGTCTCTTATCTGTCACGCACCTGTATTCACACATAATGCAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2121
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087064 | Nonsense | 288 | 483 | 6 | 14 |
ENSDART00000113890 | Nonsense | 288 | 483 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 26870471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26033765 |
GRCz11 | 3 | 26164636 |
KASP Assay ID:
554-3278.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCAAGATCTACAGAAATCTTTTAGCATGTCACAAAATGCTGTTCAGTG[C/A]AGATTGGTGAGYAGCATGTGACTRAACCAATYAGAAGCTAGCATTAGCAG
Long Flanking Sequence:
ACTCTAATATGACAGTGCATGCACTATACGTACACACATTTCTGTCCAAACAGCTTACAAAAGTCAATTTTCATCATAGGTACCCTTTGAAACACAAAAGACTAATTTAAAATGTTTTTAAATATACAGTCAAGCCCGAAATTATTCATACCCCTGGCAGATTCAGACTTAAATTTACTTTTATTCAACCAGCAAGGTTTTTTTTTTTGACTGGAAATGACTACACAGGCTTCTCCCAAAACATAAAATGATACACAAAAGGCATAACTATGAAAAAAAATAGATAATAAAAGTTAATAAATAAATATAATAGTTTTACTAGAACCTTGACATAGCATGTCTGCAGAGGATTTCTTTCTAAATAAACACTTGTATATTAATATATCTGCGTGTTCTTGTCTATGGCAGTTGTCAGTGCTTCAGTCTCAGGTGCAAACTTCTGAAGCCCTCCTTCAAGATCTACAGAAATCTTTTAGCATGTCACAAAATGCTGTTCAGTG[C/A]AGATTGGTGAGTAGCATGTGACTGAACCAATCAGAAGCTAGCATTAGCAGGATTTCCGAGCTACTACCCTGATGAGATCACACGCTCTTTATGAAACTTTTTCTTTGTGCATTTTCTCCACTCAGGCAGAGCTGTCTTACTCGCAGAAGAGAGTCTGTAATGAACTCTCCAAGCTGAAGGGAGAAGACGGTGACGTGGATGAAAAAACCGAGAACAGCCTGCCACCCCCCAGTCCAACACTAGAGGTAAACGAGTGTGTGAGTGTACGTGGATTTGTTGAAAGGTGTGGAGGAACTGAATGGTGTGTGTTTTTCTATTAATGTGTATCTCTATAGGCAGCTCACTGTGAAGAGAGGCTTCGTATTGAAATAGTCAACCTACAGGAACAGCTGGAGACGCGCACAGAGGAGAGCGGTCTGTCTATATTGTTACATATTTATTTACATATATTTTTATACTAAATGTTTTACAGTGCGTATAAACTATACACATGGGAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1964
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087064 | Nonsense | 298 | 483 | 7 | 14 |
ENSDART00000113890 | Nonsense | 298 | 483 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 26870618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26033618 |
GRCz11 | 3 | 26164489 |
KASP Assay ID:
554-0293.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTTTCTTTGTGCATTTTCTCCACTCAGGCAGAGCTGTCTTACTCGCAG[A/T]AGAGAGTCTGTAATGAACTCTCCAAGCTGAAGGGAGAAGACGGTGACGTG
Long Flanking Sequence:
