ZMP
RBM6
Ensembl ID:
Description:
RNA binding motif protein 6 [Source:HGNC Symbol;Acc:9903]
Human Orthologue:
RBM6
Human Description:
RNA binding motif protein 6 [Source:HGNC Symbol;Acc:9903]
Mouse Orthologue:
Rbm6
Mouse Description:
RNA binding motif protein 6 Gene [Source:MGI Symbol;Acc:MGI:1338037]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20795 | Nonsense | Available for shipment | Available now |
sa40771 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40772 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33940 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20795
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 |
---|---|---|---|---|---|
ENSDART00000097273 | Nonsense | 673 | 1393 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 42607372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42678426 |
GRCz11 | 6 | 42675962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTAACTAACGCAAATCCATCTGTATTTCAAATGCTGTTCCCAGGTTA[C/A]AGCTTCGATACGGCCTATGTGGAGTTTTTAAACCTCGAGGATGCTGTCCA
Long Flanking Sequence:
CTAATACATTTTTACAGAATCTTTACTAACACTTGCAGTGATATTAACATGTTTAGACATGACATCCTTATTGTTAATGATTTTTCAAACTTCGTTTTTAAAATACTTTTTCAGATTGTCCATATACTTATTCCTCTTTGAAATGATGCCAGTTTTATGTAAAAATGGGCCATCTTTTCTGTTTTTGCTATATATTGCTATATATAGGATTAGACTTAAAAATTTCTAGCAAATCAGTTTTCATTTTGGGTCTGTATTACACTCAGTATTACATTCATGTATTTATTTGGCCTTATAAATGTATATCTTGGTGAGGCTACTCTGATTCTTTGAGTAACCAATAAAAGTAAATTCATAATGAAAAAGAAAGCAGCGTTAACATCCTGTTTGAATTTCGCTTTGTTTCGTGAAACAACTGCCTTTTTACTCTTGAAATACTTTTATTTACCTGCATTAACTAACGCAAATCCATCTGTATTTCAAATGCTGTTCCCAGGTTA[C/A]AGCTTCGATACGGCCTATGTGGAGTTTTTAAACCTCGAGGATGCTGTCCACTTCATGGAGTCCAACCAGGTGGCCCATCCTCGCCCTTCTACAACGACTGCTAACAAGAAGGAGGCTTGGGCTGGGGAGGGGGAGGTGGCTGGGTTCAGGGTGGGAATGGGGTAGATGGTACATGAGACTTTCAAGAAAGTCGTTATTAAACATGACCAGTGAAAACACGCCACTTAGTTTGCAACAGCAACTTTCAGATGTAACGAGTGAGCATAGTGTTAAAGAGTTTTTATTGATGTCTGCCGTAGGCATATAAGCTGAATGATCGTTCACTACCTTTTAATGTGTAGTTTTTTGAATAATTACTTGGCATGCTAAGTTTGGAATTGCATTTGCATTTTTGCAAAATTTTCTTCAACTTCACACCATTGTTGTTTCAGTCTACTGTTTACAACAGTATAATACTTCATTTTCATCATATGGCCTTCTTGATTCCATGGTCTTCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40771
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 |
---|---|---|---|---|---|
ENSDART00000097273 | Essential Splice Site | 817 | 1393 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 42611647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42682701 |
GRCz11 | 6 | 42680237 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCACGCCAAAACTTACAGTACTCTGATCCAGTTTTTAAAGAAAGCAAAA[G/T]TAAGTCATGTCAGCTGCGACTGAGATTTTTCAATTAAGGAAAATGGTAGA
Long Flanking Sequence:
ACATTTAAAAAAACATTCTTTTTATTTTCTAGGGATCTGTTAAGGTTGGTGACAAGACTGCTCTGCTTAAATATGTCCAATCTGACAAAAATGGGAAAGAGCAGGTGAGTCTCCTTGTTTGATAGAGCTTGATTACTTACCTTTACTATGATTTGATTATTGTTTGAAATTCTTTCATGTAATAACTGCATTGTAATTTGAATTGCAGCTCCATGAACCACCCACTAAGGCTACACCAGCTAGTGATGATGGTTTGTTACCAAATCCAGTCCCTCCACCAAACAAACAGGAGGAAACCGCTGTCAAGCCTCTACTGGATGCTGCTTCTCAAGGTGTGTGGCAGAGAAGCTCAAACTTGACTCCTGAAGCATGGCAACAGCAAGTGGACCAACAGCAACAACAGCAGGAACTGGAGCAACAACCCACAGAAGAATGGACCAATCAGAGAGCATCACGCCAAAACTTACAGTACTCTGATCCAGTTTTTAAAGAAAGCAAAA[G/T]TAAGTCATGTCAGCTGCGACTGAGATTTTTCAATTAAGGAAAATGGTAGAGGATTATACTTAAATTTCATGTCTTGTTTTAGCAATGATCATTAAGAACATTCTCCCTACCACCACCGTGGAGACCATTCTGAAAGCACTTGATCCATTTGCTTACCTGGATGAGCGCAATGTACGTTTGGTCAAAGGGAAATCACCTGGATCCAAATGCTTCTGCTTTGTTGATATGGATTCACATGAGGTGAGATGTACAGAATTATGATTATAACAAAGACAATATGATGTCTCAAAGTCCCGATAACACTATTTTTGTGTGCAGCATGTGACACGGTTGGTGGAGCTGCTCACAAAGCCTCGGCCAATCATGATTGATGGGGTCAGAGTTTATGCTGAGGTTGCAAAGCCTTTGAAAAATCAAAAGTAAGAAATTACGTTTTTTTTTATTGGTTTCCTCTTAACATAGCATATAGTACCATACAAAATGCACATAAATTCTTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40772
