ZMP
LOC571586
Ensembl ID:
Human Orthologue:
JMJD1C
Human Description:
jumonji domain containing 1C [Source:HGNC Symbol;Acc:12313]
Mouse Orthologue:
Jmjd1c
Mouse Description:
jumonji domain containing 1C Gene [Source:MGI Symbol;Acc:MGI:1918614]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23163 | Essential Splice Site | Available for shipment | Available now |
sa11990 | Essential Splice Site | Available for shipment | Available now |
sa10357 | Nonsense | Available for shipment | Available now |
sa14737 | Essential Splice Site | Available for shipment | Available now |
sa32173 | Nonsense | Available for shipment | Available now |
sa17049 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23163
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114523 | Essential Splice Site | 106 | 2603 | 3 | 27 |
Genomic Location (Zv9):
Chromosome 17 (position 43805191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12943964 |
GRCz11 | 17 | 43760121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGTCTTGTATCGAGATGGACTGATTGGTTGTGATATTTTGTTTGACA[G/T]AAATTCCGGCCTCTGATTGGTCAGTCATGCGTGGGAGGCCTGTCTGTGGT
Long Flanking Sequence:
CTACAAAGTGTTTTATCACTGATTTCTCACTGTGTCTTTAGTAAATCTGGTCCTTTTATGTTAAAAAATGATCTTCGAATACCACAGAATTTGTAAAATGTCATGTGATGTAGTTCCCTGAAAAACGAATGACATTTCTGACTAAATAATGATGTAAAGAATACTCCATCGCTTGAAAAATATATTGTTTATGCAAAAATAATGCTCCAAAAATGGGCGGCATGGTGGTGCAGTGGGTAACGCTGTTGCCTTACAGCAAGAGGGTCGCTGGTCAGAGTCTTTGTTGGGTCTTGGAAGGGCATCCGCTGTGTAAAAAAATATGCTGGATAAGTTGGTGGTTCATTACGCTGTGGTGACCCCAGATAAATAAAGGGACCAAGCCTAAAAGAAAATGAATGAATACTCCAATTGGTGAAGTAGATGAAGACTGTTGTGGTTGTCACGAATAGTCTTTGTCTTGTATCGAGATGGACTGATTGGTTGTGATATTTTGTTTGACA[G/T]AAATTCCGGCCTCTGATTGGTCAGTCATGCGTGGGAGGCCTGTCTGTGGTGGAGTTCATGTGTGACAGACAGCTGGAGTTTTACACAGAAAAGGAGGAGCTCCAGCCGTTTAAGGTGCGTGTACAGAAAGTTATTATTATTTACATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTGTTATTGTTGCATTTTTGAAACTTTGTATACTTGGCATTCATTGTATCAAAATTACACTTCATTATTCAAATGAAAAATATTTTGCTAGATTTTTTTGTAAAACTCCATAGAAAAATCATCTCTTGGGCTTTTGGAATTCTGGGATATGTTAGCAACTAACTATGTAATATGTAAATATATATATATATAAGAGTTTAGATGCAAAAACCTCTAAATGCTGTCTGAACTTTTCCTCTAAAATGAGCATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11990
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 |
---|---|---|---|---|---|
ENSDART00000114523 | Essential Splice Site | 313 | 2603 | 8 | 27 |
Genomic Location (Zv9):
Chromosome 17 (position 43767143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12981918 |
