Busch Lab

ZMP

uba2

Ensembl ID:
ENSDARG00000077024
ZFIN ID:
ZDB-GENE-040426-2681
Description:
SUMO-activating enzyme subunit 2 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXG4]
Human Orthologue:
UBA2
Human Description:
ubiquitin-like modifier activating enzyme 2 [Source:HGNC Symbol;Acc:30661]
Mouse Orthologue:
Uba2
Mouse Description:
ubiquitin-like modifier activating enzyme 2 Gene [Source:MGI Symbol;Acc:MGI:1858313]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa15421 Nonsense Available for shipment Available now
sa24623 Essential Splice Site Available for shipment Available now
sa12884 Nonsense Available for shipment Available now
sa44250 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15421
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109358 Nonsense 31 651 1 17
ENSDART00000110459 Nonsense 31 650 1 17
ENSDART00000144042 None None 371 None 10

The following transcripts of ENSDARG00000077024 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 13126484)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 12727975
GRCz11 25 12824480
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCTCTCCTCCTGCCGGGTGCTGGTGGTCGGGGCGGGAGGCATYGGCTG[C/A]GAGCTYCTGAAAAACCTGGTGCTCACCGGCTTTAAGAAWATTGAGGTGGT
Long Flanking Sequence:
CTCTCCCTCGTCTGGTTTCAACCCTATGAGTAAATTCTTTATTCCAGTGAACACAAAAGAAGATATTTGCTAGATATTAAATAAAACTGTAACATAGTACAAATGCTGTGGAAGTCAATGTTTACAAGTTTCCAGCTTTCTTCAGAATATCTTCTTATTTGTTCAAAAGAAACACGTAGAGGTTTGCAACAAGTACAATGTGAGTAAATGATGACAGTTTTCCGTTTTGGGTGAACTATCCCTTTAAACAACACATTTCTGCAGCTCAGCCGAGCCAACAGAGGTCGCCAGTTAAAACCTTATACGACCCTCGCGCTTTTTAGCAGTCTCTGCGCATGCGCACCCACTTCCCTCCCCGCAGGATCAAACCGCTGCTCGTCCGCGCGCCGCCGAAACGCTGAGCCGACAATGGCAGAACTAGTCGGTCCTCTCCGAAAACAGCTCGCTGACTCCCTCTCCTCCTGCCGGGTGCTGGTGGTCGGGGCGGGAGGCATCGGCTG[C/A]GAGCTCCTGAAAAACCTGGTGCTCACCGGCTTTAAGAATATTGAGGTGGTAAGTTGGAGGAAGGCGGACTCTCTTTGTGCTGGAGGAATCAGGCCCATCATCGCCGAGTATCAATTATAATAACCTGCAATGAAAACCACAGACTTGGAATGTGTTTATTAATGCATTACACGTTACTTTAAAATTCTTAAAAGCGTAATGCTGTTCATTATCTCATAGTGAACACAGAAATCATGTATTTGTTTGATTTCGCGCCATGTTTTTTCTGTGCTGTAAACATTGAGCACGGTGGCCACACTTCACGCCAAACTGTTGAAGGAAATGTTCCCGGGCCAGTCAAAGATTAAAAACATAACCTCTTTAAGATTTTTTCTTTCCAGTAGATAAATATAACATTTAGTCCTAATAAACAGCGTTTTTTAGTCTCTATTAAAGGTAAAGGCTGACGTGATTAATAGGATTGAGGTAAAGTTGGTTTTATATTCAGACTTTCTTTTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24623
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109358 Essential Splice Site 99 651 3 17
ENSDART00000110459 Essential Splice Site 99 650 3 17
ENSDART00000144042 None None 371 None 10

