Busch Lab

ZMP

KDM6B (1 of 2)

Ensembl ID:
ENSDARG00000088087
Description:
lysine (K)-specific demethylase 6B [Source:HGNC Symbol;Acc:29012]
Human Orthologue:
KDM6B
Human Description:
lysine (K)-specific demethylase 6B [Source:HGNC Symbol;Acc:29012]
Mouse Orthologue:
Kdm6b
Mouse Description:
KDM1 lysine (K)-specific demethylase 6B Gene [Source:MGI Symbol;Acc:MGI:2448492]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa16587 Nonsense Available for shipment Available now
sa8805 Nonsense Mutation detected in F1 DNA Not yet available
sa18869 Nonsense Mutation detected in F1 DNA Not yet available
sa26939 Nonsense Mutation detected in F1 DNA Not yet available
sa40872 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa16587
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127719 Nonsense 81 1955 3 20
Genomic Location (Zv9):
Chromosome 7 (position 22933626)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21498811
GRCz11 7 21765149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTATCTTTSTGTGTWTCCAGACCCATACATCGAGGGGATAAGCAAGAC[C/T]AGTCTCAGGCTTWGATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCC
Long Flanking Sequence:
AGCGAATCATTTTCCTTGCATTTAAGATGGGTAAAAAGCTTCATAACAAAATAGTTTTTGTTTATTGTCTAGGCTGGATGCATCACACAGCAGAGCAGTTCACCGGGTGCAGCACACGGGACCCTTTTCCTCTGGACGGACTCAACCGGGGACCATGGGCTCCCGTGGGCAGCCGTGCCTGGCCACCTCCTTCCAGGTAATTTACCTCATCATCAGGGCTCATTATGCTTTTAAGGACGTCATTGATACATGTTAATTAAGAAAACAACTGAGTTGATTCCTCTTCTCTTGATAGGTGCTTAACTGGTGTCAATCAGCACCAGCTTCTTCCCCATATGCCCAGTCACATGACTGGGCTAAATCATCCTAGTAAATTCTTGAACAATGGGTGAGTTTCTGTTAATCTTTGCTAACACTTCTGGTAAAATGCACTTTTTGCATTGTTTGCTGATTTATCTTTCTGTGTTTCCAGACCCATACATCGAGGGGATAAGCAAGAC[C/T]AGTCTCAGGCTTTGATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCCAGGCCTTGGGATCCAACCAGAGCTGGCCAAGGGTATGAGCCATTGCCTGGTGATAACCACAACAGATTGCGCAATAGCTACAATGCAGGGCCTCCTTCACACCTTACAGCTCGAGCCAATCAGCTACTGAAGGTAAAAATTAGATGTTAATATCTTTACCAAACCTTTTTTATGTGCTTTCTTATGTAAATAGAAGTTGTTCATGCAACAATAATCAGTATTTTTAAATGTTTATGGATTTCTGGCATTGTATTACGGTGACATTGTGCTGTTGTGCATTTAATTGCATTTCTTTTGCCAACCTCTCTTTTTCTTTCTCAAAGTTTGGTGCTCCTCATCCTCAATTGGCAACCCATGGATCACGGCCCATTCATCCATTACCTGATTTATGGACTCCACCTGAAAATCAGCAGCAACCCAGGGGAACTCACTCTAATTCTGGACAATTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8805
Status:
Mutation detected in F1 DNA
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
ENSDART00000127719 Nonsense 85 1955 3 20
ENSDART00000127719 Nonsense 85 1955 3 20
Genomic Location (Zv9):
Chromosome 7 (position 22933639)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21498824
GRCz11 7 21765162
KASP Assay ID:
2259-8713.1 (used for ordering genotyping assays)
KASP Sequence:
TGTWTCCAGACCCATACATCGAGGGGATAAGCAAGACCAGTCTCAGGCTT[T/A]GATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCCAGGCCWTGGGATC
Long Flanking Sequence:
CCTTGCATTTAAGATGGGTAAAAAGCTTCATAACAAAATAGTTTTTGTTTATTGTCTAGGCTGGATGCATCACACAGCAGAGCAGTTCACCGGGTGCAGCACACGGGACCCTTTTCCTCTGGACGGACTCAACCGGGGACCATGGGCTCCCGTGGGCAGCCGTGCCTGGCCACCTCCTTCCAGGTAATTTACCTCATCATCAGGGCTCATTATGCTTTTAAGGACGTCATTGATACATGTTAATTAAGAAAACAACTGAGTTGATTCCTCTTCTCTTGATAGGTGCTTAACTGGTGTCAATCAGCACCAGCTTCTTCCCCATATGCCCAGTCACATGACTGGGCTAAATCATCCTAGTAAATTCTTGAACAATGGGTGAGTTTCTGTTAATCTTTGCTAACACTTCTGGTAAAATGCACTTTTTGCATTGTTTGCTGATTTATCTTTCTGTGTTTCCAGACCCATACATCGAGGGGATAAGCAAGACCAGTCTCAGGCTT[T/A]GATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCCAGGCCTTGGGATCCAACCAGAGCTGGCCAAGGGTATGAGCCATTGCCTGGTGATAACCACAACAGATTGCGCAATAGCTACAATGCAGGGCCTCCTTCACACCTTACAGCTCGAGCCAATCAGCTACTGAAGGTAAAAATTAGATGTTAATATCTTTACCAAACCTTTTTTATGTGCTTTCTTATGTAAATAGAAGTTGTTCATGCAACAATAATCAGTATTTTTAAATGTTTATGGATTTCTGGCATTGTATTACGGTGACATTGTGCTGTTGTGCATTTAATTGCATTTCTTTTGCCAACCTCTCTTTTTCTTTCTCAAAGTTTGGTGCTCCTCATCCTCAATTGGCAACCCATGGATCACGGCCCATTCATCCATTACCTGATTTATGGACTCCACCTGAAAATCAGCAGCAACCCAGGGGAACTCACTCTAATTCTGGACAATTAAAACGTCCTGGTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18869
Status:
Mutation detected in F1 DNA
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
ENSDART00000127719 Nonsense 85 1955 3 20
ENSDART00000127719 Nonsense 85 1955 3 20
Genomic Location (Zv9):
Chromosome 7 (position 22933639)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21498824
GRCz11 7 21765162
KASP Assay ID:
2259-8713.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCCAGACCCATACATCGAGGGGATAAGCAAGACCAGTCTCAGGCTT[T/A]GATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCCAGGCCTTGGGATC
Long Flanking Sequence:
CCTTGCATTTAAGATGGGTAAAAAGCTTCATAACAAAATAGTTTTTGTTTATTGTCTAGGCTGGATGCATCACACAGCAGAGCAGTTCACCGGGTGCAGCACACGGGACCCTTTTCCTCTGGACGGACTCAACCGGGGACCATGGGCTCCCGTGGGCAGCCGTGCCTGGCCACCTCCTTCCAGGTAATTTACCTCATCATCAGGGCTCATTATGCTTTTAAGGACGTCATTGATACATGTTAATTAAGAAAACAACTGAGTTGATTCCTCTTCTCTTGATAGGTGCTTAACTGGTGTCAATCAGCACCAGCTTCTTCCCCATATGCCCAGTCACATGACTGGGCTAAATCATCCTAGTAAATTCTTGAACAATGGGTGAGTTTCTGTTAATCTTTGCTAACACTTCTGGTAAAATGCACTTTTTGCATTGTTTGCTGATTTATCTTTCTGTGTTTCCAGACCCATACATCGAGGGGATAAGCAAGACCAGTCTCAGGCTT[T/A]GATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCCAGGCCTTGGGATCCAACCAGAGCTGGCCAAGGGTATGAGCCATTGCCTGGTGATAACCACAACAGATTGCGCAATAGCTACAATGCAGGGCCTCCTTCACACCTTACAGCTCGAGCCAATCAGCTACTGAAGGTAAAAATTAGATGTTAATATCTTTACCAAACCTTTTTTATGTGCTTTCTTATGTAAATAGAAGTTGTTCATGCAACAATAATCAGTATTTTTAAATGTTTATGGATTTCTGGCATTGTATTACGGTGACATTGTGCTGTTGTGCATTTAATTGCATTTCTTTTGCCAACCTCTCTTTTTCTTTCTCAAAGTTTGGTGCTCCTCATCCTCAATTGGCAACCCATGGATCACGGCCCATTCATCCATTACCTGATTTATGGACTCCACCTGAAAATCAGCAGCAACCCAGGGGAACTCACTCTAATTCTGGACAATTAAAACGTCCTGGTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26939
Status:
Mutation detected in F1 DNA
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
ENSDART00000127719 Nonsense 135 1955 3 20
Genomic Location (Zv9):
