ZMP
rcn1
Ensembl ID:
ZFIN ID:
Human Orthologue:
RCN1
Human Description:
reticulocalbin 1, EF-hand calcium binding domain [Source:HGNC Symbol;Acc:9934]
Mouse Orthologue:
Rcn1
Mouse Description:
reticulocalbin 1 Gene [Source:MGI Symbol;Acc:MGI:104559]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25356 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45271 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20882 | Nonsense | Available for shipment | Available now |
sa1699 | Essential Splice Site | F2 line generated | Not yet available |
sa20881 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25356
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102363 | Nonsense | 124 | 328 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 16595617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15578315 |
GRCz11 | 7 | 15826201 |
KASP Assay ID:
554-7505.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGAAGCGCTACGTTTATGAGAACGTTGCAAAAGTCTGGACTGACTA[T/A]GACCTGAACAAAGACAACAAGATCTCTTGGGATGAATACAAGCAGGCGAC
Long Flanking Sequence:
GCAGGATATGGTGTAAATAAATACACTAAAGACATCTTAAAATAAATTGTTACCCTTATTTTCTTTCATTCTTGACTTGACAAAACATAAAAAGCCAAATCATAATATAATTCTTATTTGAAATTAATAATACACATTTATTATCTAATCGTGACTAGATCAAATAACCAAAATAAGATGGTAATTTTTACATAAATAAGTAATTACGACAGGCCTGTTGTGCAATATACTCTGGCCATGTTTTCAAAGGATCCACCCTGTCTGAGCTGAAAAGCCGGAGATTTCTATGAAAACCTCATTCAAAGTGTGTTCTGAGCAAGTTGAATTGTATTAACTCTTTCAATTCTATGCATTTTTTTTTTTAAATGTCTTAGGAAAATTGTTGAGCGTATCGACAGCAATGTTGATGGATTTATCACCACTGATGAACTCAAAGCCTGGATCAAAAGAGTTCAGAAGCGCTACGTTTATGAGAACGTTGCAAAAGTCTGGACTGACTA[T/A]GACCTGAACAAAGACAACAAGATCTCTTGGGATGAATACAAGCAGGCGACTTACGGTTACTACCTCGGTAAGACAAGCTGTATCTGAAACCGTCAATTTAGATATTTCAGGTTTGAAGTTTGATATTCATCCAGTGTTTATATGAGATTCATTGTGTCCTTTTTTCCCAGCCAACCCAGAGGAGTTTGAAGATGCTACAGATCAGTTTAGCTTCAAGAAGATGCTTCCACGAGATGAACGCAGGTTTAAAACCGCAGACCTCGATGGCAATTTGGCTGCAGACAAAGAGGAGTTCACTGCTTTCCTCCACCCAGAGGAGTTCGCTCACATGCAGGAAATTGTGGTTCTTGTGAGTATGTTTATGATTATGGTGTTGTAGACAGTGGTAGTTACTGTCAGTTTAATTATGAAGACTACTTAAAACAACCATCATGATATTTCTAGAAATAATATAGATCTGTCTCCTCTGCTTTACCAGGAAACTCTGGAAGACATTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45271
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102363 | Nonsense | 225 | 328 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 16595082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15577780 |
GRCz11 | 7 | 15825666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAAGACATTGACAAAAATGGCGATGGTCATGTCGATGAAGATGAATA[C/A]ATTGGTAGGTGCTGATGTATTTTTGTGTGACCAATAGAATGCACCATAAA
Long Flanking Sequence:
AATACAAGCAGGCGACTTACGGTTACTACCTCGGTAAGACAAGCTGTATCTGAAACCGTCAATTTAGATATTTCAGGTTTGAAGTTTGATATTCATCCAGTGTTTATATGAGATTCATTGTGTCCTTTTTTCCCAGCCAACCCAGAGGAGTTTGAAGATGCTACAGATCAGTTTAGCTTCAAGAAGATGCTTCCACGAGATGAACGCAGGTTTAAAACCGCAGACCTCGATGGCAATTTGGCTGCAGACAAAGAGGAGTTCACTGCTTTCCTCCACCCAGAGGAGTTCGCTCACATGCAGGAAATTGTGGTTCTTGTGAGTATGTTTATGATTATGGTGTTGTAGACAGTGGTAGTTACTGTCAGTTTAATTATGAAGACTACTTAAAACAACCATCATGATATTTCTAGAAATAATATAGATCTGTCTCCTCTGCTTTACCAGGAAACTCTGGAAGACATTGACAAAAATGGCGATGGTCATGTCGATGAAGATGAATA[C/A]ATTGGTAGGTGCTGATGTATTTTTGTGTGACCAATAGAATGCACCATAAAAATTTGGTGTGGTTTGCGTTCAAGCTGCCATTTTTGCTAGTGAACTAGAAACAAAAGCACCCATGTGCTAAAGTCAAACGTTAATTGGATAGAAATGCTTGCAATCCTGTGGTGTATGCCGTAGGGTTTCACGTTTTACTGGTATTACTGTGATACTATGGCTTCAAAATACTGGCCATGCCATTGTAGTTTTTAAACAGTAATATTCTCATTAATGGTAGCGTCAACGGTAGGGGTGTCAAAATTAATCGTTTCTTCGGTGCACTGCGATGCAGACGTGGACGATTCGGTATCGGTTCAGTAATAATCATAACCTGTTTTTACTGACGTCATTTACCTCATATGCGCTCTGTCGCGAGGGAGGCGATCACGAGTATTTACAGTGCTTAAACTACTTAAAACTCATAAACTGTGCATAATTTCACTGTGTGTGTTTGCTGGATCAGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20882
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 |
---|---|---|---|---|---|
ENSDART00000102363 | Nonsense | 273 | 328 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 16592575)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15575273 |
GRCz11 | 7 | 15823159 |
KASP Assay ID:
2259-8550.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAAGATGGGAAGATGGACCTAGAAGAGATTCGTCACTGGATCCTGCCA[C/T]AGGACTATGATCACGCACAGGCAGAAGCCAGACATCTGGTGTACGAGTCA
Long Flanking Sequence:
CAAACTACGGGATATTCTTGCAGATTAACGCAGAAGTTTATCATAGGAATTTTATCGACCCATTTTTCCACAGTTGGCATTAAGGAACAAATAAACACTCTCTGACTAACAAGCAGCAGCTAAATGTGTCTGGAAAATGATTCAAAGGGCTTTTATTTTCATAAACGGTGCAGATATAAATGTCATCCATATAAGCATGTTCTGATTGGCCGGAGTAGACATCGAACGAATTTACAGGGATTTTCTAAAAGGGCCTGTTCACATGATCTCATTCTGAAAAATTGATGGTAATTGTTCTAAAAAGTCTGCATGTGTGAAAGCGGCTTATAACTCCAAGTAAAAACATTTTTCTATTGTTTTCAGCGGACATGTTTGCACATGAAGATGCTGGTCCAGAGCCAGACTGGGTAAGGACTGAGAGAGACCAATTTTCAGATTTCAGAGATCTGAACAAAGATGGGAAGATGGACCTAGAAGAGATTCGTCACTGGATCCTGCCA[C/T]AGGACTATGATCACGCACAGGCAGAAGCCAGACATCTGGTGTACGAGTCAGACACAGACAAAGTAAGAACGGGCTAGGATACTGTTAAGAATGGTTTCCAAAACAACCTTGTAGGATGTAACGATTCACAATAATAATCTCACGATTTAGTGACGTTATTTATACAAAATTATCTGACATTTAGGGTGAACACAAAAGCCCTTTAATTTTTTTTCTAAAATGCTGCACAATTTTTACAAAATAAAATCTTTTCTGCAGTACCTCAAAAAAATTCTTTAATATGAACAAACTAAAACTTTTGACTGTGCAGTTACATTACAAATTTAAAAAGAATTCCAAATAAAAAATAAACAATACAAATTAAAGAAGGCACTTTTAATTTAAATTTTTTTTATTAATAAATATGCGTAAACTAATTACTGAAATATGCGGAAACTAAATTTAAAAAGAAAGGGTAAAAAAGAAATCTGAAATGTATTCATACTTTCGCTATGAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1699
Status:
F2 line generated
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102363 | Essential Splice Site | 293 | 328 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 16592511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15575209 |
GRCz11 | 7 | 15823095 |
KASP Assay ID:
