Busch Lab

ZMP

orc1

Ensembl ID:
ENSDARG00000039217
ZFIN ID:
ZDB-GENE-030131-6960
Description:
origin recognition complex subunit 1 [Source:RefSeq peptide;Acc:NP_956227]
Human Orthologue:
ORC1
Human Description:
origin recognition complex, subunit 1 [Source:HGNC Symbol;Acc:8487]
Mouse Orthologue:
Orc1
Mouse Description:
origin recognition complex, subunit 1 Gene [Source:MGI Symbol;Acc:MGI:1328337]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa20735 Nonsense Available for shipment Available now
sa40726 Nonsense Mutation detected in F1 DNA Not yet available
sa38557 Nonsense Mutation detected in F1 DNA Not yet available
sa13649 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa20735
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057293 Nonsense 178 912 5 19
ENSDART00000130492 Nonsense 178 912 5 19

The following transcripts of ENSDARG00000039217 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 33634941)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33952606
GRCz11 6 33937296
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCTTCCAAGCGGTGGATCCTGAGCTGATAGAACCTCCTCCCAGCCCT[A/T]AATCTCCCCCGCCATCTTCACGGGGCCCTCAGGCTCGTCCTCTTCCAACA
Long Flanking Sequence:
AGCATTCTTGCGCCAGTACAGGTGAGCATAATAGAGTTGTAGGAATCGTATCATGAAGAGATCACATTTTTATACAGTAAAAAAAAAAAAAACGGACTCTAAAATCAAGAATTATCAATACAATTATTTTTTTATGATTTATATTTATTATTAGTATTATTATTATGTTTTCTAATTATTTCTAAATATCGTATTTTATGTTATTATTAATGTACCTATTTTAAATTTTAAAACTTTTTATTTAAATGCATGGGCCTTATTTATTGTATTTGTTTTTTTAAAGTTCTATTATTTAGTAATTTAGTCATATTTCACTTCCTTTCAGTAATATTTAATAGTAATATTATTATAAAAAACTTTGAATTTAGATCATGTACATCGCACCTGAGCATCCTTTTCCAGAGGGAAAGAGCAAAGACATGCTATTTGTCAAACACTCATGGGACACAAAATCCTTCCAAGCGGTGGATCCTGAGCTGATAGAACCTCCTCCCAGCCCT[A/T]AATCTCCCCCGCCATCTTCACGGGGCCCTCAGGCTCGTCCTCTTCCAACACCAGACCCCTCAATAATGAAAAGGGCCATAACAGGTGCTATTACCCGCGGCAGCATGAGCACCGGAAAAATGAGCTCCACTGAAGCAGAGTCTCTCCATTCTGCTTCCAAGCTCTCAGCAGCTAAAGCTCTTAGTGCAAAGAGGAGGAGCAGAGCTTCCTCGGGGCCACATGTTCGTAAAAAGCTGGAGCTGTGCAGTGAGTGCCATTCATCCACATATTTATAATGCTTTTAATGGTTTCGATTGCAGTGAACTGAATGTCTCTGATTTATTTTCATTGTGTTAGGTCCAAGCAAAAACATGTCCCGAGATGATGTTCTGGGGGAGATTTTAGATAAACACATCGATACAGACAAAACACTGATGTCTAAGATGAACACGTCTCCATCAGGCCGCATTTCTATTTCTATTAGACTGACTCCACTTAAATGTAATGAGGAGCAGCAGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40726
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000057293 Nonsense 267 912 6 19
ENSDART00000130492 Nonsense 267 912 6 19

The following transcripts of ENSDARG00000039217 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 33635298)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33952963
GRCz11 6 33937653
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTCTCTGATTTATTTTCATTGTGTTAGGTCCAAGCAAAAACATGTCC[C/T]GAGATGATGTTCTGGGGGAGATTTTAGATAAACACATCGATACAGACAAA
Long Flanking Sequence:
TTTGAATTTAGATCATGTACATCGCACCTGAGCATCCTTTTCCAGAGGGAAAGAGCAAAGACATGCTATTTGTCAAACACTCATGGGACACAAAATCCTTCCAAGCGGTGGATCCTGAGCTGATAGAACCTCCTCCCAGCCCTAAATCTCCCCCGCCATCTTCACGGGGCCCTCAGGCTCGTCCTCTTCCAACACCAGACCCCTCAATAATGAAAAGGGCCATAACAGGTGCTATTACCCGCGGCAGCATGAGCACCGGAAAAATGAGCTCCACTGAAGCAGAGTCTCTCCATTCTGCTTCCAAGCTCTCAGCAGCTAAAGCTCTTAGTGCAAAGAGGAGGAGCAGAGCTTCCTCGGGGCCACATGTTCGTAAAAAGCTGGAGCTGTGCAGTGAGTGCCATTCATCCACATATTTATAATGCTTTTAATGGTTTCGATTGCAGTGAACTGAATGTCTCTGATTTATTTTCATTGTGTTAGGTCCAAGCAAAAACATGTCC[C/T]GAGATGATGTTCTGGGGGAGATTTTAGATAAACACATCGATACAGACAAAACACTGATGTCTAAGATGAACACGTCTCCATCAGGCCGCATTTCTATTTCTATTAGACTGACTCCACTTAAATGTAATGAGGAGCAGCAGATCTTGCCTCTGTCATCACACAGCCCTGATAAACCCACACTGACTGCATATGGAAGTGACAGTGCGACCAGGTACATCTTTTTGCATCTGATATTTTCTTTTGTTTCTTAATGTAATGTGTCAAAGTCATTTAAGGGTTAAGGCCAGATGGGTTGAAAATGTCCCAATAAATTATCTTAGAAACCATAGATGGCTGGTAATTATATTTATGTAATATATTAATATTAACTTTCACTGGGGACAGGGGAATGTCTACTGGGGACATGCAAACCCCCCTCCACCCCCACCCCCGGGGTGTTTTAAGATTTTTTTATTTTCAATATGTGTGCTGTTATTGTTACGAATGGACAGAGAGAGTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38557
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
ENSDART00000057293 Nonsense 330 912 6 19
ENSDART00000130492 Nonsense 330 912 6 19

