Busch Lab

ZMP

ube4b

Ensembl ID:
ENSDARG00000037017
ZFIN ID:
ZDB-GENE-020205-1
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
sa45005 Nonsense Mutation detected in F1 DNA Not yet available
sa44010 Nonsense Mutation detected in F1 DNA Not yet available
sa11598 Essential Splice Site Available for shipment Available now
sa24363 Nonsense Available for shipment Available now
sa24362 Nonsense Available for shipment Available now
sa45805 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45005
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053804 Nonsense 39 1183 2 27
ENSDART00000064236 Nonsense 39 821 2 21
ENSDART00000121475 Nonsense 39 1181 2 29
ENSDART00000122920 Nonsense 39 821 2 20
ENSDART00000126384 Nonsense 39 1362 2 29
Genomic Location (Zv9):
Chromosome 23 (position 29793368)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29623935
GRCz11 23 29550476
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCACAGCCCAGCACCCCCCTCAGCACCCCTCTGACATCCCCACAGAGA[G/T]AGACTCCCCCAGGACCTTTGCCAGGACCCTCCGGGGCCTCATCACAGCCT
Long Flanking Sequence:
AGCTATATAAACGTGAAATGACTTGTGAAAGCAGTTTGTCTGTGAACTGAGATGAATAGCCGTTTGATTCAAGCGAGTTTTACTTCGCAGTTTTAATTCGCTCAGTCATGGATTTACATTTTTTCCATTTCACTGACAGTTTTTGCTGTAGAAGCCGAGGCCTTCAGTTTACCTTCTCCATCCTGAATGACTCACTCCACAGTGTAGTAAAGCTTCTTCACTGCTGGAAATAATGCCGATGCTTCAGGACTACTGTTTGCCTGAATAATGTGTTATTTTAGGGTATCGAAATAGAGCATAGAAGTTCTAGCTTTGCTTTACCCATTCACAGCAGTTAAGGGCATACTGTGAACTATTGCTCATTACTGATCTGTGGTTAGATTAAGTTGTAATTAATGCGTCTTGTTTAGATCCGTAGAAGGCGGTTGGCCCGGTTAGCTGGAGGCCAGACATCACAGCCCAGCACCCCCCTCAGCACCCCTCTGACATCCCCACAGAGA[G/T]AGACTCCCCCAGGACCTTTGCCAGGACCCTCCGGGGCCTCATCACAGCCTGTCCCACCAGCTCCATCTCACACTCTCGCACTAAATGCCCAAAATGTCACCCCTGCCACCTCTCCTATGGGGGCCTCAGGTAAGTGCTGTGCAGGTTTTATCAATCCAAAACGATCGATGTGGCTAAATGGCCGTTCAAAAGAGCATGTATAAGCATTGATTGAGTGTTTACATGAAATGTGAGATGTTGATTTAAGTTTATGGTGTTACAATAAGTAGTAAAGTTAAAGTTTGTTAAAATAATAGACCTTACATTACAATATCATAACAGCATTCCTTGTTTGAATTTTCTAATATAATGAACAGAATTTGAAAGATTAGACTGGTATTATTTAGAAAGTAGCTAAACACAAAGCATAAAAATCATTAAAAGATACATTTTTGGATTAACGATTAAAATGCAGGCAGTTTCATCATCGATATCGCAATGTGTGCATTCACAATAGTCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44010
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053804 Nonsense 115 1183 3 27
ENSDART00000064236 None None 821 None 21
ENSDART00000121475 Nonsense 115 1181 3 29
ENSDART00000122920 None None 821 None 20
ENSDART00000126384 Nonsense 115 1362 3 29
Genomic Location (Zv9):
Chromosome 23 (position 29787112)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29617679
GRCz11 23 29544220
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTCCATCTAACAGCCTGGAGACACAGTCCCAATCCCTATCCCGCTCC[C/T]AGAGCATGGACATCGACACAGCCTCCTGCGAGAAGAGGTGAGATACCTTT
Long Flanking Sequence:
TCGAGAATTTCAAAATAAGGAAAAAAAATAGTGTGTGACTGATGGCAGCCATAGGAGAGAGTAATGTAAATTTACTCTCAGCCCCATAAACTCTGTATTAGAAATACTTTGTATAAGCGGTAATTCATTTGTTGTAATTTGACACAAAGATAAAATAATACATGCATAAATGTACATATATTTTGAAAAAATCTAAATATTAAAAACTTTCAAGGGTTTAAGATTATGATAATGACCGTTAAATGCGTCTTGTAAAAAGGGTCTGCTGATGACTATTACAGAAGCATACATTGCGATATTGATGCTGAAACAATATATTGTGCAGTCACATTTTTTTTCTATGACACAATCATAAGTTTGTACTCAAACACAGAGCCTTTTTTGTGTTTTGTGTTACTGTAGGGGTTGCGTACCGCAGCCAGAGCAGCGAGGGGGTCAGTTCTCTCTCCAGCTCTCCATCTAACAGCCTGGAGACACAGTCCCAATCCCTATCCCGCTCC[C/T]AGAGCATGGACATCGACACAGCCTCCTGCGAGAAGAGGTGAGATACCTTTTGAGGAGAGTGTTTTATCAGAGACAGTGTGACATAAGAGATTGTTCTGGAGATGAAGATGTGTATCTCTCTTGCTGAATGCCTGAGATCTCTCTCGCTCTTTATGCAGTCATTTTGTTCTGTACTGTTAGACTGCAAATGACCCATTGCTCTTTTGTGCTTCAGCCTCATAATCCCTAAAGTGCATAAAAAGGATAATACTTTTAGCTGTATATGAGCAATTCCATCCAAATGTCAACCTTGCCATGAAAAAAAATCACCAAAATAGTACACACAAGAAGTTTTTTGTATGTAAGCAAGTATTTTAAAATACTTTAAAAATACTCTTAAATGTCTCTGTCACTGTTTTCAAACAATTTTATTTGATTTACCAGTCACAAAAGTGGCAATTTCACATCTGTCACATCTATAAAGGTTGTCATGATACTATACCAGCTGAAGTATCTTTATG
Associated Phenotype:
Not determined

