ZMP
fgd6
Ensembl ID:
ZFIN ID:
Description:
FYVE, RhoGEF and PH domain-containing protein 6 [Source:RefSeq peptide;Acc:NP_001093450]
Human Orthologue:
FGD6
Human Description:
FYVE, RhoGEF and PH domain containing 6 [Source:HGNC Symbol;Acc:21740]
Mouse Orthologue:
Fgd6
Mouse Description:
FYVE, RhoGEF and PH domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:1261419]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33478 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45178 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33477 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33476 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40307 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33478
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 |
---|---|---|---|---|---|
ENSDART00000066949 | Nonsense | 942 | 1315 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 24966015)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25889684 |
GRCz11 | 4 | 25878882 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGATTATTTAAAAAATCTTCCTGAGGATTCTTCCGACTACAAAGACACA[C/T]AAAGTAAGAGCACATCATTAATAAAATAACCAGAGACCAGTGAAAAAAAT
Long Flanking Sequence:
TAGCCCTGATTAACTCAATCAGGAACTAATGAGGTGAAAGAGTAAAATAAATTTAGGGTTTACATTTCTAGAATTTATCTGTAGAGCCCTGGATAGAATCTAGAGAGAGGAAACCATAAGATGTGTTAACCAAATGTTGGAAAGGTGAGGAGTTGCAATGAAGCAAAATGCTTTTTAAATAGAACTCTGATGTCATATTGGCTTGGGTGCACACCAAAAGAGCTAGTGTGAAGTCACCCTTAGAGAAATGAAGCAAACCTGCATTATATATCATGAGAAAATAAAAACACATAATATATAATGTTCATATAATTCTATTACATTATAACATATAATTCTATGTTATAATGTAATAGAAGACCTCCTAAGCAAAATAGAAACCTTTAAAATAGCATAATGAATGTCATTTTAATAAAACTAATATCTTTGACCTTTTTTTGTCTCTTTTTTTAGATTATTTAAAAAATCTTCCTGAGGATTCTTCCGACTACAAAGACACA[C/T]AAAGTAAGAGCACATCATTAATAAAATAACCAGAGACCAGTGAAAAAAATCTAATAAAATGGCCTGGTTTTATACAGAGTAACACAAATTCAGAGTGAATGTTTATCAGTCTGACTGTTAATTATTTACTAAAACATAGTTTAAGTATGTTTAGATCAAGAACCATTTGGTGAGATTAAAAAAAAAACTTTACTTAAAGGGCACCTATGATTAAAACATGTTTTGTAAGCTATTTGAACAGAACTGTGTGTAGGTATAATGTGTCCACAGTCATATTGGGGTGATCGAAACACAATAAGCATGTATTGCATAGGAATGTGGTTTCCCTGCCTACCGATTTGATTGGCAGTCACGTATAAACATGTCTCTGTAGTAACGCGTATAATCATATTAACAAGACAGGACGTGCGCAAAGCAACAGGGATTAAAAGATCTTTTCAGCTTGTTGTGATCATCAATCAGCATCAAATGTGATCAACAATGAGTTTTAATAGTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45178
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 |
---|---|---|---|---|---|
ENSDART00000066949 | Nonsense | 1094 | 1315 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 24963095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25886764 |
GRCz11 | 4 | 25875962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGCAATAGATGATTACACCAGAAAGAAGATTTCGTTCTTCTCCAGT[C/T]GAAGCCAAGAGGTGTGTGAAATTTAAGATGCGTTCTTGTGTTTGTGTGTA
Long Flanking Sequence:
CTGAATAAGCTAGCACTTGTTTTTTGATACCCAGTCAATGTTCATTCTCTCAACAGTTTAATGACATCCTGCTGTACACAACACCAGTGCAGTCTGGACAGTATAAAGTCAACAGTATGCTCTCTCTGGCTGGCATGAAGGTCAGATATCAATTATCCATAATATGTCCACTCTCTCAAACACGCATTCATATGACATTTTATATATAAGTGTTTATGTTCCATGTCTTCAACAGGTGAGCAAACCCAGTCAGGAGGCGTATCAGAATGAGTTAAACATTGAGAGTGTTGAAAGATCCTTCATACTGTCTGCCAAGTAAGAAACACACACAAGCATGTGATTTTCAGCTATGTCAAAACTGGAAATCATTTTGAATCGAGTTGAAATGACTGACTAAACGTGATGTTTGCAGTTCAGCGACTGAAAGAGATGAATGGTTGGAAGCCATTGCTACAGCAATAGATGATTACACCAGAAAGAAGATTTCGTTCTTCTCCAGT[C/T]GAAGCCAAGAGGTGTGTGAAATTTAAGATGCGTTCTTGTGTTTGTGTGTAGGGTTATTGTTCTTGTGCGTATGCCATTCCGTCAACTGGCAATATTTGCTTTCTTTAATTGATTTCCACAGCCATTTTTTTAAACGACAATTTTCTTTTGTTTTATTTACATCAAGTACTTGAATTTAACTAGTTAAAAACATTCAGAATACTATGAACTGTTATAAGTAATAATAAACAGTTTTATCGTGTTTATCTGAGATGCAAAATGGCATAAGATACAAGTCTTGTTAGTCTGTCAATATCTGTATCTGCTAAAAGGTGGATACAAAGGCTTTCATTTATTATTTTAATTTATAATATTAATTTATCAATTAATATTAATCACATATTTTTGGAAGTCATTACTTTATAATAGCCAGTTTAATGCTTTAAAATTCAGTGAAATAATACAACACAAAAAAAAAAAATTATATTGGAATTAATAGTTTTTTTTTTCAAACAATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33477
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066949 | Nonsense | 1151 | 1315 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 24959781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25883450 |
GRCz11 | 4 | 25872648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGATAAGAGATTTGTTTACTTTGGCCACAGGTGGTGTGTCAGGCATG[T/A]TCGTCTAATAAATTCTACCTGGAATACCTGAAGAATCAACTGGCAAGAGT
Long Flanking Sequence:
TTAAGGTCAAAATTATTAGCCTCTTTAAGCTATAGTCTATAGTCTACAGAACAAACCATCATTATACAATAACTTGCCTAATTACCCTAACCTGCCTAATTAACCCAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAACATATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTTAGAAATACGTTTTCTGTTAAACAGAAATTCTGGATAAAAATAAAGGGGGGCTAATAATTCAGATTTCAACTGTAGATGTTTTTATATTTGTATACTCTGATGCTATTTAATGCTCAATCTTCTTTTTGTTAATTGTGTTGATTGTTATATTGTAAAACGATAAATCATAATTAATAATAATAAAAATGAATTTACAGAAATTGTTCTATGTTGATGTACATATCATAATCAGGGCTTGAGATTATTTACATCATGATAAGAGATTTGTTTACTTTGGCCACAGGTGGTGTGTCAGGCATG[T/A]TCGTCTAATAAATTCTACCTGGAATACCTGAAGAATCAACTGGCAAGAGTGTGTGACCATTGCTATATTAAACTACAGCACAAGGGTATGTGATTTCTGTTGTTTATCTATCTCTGGACTGTTCCATGGCTCCATCATCTATAGTAGTAATAGTGTTTATTGTTCTATTTTTAATGTGGTTATGCTTAGTGTTCAGTTCTTATGCTTAAACGGTCCTTTCACCCCAAAATAAAAATTGTCCTTATTTACTTGTTCATCTTCAGAACACAAATGAAGATACTTTTTTCCCCTAAAACATAATTTATTGGATTTTTTTTTCCGAACAAAGTATTGACCTTATTCTTCAATGCGGAAGTGCGCTCGTTTTTGCGTTGTTTTAGAACTTTTGATTCAGTTGCCAGGTAGAAATAGCTAAAACGGTCAAACTACTTGCTCTTCCAACAAGTGTGTGCATGACTATACAGACAAAGCAGAATAATATAATAGGAAAATATCAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33476
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 |
---|---|---|---|---|---|
ENSDART00000066949 | Nonsense | 1200 | 1315 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 24955462)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25879131 |
