ZMP

LOC558410

Ensembl ID:

ENSDARG00000013009

Human Orthologue:

UBIAD1

Human Description:

UbiA prenyltransferase domain containing 1 [Source:HGNC Symbol;Acc:30791]

Mouse Orthologue:

Ubiad1

Mouse Description:

UbiA prenyltransferase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1918957]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31690	Nonsense	Available for shipment	Available now
sa34525	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31690

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000015554	Nonsense	71	336	1	2

Genomic Location (Zv9):

Chromosome 8 (position 55643260)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	53590918
GRCz11	8	53921998

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCTTCAGCGCGTCTCTCACGCCCGTGGCTCTGGGCAGCGCTCTGGCCTA[C/A]AAGCTGGAGGGCTCGGTGGACCTGCTGCTGCTGCTGGTGTGCGCGGTGGC

Long Flanking Sequence:

GCAACTGTAAAATCACAACAGATCAATTACTATAGTTGTTGTTACCATAGCAACTGTAGAATCACCACAACAGATCAATTACTATAGTTGTTGTTACCATAGCAACTGTAGAATCACCACAACAGATCAATTACTATAGTTGTTGTTACCATAGCAACTGTAGAATCACAGCAACAGATCAATTGCTATAATAATATTGACCTGAAAACTATGTAATGTCCCCACAGTTCACAAAAATAAGCCTGTGTGTGTTGTGATCGGCAGCTCTGGTCTCTGAAGCGCTCCTGGATGCAGGAGATGAAGCCGGCTGCGCTTTCGGGCTCCAATGGCCTGAATGGAGCTTCAGGATCGTCGGTGCGTGTCCCCTGCAGCCGTCTGTCCCGCGCGGGCCGCATGGCGCTGGATCTGCAGAGTAAGTGTGCTGCGTATGTTCTGGCTCTGCGGCCGTGGAGCTTCAGCGCGTCTCTCACGCCCGTGGCTCTGGGCAGCGCTCTGGCCTA[C/A]AAGCTGGAGGGCTCGGTGGACCTGCTGCTGCTGCTGGTGTGCGCGGTGGCCGTGCTGCTGGTCCACGGAGCCGGAAACCTGGTCAACACCTACTACGACTTCTCCAAGGGAATCGACCATAAGAAGAGTGACGACCGCACGCTGGTGGACCAGATCCTGAAGCCGCAGGACGTGGTGATGTTTGGAGCGGTGCTGTACTCTGCAGGATGTCTGTGCGCCACGCTGCTCTACTTCCTGTCCAGCCTCAAACTGGAGCATCTGGCGCTCATTTATTTTGGAGGACTGTCCAGCTCGTTTCTCTACACCGGAGGTGAATATACCGATTGGCTTCCTTTAACTCCACTCGGGGCTCTTAAAGCGATTTTTATTGATTAACTGGAATGTGTAGGTCAGCATTTCCCAGCCCTGTTCTTTTCGGCACGCCAACAGTGCATATTCTGGAGGTCTCCCTTATCTGACCCAGGCTTTGGGGGATGTTCTGATGAGTTGATTCAGGTGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34525

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000015554	Essential Splice Site	175	336	1	2

Genomic Location (Zv9):

Chromosome 8 (position 55642948)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	53590606
GRCz11	8	53921686

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCGCTCATTTATTTTGGAGGACTGTCCAGCTCGTTTCTCTACACCGGAGG[T/G]GAATATACCGATTGGCTTCCTTTAACTCCACTCGGGGCTCTTAAAGCGAT

Long Flanking Sequence:

CTTTCGGGCTCCAATGGCCTGAATGGAGCTTCAGGATCGTCGGTGCGTGTCCCCTGCAGCCGTCTGTCCCGCGCGGGCCGCATGGCGCTGGATCTGCAGAGTAAGTGTGCTGCGTATGTTCTGGCTCTGCGGCCGTGGAGCTTCAGCGCGTCTCTCACGCCCGTGGCTCTGGGCAGCGCTCTGGCCTACAAGCTGGAGGGCTCGGTGGACCTGCTGCTGCTGCTGGTGTGCGCGGTGGCCGTGCTGCTGGTCCACGGAGCCGGAAACCTGGTCAACACCTACTACGACTTCTCCAAGGGAATCGACCATAAGAAGAGTGACGACCGCACGCTGGTGGACCAGATCCTGAAGCCGCAGGACGTGGTGATGTTTGGAGCGGTGCTGTACTCTGCAGGATGTCTGTGCGCCACGCTGCTCTACTTCCTGTCCAGCCTCAAACTGGAGCATCTGGCGCTCATTTATTTTGGAGGACTGTCCAGCTCGTTTCTCTACACCGGAGG[T/G]GAATATACCGATTGGCTTCCTTTAACTCCACTCGGGGCTCTTAAAGCGATTTTTATTGATTAACTGGAATGTGTAGGTCAGCATTTCCCAGCCCTGTTCTTTTCGGCACGCCAACAGTGCATATTCTGGAGGTCTCCCTTATCTGACCCAGGCTTTGGGGGATGTTCTGATGAGTTGATTCAGGTGTGTTTGATCAGGGAGTGGTTGAACATGTACTGTAGGTGTGGCTTCAGGAACAGGGTCGGCTGTGGTTTACATTGATTTATTTGAATGTTAATTAGGCGTGCGCTGATCAGAGCATTTGCATTGACTTAACATGTAAATCACTCGCGCTTGATGCGCGTGCCGCGTCTGGTGTAAACACAGCATAATAACTGTTTCGTGTGGACATGTGATGGTCAGAAGTAGGGTTGGGCCGATAGACGATGCCATCGCTGATGGCTGACAGACACCATGATGCTGAGCCGGCATTGCGATCCTCCGCCCCGCCCCCGTTACAA

Associated Phenotype:

Not determined