ZMP

orc3

Ensembl ID:

ENSDARG00000008805

ZFIN IDs:

ZDB-GENE-030131-6247, ZDB-GENE-030131-6247

Description:

origin recognition complex subunit 3 [Source:RefSeq peptide;Acc:NP_997892]

Human Orthologue:

ORC3

Human Description:

origin recognition complex, subunit 3 [Source:HGNC Symbol;Acc:8489]

Mouse Orthologue:

Orc3

Mouse Description:

origin recognition complex, subunit 3 Gene [Source:MGI Symbol;Acc:MGI:1354944]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16022	Nonsense	Available for shipment	Available now
sa43005	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16022

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000047857	Nonsense	33	706	3	20
ENSDART00000112806	Nonsense	39	712	4	21

Genomic Location (Zv9):

Chromosome 17 (position 49495255)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	49256339
GRCz11	17	49339314

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGTACTTCTTTCAAYGATCACTATTTTTATTCATTACATGTAGACGAATA[T/G]TTAGTGGAGGCTGACGACGACAGCGGCAGGGATCGATTTAGRATCTGCCA

Long Flanking Sequence:

TTAAAGACAGGGGGCTGATTAGATTGAAAGATTGATTATTTGTAAGGTTAATGTTGTTATTAATGGATCATTTTCCCCTTGACATCGACGCTAGTTGCTAGATGGCAGTATAGGCACTTGTTGGTTTGCCGACTTACAAAGAAGAAGACGAAAAAGCGGTAACTGAAACGCATGGTTTACTGAAAGTTTGTCAAATTATATGTTTTTTTAAGAAAAGAAATGAACGAAACACTCACGACTTCATCAGTGTCAAAGGTAAATGAGCGCTGTCTGCAATAAATGCATGATAACTTATTAAACTTGACACGCGTCCAGACTTACAGATCGTTATATGTATTTCAGGGATGTTTTGTTTTTAAGTCAGCCTCTAAAAAGAGAAAGCGACATGTAGGTCTTGGTAAGTAATGATTGTCATTATTACAAATATCAACGTCTTCACTTCCATACACACGTACTTCTTTCAACGATCACTATTTTTATTCATTACATGTAGACGAATA[T/G]TTAGTGGAGGCTGACGACGACAGCGGCAGGGATCGATTTAGGATCTGCCAGAAGTTATGGGAGACGGTTCAGACAAGCACTGAGGTATGTATGTTTGCCACATGGAAAAAAATACTGTAGTAAATAGTGTGTTTTTGAACTACAGTTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCAAGTTGTCTGTCTGTCTGTCTGTCTATCAAGTTGTCTATCTGTCTGTCTGTCTATCTATCAAGTTGTCTGTCTGTCTGTCTTACTGTCTGTCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCAAGTTGTCTGTCTGTCTGTCTATCAAGTTGTCTATCTGTCTGTCTGTCTATCTATCAAGTTGTCTGTCTGTCTGTCTTACTGTCTGTCTATCTATCTATCTATCTATCTATCTATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43005

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
ENSDART00000047857	Nonsense	641	706	18	20
ENSDART00000112806	Nonsense	647	712	19	21

Genomic Location (Zv9):

Chromosome 17 (position 49471332)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	49232416
GRCz11	17	49315391

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCATTGTATACAAGCTTCATCTTGAGTGTGGGAGACTCATAAATCTCTA[T/A]GATTGGCTTGAGGTACTGTATGAACATGGTTAAAATCAAAATGACACATA

Long Flanking Sequence:

TGCAGTGTGACTTCAATCGACCGGCATGTTTGTGTGTGTGTGTGTTTGTGGGTGTGTGTGTGTGGGTTTCTGTGTTAGAGGGCGGGGCCGCAGGTTTCAAATCTCCCGGGTTTGCGCGTGCATAACTTGCTTTCGTTAGTACGTCATGGCGAAACACCTAATGACTCGGTATCAAGGCGACTCGTTTGAAGCACTATGAGTCGACTCTTTTATAGATGAATCAACCGTTTAAAACACTGTACTCTTACAGATTTAGCTGGATACTTAACTTCACTTAGAGCTGTGTTACACACTACATGGAGGGGAATTTTCAAAAACCCATAATATGGGCTCTTTAAGTTTCCCAGCCCTAATATATAGATCCAGAGTTGTTACTGTGTTCTGTTGTTGTTGCAGAATGAAAGTCTGAAAACTAATGCTGGCACAATCTCCAGCGCTGCTCCAGACCTCTGCATTGTATACAAGCTTCATCTTGAGTGTGGGAGACTCATAAATCTCTA[T/A]GATTGGCTTGAGGTACTGTATGAACATGGTTAAAATCAAAATGACACATACTGTAGAGGTGGTTATCTTTGTGCATGTTGATGGCAGATATCCATGTTGTATTTCCAGGCATTTGTAACTGTGCTGTCTGCCGCTGAGGACCAAGATGCTGATTCTGGGGATCATGGACAGCTTGATAGCCTTAAACAGTATCCTTTTACTTCTGACATCTTATATTAGCAATGAATGTGTTCCTAATTGAATATATGTCAATTTTAGCTGTGTCTGTCATAAATCTAATATTAATTGTATGGTTATTCCTGTAGTACAGGGGTGTTCAAACTTTTTGGGCCGAGGGCCAGATGCAAAAAAAAAATACGTTGTCGCGGGCCAAATTTTACATACATAACACAGACACGCATATATAAATGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTTGAA

Associated Phenotype:

Not determined