554-1645.1 (used for ordering genotyping assays)
KASP Sequence:
CGCACAGGCAGAAGCCAGACATCTGGTGTACGAGTCAGACACAGACAAAG[T/A]AAGAACGGGCTAGGATACTGTTAAGAATGGTTTCYAAAACAACCTTGTAG
Long Flanking Sequence:
TTTCCACAGTTGGCATTAAGGAACAAATAAACACTCTCTGACTAACAAGCAGCAGCTAAATGTGTCTGGAAAATGATTCAAAGGGCTTTTATTTTCATAAACGGTGCAGATATAAATGTCATCCATATAAGCATGTTCTGATTGGCCGGAGTAGACATCGAACGAATTTACAGGGATTTTCTAAAAGGGCCTGTTCACATGATCTCATTCTGAAAAATTGATGGTAATTGTTCTAAAAAGTCTGCATGTGTGAAAGCGGCTTATAACTCCAAGTAAAAACATTTTTCTATTGTTTTCAGCGGACATGTTTGCACATGAAGATGCTGGTCCAGAGCCAGACTGGGTAAGGACTGAGAGAGACCAATTTTCAGATTTCAGAGATCTGAACAAAGATGGGAAGATGGACCTAGAAGAGATTCGTCACTGGATCCTGCCACAGGACTATGATCACGCACAGGCAGAAGCCAGACATCTGGTGTACGAGTCAGACACAGACAAAG[T/A]AAGAACGGGCTAGGATACTGTTAAGAATGGTTTCCAAAACAACCTTGTAGGATGTAACGATTCACAATAATAATCTCACGATTTAGTGACGTTATTTATACAAAATTATCTGACATTTAGGGTGAACACAAAAGCCCTTTAATTTTTTTTCTAAAATGCTGCACAATTTTTACAAAATAAAATCTTTTCTGCAGTACCTCAAAAAAATTCTTTAATATGAACAAACTAAAACTTTTGACTGTGCAGTTACATTACAAATTTAAAAAGAATTCCAAATAAAAAATAAACAATACAAATTAAAGAAGGCACTTTTAATTTAAATTTTTTTTATTAATAAATATGCGTAAACTAATTACTGAAATATGCGGAAACTAAATTTAAAAAGAAAGGGTAAAAAAGAAATCTGAAATGTATTCATACTTTCGCTATGAAAACACTAGCTATGTTTCCGTTTTAAAATGCAAATTAATTTTATGCGCAAAACTAGATTATCGCATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20881
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102363 | Nonsense | 317 | 328 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 16589048)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15571746 |
GRCz11 | 7 | 15819632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATACTTGAGAACTGGAACATGTTTGTTGGCAGCCAAGCCACCAACTA[C/A]GGTGAAGACCTTACCAGGAACCACGATGAGCTCTGAGCCCAACTGACCTC
Long Flanking Sequence:
ATTCATTCAACATTTGCACCGTTTTGAATCGTCACAATGTTGTGAGCAGTGTTTCAGCATAGAAGAGCGATTTCTACAAGTTTATGCAAGACTGAAGGCTAGAGTGTTGATGCAAAAAAATAGTATTGCATACTAGTGTTGTTTATGAAGTTTAGACAACTGTATTGTTTTCAAACATGTGCAATTTGAAATATATTTTCCAAAAGTATATTTTTTAAGGCCATTGCAAATTAACAAATGCATAAAGAGAGAGTTTTTTAGCCGACAGTTATTAGCCAAAGTGTTCTGTAAATGCCCTCTGAAATAGTACCTTTACTGAAATACGATTGTTTTACCAGCAATATCAAGCAATAAAAGATTGTTAAATTGAAGTGGCTGATGGTTGAGAAACATGCACACTTTTCATGACGGCTGTTCGTGTTTTTGTAGGACCAGATGTTGAGCAAAGAGGAGATACTTGAGAACTGGAACATGTTTGTTGGCAGCCAAGCCACCAACTA[C/A]GGTGAAGACCTTACCAGGAACCACGATGAGCTCTGAGCCCAACTGACCTCTACCTGAAAACACAGGTATCCGAAACTCAAACTCCATGGCATCCTTCCTTTCAGAAGCCATGCAACTGACTGATGAACTGCAGCTCTACCTCACAGACTGGACATAGAGGACCACTGACTGATGGCCATAGTCCTGATACAATACAAGGAGATTCTCCTTCGCTCTATGTTCGTTTTGTGGGTGCTCAAGAAACTCTTGAGAGTCTGCTTGAGCTGCTACAGATTTCTGAGCCTTTCATCTCCAACGTGTTTCATTTTTAAATCGGTCCTAGTCCAAAGCTTGTACCTGTACAAGCAGTGCAGGTTTTTGTCTGATCAAATAGTCTATTTATTTGGAATTTGAATTGAATTTCTTGCTTTGAAATTACAATGCTTTTACTCCCTCAAACACAAGTCACTTCAAACACTACAAGTGTTGATAAACATAACATGAATACATGAATGTGTAAT
Associated Phenotype:
Not determined