ZMP
jhdm1da
Ensembl ID:
ZFIN ID:
Description:
Lysine-specific demethylase 7A [Source:UniProtKB/Swiss-Prot;Acc:Q5RHD1]
Human Orthologue:
JHDM1D
Human Description:
jumonji C domain containing histone demethylase 1 homolog D (S. cerevisiae) [Source:HGNC Symbol;Acc:
Mouse Orthologue:
Jhdm1d
Mouse Description:
jumonji C domain-containing histone demethylase 1 homolog D (S. cerevisiae) Gene [Source:MGI Symbol;
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15622 | Essential Splice Site | Available for shipment | Available now |
sa9752 | Nonsense | Available for shipment | Available now |
sa10471 | Nonsense | Available for shipment | Available now |
sa10721 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15622
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002851 | Essential Splice Site | 154 | 613 | None | 14 |
ENSDART00000113426 | Essential Splice Site | 154 | 846 | None | 21 |
ENSDART00000123801 | None | 154 | 188 | 4 | 4 |
ENSDART00000130409 | Essential Splice Site | 154 | 875 | None | 19 |
Genomic Location (Zv9):
Chromosome 4 (position 21441677)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22785012 |
GRCz11 | 4 | 22505987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACTGCCCCCYCCATCAKTCTCTGTCAGTGATGTGGAGCATWACGTTGG[T/G]AAGATTTWAGAGTGTGTGTTTGTGTGCRTTGAATTTAMTGTCTACCTGAT
Long Flanking Sequence:
AATTATTGTCCATGCAGTTTGTTATACAGCTCTAAGTGATAAAAAACATCCAGTTGAGGTTTTGATTCTCAAAAAATAGTGGACTTGTTGTCATTTATATGAATAGTCTAATGCCTCATTCACACTAGCAGAGAATGTGGCCTGCTCCTTTAAAAGTATGCATAAGGAGACTTTTATCCAAATAAAAGTACATTCTTTCTATCAGTTTTTGTCTCTCTTTGGTATCAAACCCACAGCTTTTGCTATACTAGCACACAAACTTTATTATTTTGACTACAAAAACCAATAATGACATTATTGCTCTTACTCGATCAGACTTTTGAATGTTGCCTCTTCCACAGCGGTGATATTCTGGTGCAGATGCAGGGGAATCAGGTGACCAAACGCTTCTTGGAGAAAGAGGGCTTCAATTACCCTATAGTGGTGCATGACCTGGATGGACTGGGGCTGAAACTGCCCCCTCCATCATTCTCTGTCAGTGATGTGGAGCATTACGTTGG[T/G]AAGATTTTAGAGTGTGTGTTTGTGTGCATTGAATTTACTGTCTACCTGATGACTCCCAGGAGAGTATTTGGGCTTTTGGGACACTACAGTGATATTAGTATTTAAATCAATAACACATTGGAACTTGTACAAAATGGTTTGCCTGTATATGGTTTTCTGGCCTCAAAAAGTGTAATGCTGCTTTATTTTTACCATTTATTAATATTTGTATTGCATATTTGCTTTATTCTGTGCTAAAATAATGGCCTATCATATGTTTTTGCTGTGGTTTACTGGAGAAGTACTGCAATGGCATTCAGTGTAACAATGTTGTTTTTTTATTTTAATTAATTTTCATTTTATTAATTATAAAGTGTTTAAAATGTAACAACGTTTACTATTATCCATTATTTTTTTTATTCGTTTTGAAGAAATAACTTATAAGTATTAGTTATGACCATGTGACTTGAGTTATGATGATGAAGTTTATCTCTGAAATCCCAGGAATCCATTTAGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9752
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 |
---|---|---|---|---|---|
