ZMP

ect2

Ensembl ID:

ENSDARG00000007278

ZFIN ID:

ZDB-GENE-040831-2

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.

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.

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