GRCz11 | 4 | 25868329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATGTGACCTTTTCCCCTAGTGGGCGGGGCTCAACATTCGCTTTTTCT[A/T]GAAAACAGAAGAAGATTCCATCAGCTCTCAAGGAGGTAATCTAAAGTTAA
Long Flanking Sequence:
CGTTTCCATCTTCTTTCTGGCCTTAAATGAAAAGCAAAAAAGAACTTCATTTGAAGTATGCCTTTAGTAGCTGAGACTGAGCATTTATATACAGCTACTCAGCTACTGGAATCTGGCTTAAATGCGCAGTAGCAGTGTGTGGATGCTGATGTTGAGGATGATTTGCAGTGCTTCTTTTATACTCACTTGTAGGTCACTTTGGATAAAAGAATTTGCTAACTGAATAAATGTAAAATGTAAATAATCAAACCCCAGATAAAACACTAAATCGGAATGTGACCCAGAGGACTCTGAAAACTCTTTTGACAGGTGAAAACCTGGCAATCGCACAATATGCTATTGCAACCGCATATTATTATTTACTTACAACAATCTGGCAAACAAGTTGTGTGACAGCAAATGTTTTTTTTATTTTTCAACCATGCTTTTTTTGTTTCTTAGGCGACCAATCCAATGTGACCTTTTCCCCTAGTGGGCGGGGCTCAACATTCGCTTTTTCT[A/T]GAAAACAGAAGAAGATTCCATCAGCTCTCAAGGAGGTAATCTAAAGTTAAACAATACTTAAAGGGATAGTTCACCCAAATGTCACTAAACATTACACTTGCTCAATAACTTGATTCAACTCTAAGTTGAATACAAAGAATTTCTTTTGAAGAATGCTGGTTGATGGTACCCATCATGATGACTTTTTTCCAGTGGGTACTATCTAACAGCAATTCTCTAAAGATCTTCTCTTGCGTTTAACAGAATAAAAACTGCTGTTTCCAAAATAACACTAATGTCATTTTTATAGTTTATTAATATGACATCGTTCTCACAGGTGTCTGCCAACACTGAGAACTCCTCCATGAGTGGATATCTGCACAGATCTAAAGGCCACAAGAAACCATGGAAGAGGCTGTGGTTTGTCATTAAGAACAAAGTCCTCTACACTTATGCTGCCAGTGAAGTAAGCTGAATTTATTCAACAACTTATCAACTGTTAAAGAAACAAGCTTTATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40307
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 |
---|---|---|---|---|---|
ENSDART00000066949 | Essential Splice Site | 1211 | 1315 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 4 (position 24955426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 25879095 |
GRCz11 | 4 | 25868293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCGCTTTTTCTAGAAAACAGAAGAAGATTCCATCAGCTCTCAAGGAG[G/A]TAATCTAAAGTTAAACAATACTTAAAGGGATAGTTCACCCAAATGTCACT
Long Flanking Sequence:
AAAAAGAACTTCATTTGAAGTATGCCTTTAGTAGCTGAGACTGAGCATTTATATACAGCTACTCAGCTACTGGAATCTGGCTTAAATGCGCAGTAGCAGTGTGTGGATGCTGATGTTGAGGATGATTTGCAGTGCTTCTTTTATACTCACTTGTAGGTCACTTTGGATAAAAGAATTTGCTAACTGAATAAATGTAAAATGTAAATAATCAAACCCCAGATAAAACACTAAATCGGAATGTGACCCAGAGGACTCTGAAAACTCTTTTGACAGGTGAAAACCTGGCAATCGCACAATATGCTATTGCAACCGCATATTATTATTTACTTACAACAATCTGGCAAACAAGTTGTGTGACAGCAAATGTTTTTTTTATTTTTCAACCATGCTTTTTTTGTTTCTTAGGCGACCAATCCAATGTGACCTTTTCCCCTAGTGGGCGGGGCTCAACATTCGCTTTTTCTAGAAAACAGAAGAAGATTCCATCAGCTCTCAAGGAG[G/A]TAATCTAAAGTTAAACAATACTTAAAGGGATAGTTCACCCAAATGTCACTAAACATTACACTTGCTCAATAACTTGATTCAACTCTAAGTTGAATACAAAGAATTTCTTTTGAAGAATGCTGGTTGATGGTACCCATCATGATGACTTTTTTCCAGTGGGTACTATCTAACAGCAATTCTCTAAAGATCTTCTCTTGCGTTTAACAGAATAAAAACTGCTGTTTCCAAAATAACACTAATGTCATTTTTATAGTTTATTAATATGACATCGTTCTCACAGGTGTCTGCCAACACTGAGAACTCCTCCATGAGTGGATATCTGCACAGATCTAAAGGCCACAAGAAACCATGGAAGAGGCTGTGGTTTGTCATTAAGAACAAAGTCCTCTACACTTATGCTGCCAGTGAAGTAAGCTGAATTTATTCAACAACTTATCAACTGTTAAAGAAACAAGCTTTATATAATTTATCAGTGTTAGCTCATAATATGAATGTTGACA
Associated Phenotype:
Not determined