ZMP
zgc:56556
Ensembl ID:
ZFIN ID:
Description:
UPF0489 protein C5orf22 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q7SZF1]
Human Orthologue:
C5orf22
Human Description:
chromosome 5 open reading frame 22 [Source:HGNC Symbol;Acc:25639]
Mouse Orthologue:
6030458C11Rik
Mouse Description:
RIKEN cDNA 6030458C11 gene Gene [Source:MGI Symbol;Acc:MGI:1925127]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38336 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11848 | Essential Splice Site | Available for shipment | Available now |
sa12758 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38336
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020367 | Essential Splice Site | 344 | 439 | 7 | 9 |
The following transcripts of ENSDARG00000011723 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 28134196)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 28310681 |
GRCz11 | 2 | 27966317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTGTACACAGTCTTAAGAATCGACCATCACCTCCGGACTATGAAATG[G/T]TGTGTTTGTTTTATATTTTAGTGGATATTTTAATCATGCTTTTAGTGTAT
Long Flanking Sequence:
TGAAGAAAATTAGATGGATGGGTCAAGGAAATTCAGCTTTTCAGGAGAAAGCCGGGGAATTTGACATTTGGCTTAGAGTGGGAGTCCTGCAAATAACAGTCTTTACACATCCATGTGTGTTTGGTTTTCAGGAGGAGCTTTTAGAATGTGTGGAGAGACGCACGCGTCAGCTTGAAGACCTGGAGGCTGCGTTCGCTGACCTGCTTGAGGATGACGGCCAGGAAACTGTTGAACGTTTAGCAGCAAACCCAGGGTACACGTTACTGCTGTCACTGACACTGTGTTTTGTGTTTTTTTTTTTTTATTATTATGGCTTCATATCAGTACACCACTGGCCTTGATTTATTACTGTACATTGTCCGTGTTCATTTGATCAAGCAGAAGATGGCATGGCTTAATGCATTGATTTTTTTTTTTTTCATTTTCTTTGCAGAATGAAATCTCTTTTCGGACTTGTACACAGTCTTAAGAATCGACCATCACCTCCGGACTATGAAATG[G/T]TGTGTTTGTTTTATATTTTAGTGGATATTTTAATCATGCTTTTAGTGTATGTCATTTCATATATCCCAAATAGTGTCTTTTTCTTTATTTTATTTGAAGAAGAAAAATAGTATCTATAACTTCAGTGACCTCTTGTTTAACCTTCATATTCTTTTAATAAGTTCCTCTGAAATAATCAGAACTCAGCCGGCAGCTGATATTGAATCTTTATCCCTCTTTTACAGTAGAGTACACATTCATTTTTCAGACATTTACCTCACATCTATTCTAGTCACGTTGTTTCAGCTTGGGGCCAATTTGACACTGAACAATGTTGAAAAATACACTAAAAGAAATGAGAATAAGCATCTGTTGGGAGTGTATTGCTACATGTAAACAAATTAGAATTTTAGGAATTAGTTCATTTTATGAACTATTAACATAAAACTAGTAACAGGCATGCTTTAAAGTTTGAAGTTAACAAATCATAATCATCAAAGTTTATAAAGCTAAGAATATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11848
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020367 | Essential Splice Site | 344 | 439 | None | 9 |
The following transcripts of ENSDARG00000011723 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 28134195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 28310680 |
GRCz11 | 2 | 27966316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTGTRCACAGTCTTAAGAATCGACCATCACCTCCGGACTATGAAATGG[T/G]GTGTTTGTTTTATATTTTAGTGGATATTTTAATCATGCTTTTAGTGTATG
