ZMP
rhobtb2a
Ensembl ID:
ZFIN ID:
Description:
Rho-related BTB domain containing 2a [Source:RefSeq peptide;Acc:NP_001093444]
Human Orthologue:
RHOBTB1
Human Description:
Rho-related BTB domain containing 1 [Source:HGNC Symbol;Acc:18738]
Mouse Orthologue:
Rhobtb1
Mouse Description:
Rho-related BTB domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1916538]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26551 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15510 | Nonsense | Available for shipment | Available now |
sa40537 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26551
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051114 | Nonsense | 16 | 709 | 1 | 11 |
ENSDART00000111587 | Nonsense | 9 | 716 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 45089150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 42870415 |
GRCz11 | 5 | 43470568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCATCTCTTGTAGGGCCCTCTCCATGGATATAGACACAGATTATGAG[C/T]GACCTAATGTGGAGACCATAAAGTGTGTGGTGGTGGGTGATAACGCGGTG
Long Flanking Sequence:
TGAAGCTCAATACTTTAAAATCATTCAGGAACCAGATCGAACCTCATAATTCCAAGGCAACGATTTGCCCGTAAGCTTTGACCTCAGATAATTTAATTTTTATTCGCCAAAATAGAAAGAGTTTAAAATGCACTTGTTAGTGACTTTGAAACTCACACACTTTAAAAATGCGTTATAGCCAAGTGCAGAATTGTGTTGTCTATCTTTGTAGTTCCTTCCTCAGACAGAAATAGCTCCTGACCTAGATTTTAGTTTAAACTTTGAACATTTGGCGAATGACTAGTCAGTATTGATGACACCATTCATTAATGTGGATGTTGTTTTGAGTCACCGATGTGAATGCATCAAATTATCTTTTTCCGACTGATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTTTAGAAAAGTGTGTTAATTTTCTTTCTCCATCTCTTGTAGGGCCCTCTCCATGGATATAGACACAGATTATGAG[C/T]GACCTAATGTGGAGACCATAAAGTGTGTGGTGGTGGGTGATAACGCGGTGGGCAAGACCCGGCTGATTTGTGCCCGTGCCTGCAATGCCACCCTTACTCAGTACCAGCTGCTTGCCACCCACGTGCCAACTGTCTGGGCCATCGACCAATACCGAGTGTGCCAGGAGGTGGGTAGACCTTTGGCATATTGTGTACATGTTGAAGAGCAATAAGTGTTGATGTAAATTCTGTACATCTCAATTGTCAGAAGGCAAATCAGTGAAGTGACAAAGATAAAGTACATATAAACATGGCAATGGATTACAGCCTGTTTTACCAGTGTATTTATAAACTTGAGTAAAAATAGAACGGTTGTAAATAGGGCTTGGTAATTCATTCGAAATGATGTCGCAAATGTGATTAAGCAAAGCTGGTATTGTTATGCACATGTTATTTGGGAAGCACAACTCTATGATCAGTAGTAAATATCCCCTGAGAGTCAGAGGGCGCTCTCATGTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15510
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051114 | Nonsense | 434 | 709 | 6 | 11 |
ENSDART00000111587 | Nonsense | 435 | 716 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 45098354)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 42879619 |
GRCz11 | 5 | 43479772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGATTGTCTCCTCTTTTGGCTYTTTCAGGCAGTGCTGCAGTACCTTTA[C/A]ACTGGTCATCTGGATGAGAGACGTGGGGACCTRAWGCAGGTGGCCACCAT
Long Flanking Sequence:
