ZMP
robo4
Ensembl ID:
ZFIN ID:
Description:
Robo4 [Source:UniProtKB/TrEMBL;Acc:A4JYG5]
Human Orthologue:
ROBO4
Human Description:
roundabout homolog 4, magic roundabout (Drosophila) [Source:HGNC Symbol;Acc:17985]
Mouse Orthologue:
Robo4
Mouse Description:
roundabout homolog 4 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1921394]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8702 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21760 | Nonsense | Available for shipment | Available now |
sa24878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6175 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38805 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8702
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 |
---|---|---|---|---|---|
ENSDART00000004127 | None | None | 1093 | None | 19 |
ENSDART00000123267 | Essential Splice Site | 60 | 591 | 1 | 11 |
ENSDART00000145562 | Essential Splice Site | 60 | 1134 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 32257166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 31358515 |
GRCz11 | 10 | 31244855 |
KASP Assay ID:
2260-3393.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGATGCATCAGCGAGCAKCACACAGAGACYGGGCCCATCGCAGGAAAG[G/A]TAAAACWAATGGCTTTTRTTGGATTATTAAACTTAAGCATTATAATAAAA
Long Flanking Sequence:
TTGGAGGAGACAGTCCCCATCCCTCTCCTCCTCTCCCGCACTCCCAGCATGGGGCCTGAAACTTGTTTTTCAATCATTGTTTCCGCCAACTTCTTTCCCAAAAGAGAAAAGCGAGGCGAGAAAGAGGAGGGAGAGAGCGGAGGGAGCGCTAAATAAAAGAGGGAGGGAAAGTAAATACAAAGCATTTGTGGAATATAAAGAAAAAACATTCTTTATAACAATCTCTCGATAATTTAGGACTGTGGGGAGAAGGGTGGACCACAGTTGGGATGGTGTAGCGGAGGGTGCAGGGCCAGAGGAGAGGAGATTTAGGCTGAAGATGCAGGTGTCTGCATGGATGTTGTGGGTGGCATGGCTGTGTACTTGCAGCAAGGCGGTGCGCCAGTGCGCGTGCCCACCTGATGAACAGGTGGCACAGAGGTCAGAGGGAAAAGGACACCTACGCCATCGTCTGATGCATCAGCGAGCATCACACAGAGACCGGGCCCATCGCAGGAAAG[G/A]TAAAACTAATGGCTTTTATTGGATTATTAAACTTAAGCATTATAATAAAATCATTTTCTTTCTCTCCAATTTCCTGACAAATGACAAAAAGTTAAATATTTTTATGTTGCTTTAACTTATTTTAATAAGGTAATCAGGATTAATTTTTTTGAGTTATACAAAGTTTAACTTCATATTTTTAGTCAGTTTGATTAAACTAACAAATTTAAGAGGGCAAGATTTATTTTTATACTATAGTTTAGATTTAGTGAATAATTTATTACTGCAACATTTATATTAGTTTTTATTTAAAAAAAAAAAAAACAATATTTAGAAATCAATGGTAAATTTATTCAGAAATGAATGGTTTGAGCATCCGCTCGCTCTGCGTATCAGCATGGGGTCCACAGCATGAAATCAGAAAGACAGTGATAACTTGATAAACCCTTTTTTTCACTTCGTGATTTTCACTCGTGGTCACTGCTGATTTAATTTACATGTGAAAAATACAGTTGAAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21760
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004127 | Nonsense | 63 | 1093 | 2 | 19 |
ENSDART00000123267 | Nonsense | 104 | 591 | 2 | 11 |
ENSDART00000145562 | Nonsense | 104 | 1134 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 32262544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 31363893 |
GRCz11 | 10 | 31250233 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCACATTGTCGTGCAGGGCAGAGGGCAACCCTGAGCCCACCATACAGT[G/A]GCTCAGAAATGGCCAACCTCTTGACACGGACAAGATGGATGCGCAGTCAC
Long Flanking Sequence:
