ZMP

LOC100001302

Ensembl ID:

ENSDARG00000061222

Human Orthologue:

UBA7

Human Description:

ubiquitin-like modifier activating enzyme 7 [Source:HGNC Symbol;Acc:12471]

Mouse Orthologue:

Uba7

Mouse Description:

ubiquitin-like modifier activating enzyme 7 Gene [Source:MGI Symbol;Acc:MGI:1349462]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16823	Essential Splice Site	Available for shipment	Available now
sa16325	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa16823

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
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Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087080	Essential Splice Site	152	1016	4	24

Genomic Location (Zv9):

Chromosome 6 (position 52905718)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	52954723
GRCz11	6	52953052

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CACTCAAACAATATAAAGTTTATTGTGGCTGACACCAGAGGACTYTGTGG[G/A]TAAGAAGCATCWCATGAATCAATACAMCACATCAATATTTATAGCGGTRC

Long Flanking Sequence:

CACAGTTTTATTTATAACTTATTTTTCAGGACACAAAAAAATCATAAAACATTAATTTGGCATTAATAAATGTTCAGCACCCGTGTAAACATCTGAAATATTTATTTGACATGTACTGACAAGTCTATACCAACTTCATCTGCAGTTAAGAGAGCAGCACAAAGCAATAGACTCATGATATCAGGTGAAAAGGGTCGATAAAAAGCGAAGATTTTAATAAATATAATAATTTACACACCATGCTATTATTGCATCCTTTTAATGTACAACAGTACTAAAGTGCAAAATGTATAAATCAGCCAATATAAAATATACAAAAATTAAATCAAATAGTTTTAACCCACTTTTAACTCTGTAACCCTTTTTTTGCATCCTATTTGTTTATCACTGAAGGTTGTGGTGCTCACAAGTTCACCTTTAGATGAGCAGCTACGTGTGGGAGCGTTTTGTCACTCAAACAATATAAAGTTTATTGTGGCTGACACCAGAGGACTCTGTGG[G/A]TAAGAAGCATCTCATGAATCAATACAACACATCAATATTTATAGCGGTGCTGGATATTATTCTGAGTTTTGTGTTTGGTTTGCAGGCAGTTGTTCTGTGACTTTGGCGAATCGTTTGAAGTCATTGACACAAATGGAGATCCTCCAGTTTCAGCCATGATTTCACATATCAGCAAGGTGACACAGGACATAAATCACGTTTCACTTTCACTTCTGTCCTCTTAAAGAAATACTCACCCACATGGCATTTAAAAATCAGTAATGCTTTCATTCATCATCAGAATACAGACGTTTTAATTCTGATCATTCTACCAAAAGATTAATGCTTCAAAATGTATAATGGCGTCCTTACTGTAAGCTTTAAGTTTAATTGTAGATGCAAATTTCAGCTTCTGTTAATGCTACATAATTTATTAGCTTCATGATTGCATGTATATGTTAGTAAAAACTTACTGTTATTATTGTAACAGTCTGAAGAAGGTCACTAAACATTTACTCGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16325

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
ENSDART00000087080	Nonsense	541	1016	14	24

Genomic Location (Zv9):

Chromosome 6 (position 52918003)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	52967008
GRCz11	6	52965337

KASP Assay ID:

2259-8205.1 (used for ordering genotyping assays)

KASP Sequence:

AACTTAACTAGCTGTCTTAACTTTTATTTTCCTTGTCCATTAGGGGTTTA[T/A]CTTGACCAATGTTGTGTGCGAAASAAAAAGCCCATGCTGGAGGGAGGAAC

Long Flanking Sequence:

ATTAAAACATTGTTTTCCAGCCGCGCTTCATTCTCAAAATGTATAGTTTGTCTAAAGTGATGCATATACACTGTATAGCATACTATGAGGAGGGACACAATCAGCCAGCACAGTCGTCTCTCCATAGTCAAAAGTGTCATTTTGTGTCTGTCGGGTTTTTTTTTTGCTTGTGGGAGCTCCACTGGAACTTCCCACATGTTAATTCTGACCAATCAAAAAGCAGTTTAGGAAATACCTTCAAAAACATCTGGCCAATGAATGATGTGGATTTTGTCACATGACTGCTTTTTGGTTCTTTTCAACTGGTTCGGACCAAAGCAATCAGTGTGGTGTGAAAAGGAACCAAAAATGGCAGAAAAATGCTACAATGTATAATTTGTTGCCCTTGATCCGAACCAAATGAACTGAACCACAGATGTGAAAGCACCCTACACCTAAAACAAGAAAGCAAACTTAACTAGCTGTCTTAACTTTTATTTTCCTTGTCCATTAGGGGTTTA[T/A]CTTGACCAATGTTGTGTGCGAAACAAAAAGCCCATGCTGGAGGGAGGAACTCTGGGTAGCAAAGGCCACACTATGGTTGTAGTGCCACGCCTGACCGAATCATACGGACTCTCCTCATCTGGAGGACAGAAAGCCATTCCCATCTGCACACTCAAGAACTTCCCTCACCGTATAGAGCACACACTACAGGTGAGAGGACAATTTTTACAATAAATGTATGATTTATTCCATTTTTGAGCAAAGCTGTCCTATGTTACTCCAAATACTGATTAAAGATCCATTCACACATACAGTATACTCTCAGAAATAAAGCTATGAGAGCTGTCACTGGGGCGGTATATTTTCTAAAGAAATACATTTTAGGACCATATTGGCACCTCAAAGGTAAAAAGTACAAAAGTTATCTCGGAGGTTCCAATATGGACCCTTTAAGGCACAAATGTGTACCTTTGTGTACACAATGATGGTACCTTTCATCCTGAAAACATAGAGCAATAGCG

Associated Phenotype:

Not determined