GGAGAATGAGCATGAGGAAAGCTCTGAGGGGAGCGAGGAAGAGGAGCAGAGCCGAAGAGGAGCCAAAGAACAGGCTGGACGAACCAAGAGTCTGGACATTGAAAAGGAGGGGGATGGGGGCACTAGAGGGGCGAATAGGTTGCTTATGTTACAGCAGGGCTCACTGAGGACTTCACAGAGTGATAACGCTCTGCCTGCCAAGGGTCAGTACTCTGCGGGAACCCTTGGAGCAGGCCGTGCCCTTTTAGGATGGGGCCGTGGTTTCTTGGGAGTGTACCTGGAGATGGTGGACGACCCTGTGACAGGTCGGCCGAGACTGATGACAGTAGTGTCTATGGATGATCTCATTCAGAAAGGGCCTTTTCAGGTAAGAACAAACTTCGATTGACCTGTGATGTCATTGCATGTTTTCTAAGAATCTCCTTAAATTGTCAACCGCAGCATCACATTACAGATTGTCTCCTCTTTTGGCTTTTTCAGGCAGTGCTGCAGTACCTTTA[C/A]ACTGGTCATCTGGATGAGAGACGTGGGGACCTAATGCAGGTGGCCACCATTGCTGAGCTTCTGGAGGTCTTCGACCTGCGTATGATGGTGGCTAATGTGCTGAACCGAGAGAGCTTCATGAACCAGGAGATCACCAAAGCCTTCCATGTGCGTCGTGCCAACCGCATCAAAGAGTGCCTGAGCAAGGGCACATTTGCTGGTAGGTAATCCCATATCAGTGACAACCTTGTATTAGATATCTATCTTATTGCCAACAGAGTCAGACAAACTATATTTTATTGAAAATGGTTTAACATCCAGGACAAAGTAGCCTCAGTTTTCTGACAAACTGTAACAAATTCTGATAAATGATCTGTTGTTGTACCGTTTTACACTGAGAAACTGAATCAAGTCTTTTGTTCAGTTTTTAACTTCTAACTCCAGTAACTGCTGTTGCTAATTGAATTAATAAACAATTCACATTGATTTTGTTTACTAATTAAAGGAACACTCATTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40537
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051114 | Splice Site, Nonsense | 592 | 709 | 9 | 11 |
ENSDART00000111587 | Splice Site, Nonsense | 593 | 716 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 45117611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 42898876 |
GRCz11 | 5 | 43499029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGATATATTAACACTTGTTGTGTGGTGTTTTGTCATGGTCTACAGAG[C/T]AACACGCCGTTGAGGATCTGTTGCAGTTGTCCGTTAAAGGGTTGGACATT
Long Flanking Sequence:
TAAAAAAAAACACACAATACTCAACTTACTTTACCCCAAAAATTAAAAGTCTTCATTTAATCAGCATAATCAATTTGTTCATGTTTTTATCGGCCCTCTATTAAAAATCCTCACCTAAAACGTTAAATAATTTAATAAAGGGATAAAGTGACAATGTCCATATGAATAATCTGTTTAATCCAAGTCTTCTGAAGAGATGTGATCTCTTTAGTTGCTGAACAAATTTAATTTTGCATTAAAACATGTGAGGGATTTATTATATATCTTAATTCATGTTTTGAAGATGAACAAATGTTTTACTGTTTTATAACAACTTAAATGTAAGAAAAAGGTGGAAGAAATTACATTCTGGGGTTGACTTAGCATTTAAAAACACAGTCGTGAAGGTGAGACATTTTTCACTGTTGACGATTTCGGAGTTGTTTGCACATTGTTAAACATTAAGCCTATGGCTGATATATTAACACTTGTTGTGTGGTGTTTTGTCATGGTCTACAGAG[C/T]AACACGCCGTTGAGGATCTGTTGCAGTTGTCCGTTAAAGGGTTGGACATTGATGGACATGTGCTGGCCTATCTGGAGATGGCTCAGGTAACGTTTATAAAGATGAAGCAAACAAAGCCTTTAATAGAATGCAAAGCACACTAGAAATGAGTAATCAAGTGGCAATACAAGCAGTGGAGCACATTAGAGAATTACCATTCATTTGTAGCCTACTTTATTCTAGTTCAAAGGATGAACACACTTTGCTTTTCAAATGAGCCTCATTGAGAGAAATCATGCTGTGCTGACTCCGCTTTCTGTCTGCTGTAGTTCCACAATGCCAAACAGCTCTCTGCCTGGTGCCTGCATCACATCTGCACCAACTACAACAGTGTCTGTCGCAAATTCCCTAAAGATATGAAGATTATGTCTCCTGGTAAGAGACAAGAAATGTTTTGATTGATTGATTGATTGATTGATTGATTGGTTGGTTGGTTGGTTGATTGATTGATTGATTGATTG
Associated Phenotype:
Not determined