TTTTAAAGACACCCTCTCATGCACATGTGATTGGCATGTTTTGGCGTGCGAGTACAAAGAGACATTGTAGGACATTGTAAGTGGGCCTATAATAGCAGAGGACCATTCCTACACTTGGTGCACAGGTGACGGATGTCCTGTTGGTCTGTAACTTTGTTTGTGAGTGCTGGCCCTTTGTTCCTCTCGGAGTGGGAAAAACAGCCTGCTGCACTGACTCCATTTCCGCTCCATACAGGAAATGTGTTTCCTTTACTCATCGTGGACTCATCTAAGCACCCTACACAAAACAATTCAGAATTCATTCTCAAGATTGGAATTTGTTTAATGTATTTGATGGGTTAATGTGACTGTTTATTTTTGTTCTCCCCCAGGTTCCAGACTTGTTTCAGAAATTAACCTACCTCGTATTGTTCACCATCCTTCCGATGTGGTGGTCCGAGTGGGCAGCCCGGCCACATTGTCGTGCAGGGCAGAGGGCAACCCTGAGCCCACCATACAGT[G/A]GCTCAGAAATGGCCAACCTCTTGACACGGACAAGATGGATGCGCAGTCACAGCCTATCGTTCTACCAGATGGAAGTTTGTTCTTCTTTAGTGTGGTCCCGGGCCGGAAGGGTCAGTCCCATGAAGCGGTGTATGCCTGCATCGCTCACAACAGCATTGGAAATGCAACCAGCAGAAATGCTTCTCTTCATATAGCAGGTTTGAATAAAGTTAAGAATCAAAATTATTTTCTTTAAAAACAGATTCTGAATAAACAAAACAAAATTTCATAATTTAATAAAAGTTGTTGCAGGCTTTTGTATGGCTATATTTATTAGTTTAATTATTTTAAATTAATGATATGATATTGTTAGAGCAAAGTCGTTTTAGCATTAAAACAATACTGTCAAAAGGCTATTTACTAAACACATGCAGTGAGAAATAAAAGAACAACAGTAAATTTAAAGTAATACAATGTGATTCACTAACATTTGCAAATTACAGTATTTGCACCCTTATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24878
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004127 | Nonsense | 419 | 1093 | 8 | 19 |
ENSDART00000123267 | Nonsense | 460 | 591 | 8 | 11 |
ENSDART00000145562 | Nonsense | 460 | 1134 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 32275713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 31377062 |
GRCz11 | 10 | 31263402 |
KASP Assay ID:
554-7662.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGTGCGGCCCTACGGCAGCAGCCTGTACGGCAGAGAGAGCAACACC[A/T]GACACTTACGAGTGCCAGAGATTGGTGAGAATTACAAACAAACTACTGTG
Long Flanking Sequence:
TTATTTTCAGATGATAATCTTAATATGGAAAAAATAGGATGGGTTTCTTACACAGAGTTTTCACATTGTTGAATAGAAATCAATGGCCAAGACTCTTCAAAATATATACTTTTGTGTTCATTAGAAGAAATAAATTTATACAGGTTTGGAACTTGAGGGTCAGGAAATGGGGATTCAACTTAATTTGAGTGAATTATCTCTTTAAACACCATCAAATCATGATCAGTTCTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTCTTCTGTATAGTTGCAGTCATTTGGTTCACAGCCTCATTATCTTGAAGGCTTTGAGGTGCTGTATCGCTCTCTCCTGCCTGCCAGCTCAGACTGGACGGCTCAAAGGGTTCCTCAGCCTAGCCTTCACACCCATGTTGGACCTCTGAAGAGAGGCTACAAGTATGAGTTCAAAGTGCGGCCCTACGGCAGCAGCCTGTACGGCAGAGAGAGCAACACC[A/T]GACACTTACGAGTGCCAGAGATTGGTGAGAATTACAAACAAACTACTGTGATGATACCATAATATAAAAATGGTAAATATAAATGATTACCATTTTAATATTTTATGCCATAGTGTTTGCATGTTACTAAAAGAACTAAAAAAATAAATAAAATAAAAATGGTTGGTGGTAAATTCATGTTGTGTAGTACTGTTCAAAAGTTTAGGATTGACAAGGATTTATTATTTAAAGAAAAGGATACTTGTTTTTATACTTTTAAATGTTTTAATCATCAAATATTATGAAAAATAAAATTGATAGTGACAACACATAAATTGGTTCTGCTTTGAATTAAATAAATTACTTTTAAAAACATTAAAATGGAACATTGTCATCATACTTAAAGATATCAATGTTTTTATTATATGAAGCTGATGTATTTGTGAACATAAGATACCATAGCAAACAACTGGACAATTAAAACCCACCAGTAAGCATGTGTTGTGTTGTCAGTCCCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6175
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004127 | Nonsense | 574 | 1093 | 11 | 19 |
ENSDART00000123267 | None | None | 591 | None | 11 |
ENSDART00000145562 | Nonsense | 615 | 1134 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 32278725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 31380074 |
