ZMP
kdm5c
Ensembl ID:
ZFIN ID:
Description:
lysine-specific demethylase 5C [Source:RefSeq peptide;Acc:NP_001116706]
Human Orthologues:
KDM5C, KDM5D
Human Descriptions:
lysine (K)-specific demethylase 5C [Source:HGNC Symbol;Acc:11114]
lysine (K)-specific demethylase 5D [Source:HGNC Symbol;Acc:11115]
lysine (K)-specific demethylase 5D [Source:HGNC Symbol;Acc:11115]
Mouse Orthologues:
Kdm5c, Kdm5d
Mouse Descriptions:
lysine (K)-specific demethylase 5C Gene [Source:MGI Symbol;Acc:MGI:99781]
lysine (K)-specific demethylase 5D Gene [Source:MGI Symbol;Acc:MGI:99780]
lysine (K)-specific demethylase 5D Gene [Source:MGI Symbol;Acc:MGI:99780]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41261 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15146 | Essential Splice Site | Available for shipment | Available now |
sa17413 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41261
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098657 | Nonsense | 547 | 1578 | 12 | 27 |
ENSDART00000127053 | Nonsense | 547 | 1578 | 13 | 28 |
ENSDART00000131117 | None | None | 544 | None | 7 |
The following transcripts of ENSDARG00000006124 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 38117308)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 36972723 |
GRCz11 | 8 | 37005157 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAGGTGCCATGGCTATATGTGGGCATGGTGTTCTCTGCTTTCTGTTG[G/A]CACATAGAGGACCACTGGAGTTACTCCATCAATTATTTACACTGGTAATA
Long Flanking Sequence:
TTTTATGGTTTTAGATGGTTCCCACAGAGCTGGTTGAAAAGGAGTTTTGGAGGTTGGTTAGCAGTATTGAAGAAGATGTAACTGTAGAATATGGTGCCGATATTCACTCAAAAGAATTTGGTAGTGGTTTTCCTGTCAACAACGGCAAGAGACAATTATCAGAGGAGGAAGAGGTTAGTTACTCTTATTTTCCGTTTCAGATGTTTTGAGTGGTAAACTGAGGAAAAAAAAACGTAGACAAGTAACTTATTTATAAACTGCTTATCTGCTGATTTCGAAGTGCTTCTTTTATCCTCACTTGTAAGTCGCTTTTGATTTAAAAGCGTCTGCTAAATGAACTACTCTGTTCTGTTTCTGTTGCAGGAATATGCCCGCAGCGGCTGGAACCTAAATGTTATGCCAGTGTTGGAACAGTCATTGTTGTGCCACATCAATGCAGATATCTCTGGCATGAAGGTGCCATGGCTATATGTGGGCATGGTGTTCTCTGCTTTCTGTTG[G/A]CACATAGAGGACCACTGGAGTTACTCCATCAATTATTTACACTGGTAATACATAAGCTTTTATGTTAATATGCTTTGTAGTATTTATCTGGAACTCATTTTCCTACTTTTTAGTCCTCTGTGATCACATGTCTGCATTTTACACCTAGTAGTTAGTATGTGTTTTTATTATTACAATTACAAGTGGACAGTTCTAAGCTTGGGTGTAAACGAAGTTGAAAACTCAGCATTTGATGTGCTATTATAGGCCTTCCTTTGGCTCAAATAGTAGTGCATGGCCCTTGCAATGCTAAATTTGTTGAATTTGATTAACCGGGAAAGCAAAAGCTGATAAAAATGTGAACCTTCAATAAGGGCTGCACGATTCTGGCTAAAATGTGAATCACAATGTTTTTTTGCTTAAAATCAAGATCACGATTTTCTCACGATTCTTTAAATGTAAAATAAAGGTTAATCTTAGTAGGCTATTATTATTGTTAATTCTCAAACATATCGTCACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15146
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 |
---|---|---|---|---|---|
ENSDART00000098657 | Essential Splice Site | 824 | 1578 | 17 | 27 |
ENSDART00000127053 | Essential Splice Site | 824 | 1578 | 18 | 28 |
ENSDART00000131117 | None | None | 544 | None | 7 |
The following transcripts of ENSDARG00000006124 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 38122861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 36978276 |
