ZMP
zgc:123251
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Zgc:123251) [Source:UniProtKB/TrEMBL;Acc:B8JJR0]
Human Orthologue:
WDR27
Human Description:
WD repeat domain 27 [Source:HGNC Symbol;Acc:21248]
Mouse Orthologue:
Wdr27
Mouse Description:
WD repeat domain 27 Gene [Source:MGI Symbol;Acc:MGI:1918932]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42249 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35546 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35547 | Nonsense | Available for shipment | Available now |
sa38958 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14036 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42249
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075414 | Nonsense | 29 | 450 | 2 | 13 |
ENSDART00000112947 | None | None | 255 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 35750627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35403203 |
GRCz11 | 13 | 35529035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTCTCTGTAACCTGCAGTAAGCCGGTTTCCCATCTTCAGTTGGCGTG[C/A]TGTCCTTCTCATTGTGCCATCCCATGGAAGGACAAGAATATTAGGATTTA
Long Flanking Sequence:
AATATTTAATTAAAGAAACTCGCAATCCGACAGTGCAAATTAATTGTCCCTCCTGGTGTGCCGTCCCAAGTAGGTCCCGTTTCCAAAGCAACAGCGACACTATCACAGACGCCACAAGTTTATGAGCGTTTTACTTTCAGGTGAGTGATGATAAACGGAATTAATTAATTAAGTTTTGCTGCTGATGTTTTTTTCACGTCTCACAAATTCAAAAAACGTTGAACATTCGAGTAAAGGTAAAAAAAAAAGTCTAACGTTAATCTTCAGAAAACCACCTGTCTGAGGTGCTAACGTTAGCTAACGGTAATAATAGTAGTTTGCTACGTTAGCTGTTATCTGCTCTGCAAAACATCTAAACACTTTTTCTCAGCCAGACTTTATCATTGTCTGTTACAGGGGAATGTTGGAGACAGCATGGCTGATGTGACCTCAGAGCAGTATTTTATTGAAAGGTTCTCTGTAACCTGCAGTAAGCCGGTTTCCCATCTTCAGTTGGCGTG[C/A]TGTCCTTCTCATTGTGCCATCCCATGGAAGGACAAGAATATTAGGATTTATGAAAACAAAATCAACAACCTGGAGGTTATTGTGCACTAATAGTACATCTGGTCTCACCAATCAGTTCATAGGAACCTTGAGTTTACTGGATTTTATCACATTTGTCCTCCACTATTGCTTTAATTCATCATGGCATGTTATCAAAAATGTATTATTTTTTCAATTACCTATTCCCTAAAAACTTATTTAAGGCAGACCAGCCCTCTAGCACTGTTTTCCCGTTCTCTCAAACCCAACCCCTCCCTCCCTTCCTCCCTCTATTTCCTCGCTTTCCATTAACAATTCTATACCCCTCTTTCCGATTCTCTAGGTTGAATCGGGGAGTCCAATCCCTCTACCAAAATATTACAGAGACGGTACCCCCACTCTTGAGTCTCACTCTTCCCTTTCTCTGCGTCCCACTATTCCCTTATCATCCCTTTCATCTCTGCATCCCTACAATAAAGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35546
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075414 | Nonsense | 225 | 450 | 8 | 13 |
ENSDART00000112947 | None | None | 255 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 35754251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35406827 |
GRCz11 | 13 | 35532659 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACAGTACAGCACCTGTGTTAACTGAATTTTCATTGTGATTCAAGCTTT[G/A]GTGCTACACTCTCCCTGTGGACCACAAATGTCGCTTGGTGACAAAACTGG
Long Flanking Sequence:
ACATATTCTGGATAAGTTGGCGGTTGATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTAAGCTGAAAAGAAAATGAATGAATAAACCAAACCAGCAAAACTTAACTCTTATTTTTTCATATATGTTTATCTAAATTATTAATACTTTTTATATATACCAGATATGGGATGTGAAGAAGGGGGGTATCCTCTTTGAATCTGCTGTCCTGTCAGGTAAGTGTGTAAAATCTAGCACCATATTTACACAACAGAAATTGAGTTTCTTCACACATTATAGCCTGTAAATGTAGAGAAATTGAAGATGCTTACATTTTATTTTCACAGCATATCCACTGTTAAGTCTGTCCTTCATGAAGCAAAATGGTCAGTTCATCACAGGATCTGGTGATGGACAGGTCAGTCACACACACATAAACACACAAACACAGGCTTTGACCTCTGTATTTCATACAGTACAGCACCTGTGTTAACTGAATTTTCATTGTGATTCAAGCTTT[G/A]GTGCTACACTCTCCCTGTGGACCACAAATGTCGCTTGGTGACAAAACTGGACCTTTCAAAACTTGAACAAAAGCATGAGAGAAACCTCCGGATGATCAGCCCTCCTCAAAGTAGAACAGATGGTTAGTAAAACCATAAGCCACATTTCAGACTACATATGACTACTGTTTTCACATGCCTATCTCACTGTGGAAACAATACATCTGTTTGAAGTGAAAAAGATCTTCGGGAGCCTCATCTGTGTACTTTTCTAGGAACGGCTCGGTGTGATGAGAGAGGAGCAGTCGAGACAGCAAAGCCTGTACTGAGAATCTGGCCACAGACACCAAAGATTAACCATGCTAGCTTGCAGCAGAGGTACTGTCTTTGGTCTGTTTTTGTTGTTCACCTTTATCTGATTGAGCTCCTGAGAAATGATTTAATGGTACTGTATGTTTTGTAATAGGACTGTCACAAGATTAAATTTTCACGACATGCTTTTCAACAGTCAATAGGTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35547
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075414 | Nonsense | 235 | 450 | 8 | 13 |
ENSDART00000112947 | None | None | 255 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 35754282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35406858 |
GRCz11 | 13 | 35532690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTGTGATTCAAGCTTTGGTGCTACACTCTCCCTGTGGACCACAAATG[T/A]CGCTTGGTGACAAAACTGGACCTTTCAAAACTTGAACAAAAGCATGAGAG
Long Flanking Sequence:
GCTGTGGCGACCCCAGATTAATAAAGGGACTAAGCTGAAAAGAAAATGAATGAATAAACCAAACCAGCAAAACTTAACTCTTATTTTTTCATATATGTTTATCTAAATTATTAATACTTTTTATATATACCAGATATGGGATGTGAAGAAGGGGGGTATCCTCTTTGAATCTGCTGTCCTGTCAGGTAAGTGTGTAAAATCTAGCACCATATTTACACAACAGAAATTGAGTTTCTTCACACATTATAGCCTGTAAATGTAGAGAAATTGAAGATGCTTACATTTTATTTTCACAGCATATCCACTGTTAAGTCTGTCCTTCATGAAGCAAAATGGTCAGTTCATCACAGGATCTGGTGATGGACAGGTCAGTCACACACACATAAACACACAAACACAGGCTTTGACCTCTGTATTTCATACAGTACAGCACCTGTGTTAACTGAATTTTCATTGTGATTCAAGCTTTGGTGCTACACTCTCCCTGTGGACCACAAATG[T/A]CGCTTGGTGACAAAACTGGACCTTTCAAAACTTGAACAAAAGCATGAGAGAAACCTCCGGATGATCAGCCCTCCTCAAAGTAGAACAGATGGTTAGTAAAACCATAAGCCACATTTCAGACTACATATGACTACTGTTTTCACATGCCTATCTCACTGTGGAAACAATACATCTGTTTGAAGTGAAAAAGATCTTCGGGAGCCTCATCTGTGTACTTTTCTAGGAACGGCTCGGTGTGATGAGAGAGGAGCAGTCGAGACAGCAAAGCCTGTACTGAGAATCTGGCCACAGACACCAAAGATTAACCATGCTAGCTTGCAGCAGAGGTACTGTCTTTGGTCTGTTTTTGTTGTTCACCTTTATCTGATTGAGCTCCTGAGAAATGATTTAATGGTACTGTATGTTTTGTAATAGGACTGTCACAAGATTAAATTTTCACGACATGCTTTTCAACAGTCAATAGGTTTTCAAATTTTTTATTTTTTTTTATGTCATTGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38958
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 |
---|---|---|---|---|---|
ENSDART00000075414 | Essential Splice Site | 265 | 450 | 8 | 13 |
ENSDART00000112947 | None | None | 255 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 35754374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35406950 |
