ZMP
B0S4W0_DANRE
Ensembl ID:
Description:
Novel protein similar to vertebrate zinc finger, FYVE domain containing 1 (ZFYVE1) [Source:UniProtKB
Human Orthologue:
ZFYVE1
Human Description:
zinc finger, FYVE domain containing 1 [Source:HGNC Symbol;Acc:13180]
Mouse Orthologue:
Zfyve1
Mouse Description:
zinc finger, FYVE domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3026685]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35822 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32020 | Essential Splice Site | Available for shipment | Available now |
sa28413 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8402 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35822
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 |
---|---|---|---|---|---|
ENSDART00000111385 | Nonsense | 242 | 654 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 13809184)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14452527 |
GRCz11 | 15 | 14388484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGGGCCAGAGCACAGACGCCTTCAGTTCGGTTCAGTATGTGGGCACA[C/T]AGACCATCACTCCCCCCACAGACTACTCACAGCTACAGCACACGGTCCAG
Long Flanking Sequence:
CATGTATAAACGCTTACTATACAGTAAAATATTTGATTTGGTCACATTTTCAAAGGCCACAAAAAGTACTTTTTGTCATTTCTCCGACAGAATTGAAAACATTAAAAGCAGCACAATGGTTAATCAGCTTGTTATCTAACCCAGATTTCAGGTAAATCCCAAAGGCAATGACTCAGGTGCTGTAGACATCACAATACAGCTTAACAACAGTGATGCCCTTGGGCAAAACCCCCTGTTTTCATGCTGTAAATCCTCCTTCACGAAAAGAATTGTAAAATCACATAAGCTGTTAACGCTCCTAAAACTGTCGTTCATCTTTTTTTATTTTGAAATGATTGAATTAGTGTCATCTGAAGAGGTGTGCCAGGCTTCTAAAATGTGTGTTTTGATGTCTTCCAGACGTCTCAGGCCTCGGGCAGGCAGACACGCTGCTGCAGAAGCGCTTTCATGACCTGGGCCAGAGCACAGACGCCTTCAGTTCGGTTCAGTATGTGGGCACA[C/T]AGACCATCACTCCCCCCACAGACTACTCACAGCTACAGCACACGGTCCAGCAGCAAGTCAGCAACACATCTCAGAGAGCCCCGCGCCAGCCTGCCATTGTGTTCAGTGCACTGCAGGTATACGTGTGTTTTTGTAAGAGTGGCCTCAAAAACATTTTAGACACTTAAAGGGGGTAGTTCACTTTAAAAGAAAAATGTACTCATCATTTTTCAAGTGATTCCAAAGCTGTCTTTTTTTCCTCTGTTGAACCCAAAAGAAGATATTTAGAAAAATGTTAGAAAGCAATGACCATTGGCATCTATAGTATGAAAAGATATTGTTCATTCATTCATTTATGAATTTTTCATTCCCTTATTTATCAAGGGTTGCCACAGCGGAATGAACTGCCAACTAATCCAGCATATGTTTTTACGCAGTGGATAGCTTTGTTGGGAAACACACACACTCATACACTATGGCCAATTTAGTTCATCCAAATCATCTATAGTGCATGTTATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32020
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 |
---|---|---|---|---|---|
ENSDART00000111385 | Essential Splice Site | 385 | 654 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 13786875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14474836 |
GRCz11 | 15 | 14410793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCACAGACAACCCGTGGTTTGGTCTGGCCAAGTATGCGTGGTCTGGG[T/C]GAGTGAGATGCTGTATTCTGCTGTCTATGAAGCTGCTCCTCATACACATT
Long Flanking Sequence:
TATTTGGTGTTTTATTTAAAAAAATATTTTTTTGTTTATTGATTTATTATTTTATTTAACTTAATTAATTAATTATTTTTTTTTTTGTTTTATCATTTACTCGTTTGTTTAATTTATTTTACATATTATTTTAAATATGCTATACTATCAAAAAAGTAATTGCCCAATTTATTAGCTATGCTGCAAACATGCATTTGTTCATATCACTAATTCACACAAAGTGGAACTGAGTAGAAAATAAAGACCAGCCCTGTACATTGATTTGCCAGTAATTTTCTCAGTTAATTATGTCTTCAGTTTAATATGTTTCCAATAGCAGTCCACTTTGGATGAAACTACTCAATTTTCATCAAAAGAATGATTTAATAGCCTCCATAAACCATTTCTTTTGCCCCTTCCAGAAGTGCTATGAGGGCGGAAGGGAAGTGATTGTCATCCCCAAAACATCTGCCTCCACAGACAACCCGTGGTTTGGTCTGGCCAAGTATGCGTGGTCTGGG[T/C]GAGTGAGATGCTGTATTCTGCTGTCTATGAAGCTGCTCCTCATACACATTCCTCATCCAGCTCTTGTTCTTCAGGTACGTTTTAGAGTGTGCAAGCTGTGGCATCATCTACCGCAGCAGACAGTACTGGATGGGCAACCAGGACCCGGAGAGCAGTGTGGTGCGGCCAGAGGTCAAGCACGTCTGGCAGGGGGTGAGTGTTTCTGTTCATGTGTTCAGTCTGCTGATGCTCACAGTGGTTAATGTTGTGTTTGTGCTTGTAGACTGATGCCTTCCAGACTGACCATCAGAATGCTGCTCAGCGGGTTTTGGATGGAATGAACTACATTATTCAGTCAGTGACAGAATACAGTTCAGGGCCGACCAAAGCTGTCGCTGCGTGGCTCACAGACCAGGTGGCTCCACCTTACTGGAAACCCAATGCTGAAATCAGCGTGAGTTCATGTGCTCGGTTGGAATATGAGAGAAAGATTGTTGAGCTGCAATTATGGTGGTATGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28413
