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 are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36737 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23391 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36737
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017798 | Essential Splice Site | 89 | 244 | 3 | 14 |
ENSDART00000097333 | Essential Splice Site | 89 | 372 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 18 (position 49540909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 50609525 |
GRCz11 | 18 | 50606090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGTGCACTCATGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCA[G/T]CTCCTGCAGCAGCTGAAGAGGCTGATCTGTGACCTGTGTCGCCTCTATAA
Long Flanking Sequence:
TTAAACTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTGAGGGAGCGTCAGGGCTGTTGATTGGACGGCTCTCTTCATTCTCAGTCTGGTATTCATTACACACACGTGAAATGTGATCAGCTTCTGTTGTGGTTTAGTGACTGAACGCAAACACACTGACGACTGAAAGAGGAGCAGCTGATCTTTATCACGGAAACAACAGATCTGGAGCACAAATTACCCATAATGACCTGCTAATCTCACACACGTGACCGTATGCGCATACACACAGTAGAGCTCAACATTATTAAAGCTGCTGTCAGAATAATTACTGCTCAGATATGTCAAACAGTTGTAGTAATAGTATTTGGCCTTCAGCTGAATGTTAGTGTGGCTCCATCATACTCACTGTGCACTCATGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCA[G/T]CTCCTGCAGCAGCTGAAGAGGCTGATCTGTGACCTGTGTCGCCTCTATAATCTCCCTCAGCATCCAGATGTGGAGATGCTGGACCAGCCGCTGCCTTCAGGACATCATACACACGACAGAAAGGTCAGCATTATTCACACACACACACCTGCAGGACACTGAGCGTACGGTGTGTGACACAATAAACCATGATCATACACCAATACTGAGGTCTATAGTCCAGTGAACTCATTAATTATGCATGATCAGGGTTCAATTAGCCAAAAGCTGAAGACGGACACACACTTGACTCGGATTTTGAGCACACTTGGTTTGTGTTCTTGCTTGGATTGCACTGTCATAACGTGTGTGTGTGTGTGTGTTTTATCCTGCAGCTGGGCACGACAGATGAGGTGACATCAGAGGAGGAAGAGGAGGAGGACATGGGAGAGGTGTGTGTGTGTGTGTGTGTGTGTGAGTGCGCAAGTTTCTCTGTGTTTAACTGTGAATGGGTGTATGTT
Associated Phenotype:
Not determined
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