ZMP
im:7163548
Ensembl ID:
ZFIN ID:
Human Orthologues:
KDM3A, KDM3B
Human Descriptions:
lysine (K)-specific demethylase 3A [Source:HGNC Symbol;Acc:20815]
lysine (K)-specific demethylase 3B [Source:HGNC Symbol;Acc:1337]
lysine (K)-specific demethylase 3B [Source:HGNC Symbol;Acc:1337]
Mouse Orthologues:
Kdm3a, Kdm3b
Mouse Descriptions:
KDM3B lysine (K)-specific demethylase 3B Gene [Source:MGI Symbol;Acc:MGI:1923356]
lysine (K)-specific demethylase 3A Gene [Source:MGI Symbol;Acc:MGI:98847]
lysine (K)-specific demethylase 3A Gene [Source:MGI Symbol;Acc:MGI:98847]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10590 | Nonsense | Available for shipment | Available now |
sa15916 | Essential Splice Site | Available for shipment | Available now |
sa35680 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35679 | Nonsense | Available for shipment | Available now |
sa42386 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8914 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22464 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10590
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 |
---|---|---|---|---|---|
ENSDART00000089845 | Nonsense | 461 | 1776 | 9 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22656985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21358473 |
GRCz11 | 14 | 21655718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTCAGACCCCTAAAGCCCCTGTTCTAGCTCCTGCTGGATTTGGTAAA[C/T]AGTCCAGTGGAGGGGTGTTTGGGAATGTCTCAACACAGACTAATGGATCT
Long Flanking Sequence:
AGAATGGCAGTTTTATCCCAAACCAAGAAAGGATTTCTTCAGTATCTGCAGTGCTTCCTGCTTCTACTCCAACGCCACCTCCTTTGAAGCCTGCCCCATCACCTTTTTCTAACACTTTTCCTTCTTTGGGTCAAATGCCCAACTTGGTGCCCGGGGCCCCTGCCCCGAAATCATCTCCCACACTCCCATCGTCAGAGAGGGAGGAGGGAGGTGTTCTTTCAGGGTATCCTAAAACAGCTGCCCTGGTGTCTCCAGGTCCTGTGACCATTTCATCACCTTCCCAAGAAAACACTTCAAGTGTGGCTCTCACTGCTCCTGTTGATGCGAACCAAAAGCCCAGTATGTGGGGATCAACCTCAGAAGGAAATCAGGTGGGGCTTTTACAAGAACAGAATTTTTTATTTATTTATCATGCGTTATTCTCTGATGCTTATTTATATCTCTTTTTTGTATTTCAGACCCCTAAAGCCCCTGTTCTAGCTCCTGCTGGATTTGGTAAA[C/T]AGTCCAGTGGAGGGGTGTTTGGGAATGTCTCAACACAGACTAATGGATCTTCCCAGGGGGACAAACCCTTTGGGTTTTCATTTAGAGGTGCAAAGGACTCGCAAAGGCAGGACTCTGATACGTCACAGAACCTGTTCTTCCAATTCATCTCTCAGAACCAGAGCAACACACAAGGCCAATCAAAAGCCTTCACATCTTTGTCCGAGTGCCTGAACAAGGAGCCGCCCAGCCTGTTCAAGTCTGCTGCTCCCTCTGAGGGTTTCAAAAAAACTGTTGTGGCTTCTGCATCCACTGGACTGTTTGGTTCAGCACCTGCCAGTGGCCTGGCACCACTGAAAGAGCAGCCAAAAGTGCCTGATATCAAGCCTGCAGGCAATGGGATCCTTATGAACAAGCCTTTTGGTGCTGTAGGGGAGGCACAGAGCAAACTCCCAGCCACTTTTTCTTCTGCCATAATTCAAGCTGCAAGCTCTACAGAGGTGCTGAAACCCTCGGGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15916
