ZMP
zgc:122989
Ensembl ID:
ZFIN ID:
Description:
Zgc:122989 protein [Source:UniProtKB/TrEMBL;Acc:Q567J1]
Human Orthologue:
RAB11FIP1
Human Description:
RAB11 family interacting protein 1 (class I) [Source:HGNC Symbol;Acc:30265]
Mouse Orthologue:
Rab11fip1
Mouse Description:
RAB11 family interacting protein 1 (class I) Gene [Source:MGI Symbol;Acc:MGI:1923017]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34455 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44692 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27245 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41264 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34455
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 |
---|---|---|---|---|---|
ENSDART00000067809 | Nonsense | 96 | 360 | 2 | 3 |
ENSDART00000124549 | Nonsense | 74 | 994 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 39113556)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37968681 |
GRCz11 | 8 | 38001620 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAGCGAAGGAGAAGGAGAGGGCAGTTCAGACTCTCCAAAGAAGAAAT[C/A]AAAGCTGAAATCCCTGTTTGGGCCAAAAACTAACCTCCAAAGGAATGTGT
Long Flanking Sequence:
ATCTTGCAATGTGACTGTTGCTGGTTTGCACAATATATTTTGCGGCCCGAATTTGTCATTTAGCCAGTGGCTATAACCTAAACTATTTATAAATTTTTTGTAGAATAATTGTAGTTAACAATTCTTATGTGTGATGATTAAAATCTTTAAACTAGCTAAAATAAATGGTCCTTCACAAGTTGTCTGCCACGCAATTTAATGAATACCATTTGTTTTTCTTTGAAGCTGGTACAAGCTGGTGGATAAGCATGGGAAGCAAGAGAAGGACCGTGGGGAAGTTATGCTGGACATTCAGTTCATGAGGAATAACATGACAGCCAGCATGTTTGACCTCTCCATGACAGAGAAGCCTCGCTCTGGAATCGCTAAGCTCAAGGATAAAATTCGTGGAAAGAAGAAAGACGGCCTGTCAGATTCTGCTTCTGCGATTGTGCCCTCATCAATGGAAACAGACAGCGAAGGAGAAGGAGAGGGCAGTTCAGACTCTCCAAAGAAGAAAT[C/A]AAAGCTGAAATCCCTGTTTGGGCCAAAAACTAACCTCCAAAGGAATGTGTCTCAGTCCATGTCAACCCTCGGCACCCTACCTGAGAAGAACAGTTCACTTAGCAGCAGCAGATCATCAGGCCTTAATGTGGATTCTCCTGATGGTAAAATAAATGATTATGCATCTTGTTAAGAATACTTTATTTTTATTTATTTTTATTATTATTATTCTTAGGTGAGTTTTGTTATTGTAAGCTATTGAGTACTTATTGTAAGTACAAAGTAAAAAAACATTTAGGCCATGTGTAATTTGTAAAACATTCATTCTTAAATCATTTCAAAACGTTTTAATATAGATATTAAGGAGCATGTCACACTGTAGAATAGAGTAGTGGTTCTCAACCACGTTCCTGAAGGACCACCAGCACTGCATGTTTTGGGTGTCTCTTTTGTCTGTCACACCAATTTAAGGTCTTCAGTCTCTGCTAATAAGCTGATGATCTGAATCTGGCAAGTTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44692
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 |
---|---|---|---|---|---|
ENSDART00000067809 | Nonsense | 128 | 360 | 2 | 3 |
ENSDART00000124549 | Nonsense | 106 | 994 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 39113460)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37968585 |
GRCz11 | 8 | 38001524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTCTCAGTCCATGTCAACCCTCGGCACCCTACCTGAGAAGAACAGTT[C/A]ACTTAGCAGCAGCAGATCATCAGGCCTTAATGTGGATTCTCCTGATGGTA
Long Flanking Sequence:
TTTGTAGAATAATTGTAGTTAACAATTCTTATGTGTGATGATTAAAATCTTTAAACTAGCTAAAATAAATGGTCCTTCACAAGTTGTCTGCCACGCAATTTAATGAATACCATTTGTTTTTCTTTGAAGCTGGTACAAGCTGGTGGATAAGCATGGGAAGCAAGAGAAGGACCGTGGGGAAGTTATGCTGGACATTCAGTTCATGAGGAATAACATGACAGCCAGCATGTTTGACCTCTCCATGACAGAGAAGCCTCGCTCTGGAATCGCTAAGCTCAAGGATAAAATTCGTGGAAAGAAGAAAGACGGCCTGTCAGATTCTGCTTCTGCGATTGTGCCCTCATCAATGGAAACAGACAGCGAAGGAGAAGGAGAGGGCAGTTCAGACTCTCCAAAGAAGAAATCAAAGCTGAAATCCCTGTTTGGGCCAAAAACTAACCTCCAAAGGAATGTGTCTCAGTCCATGTCAACCCTCGGCACCCTACCTGAGAAGAACAGTT[C/A]ACTTAGCAGCAGCAGATCATCAGGCCTTAATGTGGATTCTCCTGATGGTAAAATAAATGATTATGCATCTTGTTAAGAATACTTTATTTTTATTTATTTTTATTATTATTATTCTTAGGTGAGTTTTGTTATTGTAAGCTATTGAGTACTTATTGTAAGTACAAAGTAAAAAAACATTTAGGCCATGTGTAATTTGTAAAACATTCATTCTTAAATCATTTCAAAACGTTTTAATATAGATATTAAGGAGCATGTCACACTGTAGAATAGAGTAGTGGTTCTCAACCACGTTCCTGAAGGACCACCAGCACTGCATGTTTTGGGTGTCTCTTTTGTCTGTCACACCAATTTAAGGTCTTCAGTCTCTGCTAATAAGCTGATGATCTGAATCTGGCAAGTTTGCTTAAAGGTCCATGAACCCCCCTCTCTCAGCAAGGTGTTTTCACACCTCTTACTTTTGAAAAAGTAAGGAAAGTGGGTGTGTCCAGTTTTGCATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27245
