ZMP
uba2
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
---|---|---|---|---|---|
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.
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 |
---|---|---|---|---|---|
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.
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