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 |
---|---|---|---|---|---|
ENSDART00000089845 | Essential Splice Site | 929 | 1776 | 10 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22653936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21355424 |
GRCz11 | 14 | 21652669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGATGATGAYGACCCAAATGTAGYCTGTCGATTCTTTCACTTTCGCAG[G/A]TGAATATGATTCTGGTATATTTAGCTTTACTTATATCTGAACTGTGATAC
Long Flanking Sequence:
AAAAAATACCATTTTTATTTTGCTAGCTTACATTGTTAGACTTGAGGCTAAAAATTAAGCTGTGCAAGTTGATGCACAAAAAATGGTATGATCTTTTATTAAAATCTAATCATTTGCTTCTGTTTGATGGCTTTGTTAGCCATGGCCCTACAACAGTTAGTTTGCTGTGAGTCTAGAATGACAAAGCTTTACAACAATAAAACAATATTGGCCACCACTAATCAATATTTCATAGTGATATATCTATTAACATTCACAGGTTGTAATTTGGGTTTATATGTCATCTCTGTAGTTGGACAGTCTGTGTTGAAGGACCAGAATAAGGTACGGCGCTTGAAGCAGTCTGGAGAGGCCTTTCTACAAGATGGCTCCTGCATTAACGTGGCTCCCCACTTGCACAAATGTCGTGAGTGCCGTCTGGAGCGCTACAGGAAATCGCGTGAGCAGGACTCTGATGATGACGACCCAAATGTAGCCTGTCGATTCTTTCACTTTCGCAG[G/A]TGAATATGATTCTGGTATATTTAGCTTTACTTATATCTGAACTGTGATACTGATGAATTTGACTTGTGTTATGACAGGTTGGCTTTCACTAAAAAGGGAGTTCTTCGTGTGGAGGGTTTTCTGAGCCCACAGCAGAGTGACAGCATGGCAATGGGCCTGTGGCTTCCTTCCATCACAATACAAGAAGGACTTGACCTGGACACGTCCAAATATATTTTAGCAAATGTGGGGGACCAGTTTTGCCAATTGGTCATGTCAGAGAAAGAAGCCATGATGATGGTAGAACCACATCGTAAGTAACAATTTTAACAGTTATTTAAAATTCATTTAAGGCTCATTTATACCTAATAATAATCTAAATTATTTCCAAGAAAGTTTTATATAATACCAAGGGCATGGTTTGCACTTGACATTGGTGGGGATAGGTGAATACAATAATACTATTTATCAGAGTAGCACGGTTTGTGCTTATTTTAAATGTAAAATATACATTTTTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35680
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089845 | Essential Splice Site | 1001 | 1776 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22653642)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21355130 |
GRCz11 | 14 | 21652375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATTGGTCATGTCAGAGAAAGAAGCCATGATGATGGTAGAACCACATCG[T/C]AAGTAACAATTTTAACAGTTATTTAAAATTCATTTAAGGCTCATTTATAC
Long Flanking Sequence:
GGACAGTCTGTGTTGAAGGACCAGAATAAGGTACGGCGCTTGAAGCAGTCTGGAGAGGCCTTTCTACAAGATGGCTCCTGCATTAACGTGGCTCCCCACTTGCACAAATGTCGTGAGTGCCGTCTGGAGCGCTACAGGAAATCGCGTGAGCAGGACTCTGATGATGACGACCCAAATGTAGCCTGTCGATTCTTTCACTTTCGCAGGTGAATATGATTCTGGTATATTTAGCTTTACTTATATCTGAACTGTGATACTGATGAATTTGACTTGTGTTATGACAGGTTGGCTTTCACTAAAAAGGGAGTTCTTCGTGTGGAGGGTTTTCTGAGCCCACAGCAGAGTGACAGCATGGCAATGGGCCTGTGGCTTCCTTCCATCACAATACAAGAAGGACTTGACCTGGACACGTCCAAATATATTTTAGCAAATGTGGGGGACCAGTTTTGCCAATTGGTCATGTCAGAGAAAGAAGCCATGATGATGGTAGAACCACATCG[T/C]AAGTAACAATTTTAACAGTTATTTAAAATTCATTTAAGGCTCATTTATACCTAATAATAATCTAAATTATTTCCAAGAAAGTTTTATATAATACCAAGGGCATGGTTTGCACTTGACATTGGTGGGGATAGGTGAATACAATAATACTATTTATCAGAGTAGCACGGTTTGTGCTTATTTTAAATGTAAAATATACATTTTTACTTGAAAAATTTTATTTATTTAAAAAGGTGCCAATGGGATTTTCCTTTTTTGAAATGTATGAATATTCCAGGTACAGAACAAACATCAACTTTAGGCTCTTCTATATATAGAGGTTTTCCAAGATCTTGTTAACTTTGGTTGGTCAAAGCAAAAGTTAAGATTTTGTTGTTGAACCACTGCACTATTTTGACATTTAAAAATATAAAATACTTAATTCATAAAGATAATTTAAATAAAAGCATTTTCCCTCAATAAATTATGCACTCTCATATTTTATGACTAAATCAGAATCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35679
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 |
---|---|---|---|---|---|
ENSDART00000089845 | Nonsense | 1241 | 1776 | 15 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22647162)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21348650 |
GRCz11 | 14 | 21645895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGCAAGAGCAGTTCTTCAGCACTTCACTGGCTGGCAGATCTGGCCACA[C/T]AAAAGGAGCCCAAAGGTGAGACTCGAATATAGAGCACTTTACAGTGAGTG
Long Flanking Sequence:
AAACATAAGGTTAGGAATACACAGGATTAATTGTTAACCCCAATTAGCGTGAAGTGTAACAAAGAAACATTATGAGTTTGGATTGAACCATGTTTCACTGTTTTAAATGTGAAAAACTTGCATCTTGTATTTTCTTAATTGGTCCTGTGTTTTATTTGGTGCAGTCGGGTGCAGCTCACAGTTCGGGGAATGGAACCACGTCTACTTCATCCACAACCCGTCCAAATGAAGAATCTGCAGCTGGTGTTGTAGTCAAAACTGAACCCGTTGAAGAGCCTACAAGTGCTGATACCACATCAAGTACCAGTGGGACAAATAGCAGCACATCTAGCCCTGCTCCTGCTCCAACTTCTGCTCCTACTCTTCTTCCTCCTTCTCTTCCTCCTCCTTCACTTCCTCCTCCTTCACTTCCTCCTGCTCCTGCACTTGTACCTACACCTCCTGCAAAGGATAGCAAGAGCAGTTCTTCAGCACTTCACTGGCTGGCAGATCTGGCCACA[C/T]AAAAGGAGCCCAAAGGTGAGACTCGAATATAGAGCACTTTACAGTGAGTGGATGGAAAGTGATTTGCTTTGCATTTGTGTGTGTGTGTGTGCGCACTCGGAGGAGATGTGTGTCTGTGGTCTTTTACTGACTCGATGAATGCAGAAAAGTGTCAAACAGCTGAGTGTGTATGGCTTATCTTGTCGCAAAATGCAGATAAAAGTCCTACAAAACAGTAATAGTTTGATTACATCATTTTCATGTCTGTACTGCACTTTAATAATGCGACTGAAATAGAAATACTCCATATGTCTTAATTTGATTAGTGTTTATGACGATTATGGCTTTAAGCATATATAAAGTGCTATTCCATCCTATGTTGGTTAATGGTTAATGCGTGTGGCTGCAGTTGTAGTAGTTTCTGCTTTTGAAAGCTACAACTCCGGTGAAGAAATAATTGGTTACATAACAGTGACCTGCTCTAAATGCGTGAACCACAACTTCGAGGCCAGCCTATCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42386
