ZMP
ube4b
Ensembl ID:
ZFIN ID:
Description:
ubiquitin conjugation factor E4 B [Source:RefSeq peptide;Acc:NP_919343]
Human Orthologue:
UBE4B
Human Description:
ubiquitination factor E4B (UFD2 homolog, yeast) [Source:HGNC Symbol;Acc:12500]
Mouse Orthologue:
Ube4b
Mouse Description:
ubiquitination factor E4B, UFD2 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1927086]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11598 | Essential Splice Site | Available for shipment | Available now |
sa24363 | Nonsense | Available for shipment | Available now |
sa24362 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11598
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053804 | Essential Splice Site | 361 | 1183 | 9 | 27 |
ENSDART00000064236 | None | None | 821 | None | 21 |
ENSDART00000121475 | Essential Splice Site | 361 | 1181 | 9 | 29 |
ENSDART00000122920 | None | None | 821 | None | 20 |
ENSDART00000126384 | Essential Splice Site | 539 | 1362 | 11 | 29 |
Genomic Location (Zv9):
Chromosome 23 (position 29774041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 29604608 |
GRCz11 | 23 | 29531149 |
KASP Assay ID:
2261-7947.1 (used for ordering genotyping assays)
KASP Sequence:
AATACATTKTGAATGACACTGCCACCCCCTCTCTGTCTTTGCCCTCAAAC[A/G]GAGCCCCTCTTCAGYCCTCCCTGCTGGYTCCCTACATGCTGTGCCGGAAC
Long Flanking Sequence:
AATTTGTGCAAGTAAACATTAATATAGATTTTTAATTTGCTCTAATCTAGCATCTTGTCTATTAAGAGATGGGCTTGAAATATAAAATAATGTCAATCAGCAGGGACGTTTTAATATAGTTTATCTCTTAATGTTTTTTGCAGCACAGTACTTCTATATGTTAGACTACAGCAGCAACACCTCATAAATAAATGTAAAAGCGGCATGTGTTTTGGGTAAATTACCTCCTAAATTAATTTTTAGCTTTGTGTAAGAATATTTTTGCTGCTTTCTCTATGTGTATTGATTAGCTTCAGGGGTAAACGTTGACACTGGTGAATAGTCACACTGTTGATGCAAATGTGCAATCTGATAAGAGGAAGAAAATCAGAATCAAGCTCCTATTCAAACCAAGTGTTAAAATGCCCAAGTTGCACTCTGAAGTCTGTCAGTTTGAATGCATACCAGCACAATACATTTTGAATGACACTGCCACCCCCTCTCTGTCTTTGCCCTCAAAC[A/G]GAGCCCCTCTTCAGCCCTCCCTGCTGGTTCCCTACATGCTGTGCCGGAACCTTCCATACGGTTTCATCCAGGAGCTGGTGCGCATGACTCACCAGGAGGAGGACGTGTTCAAACAGGTGGGAGTTGCAGCAGATTATGTCGACGGGCCACACGCTGGGCCGTTTGACTTCATTATTGATGCCAAACTCCTAGGGATAGAAGGCATATTGTTGAGTGTTTCAGCTATTTGTTTGGTAACACTTTACCATAAGGTTACATTTGAGTTATGCGCATTAATTGACATGAATGGTGTTTGAGTCTTTACTAACATTTTTTTATTAGAAATGCAATGATTTACTGTTAGTTCATGTTAGCTCAGGTCATTTTAATTGTATTAACAGTAAGAACTAAATATTTTAACAATGTAGAAGTAAAGAATTTTTAGGGATTGGTTTTTTATAGGATGCAAAGCAATGTGTGCTCATGCCTCACTTGTAGAAAATTATGTTATTTTTTCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24363
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 |
---|---|---|---|---|---|
ENSDART00000053804 | Nonsense | 970 | 1183 | 23 | 27 |
ENSDART00000064236 | Nonsense | 608 | 821 | 17 | 21 |
ENSDART00000121475 | Nonsense | 968 | 1181 | 25 | 29 |
ENSDART00000122920 | Nonsense | 608 | 821 | 16 | 20 |
ENSDART00000126384 | Nonsense | 1149 | 1362 | 25 | 29 |
Genomic Location (Zv9):
Chromosome 23 (position 29757503)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 29588070 |
