ZMP
rbbp6l
Ensembl ID:
ZFIN ID:
Description:
retinoblastoma-binding protein 6 isoform 2 [Source:RefSeq peptide;Acc:NP_001003873]
Human Orthologue:
RBBP6
Human Description:
retinoblastoma binding protein 6 [Source:HGNC Symbol;Acc:9889]
Mouse Orthologues:
AC099701.1, AC158570.1, Gm9343, Rbbp6
Mouse Descriptions:
predicted gene 9343 Pseudogene [Source:MGI Symbol;Acc:MGI:3645198]
retinoblastoma binding protein 6 Gene [Source:MGI Symbol;Acc:MGI:894835]
retinoblastoma binding protein 6 Gene [Source:MGI Symbol;Acc:MGI:894835]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33231 | Essential Splice Site | Available for shipment | Available now |
sa33232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33233 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13575 | Nonsense | Available for shipment | Available now |
sa20073 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33231
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 |
---|---|---|---|---|---|
ENSDART00000055266 | None | None | 142 | None | 3 |
ENSDART00000102994 | Essential Splice Site | 314 | 1631 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35500624)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35285820 |
GRCz11 | 3 | 35415328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAGATGTATCCCCCGATGCCTTGATTGCAAACAAATTCTTGCGCCAA[G/A]TAAGATATCCTTGTTTTAATTGTTGGTTAGCACATGTCTCTAGTTTTTAT
Long Flanking Sequence:
ACAGTGGAATATATGCCATTCCTACTATTGATGCGTGAGTATGCTTGGCCTTGCTGTAAATGATTGTGATAATTTCTTGTTTACTTGTAGTATACTTGTAGTTTACTTTGTAGTTTTTAATTATATTTTGCTTGCTATGTATAGTGAGGCCTATGCCATTGGCAAAAAAGAAAAGCCACCATTCTTGCCCCAGAATCAGTCCTCATCCTCAGAGGAAGAAGATCCAGTACCTGATGAGCTGCTGTGCTTGATCTGCAAGGATCTTATGACAGATGCTGTGGTTATTCCCTGCTGTGGAAATAGTTACTGTGACGATTGTAAGTGTCTATATCAACAAATGTCAAAAAGGTAAAGTGTTTTTGACCTTGGAAAGCTAAAACTGTATTGTGACCACAGGTATTCGAACATGTTTGCTGGAATCTGAAGAACATGTTTGTCCAACCTGCAAACAATCAGATGTATCCCCCGATGCCTTGATTGCAAACAAATTCTTGCGCCAA[G/A]TAAGATATCCTTGTTTTAATTGTTGGTTAGCACATGTCTCTAGTTTTTATCTAATATTGCAACATTAAGACGACTTTATCATTCTTTTTTTTTTTCAACTTAAGGCAGTGAATAACTTTAAGAATGAAACTGGATATACCAAGAGGATTCGAAAAGCTACAGCTACTCAAGCAGTTGCTCAAGGAGCTCAAAAACAAGCTCCTGCTCAACGTCCTCCTATGAGACGCCAGCAGGATCCTCTGATACCCAGTGTTCCAAGCTCAGCGGCTGATAGCACCCCTCCACAAAGCACACCTGCTGCCCCTTTATCTCCTGTTAGCACTCACGAGCCTTCCAGCACCCCACCTTCTTCCAGCAGCTCTACTGTACACAGCAGCACTGCACCTGCAGGGTCAAACTATAGTCCTGTGGTAAACTCTCCTCCGCACCCTACTAGGCAGGATGACCCTCCTCCATCCAAGTAAGAATTTTATAGCACTTCAGATGATCGCTTGGTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33232
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 |
---|---|---|---|---|---|
ENSDART00000055266 | None | None | 142 | None | 3 |
ENSDART00000102994 | Nonsense | 637 | 1631 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35502110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35287306 |
GRCz11 | 3 | 35416814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAGCTGCACCTTTTCTATCCAAGGAGGAGTTTTATCGTCAGCAGCGT[C/T]GATTGAAGGAGGAGTAAGTAGTTATTGGGTTTTTAAGTATTGTCTGTAGA
