ZMP
mrpl39
Ensembl ID:
ZFIN ID:
Description:
39S ribosomal protein L39, mitochondrial [Source:RefSeq peptide;Acc:NP_956209]
Human Orthologue:
MRPL39
Human Description:
mitochondrial ribosomal protein L39 [Source:HGNC Symbol;Acc:14027]
Mouse Orthologue:
Mrpl39
Mouse Description:
mitochondrial ribosomal protein L39 Gene [Source:MGI Symbol;Acc:MGI:1351620]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8652 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24833 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8652
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 |
---|---|---|---|---|---|
ENSDART00000060944 | Nonsense | 46 | 342 | 12 | 20 |
ENSDART00000147633 | Nonsense | 46 | 342 | 2 | 10 |
The following transcripts of ENSDARG00000041570 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 457036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 587160 |
GRCz11 | 1 | 582339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTTCTGGCTCAGCGCAGTGCTCAGTTCTCCAGAGAGCAGCTCCGYCAG[C/T]GAGCGCTGCAGCCGCGGGTGGAGAAGGTGGAGGTGCAGCTGCAGGGGCCG
Long Flanking Sequence:
GTGGTGCAGTAGTTAATGCTGTCGCCTCATAGCAAGAAGGTCGCTGGTTTGAACCTCAGCTCAGTTGGTATTTCTATGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGGTACAGGTGAATTGGGTTGGCTAAATTGTCCGTAGTCTATGAGTGTGTGTGTGGATGTTTCCCAGAGATGGTTTGCGGCTGGAAAGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCTGGATTAATAAAGTGACTAAGCCGACAAGAAAATGAATGAATGAATAATGTGTGTGTGTGTGTGTGTGTGTGCACTGCATTGTGGTGTGTGTTTTGTGTGTAGGTATGGTGTCCAGCGCTGCAGCTGCTCCTCGTCTGTCGTCTGCAGCGGTTCTGGCTCAGCGCAGTGCTCAGTTCTCCAGAGAGCAGCTCCGCCAG[C/T]GAGCGCTGCAGCCGCGGGTGGAGAAGGTGGAGGTGCAGCTGCAGGGGCCGGGTCTGCAGGGGACGCTGCTGGTGATGAACAGAGGCCTGTCTACACCATACAGCTGCGCACGCCGTGAGTCTCATTCACACACACACACACACACACACACACACACACATATATATATATCGCACTCATACTCATGCTCCTCTGTAGACCCTTCACTCTTGTGTGCTGTTGGGTCATTTTCATCCACAGCTGTCTCTGTGTTTCAGCAAATGTGATGATTTTTGGTGACAGACACTCCATTATTAATCACAGTTATTGATTGTAAAGTCAAGACAGCAGATAAGCATGCACTTTTGGTCGATGCTGGTTTTCCCTGTTGTGATTTAGAGGGACGATCTGTCATTTTACTTTATGAAATTAAATTCAAAGGGCATGACCAATTATAGACTCCAACTGCTCTGATTGGCTGACAGTTTTGCATATTAACAGGGCTAAACAGGCAGTGCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24833
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060944 | Nonsense | 182 | 342 | 15 | 20 |
ENSDART00000147633 | Nonsense | 182 | 342 | 5 | 10 |
The following transcripts of ENSDARG00000041570 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 461924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 592048 |
GRCz11 | 1 | 587227 |
KASP Assay ID:
554-7610.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGGTGCTTTCTGCTGTGATCTGCTTCTGGATCCGCTTCTGGACTCCTG[G/A]AAGCCCACAGAGGTCAGAAACACCTCCTCAACACTGATTTATTCTCATCT
Long Flanking Sequence:
TAGTTGATGCAGTGTAAAGTGTGTGTGTTTCAGGCGTACTGGCGCTCCTGTGCGGCTCTTCTGGGTCTCGTCCTGGAGTCAGCCTTTAAGGATCAGTTCAGTGTCGAGCTGCTCAAGACTCCTGAAGTGCCAGGTCAGACTGATCCTCACTGTGTGTGTTTATTTTCAGCAAAGGACATTTAAAAGAACTTGTGTTTTTATTTTATGCTGAAATCTAATTGAATTTGTTCTGTTTTATTTAATTTTTATCCGTTTTATTTAAGCATGTCTGAAATTTAGTGATTTTTATTTTATTTTATTTTTTAAATTTTATTGTTTTCACTTTCATAGTTTTATTAATGAATTACTTACTTTATAATGTTGTGCTTTCCTTTTTCATTTCTCTAGTTTTTATATTTAAAGTTTGAATGTGCACAAATAATAAACCCCCTGGTTGTGTTTGCAGTGACGGCCGGTGCTTTCTGCTGTGATCTGCTTCTGGATCCGCTTCTGGACTCCTG[G/A]AAGCCCACAGAGGTCAGAAACACCTCCTCAACACTGATTTATTCTCATCTCACTCTGCATCTCATTTGCTTTCAATTATGATTCAGGGTTTTCTGTGGAAACTAAAAGTATTGAGGAAACAAAAACACATGATCATTTTGTAAAAGTAATTTGAATAATTGAATAAGTAATTTTCATTTGGCTCAGTCCCTTATTCATCAGGGGTCACCACAGCGGAATGAACCGCCAACTATTCCAGCGTATGTTTTACTCAGCAGAAGCTCTTCCAGCTGCAAAAAAAATCTTCTTTTGTGTTTAAAAGAAAGAAAGAAACTCATAAAGGTTTGCACACACTTGAGGGAGAGTAAATAGTCAATATATTGAATTTTTGGGTGAACTGACCCTTAATAACTCCAACATGAACACACACATCGAATACAAATAAAAAAGTCAGCTGAAATAATAAACCAGTTTAAATGTAAAATATAAGAGCTGTTTAACCGAGAGGGTTTTTACTTCAT
Associated Phenotype:
Not determined