ZMP
LOC557995
Ensembl ID:
Human Orthologue:
RNF19A
Human Description:
ring finger protein 19A [Source:HGNC Symbol;Acc:13432]
Mouse Orthologues:
1700001J11Rik, Rnf19a
Mouse Descriptions:
RIKEN cDNA 1700001J11 gene Pseudogene [Source:MGI Symbol;Acc:MGI:1919474]
ring finger protein 19A Gene [Source:MGI Symbol;Acc:MGI:1353623]
ring finger protein 19A Gene [Source:MGI Symbol;Acc:MGI:1353623]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23479 | Essential Splice Site | Available for shipment | Available now |
sa14753 | Nonsense | Available for shipment | Available now |
sa23478 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23479
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024193 | Essential Splice Site | 464 | 913 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 12669000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12127346 |
GRCz11 | 19 | 12046874 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCCATACCCGCGATGATCATTGGGATACCGGTGTATGTGGGAAGAAAG[G/T]TGGGTGGTCGTCTTTAAATGTTAAAAATGAAGGGTGAGGTGTACATGATG
Long Flanking Sequence:
TGAAAACATCTTGCGTCATGTCAGCAAAGAGTGCTCTTAACTGTTTTGTTTGTCTCCCTAAGCTGACGACATTAAGCCATGTCCCCGCTGTGCGGCCTACATCATTAAGATGAATGATGGGAGCTGTAATCACATGACCTGCGCAGTGTGCGGCTGTGAGTTCTGCTGGCTGTGTATGAAGGAGATCTCTGACCTGCACTACTTAAGGTCAGTGAGCGGGACACCACTGCGGTGTTCACAATATACAACCATGTGATATAGAATACCATGTGTTTAAAAAAACTGAATTTTTAGCTAATTTCATATATTTTGTGTTTGATTTCCGTTTCTGGCACAGTCCTTCGGGATGCACATTCTGGGGTAAGAAGCCCTGGAGCAGGAAGAAGAAAATCCTGTGGCAGTTGGGCACGCTAGTGGGAGCTCCCGTTGGCATTGCACTGATTGCAGGCATTGCCATACCCGCGATGATCATTGGGATACCGGTGTATGTGGGAAGAAAG[G/T]TGGGTGGTCGTCTTTAAATGTTAAAAATGAAGGGTGAGGTGTACATGATGGCTCTTTGTGTAATTCTACATTGCGTAATTTTTAAACCTAGTCTGTTAAACTATTTGTATTAAACAGTCATATTTGGTGTGTTCGCATTGGTTACTATAGTAAGTGTCTCCATAGTGCCAATAGAGATTTTCTTCTAGGACTGAGAGAAGCTGTAATTCTCTAAAACCTTTTAATATCACCTTATTGTGATATTATTGCAGGATGCAAAACTCATTACGCAAGTGGACAATCATCAATGGAGGCATTACTTGGGTTGGCAGCTAGCTCTCTGCAACTCTCACATGGTCATCCACAGAAGCTAAGCAGGGCTGCCTGCAGGGTCAGTACCTGGATGGGAGACCTTATGGGAAATCTAGGTTGCTGCCGGAGGTGGTGTTAGTGAGGCCAGCAGGGGGCGCCCAACCTGCGGTCTGTGTGGGTTCTAATGTCCCAATGTAGTGACTCGATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14753
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 |
---|---|---|---|---|---|
ENSDART00000024193 | Nonsense | 887 | 913 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 12655409)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12113755 |
GRCz11 | 19 | 12033283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTACATTGCAGAGGAGAATGTGAGTTTAATGTGTGCGGCTAATGCGAGC[C/T]AGAGCTCGCCTAAAGAACGCAATAACAAYCTTCCTCAGCCAGCTAGCCCT