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 |
---|---|---|---|---|---|
ENSDART00000097273 | Essential Splice Site | 870 | 1393 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 42611888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42682942 |
GRCz11 | 6 | 42680478 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCACCTGGATCCAAATGCTTCTGCTTTGTTGATATGGATTCACATGAG[G/T]TGAGATGTACAGAATTATGATTATAACAAAGACAATATGATGTCTCAAAG
Long Flanking Sequence:
AGTGATGATGGTTTGTTACCAAATCCAGTCCCTCCACCAAACAAACAGGAGGAAACCGCTGTCAAGCCTCTACTGGATGCTGCTTCTCAAGGTGTGTGGCAGAGAAGCTCAAACTTGACTCCTGAAGCATGGCAACAGCAAGTGGACCAACAGCAACAACAGCAGGAACTGGAGCAACAACCCACAGAAGAATGGACCAATCAGAGAGCATCACGCCAAAACTTACAGTACTCTGATCCAGTTTTTAAAGAAAGCAAAAGTAAGTCATGTCAGCTGCGACTGAGATTTTTCAATTAAGGAAAATGGTAGAGGATTATACTTAAATTTCATGTCTTGTTTTAGCAATGATCATTAAGAACATTCTCCCTACCACCACCGTGGAGACCATTCTGAAAGCACTTGATCCATTTGCTTACCTGGATGAGCGCAATGTACGTTTGGTCAAAGGGAAATCACCTGGATCCAAATGCTTCTGCTTTGTTGATATGGATTCACATGAG[G/T]TGAGATGTACAGAATTATGATTATAACAAAGACAATATGATGTCTCAAAGTCCCGATAACACTATTTTTGTGTGCAGCATGTGACACGGTTGGTGGAGCTGCTCACAAAGCCTCGGCCAATCATGATTGATGGGGTCAGAGTTTATGCTGAGGTTGCAAAGCCTTTGAAAAATCAAAAGTAAGAAATTACGTTTTTTTTTATTGGTTTCCTCTTAACATAGCATATAGTACCATACAAAATGCACATAAATTCTTGACAGTTAAAGAAAATAAAAAATAAAAAAAAATAGAAAAACTGTATCAAATGCATAAAGTTAATACTACAGAGCACAACAGGTAAGATGCATCTATAGTTTAAGTGAAGAAATTAAATTTTCCCTCATATCAGCTTTCATATGATTACTAGACACGTTCTCCGGGGTTTCCGCAAGGTCTTAAAAAGTCTTAATTGTGATTTCTCTCAGATCGCATCTTTGATAGTTCACACTGTGTGATTGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33940
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097273 | Nonsense | 1105 | 1393 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 42614422)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42685476 |
GRCz11 | 6 | 42683012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTCCTGTGACTCCTGTTGCTGAGGTTATAGCTGTACCCATTAAAGAA[G/T]AGGAAGCCAAGGCGGTTTCAGAGGCTTTGCCAGAGGTGCGGGTGGAAGAG
Long Flanking Sequence:
TCCATCATAGACACTGGTATCAGTAATAGCAGTTAAGACAGTGTTTCGTAGTATGTATGAATGAATGATAGACAACTGGTCTAATAATAATACTTATAACTGTAGGATCTGAAGCTCCAGATTTGTCAGCCTTCCTTTACGATGCTACATCTGGCTTTTACTATGACCCTCAGACTACGCTTTACTATGATCCCAACTCAAGGGTAAGTTTATATATTCCCTTTTGAATAAAAGCATCTGTTAAATGTAAATATAAATAGCTCTTTAATTCTCAATTAAATGAAATGCTATATGAAATGGTTTAATGTATATGTTTGCTTGTGCAGTATTTCTACGATGCTCAAAATCAGCAGTACCTGTATTGGGATAGTTCTTTAAAGACCTACATCCCAGTCCAGAGCTCTTCCACTGATGGTCAGAATGTTCCTGAAGTTCCGGCCCCTGAAGTTCCTGCTCCTGTGACTCCTGTTGCTGAGGTTATAGCTGTACCCATTAAAGAA[G/T]AGGAAGCCAAGGCGGTTTCAGAGGCTTTGCCAGAGGTGCGGGTGGAAGAGGAGCCTGGGCAACGTGGAGAAAAGAGAGAGAAGGAAAAAGAGGAAAAGCCCAGGAGTTTAGCAGCTTTTAAGGTCTTAACAGTACTTTATTGCACCACATGTTCAGTGATTAATTCAAAATTATGAGAGTAATATATTAGATCTGTGTAGTAATTTTGGATGTGGTCATCAGATAATGAAAGACATGGAGAGATGGGCGAAAATCCAGAACAGTAAGAAAGAAAGTGTCCGAGCTCCTTCCCCTGTCCTCAAGTCTGGAGATGACCACAGACCTTCAAAGGCAGCTGATGCAGCCTTCGCCATCTTTGAAAGGAAGGTCAGATCACCTTTTACGCTTTGTTTTTGTTCAACCCTCTCACCTGATCATTAAACTTGTGGTTGGCATACTATGCTTTTTTTTTAGGGAAATTGAAAAATAAACCTAAAGTACTCGAGTACCAGACCAATTTG
Associated Phenotype:
Not determined