Chromosome 7 (position 22933788)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21498973
GRCz11 7 21765311
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATTGCGCAATAGCTACAATGCAGGGCCTCCTTCACACCTTACAGCT[C/T]GAGCCAATCAGCTACTGAAGGTAAAAATTAGATGTTAATATCTTTACCAA
Long Flanking Sequence:
CCGTGGGCAGCCGTGCCTGGCCACCTCCTTCCAGGTAATTTACCTCATCATCAGGGCTCATTATGCTTTTAAGGACGTCATTGATACATGTTAATTAAGAAAACAACTGAGTTGATTCCTCTTCTCTTGATAGGTGCTTAACTGGTGTCAATCAGCACCAGCTTCTTCCCCATATGCCCAGTCACATGACTGGGCTAAATCATCCTAGTAAATTCTTGAACAATGGGTGAGTTTCTGTTAATCTTTGCTAACACTTCTGGTAAAATGCACTTTTTGCATTGTTTGCTGATTTATCTTTCTGTGTTTCCAGACCCATACATCGAGGGGATAAGCAAGACCAGTCTCAGGCTTTGATGCCGGCATTGCAAAGAATGCCCCCTGCTCCTCCCAGGCCTTGGGATCCAACCAGAGCTGGCCAAGGGTATGAGCCATTGCCTGGTGATAACCACAACAGATTGCGCAATAGCTACAATGCAGGGCCTCCTTCACACCTTACAGCT[C/T]GAGCCAATCAGCTACTGAAGGTAAAAATTAGATGTTAATATCTTTACCAAACCTTTTTTATGTGCTTTCTTATGTAAATAGAAGTTGTTCATGCAACAATAATCAGTATTTTTAAATGTTTATGGATTTCTGGCATTGTATTACGGTGACATTGTGCTGTTGTGCATTTAATTGCATTTCTTTTGCCAACCTCTCTTTTTCTTTCTCAAAGTTTGGTGCTCCTCATCCTCAATTGGCAACCCATGGATCACGGCCCATTCATCCATTACCTGATTTATGGACTCCACCTGAAAATCAGCAGCAACCCAGGGGAACTCACTCTAATTCTGGACAATTAAAACGTCCTGGTCCCCCTCTCGGAGAACATTCTGTTATTCAGCATACACCTCCTCCCTCTCTACACCGGCCCATAGAAGACCTCCCCAGTCCGAGCAAGAGGAAGAAGAGCTCTGGGTCTGAACAGGTTGGTCAAGAATTATCATACATTTATTTACATCTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40872
Status:
Mutation detected in F1 DNA
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
ENSDART00000127719 Essential Splice Site 280 1955 5 20
Genomic Location (Zv9):
Chromosome 7 (position 22935446)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 21500631
GRCz11 7 21766969
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCACCCTGGAACCCAACTGAACACAAAAGTGGACCCATTCATTTCCAG[G/A]TCTGCCGTCACTCATCAGAATTTATATTAAATTTTATTTTCTTCTATTCT
Long Flanking Sequence:
AATGCTTTACTTTTTGCATGTGCGCGTCGGATGTTCAGTTTCCCTTTGTTGAAAGAGAAAACTGCCACCCACATGTGCGGAAAGACAAATCAGGACATGTGCTCTTGAATCAGTCTGCTGCCATCTGATTGGTGTTCACTCTCAGCTTTTTAGTCCAGACTGGACCAGAAGCGAGCTAACATGATGCAACAACACAGTTAATTTTCATTTACGCTAGTTGTTTGATGTAGGTTTGGTGTGTCCTGGCCCTAAGACCTCAGCTCTGAATTTTCTTTCCAAAACCTTTTCTTCGGGAAGTGTTGTAAAAAGTTGTCTCTTTTTCTGTCTTACAATAGATTGCGCATTCAGCCATGCAACGTTTATCTGGACCAACTGTACATTTGAATCAACAGCCATCCTCCCACTATCCCCCACCTAAACCTGGCTTTTGGAACCCTTTGCACAAAGTGGGAGCACCCTGGAACCCAACTGAACACAAAAGTGGACCCATTCATTTCCAG[G/A]TCTGCCGTCACTCATCAGAATTTATATTAAATTTTATTTTCTTCTATTCTCTCTATCACTGTTGCAATTGCAAAATATTTTTTCTAAGAATTTTCTTTTTACCTAAAGTTAATAGTAATCACAGACTATTGGCATTGTCATATGACATCAAGCAGTCATGAAGTGTCGTTACGGACATTTAAATTTTTCAATTTGTGTCGTGTTTACTGCATTTAGCTATTTACTCTTCTCTTTCACAGGATTCAGCTAAGCCAGAAGTTGAAAGTATCCCCTATAAAGCACCTCCTATAAGTCTATCAACCTTATCTTCTCCCACCATTAACACCACAAGTGGCTATGGACAAAGCAGGGCCTCTTCATCACAGTCACAAAAGGCCACTCAATCACCACAGTCTCTGGGACCACCTTTACAGAGCCCTCACATCCACCATTCAGCATACTCTTATTCCAACAACAGACCTTCAGACCAGTCCCAAGGAGAACCACATGGTACTACTCCA
Associated Phenotype:
Not determined