ZMP
zgc:154110
Ensembl ID:
ZFIN ID:
Description:
JmjC domain-containing protein C2orf60 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q08BV2]
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 |
|---|---|---|---|
| sa13117 | Nonsense | Available for shipment | Available now |
| sa17249 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13117
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 |
|---|---|---|---|---|---|
| ENSDART00000101571 | Nonsense | 106 | 326 | 4 | 8 |
The following transcripts of ENSDARG00000069672 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 25152297)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 24308083 |
| GRCz11 | 9 | 24118952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTTGAGTGATTAACTAGGATCTTGTTGTTTCCACCAGGATGAAAGTTA[T/A]TATTTGCGCTCACTTGGAGAAGATGCCCGCAAGGTAGTCTGAAGGACTTT
Long Flanking Sequence:
CATGTGACAAGAACCGACTGATCAGCTTCATATTTTAATGGAATATAATTTCATTAGACTAATTATCTCAGACAAACACAGAACACCCAAACACTGCAGTGGTTTTTAATTTTCTTCATGAATAAAACTAGCATCAGAGTGCAGCAATGTTTTGTTAGCTTGACATCCTCTGAGAAAAACAGGTTCCCAAGCAATCTACATACAAGCTAATGTTTAGATTTCAAAAACTTTTACAAATTTGTCATATGTACATGCAATATATATTTCAAAATTTATTTAAAAATTGTATAAATATGAATATGACTTAATTTGGCCAACTACGCTACATTATTTCAATTTTGGTCATTTTGGTGAAAAAAGTTTGAGAACCACTGCTGTAAATTATTTGATTGTAATTTAGTGTTTCATCGTGGCCATTTAATGTAGGTATTGATGTAGTGAACTGACTTATTGTTGAGTGATTAACTAGGATCTTGTTGTTTCCACCAGGATGAAAGTTA[T/A]TATTTGCGCTCACTTGGAGAAGATGCCCGCAAGGTAGTCTGAAGGACTTTTGAATTAAAGTAATTAATCCAGATGTTAAGGCTGTAGAGTTTGATTTGAATATTGGAAATTATATCTGATTTGTTTGGACATTATTACTGCATCATTGTCTTTCCTCATGAAGGAGCCTGCTGATTTAAGGAAGCAGTTTCCTGAGCTGGCGGAGGACTTCCATGTACCCCAGTTCTTTGAGCCGGAGCAGTTTTTCTCCAGCGTCTTTCGTATCAGTTCCCCTGGTCTGCAGCTGTGGACACACTACGATGTGAGTTTTTCACCCCAAAATATGTTACAAACTAATGTCATGCTGATCATCTGAAAGATTGTGTTATTTTAAATCTATTTTTACATTGAGTTCAAATATATTTTCGCAAACCTCACTTTGCTCTTCGTTTAATTCACCTATAAGAAAAAAAATAGACCACCTTGTGTGAAGAGCATCCATCACTTTCTGCTCAAACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17249
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 |
|---|---|---|---|---|---|
| ENSDART00000101571 | Nonsense | 199 | 326 | 7 | 8 |
The following transcripts of ENSDARG00000069672 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 25150752)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 24306538 |
| GRCz11 | 9 | 24117407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGGATGAAACAGTAATTGTGATGTTTTTAGGGGACAAGTCTGAAGTTT[T/A]GGACATCGACAGTCCAGATCTGCAGCTTTATCCAGAGTTTGTGAAGGCTC
Long Flanking Sequence:
GTTCTTCCCATGTTGGCGTGGGTTTCCTCTGGGTGCTTCAGTTTCCCCCACAGTCCAAAGACATGCGCTAATAGGGGAATTGGATTAACTAAATTGGCCCTGATGTGTGTGTGTGAATAAGTGTGTGGATGTTTCCCAGTACTGGGCTGCAGCTGGAAGGGCATCCGCTGCATAAAACATATGTTTGATAAGTTGGTGGTTCATTCCGCTGTGGCGACCCCTGATGAACAAAGGGATTAAGCCGAATGAAAACAGGAATGCTACATCTGTTTTTTTTAACCCTGCTTGTTTTCAGGTAATGGACAACCTCTTAGCTCAGGTTACAGGAAAAAAGCGTGTTGTTCTCTACAGCCCTGAAGATGCCCTCCATCTCTACCTCACAGGTGAACTTCAGCACTTCTTAAAGTGTGTGCAGGAAATAGAATTGACTTTATATACACCTTACTGATGTGTGGATGAAACAGTAATTGTGATGTTTTTAGGGGACAAGTCTGAAGTTT[T/A]GGACATCGACAGTCCAGATCTGCAGCTTTATCCAGAGTTTGTGAAGGCTCGTCGCTACGAGTGTTTTCTGGAACCTGGAGACCTGCTCTTTATTCCAGGTGCTCCCTTTATGAACCAGGCTTATTGGTTTTACAGTGAATATTTTTTATATTGTGAACCAAACATCTAAGTGTTCTTAATAAGTGATGAACTGCATTTCTAAAAGTGCTGCATGCGTTTGCTTTTCCTCAGCTCTTTGGTTTCACAATACTCTGGCTCTTCAGTTTGGAGTCGGTGTCAATGTGTTCTGGAGGCATCTGCCATCTGAGAGTTACGATAAGAAAGACCCATATGGAAACAAAGACCCAGTAGCAGCCACGCGAGCTCTGCAGTCACTGGAGAGGACTCTAGGCATCCTAGATGAACTGCCACCTGATTATCGGGATTTCTATGCTCGTCGAATGGTGCTGCGCATTCAAAGCAGAGCTTATATTAGGAAACCTATAAATGCAGCACAGGAA
Associated Phenotype:
Not determined