ZMP
RNF138
Ensembl ID:
Description:
ring finger protein 138 [Source:HGNC Symbol;Acc:17765]
Human Orthologues:
RNF125, RNF138
Human Descriptions:
ring finger protein 125 [Source:HGNC Symbol;Acc:21150]
ring finger protein 138 [Source:HGNC Symbol;Acc:17765]
ring finger protein 138 [Source:HGNC Symbol;Acc:17765]
Mouse Orthologues:
Rnf125, Rnf138
Mouse Descriptions:
ring finger protein 125 Gene [Source:MGI Symbol;Acc:MGI:1914914]
ring finger protein 138 Gene [Source:MGI Symbol;Acc:MGI:1929211]
ring finger protein 138 Gene [Source:MGI Symbol;Acc:MGI:1929211]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16816 | Nonsense | Available for shipment | Available now |
sa23634 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16816
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 |
---|---|---|---|---|---|
ENSDART00000117777 | Nonsense | 333 | 343 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 6592600)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 6497674 |
GRCz11 | 20 | 6487621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGWGATTTCCRATCCGCAGCCCCTCCAGCAGTCCGATGAGGTGAATCTG[C/T]AGCTYGCGCTTATGGCGTCWTATCAACAACATTAAACCGCATTTTCAGTT
Long Flanking Sequence:
GAATAGATACTTTGAAGAGAGATGGAAACTGGTAACCATATTTAGTTTTTTGTTTTCCAACTGATGTCAATGTTCACACCTTTTCAGCTTTCTTTCAAATATCTTCCTTTGTGTTCAAACTCAAAGGTTTAAAAACCACTTGAGGGTGTGTAAACAGTGAGTATATTTCCATTTCATTTTTTGAACTGTCACTTCAGGGCCTAAGCAGTGAAAATCCTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCGTCCTCTAGGTGTGTCCAGTGTGTGTAGCGACACCTCACGGAGATCCACAATACTACAGCCGCAACTTCATCGGCCACCTCAACCATCGCCACTGCTTCTACCTGGAGGATATAACTGTAAGCCTGTCACCATCATAAATAAAATAACTTCTCCATAATTCTGATAATTTCTCAAATGTCAGTGCCTAACTGAGATTTCCGATCCGCAGCCCCTCCAGCAGTCCGATGAGGTGAATCTG[C/T]AGCTCGCGCTTATGGCGTCTTATCAACAACATTAAACCGCATTTTCAGTTCTCAGACATGGTCTGGACAGCAAAAACGATGACATTCATGAATCACCAGGATATTAATAAACTAAAGAGATGGCGGTGAAAGATTGAAGATATGATGATGAGGTATATTATCGATTATATAATGGCGTCCCACATGGAAATAGGCTATTACAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCTTTTCTTGGAACGCAAAATTACCCATTATGCTTTGCGTGTATGAGCAAGGAGAATGCGAAGAACTTCCAGTCGGCAGCTGATGCGTGTAAACAGTCACATTTGGACAGCTTTGAAACGATAGTTTTAATCTATTTTACTTGCTTTTATCCTCTTTGAACTGATACTGTTGTCCATCAGCACCGTCTCCTGGACTGATCACTTAAAGAAATGCGATCTAATAGGATGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23634
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 |
---|---|---|---|---|---|
ENSDART00000117777 | Nonsense | 340 | 343 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 6592623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 6497697 |
GRCz11 | 20 | 6487644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCAGTCCGATGAGGTGAATCTGCAGCTCGCGCTTATGGCGTCTTA[T/A]CAACAACATTAAACCGCATTTTCAGTTCTCAGACATGGTCTGGACAGCAA
Long Flanking Sequence:
GGAAACTGGTAACCATATTTAGTTTTTTGTTTTCCAACTGATGTCAATGTTCACACCTTTTCAGCTTTCTTTCAAATATCTTCCTTTGTGTTCAAACTCAAAGGTTTAAAAACCACTTGAGGGTGTGTAAACAGTGAGTATATTTCCATTTCATTTTTTGAACTGTCACTTCAGGGCCTAAGCAGTGAAAATCCTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCGTCCTCTAGGTGTGTCCAGTGTGTGTAGCGACACCTCACGGAGATCCACAATACTACAGCCGCAACTTCATCGGCCACCTCAACCATCGCCACTGCTTCTACCTGGAGGATATAACTGTAAGCCTGTCACCATCATAAATAAAATAACTTCTCCATAATTCTGATAATTTCTCAAATGTCAGTGCCTAACTGAGATTTCCGATCCGCAGCCCCTCCAGCAGTCCGATGAGGTGAATCTGCAGCTCGCGCTTATGGCGTCTTA[T/A]CAACAACATTAAACCGCATTTTCAGTTCTCAGACATGGTCTGGACAGCAAAAACGATGACATTCATGAATCACCAGGATATTAATAAACTAAAGAGATGGCGGTGAAAGATTGAAGATATGATGATGAGGTATATTATCGATTATATAATGGCGTCCCACATGGAAATAGGCTATTACAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACCTTTTCTTGGAACGCAAAATTACCCATTATGCTTTGCGTGTATGAGCAAGGAGAATGCGAAGAACTTCCAGTCGGCAGCTGATGCGTGTAAACAGTCACATTTGGACAGCTTTGAAACGATAGTTTTAATCTATTTTACTTGCTTTTATCCTCTTTGAACTGATACTGTTGTCCATCAGCACCGTCTCCTGGACTGATCACTTAAAGAAATGCGATCTAATAGGATGGAAAACAGCTGCTGTGAGGCATTTTCC
Associated Phenotype:
Not determined