ZMP
jarid2a
Ensembl ID:
ZFIN ID:
Human Orthologue:
JARID2
Human Description:
jumonji, AT rich interactive domain 2 [Source:HGNC Symbol;Acc:6196]
Mouse Orthologue:
Jarid2
Mouse Description:
jumonji, AT rich interactive domain 2 Gene [Source:MGI Symbol;Acc:MGI:104813]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16122 | Essential Splice Site | Available for shipment | Available now |
sa22844 | Nonsense | Available for shipment | Available now |
sa16781 | Nonsense | Available for shipment | Available now |
sa30687 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16122
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 |
---|---|---|---|---|---|
ENSDART00000086333 | Essential Splice Site | 105 | 1171 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 27685084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25530771 |
GRCz11 | 16 | 25445803 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAAGAGCGCAACCATGAGTTCTCTATGGACGGGCCTGCCAGGAAGAAG[T/C]GAGTTTACTTAGACCTGCACTTTATTGTGGTTTTGTGTCATTCTGTGTTA
Long Flanking Sequence:
AATCAGTAAGGGGATAGATGAACTATTTATTTTCTATTTATCTATTTTATTTTTGCCCAATTTAACACTGAAATCTTAGATAAACGTAACAGGACACTATACACACTTTGATTTTGCTCTTTATTTCCTGTCAGTTCATTCTGAGTGTCCACTCATGTTTGTTCACCACAGTGCTTACACTTAGTGATTTGAAAAATCCTCTTCTCCATTTCAGAGACATTTTAAAGTGTTTCTGCTCCCTTTGGATTAGTTTATTTCTTGCGAACAGATCGGCTTAAGAACAGCATGGAGGAATTTGTTTGCTTTTCTGTTCATGTTTGCCTGTTTATATCTGAACCACATCTCCTTCCCCAGGCTCCTTTGCTAATGGTCATCTGAATGGATCGGGCACTAAAGCTGGCCTGTTTGTGGGAAGCTGTAAGTCAGAACGGACCCAGCATGCAGTGCAGAGCAAAGAGCGCAACCATGAGTTCTCTATGGACGGGCCTGCCAGGAAGAAG[T/C]GAGTTTACTTAGACCTGCACTTTATTGTGGTTTTGTGTCATTCTGTGTTAGTGCATGGTTAAAAAGAGCTTTAATGGATGAATAAATCATCATTCATGAACTAAGTGGGAAAATAGCAGTGAATGGACTGAAATGCTATCCCTTTATGTATCTTTCAGTGGTAAAAGATATAATGTTTCTTTCTAGGTTGAATCAGTGATTGTTCATCAGCAAAATGTAACTGGTTTTTGAGCTAATCAATGATGGATATCCTGCTTGGTTGATTCTTGTTTGAACATCAAGTGCTTGGAAGAAGCATCAAAGCACAACATATGCTCTTGGCCAATTAAAAATGACTTGCACAGTCAGGCTTTTTGCTTAGCTTTTATATATCAGACCCAAGTGCTTCCCTCCGCAGGTCTTCTGTATGATTAGATTAGCATCTCTTTTCCCACCAAATGATTCAGATCATTGTGCTTCTGTCCTTTTCCTTTTTATGGACTTTGAGTCAATAAACTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22844
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 |
---|---|---|---|---|---|
ENSDART00000086333 | Nonsense | 374 | 1171 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 27716698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25562385 |
GRCz11 | 16 | 25477417 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGGCTCAGTGGGACAGACACTTTCCCCCCGAGACGAAACGGACTTCGG[C/T]AGTCAAAGAGGCAGCTGGAGTTAGCCGGAGCAGAGGTCGAGGTGAAGAGG
Long Flanking Sequence:
TAGTCCAAAAAAATGAAAGAAAATGAGGGAATCAGTAGGGAATTGGTCTTTGGGTTTTAACAGCAGCACTCCATAACAGCCCTGAATTAGATAAAAGTAAAAAATGACACACAACAGCTTGAAGTATGTGTTTTATATACATGTTTACTGTTGTGTGTGTGAGTGAACTAAAAAGAAGCTTTTCTGTCATCCCTTAGGCCTCCAAAATGAACGGGACATCGGGAGCCTCCGCCGTCAGTTCTCGAAAGACGAGAGAACTGCGAACTCCCCCGACCAAAGCTGTGAAATACCCCAAGGGCCACGTGACGTACACCAAAGCCAGACTGCTCAAAGAGGCCAAGCTCAGCCTGAGCACACACACACACACACACTCTCAGACCTCCAACTCAGGAAAAGCCCAAACCAGCCACGCCAAGATGCAAAAACAGGTGCTATCACCAGCAACCGCTGGACGGCTCAGTGGGACAGACACTTTCCCCCCGAGACGAAACGGACTTCGG[C/T]AGTCAAAGAGGCAGCTGGAGTTAGCCGGAGCAGAGGTCGAGGTGAAGAGGGTCAAGGTGCACGTGGTTCCTTTGGAGACCCGCAGTAGGAAAGCAGCTCAGGAGACGCAGGCCAGACCGCAACCGGCGGGATCACAGCGGCCCAAACGGGCATCGGCCGGGAAGCTCATGTTCACTAAACAGATGCACTGCAAAGCCAGCGTTCTGGCCAAGAACAGCCCCACTACCTCAACACGAGACATTCTGAGACCAGCCAACTCCCCCAAACTATCAGAGACCCCCAGAACAAGCAATGCTCTAAAACAAGGCCATCCTTCAAATATGACTGAGCCCTTCTCATCTGAGCCCAAGGAGCGAGGCCGGCGCAGTGCCGAGATCACGGAGCTGCCCGTCTTTTATCCCAACACACATGAGTTTCATGACCCGTTGACTTTTATGGAGTTGGCACGGGGGCAGGCCGAGGCGTTTGGGTTGTTCCGGGTTGTTCCGCCAGCAGGCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16781
