ZMP
zgc:77778
Ensembl ID:
ZFIN ID:
Description:
UPF0762 protein C6orf58 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q4QRF7]
Human Orthologue:
C6orf58
Human Description:
chromosome 6 open reading frame 58 [Source:HGNC Symbol;Acc:20960]
Mouse Orthologue:
2310057J18Rik
Mouse Description:
RIKEN cDNA 2310057J18 gene Gene [Source:MGI Symbol;Acc:MGI:1914969]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1814 | Missense | F2 line generated | Not yet available |
sa6612 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10898 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1814
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:
G > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002242 | Missense | 67 | 364 | 1 | 6 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 1422243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 1378108 |
GRCz11 | 20 | 1398934 |
KASP Assay ID:
554-1806.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCAGGTAAACCCGTGGGTCTACTCCCAGAGGATGACCATGTTGAAAAT[G/T]GTGATCAACGCTACTAATGCCTACATGAGCTCCATGGGCCCCGGGGAGCA
Long Flanking Sequence:
CCGGATGTGAGGCACATGAATTTTGCTAGCTGGGATTGATGAAGGCTCATAACTGAATCGATTGGTTTTTCTTTTCTCCCGTGATTCGTTTAATGAGTTATTGAGTGTGACCTTCTTTGGTATTTGCCATTTGTCGATATTTGGCATGGAAACGAGACTAAAGTATGTTTTTGTGCCGTGGGTGTGTTTTTCTCCACCCACACTGGTTTGGTTTTGTCTCCATGTGGGATCAAAGTCCATGTGCTGCCCATTGATTAAAGCTCCTCTCTGCTGGACTCAGTGTTTCAGCAGTCCTGCTAGATGTCTGAGATGGGTTTCCTGCGATCAGTGGCCGCTGTGCTCTTGTTGGCTGTGTTTAGCCACGCAGCAGTAGTGACTGAGAATGGACTGCCGATTCAATGGAGAAAAGCTCCCAGCGATCTCTCCCACCTGCCCATATCGAACACGGGGGTCCAGGTAAACCCGTGGGTCTACTCCCAGAGGATGACCATGTTGAAAAT[G/T]GTGATCAACGCTACTAATGCCTACATGAGCTCCATGGGCCCCGGGGAGCAGGAGAATCCGCTCTGGAGTCTTCCTCTGCAGCTCGGCTGGAAACTCAAATCAGGTGCCCTTTATTTTGCACTGTAGGAAACAACACCCTAGCTAATTGGCTGTGATTTCAATGCCTGGTTAACAGGAAGTTTCATTAATATATAGTTAAATTCTGAATTATTCTGCCCCCATTTATTTTCCCCCCAATTTCTGTTTACCAGCACATTTCTAAACATAGTTTTAATAACTCATCTCTAATAACTGATTTATTTAGTCTTTGACATGATGACAGTAAATAATAAATAACTAGATATTTTTAAAGATGTTTTGGATTCTTGTTGTGGTCATTATTATTATGGTGGCTTGAGAAAGCCACCATTTTGATATTCTACATAACCTTATAATTATTCTTCCGTCTTCTGAGACTAATTTTAAAGTGTATCTCCTCCTAAGCCTTTCTAGCTACATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6612
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 |
---|---|---|---|---|---|
ENSDART00000002242 | Nonsense | 178 | 364 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 1425366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 1381231 |
GRCz11 | 20 | 1402057 |
KASP Assay ID:
554-4842.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGTCCCAGCAGAAGTGGCTCAGGATTACTGCTCCAGCTACAGMGACTG[C/A]TMCACCAAACACCCCRACRCCATKGCCAAATGGCACCTCTYTTTTCAGGT