Long Flanking Sequence:
TAGGACCCCAAAGGAGTAGTGGTCAAAGGCCATCTGGAAGTCGTTCTGGATGGGATCCGTAAGTATCAAAGTGTAATCTAATACATTTTAGTTTTAAACAACAAATGTGAAAAATCCTGACTTTTATTTATCCTACCAGGTCCACGAGTAGAGGTAGACTTCAGAGTGAGAGGCCACCAAGAATACAGCCTCAACCAGTGCAAAATCTTCCTCCTGTAGTCCCTCCAGTATTTGTGCCCCCTGCTCTTTTTCCACCTCCTCCACATCCTATGCCACAGCCACCTGTTGTTGTTTCTCAGCAATATCCCATACAATTTCCTCAAGGACAGCAGCCACCACCTCCTTCCTTCAACATTCCTCCTCCTGTATTTCCTCCTGTTCCACCTAATGTGACTGCTCCATGGGTGCCTCCTGGCCCTCAGCCACCTATAGCCAACCCTATCTCTGCTATGCCAGCTGCACCTTTTCTATCCAAGGAGGAGTTTTATCGTCAGCAGCGT[C/T]GATTGAAGGAGGAGTAAGTAGTTATTGGGTTTTTAAGTATTGTCTGTAGAGTATTATTCTTCTTTGCCCGTGCTTATTGTCATTTCTGTTGTAATGTATTTCCAAGGTTTAACTGCAAAGTTTTATTTCCTTCCTGTCTTTGATAAATAGTTCCCAATGTCGATTCGTTACCAGGGAGAAGTCCAAACTTGAGGAGTTCACCAATGACTTTGCCAAAGAGCTTTTGGAGTATAGAAAAATCCAGAAGGAGAGAAGGCGATCCTACTCGAGGTAAAAATTAAATTGACAGATTGACCCACCAAACTGTCAATTTTGTTAAATGATGTCTGGCATCAACTAAATTTTCAATTACATTTTTTCCAGATCCAAATCCCCTTACAGGGGTTCCTCCTACAGTGGTTCTTCATATTCCTATTCAAAATCTCGCTCTCGTTCCAGATCACCTCGCTCCTATTCTCGGTCACTATCCCGATCACGGTCAAGATCCCGTTCACGGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33233
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 |
---|---|---|---|---|---|
ENSDART00000055266 | None | None | 142 | None | 3 |
ENSDART00000102994 | Nonsense | 683 | 1631 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35502504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35287700 |
GRCz11 | 3 | 35417208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAATTACATTTTTTCCAGATCCAAATCCCCTTACAGGGGTTCCTCCTA[C/A]AGTGGTTCTTCATATTCCTATTCAAAATCTCGCTCTCGTTCCAGATCACC
Long Flanking Sequence:
TGCTCCATGGGTGCCTCCTGGCCCTCAGCCACCTATAGCCAACCCTATCTCTGCTATGCCAGCTGCACCTTTTCTATCCAAGGAGGAGTTTTATCGTCAGCAGCGTCGATTGAAGGAGGAGTAAGTAGTTATTGGGTTTTTAAGTATTGTCTGTAGAGTATTATTCTTCTTTGCCCGTGCTTATTGTCATTTCTGTTGTAATGTATTTCCAAGGTTTAACTGCAAAGTTTTATTTCCTTCCTGTCTTTGATAAATAGTTCCCAATGTCGATTCGTTACCAGGGAGAAGTCCAAACTTGAGGAGTTCACCAATGACTTTGCCAAAGAGCTTTTGGAGTATAGAAAAATCCAGAAGGAGAGAAGGCGATCCTACTCGAGGTAAAAATTAAATTGACAGATTGACCCACCAAACTGTCAATTTTGTTAAATGATGTCTGGCATCAACTAAATTTTCAATTACATTTTTTCCAGATCCAAATCCCCTTACAGGGGTTCCTCCTA[C/A]AGTGGTTCTTCATATTCCTATTCAAAATCTCGCTCTCGTTCCAGATCACCTCGCTCCTATTCTCGGTCACTATCCCGATCACGGTCAAGATCCCGTTCACGGTCTCGTTCTCGATCACGCTCCTTCTCTCGCTCACCATACTCCCGCAGGCCTCGAGGTCGAAGTCGTAGCTATCGATCAAGGTCACGCACTCCAACATTCCATCGTTCTCGCAGTAGATCTCCATCATATAGAGGTCGTGAGATGAGTGGGATGGTAAGTGGCATCTACCGTTCCCGCTCTCGATCCCCCATGTATAGAAATCATAGTCCTGGCAAGAAACTCCCACCACCAGCTCAACTGGAAGGTGAGCGCAAATATACAGGAAGGTACAGAGAACTCCCGCCTTATGATGCTAAGGCTTATTATGGCCGAAACGTAGACCAGAGTGACCCTTATGAAAGAGAGCGATACAGAGAGTGGGAAAGAGAGTACAGAGAGTGGTATGACAAGTATTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13575
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 |
---|---|---|---|---|---|
ENSDART00000055266 | None | None | 142 | None | 3 |
