ZMP
ect2
Ensembl ID:
ZFIN ID:
Description:
protein ECT2 [Source:RefSeq peptide;Acc:NP_001003883]
Human Orthologue:
ECT2
Human Description:
epithelial cell transforming sequence 2 oncogene [Source:HGNC Symbol;Acc:3155]
Mouse Orthologue:
Ect2
Mouse Description:
ect2 oncogene Gene [Source:MGI Symbol;Acc:MGI:95281]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35030 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41785 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35030
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 |
---|---|---|---|---|---|
ENSDART00000011087 | Essential Splice Site | 506 | 878 | 15 | 24 |
ENSDART00000081827 | Essential Splice Site | 538 | 976 | 16 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 10485368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10437682 |
GRCz11 | 11 | 10421374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAATGGCAGCTTTTGTGATCTCTCTTTATTTTTTCAAATTCCCTCTCA[G/A]TCTGGAGAGCTGGTGAAGGCCTACCCACCATTTGTCAACTTCTTTGAGAT
Long Flanking Sequence:
AATCGGTTCCTTTAGTGATCCCGCAGGAATGCAGACCTTTACCGTCAAGTCCTGCTCCATTAGCGAACATATCGGAGTCCATCCTGGCTTGATCTAATTTCCTTTGTTCATGGCTCCTTTCAGCTCTTCAAATATCCGCTGGAGAAAGAGGGGCAGGTGGGCGGCCCCATTCTGGCTCAGGAAGAGATCAAGACCATCTTTGGCAGCATTCCAGACATCTATGAAGTGCACACCAGAATAAAGGTAGGCAATAACCTTTCTAAAACGCTGAGTTAAAGGCTGTGTTGTGCGTGTTGGCTGATGAATGTGCTTTGACAGGCGGATCTGGAGGAGCTGGTGATGAACTGGTCTGAAGAGAGGAGCGTTGGAGACATTATCCTGAAATATGTGAGTGCGATGAAGCTTTGAACTCGACCTCCTCCGGCGTGCAGCTCATAACGCAGTCAAAGGCTGAATGGCAGCTTTTGTGATCTCTCTTTATTTTTTCAAATTCCCTCTCA[G/A]TCTGGAGAGCTGGTGAAGGCCTACCCACCATTTGTCAACTTCTTTGAGATGAGCAAAGAGACCATAGTGAGATGCGAGAGACAGAAGCCCAGGTTTCATGCCTTCCTGAAGGTACTGTCAGCTCTTTTTAGTGCATATGAAGAGATTCTTTTCTTTCTTTCTTTCTGTCTGTGGTAGAACCTTAGGGTGATCATGCTTCTGATGGTTTTAGAGTGTTAAAATGTAGTCAAAAACAGTCATGTTTGAATGGGTTTCTGTCAGAAATGACAGCTATTAGATGACACAGCTGATATGTTGAATAGACTATCTTTCATACAGTTATTTATTTATTTCCCCCTATTCTTTCTTTCCTAACTTTCTTTTCTTTTCTACTTTTATTTCTTTTCAACTTTTTTCTTTTCTTTCTTTTACTTTCCCCCTACTTTTTCTTTCTTTCCTTCTGTCTTTCCTTCCTTCTTTCTTTCCTTCCTTCCTTCCTTCTTTCTTTCTTTCCTTCCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41785
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000011087 | Nonsense | 595 | 878 | 17 | 24 |
ENSDART00000081827 | Nonsense | 627 | 976 | 18 | 26 |
Genomic Location (Zv9):
Chromosome 11 (position 10482768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 10435082 |
GRCz11 | 11 | 10418774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACACATCAGATGACAACCCAGATAAATTGACACTTGAAAAGGCCATC[G/T]AGTCTCTCAAGGAAGTGATGACGTGAGTCCTTATTGTCCTTATATAAAAA
Long Flanking Sequence:
TCTTCCTACTGTCTTTTTCCTTTTTACTTTCTCCATCTTTCTTTCTTTCTTTGTTTCTTTCATTTTAACGAAGACTGTATATTTACATTTTTCTGCCTCATTTTGTTATTCAGATTAATCAGTCTAAACCTGAGTGTGGCCGTCAGACTCTCGTTGAGCTTTTGATTCGTCCCGTGCAGAGACTGCCAAGTGTCGCCCTCCTGCTGAATGGTAACCCACATAATATGGCTTTGGCATGATGCAACTGATAGACACACAAACAGCTGTTCCTATTCAGTAAACTGAGCTGAATCCATAGGGTCTAAACAGAGTTTACGATCAATTCAGTTTGTAAAGTAATTTAATATATCACATCCTGTACACGTTTTTCATAATTAATGTTGAGCCAGTGTATGCTTATAGTAATAAACAAGCTTTTGGATGTATTTTTGCTCTTTGCAGATATAAAGAAACACACATCAGATGACAACCCAGATAAATTGACACTTGAAAAGGCCATC[G/T]AGTCTCTCAAGGAAGTGATGACGTGAGTCCTTATTGTCCTTATATAAAAACCATCCTTGAAACAAAGTAATGTTGCGCTGAGAACTAATTTCAGCAACCAGAACATGTTGAAAGGCCAAAATCATTGACTAAAACAGTGGCTTTTAGGTAAAGAGCTGTATATTTCTCTCTCTCTCTCAAATTCACAGCCACATAAATGAGGATAAAAGGAAAACAGAAGGACAGAAGCAGATCTTTGATGTTGTTTATGAGGTGGACGGCTGTCCTGTAAGTAATTTTGTTTTTACTTCTCAGGAAGTTTTCCACATTCACACACATCTTTTGAGTTTAAAGGAATCACTTTCCCACAGTGCTGTCATTTGCTTGACTTCATACAAGTCGTGCTACATTCCAAGTCTTTTGAAGCTTTGAGTCGACAGATCGCAATGAAAGATGTTATTTCAGTGGCCGTTACAGCTTTCAAATAACTCAAATCATTTCCACACCCCTTCAACCAACAG
Associated Phenotype:
Not determined