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 |
---|---|---|---|---|---|
ENSDART00000086333 | Nonsense | 840 | 1171 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 27732001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25577688 |
GRCz11 | 16 | 25492720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGCATGGATGGAATCTTAATGTCCTTTCCAATAACTCAGGATCCATCT[T/A]ACGTCATCTTGGTGCTGTGCCAGGTAACATTTCAACCATTTCCTGAGAGC
Long Flanking Sequence:
ACGTCAAATTATTATTTGTTGATCCTAAAACTTGGATAGGCGACAAGACTTTTGTCTGGTAGTATAATTAAACTAAATTACACCACAATAAAATACAATTATTATTCATTTAAATGTGTTTAAAACAACTCCTTCTCCACACCTGTTTGAGTTTCTTTCTTCTGTCGAACACACAGGAAGTATACTTAGGAATGCTGGGATAAAAACAGCTGTTGGCTTTTATTGTAATTTTTGTTTCCACTTTGTCTACTTTGTTTTCCCTCAGCATTCATCAGAATATCTTGTTCAACAGAAGAGTGAAATTCACAAAAGTTTAGTTTGATTAAAATAGAGAGAAAATTAGCATTTTGGGTAAACTATCCTATAAGATCTATTGTAAAGTGTTCATTAATTAAATTCATTGTGCATAAAACATTGTTTGCTTTCCCCTGATTTGTTTGTCTCGTTCTCAAGGCATGGATGGAATCTTAATGTCCTTTCCAATAACTCAGGATCCATCT[T/A]ACGTCATCTTGGTGCTGTGCCAGGTAACATTTCAACCATTTCCTGAGAGCTTTACATTCCACGCATGCAATAAAACACCTTGACGATCAAGTGTTAAATCATCATCCTGAAATGAATGTGTGCGTGTGTGTTTGTCTGAAGGGGTGACCATCCCCTGGCTGAACATAGGCATGGTCTTTTCTACCTCATGCTGGTGTCGGGACCAGAACAGCCTTCCGTATATTGATTATCTACACACTGGTGCTGACTGCATTTGGTGAGTCTTTATTTACAGCTGCCAGAAATGAGATGAAGGTGGGTGGAGCAGAATGTTTGGGCATGTTTGATGGTGACTGTGCTTCTTGTCTTCAGGTACTGTATTCCAGCTGAAGAGAAATCCAAACTTGATAAAGTAGTTCACACACTGCTACAGGCTAACGGCACTCCAGGGCTGGAGATGCTGGAGAGGAACATTATGGTGAGAGATCAACATTGTTTACTTTCTCTCTCAATGGGGCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30687
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086333 | Essential Splice Site | 1024 | 1171 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 27735118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 25580805 |
GRCz11 | 16 | 25495837 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAAGCAGCTCATGACTGCCGTCTCCAGTCTCTTCAGAGATCTCAGG[T/C]TTGTGGAAATCTGCTCTCACTGGACTCTTATTGTCACAACAACCACATCC
Long Flanking Sequence:
TATATGTTGTAAACAGGGGCATAATAGATCCACTTTAAGTCGTTCATCTTTCAGTAATCTGTAAAGAGAATGTTTTGAGCTGATGTTCCTGTGTCCTCCTCAGATTTCTCCAGAGGTGCTCCGTCGTAAAGGGGTGAAAGTGTACCGGACAGTGCAACACAGTGGCCAGTTCATGGTTTGTTTCCCAGGGACGTTTGTGGCTAAAGTGTGTTGTGGCTACAGCGTCTCAGAGACCATGCACTTTGCCAACCTCCAGTGGATGAAACTGGGCTATGAGGCAGCTAAGGTGACTGACACTTTACCTCTCATTCAGCTGCTTTCAGAAGTGAGCTTTAGCCAGTCTTTCACACTCGGGTGCCGCGTTTGCTTTGCAGGATCTGAAACGGCGTCGTATTGAGGAGCCTTTTTCAACAGAGAAACTGCTCTACCAGATCACCACATGTGAGCGGGACAACAAGCAGCTCATGACTGCCGTCTCCAGTCTCTTCAGAGATCTCAGG[T/C]TTGTGGAAATCTGCTCTCACTGGACTCTTATTGTCACAACAACCACATCCATCTTGGAATTTGACACAAAAAAAGACTTATAATTAATTATTATTAGTAGTAGTGTATAAATATTGATCATAAAGTACTGGGCAATTACCAACCGAGATAACAAGCTTTTCCTCTATCTTATCTATACACTAAAAAAAGCTGGATTCCGCACTGTTCCTTTATGTTGTCCCAAAACAAATGGATAACGTTAACCTAATTGTTTTTACAAATTGAAGTGGACTGAACATAAAACAATAAAGTTGTCCCCCCAAAAACTCATAAATTGTGTCGATCCAGCTTATTTTAATTAAGTAGTTTAAACAAGCAGCAACAATCATTCTTTGAATGTACCGTTATTCTCCAGTATGGGATAGCTAGCATCTGCACTAATATTTGCGTAAAGCAATCTGATTGGCTGACACTTCTGTTGTGCTTAAAGTTGAACATTTTTCAGCATCTGCCAAAGCAAC
Associated Phenotype:
Not determined