The following transcripts of ENSDARG00000077024 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 13127991)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 12726468
GRCz11 25 12822973
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTTGTCCATCTGCAAACATCACTGCCTATCACGACAGCATCATGAAG[T/C]AAGTGCAGTAACGTTATTGCCAAAAAAAACTTTGTAAATTTGTTTGTTTA
Long Flanking Sequence:
AAAAAACTATAGTTGCATTGTATATTTTTCAAGACCTCTAGCGAAGGTACAGTCAATCCGATGCAAAGCATTCAAGCATTTTTAAAATGACAATGTGAAAATGTGACAATGGGAAAAGTTTATTAAATTTCAATGTCACACATCCTGTGTGTTTTGGGTAGTCATTAAAAAAACGCATAGTAATATTATTGATTGGCTAGTATGTTTAAACGGTGTCTACTAATGTCTCATAGCGTCTTGGTTTTCTATTTATCCTCTTTTGCAGATTGACCTGGATACCATTGATGTCAGCAACCTCAACAGACAATTTCTGTTTCAGAAGAAACATGTTGGAAAGTCTAAAGCTCAGGTGAATGATACAAACTAACTTCGGCTCATTTGTAATATTCAGAAATGTGCAACAGACCTTTGACGACTGTGCATTTCAGGTTGCCAAGGAGAGCGTGCTTCGGTTTTGTCCATCTGCAAACATCACTGCCTATCACGACAGCATCATGAAG[T/C]AAGTGCAGTAACGTTATTGCCAAAAAAAACTTTGTAAATTTGTTTGTTTACTGTGTGAAGCAATAATTTAATAACCTTGATGTTTTTTCTTCTTGCAGCCCAGATTACAATGTGGAGTTCTTCAGGAATTTCCAGCTTGTAATGAATGCTTTGGACAACAGAGGTGTGAATTAGTTTCTGCAAATATTAACGTGAAGGATCATCTTGCTTCAGTATTAAAAGTCTTTTGTCTTATATTTGCAGCGGCCAGAAATCATGTGAACCGAATGTGTCTGGCAGCTGACATTCCCCTTATTGAGAGCGGCACGGCTGGCTATCTGGGACAAGTCACGGTTATCAAGAAGGCAAGGCTCTTTTATTAAAGGGATAGTTTACCTAAAATCAATTTTTACTCACCCACATTTTCTGCTAAACACAGAACATATTTCGAGGAATTTTGGCAATCAAATAGTATCATTTTCATTGTAGAAAAAAAAATGACTATGGAAGTCGATTGGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12884
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109358 Nonsense 117 651 4 17
ENSDART00000110459 Nonsense 117 650 4 17
ENSDART00000144042 None None 371 None 10

The following transcripts of ENSDARG00000077024 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 13128143)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 12726316
GRCz11 25 12822821
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATTACAATGTGGAGTTCTTCAGGAATTTCCAGCTTGTAATGAATGCTT[T/A]GGACAACAGAGGTGTGAATTAGTTTYTGCAAATATTAACGTGAAGGATCA
Long Flanking Sequence:
TTTGGGTAGTCATTAAAAAAACGCATAGTAATATTATTGATTGGCTAGTATGTTTAAACGGTGTCTACTAATGTCTCATAGCGTCTTGGTTTTCTATTTATCCTCTTTTGCAGATTGACCTGGATACCATTGATGTCAGCAACCTCAACAGACAATTTCTGTTTCAGAAGAAACATGTTGGAAAGTCTAAAGCTCAGGTGAATGATACAAACTAACTTCGGCTCATTTGTAATATTCAGAAATGTGCAACAGACCTTTGACGACTGTGCATTTCAGGTTGCCAAGGAGAGCGTGCTTCGGTTTTGTCCATCTGCAAACATCACTGCCTATCACGACAGCATCATGAAGTAAGTGCAGTAACGTTATTGCCAAAAAAAACTTTGTAAATTTGTTTGTTTACTGTGTGAAGCAATAATTTAATAACCTTGATGTTTTTTCTTCTTGCAGCCCAGATTACAATGTGGAGTTCTTCAGGAATTTCCAGCTTGTAATGAATGCTT[T/A]GGACAACAGAGGTGTGAATTAGTTTCTGCAAATATTAACGTGAAGGATCATCTTGCTTCAGTATTAAAAGTCTTTTGTCTTATATTTGCAGCGGCCAGAAATCATGTGAACCGAATGTGTCTGGCAGCTGACATTCCCCTTATTGAGAGCGGCACGGCTGGCTATCTGGGACAAGTCACGGTTATCAAGAAGGCAAGGCTCTTTTATTAAAGGGATAGTTTACCTAAAATCAATTTTTACTCACCCACATTTTCTGCTAAACACAGAACATATTTCGAGGAATTTTGGCAATCAAATAGTATCATTTTCATTGTAGAAAAAAAAATGACTATGGAAGTCGATTGGGACCAACAATAGTTTGGTTAATGGTATTAAACTTTTCTTTTTTTTCTATTATAATAAGAAAAAGGTTGGATCAAAGTGAAGAGTGAGTAAATGATGATGTTTTTAATTTTTAGGTAAACTGTCGCTTGGGTGAATTGATCTCAATGTCATTCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44250
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
ENSDART00000109358 Nonsense 316 651 10 17
ENSDART00000110459 Nonsense 315 650 10 17
ENSDART00000144042 Nonsense 147 371 5 10

