ZMP
eea1
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to H.sapiens EEA1, early endosome antigen 1 (EEA1) [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
EEA1
Human Description:
early endosome antigen 1 [Source:HGNC Symbol;Acc:3185]
Mouse Orthologue:
Eea1
Mouse Description:
early endosome antigen 1 Gene [Source:MGI Symbol;Acc:MGI:2442192]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29005 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36607 | Nonsense | Available for shipment | Available now |
sa44886 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29005
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 |
---|---|---|---|---|---|
ENSDART00000091349 | Nonsense | 242 | 1398 | 9 | 30 |
ENSDART00000141800 | Nonsense | 242 | 811 | 9 | 19 |
ENSDART00000142527 | None | None | 255 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 15531445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15883857 |
GRCz11 | 18 | 15852369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGACCCGAGAGCGAGAGGAGGAGTCAGAGCGCCTCAAAGGCCAATA[T/G]GAGCAGCTGCAGGCCAACTTCACTACCTCAGAGGTACAGATGGCTAAATA
Long Flanking Sequence:
TTGAACAAAAAGCTGCTCAGCTTGCGACCGAGATAGTTGGTAAGCTTAGAAGGAAAGTTCCAGCATTTTATATTTACAGTAAATATAAAGTAAATCCGGCCTGTCCAATTTTCCCATCTCAGACATCAAATCTCGCTACGATGAGGAGAAAAGTATGAGAGAAGCTTTGGAGCAGAGACTGGCCAACTTAAACCAAGATATGCAAAAAGAAAAACAGGAGAAGGAGAAACTGTCGGCAGAGCTGGTAACGTCACACTTATTGTCTGGTGGTAATGAATGAGCTTGCATTCTCTCAGCTGCTGCTGCCCATACTTCATCAACTTCTTACCTCATCAATCTTTCCCGGCCTAATCCTGTCTGTCACTGGCTCTCCTCCAGCTCCAGAGGCCGGGTGTGGAAGATGTGGAGGTGTTGAAGAAAGAGCTGGTGCAGGTGCAGACGCTCATGGACAACATGACCCGAGAGCGAGAGGAGGAGTCAGAGCGCCTCAAAGGCCAATA[T/G]GAGCAGCTGCAGGCCAACTTCACTACCTCAGAGGTACAGATGGCTAAATATTAAAATTGTTAATAATCCTTTTAATTCATTTCAACTGTGTTTGTATAGCACTTTTAACAATATTTATTGATTCAAAGCAGCTTTATAAAAGGTGCACATTATTCAAATCAGAAAAGTCAGAACACCTCAAATCATACACCTTAGCAGTAGTCAGACTTTTTTAACATGTGTATTTTTGAGCTTCATGCGGATTATGTGCAAAACATGTATAGCAGGTGTGAAGTGCACACGAGTTTATTAAAAGCTTTCCAGTAGTGCGCTTGGGGTGGTGCATTCATTGCGGTCAGCATTATCAGCTTGTTTGTTATTTGAAATATATTAGCATATGATCCATCTGAACTGGAACATGTATTAATATTGAAATTTTATTCATGTGAGGTACATAAAGACAGGTGAAGTGGGCTACTGACTAAATGTCAGAAGCCTTTAACACACCTTGAACATTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36607
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091349 | Nonsense | 395 | 1398 | 11 | 30 |
ENSDART00000141800 | Nonsense | 395 | 811 | 11 | 19 |
ENSDART00000142527 | None | None | 255 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 15542653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15895065 |
GRCz11 | 18 | 15863577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGCAGAGCGGAAACAACTTCAACAGCAGAGGGAGGATAAAGAAAAC[C/T]AGGGCCTGCAGCAACAGAGTGAGATCAGCCAGGTCAGTAAGAGATGCTAA
