ZMP

ECT2L

Ensembl ID:

ENSDARG00000091471

Description:

epithelial cell transforming sequence 2 oncogene-like [Source:HGNC Symbol;Acc:21118]

Human Orthologue:

ECT2L

Human Description:

epithelial cell transforming sequence 2 oncogene-like [Source:HGNC Symbol;Acc:21118]

Mouse Orthologue:

Ect2l

Mouse Description:

epithelial cell transforming sequence 2 oncogene-like Gene [Source:MGI Symbol;Acc:MGI:3641723]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23127	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42970	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23127

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
ENSDART00000123093	Essential Splice Site	236	761	6	18
ENSDART00000129416	Essential Splice Site	305	907	8	22

Genomic Location (Zv9):

Chromosome 17 (position 33606835)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	33448566
GRCz11	17	33401077

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCCTCTTCCTCACTTTCTACTCGTGTCATCCAAAGTCCCTGGATATGAA[G/A]TAAGACTTGTTCACAACATTCAGTTGCTTCACTTCTTGAATGACAACAGT

Long Flanking Sequence:

GAAGCGACCCCGGATTAATAATGGGACTAAGCCAACAAGAAAATGAAAGAATGACTGATTTTGTTCCTCAAGATTTGATTGGGTTGTTGTTTGATTAATCAGATTAATTTAAGTGCTTAGTGTTACAGAAACCCAGCTAAAGTCTGATCACATGTCTCAGAATTACAGTTATACATTTGGTAAACCCTTTTTATCTCTTAAACACAGGAAAAGTGTCGTTTGAAAAATTCACTCTCCAGTGTGGAAATAAGGAAACCACGGCTTGATTTGAGCATGAAGAGTACTCTCGATAGCACAAGTTTATTGAAAACCACAAGGTCAGTAATGAATCTCGTCGTGAATATATAATATTTACATGCAATATTAGCTTCATCTAGCACCAATAATTCTGAAGATGCATGCTGTTTCCTTACAGTTCACTGTTCAACAGACCAGTCATGTCCTCCTACTATCCTCTTCCTCACTTTCTACTCGTGTCATCCAAAGTCCCTGGATATGAA[G/A]TAAGACTTGTTCACAACATTCAGTTGCTTCACTTCTTGAATGACAACAGTTGTTTATGAACTGAGCAATCTTCTTTTTTCTAGCTGCTTCTGGCTGCTGTGCAAGTGTCTGTGTTGGTTTTGCCATATGACTCGCAAGGCATGACCTTAGAGGTCTTGTTTTCTCTGGCGGAAAGAGTGATCCAAGGCAGGATGCTGCAAAGCGTTGGCATTCTTGTGCCAGGAAGCACAGATGACATAATGCTTACAGATGGTAATCCTTTAGGATTAATGCAACATTTTATTTTATTAACAGATTATAAATGACGGATGAGAGTAGATTTATTAAATCACCTAAAAGATAGAGTGCTGTCAAATCCCTGACAAATATTTTTCAATTGCCAAAATGACATAAGCAGCGGTTAATGATTATTAAGTTATCATAACACAACAATTCGTTCATTTTCCTTCGGTTTAGTCCCTTTATTCATCAGGGGTCACCACAGCAGAATGAATCGCCAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42970

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123093	None	None	761	None	18
ENSDART00000129416	Nonsense	706	907	18	22

Genomic Location (Zv9):

Chromosome 17 (position 33598729)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	33440460
GRCz11	17	33392971

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAAGTTTTACAAGAGTGATAAGCAACCTTCCGATTCTCCATTCAGTCTC[C/T]AGGAGTTGCTTCTCACACCATCCGCACGAGTGGAGGAGTACGTGGCTTTA

Long Flanking Sequence:

TTTAAGACATAATGAAGCTATAATATTTTAGGAATTAGGTCAAAATATTACAAGAATAAATGCAAAACATTTGAAAAATAAAGTAAAAATGACAAAAATAAAATCTAAATATTGTGAGAATAAAGTGGAAATTACAGTAGTACAAAATAAAAATAATATTTTGAGAAAAAAGTAGCAGTATATAATTTTACTTTAATTTAATTTTATTTTATTTATAAAGTTTAAACTTTAATCTAAGAACAATCATAGAATTGGAAAAAACAAGTTAAATGGAAATGGTGGGTTTGGTTAAATAACAATTTGACTCATAATATTCTATTTTCTACATGTTTTGTAGTGCCGTGAGATGCTTCCTGTATTCCGCAACTTTCTAAAGAGATACGATCGAACCATTGCTACTAGAATGCTGAGGTACAGTAAAGGCTTCAGCTCTAAAAGTCTTCTAACAAATGAAGTTTTACAAGAGTGATAAGCAACCTTCCGATTCTCCATTCAGTCTC[C/T]AGGAGTTGCTTCTCACACCATCCGCACGAGTGGAGGAGTACGTGGCTTTACTTCAGGCGTTAACACTACACACACCACCTGAACACCCAGACTACACACAGCTCACATCCGCCCTCGACACACTGATGACCTACAGAGGCTTCATTCATAAGGTGCGTTAAAAACAAACAAGCTCTTGTATTTTTCAGTCTAATGCAATGAAAAAATCCAAAATACATTTTATGTCTTTTAGGCCGTTTTTTTAAATGCTGAAATGATGACATAAACTCACTGGCCACTTTATTAGGTACACATTACTAGTACCGGGTTGGACCCTTTTTTTGGCCTCAGAACTGCCTTAATCCTTCTTGGCATAAATTCAACAAGGTACTGGAAATATTCCTCAGAGATTTTGGTCCATATTGACATGATAACATCACACAGTTGCTGCAGATTTGGTGGCATCCATGATGCGAATCTCCCATTTCACCACATCTGAAAGATGCTTTACTGGATTGAGA

Associated Phenotype:

Not determined