ZMP
jmjd7
Ensembl ID:
ZFIN ID:
Description:
jmjC domain-containing protein 7 [Source:RefSeq peptide;Acc:NP_001017615]
Human Orthologues:
C2orf60, JMJD7
Human Descriptions:
chromosome 2 open reading frame 60 [Source:HGNC Symbol;Acc:26754]
jumonji domain containing 7 [Source:HGNC Symbol;Acc:34397]
jumonji domain containing 7 [Source:HGNC Symbol;Acc:34397]
Mouse Orthologue:
1110034B05Rik
Mouse Description:
RIKEN cDNA 1110034B05 gene Gene [Source:MGI Symbol;Acc:MGI:1915986]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36341 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13433 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36341
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051526 | Essential Splice Site | 229 | 311 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 10587248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10570337 |
GRCz11 | 17 | 10726371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAGACGACGGCACCTTTGAAATAGTGGATGAAGAAAACTCACCCAAA[G/A]TAAATGTTTTACGGTTTTTCTCAGTCGCTTTGGTGCATTTCTTACAACAC
Long Flanking Sequence:
TGCCGCAGATTGTCTTGACCATGTCTACATGCCTAAATGCATTGAGTTGCTGCCATATGATTGGCTGATTAGAATTTTCAGAGCACTTGGACAGGTGTACCTAATAAAGTGGCCAGGGAGTGTATATAATGGATATAAATCCATTCATTTATTTACTTGTGAGTGAACTTATTATAATTGTTATTTTTTTATCTGCAGTGCATAAAGATCATTATGAGAATCTATATTGTGTGATTTCTGGACAGAAAGAGTTTGTTTTACTTCCTCCGACTGATAGACCTTTCATACCGTATGGTAAGAAGACCTTCATCAATATAATATAATACTATTATTGTGCTAATAATTATTGAAAATGAGTAGTTTTTAATATTGAAATGGCCTCAGGAGGACTTTTTTAGCATTGTATTTTCTTCCTCTTCACAGAGCTCTACCAGCCAGCAACATACAGACAGAAAGACGACGGCACCTTTGAAATAGTGGATGAAGAAAACTCACCCAAA[G/A]TAAATGTTTTACGGTTTTTCTCAGTCGCTTTGGTGCATTTCTTACAACACTATTTACATTTGCACAACAGTTAATGCATTTCCTAAAACAATTAGTCTTTTGTGCACATCATAGTGGCAGTTTCTCATTCCTTCCAACAAATTGCAGATGCTTTTGATCATGCATCAATTGCTTTCATACAACTCTCTGCTGTTTTATAACATTATCATTTGCTTATGTCATGTCAGTCAAAATTAACTAAACTTGTGAATGCTGAATAGTCATTCCATATAAAACTAATAGTCCTCCTTTCATTGCTTGAGTCATCAATATAAAAAAACTTACAGATGCCACAAATCTAATACCTTTAGAAAAGAAGTCCATTCACATTAATATATAATAATATGCAAACTAACTATACCTGTTACAATTTAATAATAGTCATAGGCCATACTCACACTAGGTACAGTTGCCTCGAACCGGGCCAAAGCACGCTTGTCCCCCCTCCCGTCTCCCCAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13433
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 |
---|---|---|---|---|---|
ENSDART00000051526 | Nonsense | 265 | 311 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 10578619)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10561708 |
GRCz11 | 17 | 10717742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACATGCCAAAGCTCTGCACTGCACWGTTAAAGCAGGAGAGATGTTGTA[T/A]CTGCCCTCGCTCTGGTTCCATCATGTGCGACAGTCTCACGGCTGCATAGC
Long Flanking Sequence:
TGTCGCCAAAATCTGCATTTTTTGCATTGGAGAAAACTTTACAGAGTAAACTGTTGACTATCAGTGACTAAGCATTTGATTATCTTGTTCATAAACAATGATGTCAGGACTTTTCATCTTGATGACACTGCCACTTTTATTGACATCAATACTTGCTTTCGAGGAATGAGCTGTCGATTTTGAGCAAGAGACACACTTTTGCAGGTTTTCATCTAGGTTTTGCAGTTTGTACTAACTGTTTTGAGAAATGCATTAACTGTTGTGCAAATGTAAATAGTGTTGTGAGAAATGCAACAACGCCACTGAAAAAAACTGGAAAACATATTTTTGCTTGTTTTATAGGTAATCAGTGATGGTTGTATAACTTGTATTAATAAGTACCATGTCTGTCAGGTGCCATGGATCCCCCTAGACCCACTGAAGCCAGATTTCGAGCGTTTTCCCTCATACAGACATGCCAAAGCTCTGCACTGCACTGTTAAAGCAGGAGAGATGTTGTA[T/A]CTGCCCTCGCTCTGGTTCCATCATGTGCGACAGTCTCACGGCTGCATAGCAGGTTAGTAATTTCTGTTCTGCAATTAATATTTCTGATCATGATTTTTTAATTTTGTTTATAAATGCACCTTTTGGTTACAGTTTATACGTTTTGCATCAACACAGCCGAAATGATCACAACAATTTTAATAAATTAAACAAGACAAAATTCATAATGGGTTAAATATGCGTCAGTGTCTGCGGAGACTTAAAAATATTACAAGTTTATAAATCAATTTAGAGAAATGTAAGGCCCATAAAAGGAATTAAATGCTAGGTATTACATTTTGTAACATCCTTGATCATACAATGTATAGTTGTCTGCTAAAGCCTAGTTCACACTACATGACTTTAAACATCGGCAGATCACTGTGCCGTTCACACTACATGACTTGATGCTGTGCCTTTTAATTGCTGTGGTGTTCACACTACGTGGCACTATGTAAATAATCCACAAGAGGGGGGGGGTC
Associated Phenotype:
Not determined