Busch Lab

ZMP

uba1

Ensembl ID:
ENSDARG00000037559
ZFIN ID:
ZDB-GENE-040426-2009
Description:
ubiquitin-like modifier-activating enzyme 1 [Source:RefSeq peptide;Acc:NP_998227]
Human Orthologue:
UBA1
Human Description:
ubiquitin-like modifier activating enzyme 1 [Source:HGNC Symbol;Acc:12469]
Mouse Orthologues:
AC007585.1, Uba1, Ube1y1
Mouse Descriptions:
Ubiquitin-like modifier-activating enzyme 1 Y [Source:UniProtKB/Swiss-Prot;Acc:P31254]
ubiquitin-activating enzyme E1, Chr Y 1 Gene [Source:MGI Symbol;Acc:MGI:98891]
ubiquitin-like modifier activating enzyme 1 Gene [Source:MGI Symbol;Acc:MGI:98890]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa44999 Nonsense Mutation detected in F1 DNA Not yet available
sa37679 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15137 Nonsense Available for shipment Available now
sa37680 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44999
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
ENSDART00000054691 Nonsense 141 1058 5 26
ENSDART00000133131 Nonsense 141 195 5 6
ENSDART00000147382 None None 93 None 4

The following transcripts of ENSDARG00000037559 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20939076)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 20724183
GRCz11 23 20650526
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAACCGTGCTGATGTCAGTCAGCCTCGACTGGCAGAACTGAACAGTTA[T/A]GTGCCTGTAACCTCCTACACTGGCACCCTCACCAATGAATACCTGACCAA
Long Flanking Sequence:
GCATGATGGTAAAACTTGAAGGCTGTTATGAATGTATTAAAACGTGTTTGTCGTAAAAATTCGTAATAATGACAAAAAATATGAATTTGTGCATCTCCTGATTCCGGGTGAAGATATGCTGCCATTGTAGAATTGGGATGAAAAAAAAATTAAATGAATGAATAAACGTGTACGTCAGTTCAAAATATTACTGTTATTATTATTATTATTATTATTATATATAGATTTTTTTAAAGGCAATGTTGGTGAGCACAAGAGACTTTTTCTAAAATAATTTTTAAAATCTTACCAAACCCAAACTTTTGTACTGTTCTCTACATAAACAAATGAAAAAAAATCCATATATTGTTTCTGGAAGTGTAAGAATAAACATTAATAATCTACAGTAGTAGAAATACAATTTTGTTTGCTTCATGTTCCTAGTTTTACCTGCGTGAGGAGGATCTTGGGAAGAACCGTGCTGATGTCAGTCAGCCTCGACTGGCAGAACTGAACAGTTA[T/A]GTGCCTGTAACCTCCTACACTGGCACCCTCACCAATGAATACCTGACCAAATTTCAGGTACTGCTGCTATTGCTCCACTGGACTTTAACTTTGATCTCTTATAAGGATTACAAATTATTTTCTCTAAATGCATATTAAACTTTGCATTATAGCTGAACTGAAGTTTGAAGCTGTTAGCTAATAGGTCTTTGTATGCTTTTGTCCAGGTTGTTGTGCTCACCAACTCTAGTCTTGATGAACAGACACGTATCGGGGAATTTTGCCACAGTAATGGCATCAAGTTGATTGTGGCAGACACACGTGGACTGTTTGGGTATGAATATTTAAAAGATATGACATTTTTTAAGGTTTTTTTTTTCCTCCATGTAACTTTTTCATAAACATTCTGTTATTTAATAGGCAACTGTTCTGTGATTTTGGGGAGGAAATGATAGTATTCGACACAAACGGAGAACAGCCATTGAGCGCCATGATCTCAATGATCACAAAAGTAAGAGCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37679
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054691 Essential Splice Site 304 1058 10 26
ENSDART00000133131 None None 196 None 6
ENSDART00000147382 None None 93 None 4