Long Flanking Sequence:
GAAGAAAATTAGATGGATGGGTCAAGGAAATTCAGCTTTTCAGGAGAAAGCCGGGGAATTTGACATTTGGCTTAGAGTGGGAGTCCTGCAAATAACAGTCTTTACACATCCATGTGTGTTTGGTTTTCAGGAGGAGCTTTTAGAATGTGTGGAGAGACGCACGCGTCAGCTTGAAGACCTGGAGGCTGCGTTCGCTGACCTGCTTGAGGATGACGGCCAGGAAACTGTTGAACGTTTAGCAGCAAACCCAGGGTACACGTTACTGCTGTCACTGACACTGTGTTTTGTGTTTTTTTTTTTTTATTATTATGGCTTCATATCAGTACACCACTGGCCTTGATTTATTACTGTACATTGTCCGTGTTCATTTGATCAAGCAGAAGATGGCATGGCTTAATGCATTGATTTTTTTTTTTTTCATTTTCTTTGCAGAATGAAATCTCTTTTCGGACTTGTACACAGTCTTAAGAATCGACCATCACCTCCGGACTATGAAATGG[T/G]GTGTTTGTTTTATATTTTAGTGGATATTTTAATCATGCTTTTAGTGTATGTCATTTCATATATCCCAAATAGTGTCTTTTTCTTTATTTTATTTGAAGAAGAAAAATAGTATCTATAACTTCAGTGACCTCTTGTTTAACCTTCATATTCTTTTAATAAGTTCCTCTGAAATAATCAGAACTCAGCCGGCAGCTGATATTGAATCTTTATCCCTCTTTTACAGTAGAGTACACATTCATTTTTCAGACATTTACCTCACATCTATTCTAGTCACGTTGTTTCAGCTTGGGGCCAATTTGACACTGAACAATGTTGAAAAATACACTAAAAGAAATGAGAATAAGCATCTGTTGGGAGTGTATTGCTACATGTAAACAAATTAGAATTTTAGGAATTAGTTCATTTTATGAACTATTAACATAAAACTAGTAACAGGCATGCTTTAAAGTTTGAAGTTAACAAATCATAATCATCAAAGTTTATAAAGCTAAGAATATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12758
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020367 | Nonsense | 397 | 439 | 9 | 9 |
The following transcripts of ENSDARG00000011723 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 28125976)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 28302461 |
GRCz11 | 2 | 27958097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTTTCCTGAACTTCTATTTGTTCTTGTCAGATCCAGTTTGGATGAGTA[T/A]TGTCCAGCTGAACAAGTGGATTCCATCCAGATCAGARTGCTGAAYATTCT
Long Flanking Sequence:
GCAGATTCTGTTTTTCTAGTGTATTCAGCACTGAACTCCACTGTTATAAATGTCATTGTTTGTTTTTATTGCAATAAGTTATCATTAAAAAAGTTATACTGATTGGTTAATATTCTTTAAAATAATGTTTTCTATTTATTTTGAAATGTTAAATAGGCCTAAATTACAAAAATAACCATGGCAACATTAATTAAATATAGTTTGGTATATTTACCTTCGGCTCTTAATGACATTTATTTTTTGGCCCTTCATACGAAAAAGTTTGGGCACCCCTGCACTAAAGCATATCATATTTACCTTTTGTTACCTTCCACTTCATTATCAGTTTTTCATATACTGTTTCAATGACTCACATTTGGTGCTTGGTGAGCATTTATTTTATGCTCTATACGGTTCAATATAAACGTTTTCAGTTGTAATAAAATCAGAAAAGTATGTAGTAGTATCAAGGTGTTTCCTGAACTTCTATTTGTTCTTGTCAGATCCAGTTTGGATGAGTA[T/A]TGTCCAGCTGAACAAGTGGATTCCATCCAGATCAGAGTGCTGAACATTCTAGAGTCCCTCTTCGGCTGCTTAGATGTTCACAGAGATTACGAATCAATACCAGCAGAGAGCACATCACACACCGCATGAGGAGAGAGGTTAAATTCATCATCAGCTGCAGCATCTTTTTTTTTTTCAATGACTGTTTTCAGATGCTGAACCATGCTAAGATTTGCCCTGCACTATTTTGCGGTTGAGTGCATATCTCACAACGAATGTATGGATGTGAATGGAAAAGAAAATTAATTTCCAGCTGGGAAATGGGCTTTTAATTCAAGAGGTTTTCGTGTATATGTTTGAAGTGCATTCATTCATAATACGAGCCCCTGCCACTGTAGAGTGGATATACTGGAAAACCTTGGTAATAATGTATCTGTATTGTCGCCAGAACAACAAAATAAAAAGCCCAAGATTTCCATATGAATTCTGTGCTGCAGTCATTCATCCCCAATGCATTCAGG
Associated Phenotype:
Not determined