Long Flanking Sequence:
TTTTGTCAGCATTCAAAAACACTGTTATAAAATGCTCATGTTTTGGTATTCTGTGCTGGCGGCCGGTGGTCTGATGAAAAAGCTTGTTGTATTGCATTCTTACTGTTGCCATGAAACAAAAGTTTGTATAAATGAATTGGTCATATTAAAAAAAACTGAATAGCAATGAATGTAATCACTCTGCCACTCCTCAGGCTTTGTCAGAGAAATTATCTCGTAAAGAGAAGGAGAATCAGGAACTGGAGGAGCGTCTGGGTCACGAACAGGCCTCTAAGAAGAGTCTTCAGGCTAATCTGCATCAGAAAGAGCTGGAGCTCCAGGAGAGTCGAGCACGGGTGTCTTCAGGAGAAGCAGCTCTCAGTCGAGCACAGGCTGAATTAACTGAACGTGGGGAAGAGGCTGCACGACTCAGACGAGAGCTGGGCGAGCTGGAGAAGAACCAGCAGGAGCTGAAGGCAGAGCGGAAACAACTTCAACAGCAGAGGGAGGATAAAGAAAAC[C/T]AGGGCCTGCAGCAACAGAGTGAGATCAGCCAGGTCAGTAAGAGATGCTAATAAAAGATGATTCAACCCTTTTCTTCAGAATCAGATTAATCTGTCCTTTTAGTTTAGAATCTAATTTATTATGTCGAAATCAGATCTATCTATACTTTAGTTCAGAATCCATCCATTCTTTAGTACTGAATTAGATCCATCCATCCTTTTGTTTAGAAACTAATTCATCAATTCTTTGAATTTAATTGAAAGGGTCTTTAAAGGTATAGTTAACTAAAAAACTTAACATTTCTTCATCATTTACTCATATTCAAGTGGTTGGAAAAAAGAAGCCAATGACATTCTTATTAGGAATGAGCTAAAAATAAACTATGGTAGAAAATGGCTGTTTTTCCCAACGTTCTTTAGTAAATCTTTTTGTTCAACAGAAGAAAGAAACAAGTGGCAGGATAAGTAAACAACTTGTTTCTTTAAGTTTAGAAACAAATACATCAATTTAGAATCAAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44886
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 |
---|---|---|---|---|---|
ENSDART00000091349 | Essential Splice Site | 1143 | 1398 | 24 | 30 |
ENSDART00000141800 | None | None | 811 | None | 19 |
ENSDART00000142527 | None | None | 255 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 15554276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15906688 |
GRCz11 | 18 | 15875200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACAAACTGTCTGCTGATCTCAAAACACTGGCTGAGAAGAATGAGAAG[G/A]TTAGACCCCAAAACACATTGAAATTCACATTAACAATCATGTAATGTGTA
Long Flanking Sequence:
TATTGGCCATGCAGGTGTGCGAGGAGAAGTTGGTTCTTGCTCAGGAGGAGCTGGTGACCAACAGGAACCAGCTCAGTGCTTACGAAACCCAAATCCAGGAGCTGAAGACGGGCCACACAGCGATGGAGATAGACCTGAGCAAGAGAGACGAGAAGATCAAACAGCAAGTGGAGACTCTGCAGAAGCTCCAGAAACAACAGGTAACAGAACAAGCCTGAGAAATCACACTTGTGCCCTCAAGCAAGACTTTGAATCACAGATTCTGAAGGTTACAGAAATATTTGTCAGTCATAAATTATATTTGCAGATTAGCACAGACAAATCGTGTGCTATTTTATGATCTGACTGGGTCTTTGTGTCTTTTGAAGGGACAAACAGAGGAGCAGCTGAAGAAGGAGAAAGCTCAATGCGAGGAGCTGAGAGAGAGTCAAAGCGCCCTGGAAAAGGACAAAAACAAACTGTCTGCTGATCTCAAAACACTGGCTGAGAAGAATGAGAAG[G/A]TTAGACCCCAAAACACATTGAAATTCACATTAACAATCATGTAATGTGTATTTATATAGCGCATTTATTGTGTGTGGTCATACACCCAAAAATCTTCACAGTCATTAGTGGAGTCTCCCCACACCACCACCAGTTTGCAGCATCCACTTGGATGATGCGATGGCAGCTACAGAACAATGGTGCCAGTGCACTCACCAAACACCAGCTATAGGTGGATTGGAGAGCCCTAATAGTAAGGGCAGATAGAGGGACTTTGGCCAGAACACCGGGGTTAAACTCCTACTCTTTACGAGAAGTGCCATGGGATTTTTAATGACAACAGAAAGTCAAGACCTCGGTTCAACGTCTCATCCGAAAGACGGCGCCCACTGACAGTGTAGTGTCCCCTTCACTTTTACAGGGGCATATGGACTCACACAGACCAAAGGTTGAGCGCTCCTTTCTGGCCTCTCTAACACAACTTCCAACAGCAACCTAGTTTTCCCATGTGGTGTCTTGTC
Associated Phenotype:
Not determined