ZMP
ube2q2
Ensembl ID:
ZFIN ID:
Description:
ubiquitin-conjugating enzyme E2Q 2 [Source:RefSeq peptide;Acc:NP_998152]
Human Orthologues:
AC011295.5, UBE2Q2, UBE2Q2P2
Human Descriptions:
ubiquitin-conjugating enzyme E2Q family member 2 [Source:HGNC Symbol;Acc:19248]
ubiquitin-conjugating enzyme E2Q family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:37440]
ubiquitin-conjugating enzyme E2Q family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:37440]
Mouse Orthologues:
E330021D16Rik, Ube2q2
Mouse Descriptions:
RIKEN cDNA E330021D16 gene Gene [Source:MGI Symbol;Acc:MGI:2141773]
ubiquitin-conjugating enzyme E2Q (putative) 2 Gene [Source:MGI Symbol;Acc:MGI:2388672]
ubiquitin-conjugating enzyme E2Q (putative) 2 Gene [Source:MGI Symbol;Acc:MGI:2388672]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15381 | Nonsense | Available for shipment | Available now |
sa30279 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15381
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 |
---|---|---|---|---|---|
ENSDART00000016117 | Nonsense | 23 | 182 | 1 | 6 |
ENSDART00000124645 | Nonsense | 23 | 373 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 30453272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 29020633 |
GRCz11 | 25 | 29463640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGGCCGAAKTAAAGTTCCTGGAGTCAATCTTTGACCCAAACCATGAG[C/T]GATTTCGAATAATCGACTGGAAGCMAGACGAACTGAGYTGCCAGTTTAAT
Long Flanking Sequence:
TTTTTATCTTTTTATTAATATTGTATCTTTGTAAATGTTCTTTCTTGCATAATAAAAATAAATGCATATTATTATTATGTGTTTTTTTATTTTTATATGTTGGATAATGCAAGAGGACTGTCATAGACAAGAATGAAGACGAAGAATGGTCAACCACACGTTCACAAAACACAATTGGCGTCCCAGTAGTCCACGCAGATCTCGATCACCCACTTCCCCTCTCTCGCATTATTTCTTGGCGGGCGTTGTTTTGTCGTCTCTCCGGCCTCCAGTTCGCCTCTCTCTCCCCGCCCCCTCTTTGTTGTTTCTCTCCTCCAGCCTCCCTCCGCCGCCGCGCGCTCACACACACGCACTCTCGCTGGATCAGCTGCGCGCTCGCGGTCTCCGTGCGTCCCTTCCCCCCGCGGCCTGGCTGCTGATGAGATGAGTGGAAGATGTCGGTGTCGGGGCTGAAGGCCGAATTAAAGTTCCTGGAGTCAATCTTTGACCCAAACCATGAG[C/T]GATTTCGAATAATCGACTGGAAGCCAGACGAACTGAGCTGCCAGTTTAATGTGACGGGAGAAAAGCTGCTGATTATTCACTGCAACATCACGGTAAGATCCACCAGCCCCGTGTGTAGGTTTACATGCGAACAAGGCAAGGCCGAGTGAAACAACACCACCCACAAGCCCCTGTTTGCTCGAATAAAGCCACGATAGTGCGAATAAAAGCATTTAGGGTGATCAGTGTTCAGTTTTATAATCAAAAAGATGTCAAAATCACTGCTAAACAAGCAGCGCGAGCTACGCTTAGCTTGCTGGTGTATTAGCTAACAAAGTTAACTGCGTTTGCTCTCGGTTTCACTTTGTTGGCTTAATAAAACCATCAGCTAATCGTCAACGTTATTTATTCTTGTGTACAGGAGATGGTTGACCAAGACCTGTGGATGTTTTGTATTCTGCGTCACTTTAAATTAGTTGTCATGTAATTAGCTTGTGTGCTAATTTGGCTTAGCTGGTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30279
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 |
---|---|---|---|---|---|
ENSDART00000016117 | None | None | 182 | None | 6 |
ENSDART00000124645 | Essential Splice Site | 243 | 373 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 30427630)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28994991 |
GRCz11 | 25 | 29437998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAGCTAGTAAACGATAGCCTGTATGAGTGGCATGTCAAGTTAAGGAC[G/A]TAAGTATGCTTATCATATAAGAAATAGCGTGTTGAATGATTACAGTTTGA
Long Flanking Sequence:
CTAAAGTTTGCCTAAATTTAATCCTAGAATATTCGATATTGAGTAGTTTTTCAGAAATCAATAAAATCCTGCTAGATTTGACTTCAAGCTGATTTGTTTACTGCAGTAACCAGGGAAACGCTGTTATACATATAGCGCCACCTGCTGGATTAGCATTTTTATATAGCATATGAATACTGTTTTAGTTTAGGATATACTGTTAATGTCGCAGATGAGGAAAAAGAGTCTTAAAAAAAACTAAAAGGTATTGAATTTCATTCTTTGGTTCCTGTATATACCCTGATTGATATTTTTCCACTCTTTAACCGTTGTCTAAAAAGTTAGGCACAGGGAACATTGGTGTGGTGTGAAATCTGTTGGCATGCGAATGAGTCTTAGTGAAAAGAATGTTTCAGGTTTGCATGATCTGTTTGTTTACATTATATTCTTTTGGTTCCAGGTATCTATTCAGTGGAGCTAGTAAACGATAGCCTGTATGAGTGGCATGTCAAGTTAAGGAC[G/A]TAAGTATGCTTATCATATAAGAAATAGCGTGTTGAATGATTACAGTTTGAGTCACTAATGTGTAAAATGACTCTGTTTGGTTTATAAGGGTTGATCCAGACAGTCCCTTACACAGCGACCTACAGGTTTTGAAGGAAAAAGAAGGAATGGACTACATTCTGCTCAATTTCTCTTATAAAGTGAGCATTGTTGTTATTTTTTTATTTTATTGTTTTTTTTTTTGGTGTACAAATGAAAAGAGATAACAATTGAATTTTGGTTTTCTTGTGATGGCAGGATAACTTTCCTTTTGATCCTCCCTTCGTACGGGTTGTGTCTCCTGTCCTGTCTGGAGGGTGAGCTTGAGAACTTTGCTGAACCTATCTTGTATAATTATTTCTATATTTAATGGTTGCATTTACTTTGGTGCGAATTTAATGGGAGCATAGTAATATTTTTGATGTTACATAAAATGTCTTGTTTTCATTGCACAAAATATGTAGTAAAATTATGTTTTAGTT
Associated Phenotype:
Not determined