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089845 | Essential Splice Site | 1421 | 1776 | 18 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22641586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21343074 |
GRCz11 | 14 | 21640319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCAGTTGCGTTCTGCTAATGCTAATGAAGTGTTTTTCCTCTTTTTTTA[G/A]CCTGTGCTGGTCTCAGGCATACACAGGAAGCTGAAGGAACACTTATGGAG
Long Flanking Sequence:
TAATGCTATTTTTTCCACTAAGTTTAAGCTTTCGAGCTGTTTTAAATATTTTAGGTCATTTTTTTTTCTCAAGTGAAAAAAAGTCTGTCCCAACTACTATCTAACTTTATAAATATATTTCTTTCTCTCCCTCTTTAGCAGGCTGATAAAATGAAGGGAGGTCTTCCTAACTTCCTGGATCATATCATTGCATCAGTAGTGGAGACTAAGAAGTCAGAGGTTCGTCGTGCATCAGGTTCAGCAGAAGTCATCGAGTCTGCCACTGCTCCTCGCAGAGAGGGGGTGATGGGGCTGAGTGTCCTGGATCCACACACTTCACACTCTTGGCTTTGTGACGGCCGTTTGCTCTGCCTGCAGGACCCCAGTAACCCCAACAACTGGAAGATCTTCAGAGAGTGCTGGAAACAAGGACAGGTGAGCTGTGAAGGGCCAGTGGAGATGCTCTTGTATGATCAGTTGCGTTCTGCTAATGCTAATGAAGTGTTTTTCCTCTTTTTTTA[G/A]CCTGTGCTGGTCTCAGGCATACACAGGAAGCTGAAGGAACACTTATGGAGGCCTGAGGCCTTCAGCGAGGAGTTTGGAGACCAGGACGTGGACCTGGTCAACTGTAGGAACTGCGCCATCATCTCTGATGTTAAAGTCAGGGAATTTTGGGATGGCTTCCAGGTCATTTCCAGTGAGTACAGATGCTTTAAACTCCCAAGGAAAAAAATTGACTTTCAAATCTGTTAAAATGATTGGTAACTGTTAAAAAGCACTGCATCTTAGATCCCCCCCAGCTCTAATTGTACCCAGACCTAATAAAAAAATCAATTAAATCTTTCCATCACATTCAGAATTTTTTCAGCAAAATACTAATATTTTTTAAATTACATAAATGTATCAGGTGTTATCAAATGTGAGGAAAGTTTTAAAGTAAAAAAGATTTCAAAATGTATCATTTTAACTTGGTCTTCAAATCAGGACATTCAAATATATGTTCAAATGCATGCTCCATTTCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8914
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089845 | Essential Splice Site | 1592 | 1776 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22638163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21339651 |
GRCz11 | 14 | 21636896 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTATGGTGTATGTGGGCATCCCAGAAGGAGAGAATGACCAAGAAAGTGG[T/G]AAATATRAGTCARTTTTATTTTTGAAAGCAGCATCATTTAGAATATTACA
Long Flanking Sequence:
