ZMP
rnf44
Ensembl ID:
ZFIN ID:
Description:
RING finger protein 44 [Source:UniProtKB/Swiss-Prot;Acc:Q08CG8]
Human Orthologue:
RNF44
Human Description:
ring finger protein 44 [Source:HGNC Symbol;Acc:19180]
Mouse Orthologue:
Rnf44
Mouse Description:
ring finger protein 44 Gene [Source:MGI Symbol;Acc:MGI:2145310]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18224 | Essential Splice Site | Available for shipment | Available now |
sa42444 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18224
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099235 | Essential Splice Site | 232 | 448 | 5 | 11 |
ENSDART00000146134 | None | None | 83 | None | 3 |
The following transcripts of ENSDARG00000068582 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 47759135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 45802335 |
GRCz11 | 14 | 50953567 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCGCCGATCAACCAGTTCGTCCCCATTCAGCCGCAGCACCCGCGCATGG[T/C]GAGTAACACTCMGGCAACACAAACTACCATAAATCATACCYGTCAACCCT
Long Flanking Sequence:
AATTAATGTATGTGATAGATTATTTCTAACATATAAATGAATGTTTTTTTTTGCATTGTATAAATTGTGTATACATGCATCACGTTTTCCCAGTACTATGCAGGATTGCTTATCATTAAGCCTGATGCTTTTGAAATAATATATTGGATTGCTACACAGTGCAAAAGTGAGATCTTTTCCAGAGCATTTGACCATGTCTCTTTCTCAGCGTTATTAGAAATATACAAACACGCTTTCAAGTCACAGTCCATTTCAGTGTTCTCTCTCTCTCTGTGTGTGTGTGTGTGTGTGTGTGCAGCTCATTCAGGCCTGCACCATGCAGCATCTGCCGGTGTCCTATCAGGCGTTCCCTCCGCTGATCTCCAGTGAGCATTTCATCCTGCACCCCAGTCCTGCAGTGGCGCCCCACCAGCCTCCACCTCACCCTCCTCATCCTCCTCCTCCTCATCTGCCGCCGATCAACCAGTTCGTCCCCATTCAGCCGCAGCACCCGCGCATGG[T/C]GAGTAACACTCAGGCAACACAAACTACCATAAATCATACCCGTCAACCCTCCAGTTAGTATCAGGATTCTCCGGTATTTTACACTTCTATCCCGCTATCATCCTGTATTTTTAATCTTTCTATGAAGGGTGGCAATAAACATTAAAGCTTCAATCCTCCCTATACACAACCCATACCGCCGAACCACCAGGGGCCGCCCCTCACTCTTAAATGCGAGTCTGTTCTGTGCTTTCGGTTTGTTTAGGCATGAAAACACTTTAAAATAAATGTAAAAACGGCGGGATTCCCTTTTCTTTCCATTCCAGGTGTCATTGCCTCTCCTATGCAATCCTCAAACCAGTCAGTTCATATAGCAGTGCGTGACTGTCAGCTGACGTGCTCCATAGTGATAAATAGACGCTGCTTCCCAAACGGATTCTGCACACGTGATTAAAGCAGAGCGAAAGTGGACACACTGGGTTTTGGGTGCGTGTTTGAACAGACATATGTACATATTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42444
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099235 | Nonsense | 299 | 448 | 7 | 11 |
ENSDART00000146134 | None | None | 83 | None | 3 |
The following transcripts of ENSDARG00000068582 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 47748501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 45812969 |
GRCz11 | 14 | 50964201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGTTTCCTCAGCCATATCCACACATGCTGCCGAGGCGTATAACGGGA[C/T]AGAGGTATCGGTTACAGCAGCCTCTGCCTCCGCCGCCGCCTCCACCGCCG
Long Flanking Sequence:
AGGAACGAAGCTATTTCTGTAATGCGGAGTCCTGCTAATATCCCTCTGAAAGTGGATAAGCCGTAAGATCTGCCTACTATACATTCAACATGCAACACCGCAATCACTGTAATCAGGTCAACACTCATCGCAATCGGCAGCATTTGCATAAGCAGGTAATCAAATTATGCTAAATAAAAATGTCTAGTCATGTAAAAAAGTGGTTCCTAGATTGGGGTTGGGACCAGGGTGAGAGTTATACATTGACAATCGGGGGTCAACAACTTTAATGATGTTAGTTTGCGTAATACATGTGGTCACTGACAGTTTCTTTGTATACTCGGCACTCGTTGCGTGTATTGCCTCTTCTTGTTGAATCATTGAATGCCTCCTCAATTGTACGTTGCTGTGGACAAAAGCGTTTGCTAAATGTTAATGTAATTGTGCATTGTGCATGTGTTGTGTTTGCGTCTGTGTTTCCTCAGCCATATCCACACATGCTGCCGAGGCGTATAACGGGA[C/T]AGAGGTATCGGTTACAGCAGCCTCTGCCTCCGCCGCCGCCTCCACCGCCGTATTACCCCGGCTTCCTACCATACTTCCTGTGAGAATCCCTAACATGCACATCAGATGTTTCTACACTGTTCAAAGTCGGAGTTTAACTCTAAAGCATTTGTTTGTGCCCTGTTGAACAGCTCGATGCTTCCTGTGCCTCCAACTGCTGTGGGTCCTGCTATCAGTCTGGACCTGGATGTAGACGATGTGGAGATGGAGAACTATGAGGTAAATGGAGGATATAGAAAATGCTGCCAGCCATCATCAGACTATTTTCAGCTGGGAGTACATGAGCATATTAGGGCTGTGCAATTAATCGAAAATCCGATTTCGATTTCGATTTTGGCTTTTAACGATTATGAAAAACCATTAATCGAGATAAACGATTATTCCATCACGTACCGCCTCCTTTCCAGTTGTACACGTGTGAAAACTCTTTGCCTCTGCAAAGCTCAGTTCCACGTGAAAAT
Associated Phenotype:
Not determined