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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

Mutation Details

Allele Name:
sa45805
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053804 Nonsense 1045 1183 24 27
ENSDART00000064236 Nonsense 683 821 18 21
ENSDART00000121475 Nonsense 1043 1181 26 29
ENSDART00000122920 Nonsense 683 821 17 20
ENSDART00000126384 Nonsense 1224 1362 26 29
Genomic Location (Zv9):
Chromosome 23 (position 29755165)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29585732
GRCz11 23 29512273
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAAAAGCTTCTGGATCAGCTCACTGACATCTACCTGCAGCTAGACTG[T/A]CCCCGATTTGCTAAAGCCATCGCAGATGACCAGGTCTGTTTTTGGTCTGT
Long Flanking Sequence:
TCACAAGTAGAATAGTAGAAATAATAGTTTGTAATATCAAGCAGCATGATGAGCAGTTACTAATGTCAATAGCAGTGAATGAGACCGGAAGTCTCGAGCCAAAAAGTTTTGATGGCTCCGCCCACTCATACATTAAGAATAAGGTCAATATAGAAGAAGATAATTTTCTGCGCTCTCAGGTATTTATAGTCTTCAGGGAACACTGAATCACTGCCAGTGTCAGAACATTGAGTTTTTTCAGAGGAGGCGTTAGCAAAGGCTCCTCTAATGACACTAAGAAGACAATACTATATTTATAGGCTTTGTTTGTGAGTGACTCGTGTGTTCTGTTATATTAAATAGGAACTGGGTCCTCGTCTGGCTGCCATGTTGAATTATAACCTGCAGCAGCTATGTGGGCCTAAATGTCGAGACTTGAAGGTGGAAAACCCTGAAAAATATGGTTTCGAGCCAAAAAAGCTTCTGGATCAGCTCACTGACATCTACCTGCAGCTAGACTG[T/A]CCCCGATTTGCTAAAGCCATCGCAGATGACCAGGTCTGTTTTTGGTCTGTTTCTAAAATCTTAACCGTTGTTTGTTCAATGGTTGTAACTGACTTTTTTTCTTTATGTTTTCAGCGGTCGTATAGCAGGGAGCTCTTTGAGGAGGTCATTTCCAAAATGAGAAAGGCGGGTATTAAATCCACCATCGCTATTGAGAAATTCAAGCTTCTGTTGGAGAAGGTGGAGGAGATTGTAGCCCGCAATTCTCAGTCAGAGATGGATTACAGTGACGCTCCGGATGAGTTTAAAGGTCAGTGTTCTTCATCAAAGAATTAGTTCACCCATTTACTCATCGTCTACTTGTTTCAAATCTGTTTGAGTTTCTTTTTTCTGTTGAACACCAAGAAAGATGTACTGAAGAATGTTGGAAAAAGCTGCCATTGACTTCCATAGTATTTTTTGTTCTTACTATGAATGTCAATGACTGCTTTTTTTCCCAACATTCTTCAGTATAACTTTTG
Associated Phenotype:
Not determined