GRCz11 | 17 | 43722167 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGAAAAAGAAGGAATGAGGGAGGAAAAGAGGAGTGATGAGRGAARAG[G/A]TGAGTTGGAGCTGTAGATAATGATTATGAGGATGTTAAAAGCACTATCTG
Long Flanking Sequence:
TGGGATTTTTGTTTTGTATGTGTGCACATACTAGTTTTGAGACAAGATATTTCCCTAAAGTATGGCAAAGCATTTGCTGAAAAAGAAATTGGATATAAAAAATATTTATCAATGTTTAATAATATATATTTTCTTAACAAATCAGCATTAGTATACATCATGGTAGAAGTATATTTGGATATATAGGATATATCCACATTTGGGTTTTAGCCAAATAAAATGTATGCTATTTGTGTCTTACTTGCATCTTTACCGTCTGCTTCCAGGGTACAGGAAGTAAAACAAACACTACAACAAATGACCAGGTACAGACTTTAACATGCTTTCAAATACATGGCACCAGTCTCATTCATTCTCTAGTTTAAAAACACACTCCGTTTCTCTGCTGAAGGTATGCAAGCCAGTGCAACACCAGTCTGAAATAAGCACACACAACTGCAGCATGGAAAAAGATGAAAAAGAAGGAATGAGGGAGGAAAAGAGGAGTGATGAGGGAAAAG[G/A]TGAGTTGGAGCTGTAGATAATGATTATGAGGATGTTAAAAGCACTATCTGTAAAAATTACTAATAGTGTGACTGAGATTTATGTCATAAGACTGATAAAGAATACAGATTTTCTCAAGTTTTTACAGAGAATCTTAGATTGTGCTGTGCAAACTTTTACCTCAGTATTGTTGATCTTTTTTTGTATACCTAGATTCTTCCAAATCTAAAAACAGTCATTGTGAGAGAAAAAGAAAGAAGGAAGATGAGGAGAAAGATGACCAGCAGAGAAATAGATGTGGGCTGAAGAGGCTGAAAGGGGGCAGTGTGTCTGACCTGTCTGAGAACAGTGATTCTGAAAATTCCAGCTGCAGAGTGCCAGATTCATCCTCAGATTTAGGATCAAAGAGACAGCTGAAACAGCGTTACACTTCAAAGAGACCATTGGATTGTGAGGTTCACCCCTCCCACAGAGGTGGAAAACTTTCCTCCAGCCAATTAGGAGAGACTGAGATATTGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10357
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114523 | Nonsense | 1463 | 2603 | 11 | 27 |
Genomic Location (Zv9):
Chromosome 17 (position 43761434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12987579 |
GRCz11 | 17 | 43716506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTCCCTCATTTGAAAAAACACAGAGCTGGACTAACTGCTGCTATCTCT[A/T]GAGCTAACACACATACAATTCAGCCTCAACACACTACATATCCTTTGMAT
Long Flanking Sequence:
AAAATGGCGGCGTTGTCAAACCACAGGTGGCTACTGCATCAGTTATTGTGCGTCCAACAAGCCACACCCATACAATAATAAATTACACAGTGTCTGACAGCTCAGTTTCACAGATGCATTGCAGCCCCATAAGGCCATTGGAAAGCATGTCCAACTTAAAGTCTAAGGAGGGCAATGTTCAGCATAAGAGAGGTGTCCTGTGGACCCCTCTGGATACTGTCCATCCAATCAACATGACAACTCAAAAGGAAGATCTCAGTACTCCCATAAACATGACAATGAAGCTAATTAACACAGCTCATCCGAGTCATGGAGTGACACACCCCTTAACCAACATGAATGCCTCACATTCTAAAATAGACCTAATTGCAGAGCAATGCAAGAAGAGAGACAGTGGAGCCATTCAACCAAAGACGGAGCCCTCTTCATCTTCTTACTGCACTACAAGAGACTTCCCTCATTTGAAAAAACACAGAGCTGGACTAACTGCTGCTATCTCT[A/T]GAGCTAACACACATACAATTCAGCCTCAACACACTACATATCCTTTGAATGCTATGACCAATAACTCTCACCTCTCAGAAAGTCATTTTGAGTCTCTTACTGCACTCACTACCCACACCGTGTGTTCTGCACATGTTTTAGAAAGAGAAAAAGAGCCTGTATTCAACACTAGCACTTCTGAATCTCTGGCATCAGGGACTTCCTGCCCTGCACCAACAGACAAACAAGGTTCGCCAACCAATGGGTATACAGCTGGATCAACAATAATCAACCAATCAGCTCAATCCGGTCAGAACAATTACCATAAACTTAAAAAAGCCTGGCTGACCCGCCATTCTGAGCAAGATAGAGGCAGTACGGACTCCCAAACACTAGATGGTACTAAGTCTGCTGTAATTCTGACGAACACAAGCACCTATATACCAGCCAAGCAGGAAGTGAATGGACTGATGGACAATTTGGAGGACAAAAACTCACTTGACAGCAAAAAGCCCAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14737
