ZMP
kdm4b
Ensembl ID:
ZFIN ID:
Description:
lysine-specific demethylase 4B [Source:RefSeq peptide;Acc:NP_001076274]
Human Orthologue:
KDM4B
Human Description:
lysine (K)-specific demethylase 4B [Source:HGNC Symbol;Acc:29136]
Mouse Orthologue:
Kdm4b
Mouse Description:
lysine (K)-specific demethylase 4B Gene [Source:MGI Symbol;Acc:MGI:2442355]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44979 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15777 | Essential Splice Site | Available for shipment | Available now |
sa17996 | Nonsense | Available for shipment | Available now |
sa10758 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44979
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 |
---|---|---|---|---|---|
ENSDART00000034084 | Nonsense | 165 | 1134 | 2 | 21 |
ENSDART00000128161 | Nonsense | 165 | 1134 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 3899192)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 3944309 |
GRCz11 | 22 | 4397157 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTGCTCCCATCATGCAAGTGGTGACCGGCCAATCTGGGCTCTTCACA[C/T]AGTACAACATCCAGAAGAAGTCCATGACCGTTGGAGAATATCGCAAACTG
Long Flanking Sequence:
ATTTTACACTACTGCAGAAATGTTGCGTCGCGTGTTGTTATAAATCCCTCAGCATCAACTTTTATTAATATTCATGAGGTTTAATATTTATTCATTTGATTTTTAACCTGTCTATTTCGTTGGGAGATTGTTGGTATTGTTTTATTTGGTATTTAAAAGTTTCTGTCACGTTGCGTCTGGTGCGGACAAACAATTGAATTATTACTGGAATATTGTTGGAATATATCAAGTTATGCTGTGTGCGGTACTATACTGAATCATAATGCTCAGTCCAAACAAGTCATATAAAATATCATGCAGGGACTTGAACGAATGAGCGATCTTTTGACTGACTGTATATTTACTTTTATGTTTATGTTTTCTTCGTTCTCTCGTCTTGCGATGCTCAGGTTATTCCGCCGAAGGAGTGGAAACCGCGCCGTTCCTACGAGACCATCGAGGATATGGTCATTCCTGCTCCCATCATGCAAGTGGTGACCGGCCAATCTGGGCTCTTCACA[C/T]AGTACAACATCCAGAAGAAGTCCATGACCGTTGGAGAATATCGCAAACTGGCCAACAGTAAAAAGTACGGTTTACACTTGCATTTCTTTTACCTTTATTTCTAAATGTAAACAATAAAGTCCCTTATAGGATCACTTCACCTCACTTTATATTGAAAAGAGCTCATTTTACAACTCTCCACAAGTTAAAGAGGGAAGGTTTATCGTTTTTGACTCCATTGAGCCGATCTCTAGGGAGTACTATTATAATTAGAAATAAAATAAAATTTTTAGCTTAGCATAGTTCATTGAATCAGGTTAGACCATTAGCATCTCACTCAAAAATGACCAGAGTTTTGTAAATTTTTCTATTTAAAGCTTGAGTTTCTGTAGTTACACTGTGTAGACGGACTGAAAATGATAAAGTAGCTAATAAGTAATAAAAAAAACACTTTTTGCTTAGCTTAGCATAGTTCATTGAATCAGATTAGACCATTAGCATCTTACTCGTCAATGACCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15777
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034084 | Essential Splice Site | 306 | 1134 | 5 | 21 |
ENSDART00000128161 | Essential Splice Site | 306 | 1134 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 3922489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 3921012 |
GRCz11 | 22 | 4373860 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGCCATTCCTCCCGAGCACGGCAAGAGGCTGGARAGGCTGGCGCAAGG[T/C]AAGACCTCACATCCGTTTGTTATCGTGTCTTCAAGCTRAAAYGAAACCTC
Long Flanking Sequence:
CAATGTCAATAACAACGTCAAGCGAATTGAACCCTTCAGTAAAGCGCACCCCACACCAAAATCATTGCAAATTTAAAGCAGCACCGTCTGCAATTTGGGCTGGAAAATTATTAGCGCGCATGTTTGAGCCGATTAGGCAAAATGAATTGGCTGGCGCGCTGTAATTTTCCAGGCTTTGTCTTAGTGACATTTGAGCACTTTTGTCTTTAAAGCAGCGTGTGACTGCTGAATGTGAAATAGGGGTGAAATTTGTGCTTTTGTGTGTTTCCCGGAGCAAAGAAACGGCTGTGTTTTATGTTTTCGGAGGGCTGCAGAAGAAGCCTGTGATGATCAGAGGCTGCTTCTCTCAGAGGCGTCTCGCTGCGCGTCCCTCCAGTGTCTTTCTCTCTCCTCTTTTCTATTGATCCCATTAATTGATCTAGTTTTTTTTTTCCTCCTCTTCACCGCAGGTATGCCATTCCTCCCGAGCACGGCAAGAGGCTGGAGAGGCTGGCGCAAGG[T/C]AAGACCTCACATCCGTTTGTTATCGTGTCTTCAAGCTGAAACGAAACCTCGTGCCTCAGCCGATTTAAAAACTGAGCTCATTTACATACACGAGTCTTGAAGCTGTGCCTGAAGAAGTGAGAATAAATCTTGTACCAATTAACTTGCTTGCAAGAACTTGAGATATTTCACTAAATGTTCAAGCTGCTCCCTTGGCATTGGCTAAAATGGGAAAAAATGCAGTTTAAATGCAGCACACTGACCGGCCACTTTATTAGGTACATCTGACTACTACCGCGTTGGTCCCCCTTTTGCCTTCAGAACTGCCTCAATCCTTGGTGGCATAGATTTAACAAGGTACTGAATATATTCCTCAGAGATTTTGCTCCATATTGACATGATAGCATCAAGCAGTTGCTGCAGATTTGTCGGCTGCACATTCATGATGTGAATCTCCCGTTCCACCAGAACCCAAATGTGCTCTATTGGATTGAGATCTGGTGACTGCGGAGGTCGTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17996