ENSDART00000002851 | None | None | 613 | None | 14 |
ENSDART00000113426 | None | None | 846 | None | 21 |
ENSDART00000123801 | Nonsense | 183 | 188 | 4 | 4 |
ENSDART00000130409 | None | None | 875 | None | 19 |
Genomic Location (Zv9):
Chromosome 4 (position 21441590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22784925 |
GRCz11 | 4 | 22505900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AMTGTCTACCTGATGACTCCCWKGAGAGTATTTGGGCTTTTGGGACACTA[C/A]AGYGATATTAGTATTTAAATCAATAACACATTGGAACTTGTACAAAATGG
Long Flanking Sequence:
TTGTCATTTATATGAATAGTCTAATGCCTCATTCACACTAGCAGAGAATGTGGCCTGCTCCTTTAAAAGTATGCATAAGGAGACTTTTATCCAAATAAAAGTACATTCTTTCTATCAGTTTTTGTCTCTCTTTGGTATCAAACCCACAGCTTTTGCTATACTAGCACACAAACTTTATTATTTTGACTACAAAAACCAATAATGACATTATTGCTCTTACTCGATCAGACTTTTGAATGTTGCCTCTTCCACAGCGGTGATATTCTGGTGCAGATGCAGGGGAATCAGGTGACCAAACGCTTCTTGGAGAAAGAGGGCTTCAATTACCCTATAGTGGTGCATGACCTGGATGGACTGGGGCTGAAACTGCCCCCTCCATCATTCTCTGTCAGTGATGTGGAGCATTACGTTGGTAAGATTTTAGAGTGTGTGTTTGTGTGCATTGAATTTACTGTCTACCTGATGACTCCCAGGAGAGTATTTGGGCTTTTGGGACACTA[C/A]AGTGATATTAGTATTTAAATCAATAACACATTGGAACTTGTACAAAATGGTTTGCCTGTATATGGTTTTCTGGCCTCAAAAAGTGTAATGCTGCTTTATTTTTACCATTTATTAATATTTGTATTGCATATTTGCTTTATTCTGTGCTAAAATAATGGCCTATCATATGTTTTTGCTGTGGTTTACTGGAGAAGTACTGCAATGGCATTCAGTGTAACAATGTTGTTTTTTTATTTTAATTAATTTTCATTTTATTAATTATAAAGTGTTTAAAATGTAACAACGTTTACTATTATCCATTATTTTTTTTATTCGTTTTGAAGAAATAACTTATAAGTATTAGTTATGACCATGTGACTTGAGTTATGATGATGAAGTTTATCTCTGAAATCCCAGGAATCCATTTAGTTTTTAAATATGTTCATATAGTCATCAACAGTTAAATTATTGAATAAATACTGTTTTTGGTGAACTCTGGAAGTACTCTAGTATTTTAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10471
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002851 | Nonsense | 337 | 613 | 8 | 14 |
ENSDART00000113426 | Nonsense | 337 | 846 | 8 | 21 |
ENSDART00000123801 | None | None | 188 | None | 4 |
ENSDART00000130409 | Nonsense | 337 | 875 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 4 (position 21432285)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22775620 |
GRCz11 | 4 | 22496595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGCTGTTCTCACTTCTCAGGACTCGATGGCGTTTGGAGGAAACTTCT[T/A]GCATAACTTAAACATAGACATGCAGCTCAGGTGCGATCCTTCAGTCGSGG
Long Flanking Sequence:
AGTTTTATAAATTTATATATTTAAAATATTTAGGTGTTCCTTTCTGACCAGCCTGGAATAAATTGAAACAAAATAAAATTACATTTAAAATTACATTTCAATATGTTTAATGTCATTTATTTAATCATTAGATTTTTAAACAGACGTGTACAAAGTAAAACTACAATTAAATAAAATGGTAAATCTATTTGAAAATAATTATTTAATGTTTACTCATTTGATCTGATTCAAATTAAATGTATTTAAATTAATGTGATGAATCTTTCTAAATAAAATGTATAAATTAATTTTAATACTTGATGAATATAATGAATAACCTTAATGAATATGTCTGATATATATGCAGAGACATTGCTAAAAACTAAAAGGTTGAAAGTTTTTTTTTTAACTGGAATTGATGATTAGAGTAAGGTTAGCTTATGTGTGTTTGTCTCCCTCTACAGGCTGGATTCATGCTGTTCTCACTTCTCAGGACTCGATGGCGTTTGGAGGAAACTTCT[T/A]GCATAACTTAAACATAGACATGCAGCTCAGGTGCGATCCTTCAGTCGCGGTCTTTCTGAAAATCTTATACTTACACACTCAGCGTGTGTGTGTTTATAGATGTGTGTTTTCCTGACAGATTTGATCTGATTTCAGGTGTTATGAGATGGAGCGCAGACTGAAGACTCCAGATCTCTTTAAGTTCCCATATTTTGAGGCCATCTGCTGGTATGTGGCCAAAAACCTGCTGGAGACTCTTAAAGGTGAGGTGCATTTTATCATTGAAAAGTTAAATGTTTCAAATGAAAACAATGTAATATATTGTATTATACAAGCATGAAGAAAATTTGTTGTTGTTTTTATTTAGTTTGTGTGTGTATATTCGTATGCTGACTCTCTTAAGATGGAGTTAATAAACTGTTGTAAATATTTAATACATTTTTGTGTGGTTTAAAAAAAATAAATGACTAAAATGAATGCTCATTAAATTAAATCGATTCATAAAATGTGGAAAAAACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10721
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 |
---|---|---|---|---|---|
ENSDART00000002851 | Essential Splice Site | 531 | 613 | None | 14 |
ENSDART00000113426 | Essential Splice Site | 508 | 846 | None | 21 |
ENSDART00000123801 | None | None | 188 | None | 4 |
ENSDART00000130409 | Essential Splice Site | 531 | 875 | None | 19 |
Genomic Location (Zv9):
Chromosome 4 (position 21430176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 22773511 |
GRCz11 | 4 | 22494486 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACACACTGGAGGTGTTGAAGAGACTRGAGGTTGGCCAGCTGAAGGAGG[T/C]CAGTGCTGTGGACACTYTATTCTTTATCAMGTTTTTTTTTNNNTGTTTGTTTG
Long Flanking Sequence:
TATTTGAATTACATTGTATTAAAATGATTTTGTTGATTTTGAAATGTGAAATGTTGAATTCTCTTTTTTGTAAATTATTAAACTAAAAATGTATTATATATTTATTAATGAATTCAAAAAATGAAAATAATAATGTTTTTGTTTTAATAAGTCAGTGTATATTAATACAAGATGTAATTGGGCTCTTAAAACAGCTCTTAAATGTGATTTGCTGTGTTGTTTTCTTTAACAGGACGATTCCAATAAAGCTGTGAAAACTCAGGGAAGTGCTGAATGTTCTTTATCCCGCTCGACACTGGAGAAAGGAGATCAAGCCCAACAGGCTGCTCGGCGACTGCAAGATCATCATCATCACAGACGCCGCCACCACCATCACCACCATCATCATCATCATCACCACCACCATCATCACAGCCGAAAACTGCCCTCAAACCTGGACGTGCTGGAGCTCCACACACTGGAGGTGTTGAAGAGACTGGAGGTTGGCCAGCTGAAGGAGG[T/C]CAGTGCTGTGGACACTCTATTCTTTATCACGTTTTTTTTTTGTTTGTTTGTTTTCTGTATGTTAAATATGCTTAATGGCATTATATCATTTGTATTGTTTTTTTTTTCTATAGACAAGATTTTGTCTCTCTTTCTATCACTCTATTCTTAAAAAAAATACTGCAAGCTGCCAGAAAAACAAAAACCTTTTGGTAGAATCAAATGTTCATAATCTGGCATGTTGTGTGTGAACATGTTCAGAATACAGATGGGAATATACCTGTGCAGTCTGGTGTATGTAGAAGCTGCTGAAGTGGAGATTTATGACTCTAAAACCTCTCAAGAAACCTTTTATAAATATGTATTGCAATTAAAATCTACAGACACAAATTGATCAAATGCAACAAAAGAAAGACTAAAAAGTGTATTTTTTGTTGTTTGCAATTAGGCTAAATTTTGTTTTGTTTTTTATTTAAAAGCCCAAAGTCTCAGCTCAAAGTCAAAACTGACAGGTGCATGAA
Associated Phenotype:
Not determined