GRCz11 | 23 | 29514611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTCTCAGTTGACTCAGGATGAGCGAGTGTCACGGTCTTACCTGGCTT[T/A]AGCCACAGAAACGGTGGATATGTTTCATATCCTCACCAAACAGGTCCAGA
Long Flanking Sequence:
TGTTTTTGTTACAAGTTAATCGTACCTTTTCTTCTTTTGTTCATTCCGCAGCTCCGGTAAACAGTTTGTGCGCTACATCAACATGTTAATAAATGACACAACGTTTCTGCTGGACGAGAGTTTGGAGTCTCTGAAACGCATCCATGAGATTCAGGAGGAAATGAAGAATAAGGAGCAATGGGACTTGCTTCCCAGGGTCAGCACATCTCACCAATTCACTAATAAATCACTCACACACCCTTTTAACTGCATTATGTGTAATGGATTTAATGCATTATCTTATCCGCTATAAACCATTAGCATTAAGGCTGAAAAACAGAAGGGTGAAGTTTAAAGTGAATGAAACAACGGGAGCGTTTGTGCTTTCATGAACAATTTTTGTTCTGCGTTTCCAAATTGGATGTGATTGAATGTGAAATGTTGTGGTCTTCAGGAGCAGCAGCAGAGCAGACAGTCTCAGTTGACTCAGGATGAGCGAGTGTCACGGTCTTACCTGGCTT[T/A]AGCCACAGAAACGGTGGATATGTTTCATATCCTCACCAAACAGGTCCAGAAGCCGTTCCTCAGGCCTGTAAGTACACAGTTATGTCACATTCATATGTGCTATAAAAATTACACCTTGATGTCATGTGTGCAGACAATAATGTTCAAAAATGTAGAGTTAATATGATTTTTTTCATTAGTATTTTTGGAAGTTGTCTTATACATAACAGGTCTGACCCTAGGAAAACAAAAGACTGTAAAAATAATATTGTGAAATAGTAACGGTCTTTGCACGCTGAAATCTGAAATTTTCTTATGCATTTTTTTCGTATTCATATGCAAACAAACCGATGCATATTAATTAATCCATTAGGAAAAAACACAATACATTTCGGAGTCAGTTCAAGCAGTGATGCACTGTTCTCCTCTCTTCTCCAAAGTAGAAAAAGAAAGAGGAGTAGGCTACATATTGTGTTCATCCAATACTAGAAGAAGGAGAGTTCATCTCATTATCAAAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24362
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 |
---|---|---|---|---|---|
ENSDART00000053804 | Nonsense | 1014 | 1183 | 24 | 27 |
ENSDART00000064236 | Nonsense | 652 | 821 | 18 | 21 |
ENSDART00000121475 | Nonsense | 1012 | 1181 | 26 | 29 |
ENSDART00000122920 | Nonsense | 652 | 821 | 17 | 20 |
ENSDART00000126384 | Nonsense | 1193 | 1362 | 26 | 29 |
Genomic Location (Zv9):
Chromosome 23 (position 29755258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 29585825 |
GRCz11 | 23 | 29512366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTGCCATGTTGAATTATAACCTGCAGCAGCTATGTGGGCCTAAATG[T/A]CGAGACTTGAAGGTGGAAAACCCTGAAAAATATGGTTTCGAGCCAAAAAA
Long Flanking Sequence:
AGAACTTCTGATTCAGTTGCCCTTGGGAGACATGACTAGGAATAATAAACGGCAGAAAACCTTCAAATGACTTGCTGTGGTCATGACTATACATCACAAGTAGAATAGTAGAAATAATAGTTTGTAATATCAAGCAGCATGATGAGCAGTTACTAATGTCAATAGCAGTGAATGAGACCGGAAGTCTCGAGCCAAAAAGTTTTGATGGCTCCGCCCACTCATACATTAAGAATAAGGTCAATATAGAAGAAGATAATTTTCTGCGCTCTCAGGTATTTATAGTCTTCAGGGAACACTGAATCACTGCCAGTGTCAGAACATTGAGTTTTTTCAGAGGAGGCGTTAGCAAAGGCTCCTCTAATGACACTAAGAAGACAATACTATATTTATAGGCTTTGTTTGTGAGTGACTCGTGTGTTCTGTTATATTAAATAGGAACTGGGTCCTCGTCTGGCTGCCATGTTGAATTATAACCTGCAGCAGCTATGTGGGCCTAAATG[T/A]CGAGACTTGAAGGTGGAAAACCCTGAAAAATATGGTTTCGAGCCAAAAAAGCTTCTGGATCAGCTCACTGACATCTACCTGCAGCTAGACTGTCCCCGATTTGCTAAAGCCATCGCAGATGACCAGGTCTGTTTTTGGTCTGTTTCTAAAATCTTAACCGTTGTTTGTTCAATGGTTGTAACTGACTTTTTTTCTTTATGTTTTCAGCGGTCGTATAGCAGGGAGCTCTTTGAGGAGGTCATTTCCAAAATGAGAAAGGCGGGTATTAAATCCACCATCGCTATTGAGAAATTCAAGCTTCTGTTGGAGAAGGTGGAGGAGATTGTAGCCCGCAATTCTCAGTCAGAGATGGATTACAGTGACGCTCCGGATGAGTTTAAAGGTCAGTGTTCTTCATCAAAGAATTAGTTCACCCATTTACTCATCGTCTACTTGTTTCAAATCTGTTTGAGTTTCTTTTTTCTGTTGAACACCAAGAAAGATGTACTGAAGAATGTTGG
Associated Phenotype:
Not determined