Long Flanking Sequence:
GTCTTCACGACGGCAAATGCGTCACTTCTCGCTGGGCCAAGGAGCCATCCTCCACTTCATCCTCATCATCTGGCAAGAAGAGTAAAGGAAAGCTGCGCAAAAAGAGCGGCGGAACCAAGATTAATGAGACACGCGAAGACATGGACGCACAGCTGCTGGAGCGCCGCAGCACCAACTCCAGCGAACTAGACTCTCCTTCTCTGAGCGGCAGCCTTCCGTCTGTGGCCGACTCGCACTCCAGCCACTTCTCAGAGTTCAGCTGCTCTGACCTGGACGCCTGCAGACCTACATGCTACGAGTCTCACATCCGCCATCCCAACACAGGCGGAGCGGTCAGCCCTCTTCCCGAAGTCGAAAACGACCGGCTGGAAAACTGTCCTGCTTCTGGGAGCCTCCCTCAAGCTATGGTAGCCCCAATCTCCCCCGATGGGGCGGCAGAGCGTCCTCTGTGCTACATTGCAGAGGAGAATGTGAGTTTAATGTGTGCGGCTAATGCGAGC[C/T]AGAGCTCGCCTAAAGAACGCAATAACAACCTTCCTCAGCCAGCTAGCCCTGTGCGCAACACCTGCATTCAAACCGAGATATAACCAGACGGGTCGACTTCACCCAAAATGCTTTCACAGCTAACCTCAACGCCCATTTTATTACCAAGGATTGCACACTGAATTGAAGATTTTGTTTTGGTGTTCTTCTTCGGGGGTTACGTGGAGGTTTTAACGTCCTGGTCTGATGGTCGATTGTTGAAATGTTGGAGAAGGCGCACCACTTTTTACACTGGTCAAGGGCAGGTTGTGCCTTGAGGTTTCAGAAAGTTGACCAAAGGTTACAGTTTGATTACCAGGCTTTGTTAAGACCTGTCGGTCTGCGCTTCTAGTTGGTCTAAAGCTTGGATATGGTTCGGAAAGTCAACAGATGAATGTAAGGCGGCAAGTGATGCACAGATACTGAGGATGATGATGCTGTTGATGATGTAGCTGTCAATCACATATGCCTCTTTCAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23478
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024193 | Nonsense | 912 | 913 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 12655334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 12113680 |
GRCz11 | 19 | 12033208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACCTTCCTCAGCCAGCTAGCCCTGTGCGCAACACCTGCATTCAAACC[G/T]AGATATAACCAGACGGGTCGACTTCACCCAAAATGCTTTCACAGCTAACC
Long Flanking Sequence:
AGAAGAGTAAAGGAAAGCTGCGCAAAAAGAGCGGCGGAACCAAGATTAATGAGACACGCGAAGACATGGACGCACAGCTGCTGGAGCGCCGCAGCACCAACTCCAGCGAACTAGACTCTCCTTCTCTGAGCGGCAGCCTTCCGTCTGTGGCCGACTCGCACTCCAGCCACTTCTCAGAGTTCAGCTGCTCTGACCTGGACGCCTGCAGACCTACATGCTACGAGTCTCACATCCGCCATCCCAACACAGGCGGAGCGGTCAGCCCTCTTCCCGAAGTCGAAAACGACCGGCTGGAAAACTGTCCTGCTTCTGGGAGCCTCCCTCAAGCTATGGTAGCCCCAATCTCCCCCGATGGGGCGGCAGAGCGTCCTCTGTGCTACATTGCAGAGGAGAATGTGAGTTTAATGTGTGCGGCTAATGCGAGCCAGAGCTCGCCTAAAGAACGCAATAACAACCTTCCTCAGCCAGCTAGCCCTGTGCGCAACACCTGCATTCAAACC[G/T]AGATATAACCAGACGGGTCGACTTCACCCAAAATGCTTTCACAGCTAACCTCAACGCCCATTTTATTACCAAGGATTGCACACTGAATTGAAGATTTTGTTTTGGTGTTCTTCTTCGGGGGTTACGTGGAGGTTTTAACGTCCTGGTCTGATGGTCGATTGTTGAAATGTTGGAGAAGGCGCACCACTTTTTACACTGGTCAAGGGCAGGTTGTGCCTTGAGGTTTCAGAAAGTTGACCAAAGGTTACAGTTTGATTACCAGGCTTTGTTAAGACCTGTCGGTCTGCGCTTCTAGTTGGTCTAAAGCTTGGATATGGTTCGGAAAGTCAACAGATGAATGTAAGGCGGCAAGTGATGCACAGATACTGAGGATGATGATGCTGTTGATGATGTAGCTGTCAATCACATATGCCTCTTTCAGTGTTCTGGGTCGCTCTGATGAACAAGTACATAGATGAATCTCGCAAAAACGTCTTGCATAGTTCAACCCAAAATTAAAA
Associated Phenotype:
Not determined