AGTTATTTTAAATGTCTGGGTAAAAACCAACATATTTGTTTCCCCATTGAACACAATATATTTTATATTATGAAACATTAAAAATATTTTTAACCAGTAGCTTTTTTCGCCCTAAAAAACAAAATAAAATAGTTGTGAAAAACGTAAAAACATATACCTTGGAAACGCTATAACAGAAAACTTTGACTTTTCCAAACCGCAGTACACCTTGAAACTGGTTATCGTTCTATGCCTAGTCTACATGCACCTACATGCCTATTACCACAAGGAAAACACAAAACTTCATAAAATCTGTTGACCACATGTGGCAAATGACTGTAAACAAGCATGCAAAATTATGTGGCGCTATAGTTAAAAGTGTCTTTCATGTTTTTTTCAGGTCTGATCTCCACAGAAGACAGGAAGGTCGGCACCACTAACTTGCATTTGGATGTGTCTGATGCCGTCAACGTTATGGTGTATGTGGGCATCCCAGAAGGAGAGAATGACCAAGAAAGTGG[T/G]AAATATGAGTCAATTTTATTTTTGAAAGCAGCATCATTTAGAATATTACAGGATTTCTTGCTCAAATAATTAAGCTGTTGTTTGTGTTCACTAAAATTGCTGCAAATATTTTAGTTAAACAGGATAAAGTAAAAACTTTGTAACCATGAATATTTGAGTGATTTCTTTTTTTGAAGGTAAATTTTGAAGGTAAAAGGTAAATTAATCAAAAAGTCACTCAAGATAAAATAAAAATAAAAAACAAGATGATGTGTAATTTAATTTTTAGGTTTTCTTTTATTTGAAAATTCCACATCACCACGGACAGTTTCATATTTTTTTTAATGAAAAATGAAACAAATAAATAATTTTCCCTGAAAATTCTCCCTGTCCTTAAAGCTAGTTTTACTAAATGAAAATGTTTTCACATTCATGTTTTTTTTTTTTAAACTGGGGATAATGAGTTTGTAAGCGATTAAAGTGTGTTTGTGGATTTTTATTGTAGTTTATCAATTAGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22464
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089845 | Nonsense | 1667 | 1776 | 24 | 26 |
Genomic Location (Zv9):
Chromosome 14 (position 22631408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 21332896 |
GRCz11 | 14 | 21630141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGGTCAAGAGAACCCACCAGACCATGATCCTATCCATGACCAGAGCTG[G/A]TACCTGGACCAGACGTTGCGTCGCAGGCTGTATGAGGAGTATGGAGTCCA
Long Flanking Sequence:
TCCAAATTAGAATCTGAATTAGGTTTTATGTGTAAAACTGGAATATCACATGAAAAATTTGATAATCACATAATCTATGAAACAAAATCCTATGCATTTTATATGCGTATGCTATAATTTCTTCAGTAAAGTTTCCATCAAAGTTTAAGTGCATTTTTTTTTTATCGAATTAAAAATTTATCCTACTCAATTGAGCATACTTTTTATTATTATGGGTATTTTTAAAGTTATGCACATCTTGCTGTTTCCATTAAGCATTTTTATGCAATAATCCAAAATGCACATAAACATAGGTGGATGGAAACATATCTACTGCCTGTATGAGGTTTTATGATTCCTAATAATAAATCTTAACATTTGCAGATTCCTGGTGTTCCACTTTTTATTTGTTAATACAGTGATTGACTGAAGTTTTTCTGAAATTTCTGTTAATTGCAGGTTGGAGAGGAACAAGGTCAAGAGAACCCACCAGACCATGATCCTATCCATGACCAGAGCTG[G/A]TACCTGGACCAGACGTTGCGTCGCAGGCTGTATGAGGAGTATGGAGTCCAGGGATGGTCCATTGTGCAGTTTTTGGGAGATGCAGTGTTCATCCCAGCTGGAGCACCACATCAGGTTCGTTTTGTGAGAAAAACTCTAGTGCTACATTGTAGCAGTAGCAATACATTGCATTTTCAAAACTACATTCAGAACCTCCCAGAACACCAATACATAGTGGCCATTGTGTTTTCGTTACATTTCATTATTTGATGCTTAGTTCAGAACAATAAAACGCACAAAAATCGAGTGGTTTTAAACAGTAATGAGTATTTTTCTTCTGCTGAACACAAAAGAAGATATTTTTTAATGTTGGTCCTCAGTAGGCAGCCATTGACTTCTATGATATTATTGCCCAATGCTTGTAAAGTACTACAGTTTTTTTTCTTAATATTTAAAAACTTTCTGCAAAAAAAATTTGATGGGATGTAAATGAGGAGTAAATTTTCATATTTATTAGATAA
Associated Phenotype:
Not determined