ZMP
rqcd1
Ensembl ID:
ZFIN ID:
Description:
Cell differentiation protein RCD1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6NWL4]
Human Orthologue:
RQCD1
Human Description:
RCD1 required for cell differentiation1 homolog (S. pombe) [Source:HGNC Symbol;Acc:10445]
Mouse Orthologue:
Rqcd1
Mouse Description:
rcd1 (required for cell differentiation) homolog 1 (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:192890
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43792 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37457 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43792
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047464 | Nonsense | 34 | 298 | 2 | 9 |
ENSDART00000143574 | Nonsense | 34 | 298 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 12899147)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12735077 |
GRCz11 | 22 | 12759854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGGGAGAAGATCTACCAGTGGATCAATGAGTTGTCCAGTCCAGAAACA[C/T]GAGAGAACGCCCTGCTGGAGCTCAGCAAGAAGAGAGAGTCTGTGACTGAC
Long Flanking Sequence:
TTACTACATATTTTCAAGACACTTCTATACAGCTTAAAGTGGCATTTAAATGCTTAACTAGGTTAATTAGGTTGACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGAATAATGATGGTTTGTTCTGTAGACTATTGAAAAAAATATACAGCTCAAAGGGGCTAATAATTTTGTCCTTAAATTGGTGTTTAAAAAATTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATCAGACTTTCTCCTGAAGAAAAAAATATTATCAGACATACTTTAAAAATGTCTTTGCTCTGTTAAACATAATTTGGGAAATATTTAAAAAAAAAAAGAACAAAACAAAAAAATCAATGGTGGGCTAATAAATCTGTCTTCAACTTTATATATGATGACTAAAGAAGTGCTCTCTCACTCTCACAGACTGTAAGCACAGCGGGTCTGGCGCAGGTGGACCGGGAGAAGATCTACCAGTGGATCAATGAGTTGTCCAGTCCAGAAACA[C/T]GAGAGAACGCCCTGCTGGAGCTCAGCAAGAAGAGAGAGTCTGTGACTGACCTGGCCCCAATGCTCTGGCACTCCTGCGGGACCATAGCAGCTCTACTGCAGGTCTGCTTCAGTTTCTTTCATTCTAGACACAATTCTTTTTGATTTAAAGAAATATTAATTGAATTGAATAATTGTGTAATTATTATTATTATTTTACATATAAATAAATATTAAGTGGCATAACTGTATGTTTTTTTAATATATATCTGGTTAATTAATTCATTATGCAATTAATAATACAATAAGTAAAAATTAATTACAAAATTATTTTAGGTAATATTAAGAGGGATTTGTAAATGTAGGTTTTTTTGTTCAATGTTTTTATTCAATGTACACAATTTTGATTAATCTTTTTGATGAAAATGACATTTAAAATGAATTTTAAAGCAATAAATTGACAAACAATTGTTTAGTAAAACATGAATTATTTCAGATATTTGAAAAATTATGGAATGGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37457
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047464 | Nonsense | 237 | 298 | 7 | 9 |
ENSDART00000143574 | Nonsense | 237 | 298 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 12893410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12729340 |
GRCz11 | 22 | 12754117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAGGAACCCTCGGCTCGTCTGCTTAAACATGTTGTGCGCTGTTATTTA[C/T]GACTTTCTGACAACTCCAGGTATTTTTATACGGTTTGCATGAATTTTACA
Long Flanking Sequence:
TCAAAAACAACAAATGTTTTCGTCGTAGTCAAACTTTATTGAAAACTCGGGTATCAGCATAATATTTTTGTAATGATGTGTAAATTTGCAAAAACAAATACATTAATTTATGAATTTTCAATTCACATGCTAAAATAATAAAGGTGTGATTTTTTTTATTTATTTATTTATTATTTTTTTTATTGATTTATTTATTTATTTTTTGCAGCAGATGATTAGTACAATTAGTACAACTGATGTCTACTTTTAAACAATAGAAAAAAAGCAGGATGAAAATAGGCTTGTCTGTAAAGGTTTATCAGTAATTATTAAAATCAGTTATGGAGAAAACCGTTCCTTTGTTTGAGCAGAAGGTCTCTGATTGGCTGGCTAATTGCATGACTGAAGTGGTATTTAAACTAATGACTATATGTTTTGTGCTCTTGCAGGGGAAGATGGTTCTTCAGTTGTCTAAGGAACCCTCGGCTCGTCTGCTTAAACATGTTGTGCGCTGTTATTTA[C/T]GACTTTCTGACAACTCCAGGTATTTTTATACGGTTTGCATGAATTTTACAAAAACAATATATATTTATATTTATATATTTTATCTAATTTCAACTCCAAAATTGTATATTACTTGTTTAAAAGATTGTTTTACATTTATTTTAATTTACACATAATACATAATGTTTACTTTTAATAATTTTAATTAAAATGAAACTTTATTAGTTTGTGAAATATTTGCATCAATTTTATGTTGTTATATATTTAAAAAAATCTAATATTTGTAAAATTATAAAAACATAATCAGTTATGTTTATTTGTATTTTTTTAATTCATGTTTTTAATAATTTTTTTAATCTATGTTTCTAACTTTTTTTTTTGTAATTTGTTTAAAGTCTGTGCAAAATCAATATTGAAAATGTTTATTTTGCTAGCGCACTTCATTATTCTTTAGGTCAGGGGTGCTCAATCCTGTTCCTGGAGATCTACCTTCCTGCAGATTTCAGTTGCTACCCATATCA
Associated Phenotype:
Not determined