ATACCCCTGGCAGATTCAGACTTAAATTTACTTTTATTCAACCAGCAAGGTTTTTTTTTTTGACTGGAAATGACTACACAGGCTTCTCCCAAAACATAAAATGATACACAAAAGGCATAACTATGAAAAAAAATAGATAATAAAAGTTAATAAATAAATATAATAGTTTTACTAGAACCTTGACATAGCATGTCTGCAGAGGATTTCTTTCTAAATAAACACTTGTATATTAATATATCTGCGTGTTCTTGTCTATGGCAGTTGTCAGTGCTTCAGTCTCAGGTGCAAACTTCTGAAGCCCTCCTTCAAGATCTACAGAAATCTTTTAGCATGTCACAAAATGCTGTTCAGTGCAGATTGGTGAGTAGCATGTGACTGAACCAATCAGAAGCTAGCATTAGCAGGATTTCCGAGCTACTACCCTGATGAGATCACACGCTCTTTATGAAACTTTTTCTTTGTGCATTTTCTCCACTCAGGCAGAGCTGTCTTACTCGCAG[A/T]AGAGAGTCTGTAATGAACTCTCCAAGCTGAAGGGAGAAGACGGTGACGTGGATGAAAAAACCGAGAACAGCCTGCCACCCCCCAGTCCAACACTAGAGGTAAACGAGTGTGTGAGTGTACGTGGATTTGTTGAAAGGTGTGGAGGAACTGAATGGTGTGTGTTTTTCTATTAATGTGTATCTCTATAGGCAGCTCACTGTGAAGAGAGGCTTCGTATTGAAATAGTCAACCTACAGGAACAGCTGGAGACGCGCACAGAGGAGAGCGGTCTGTCTATATTGTTACATATTTATTTACATATATTTTTATACTAAATGTTTTACAGTGCGTATAAACTATACACATGGGAACATAATTAATCCCACTGGTGCTTGAGCCACAGAAAACTTTTTTATTTTATTTTGCTTTTCATCATTGCTCAAGCACAGTATTAATTCATCCTCAAGTGGTTCCAAACCTTTCAGGTTCCTTTTTTCTGCTGAACACAAAAGAAGATATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38390
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087064 | Essential Splice Site | None | 483 | None | 14 |
ENSDART00000113890 | None | None | 483 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 26877591)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26026645 |
GRCz11 | 3 | 26157516 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACATGGAAAATGTGCAGAGCTGGTGGTCCTCCAGGAACTTGGTTGAGA[A/G]ACACTGCTTTAGAGTAAATTCATTATGACTTTGCACAGCATAAGTGCATT
Long Flanking Sequence:
TAAGATTGTTCAGTGATGAGCAATCAAATTTTTATGTTACTATTAAAATATGGCATTAATTCTTTTAGTTAAAATCTTAACATGTTACATGAGATGCAAACTTTTTCTAAAAATATTTTAAGGACCGTTTGTTGACTATTCTAGTGCCCTATTTATTTGTTTTAAAGAGTGCATCTTTTAATTCATACCATTTTTATTCATAACTAGTGTTACAATTGCTCCTAGCTTCTGAGTCAGGATAACTGTAATGATAGCTAGTTATTAATGCTAGCCACCAGCGAGCAATAACCAAGAAATTAAATATATGCGTTAGATCAGTGTTTCTCAACCACGTTCCTGGAGGACCACCAACACTGCATGTTTTAGATGTCTCCTTTGTCTGTCACACCCAATACAGCTCTTTCAGTCTTTAATAAGCTGATGATCTGAATCAGGTGTGTTTGGTTAGAGAGACATGGAAAATGTGCAGAGCTGGTGGTCCTCCAGGAACTTGGTTGAGA[A/G]ACACTGCTTTAGAGTAAATTCATTATGACTTTGCACAGCATAAGTGCATTTCACATCTACAAATATTTGAGTTTATTGAATCTGTCACTCAAAGTGAAATATTCGTATTGTTCTCAGGCTAAACTGAACTGCTTTCATCACTCTAGACTGAATATTTTTTGTGTAAATTTTACTCTTAGTGTAATACTACCTACTGAACACTGTAATGAGATTTGCATCGAGTTTATGGCCAAAGTCACTTTATCAGAAAGAGGTCTAGTTTCATTTTGATGTATCTGGTGCCTGAGCCAATGAGCAGTGGAAGATCAATTTGGTGATGAAACACTAAATCTATTTGGGGCTAATACATGTTAATGAAGTGCTATGAATGCAGCACCATGTTAGAAACAATTCTGAATGAATTGTGTATGTATAAAACAAATAAACTAAAAGACTGTAACAGACAAGGCTTGTTTTATACACATCTTTATTTTAAGAATAGCATTTTCATTAGAATATAC
Associated Phenotype:
Not determined