ZMP
ube2q1
Ensembl ID:
ZFIN IDs:
Description:
ubiquitin-conjugating enzyme E2 Q2 [Source:RefSeq peptide;Acc:NP_001018415]
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 is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23391 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23391
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 |
---|---|---|---|---|---|
ENSDART00000017798 | Nonsense | 243 | 244 | 8 | 14 |
ENSDART00000097333 | None | 238 | 372 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 18 (position 49539782)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50608398 |
GRCz11 | 18 | 50604963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATCTACTCAGTGGAGCTGCTCAATGACAGTTTGTACGATTGGCACAT[C/A]AAGCTGAGAACGTAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Long Flanking Sequence:
AAGAGGAGCCGGTGGAGGGGAAGAAGTCTGAGGATGACGGGATAGAGAAGGAGAATCTGGCCATCCTGGAGAAGATCCGCAAGACCCAGCGGCAGGACCACCTCAATGTAAGTGCGCACTCGGTAAGGGCCCTTTCCTTCTGCTCCTCTCCTCTTCTGTTCTGGGTCGGTGTTCAGATGTCTGCCGGGTTTATAGGTTGTTGTGTGTTGTGTTGTTCTAGGGAGCTGTGTCTGGATCTGTTCAGGCGTCTGACCGCCTCATGAAGGAGCTGAGAGAGATCTACCGCTCTCAGAGCTATAAAAACGGTAATGTGCATTACTCAGACTGCTGCTGCTGTTCTCTGATCAGTCTGTATCCTCTGCTGTTCTCTGATCAGTCTGTATCCTCTGCTGTTCTCTGATCAGTCTGTATCCTCTGCTGTTCTCTGATCAGTCTGTATCCTCTGCTCCAGGAATCTACTCAGTGGAGCTGCTCAATGACAGTTTGTACGATTGGCACAT[C/A]AAGCTGAGAACGTAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATCGTGATTGTGTGTGTATCTTGATGATGATTGTATGTCTGTGTCTTAATAATGATGATAGTGTGTGTGTGTGTGTGTCTTCATGACGATGCTGATGATGGTGTGTGTGTTCAGTGTGGATCCTGACAGTGCGTTACACAGTGATCTGCAGGTGCTGAAGGAGAAGGAGGGAATGGACTACATCCTCCTCAACTTCTCCTATAAGGTGAGTTTCACCTGCTGAAGTGGAGAATATCAGGGTTGTGGATGAACTGAGCAGTGATGGGAGGGAAATGCGAGTGTCATGTTTTCACTGTAACAAGTTCTTTACTTGCGTTCTTACCATGTGTGTTTGGCCAAAAAATACATTTTTCATTATGCTGAATGTGATATTAATTAAATATGTAAATGTCATTTTGAAAAAGTAAATAAAAACACGAGTCATTCATATTTACAAAGATTTAAAGC
Associated Phenotype:
Not determined