Busch Lab

ZMP

rnf6

Ensembl ID:
ENSDARG00000077955
ZFIN ID:
ZDB-GENE-100209-1
Description:
Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:B4F6Q6]
Human Orthologue:
RNF6
Human Description:
ring finger protein (C3H2C3 type) 6 [Source:HGNC Symbol;Acc:10069]
Mouse Orthologue:
Rnf6
Mouse Description:
ring finger protein (C3H2C3 type) 6 Gene [Source:MGI Symbol;Acc:MGI:1921382]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa6766 Nonsense Mutation detected in F1 DNA Not yet available
sa15269 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa6766
Status:
Mutation detected in F1 DNA
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
ENSDART00000109587 Nonsense 333 713 4 4
Genomic Location (Zv9):
Chromosome 24 (position 22113308)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 21360186
GRCz11 24 21505360
KASP Assay ID:
554-5327.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTTCAGCCTCAGTCTGACCCCCAGGTGGCGCCAGCTGCCCGTGAGCCA[C/T]GAAACAGTAGGACTCGTTCACGTGGTCGTGTGCGCCGGGCAGCAGGTGCC
Long Flanking Sequence:
AGCCTGGTGAACACAGCGACACCCCTGACCCAACTGATCTTCCAATGCCTCCCCCTCCTCCTCCTCCCCCTCCCCCTCCTCCTCCTCCTCCAGTGCAATCTGCCTCTCCACCCACAACCCCTTACAACCCTTCAAGGGCTGCACCCTACTCACTTCAACACCCCACGCCGTACTCCACGAGCAGACCCACCCTGGGAAGAAGAGGCGCAGTGCGCCGCACTCGCAGTAGCACCACTCCGCCTGTAATGCCCCCTATGACCTCACAGGCTCCTCCCATGCCTCTGAGAAGGAACTTGCCTACTTTGCCAAGCTCTCCACCTCCACAGGCTCCACTTGCTTTTCAGTCACAGGAGACGGATGGTGGTGCTGTTCGGAGTCAAATACAGGTCACGACCTCCTCAGTCAATACAGGAGTGGAGCAGAATGGAAGTGAAGGCCCAGACTGCCCTAATGTTCAGCCTCAGTCTGACCCCCAGGTGGCGCCAGCTGCCCGTGAGCCA[C/T]GAAACAGTAGGACTCGTTCACGTGGTCGTGTGCGCCGGGCAGCAGGTGCCGGAGGGGCTTTATCTCGTTCTTCGAGAAGAAGCCGCTCGCCTCTGGACAGAAACACCGCCTCCAGTGTTAGTCCCACCCACAGCAGCAGCAGCAGCACCCCCCCAGTGGAGTCTGCTGGGAGTACAGCTGTTAGTATGGAGATGGGCCAACCCACCGCAGAGCCAACTGCTCCTACAGATCCTCCAGAGGCAGGTGAGGAAGAGGGAGAGACGCCTGTATCAGGTGCTGGAGGTGTTCGTCGTCACCCCACAATCATGCTGGACCTGCAAGTGCGGCGCATCAGGCCAGGAGAGAACCGGGACAGAGACAGCATCGCCAGCCGCACGCGCTCTCGTGCTCGGGCTGCTGAAAACACAGTCACCTTCGAAAGCGACAGCGGTGGCTTCCGGAGAACAATCTCACGCTCAGAGCGTGCGGGTATTCGCACTTACGTCAGCACTATACGCATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15269
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109587 Nonsense 641 713 4 4
Genomic Location (Zv9):
Chromosome 24 (position 22112384)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 21359262
GRCz11 24 21504436
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCAATGAAGATGAAGAYGAGGAGCACCCACGGGGCCTCACCAAAGAA[C/T]AGATCGACAATCTGGTCACACGCACTTACGGTCAGGTCAACCTGGAGGGT
Long Flanking Sequence:
ACAGCGGTGGCTTCCGGAGAACAATCTCACGCTCAGAGCGTGCGGGTATTCGCACTTACGTCAGCACTATACGCATCCCATTGCGGCGCATTTCTGAGACAGGCCTCGGCGAGCCCAGCTCCATGGCATTGCGATCTATTCTTCGCCAGATTATGACCGGCTTTGGTGAGCTCAGCTCCCTCATGGAGACGGAAGCAGATTCAGAGACTGCGACGCCCAGCCAGGACTCTGCTCCCGCTGCTGGAGCCCAGACATATCGCGCTGCTGGTGCAGAGGGTGGAGCCACCCATGGCGGAGTTGAATCAGCACGGGAAACTTTAGGGGAGGGTGAGGAGGAAGGACAAGTGCGGGTGAGCAGGACTGGGCCGGAGGGACGACCTAGCAGCAGAGACACTAACAACCTAGTGGAAAATGGCACATTGCCCATCCTAAGGCTTGCACACTTTTTTCTTCTCAATGAAGATGAAGATGAGGAGCACCCACGGGGCCTCACCAAAGAA[C/T]AGATCGACAATCTGGTCACACGCACTTACGGTCAGGTCAACCTGGAGGGTGAGCAGGGCCGCGCTTGCAGCGTTTGCATCAATGAGTACGCGCAGGGCAACAAGCTGCGCCGCTTACCATGCGCCCACGAGTTCCACATCCACTGCATCGACCGCTGGCTCTCTGAAAACAACACCTGCCCCATCTGCAGGCAGCCCATCCTGTCCAGCCATCAGGAATGATGTCAGGCTGTAGCTATCAATCAACAGACTGAACCAGTGACTTTTATTCTGCCGTCGGTGGCAGCTGTACATAGTGCTTCAATGTTTTCATTCTCTGAGATCCATTGTATTCAAGCTAAAGGTAGAACCAAAAGCAGAAAAAGACTATAATGCAGAGATTTAACAAAGCTTTATTTTTTTAGACTCCTTTTGTTTTCCTCTTCTTCCATTTTCCATTAAGCTTTGCGGAAACATTAACAGATGGCATGACTAACTTGGATGGAGTTAGGAATGTTAACT
Associated Phenotype:
Not determined