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 |
---|---|---|---|---|---|
ENSDART00000067809 | Nonsense | 199 | 360 | 3 | 3 |
ENSDART00000124549 | Nonsense | 177 | 994 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 39110763)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37965888 |
GRCz11 | 8 | 37998827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAACCTCTGTATCAACGGCAGCCATGTTTATGCAGAGGATCAAGAACCC[A/T]AAGCCAGCTTTGGCTCCACGCTCAGCCTGAACAGCTCCGGAAAGGGTTCG
Long Flanking Sequence:
GGCCAAGTTTACAAATTGCATTGTTTCCGAATTAAAAAAAAAAAATTGTTTATTATTTTCTGCAAAGCTGCTTCTGATCATGATGTGTCCACACTAAATGGTTATAAGGGACGTGTTAAAGGGATTATATGCAACATCTTTCATTTATTCTTTTAGGAAAGGAGAAAGCTCTACTTAACGTACTTGGAGGGAAAATGTGCTTTATGCAGTGTTAAAGTTATATAAAGCTTGAAGCAGTGGCCGATAAGCATGAAATTTCTGATCAGAGCATCCCTATTTATAGCTTTGTTGAGTAGAAAATACTAAAACTTTTCCCTTATCTTTTTCCTCCTACAGTGAAAAAGAAGTTTAAAATTCTGGGACACAAGCGCACTGACAGCTCGGATAGCAAAGTGTCACTTGGCCCTTTTTCTCTTCTGAGTCGCTCTAAACAGAACATCCAGGAGCAGAATAACCTCTGTATCAACGGCAGCCATGTTTATGCAGAGGATCAAGAACCC[A/T]AAGCCAGCTTTGGCTCCACGCTCAGCCTGAACAGCTCCGGAAAGGGTTCGGCAGAGGATGTTCGTAAATTCCATCAACGGAATATTTCTGACGTCTCCATCGACTCATTTAAAGGCCTAAGTATTCCCTCGTACAAGCCTGAAGTGCAAGACAAAACTGTCCCACAGCGCCCTCTGGAGGACAAAAACTCGCAACCTGTGAAGGTGCTGGAGGAGGAGAAGGAAAAGAAACCCGAAGGAAGAAGCCTTCAAGAGATGCTGGACCGGCAGGAGGAGCAAGAGCAATGGAGGCAGCAGGAACGAGAGAGGAAGCAGGAGGAAGAGAGGAAAGAACAAGAGAGGAAGCGCAGAGAAGAAGAAGAGCTGCAGAGGAAGAGACGTGAAGAGGAGACTCAGCATGCCGAGGAGCAGCGGCACCAGGAGGAGAGCAGAGTAACTGAGCGGCTCTCCTCGCTCTTCGGCATTGGAAAGAAAAAGGAAGAGAAGAAAGAGGGATCTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41264
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067809 | None | None | 360 | None | 3 |
ENSDART00000124549 | Nonsense | 673 | 994 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 8 (position 39101076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37956201 |
GRCz11 | 8 | 37989140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACATTTACCTCAGGATATGGAAAGGAAGACTCCTGATGGCATTACCTA[T/G]CAACCCTCCCATTCAATAGATAAGCCTACACCAGCCTCCAGGGTCAAACA
Long Flanking Sequence:
TCCAGTGCTAGAAACGGGAGACAGGACTCTAAAAATACTCAAAGGCCTCCTCTTCCTCTTCCTGACTATGAAACACTTTTTCCCAAGAAGAGGCATGGGGTGATGAGTCAAACACGTTGGGACCATATTATCGCAGAGGTAAACCAGAGAAACTGGGATTTCTCGGAAGAGATGAACGTAGATGGACCAAACAAATCATTGTCGAATTCATCTGCAGTTTTGAAGGACAGAACCTCAGCCAACCTTAACCAGCTTCAAAGAAATCATGAGCCTCTTCCACCTGTCCTTACAAGGCCCAAAGAAGCCCTCAAGCCACCAAAGGTTCATGAAACATCAGAACCAACGCTTAAGACCACTGTCCAACATGACAATTTCAATGAGTCTGTATATGCTACTGTTAATAAACCTGGAAAATCAAAGAACTTTGAAAACAACCCACATCCAGCTGTCCAACATTTACCTCAGGATATGGAAAGGAAGACTCCTGATGGCATTACCTA[T/G]CAACCCTCCCATTCAATAGATAAGCCTACACCAGCCTCCAGGGTCAAACAAAATATAAATCCAAAGACTGAAGATGTGGCTAAACAGATGCCTTCAGCCAAACCCCGACAACAGTCATTAGTCAAGGACCCAGTCAGACAGGTTGAACCAGACCAGCATGTGACAACTCAGCCTGTGACTTCAGAAAATAACAAAGCTGAGAAATCAGAGAAGGGCCAAAAGGGAAGTGTTTTTACAAGTAAGTCCCACCTTAGAACTTCAGAAGTTCCAGAAAATTTGGGAAAACTTTCTAAGGATCCTGATGGAAGTGGAATGATCAACACATTCCCAGGTGATAATGTAGGTACTGAAGATCCTTGGGCTTTTATACCACAGCAAACCACAGATGAGGAGGATGTGCTCTTCACTAAAGGCCCAACGCAATTGAAAAGTATTGAAGATCAAGAGTTATCCTACAATAAAAACCTAGCAAAAAAAGATAACAGCATGGCACCAAAATC
Associated Phenotype:
Not determined