ZMP
zgc:171980
Ensembl ID:
ZFIN ID:
Description:
UPF0510 protein INM02 [Source:UniProtKB/Swiss-Prot;Acc:A7E2M3]
Human Orthologue:
C19orf63
Human Description:
chromosome 19 open reading frame 63 [Source:HGNC Symbol;Acc:27609]
Mouse Orthologue:
2310044H10Rik
Mouse Description:
RIKEN cDNA 2310044H10 gene Gene [Source:MGI Symbol;Acc:MGI:1916933]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2098 | Nonsense | Available for shipment | Available now |
sa9304 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2098
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077029 | Nonsense | 77 | 257 | 3 | 7 |
ENSDART00000133516 | Nonsense | 77 | 251 | 3 | 8 |
The following transcripts of ENSDARG00000054793 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 30398883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30116922 |
GRCz11 | 3 | 30247764 |
KASP Assay ID:
554-2722.1 (used for ordering genotyping assays)
KASP Sequence:
CGACTTCGTGGTGCTCTACAGTTCAGGGGTGGRAGGGAAAACAGTGTGTA[T/G]CTCTCACAAAACCAGCTCTCAGAGAAAGACAGGAATACACTGAAGGTGAG
Long Flanking Sequence:
GGCTTGAGACAAAATGGCTCCGATTAGAGTGTTGTCACTTGTTCTCCCCATCTTGTCAACTGTACCGTTGTTATTGACACAATTTGGCGAATGCAATAATGGTCGAAGGGTAAGATGATTGTGTCTGATACACCTCGCAGTCACAAAATCTGTATTTTACATGGCATTGCAGATGACTTGCACAGGGAGCTTGTTAGCATGCTAGACTGCTGTCTAACGTTAATCAGATGAATATGATTGAATGTCAGTTACTTTATCTGTCTGTTAGTCAGGAGACGCGGTGGACACTGATTTCAGCGGATTCTCGGTGCCATTAGAGCACTCGTTTGAAGTGGGTGAGTACAAGTTAGTCAATGAAAAGGCTTTTTGTGAATAAATTGTTGGTCTCTTTTTAGTGCAAGTGAGTCACTAACGTTATTGGTCTGTGTTTCAGATGATGTGCCAAGATTTCGACTTCGTGGTGCTCTACAGTTCAGGGGTGGGAGGGAAAACAGTGTGTA[T/G]CTCTCACAAAACCAGCTCTCAGAGAAAGACAGGAATACACTGAAGGTGAGGACATGCCATTGAGACAAAGTTGGTTTTATATTCGCACATTCAGACCTTCTTAACAATATAATTTCAGAAAAGTATTCTATGCAAGTAAATAAATAGTAAAGTCATACTAGCAGTCAATGACTTTTGAAGTTCAACACTGTTCACAGCCAAATAAATAATGCTAATGTTGTTTTGAAGTCATACTTGCATGTGATTTCAGACCGAATATTTGAAGTAGCAAAGCAATAGAGCAGCCTTGTCACAAGTTGTCACTAAACAATTGTGCGAACATAAAACCAACTTTACCTCAATGAACATGCAATGAAGGAAAACTCTGATTTAATATTATTTTTTTAATGGTTGTCCAGGAAAGGCTGTCAATTTGAAATGTTCTAACTCTGTTTCACTGGTATAATTTTGTGTTTCTCTACCTGTGTTTTTCAGGACGTGGCAGCAGTTGACGGTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9304
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 |
---|---|---|---|---|---|
ENSDART00000077029 | Nonsense | 101 | 257 | 4 | 7 |
ENSDART00000133516 | Nonsense | 101 | 251 | 4 | 8 |
The following transcripts of ENSDARG00000054793 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 30398382)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30116421 |
GRCz11 | 3 | 30247263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTCTCTACCTGTGTTTTTCAGGACGTGGCAGCAGTTGACGGTTTGTA[C/A]AGGATCCGGGTCCCAAGGGTCTCTCTACAGGTGGATCGGCAGACAGAGAG
Long Flanking Sequence:
CTCTCACAAAACCAGCTCTCAGAGAAAGACAGGAATACACTGAAGGTGAGGACATGCCATTGAGACAAAGTTGGTTTTATATTCGCACATTCAGACCTTCTTAACAATATAATTTCAGAAAAGTATTCTATGCAAGTAAATAAATAGTAAAGTCATACTAGCAGTCAATGACTTTTGAAGTTCAACACTGTTCACAGCCAAATAAATAATGCTAATGTTGTTTTGAAGTCATACTTGCATGTGATTTCAGACCGAATATTTGAAGTAGCAAAGCAATAGAGCAGCCTTGTCACAAGTTGTCACTAAACAATTGTGCGAACATAAAACCAACTTTACCTCAATGAACATGCAATGAAGGAAAACTCTGATTTAATATTATTTTTTTAATGGTTGTCCAGGAAAGGCTGTCAATTTGAAATGTTCTAACTCTGTTTCACTGGTATAATTTTGTGTTTCTCTACCTGTGTTTTTCAGGACGTGGCAGCAGTTGACGGTTTGTA[C/A]AGGATCCGGGTCCCAAGGGTCTCTCTACAGGTGGATCGGCAGACAGAGAGACAGTATGAAGGTTACCTTACCGCATTCGTTAGAGCTGTAAGTCAACTGCATGCACATACCTGCACAAAAATTTTACCAGCATTAAAAAGACCTGCAGATTAATACATTTTTTTGTCTTTTCTAAATTTCTAAAGATTTCTACATTTAGCATTATCAGCAACAGTAGTAGTAACAGTGCATTTTTCTCAATGTTGAATATTTTACAATATTCAGCTAATTATTTCTTAATTTTAATAAATTACAAGTTCTGAGTTCTATATGTTAAAACCAAAAGTTTCTTCCAGTGCTGTTTTTGTAATAAATGGAAAGCAAATTACATTTGTCTCCTCCCATTTTTGACCCCAAAAATGGGCCGATCTGTGACCAGAAAATACATAATAGGATTCGAAACATAGAACTATGATTTGTTACACCACTATGATGTATACATTATGCATGCGAAAATACAA
Associated Phenotype:
Not determined