Long Flanking Sequence:
GTTGCGTCTCCGCCCCTGCCACTTCACCCAATCCAACAGCATGTGGCACCGCCTGAGAAAAAAAGTAGAATAAAAAACAGGTAGAATAGGGATTGGGTCTTAGTCTTGAAAACATTACCGTAAAGACTCACACTAGTAATAATCAAATGTTCCCAATCACATTTATGGATTTTGCATTAATTTACAATAATAATGACCTCAGTTTACTGTAAATTACACATTAGGTGTACCTTATATCATTCCAGTTTAAAGAAAATAATTGAAAAACACCTGAAATGTACCTGCTGCTCTGGAATGGGTCATATAATTAAAGATTCTGTACATCTTCTGAATCCTATTATCATCATTTTGTTGGTGTGTGCAGGTGTAAACTACTACCTGTCTGTGCTGCCATTCCTGGCGGCAGTGGAGACTGGTGTGGTTAGCAGCGGAGGGCATCAGATGCTTATTCAGGTCCCAGCAGAAGTGGCTCAGGATTACTGCTCCAGCTACAGCGACTG[C/A]TCCACCAAACACCCCAACACCATGGCCAAATGGCACCTCTTTTTTCAGGTGCCGTTTTTATCTCTGGGTGCATACTAACCTTTAGATTTGATCCATTTGGAAGACTCTTATTGAAATTAATGTGGCTCATGCACACACATGCTTGATTTTGATTGGCTGATGGTCATTCTGAAGTGTTTGGTTATTGTCAGATAAATGCACAGCTAAAGTAGTTCCGACAGGTTTTGAGCACATTACAGCTCCGTAAAACTACGCTAAATGATTTGAGCTATTGCACAGCTACAACAGTCAACCATCACATCAAAACACAACAGAAAGATTTGGATGAGATGTGGAAGAAACTAGTGTTGCACACAGGAGCAGCTTGAGTTTGACAAAAAACCTGACAAATTAAGTCTCAAATGCTACATCTCAACAGCGGATTTAGAAGCGGGAGTCAAAGCTCAGGGTAACACTCCTGCGGGAGTCAGAGCTGCAGGGGCAAGTATCCTGCAGGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10898
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 |
---|---|---|---|---|---|
ENSDART00000002242 | Nonsense | 226 | 364 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 1427425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 1383290 |
GRCz11 | 20 | 1404116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGGACAGCATTCTGGGYCTRATGTGGGCTGCCGAGGAGGAGTCTMTA[C/T]AAACCGCCTCTGGGGCTTGCACTGAAAGGTCAGCATACATTACATTCAGG
Long Flanking Sequence:
TGTTGCTGCTTTTGTTCAATTTCTTTTGAAGTCGTTGGATGAGTATTTGCTTGATCGGTGATTTGCTTCTTTAAGGTAAAGATGGCTAAGATAAGGAAATCTGGGTGTTTATGTTTGGATTCATCTGATTAGTATATCATGTGATCACTAATGTAGGACCAGCCGTGGTCAATCATAATCCCGTGATCTTCTCTAAATTAGTTTATAAATAAACTTTACTTAGTGTTCAACAGAAGAAAGAACTTATGAAAATGTAAAACCACTTGAATGAGGAAACTGGACGAACAGTGCCCTCTCAACATCTGCTTTGTTCATATCATAAACTGGCAACTTCTGATACATAAGCCTGTTGGATGTTGTGCCAGATGAAGCATGTTTAATCGGTCAGCACTTGGGTGTGTGTGCAGTCTCTGCGGCACGTCAGCCAGTCCAAGGACAGCGATTTTAACAAGAAGGACAGCATTCTGGGTCTAATGTGGGCTGCCGAGGAGGAGTCTATA[C/T]AAACCGCCTCTGGGGCTTGCACTGAAAGGTCAGCATACATTACATTCAGGGGTTTGAGGGCCTCAGCCATCCCAGCCATGGGGCACAACAGCTCTAATGTGCAGCCTTTGTTTTTCTATACCTTTTTTGTTGCTTGTTGCTAATGTGTTAATTAACAAGCATGTACTAATAAGTGATAAGGTGATAACTTTTTATGTCAAAATCCATTTAAATTTGTAAAAAATAAAAAGTTAACTTAGTTCCTTCATGTGTGGAACCCAGTATGTTTTTGTGTGTGTACTGCTCCCTTCTCCCTCCATTCCCCGACAGTAAACCAGTGCTGATATAGTTTTAGAAAGGCTCATTTTTCATCTTCTTCTTCAGACAAAAGCTGTACTCATCTCCTGAGGTGAGCTTTCAGCAGAGCAGCGTGAACTTGGGAGCATTTATATCGGCGGCTCATTACCACGCAAGCATTGAGCGCGCTGGGAAGTTCATGTCTCATCTGCCCAGCCGAGTCC
Associated Phenotype:
Not determined