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 |
---|---|---|---|---|---|
ENSDART00000034084 | Nonsense | 579 | 1134 | 10 | 21 |
ENSDART00000128161 | Nonsense | 579 | 1134 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 3946158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 3897343 |
GRCz11 | 22 | 4350191 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTCCAGGAAGTGTTTGAGCAGWTCACCACCGCCAGCGAAATGCAGAAC[C/T]AGAGCAATGGAGCTGCCCCTCTGCAGGTGAGGAGACTCNTTYCTATCTTTT
Long Flanking Sequence:
ATCCAGAACAGGTTAAGGCTGGGTAGTCAGCATTGGTTGGCCATTTCAACAATCAACAACCCCTTTAGTAACCAATTCTCTACCCAGAGCACCAAAGCAACCAATATTTCAGTTGCTTGACAACAACACTAAATACCCTAGCAACCATCCAAAACATCTTAAGGCCTGGTAGTCAGCATTGGTCAGCCATTGCAACCTTCAACCTCTTGGTAACCAATTCTCTACCCATCAGCCAACTAAATTAACCTAGCAATGACATAGCAATCTACAAATCTCAGAACACATTAGCAACCAAAAGCCTAGCAACAAGCCAAGACTGTGTTTTGATCCTATTTCCTGTCATTTCTTTATCAGTTGAAGAAATAAAAGCCGATTTCCAGGATCCTCCAGTGGAGAACGGAGAAAAGAAGAAGAAAAAGAAGAAAAAGCTTCAACTCACAGATGAAATGTCCTTCCAGGAAGTGTTTGAGCAGTTCACCACCGCCAGCGAAATGCAGAAC[C/T]AGAGCAATGGAGCTGCCCCTCTGCAGGTGAGGAGACTCTTTCTATCTTTTCTTTGTATGATTATTAGTAGATTGATACACATATATAATATTTCATTAAATTATTTTTAGACAAATCCGTTCACGAAGCTGAAGAAGAAGGTTGAGGTGAAGAAGAGCCGAAGGCATCCAATCAGCAAACCGCCGATGCGTTCGCCTCACTCCATCGTCAAACAGGAGGCCTCCAGCGATGAGGGTAAATACTGCTTGTATTACATTTATATCGGAATGTTTGTTTGTAAACCATTTCATTAATTGTTGTGCTAAATTAAGTGTTTTACGTAAGAATACATTCAAAAAATGGCCTTAAAATCGAATATTTCATACACGCGTTACCTAAGTAATCCTTGTTTTTGTTTGTAAAACCATTTTATTGTTACGTTATTTTATTTGTTTAAAGTCCATTTTTATTTTAAAGATGTCCTGAAAAACAAATATCATACACAGAAGTCTCTAAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10758
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 |
---|---|---|---|---|---|
ENSDART00000034084 | Nonsense | 665 | 1134 | 12 | 21 |
ENSDART00000128161 | Nonsense | 665 | 1134 | 13 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 3951102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 3892399 |
GRCz11 | 22 | 4345247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGACAGCGACCTGTGGCAGAACCGTTCKCCGAACTTCCTAGCCGAGAAA[C/T]AGTTCAACGCGGCCATGTCCACCATTGAGCCGTACTGCGCCATCTGCACG
Long Flanking Sequence:
TTTAGTAGTTTCATCTGTCCGTCCATTCACCATCCATCCATTATACCATCTACCATTTATCAATCCATCCATTTTTTTAGTAGTTCATCCATTGTTTTTCATATTCCATCTATCCTTTGATTTATCTATCCATCCATCCATCAATCCATCCATTTTTTTTTTGGTAATTTCATCGATGCATCCATCCATCCTTTTTTTTGGTAGTTTTCTCTGTCCATCCATTCACCATTCACCATTCATCCATCCATTCATCAATCCATCTATTTTTTTGGTAGTTTCTATTCATTTTCCATTCAGTTTTTTTCCCTCCATTGTAGCATGTGTCACTTCTGAATTGTGTAAATTACAGTAAAACTCACATGTGTCTTTATGGCTTCTCTGTGTGATATGCAGAGCTCTACTCAGGGCTGCCAGTAGGTGGCGGTGTCACTCACGAAAGCAAGAAGCCCGAAGACAGCGACCTGTGGCAGAACCGTTCGCCGAACTTCCTAGCCGAGAAA[C/T]AGTTCAACGCGGCCATGTCCACCATTGAGCCGTACTGCGCCATCTGCACGCTCTTCTGCCCGTACACACAGGTAACGCATTGCATATGTAAAATACATGCATAAACAGGATCACTATTTCACTCCCAAATGGGTTCACACACAGACACACATAACATATGGCATCATTAATAAAGTGCTTTTGGCTTCTTATTTGCATTATTTCATGCACGTTATATTCAATTATATTAAATGTTGATTAAATTCAAGTCAAGTTGAGCTTTATTGTCATTCTGCTACATGTGCGGACATGAAAGAAGAAAGGAGGGGGAATTATATTATAAAAAATATTGTAGGAAATACTGTGAAGAAGTCCTTGCTCTGATATAATTTGAAACTAAATAGCAGTTAATGAATAAACAAATAAACTCTCTTTTTGTGTATTTTCAGTCTGTGAAGGACCCCTTCCACATCTCGGACATGTCTGGTCTGGTGTCGCGGGTCGGCTGCCGCACTCGTCCG
Associated Phenotype:
Not determined