The following transcripts of ENSDARG00000037559 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20941458)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 20726565
GRCz11 23 20652908
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATAAATTAAATCCCCTGCTGGATTTTAAACGCACTTCTTTCTTCACC[A/T]GAAATCCCTGTCCTCCTCCATGGCCGAACCAGAGTTCTTGCTGACTGATT
Long Flanking Sequence:
TACCTGCAATTTGACAACCATTTCACATGTTTAAAGTTTTTAAGCTGCTGCTGGTATCTTCTGACTGTTTGACAGCTTTTAACATTTATGCTGGCCTACTTTTTAATATGTAACTGGATCAGCATGAGGCAACACCTGTCAATTGTTTTAGCAACCAATCACATCAAGTTTCTACCCTTCTCCTAAAGAAAGAGAAACTGATGCAAAACCGAAAAGAATGTCTGTAGAATCTGAGGCCTCTTTAAAGAGTTGTGATGTTAACCATACACTGTTTACATTTCCATCTGGTGGGGTGTTTTGTGACTGATGTCTTTTGCATTCAGGTCCTTACACTTTCAGCATCTGTGACACCAGCTCATTCTCTGACTATGTGAGAGGTGGTATTGTCACACAAGTGAAGATGCCCAAGAAGATTGCCTTTGTAAGTTGATTCCCTGGCTGAGATTGTTGATAATAAATTAAATCCCCTGCTGGATTTTAAACGCACTTCTTTCTTCACC[A/T]GAAATCCCTGTCCTCCTCCATGGCCGAACCAGAGTTCTTGCTGACTGATTTTGCCAAATTTGATCGTCCAGGCCAACTCCACGTGGGCTTTCAGGCACTGCATGCATTTGAGAAGAAGCACAGTCGTCTGCCAAAGCCCTGGAATCAGGTGAAGACTTTTATTTTGTCTAGCAGTATTTCTAATCATCTAGTGTATTTTCTGGATTAGTCACTTTATAGTGTCAATTGTTTTTTATTTGTTTTGTTTTTTTATCATCTGAAATAGGGTGTGATTTTTATATTCTGAAGTGTATTTTATTTGACTTGCAAATCAAGGTTTGAGTTTATCAATTCTTGATTGTGAGTGTTGCCCTAAATGTTTTACAGTTCACAGTGTTTTCTGCTATAAGTAGTTTAAAATTATTTGTTGTGTAGTCTATTCAGAAAAGAAAAAACAGCGCTCTTTCATGACACACTACTAAATTGTGATCTGTGGGCTAAAGACCCCTGCTTTAGTCTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15137
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054691 Nonsense 374 1058 11 26
ENSDART00000133131 None None 196 None 6
ENSDART00000147382 None None 93 None 4

