ZMP
si:ch211-262l3.1
Ensembl ID:
ZFIN IDs:
Description:
Jmjd2al protein [Source:UniProtKB/TrEMBL;Acc:Q802U7]
Human Orthologue:
KDM4A
Human Description:
lysine (K)-specific demethylase 4A [Source:HGNC Symbol;Acc:22978]
Mouse Orthologue:
Kdm4a
Mouse Description:
lysine (K)-specific demethylase 4A Gene [Source:MGI Symbol;Acc:MGI:2446210]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32882 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45096 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11870 | Essential Splice Site | Available for shipment | Available now |
sa45095 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32882
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 |
---|---|---|---|---|---|
ENSDART00000024302 | Nonsense | 107 | 895 | 4 | 19 |
ENSDART00000109814 | None | None | 174 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 17310353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17817319 |
GRCz11 | 2 | 17488488 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTGATCGTGACACCATCTCTCCTTTATGTTTAAGGTTTTGCAGTCCT[C/T]GATATGATGATTTTGAAGAACTCGAAAGGAAATATTGGAAAAATGTAACC
Long Flanking Sequence:
TTAAGGCTATCCCAAAAGGCTACCATGTATTTTACAGTTTTTAAGCCCAGTATCTCAATGAATCTGAATTGACGATTTTTCCCCCAAATAGACGTATTCAGGCCATCTGGTAAAACTATTCATAATGCATTATATATGGCAGAAAAACCAAATATCACATTGTCTGATTATTTTTAATATCATGCAGCCCTACTGCTTAGGTCTTTAACAAAGCTCTGTTTTTGCGCTCCACCACAGATCGTCCCACCGAAAAACTGGAAGCCTCGAGGTTCTTATGATGACATTGATGACCTGATCATACCTGCACCGATTCAGCAGGTTGTGACTGGGCAGTCGGGGCTGTTCACTCAGTACAACATCCAGAAAAAAGCCATGACTGTGAAAGAGTTCCGCAAAACCGCCAACAGCGACAAGTATGTTCTGTTCAACTTGTTACTTGTTTTCCTGAAGAAATTGATCGTGACACCATCTCTCCTTTATGTTTAAGGTTTTGCAGTCCT[C/T]GATATGATGATTTTGAAGAACTCGAAAGGAAATATTGGAAAAATGTAACCTTTAATCCTCCCATCTATGGAGCTGATGTGAATGGGACACTTTATGACCCGGTGAGTAAACGCTTGTTGAAGTACTAATTAAATAAAAACGAACCATATTATTTTGTTGCTTTCACTCCAGTAATGAATTATATTGACTTCATTACATTTACTTGAGTAGAATTGTTAAGTAACGTGTACTTTTTGAGTACATTTAAAAATGTGTACTTTTACTCAAGTAAATTATTTGAGAAAAGTGTTTACTCTTGCTTTGCTACATGTGGTGGCGTTCCTCCGTTACTGACAAATGATAATAAATATGATTTATATGACTTATTTGCAAATATCAAGAGGCACCGCATTGGAGAGGTTGTGTCATGAGAGGTTGTTATAGAGATGCGTCTCCTTCTTTTAGTTAGAGCGCATGTGCCTATGTTGGAATGATGGCTGAAGATGTGAGAGTTTATTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45096
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 |
---|---|---|---|---|---|
ENSDART00000024302 | Nonsense | 365 | 895 | 9 | 19 |
ENSDART00000109814 | None | None | 174 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 17304615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17811775 |
GRCz11 | 2 | 17482944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGTTTTTAGGTGGAGAGGCTGGTGCTCAAGAACTCCGCATTGAGAAC[C/T]AAAGTAATGAGGGACAAAAAAAGAGGTGAAAAAACACACCCTCTTTCATT
Long Flanking Sequence:
ATATATATATATATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGTTTAAATGTTGTATAAATGTCATCATATTTAGTCAGTTTGACGTGGCATTAAGTTATATCATGTACATAAAAAAATCCATCAGTCTTTGTCTGTTTTCTTTTAGTGTTCTTGCAGGAAAGACATGGTGAAAATCTCCATGGATGTGTTTGTGAAGAAATTTCAGCCTGAACGGTACGAGCTGTGGTTGGAGGGGAAGGACAACGCACCCATTGATCACTCTAAACCCACGCCTGAAGCAGCTGAGTTTTTAGGTGGAGAGGCTGGTGCTCAAGAACTCCGCATTGAGAAC[C/T]AAAGTAATGAGGGACAAAAAAAGAGGTGAAAAAACACACCCTCTTTCATTCTCAGTTGCCTCTCGGTGTACGTCAAATTATATATAGTATTATAATATCCCTTTCAAATGTTGCTTTTGCCACTTTCATTAGCCTGGCCAAACAAAGGATAGGAACCAAAAGACACAGGGTGTGTCTGGACTTTCCAGAGGAAGTTCTTCCAAAGACTGAAACAAATGATGAGGCTGAATATGGCAAGAAGGGCCGATTGACTCCATACACAGAACAGTGCAAGGAGTATACAGGTATGTTTTGAGGATATGGCATTAATGTGTTTTAAAGGGTTAGTTCACCCCAAATTCTTTTATTATTTAATTAATTACTCGCTGTCCTTTTGTTCCAATCCCATGAGTCCTTTATATTCAGAAAATAGATAAATAGATGGATGGATGGATAGAAAGAAAACAATATTGGCATAACAATCAATATAACATACACTTCGACCACAAACACCTTAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11870