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111385 | Essential Splice Site | 424 | 654 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 13786681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14475030 |
GRCz11 | 15 | 14410987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGGAGAGCAGTGTGGTGCGGCCAGAGGTCAAGCACGTCTGGCAGGGGG[T/C]GAGTGTTTCTGTTCATGTGTTCAGTCTGCTGATGCTCACAGTGGTTAATG
Long Flanking Sequence:
TTGTTCATATCACTAATTCACACAAAGTGGAACTGAGTAGAAAATAAAGACCAGCCCTGTACATTGATTTGCCAGTAATTTTCTCAGTTAATTATGTCTTCAGTTTAATATGTTTCCAATAGCAGTCCACTTTGGATGAAACTACTCAATTTTCATCAAAAGAATGATTTAATAGCCTCCATAAACCATTTCTTTTGCCCCTTCCAGAAGTGCTATGAGGGCGGAAGGGAAGTGATTGTCATCCCCAAAACATCTGCCTCCACAGACAACCCGTGGTTTGGTCTGGCCAAGTATGCGTGGTCTGGGTGAGTGAGATGCTGTATTCTGCTGTCTATGAAGCTGCTCCTCATACACATTCCTCATCCAGCTCTTGTTCTTCAGGTACGTTTTAGAGTGTGCAAGCTGTGGCATCATCTACCGCAGCAGACAGTACTGGATGGGCAACCAGGACCCGGAGAGCAGTGTGGTGCGGCCAGAGGTCAAGCACGTCTGGCAGGGGG[T/C]GAGTGTTTCTGTTCATGTGTTCAGTCTGCTGATGCTCACAGTGGTTAATGTTGTGTTTGTGCTTGTAGACTGATGCCTTCCAGACTGACCATCAGAATGCTGCTCAGCGGGTTTTGGATGGAATGAACTACATTATTCAGTCAGTGACAGAATACAGTTCAGGGCCGACCAAAGCTGTCGCTGCGTGGCTCACAGACCAGGTGGCTCCACCTTACTGGAAACCCAATGCTGAAATCAGCGTGAGTTCATGTGCTCGGTTGGAATATGAGAGAAAGATTGTTGAGCTGCAATTATGGTGGTATGGGAAAGACCTATAGCACAGTTGAGCACAGTTTAAAAGTTTGGAGATCTCCTATAGTGGGTTTACATATTTTCAAGATCAAAAGCACCAAAATAAAATTCTGCAATCTGAGATTGTCAGATAAGCACACTATAAAAAATATGTATGTATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8402
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111385 | Nonsense | 459 | 654 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 13786510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14475201 |
GRCz11 | 15 | 14411158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATGAACTACATTATTCAGTCAGTGACAGAATACAGTTCAGGGCCGACC[A/T]AAGCTGTCGCYGCGTGGCTCACAGACCAGGTGGCTCCACCTTACTGGAAA
Long Flanking Sequence:
ATAGCCTCCATAAACCATTTCTTTTGCCCCTTCCAGAAGTGCTATGAGGGCGGAAGGGAAGTGATTGTCATCCCCAAAACATCTGCCTCCACAGACAACCCGTGGTTTGGTCTGGCCAAGTATGCGTGGTCTGGGTGAGTGAGATGCTGTATTCTGCTGTCTATGAAGCTGCTCCTCATACACATTCCTCATCCAGCTCTTGTTCTTCAGGTACGTTTTAGAGTGTGCAAGCTGTGGCATCATCTACCGCAGCAGACAGTACTGGATGGGCAACCAGGACCCGGAGAGCAGTGTGGTGCGGCCAGAGGTCAAGCACGTCTGGCAGGGGGTGAGTGTTTCTGTTCATGTGTTCAGTCTGCTGATGCTCACAGTGGTTAATGTTGTGTTTGTGCTTGTAGACTGATGCCTTCCAGACTGACCATCAGAATGCTGCTCAGCGGGTTTTGGATGGAATGAACTACATTATTCAGTCAGTGACAGAATACAGTTCAGGGCCGACC[A/T]AAGCTGTCGCTGCGTGGCTCACAGACCAGGTGGCTCCACCTTACTGGAAACCCAATGCTGAAATCAGCGTGAGTTCATGTGCTCGGTTGGAATATGAGAGAAAGATTGTTGAGCTGCAATTATGGTGGTATGGGAAAGACCTATAGCACAGTTGAGCACAGTTTAAAAGTTTGGAGATCTCCTATAGTGGGTTTACATATTTTCAAGATCAAAAGCACCAAAATAAAATTCTGCAATCTGAGATTGTCAGATAAGCACACTATAAAAAATATGTATGTATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATAAATAAATAAATATATATATTATCATATATATATATTATCTATACTGTACATTATTTCTGTTAAATGACAAGACTTTTGTCTAAGCAAAGTCAGACCTTACTGTCCTAATTAAATAATTCAAAATGAAGGCATGATCATATTTTATTTTGGTAAAATAAGTGTAATCTAGAGGCCT
Associated Phenotype:
Not determined