GRCz11 | 13 | 35532782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGAGAGAAACCTCCGGATGATCAGCCCTCCTCAAAGTAGAACAGATG[G/A]TTAGTAAAACCATAAGCCACATTTCAGACTACATATGACTACTGTTTTCA
Long Flanking Sequence:
ATATGTTTATCTAAATTATTAATACTTTTTATATATACCAGATATGGGATGTGAAGAAGGGGGGTATCCTCTTTGAATCTGCTGTCCTGTCAGGTAAGTGTGTAAAATCTAGCACCATATTTACACAACAGAAATTGAGTTTCTTCACACATTATAGCCTGTAAATGTAGAGAAATTGAAGATGCTTACATTTTATTTTCACAGCATATCCACTGTTAAGTCTGTCCTTCATGAAGCAAAATGGTCAGTTCATCACAGGATCTGGTGATGGACAGGTCAGTCACACACACATAAACACACAAACACAGGCTTTGACCTCTGTATTTCATACAGTACAGCACCTGTGTTAACTGAATTTTCATTGTGATTCAAGCTTTGGTGCTACACTCTCCCTGTGGACCACAAATGTCGCTTGGTGACAAAACTGGACCTTTCAAAACTTGAACAAAAGCATGAGAGAAACCTCCGGATGATCAGCCCTCCTCAAAGTAGAACAGATG[G/A]TTAGTAAAACCATAAGCCACATTTCAGACTACATATGACTACTGTTTTCACATGCCTATCTCACTGTGGAAACAATACATCTGTTTGAAGTGAAAAAGATCTTCGGGAGCCTCATCTGTGTACTTTTCTAGGAACGGCTCGGTGTGATGAGAGAGGAGCAGTCGAGACAGCAAAGCCTGTACTGAGAATCTGGCCACAGACACCAAAGATTAACCATGCTAGCTTGCAGCAGAGGTACTGTCTTTGGTCTGTTTTTGTTGTTCACCTTTATCTGATTGAGCTCCTGAGAAATGATTTAATGGTACTGTATGTTTTGTAATAGGACTGTCACAAGATTAAATTTTCACGACATGCTTTTCAACAGTCAATAGGTTTTCAAATTTTTTATTTTTTTTTATGTCATTGATCTCAAGAATGAAAATGTAAAAGTTATCTATATAGAAATTTAAACATTTGTTTGCTTTAATGCATGTTTTATTAATCAGTTTGTATTAAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14036
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 |
---|---|---|---|---|---|
ENSDART00000075414 | Essential Splice Site | 349 | 450 | 11 | 13 |
ENSDART00000112947 | Essential Splice Site | 62 | 255 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 35758989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35411565 |
GRCz11 | 13 | 35537397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CWTTTCCATAGCAGGCTCATGGGTGATCTCTGAAGGRCTKGATGGCAGCG[T/C]AAGTCAAATTCTGATAAYTGAAATTGAATACAAATTTTGTGTTTGCACAT
Long Flanking Sequence:
AATGTTCAAGTTTGCTCAAAAATGTTACAGCCAGGCCTTAAAAACACATGCAAATAATAAACTTTCACTCAAAGGTTAAAATGTGAAATTACTCCTCTATGGTGTTAACAGTAATGTCTGATCAACTATAATCCTGACTACAATGCAGATCCCTGCAATGTGACTATTGCTGACTCGCACATTGCTGTATCGATCCTGAAACAATATATTGTGCAGCCCTAGTAAAATGGAATAAAAAAGTAATTTTTTCATTTTGTCTCAACACAAATACATTGTGTGAAACCCAGCATTTTTACAGTATATATATATATATATATATATATATATATATATATATACATACACACACACACACACACACACACAGTATATAGGTTAGTCATTAAAGGCCTCAAAACATGAATTTTGAAAGTGTTTAGTAGCTATTTTTGTCCTTGCAGGTGACCTGAGCATTTCCATAGCAGGCTCATGGGTGATCTCTGAAGGACTTGATGGCAGCG[T/C]AAGTCAAATTCTGATAATTGAAATTGAATACAAATTTTGTGTTTGCACATAAATTTGATTGATTGAATTTCTGACTGTTGCATAATGTTTTTTTATTAACAATGAACATCCACATTTATGACAAACTATTATGATCTCCTTCAGAAAAGCTCCTTTTTTTAACAATCCCAACAGTTAACCTTAAACTGCTCTACATTCACATGTATTGCACCTTCGGTATTTTTACAGCCCTGCAATTAGCAGTTTACGGTTTCAAAAAGCCAGGATTATTTAAGATGTAAAGCTTTTACGAGGTTTGGCTGCGGTTTCCATTCTGGTAGGAAAGTAATGTGTGTGTGAGGCACAGTATAACATGATGACTACTCTCATCCTCTCTCTCTCTCTCTGGTCAGATGCGTTGTCTGGTGTCTTCTCTGTTTGAGACTTCAGTCGTTCTTTTAGTGGTTAATGGTGTCAGACTGGACGAACTCTGCTTAAGGATGGCAAAGAGCTTCTCTGTT
Associated Phenotype:
Not determined