GRCz11 | 10 | 31266414 |
KASP Assay ID:
554-5094.1 (used for ordering genotyping assays)
KASP Sequence:
GCACCCTCCTGTGGTGTGTTTTGATGATTACTGCMGTRTTTTTGTACAGG[A/T]GACATATCAGACCAGCCAACCCTRGTGGCAAAAGCTCAGGTAATCCATAA
Long Flanking Sequence:
CCAGAGCGACCCATACAAACTGCTCATAGGTACGCTAAAAAAACAAAAGTCAGACTTTATTTTGATGGTCCGTTTGTAGAATTTAGGTTACATTGCATCTACATGCCAACTAATTGTCACTAGATTATAAGGAGACAGTTAGGTTGGAATTAGGGTTGGGATTAGGGTTAGTGTAAATTGACATGTACTTGCAAAGTTTCTTATAGACAGTTAAATATCTGTTTACCAGCAGTATTAGGCTAATATCTACTAATACTCAAATGGACAATCAAAATAAATTGTTACCAAAACTAATAATCATATTAAAGTGTATTCTGCTCAATATAATCCCTGTCTGTTCTTTTTTCCAATCAGAGTCGAGACTGGAGGCGACTCCATATCAGACAGGCATACTCAGTATGTCTCATTTCGTTAGTGTGATTAAAGAGCCGGTTTTCATAGGCAGCGTTGGCACCCTCCTGTGGTGTGTTTTGATGATTACTGCCGTATTTTTGTACAGG[A/T]GACATATCAGACCAGCCAACCCTAGTGGCAAAAGCTCAGGTAATCCATAATAAAGTGTCCATTTACAACCTTTTTCGCCATAGTAAACTTATGTCTACATTTCCTATATTTTTATATTTATTTCTAGGTTTATATAGACTGGAAAGTGAAGATCTCATCATCAAACACAGGTAAAACAATAATGATATAGTACAGTGGTGAAAATACAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTATTTTTTTTTTTGTAGTGTTTATTTTTTTTAAGCATGATGGTAAAACACGAGCACGGTTATGAATGTACTAAAACATGGGCTTGTTTGTTGTAAAAATTTATTAAAATGACAAAAAATGCTAATTTGTGTATCTCTTTACTTTCGTGTACAGTAACGCTGCCGTTGTAACGTTAGCTGGTGTAATCTGGGAAATTTTCTTACCCATTGGTTTCGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38805
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004127 | Nonsense | 739 | 1093 | 14 | 19 |
ENSDART00000123267 | None | None | 591 | None | 11 |
ENSDART00000145562 | Nonsense | 780 | 1134 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 10 (position 32280592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 31381941 |
GRCz11 | 10 | 31268281 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAAACGCACACTCCCTGCCCAGCCCAACATGGGAGTCAAGAAGGAAT[C/A]ATGGGAGAAAAATGTCAAGCGTGGTGAGATGTTCATTCATTCTTTATTCA
Long Flanking Sequence:
AACATTTCAAGTTATCATTAATCTCAGCAGTCACTCTTTAGTTTTTTCCTATCGTCATCCCTCTGGATGACAGATACGTCCTCATAAAAACCTCCAAAAGATGCCTGTCACCCCTGAAGTCATGACTCCTCGTCAAATCTAATTAGCGTTGACATCTTGGCACATTATGTAAATCAGTCTGACTTTTACCTCTCTACTGACAGCTCTGCCTATTACGGTTAAAAAGGACCCCAACCCCCTGCGGTCAGCTGTCCCCATCGTGCCAGACAATTGTGGGGTCTACGGCACCTTTTATGTGGATCTAACCGGCAATGGACTGAAGACGTTTAATAGTCCCGGCCGCTGTCCCAGAATGCCTCATGGTAACTCTCAACTGCAAAACTCGGAGACCATTCGCATCACAGAGCCCATAGTCAAAACCGCCGTTGTCAGGGAATTGCAGGCATTACCATGGAAACGCACACTCCCTGCCCAGCCCAACATGGGAGTCAAGAAGGAAT[C/A]ATGGGAGAAAAATGTCAAGCGTGGTGAGATGTTCATTCATTCTTTATTCAGATTCATGAGATTCAAATAGTAAAGCATGAAGCTAGCAATGCTTAAGTTGTGGGTTCGACGTCCAGGGAAAGCACAAACTGATCAAATGTGTACTTTCAATGCAGTGTAAGTGGCATTGAATAAAAACATCTGCCAAATGCATAAATCTAAATGTAAATGTTTGTTTTTTTCTTTCAGAGCTGCATGCGGTGAAAAGCGCCCCACTGATGCCTCTGAATCAACAAGCTCTGGCAGTGTGCAGTGCACCGAACCATCAGCAGAGATTCAGTCAGCATCCTGCAGGTTTGAACAACAGCATTTCTTGTTATTCTCATTTACATATTAACAAACTGAATGTAGTTGGCGATAGCAGTTAATGTGATTTAACCAAGTAGGACATGCCCCTCATTTATGTTGATCCAGGAACAACATTCCAATCAGCCAATCAGATTTAAGGGACAATTTTTGGT
Associated Phenotype:
Not determined