The following transcripts of ENSDARG00000037559 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20942471)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 20727578
GRCz11 23 20653921
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTATGACTCTGGCTGAAGAGGTGAATGCTGCACAGACAGGATCTGCC[A/T]AGCAAGAGGAGCTGGACCAGGCAGTCATAAAAAAGCTGGCCTGCGTGGCT
Long Flanking Sequence:
TATTTGCATGCAGCAAAGTATATTCATCTAGTGGAGACATTTATTTGCCCAAATTTAAATCTGAGAGCATAAAGGGTGAAAAAACAAAAATTGTATCCGAAATCCAACGATCCGAAAATGCGTGAAGTGACAAGTAGTTGACAGGCCCACAGTCATTTGTTAGCAAACATTCTTTACTCTTTATTATTAATTTTTTTTAACTAAGTATATTCACTATAATGCAAGTAATGGAAATCCCATCCCAACTAGCCATCTCTAATTCCACTCTGAACATACTGGGCTGACCAGATTTCTCTGTTCACTTAGTGTTCCACTTCCCAGTCTAATACTTTCAAGAAGTGCACTGTTGAGCTTTAATTCTACGTGAATGCTGTACTGTGGATATCAGGCTCAGTGACTCAGCAGTGATTTTTCTCTCTCTGTCTGTCCTATTGCAGGCAGATGCGGATGAGCTTATGACTCTGGCTGAAGAGGTGAATGCTGCACAGACAGGATCTGCC[A/T]AGCAAGAGGAGCTGGACCAGGCAGTCATAAAAAAGCTGGCCTGCGTGGCTGCTGGAGACCTGGCACCCGTCAATGCCTTTATTGGTGGGCTTGCTGCCCAGGAGGTTATGAAGGTAATATGGTCTTCCATTATTGTCTTTGAACTTTAGATCTGTGAGATGCAGCATTGTGATGTGTTAGCCTCACCTATCATGCTTCTTTATTGTTTATCTGCTCAGGCCTGCACAGGGAAGTTTATGCCCATCATGCAGTGGCTGTATTTTGATGCTTTGGAGTGCTTACCTGAGCCTGAGGAAGTCATTCTTACAGAGGAAGAGTGTGCTCCTGTAAGTGCTTTATATTTTTAGCATTTGTTTAATATTTGTGCATTGTTATGGCTCGCTCAAAAGATTGTGGGTTTAAGACAGAATAATTTATTCAGTTATCTGTTTTGTACAGAGGAACTGCCGGTATGACGGCCAGATTGCCGTCTTTGGGTCCAAGCTGCAGGAGCTGTTAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37680
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054691 Essential Splice Site 882 1058 22 26
ENSDART00000133131 None None 196 None 6
ENSDART00000147382 None None 93 None 4

The following transcripts of ENSDARG00000037559 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 20949033)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 20734140
GRCz11 23 20660483
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAATCTGAGAGCAGAGAACTATGACATTCCTCCTGCAGACAGACACAAG[G/A]TTAGCAGGCCAGCGATTTCAAAGCTGTCCTGTGAGCTACGTATCATCTTT
Long Flanking Sequence:
CCAGTTATGGTCTACTACTAGACTGATACTGAAATGTTTGTACACTGCATTGTGACACAGATAACAAGGACGATTTATTGACTTGTATAGTTCACCAAAATTTTAATTCTGTTTAATCTATGCTTGTACCACCCTATTTGAGTTTCATTCAAGACATTTTGCACTGTTGAAAACCCTTAGCTGTTGTCTTTTTCAATCTAGCATTGCATATTCTGTTCTCTGCCTGTTTTCAGATGACTCGAGGCTCGAAGAGCTGAAGACACTGTTGCCTTCTTTAGAAGCATCTTCTCAATTCAAGCTCTGTCCTATTGAATTTGAAAAGGTACTACTTATAACTTGACCCCAATTTCCTGGGCAGTAGCCCTTTGGAATTGGAGTTAAAATATTAATTAACTTCTATTCCTCAGGACGATGACACAAACTTCCACATGGACTTCATTGTAGCGGCATCTAATCTGAGAGCAGAGAACTATGACATTCCTCCTGCAGACAGACACAAG[G/A]TTAGCAGGCCAGCGATTTCAAAGCTGTCCTGTGAGCTACGTATCATCTTTAAAGATTCTCACCTTTCTCTTTCATGTTTCAGAGCAAACTCATTGCTGGAAAAATCATTCCAGCCATTGCCACAACAACAGCCGCTGTTGTAGGTCTGGTGTGTCTGGAGTTGCTGAAGATCGTTCAGGGGCACAAGAAGCTCGAGTCCTACAAAAATGGCTTCATGAACCTTGCTCTGCCTTTCTTTGCCTTCTCCGAGCCTATAGCTGCCCCCAAGCACAAGGTAAGCTGCAGCAGCAGTATTCTTCATTACTGCAGTGGTTCTGTTGTTACTTTGAATTACTCAGCTGTTTTGACATTCTTGTCTGCGAATAGTACTACGAGATTGATTGGACACTTTGGGACCGTTTTGAGGTGAAGGGCATTCAGCCTAATGGAGAGGAAATGACACTCCGGCAGTTCCTGGATTATTTCAAGGTAACATTTCATGATCATTTCTAAAATGTTTA
Associated Phenotype:
Not determined