GRCz11 | 8 | 37010710 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCYAACCGCGTGAAGGAAGCCCTAGAGCAGGATGAAGGCAACAAAATAGG[T/G]AACTGTATTTMTTTACATYAGTGGTTCTCAACCMCATTCCTGAAGCCCGT
Long Flanking Sequence:
AAAAGTGACTGTAACATGAATTGTCAATTGGACACCAAGCAACTTACTATTTCAGAAGCACAATGGAGGAATAAGGCTCTACTCAATAGAGTCATGCTGAAATGTTTATATTTTGCTGATGTTTACAAATCATAAAGGATGCAAAAGCTTGTTTCTTCCTCATTCATTGAAAATTGCACAGTTGTAAGCATAAGCTTTTTAGGGTCAGTACTTCTACTTTGAATTGTTTTGTGTATAGTGTAAAAGTCGATATCAGATATGAGATCCTTAAAGTTAAATGCTCAATAAAAAACATTTAAATAATAAAATATCAGACCTGGCATCAAGACGAGTGTTCTGAAGGAAGTGTCGTATATGCTCTCTCCTATATGTAGGTATCGCTATACTCTGGATGAACTGTTGGCCATGTTGCATCGGTTGAAAGTTCGCGCTGAGTCTTTTGACTCTTGGGCTAACCGCGTGAAGGAAGCCCTAGAGCAGGATGAAGGCAACAAAATAGG[T/G]AACTGTATTTCTTTACATCAGTGGTTCTCAACCCCATTCCTGAAGCCCGTCCCCATGGACTCTGTCCTGGAGGGCCACTGTCCTGCAAAGTTAAGCTCCTACCCCAATTATGGCCCGTTTCCACTGAAAGGTTCAGTACGGGTCACCTTTATCAAGCCTGCGTTTCCACTGTCAATAGGGTACCCTTTTGGTGGGGGTGATTTACAAAAGACTATGTCATTTTTACTGAAGGAAATGTCACAGTAAAGCTGTATGGGTCGTTCACATATCAGATGAGAAGCACTTCTCACAAAACAGACACTTTATGCACATAAATACTTGTGTATAAATGTCCATTACTAACTTTTCTATGAACATAGTTGGATTGTAACTGCAGATCAATGATCAAATAGCCAAACAGCCTACTGTAACCTCTGCAATTATATGAAATAAATTAATAAATGCAACATATATGAACACATACAGACCCTTACAGTCTCTGATATGTTATCAATAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17413
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 |
---|---|---|---|---|---|
ENSDART00000098657 | Nonsense | 1374 | 1578 | 23 | 27 |
ENSDART00000127053 | Nonsense | 1374 | 1578 | 24 | 28 |
ENSDART00000131117 | Nonsense | 488 | 544 | 6 | 7 |
The following transcripts of ENSDARG00000006124 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 38129143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 36984558 |
GRCz11 | 8 | 37016992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAGGCATTAGACACTCCAGAAGTACAGGAGGYGCTAGACAGACTGCAA[C/T]AAGTAGAGGATGAMATGGTCAGTATAAAAGAGGAAGAACCAGAGGAGAAA
Long Flanking Sequence:
ATGGAGTAAGCACTGACCAGGACAGTATCAAGACAGAAAAGAAACAGAGTAACTCCATGGAGACAGATGTGCCCCTTAACTCAGACAGTCCCGTGCTGCAAAATGGAGGCTCTTCCCATTCCCTCACCTCTAGCCAAACTGTGTGTATTTGTGGTGGCCCACCTCGCCCCTTGCTTCACCGGTGCCATCTGTGCAAAGACTGGTTCCATGGAGGTTGTGTGTCCTTCCCACCATTGTTGGCCACTTCAGACACGCATCTTACAAAACCCCTCTGCTGGTGGGACTGGAACACGCGTTTTCTCTGTCCGCGGTGCCAGCGATCCCGACGGCCACGGCTGGAAACTATTCTAGCGCTGCTGGTGGCGCTGCAGAGGTTACCTGTACGGCTGCCAGAGGGAGAAGCGTTACAGTGTCTTACAGAGAGAGCTATTAACTGGCAAGGTCGAGCCAAACAGGCATTAGACACTCCAGAAGTACAGGAGGCGCTAGACAGACTGCAA[C/T]AAGTAGAGGATGAAATGGTCAGTATAAAAGAGGAAGAACCAGAGGAGAAAAAGAAATGGAATGGAGATGCTGTAATTGTGCTTTCTGACTCGGAGGAAGCAGAAGATGGTGTTATCGATCTGACGGAAGATGGGAACTCGCCAAAAAAGAATGAAAGGAACGCTGTCAATGGTACACAGGTGAGCTTGTGCGATTGGACGTAAATAAAGAAATCTATAATATACACCTTTTTCCCCAAGGCAGTTTGAGTGCTAGTTTAGAGCCAGAGCATAGTCCCAAATTGGTCCTTTGACTTTGGACTCCAAAATATTGCTGGGTAAAGGCTGATTTATACTTCTGCGTAAAACGCCGGCGTATGCTACGACACTGACGCATAGCCCTTCGCCGTGGCCGTTGCTGACGTGCACCTCTCAAAAAATGTAACTACACGTCGCAACAACTCATAGCCCAAGCTCTGCGATTGGCCGGCTTGGTAGCGATGACGAGTCTGGGCGGGACCG
Associated Phenotype:
Not determined