ZMP
orc1
Ensembl ID:
ZFIN ID:
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 |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa13649
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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