ZMP

ube2q2

Ensembl ID:

ENSDARG00000013990

ZFIN ID:

ZDB-GENE-040426-1919

Description:

ubiquitin-conjugating enzyme E2Q 2 [Source:RefSeq peptide;Acc:NP_998152]

Human Orthologues:

AC011295.5, UBE2Q2, UBE2Q2P2

Human Descriptions:

ubiquitin-conjugating enzyme E2Q family member 2 [Source:HGNC Symbol;Acc:19248]
ubiquitin-conjugating enzyme E2Q family member 2 pseudogene 2 [Source:HGNC Symbol;Acc:37440]

Mouse Orthologues:

E330021D16Rik, Ube2q2

Mouse Descriptions:

RIKEN cDNA E330021D16 gene Gene [Source:MGI Symbol;Acc:MGI:2141773]
ubiquitin-conjugating enzyme E2Q (putative) 2 Gene [Source:MGI Symbol;Acc:MGI:2388672]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15381	Nonsense	Available for shipment	Available now
sa30279	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15381

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016117	Nonsense	23	182	1	6
ENSDART00000124645	Nonsense	23	373	1	13

Genomic Location (Zv9):

Chromosome 25 (position 30453272)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	29020633
GRCz11	25	29463640

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGAAGGCCGAAKTAAAGTTCCTGGAGTCAATCTTTGACCCAAACCATGAG[C/T]GATTTCGAATAATCGACTGGAAGCMAGACGAACTGAGYTGCCAGTTTAAT

Long Flanking Sequence:

TTTTTATCTTTTTATTAATATTGTATCTTTGTAAATGTTCTTTCTTGCATAATAAAAATAAATGCATATTATTATTATGTGTTTTTTTATTTTTATATGTTGGATAATGCAAGAGGACTGTCATAGACAAGAATGAAGACGAAGAATGGTCAACCACACGTTCACAAAACACAATTGGCGTCCCAGTAGTCCACGCAGATCTCGATCACCCACTTCCCCTCTCTCGCATTATTTCTTGGCGGGCGTTGTTTTGTCGTCTCTCCGGCCTCCAGTTCGCCTCTCTCTCCCCGCCCCCTCTTTGTTGTTTCTCTCCTCCAGCCTCCCTCCGCCGCCGCGCGCTCACACACACGCACTCTCGCTGGATCAGCTGCGCGCTCGCGGTCTCCGTGCGTCCCTTCCCCCCGCGGCCTGGCTGCTGATGAGATGAGTGGAAGATGTCGGTGTCGGGGCTGAAGGCCGAATTAAAGTTCCTGGAGTCAATCTTTGACCCAAACCATGAG[C/T]GATTTCGAATAATCGACTGGAAGCCAGACGAACTGAGCTGCCAGTTTAATGTGACGGGAGAAAAGCTGCTGATTATTCACTGCAACATCACGGTAAGATCCACCAGCCCCGTGTGTAGGTTTACATGCGAACAAGGCAAGGCCGAGTGAAACAACACCACCCACAAGCCCCTGTTTGCTCGAATAAAGCCACGATAGTGCGAATAAAAGCATTTAGGGTGATCAGTGTTCAGTTTTATAATCAAAAAGATGTCAAAATCACTGCTAAACAAGCAGCGCGAGCTACGCTTAGCTTGCTGGTGTATTAGCTAACAAAGTTAACTGCGTTTGCTCTCGGTTTCACTTTGTTGGCTTAATAAAACCATCAGCTAATCGTCAACGTTATTTATTCTTGTGTACAGGAGATGGTTGACCAAGACCTGTGGATGTTTTGTATTCTGCGTCACTTTAAATTAGTTGTCATGTAATTAGCTTGTGTGCTAATTTGGCTTAGCTGGTAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30279

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
ENSDART00000016117	None	None	182	None	6
ENSDART00000124645	Essential Splice Site	243	373	7	13

Genomic Location (Zv9):

Chromosome 25 (position 30427630)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	28994991
GRCz11	25	29437998

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGAGCTAGTAAACGATAGCCTGTATGAGTGGCATGTCAAGTTAAGGAC[G/A]TAAGTATGCTTATCATATAAGAAATAGCGTGTTGAATGATTACAGTTTGA

Long Flanking Sequence:

CTAAAGTTTGCCTAAATTTAATCCTAGAATATTCGATATTGAGTAGTTTTTCAGAAATCAATAAAATCCTGCTAGATTTGACTTCAAGCTGATTTGTTTACTGCAGTAACCAGGGAAACGCTGTTATACATATAGCGCCACCTGCTGGATTAGCATTTTTATATAGCATATGAATACTGTTTTAGTTTAGGATATACTGTTAATGTCGCAGATGAGGAAAAAGAGTCTTAAAAAAAACTAAAAGGTATTGAATTTCATTCTTTGGTTCCTGTATATACCCTGATTGATATTTTTCCACTCTTTAACCGTTGTCTAAAAAGTTAGGCACAGGGAACATTGGTGTGGTGTGAAATCTGTTGGCATGCGAATGAGTCTTAGTGAAAAGAATGTTTCAGGTTTGCATGATCTGTTTGTTTACATTATATTCTTTTGGTTCCAGGTATCTATTCAGTGGAGCTAGTAAACGATAGCCTGTATGAGTGGCATGTCAAGTTAAGGAC[G/A]TAAGTATGCTTATCATATAAGAAATAGCGTGTTGAATGATTACAGTTTGAGTCACTAATGTGTAAAATGACTCTGTTTGGTTTATAAGGGTTGATCCAGACAGTCCCTTACACAGCGACCTACAGGTTTTGAAGGAAAAAGAAGGAATGGACTACATTCTGCTCAATTTCTCTTATAAAGTGAGCATTGTTGTTATTTTTTTATTTTATTGTTTTTTTTTTTGGTGTACAAATGAAAAGAGATAACAATTGAATTTTGGTTTTCTTGTGATGGCAGGATAACTTTCCTTTTGATCCTCCCTTCGTACGGGTTGTGTCTCCTGTCCTGTCTGGAGGGTGAGCTTGAGAACTTTGCTGAACCTATCTTGTATAATTATTTCTATATTTAATGGTTGCATTTACTTTGGTGCGAATTTAATGGGAGCATAGTAATATTTTTGATGTTACATAAAATGTCTTGTTTTCATTGCACAAAATATGTAGTAAAATTATGTTTTAGTT

Associated Phenotype:

Not determined