ZMP
zgc:171646
Ensembl ID:
ZFIN ID:
Description:
ubiquitin-conjugating enzyme E2 E1 [Source:RefSeq peptide;Acc:NP_001096586]
Human Orthologues:
UBE2E1, UBE2E2
Human Descriptions:
ubiquitin-conjugating enzyme E2E 1 (UBC4/5 homolog, yeast) [Source:HGNC Symbol;Acc:12477]
ubiquitin-conjugating enzyme E2E 2 (UBC4/5 homolog, yeast) [Source:HGNC Symbol;Acc:12478]
ubiquitin-conjugating enzyme E2E 2 (UBC4/5 homolog, yeast) [Source:HGNC Symbol;Acc:12478]
Mouse Orthologues:
Ube2e1, Ube2e2
Mouse Descriptions:
ubiquitin-conjugating enzyme E2E 1, UBC4/5 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:107411]
ubiquitin-conjugating enzyme E2E 2 (UBC4/5 homolog, yeast) Gene [Source:MGI Symbol;Acc:MGI:2384997]
ubiquitin-conjugating enzyme E2E 2 (UBC4/5 homolog, yeast) Gene [Source:MGI Symbol;Acc:MGI:2384997]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10112 | Essential Splice Site | Available for shipment | Available now |
sa3002 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa10112
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123519 | Essential Splice Site | None | 195 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 19345721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 17899239 |
GRCz11 | 19 | 17359097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCAGTGTTAAAGGTCAAACACGCGCCAGTAGTTGATACATCGACACGG[T/C]AACATTTATATTACCTACCATTTCGTCGATACAGCGAAACATTGTTACAT
Long Flanking Sequence:
AATCCTTTAAACATTACAAAATAGCGCATATTTATGTTATACTTACATCAGCGGTGTGTTCGAATGCTCGTATTCTCGTCTGTATTGTGACAGTCTGAAATATTTGTCCATCGATGTTAAATGAAGACTGAACCCGGACAACTACAGGGCTGACGACACATTTACTGTCTTTTTCATCATGTTCATTCAGCATATTTGTGGGATGGGGTAAAGTTTAAGTTTAGTGAACTCGACGGCGATGCGTGTTTGTGCGTTTCCTACTTAGGATTAATCTCGTGTATTTGATCGCGTGTGTAACGTTACGGATTCGATTCGATCAGACTCAGCGTTACGTTTGCGTGGATTAAAACACAAGAGATGGATATACGTCTGATTATTTTGAGGTGTTTTAACCGATATTTCGAGCTATAAATGCGGAGTGATCGCACCCACGGTATCGCAGTGTTGTTGATCCAGTGTTAAAGGTCAAACACGCGCCAGTAGTTGATACATCGACACGG[T/C]AACATTTATATTACCTACCATTTCGTCGATACAGCGAAACATTGTTACATGTGTGCTCCCATACGGCACATACAATCAAAGTGGTTAACAAATTGTATGTTATTTTTACTGCAGTGTTTGTGTTTCACTCTCATGTAGATCGGGATGTCGGATGAGGACTCGCGTGCAAGCTCTAGCTCATCTTCCTCTTCCTCCTCCTCCTCCACCCATCAGCAGCAGGAGAAAGACACACCTGGAAAAAAGAAAGAAAGCAAAGCCAACATGAGCAAGACATCCAAACTCCTCTCCACAAGTGCAAAGAGGTGAGGAAACATCATAGCTTGGGCTTTGTCAGAAAGCCAGCGTTGCTCCTGGACAGTGAAGGATTTAACAGCAAACGATATGTACAGTATACTGGATTAGAAAGGCTTTCATGACCCCAAAGCATCATATGAAATTATTTCACAAATTTAGTAAGCCCAATATTTCATTTTACTGAATGCAGCAGGGTTAAATCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3002
Status:
F2 line generated
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123519 | Essential Splice Site | 164 | 195 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 19361421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 17914939 |
GRCz11 | 19 | 17373510 |
KASP Assay ID:
554-2469.1 (used for ordering genotyping assays)
KASP Sequence:
TCCAAAGTGCTACTGTCTATCTGCTCTCTGCTCACAGACTGTAACCCTGG[T/A]AAGTCACACGTCCGTAAACACACTTCAAGCTAATCAGGACTTGTTAGTTG
Long Flanking Sequence:
ATCGCTTTCACACCAGACTATCCCTTCAAACCACCCAAGGTAAGATCTTCTTTTCAGATCCTTGTTACAATCAATTTAATAAATTGTTACAAAAAGAGTATATAGTTATGTTTCAAATAAATGTGTTCATCCAAGAATTCAAAGCACAAGTTTATTACAGTTTTAATCAAACAAATGTAGGAAACTTATGATTTGTCTATGTTTTTCTGATTGAATATCACAAAGACTAACATGGCAGAATGCACAACTTGCTTGTTTTTATTATCTAAATTCAAACAAATCCGTGTACATGCCAAAAGGTGCTAGTGTGAAAACCCCTTTAATGACAGTGGTCCTGTTTTCTTTTGTCAGGTGACGTTTCGCACAAGAATCTATCATTGCAACATCAATAGTCAGGGTGTGATCTGTCTGGACATCCTGAAGGACAACTGGAGTCCAGCGCTCACTATCTCCAAAGTGCTACTGTCTATCTGCTCTCTGCTCACAGACTGTAACCCTGG[T/A]AAGTCACACGTCCGTAAACACACTTCAAGCTAATCAGGACTTGTTAGTTGGTCATGTGCTGATGCTCCAGTGTCTGTCAGTATGTTGGAGCTTAAGCTGTTTGACCTAGACTAAAGCTGAGGCAGTTACAGGTGTGGGCAGTTATGCAGCAGCTTAATGCTCATGTATGAAACTGCATACAAACAACTTCATCTTATATTAGAGCTGTCTGTTCCTTTCAACTTGACTTTTCTGCTAAAACAAATCACATCTCAACTACTTCCTGGAGGATCACCAACACTGTGTTTATTCGGGATATACTTGTTTTTTTTTTTTTTAACTGTGCGACTCGTGCCGAGAGAGCACCCTTTGGAGTTCGGAGGAAATTTACCACTGATCACATCACCGTTCTGTACTTGCATGATGGGCAAGACAATCGCAGCTTTTGCTGAATTACAAATGTGACTTTATGTCGATATATTTTTCAGCCCTAATCCTAATCAGAAGACATGGGAAATGTG
Associated Phenotype:
Not determined