The following transcripts of ENSDARG00000077024 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 25 (position 13131957)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 12722502
GRCz11 25 12819007
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAAAAGCAGGTTCTCAGGAGCAGGTAATTGGCTCAGGGCTGAAGGAC[C/T]AGCAGGTTTTGGGAGTTCAGGGTTATGCTCAACTCTTCCAGCATAGTGTA
Long Flanking Sequence:
TTTAATGGGCCTGTTTGATTAAAGGATGTTTTTTTTTTTTTATTACCTTAGGGAATCCTGCAGATGCAGCAGCTCGAGCCACAGCATCCGATCAGGATGGAGACATCAAACGAGTGTCCACTAAAGAGTGGGCTCGTTCCACAGGCTACGACCCTATCAAACTCTTCAACAAGGTGTCAGCTTTGTCACAAACCTCACCTTACGTTAGTCTTTACTTGTTTTTTTTTTTTTTTTTGTCTGAAAGTAATTTATATATTTCCTTGCAGCTTTTTAAAGATGACATAATGTATCTGCTGACCATGGATAAGCTTTGGAAAAAAAGAAAAGCCCCGTTACCACTAGAATGGGAAGAAATCAACCAGCTTGGTGGGTATTTTGTTCTTACATGGCTATCAACAGTTATTTAAACAAATGTAATTGTATGTTAAAAAATGCATATTAAGTAAGTCTTTTTAAAAGCAGGTTCTCAGGAGCAGGTAATTGGCTCAGGGCTGAAGGAC[C/T]AGCAGGTTTTGGGAGTTCAGGGTTATGCTCAACTCTTCCAGCATAGTGTAGAAACTCTACGATCTCAGCTGAAAGAGAAGGGTGACGGTGCAGAGCTCGTCTGGGACAAGGTGAGATTTAAACAGCTTTTTTTCATAAGCTAACAGTATATACCAGTTTGGCTATCAGTCAAAATGTCTATATACCTAACCAAAATATGAGAGGTGCAGTTGTCGTTTTTAATGTGAATAAAACATTTAGATGTTTTTTTATGTGTGCTGCTGTTTTCAGGACGATCCTCCAGCCATGGACTTTGTTACAGCAGCTTCAAACTTGCGTATGAATGTATTCAGCATGAACATGAAAAGCCGCTTTGATGTCAAATGTAGGTGTATGGTTGATTTACATTTTTTAAAAACGCTTTAATAACTCGAGCTTAAGTAAGTGCGTTATTGCTTTATCGAAGGAGACACTGACTTTTGACTATGAAATTAATACCAGTACATAGGGATGGGTACCGA
Associated Phenotype:
Not determined