ZMP
si:ch211-152m4.1
Ensembl ID:
ZFIN ID:
Description:
wingless-type MMTV integration site family, member 16 (wnt16), mRNA [Source:RefSeq DNA;Acc:NM_001100
Human Orthologue:
C7orf58
Human Description:
chromosome 7 open reading frame 58 [Source:HGNC Symbol;Acc:26159]
Mouse Orthologue:
A430107O13Rik
Mouse Description:
RIKEN cDNA A430107O13 gene Gene [Source:MGI Symbol;Acc:MGI:2444814]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38426 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20221 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38426
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 |
|---|---|---|---|---|---|
| ENSDART00000067251 | Essential Splice Site | 234 | 975 | 5 | 24 |
| ENSDART00000143690 | Essential Splice Site | 89 | 839 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 4 (position 9711226)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 10647853 |
| GRCz11 | 4 | 10646702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTTCCACATCTCCACTAGAGGGAATCCAAAATACTAATGATGCATGG[T/A]GAGTTATGTCAAGTATAAAAAAAATGGTCTACCAAAAATGTTGTAAAGGC
Long Flanking Sequence:
GGCTTTTTAATATTTTTTCCACATTTTTCAAGTGCCTTAGACTTTCTTTCGCTGTTTAATAAAAACATTGTTTTACTAAAACTCTCATGGATTTTATCATAAGCAATTGAGTATTTACCGTGACACTGAAAGTCATTTTAGCATGGTGGATGAAGCAAGAAAAATGTTAATTGCACATTCCAAAACAGCATGTAGACGTTTAGCATTAAGGCAGCTCGATGTGTTTTTGAACAGAGCTCCAGTTTATTTATGACTGAACAAACCAGCATGTGTGAGAAGCTGTGACAATCAACAACACATGTCTGGAGGTCTGCATCAAATATCTTTGGTCTTCATCTCGATGCATGTGCAGTGTGTGTGTCTTCCTCTGAGAACATCAATATGGCTCAGTACTCACTCTCTGTTTTTCAATCTCAGGAGCGACATTACCCATAAACCCCTCAGCCTGCGCCTTTTCCACATCTCCACTAGAGGGAATCCAAAATACTAATGATGCATGG[T/A]GAGTTATGTCAAGTATAAAAAAAATGGTCTACCAAAAATGTTGTAAAGGCAATGTTTTCAACAGCCCTATTGTGATTTGTATCCTACAGGAGGCAGCCAATCACACACAACCATTCAGACAATCAGGGATTAAATGCGACCGTAAACGTGTACGTCCTGGTTACTTCTGCAACACCACTGACCGCTTTCCTCCACCGCACAGCCCTGGTCAGAACTCCCCAGGATAAAGCTAGTTACGCCACTGAGGTAAGAAAACATTGTCCATCCACTGAGATGGATTAAATAAAGCAATATCTCTGCTTCTCAATACCCATGAGCTCAGAAATCATTATTAGGTGCCTTTTAGCTATTTTGATAAGCGATTATGCCTTTAAATCGGATCAGAGGAGAGTTCTCCAGTCTTAATATTGCTGCTTGGGTCTCTACGCTGCCATTTACTGATGATGATGGAGGCTTGGCTAAACATTTATTCCCCATGTGATGTTTATTAGGCCTCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20221
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000067251 | Nonsense | 654 | 975 | 15 | 24 |
| ENSDART00000143690 | Nonsense | 496 | 839 | 13 | 19 |
Genomic Location (Zv9):
Chromosome 4 (position 9752279)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 10688906 |
| GRCz11 | 4 | 10687755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTTTGGAGCCCATTCCAGGAGTGAGATCTTCAGGAGAGGCCCAGGCTT[C/A]ACTTCGGCCTTGCCTCTCAGGAGATGAACCTGGTATGTTTGCTTCAGGTT
Long Flanking Sequence:
GGCCTCGAGAAGCCCCTGTGCAAAGTGTTAAGGAAGGGGGCAAAAGAAAAAAGTGAATGGAGAGCCGCTCTTCAGAAGTCGAGCCAGACCCGATGGCTCCCGTGAGGGACCTTGAGGGTCGGCGGCGCGGCTTCGGTTCTGTCATTTAGCCTGTTAGGTTTGTTTGACCCTTAGCCCCTAACAAGGGGGCAAGGGTGCAGGGCAGGCGTCAAGCGGCGCGCATGCTTTAATTTAACCTCATGTACGCGGCCACATGAAAGCGAATGGGGTGAAAAGGCTATGGAAACTTTGCAACAACTCTATCTATATCAGATTTTATTTTCTTGAAAAGTTTTTTTTTTTTTACATAAGAGTGCCACCATGAACTTACCAGACTCCAACCTGTATCTCTTCTTTTCTCACCCTGTCGGAGCAGGACTGCGGCCTAGTCGTCCGGCCAGACCAGCCCTGCGGTTTGGAGCCCATTCCAGGAGTGAGATCTTCAGGAGAGGCCCAGGCTT[C/A]ACTTCGGCCTTGCCTCTCAGGAGATGAACCTGGTATGTTTGCTTCAGGTTTTGATCACCGGCTTGTAATTAAACATCTGAAATTTGAACTTGAAAGTTGCTGTAAGATTTAAAGTCCTGTTTTTCATGCAAGGCCATTGCAAAGTGTCTGTTTTATGGTCGGATGATATATTTACCGCCCATTTTTCTTTCTGTGCACAGGATCATGTTGGCCTTAAAACTGTATATTTTAGTTACAAAGTAGTTCATCATGTGTTTGGCTATATTAGCTTGAGATTCACGGTTTATTAGCTGCTACACTGGAGAATAGGAAAGGTTTGGTAGAGAACTGAAGGTTGGTAATTTATGTGTCTGCTTTTACTGTGTGATAAAGTTCTGATTCATCGCCTGAGTTGAATCATTGCTCGATTATAAGGTTAGGACTTCCATGCTGACTTTATGAGGGAATATAATCACTTCATACAGGTTTTTTTGGAGTGAGTTGTCCTTCTGCAGGGACAT
Associated Phenotype:
Not determined