ZMP
setd1bb
Ensembl ID:
ZFIN ID:
Description:
SET domain containing 1Bb [Source:UniProtKB/TrEMBL;Acc:A5XCC1]
Human Orthologue:
SETD1B
Human Description:
SET domain containing 1B [Source:HGNC Symbol;Acc:29187]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34447 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30902 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41257 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34446 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21340 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34447
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114080 | Nonsense | 107 | 1789 | 3 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 35896608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 34825032 |
GRCz11 | 8 | 34759832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGAAATGTGTAAATGCTTTGGAGAGATTCAAGATTTGAAAGTTTTTTA[T/A]AATCCAAAGAACAAGAAACATTTAGGACTAGCAAAGGTTGTTTTTGAATC
Long Flanking Sequence:
TTTACAGGTTCACTTAAAAAATAAAATGTGTTAAATATAATTGTTTTATTAATTTAGTTTTTAAACATTTACTATTTATTATTACAATATAATCTGGTACACCCTATATACATATACTGAAGTGTTACAAATATTTTTAGAAACATTGTTGCGATATAAATTTAGCAGCATTGTGTTTGGGATCAAAAGTACAGCTTGCACAACATTTGATTATTCATTCTGCAAATTGTTATTATATTTTATTCCATAGCCCTCTGAGATGCCAAACAAGTAATTTAACAACATTCAGAGTTCAAGTTTATAATTTTATTTATAAGTTGTTTTCATCTGTATCAGAAGTACAAAATAATGTCAATATCCTTCTTTTTTTAGGTTGATGAGTATTATGTCGGAGCACCTAAGGAGTTGACATTTGCAAGACTTAATGACAACATCAGAGATGGATTCCTATCTGAAATGTGTAAATGCTTTGGAGAGATTCAAGATTTGAAAGTTTTTTA[T/A]AATCCAAAGAACAAGAAACATTTAGGACTAGCAAAGGTTGTTTTTGAATCTGTAAAAGCAGCAAATAATGCAGTAAAAAATCTCCACAAAACTTCTGTGATGGGAAACAACATTCATGTGGAGCTTGACCCTAAAGGTAAATACATTTCCACTTCCTATGAAAATCCGGCAAATAAAAGCTTTCATCAACATCTCTATGCAATTATTTGCAATTTAAACTTTTACTGTGTTTGCATTCACTGCTTGATTCCTGACTGGTTTTAGGCTTGAAGAGGCATCGATACTTCCAGATGATTGTTAATGGTTTATATACACCTTTTACTCTCCCTGTTGAAGAAGAGGCCTGGGGGCCGCAGTCACCATCTTCCATCACAGACTCCTTAATTGTGAGTCGAAGACCAAATACCAAACATTTTGTGATGTTAATAAATGGTCAAATGGCAGGAACTTGGAATGATTTTAGTTCTGTGAAGACCATTTTGTGTCAGCTAAATTAGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30902
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114080 | Nonsense | 1130 | 1789 | 16 | 23 |
ENSDART00000114080 | Nonsense | 1130 | 1789 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 35888614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 34817038 |
GRCz11 | 8 | 34751838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCCAGCTCAAATGGAAGACCCAGAGGAAGAACTGAGTGTACGAGTGTA[T/A]ATGCAGGGACTAAAACTGCCTGAGCCTCTCAGATACACCTTACAGGACCC
Long Flanking Sequence:
AGCTGTTTGATACGACAAAATATTTAGGCATCATAATTTAGGATGAATACATTTTTAATGGAAGGACACAGATTTCATATTTAATTGAAAATATCTCTATTTGTTTTAAGGTTTGACAAAAGATTTATGGGTTTGTAAAGATGTGATGGTAAGTAAATGGTTAAGGCAAACAGAGGTCATTTTGAAAAGAGCTAATCATTTAATGAACCTTTTATACCTTCACCACCTAAAATCCTGTAATATGCAGACCAATAATACAGATTTTACTATTTAAAATGGATCTACATGTTTCATTTATTGTGTTTTTGAGAATTAATATCTTTTTTTCATAGTTATCTTTAAGTTGTAGCAATCAGCTGTTAAAATAAATAATAATAATAATAAATCTTCATCTTCATGGTTTAATCATCATTGTTAAACAATATGATATGTGGTTCTGCTTCAGATTTGGATCCAGCTCAAATGGAAGACCCAGAGGAAGAACTGAGTGTACGAGTGTA[T/A]ATGCAGGGACTAAAACTGCCTGAGCCTCTCAGATACACCTTACAGGACCCTGTGAAACACTGTTTGACAAACAAACTGAAGCTTCCAGACCCTGTGATATTCTTCTCAGATCAGGAATCAGAGCTGCCAAGCCCACCTTCTCCTACATACAGAGGATTATCAGGTGCGGGTTTTATTTATTTTTTTTTTACCTGAGTAATCACTCTTTTCAAATATGTCCTAGTTTCAGATCCCTCAAAATAAACTTTCTGTAGTTATAAATAATTTTTTTAAGATAATTGTTTTTTTTTTTTTTACAATTTTGTTTTCAACATATAACCAGAGTTTTTTGCAATAATTCTTTTTATTTTTTTTCCTTTTGTCAAACACTAAAGATATTTTGAAAAAAGTAAGAAACATGTAACCATTGACATTCATAGTAGGAAAAACAAATACTATGGAAGTCAGTGCTTTTGCAGGTTTCCAAATCTTTTTCAAAATCTCTTTTTTTGTGTTCAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41257
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114080 | Nonsense | 1130 | 1789 | 16 | 23 |
ENSDART00000114080 | Nonsense | 1130 | 1789 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 35888614)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 34817038 |
GRCz11 | 8 | 34751838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCCAGCTCAAATGGAAGACCCAGAGGAAGAACTGAGTGTACGAGTGTA[T/A]ATGCAGGGACTAAAACTGCCTGAGCCTCTCAGATACACCTTACAGGACCC
Long Flanking Sequence:
AGCTGTTTGATACGACAAAATATTTAGGCATCATAATTTAGGATGAATACATTTTTAATGGAAGGACACAGATTTCATATTTAATTGAAAATATCTCTATTTGTTTTAAGGTTTGACAAAAGATTTATGGGTTTGTAAAGATGTGATGGTAAGTAAATGGTTAAGGCAAACAGAGGTCATTTTGAAAAGAGCTAATCATTTAATGAACCTTTTATACCTTCACCACCTAAAATCCTGTAATATGCAGACCAATAATACAGATTTTACTATTTAAAATGGATCTACATGTTTCATTTATTGTGTTTTTGAGAATTAATATCTTTTTTTCATAGTTATCTTTAAGTTGTAGCAATCAGCTGTTAAAATAAATAATAATAATAATAAATCTTCATCTTCATGGTTTAATCATCATTGTTAAACAATATGATATGTGGTTCTGCTTCAGATTTGGATCCAGCTCAAATGGAAGACCCAGAGGAAGAACTGAGTGTACGAGTGTA[T/A]ATGCAGGGACTAAAACTGCCTGAGCCTCTCAGATACACCTTACAGGACCCTGTGAAACACTGTTTGACAAACAAACTGAAGCTTCCAGACCCTGTGATATTCTTCTCAGATCAGGAATCAGAGCTGCCAAGCCCACCTTCTCCTACATACAGAGGATTATCAGGTGCGGGTTTTATTTATTTTTTTTTTACCTGAGTAATCACTCTTTTCAAATATGTCCTAGTTTCAGATCCCTCAAAATAAACTTTCTGTAGTTATAAATAATTTTTTTAAGATAATTGTTTTTTTTTTTTTTACAATTTTGTTTTCAACATATAACCAGAGTTTTTTGCAATAATTCTTTTTATTTTTTTTCCTTTTGTCAAACACTAAAGATATTTTGAAAAAAGTAAGAAACATGTAACCATTGACATTCATAGTAGGAAAAACAAATACTATGGAAGTCAGTGCTTTTGCAGGTTTCCAAATCTTTTTCAAAATCTCTTTTTTTGTGTTCAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34446
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114080 | Nonsense | 1296 | 1789 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 35886210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 34814634 |
