ZMP
rnf141
Ensembl ID:
ZFIN ID:
Description:
RING finger protein 141 [Source:UniProtKB/Swiss-Prot;Acc:Q6IV56]
Human Orthologue:
RNF141
Human Description:
ring finger protein 141 [Source:HGNC Symbol;Acc:21159]
Mouse Orthologue:
Rnf141
Mouse Description:
ring finger protein 141 Gene [Source:MGI Symbol;Acc:MGI:1914400]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36611 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32198 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36611
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061265 | Essential Splice Site | 173 | 222 | 5 | 6 |
ENSDART00000123898 | Essential Splice Site | 173 | 222 | 4 | 5 |
ENSDART00000136320 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 16412631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16764397 |
GRCz11 | 18 | 16753463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTCTTCCCTGTGCGCACAGCTTCTGTCAGAAGTGTATTGACAAGTGG[T/A]AAGAGCTCATCATTTAATAATGACAGTTCTTTTAGTGTTCCTTTATGTTG
Long Flanking Sequence:
ATTAATAAGTTTGACTAATTATCTAGTAACTAATAGCTTTTATAGGCAGGTAGGCTTACTATAAATATATAAACATTGTTAATATGCAATTATATAGTCTATAGGCCCACATATTAGCCCACGTATACATATTGTTTATGTATAGATGTTCAGTTAAGTGTATGTGTTTGAACTGAGAGAGTGTGTCCGAGTCTCAGACATTATCAGTAAGGTTGTTCTAGAGTTTAGGAGCCATATAAATGAGAAGGCTCGACCTCCTTTAGTGGACTTTGCTGTTCTGGTTACTAGCCAGTTATTGTTCGGTTTAACAAATCTGCATGAAATGTTATGATGCGTAATGGAAGACTCCTTGTTTACTTTAGCTAATAATGCTATCTGTGCTGTGTAACAGGGTAAAACAGTTGACTGATGAGGAAGAATGCTGTATCTGCATGGATGGGAAAGCAGATCTTATTCTTCCCTGTGCGCACAGCTTCTGTCAGAAGTGTATTGACAAGTGG[T/A]AAGAGCTCATCATTTAATAATGACAGTTCTTTTAGTGTTCCTTTATGTTGTTCTAAATCCATTTGACTTGAGCTCTTCTGTTGGGGAAAAAAAGAAGATATTCTGAAGAATGATGAAGTCAGTAGAACTGTTTAGTCATCTGCATTCTTTAAAATATTTTCCTTTGTGTTCACAAAAGAGAGACCATTAATTTAGTTCAGTTTTATTAATTTTTTATTGAACTTTAATGGATTAGTTCATCCAGATCATTAAAATGGTTTACTCACCCTCATGTTGTTCCAAGCACACTATTCATTAATTACCCTTTTTTCCTCTGTGGAACGCTAAATGACAAATTATGAAGAAGTTTTTGTTCAGGACTGGTGCTTATCATTTCCAAAATGAGTCCTTTTAGACCACCTTGAGCTGGATCCAGGGTGTCTGTATAATTATTTTTATATAAAATGTAAGACTTTTTTTTAAGACATGCACAAATAAAATGAAATTCATATGTCCCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32198
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061265 | Nonsense | 194 | 222 | 6 | 6 |
ENSDART00000123898 | Nonsense | 194 | 222 | 5 | 5 |
ENSDART00000136320 | None | None | 131 | None | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 16415133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16766899 |
GRCz11 | 18 | 16755965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAACTGCCCCGTCTGCCGGATTCAGGTGACTGCCGCTAATGAATCCTG[G/A]GTCATGTCGGATGCTCCCACAGAGGAAGATGTAGCCGGGTACATTCTCAA
Long Flanking Sequence:
CTTTCTTGAACATGACAGGGAGGTCACTGTACTCATATGGCCTCCACAGTCACCAGATGTCAATCCAATAGAGCACCTTTGGGATATGGTGGAACGGGAGATTCGCATCATGGATGACTAGCCGACAAATCTGCAGCAACTGCGTGATGCTATCATGTCAATAAGGAATATTTCCAGTACTTTGTTGAATCTATGCCATCAAGGATTAAGGCAGTTCTGAAGTCAAACCGCGGACCAACCTGGTACTAGTAAGGTGTATCTAATAGAGTGGCCGGTGAGTGTATTAACACATGCAAATTAAAGCTCATTTAATTGATTTATGAGGAAATCAGAAAGGAATTTAGAACAACATTATTATACCACACACAGCCGCAATTCCTAAATCCTTTTCATCGGCCATGACTAACCCTATGCCATTATGTCTGTGCCTCATACAGGAGCGGCCAGAGCCGAAACTGCCCCGTCTGCCGGATTCAGGTGACTGCCGCTAATGAATCCTG[G/A]GTCATGTCGGATGCTCCCACAGAGGAAGATGTAGCCGGGTACATTCTCAATCTTGCGGACGAAGCCGGTCACCCACACAGACCTTAAAAATCTAACACTGTGCCACTCTCATGCTCACCATCTCCCCATAAAAGACCACCTATATATAGTTTTCATAGGGTGACTGTGGGTATTTGTATTGTCACTCACTGGAGGCAATAACAGCTGATCATTTGAATTTTAAACACACTTTTAGGTTTAACACATGTCATAATAGATCCATAGACTGTAAACATTCAGTATGTAGGACGACAACATCTGCTGTAGCACATCATTGCCTCGTTATACTTGCTGTTTTATCTGGTTTGTGAAGTAATTGCACTTAATTGCGTTTGTTCTGTAAAGGCCTTGTAATACCTAACAAAAAGCATCACAGTGTCAGCACGTGCAACAGTTAAGTAGTATTGATGCTGTACTTTAATAACGCTGACTTTACAGTCGATGTGCGTTTATAATCTAAG
Associated Phenotype:
Not determined