ZMP
foigr
Ensembl ID:
ZFIN ID:
Description:
UPF0636 protein C4orf41 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q1RLX4]
Human Orthologue:
C4orf41
Human Description:
chromosome 4 open reading frame 41 [Source:HGNC Symbol;Acc:25751]
Mouse Orthologue:
D030016E14Rik
Mouse Description:
RIKEN cDNA D030016E14 gene Gene [Source:MGI Symbol;Acc:MGI:2444585]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22424 | Nonsense | Available for shipment | Available now |
sa30977 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22424
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 |
---|---|---|---|---|---|
ENSDART00000054809 | Nonsense | 693 | 1132 | 20 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 7305894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 7031373 |
GRCz11 | 14 | 7337782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGTCTGGTTTTGTCTTTCAGATCACCAGTGTGGGACTAATGTTAGGT[C/T]GAGAAACGGGCCGTTATGTTTATCTGAATTGGCGGGGCGGTTGGGGAGAT
Long Flanking Sequence:
CACGTTTGTATTTACCTGTAAAGTTGTTTGGGAAATTTTCTTGATATTTACTTGTATCACTGTGTGAAAGGGTCTAATGCAGGGGTGGGCAAACTTGGTCCTGGAGGACCGGTGTCCTGCACAGTTTAGCTCCAACCCTAATCACACACACCTGCTTATAGATTTCGTGTGATCTTAAAGACACTGATTAGCATGTCCAGGTGTGTTTGACTAGTGTTGGAACAAAACTCTGCAGCGACACCGGCCCTCGAGGATCAAGTTTGCCCATCCCTGGGCTAATGGCTGCTTTTTTCTAACATTCCTCAGTATATCTTGTCTTTTGTTCAACAGAAAAAAGAAACTTAAGTAAGTTTAGAACCACTTGAATCTGAGTAAATATTTTGGGTGAGCTGTCCATGTAAATTCAGATCTTGTGTTGTCACAGATTTACAGCTGATTAGTTTGTTTGATGTTTGTCTGGTTTTGTCTTTCAGATCACCAGTGTGGGACTAATGTTAGGT[C/T]GAGAAACGGGCCGTTATGTTTATCTGAATTGGCGGGGCGGTTGGGGAGATGCGGCCTCTTCCCATGAGAGTTTGCAAGCTTCCCGCTCATTTAAAAGGAGGACACGCCTCCCAGAGCAGCATGTGGACTGGGACGCAGTGTCTGTACAGTCTAGTACCATGTAAGTTAATAGAAAATCTGAAAAACTAGTATATCGCTTCAGAAATTAATGATTTAAATCATAGGTCTTAAAACATTTTTAACTCTCAAATGGTTGTTGTCAAGTCATTGGTTAGTGACTAGACATTTAAGTTTCATTCAAAATGTGCCGAGTTCAAATTAATAAGGAATAAACAGCTAAGTTTTCCTTTCTGTATTCCCTGTAGGATCATCTCTAGAGTGCCCAAAATTTCTGTACAGCTGACCCATGAGCCTCCAGCACTTACCAATGAGATGTTCTGTATGACTGTTACCATCAAATCAGAAGAGGACACTGTGGGTAAAGACATCAAACTCACTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30977
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054809 | Essential Splice Site | 898 | 1132 | 24 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 7303714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 7029193 |
GRCz11 | 14 | 7335602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAAACGGTTGTTCCCTTTGAAGTGGCTATGAAGTTTGTGTCCAGTAAG[G/A]TAAGAGGTTTCACTTGGGAGATTTCGGTAATGAAAATCCGTAGTCGTTTA
Long Flanking Sequence:
TGACGATTCTCATCCTGCCCTGCTTCCTGACATTCCCCTCGGAGATCTGCAACCTGGTCAGAAGGTACCGCTTCTTTTGCAATGATGAAAATATTCATCCAATGGTCTTGGCTCTAGTGCACTGTTGCATACGTTTTGTTATCTTGTGTGGCAGATTGTGAAGCCTCTGTATATCCGCTGTGTGAGCACTGGATCCAGAATATTCCTGTTTCATGTAGCCTATTCAGTGAGTGCCACGGTCGAGGGCAAGGACATCACTTGCAAGTGTCACAAAGTACGTCAAATTCTAACATCTTGTCATCATCATGTAATTGCTTGCTTAGGATCCCTAGGAAAAGTTTTTGTTCCAAATCACACATAAAACTTCATTTTTGAATAATATTTACTCTGGTGGTCAGTATCATTCAGAGTTGTTGTGTGTTTTTCACCTGCAGGATGAAACTGTTACAGTAGAAACGGTTGTTCCCTTTGAAGTGGCTATGAAGTTTGTGTCCAGTAAG[G/A]TAAGAGGTTTCACTTGGGAGATTTCGGTAATGAAAATCCGTAGTCGTTTACATGTTTCAAGCCCAAATTATTGTCTCTCTTCTGTGAAAAACAAAACTGTTTATCTGTATTTTTCAATACTACATACAGAGGTAGATAGGGTATATGCCGAAGCATGCTAATAGGACTTTTAATTTGCCAGCAACCTGGGTTAATCGTTTCCGGTGAACAGTCTGAATGGTCTGTTTTCTTTAAAAATCAGCGATCTCCACTGGCTGAGTGATATCCGATATAAAGTGGGTCTCAGATTGTACAAGAAGCACTGCATTAAATTACATTTTTCCCCGCCATGTCTTTATAATATGAGTATTTATTTTACCTCAGTATATTTAATGGAGCTTCTGCGCTAGCCTGCCGATTCTGATGGGCGAGTGCGAGCACACTGCTTTTTGTCTCGTTTTACTCTTGAGGAACTAAATGACTGCCAAAGTCTATTTAACTTAATGTATTTGAATTACATT
Associated Phenotype:
Not determined