GRCz11 | 8 | 34749434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACTTCCATCCTCACCCCTTTACTACGGTATTCCTCTCCTGTCATCATA[T/A]CCTGGATATGAGGAAATCCCAAAAACACCAGGCAGAGTCAATGATCCAGG
Long Flanking Sequence:
TGAATTTAGGCCAAATCGCCCAGCCCTACATTATAGCATAAACAAATAGACCTATACATACAGTAGACCAACATGTGCATAATTGGCATATCAGATCAATCAAATCAAACTGAATATCATATCTTCAACTAATTGTTAGTTGCATCATGTATCTTTGTGCTTTCAGATGATTTGGAGACCCAGTACACTACAGACTCAGAGGACCAGAGAGTCATCATGGAAGCGCTGGAGGATCCCGTGCACCTCAGACCCATCACACCCACTGGATTCTTGTCCGACAGTGACCCTGACATAGAGATGGGACGGAAATTTTCTCCTCCGGCCATCGAGGAGGTAGATCTGCCACACACTCCTGGTAGATGTCTGGAACTAGAGGATGATGAAAATAACATTCTACCACCAGGTCCACCGACACCACTACCACCTCCTCCATCTCCTACAGGCATAAAAGAACTTCCATCCTCACCCCTTTACTACGGTATTCCTCTCCTGTCATCATA[T/A]CCTGGATATGAGGAAATCCCAAAAACACCAGGCAGAGTCAATGATCCAGGTTTTGTTTTTCACTCTGAAAGAATAACACCACCACAAGAGCCTTCACGAACACTGGAAAGCCCCTGCAATCCCTTTCTGTCTTCTTTTGCTGACAGCGGGATTCCAAGGACCCCAGGGAGAGACATGTCTCTGTCTCCACCTGTGCTAAACCACAGAGAAAGACATGTTCAACACAGAGAGCTGTTGAAATATGGACAGCGTCATCGTAACAGTGATTTTGCACAGTCAGACGTACAAACAAACAATTTTAGTAAAAATAATAGTCACACACCTCGTTCAGACACGGCACGCTTGAAAAGGCGACGAGAGCGTCTTAAAAAAAGACAACGAATGATTGAATTACAACGGTCAAGACGATGCACTGATCTAAATACTCATTCATCTTTACAAGTGAGTAGTGCGACAACAAAACCTACAAATCAAAGTTTGGAGCCTTTGGACAGAGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21340
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 |
---|---|---|---|---|---|
ENSDART00000114080 | Nonsense | 1766 | 1789 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 35881327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 34809751 |
GRCz11 | 8 | 34744551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTACTCACGACAACCTATCACTGTAAATGAAGAGATCACTTACGATTA[C/A]AAATTTCCTATTGAGGATGAGAAAATCCCCTGTCTGTGTGCTGCGGAGAA
Long Flanking Sequence:
TCCTAACATCCATTCAAAAACCTTAGCAACTACATGATAGCCTCCCCAAATACACTTTCATCTGAACAAAAACACTTTACAATTACCCAGAGCATCACCATTTGGTATTGTTATCATGATTTCTTAAATTCTGTCTGTAGGTAATAGCAGACATGCGTGAAAGGCGTTATGAAACTGAAGGCATTGGAAGCAGCTATCTTTTCCGGGTGGACCACGACACCATCATTGATGCAACCAAGTGTGGTAATCTGGCAAGATTCATCAACCACAGTTGCAATGTATGACCAGAAATATTTTAGTCATTGTCAGAAAATCAAACAATTGTTTCATTTTCTTGTTTGGCTATTTGATTTCCTTTTTTAAACTTACTGTTTTATTCATGTGCTTTTCCTTCTGTAGCCAAACTGCTATGCCAAAGTCATCACTGTAGAGGCTCAGAAGAAGATTGTCATCTACTCACGACAACCTATCACTGTAAATGAAGAGATCACTTACGATTA[C/A]AAATTTCCTATTGAGGATGAGAAAATCCCCTGTCTGTGTGCTGCGGAGAACTGTAGAGGAACCCTCAACTAGACAAGAGCTCATCTAACACATTCAAAGTATTAGCAGTAAACATGAACCTGTTTTTAAGCACAACATTTTGTTCAGGTAAAGTATTGAAACATTTACTTTAACCCTGAACACTACACAAAGGAAAACACAATTTAGAACTGGTAAAACATCATTTAAAATTAAAACATAGAATCCTTCTTTAGATTAATACACTACCTGACAAAAGTCGTCGATCTCAGTTGTAAGAGAAACAAATATTAACCTGACTTCTAGTTGATCATTTGGAAAAATGGCAGAAAGTAGATTTTTCAGAGGAAACGTGTTAAACTGCATCCCGATCATCACAAATACTGCAGAAGACCTATTGGAACCTGCATGAACCCAAGATTCTCACAGAAATCAGTCAAGTTTGATGAAGGAAAAATCATGGTTTGAGGTTACATTCAGTA
Associated Phenotype:
Not determined