ZMP
mrpl37
Ensembl ID:
ZFIN ID:
Description:
39S ribosomal protein L37, mitochondrial [Source:RefSeq peptide;Acc:NP_001076324]
Human Orthologue:
MRPL37
Human Description:
mitochondrial ribosomal protein L37 [Source:HGNC Symbol;Acc:14034]
Mouse Orthologue:
Mrpl37
Mouse Description:
mitochondrial ribosomal protein L37 Gene [Source:MGI Symbol;Acc:MGI:1926268]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39779 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10750 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39779
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091479 | Nonsense | 193 | 425 | 3 | 7 |
ENSDART00000146546 | Nonsense | 198 | 430 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 10715398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11140494 |
GRCz11 | 2 | 10924093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTTCCTTCATAGCCCCATGCTTGTGCATAGACTGCTTCATCTGTGT[G/T]GAGTCCTGCAGGTCCGCCATCCGGAGCTGGCCAAGAGGATGCTAGCTGAG
Long Flanking Sequence:
CGTCCCCTCTCACCCGGCGCCTCATAATTGGCTCAACAGCTTCAATATGGAAGGTGGCATTTGGCCTGGGCCTTGTCGCTCTGATGGTGTGTTGAGTTTAATGACGGTCATTAAACACGGGCCGGTCTGCATTCCCAGCAGGCGGCGGCTCTGTAAAGCCTTTATTAATTAATACCGCTCCTAGGAGGTCTGCCATTCATAAGAGCCTCTTTGATATCTCTCATCTCCCCCGGTTAAAGTCTGCCCTTTGGTGCCTGTTTTATCTCCCAACTACTGCTGGCCCTTAACATTTTCCTTCTCACAAAAGCCCGTCACCAAAAGGCCATATTGACATTGACACCAAATGACATTACGCTCACGAACATGCGTTTGGCGAATTGGGAATGTCCGCATGCTGTTTTGTATGAGCCATCGCATAGGTAAATGTCTTTTATGTGTGTAAATAGTGTTTTCATTTCCTTCATAGCCCCATGCTTGTGCATAGACTGCTTCATCTGTGT[G/T]GAGTCCTGCAGGTCCGCCATCCGGAGCTGGCCAAGAGGATGCTAGCTGAGAAATACAATTTGGCAGCGACCTGGAGGAGAGGTGGGTGTGTGTTGTCCATCACATATGCCTATCCTTCACTCTTAGATTAAAATTAATATGGATATAATGAATGCAGAAGGCTAATTTGCTTCAATTTTTATTTGATTTAGTGAGAAGTTGTCGACCATATTTTATTTGACTTTTTATATTATTTTATTTTTAATTAAATTTATTATAATTTTTTTCGTTTATATTCATTTTATTTAATTTTTTAATTTTGTAAATTAATATAGTTGTTTCATTATTTTATTATTTTGTTGTTTTGTTATTTATTTATTTTAATATTTTATTTTTTATTTTATTTTGATTTAATTTTTATATTTTTAATATTTTATTTAATTTTTTCTTTTTATTTTAATTTATTTTTTCATTTATTATTTTTATTTATTTTTTTATTTTTTTCATTTTATTTATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10750
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091479 | Essential Splice Site | 400 | 425 | 6 | 7 |
ENSDART00000146546 | Essential Splice Site | 405 | 430 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 2 (position 10721119)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11146215 |
GRCz11 | 2 | 10929814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATGAACACGCCCAGGCCCGGGCTCACATCAAGAGGAGAGTCGTCAAG[G/A]TAAAGTCYACTTYATTCATRTTCAGTCCCTGCTGAAAAAAACAGCTKAAA
Long Flanking Sequence:
GTATATAGTATACTATAGCACAGTATTCAGGCACAGTAAAAAAGGATGCAGGAATAGTTTTATGGTCTTCTTTTTCTTTTTAGTGATGATGAAGTTATTTTTTTACAACATGGCCATATCCAAATGGTGCCATTTGTTACAATTTTGTTGAATAATAATCATTCTTTCTTGTGATGATTTTGTAGACAACTTGCTTTCATTATTTATTGTCTTTAGATCTGCATTAGTTTCACATGTTTGGTTCAGTTTGTCAGTAATGATAATCTACTTTACATGCGTTCTCTTGTCTCCGTCAGGACGAGCCCAGAGTTCTGGAGAAGCCCATTGTGGTTCAGAGTGTGGCCACAAACGGCCGTATCTTCCAGTTTGTGGTGTTTCAGCTCAACACGACGGAGCTGCAGTCGGACAGCGGAGTGAAGAATCTGGTGTGGGTGGACGAGGATAAACCGCTTTATGAACACGCCCAGGCCCGGGCTCACATCAAGAGGAGAGTCGTCAAG[G/A]TAAAGTCCACTTCATTCATGTTCAGTCCCTGCTGAAAAAAACAGCTGAAACCAGCCTAGGCCAAAACCCCTTTAAAACCAGTCTGGTTGACCAGCTAAAACCAGCCTTGGCTGGTTTAAGCTGTTTTTTTCATTAGGGGTACAGGGAATGTTCACCCAAAATATGAAAGCGTTAAAGGCCCGTGCATACCGAGACGTTTTTTGCTCGTGTTTTCCGTCGACCTTCAATGCTTTGTGATTTAAATAAAGGGCGTCAATGTGATTGTGCACACCAACGCGCAAAACAGCAGGCACAAAAGCGTCATTTAAAAAAAAAAAACGCCTCATGCTCGTTTTTTTGTTTTGACGTGAGCCTTCTCCACCAATCAGGTTGGCACTTTTGTTCACATGCATGGAGTTGTTGAAGTTACAGTAAACAGCACTTGGAGGCGCTCAAGCGCAAAACTGTCAATGCGAGCGCACATTGAAGAACATGCCCAGAGGCGATATAAACGTTTAGCT
Associated Phenotype:
Not determined