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 |
---|---|---|---|---|---|
ENSDART00000114523 | Essential Splice Site | 2089 | 2603 | 17 | 27 |
Genomic Location (Zv9):
Chromosome 17 (position 43756086)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12992927 |
GRCz11 | 17 | 43711158 |
KASP Assay ID:
2261-1479.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGAAGAACTCACAGCACGTCACACTGAGAGCGCACACTGAGAGAAGAG[G/A]TAATGACAGWAGTAATGCGCAATAATACGCTAAGATATTTTTCACAACAT
Long Flanking Sequence:
ATTCATCTACTTAACGTAAATAAAAGTCACATCCTGTTCTTCTCTGACTGGGAACCTTGTAGTAATAAGCAATGCATTGTCATTTGTCCACAAGTGTTGGCGGACATGCAGAACTCTTTGCACTCTTTGAAAGAAAAGTTTGCAATCTCTTCCCAACGTCCTGGCACTGAAACCAAATCCATGGCCACTACCAACGGACTCTCACCGGTAAGACTCTTAGTTTTTTTTATTTCATGTCAAGTCACATTTACATTTATGCACTGGCAGATGCTCCTATACATTGCTTTCAAGGGATTCAGTTTATTAGTTTATTCATTTCCTGGGAGTCTACTGGAATTATTAGATGCATTTCAAGCTCCACATGAATGACATTTAATGAACATGTTTGGTGTGACATCAGCTTTCAGACACAGATCAAAGTGACCTGAATAGTCGGCAGATCTCAGATCAGCAGAAGAACTCACAGCACGTCACACTGAGAGCGCACACTGAGAGAAGAG[G/A]TAATGACAGAAGTAATGCGCAATAATACGCTAAGATATTTTTCACAACATGCAGCCAGCCCTGTCCACCGTGAAATCTCAATTATATCCTCCACATAGTGTATTCTAAAGTGCTTTAATATGCTGTTTTCTCGCATTATCCAGAAAAGGCAGAATGTGATGGTGTGGAAGCCCAGAGTAAGAAGTCCACAAGCCCTGAACAGGGATCAACATTGCGTGACCTTTTGACGTCCACTGCTGGGAAGTTACGCCTTGGATCTGCAGGAGGTGCCTTTGCACCAGTCTACAACTTTTCTGAACAGGTTTGATATATACATTCTTGTTCATATAAAAATGTGAAGTGGAGATCAAATTTCTGGCTAATGAATTCAGAGAAGGAAACCCTGGTGTTGATGAAGGAGCTTCTGATAAACATTTGCATTCACTCTGCCATGTAGCTGTGTTTGCACCAGGTATTGAGATTTGAGATTGTATTTTTCAGTCAAATCACTAGTGGACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32173
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 |
---|---|---|---|---|---|
ENSDART00000114523 | Nonsense | 2179 | 2603 | 19 | 27 |
Genomic Location (Zv9):
Chromosome 17 (position 43753576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12995427 |
GRCz11 | 17 | 43708658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATAAGATTCCCGCTACAAAGATGGCCAAGGCAGAGCTCAAACAGGATT[C/A]GCTGCCTGAGGAGGAGGCGGGGCAGCGGCCAGATGGAGTAAAGCTTGATG
Long Flanking Sequence:
TGACACTCACTGTATATTTTCTATTTTTCGGACCATTCTCTGTAAACCCTAGAGATGATTATGTGTGAAAATACCAGTAGATCAGCAGTTTCTAAAATACTCAGACCAGCCCATCTGGCACCAACAACCATGCCACGTTGGACAGGTGTACCTAATAATGTGGTCAATGAGTGTATATGTACTTCAGAATATTTGTAACCATTGAAATATGCTTTTAAAACAGATATTTTACTACCGTAACCTAACCCTACCATTATGAATACCTCAAATAGGATTAATCTGTGACTGAACTTTAGGAAATTGTAGATTAATCACTAATTTTGATCACCACTGTAGCATACTGACAGCTAAAATCTTTTCTAATAATCACTCTTCATGCTTAATTCGCTAGGTAACCCAAAACACTCGCGTACCCAACATCCTGGATGACATTATTGCTTCTGTAGTAGAAAATAAGATTCCCGCTACAAAGATGGCCAAGGCAGAGCTCAAACAGGATT[C/A]GCTGCCTGAGGAGGAGGCGGGGCAGCGGCCAGATGGAGTAAAGCTTGATGAAAGCACATTGGCTAATCCCCATGCCACTGCACCTTATGATTGGTTGGGAAATCACCGACTGCTTTGGCTCAAAGATCACCGTCACCAAGGCAACCAAAGGCTGTTCAAAGAGAACTGGACACAAGAGCAGGTTTGTATTGCTCCCACTAGTGGAGTATTAACTATATATCTACAGATACCAGGGAGAAGCAAAACACCCTTAAAGTGAAATAAGTATTAGGAAACATTAGTTTTTGATACAGAATGAATAACCCAAAGTTGCCATTGCTCGAAAATTTTGTTATCATTGATAAGAAATGGCTTCTTGTATGACATAAAATGTTCATTTAAAATATAATGCTGCATATGATGTGTTGTCGGGATGTCTCTTCAATAGCCAGTACTGGTGTCTGGATTGCACAAGAGTCTGAACGCAAATTTGTGGAAGCCCGAGAACTTCAGCCGTGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17049
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 |
---|---|---|---|---|---|
ENSDART00000114523 | Essential Splice Site | 2295 | 2603 | 20 | 27 |
Genomic Location (Zv9):
Chromosome 17 (position 43752979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 12996024 |
GRCz11 | 17 | 43708061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACCAACTCCAAAGTCAAGGAGTTCTGGGAYGGTTTTGAAGATGCCTCAA[G/A]TGAGTGATCCAGTTTAGCAATTCTGCGCTCATCATTTKTAATTTGCTGCA
Long Flanking Sequence:
GGGAAATCACCGACTGCTTTGGCTCAAAGATCACCGTCACCAAGGCAACCAAAGGCTGTTCAAAGAGAACTGGACACAAGAGCAGGTTTGTATTGCTCCCACTAGTGGAGTATTAACTATATATCTACAGATACCAGGGAGAAGCAAAACACCCTTAAAGTGAAATAAGTATTAGGAAACATTAGTTTTTGATACAGAATGAATAACCCAAAGTTGCCATTGCTCGAAAATTTTGTTATCATTGATAAGAAATGGCTTCTTGTATGACATAAAATGTTCATTTAAAATATAATGCTGCATATGATGTGTTGTCGGGATGTCTCTTCAATAGCCAGTACTGGTGTCTGGATTGCACAAGAGTCTGAACGCAAATTTGTGGAAGCCCGAGAACTTCAGCCGTGAGTTCTCCAGCCTCCACAGTGACCTCTACAACTGCCGAGACGGGAGCATCACCAACTCCAAAGTCAAGGAGTTCTGGGATGGTTTTGAAGATGCCTCAA[G/A]TGAGTGATCCAGTTTAGCAATTCTGCGCTCATCATTTTTAATTTGCTGCATATGATTTTGCCGTTTGACTCTTAACGTTATTTGCATGCTTGTGTGTATGACTGACAGAGAGGCCGAAATCTGGTAAAGGAGAGTCAGTGGTGTATAGACTGAAAGACTGGCCATCAGGGGAGGAGTTTCTGGCCCTCATGCCTGCCAGGTACTGCTGCCCTTGGAACCATTTGAAGCATATGTTGTCTTTCAGACCTCACCAGAATTTGCATAAAACGGCACTTTGTACTGCTAATGCCTTCTCAATTTGAATACACTGTTTCCACTATTTGAATACACCTCTACTCAAGCCTTGAACTCAGACAATGCAGTAAGAGATGGCAGGAAATATGCAATGTTTTTCCAATAGAGAAATAGATTCCCTGTGAAAAATGACTTCAGATTAATGAATGATTGGTTGGTCCTTGCTTTTCTCACACTGTAGTCGTTCATTATACAACAACAGTATT
Associated Phenotype:
Not determined