The following transcripts of ENSDARG00000039217 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 33635489)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33953154
GRCz11 6 33937844
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTGCCTCTGTCATCACACAGCCCTGATAAACCCACACTGACTGCATA[T/A]GGAAGTGACAGTGCGACCAGGTACATCTTTTTGCATCTGATATTTTCTTT
Long Flanking Sequence:
ACACCAGACCCCTCAATAATGAAAAGGGCCATAACAGGTGCTATTACCCGCGGCAGCATGAGCACCGGAAAAATGAGCTCCACTGAAGCAGAGTCTCTCCATTCTGCTTCCAAGCTCTCAGCAGCTAAAGCTCTTAGTGCAAAGAGGAGGAGCAGAGCTTCCTCGGGGCCACATGTTCGTAAAAAGCTGGAGCTGTGCAGTGAGTGCCATTCATCCACATATTTATAATGCTTTTAATGGTTTCGATTGCAGTGAACTGAATGTCTCTGATTTATTTTCATTGTGTTAGGTCCAAGCAAAAACATGTCCCGAGATGATGTTCTGGGGGAGATTTTAGATAAACACATCGATACAGACAAAACACTGATGTCTAAGATGAACACGTCTCCATCAGGCCGCATTTCTATTTCTATTAGACTGACTCCACTTAAATGTAATGAGGAGCAGCAGATCTTGCCTCTGTCATCACACAGCCCTGATAAACCCACACTGACTGCATA[T/A]GGAAGTGACAGTGCGACCAGGTACATCTTTTTGCATCTGATATTTTCTTTTGTTTCTTAATGTAATGTGTCAAAGTCATTTAAGGGTTAAGGCCAGATGGGTTGAAAATGTCCCAATAAATTATCTTAGAAACCATAGATGGCTGGTAATTATATTTATGTAATATATTAATATTAACTTTCACTGGGGACAGGGGAATGTCTACTGGGGACATGCAAACCCCCCTCCACCCCCACCCCCGGGGTGTTTTAAGATTTTTTTATTTTCAATATGTGTGCTGTTATTGTTACGAATGGACAGAGAGAGTCTGTATGTTGATGCTTAGATAAAAAGAGAGGATGGCAGTTGGTTGATTCAGTGCTTTGAATAATCATATTTACGTCTACATTTGTTTATGTTCGTCTAAAGCACTTGTTGATGTTCGTCAAATGTAGTTCCTTTAGGGCCACAACTCTGCACAGTTTAATTCCAACCATAATTAAACACACCTGATTAAGCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13649
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
ENSDART00000057293 Nonsense 895 912 19 19
ENSDART00000130492 Nonsense 895 912 19 19

The following transcripts of ENSDARG00000039217 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 33645070)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 33962735
GRCz11 6 33947425
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCWCCTGTCGCTTGCTGCTGCTTGAAGGAAGCCGTCTGGACCTGTTTCTC[C/T]GAATCCGTCTCAATGTTAGTCAAGAYGATGTGCTTTATGCCTTGAAGGCT
Long Flanking Sequence:
GTATAATAATAATAATAATAATAAAATCAGTATTATGTATTATTAGCCCCCTTGGGATATATATTTATTCAGTTGTCAACAGAATAAACCACTGTCATCCAATGATTTGCCTAATTATCCAAACTTGCCGAGGTACCATAACCTAGTTATGTCTTTAAACTGAATATTAGAGTTTTGCAAAGTCAGCAGAAAAGTATTATGCACCATGTTGAAGAGAGAACTTTTTAGATTTCAAAAGTATTATGTTTAATAATGTGTTAAAATCTTCATCGTTAAGCAACATTTCACATCAGGGTTAAAAATTTTGACTGTATACCCATGGTTTAATATAACGATTTAAATGCTGAATTGTTTGTCTTCAGGTGTTTGTTCAGCACCAGGCTCTGTGTCGCGTTGAAGGTTTGCAGCCAGTGAGTGTGTCTGAAGGGTTATTGGTCTGTCAGAGGCTGGGCTCCTGTCGCTTGCTGCTGCTTGAAGGAAGCCGTCTGGACCTGTTTCTC[C/T]GAATCCGTCTCAATGTTAGTCAAGACGATGTGCTTTATGCCTTGAAGGCTGACTAAAAACTCGGCCATGCTGTCTAGCATGTTTCAGGCTATTGTGGCGATCCATAGCATAATTTTATGAACCGTTTATTGTCTAAAATGTTTAAATAAATTATCTATTTTAATGGTTAATAATTCTACACAGTTCTATAAGCACATTTTAATATGCTCATTCTTTGTGTGTTTAACTGTATCTCTTGGCTTCTAATCATGTCTTCACATTCAAGCTTAAATGTCTTTGGAAAACTTACACAAAGGCTTTATTATTAAGCAATTTAGTGTGGGAGAGCGAGACTCGCACATTTCTTTATTATCATTTAATGATTCACATAAAATATACATTTTTCATACAGTGTGCCAAAATGTTGGATGTTTCAAATTTTATGCAATAAAGCTATTGACTGAACTGATCACAAGACATTGCTACTGTGCCTTTGTCAGTACAAGGTAGACAGACAACTT
Associated Phenotype:
Not determined