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 |
---|---|---|---|---|---|
ENSDART00000024302 | Essential Splice Site | 572 | 895 | 11 | 19 |
ENSDART00000109814 | None | None | 174 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 17298903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17806063 |
GRCz11 | 2 | 17477232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTAGACGTGAGGCCAAATACACCAACTCCACCCCCAGACACACCAGAGG[T/C]TGGTAACTGCATGCAGTGTTTGTATTTTATTTTTATATGGGCATTAAACT
Long Flanking Sequence:
AATCATAGCAACCAGTCTGAAATTTCCTGTAAACCAAATCTGCCTTGTTTCAGAGTTGAAGCATGAAGACCGCACACTTCCACTGATGGGTTCAACCAGTTTAAAGATGCTGCCAGGATCCAGAAGTGCTGAATTTTCGGAAAACGTTCGGGGTGCTGGTTTTAGTGACGCAGACCTGGATGCTAAAGCAACTAGCCATATTTCAGCCTGTGCGCAGCCCTTCCCAAAGCATCACCTCTCTATCGCATCTGTCCCTACTGTCCCACACTGCTTGTCAGCTGTGCCACGGGTATCCACCAAACCAGGGGTGGCAAGCCTTCTCTTTCATCGCACCCTCAGCCCGACAGATGCCCTGCAGGTCCACAGCTACGCAGCCAAAGCTGCACTCTGTAAACCACAAACACCCAGTCCAGAGAAACCCAGAGAAGACCTACACATACCAGACATCAGTCTAGACGTGAGGCCAAATACACCAACTCCACCCCCAGACACACCAGAGG[T/C]TGGTAACTGCATGCAGTGTTTGTATTTTATTTTTATATGGGCATTAAACTGTAAAAAAGGCTAGGTTCCACTCAAATTGTTGAAGTTTATTTGATCGATTTAACAAATTCAAATGAATTGAACATGAAACGATTGAGTTGTCCCAAAAAATACATTAAAATACATGAAAATACAAATTAAAATAATTTTATAATTTCATTACAGTAAAAAAAGACTTTACAAGGCAAGCAAGACACTCTTCAAATTTATGTTTTGAGACCAGGCTTGACCAAACTGTTCATACTAGATACTGAATTAGTCATTCTAGGTTGACTCCCTTGTAGGGCTGGGTGACATTGCAAAAATAATTCTGACAGTATCATGATTCATATTATTCAATATTAGTAATTTTTTTTATATTTTTAAACAATATATTTAAGAATATTAGTTTTTTTAACCACTTTAATTTACTAACAGTTCTAATACAAATAGTTTTAATAGTCAAAAACTAAAATATTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45095
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024302 | Essential Splice Site | 609 | 895 | 12 | 19 |
ENSDART00000109814 | None | None | 174 | None | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 17295414)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 17802574 |
GRCz11 | 2 | 17473743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTGCCGCGTTTGCATCCTCTGCTCCGAGAGAACTCCAGTGATGACGG[T/A]ATCATCTGCTTTTCCGCATTTCATTTACGGTGATTCCACTGATTGTGCTG
Long Flanking Sequence:
CATTTATTTATCAAGTTTGCATTCAATTAAACGATAAATGACTGTAAAAACACTGAATGTTACAAAAGATTTCAGTTTATTTAGAATTTTCTATAGATAAGTGTAGTCTTTAATCTTTCCCAAATTAGATGGTAGATTTAGGCAGATGACATTTTCTTACATTTTCTACATTTACACGTATATTAAACAGTATCTCATTATATTAAGTTGGTTACTGCATTACACATTTAAAAAGTACTGATAAAAAAAAGCATTGTTAGTCTTATCCCACTCCTTTCTTTATTTAGCAGTATAACATCACAAATAATTATTAAAACAAGCTAAAAAACATCAAACCTCTCATCAACATGTATAAAAATGAAATGTGATGCGTCTCTGTCTTTTCCATAGCACGAAATTGAAGGTGAGAAGGAGAATAACAGCATGAAGAGGAAACTGCAGCCGCTCAGCAAGTTGCCGCGTTTGCATCCTCTGCTCCGAGAGAACTCCAGTGATGACGG[T/A]ATCATCTGCTTTTCCGCATTTCATTTACGGTGATTCCACTGATTGTGCTGTTGCTTATTATCTCCTCCACTCCGCAGAGATCCAGGAGCCAACAGCTGAGCCAGAGGAGACCGATCCCTGGGCTAAAATCCTGGCTCCCATGTGGCAGAGCAGACAACGCAACTTTCAGATCGAGAAGGAGTTCAACTTCCGCATGGGCCTGCATCCACCGTACTGTGCAGTGTGTTCCCTCTTTCACACCTACAATGAGGTAGCTCATGCTCTTACTGTCATAATCATCATAATTCATATTACTTCGTTCATTTGTTTGGCTATACAATGCAAGTTCATGCTAGCTGGGTCTGGGTATCAACCTGATTTTGATTCTAAATTTGATTGTGACTATAAATTTAATACAAATGCTATTGATATTTCATTGAGCTAGTGATTCATGCTATTAAAATTAGTGAACACTAATTTAGTATATTTAGTATATAGTATATACTAATATATATATATCA
Associated Phenotype:
Not determined