ZMP
zgc:153720
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC767719 [Source:RefSeq peptide;Acc:NP_001070125]
Human Orthologues:
VWDE, WIF1
Human Descriptions:
WNT inhibitory factor 1 [Source:HGNC Symbol;Acc:18081]
von Willebrand factor D and EGF domains [Source:HGNC Symbol;Acc:21897]
von Willebrand factor D and EGF domains [Source:HGNC Symbol;Acc:21897]
Mouse Orthologue:
Wif1
Mouse Description:
Wnt inhibitory factor 1 Gene [Source:MGI Symbol;Acc:MGI:1344332]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7384 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7384
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084891 | Missense | 76 | 189 | 2 | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 39845341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 38764740 |
GRCz11 | 1 | 39482813 |
KASP Assay ID:
554-4292.1 (used for ordering genotyping assays)
KASP Sequence:
ACGGAGGCCACGTCAAAGAGATGGTCCACCGAGAGGCAGACGARTATAGC[C/T]GCCARGKTGAGTCGCCCATGACTTCACCCMGTCCACAGGTCACATGACAC
Long Flanking Sequence:
AAACTCTCTCACACTGTCCCCTGAAAGACGGTATCTCCCAACAGTCCAGAAGGTGTAAAGGATTTCTGAATCCTGGGAAGATTGTGTACAGCCTTGTGCTGTGTGACCGCTAGTTTACACTTTTTTTTAAAAGGAATTCTTTCTGTCTCTCTTTTCCAATCCCCTCCTCTCACTCTCCAGGTAGACAACAGTAAGCTCACATTTGGGCAGAGCCTGTGGCGAGCGAGCGCTCCGATTGGTTGCCGCCTTGTGTTTCACCGCGTCATGCGGGCAGGATGGATGTGAAAGAACGCAGGCCCTACTGCTCATTGACTAAGAGCAGGAGAGAGAAAGAGCGCCGCTACACGGGCTCATCGGGCGACAGCGAGGACTGTCGCGTGCCCACCCAGAAGTCCTACAGCTCCAGCGAGACGCTCAAGGCCTTCGACCACGACTCCTCACGTCTGCTTTACGGAGGCCACGTCAAAGAGATGGTCCACCGAGAGGCAGACGAGTATAGC[C/T]GCCAAGGTGAGTCGCCCATGACTTCACCCCGTCCACAGGTCACATGACACAAACTGGAAATAACATGTGCCTAAAAACACGTCAAGAATGCGCTCTTGGACGGATCGCACTCAGCTAATAATATATGGGATGCACAACCATAATTACACATAATTAGAGGAAATTAAGTTTGGTTTGGCACAACCGAGTGCTTTCTTTGAGAAAACATTTACTTACTTTTGATTGAAAAATGAAGCAGATTCAAAAACAAATTAGACAGATTTATGGACCCCAAATTTGCTCGGCTACTTGTCTAGTCGACAGAGCGAAGAATGAAGAAATAAGGCATTTCCTTAAGATTAGCAAAACCAAAACCCCCTCATCCCAGCCTCTCATTTTCACATCCTAAGTTTCCCTTAGAACATATGCCCATGTGTCCCATCGGCAGTAATGAATGGTACCATAAAAAACATAAACAGCATTATTGCACTGCTCTGAAGTTTGCAGTGTGCCCTGCCCGG
Associated Phenotype:
Not determined