ZMP

psmd3

Ensembl ID:

ENSDARG00000018124

ZFIN ID:

ZDB-GENE-040426-1444

Description:

26S proteasome non-ATPase regulatory subunit 3 [Source:RefSeq peptide;Acc:NP_956866]

Human Orthologue:

PSMD3

Human Description:

proteasome (prosome, macropain) 26S subunit, non-ATPase, 3 [Source:HGNC Symbol;Acc:9560]

Mouse Orthologue:

Psmd3

Mouse Description:

proteasome (prosome, macropain) 26S subunit, non-ATPase, 3 Gene [Source:MGI Symbol;Acc:MGI:98858]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14257	Essential Splice Site	Available for shipment	Available now
sa36924	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14257

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027158	Essential Splice Site	43	503	1	12

Genomic Location (Zv9):

Chromosome 19 (position 49784478)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	48389213
GRCz11	19	48049490

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAGGAGGAGCAGCGCGGGGCCCGGGAACTGGACCAGACCACTCTGGACGG[T/C]CAGAACRCTCTAYAATACAGTATATTACTGACCCATAACACACAGGGGAC

Long Flanking Sequence:

CATCATCACTGAAATAAACAAACATCATCACTGAAACAAACATCATCACTGAAATAAACATCATCACTGAAATAAACATCATCACTGAAATAAACAAACATCATCACTGAAATAAACAAACATCGTCACTGAAACTTCATAAATAACAGACAGCACTGCTCTAGTTCCTCTGGCGGCTCAGCAGGGGGCAGCATCTCCTCCCGTGTCCGCCAAAACACGCACGAGCAAGAGCGCGACGGCCCAGAGTGCAGTTCGGCCGTCAGATTTGCCAGTCATCTTCAGCATCAGTTCTGAGCTGCAGCAACTCAGAGGAGCTGTTTATTTACATTACCGGAGAATTACCGACACCGAACACCGACACCGGGCGGCAACATGAAAGAGGCGACGGCGAAGAGACGAGAGAAACCGAAGGAGAAAAACACCGCAGAGCCGCAGGATGTGGAGATGAAGGAGGAGGAGCAGCGCGGGGCCCGGGAACTGGACCAGACCACTCTGGACGG[T/C]CAGAACACTCTATAATACAGTATATTACTGACCCATAACACACAGGGGACTGGACCAGACCACTCTGGACGGTCAGAACACTATAATACAGTATATTACTGACCCATAACACACAGGGGACTGGACCAGACCACTCTGGACGGTCAGAACACATTATAATAGTGGACTGTACAGTACCGCACATTGTTATTGGATGATGATGAGCAGCAGAACAGTACATGTTGTTTCGGGCTCTCGTGTTTAACAGATCTGCTACAGCTGCAGTGAGACTGGAGCAGCTTCTGTTCTGAACTCTGTGAATGTCCAGACGGTCAGACGCTCAGCAGCGGGTTGGTGATGATGAGGATGGAGTGTGTTGCAGATCTTCATCATCATCTCTGCATTTACAGACAGCAGTGCTGTCATCTGCTCTCTGCTGTCAGAGGAGTGTGTTATTACAGTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36924

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027158	Nonsense	182	503	4	12

Genomic Location (Zv9):

Chromosome 19 (position 49780891)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	48392800
GRCz11	19	48053077

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTCAGAACCGCCGTGCGCTGGATCTGGTGGCCGCTAAGTGCTACTATTA[T/A]CACTCACGTGTGTATGAGTTCCTGAACCAGCTGGACGTGGTGCGCAGGTG

Long Flanking Sequence:

TCAATAGACTCAGTGATGGGCTGGAGATCTGCAGATTTGTGTGTGTGTGTGTGTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGAGTGTGTGTGAGTGAGTGTGTGAGTGAGTGTGTGAGTGTGTGAGTGAGTGAGTGTGTGAGTGAGTGTGTGAGTGAGTGTGTGAGTGAGTGTGTGAATGTGTGTGTGAGTGTGTGTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGTGAGAGTGAGAGTGAGAGTGTGAGTGTGAGTGTGAGTGTGTGTGTGTGTGTGTGTGTTGATGAGTAATGAACGCATTGTCTCCTCCACAGGCTCAGAAAGTCTCAGATGATCTCCTTCAGAAGATCGGCTCTCAGAACCGCCGTGCGCTGGATCTGGTGGCCGCTAAGTGCTACTATTA[T/A]CACTCACGTGTGTATGAGTTCCTGAACCAGCTGGACGTGGTGCGCAGGTGAGCTGTTCACACACACACACACACACACACACACACACACACACTGCAGTTAGCTCATACTGTTCTGTTTCAGTTTCCTGCACACGCGGCTGCGGACGGCCACGCTGCGCCACGATGCGGACGGTCAGGCCACGCTGCTCAACCTGCTGCTGCGCAACTACCTGCAGTACAACCTGTACGACCAGGCAGAGAAGCTGGTGTCCAAATCTGTGTTCCCCGAGCTGGCCAATAACAACGAGTGGGCACGCTACCTGTACTACACAGGTGAGAGGATCCTCAAACAGGGGAACAGCGGTGTGTAGGGATGTCCCGATACAACATTTTAACTTCCGATACGATTCCGATAATGCAGCCTTCAGTACGAACCGATACCGATATAAATGCGATATCAGATGATGAATACTTTACTTTTACCTATTTTGTTGAGAGGAATGTCTGAAAGGCTAGATC

Associated Phenotype:

Not determined