ENSDART00000102994 | Nonsense | 778 | 1631 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35502787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35287983 |
GRCz11 | 3 | 35417491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGTCGTGAGATGAGTGGGATGGTAAGTGGCATCTACCGTTCCCGCTCT[C/T]GATCCCCCATGTATAGAAATCATAGTCCTGGCAAGAAACTCCCACCACCA
Long Flanking Sequence:
AGAAGTCCAAACTTGAGGAGTTCACCAATGACTTTGCCAAAGAGCTTTTGGAGTATAGAAAAATCCAGAAGGAGAGAAGGCGATCCTACTCGAGGTAAAAATTAAATTGACAGATTGACCCACCAAACTGTCAATTTTGTTAAATGATGTCTGGCATCAACTAAATTTTCAATTACATTTTTTCCAGATCCAAATCCCCTTACAGGGGTTCCTCCTACAGTGGTTCTTCATATTCCTATTCAAAATCTCGCTCTCGTTCCAGATCACCTCGCTCCTATTCTCGGTCACTATCCCGATCACGGTCAAGATCCCGTTCACGGTCTCGTTCTCGATCACGCTCCTTCTCTCGCTCACCATACTCCCGCAGGCCTCGAGGTCGAAGTCGTAGCTATCGATCAAGGTCACGCACTCCAACATTCCATCGTTCTCGCAGTAGATCTCCATCATATAGAGGTCGTGAGATGAGTGGGATGGTAAGTGGCATCTACCGTTCCCGCTCT[C/T]GATCCCCCATGTATAGAAATCATAGTCCTGGCAAGAAACTCCCACCACCAGCTCAACTGGAAGGTGAGCGCAAATATACAGGAAGGTACAGAGAACTCCCGCCTTATGATGCTAAGGCTTATTATGGCCGAAACGTAGACCAGAGTGACCCTTATGAAAGAGAGCGATACAGAGAGTGGGAAAGAGAGTACAGAGAGTGGTATGACAAGTATTTCAAGAATTATAACAACCCACCAAGTGGTCAAATGCGAAGCCGTGTTCCAGGCAGCAGAGATGCCTATAGCCCTGAGCGTTTTGCTCCTCCTCGACCCAGAGAGAACTCCCCCTACAACAGGGGACGCCGAGAGGATTATCCACCACCACCTCAGAGCCACAGTGCCCAATCAAGAGGCAGAGTTGCCATGACATACCAAGAGAAGTGTGCTGAGAAGTTTGGCCACCTTCATGCCAATACCACTGGAACAGGCAGAAGTCTTAACAAAGAGCCTTTGAAACCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20073
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055266 | None | None | 142 | None | 3 |
ENSDART00000102994 | Nonsense | 1441 | 1631 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 35504963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 35290159 |
GRCz11 | 3 | 35419667 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAGGCAGTGACCATGGCAGTGAGCGGAGCTCCTCTTCTCAGTCTTCT[A/T]GAGACAGGCAGGCTGATAAAGCTGAACCAAACTCTAGAAAGCCAACAGGT
Long Flanking Sequence:
AGGAGAAGATTGACTTAAAGAAGACTGTTGTGAAGACCCTGGAAGAATACACCAATGACAGCTCCACCCCTGCTGAGGATGAAATTGTAATGATACAAGTGCCCCGTTCTAAGTGGGAAAAGGAGGACTATGAATCTGAGGATGATGATTCTAAGGTTCTCAACAGGACGAGCAGTGCCGATACATCTGTCGCTGCTCCTTCAGTGGAGAACTCTGCTGTGAAATTATCTGACAAGGAGTCTCCCCATTCTGACAAAGCCCAATCTACCTTGAAAGAGGCTGATGTCAAACCTGCCAAAGACTCCACCTCAGGTGATAAGGAGAAAGATACTGACAAAGACAGAGAACGAGAAAGAACCAAAGAAAAAGATCGCAGCAGCACTACAGATCGTGAGTCAACTGATAAAAAGAAACCTAGTGTACCTAATCAGGAGAGCGCACATGCACAGGAGAAAGGCAGTGACCATGGCAGTGAGCGGAGCTCCTCTTCTCAGTCTTCT[A/T]GAGACAGGCAGGCTGATAAAGCTGAACCAAACTCTAGAAAGCCAACAGGTAGGGAGACGACTACAGGCCCCACCAGTAGGAAACCAGAGCATAGAGATGATACAAAAGACCACTTGGGTACAAGATCAAAAGATGAGAAAAATCCAATCAGGAGAATACCATCATCCCCACCATCAAGGGTGAAGGACTTGCACAAAGACTCTGGGAGAAAAAATCTTGAAGCACCTCAAGAGTCACAAAGTCCAAGTAGGACTAAGAGAGCACCAATTCAAAATACCTCTGAGCCAAAACGATCAGGTCCAGAGGACCACAGAGAGAGCCAGTCTTCTAGGCATTCTGAAGTGCGTCCCAGTAAAGACAAAGAGCACAGGACTCCACATATAACTTTGACTCCTGAGCCAAGGACTGATGCGGAGAAAAGTGCTCCACATGTAGACCATATCAAAATACCGTCTGCGCGCTTGACAAGACTCTCCTCAGATTTAGCACGGGAAACCGAT
Associated Phenotype:
Not determined