ZMP

E2F2

Ensembl ID:

ENSDARG00000079233

Description:

E2F transcription factor 2 [Source:HGNC Symbol;Acc:3114]

Human Orthologue:

E2F2

Human Description:

E2F transcription factor 2 [Source:HGNC Symbol;Acc:3114]

Mouse Orthologue:

E2f2

Mouse Description:

E2F transcription factor 2 Gene [Source:MGI Symbol;Acc:MGI:1096341]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42947	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36429	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa42947

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110903	Nonsense	171	438	3	7

Genomic Location (Zv9):

Chromosome 17 (position 27092068)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	27231987
GRCz11	17	27250378

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGGGGTTCTGGATCTAAACTGGGCCTCAGAGGTTCTGGAGGTTCAGAAG[A/T]GACGCATCTATGACATCACCAATGTTCTGGAAGGAGTGCAGCTCATCCGC

Long Flanking Sequence:

TTTGATATGCTGTGTCAAAGCTTGTCCACATACCTGAAATGCCAACTAATCCAGCCGGGCCTCAAACCAGCTACCTTCTTGCTGTGAGGCGACAGTGCTAACCACTGAGCCACCATGTCGCCCATATGAAAGATAATATTCCAAGAAAAAAAGATTATAGGTGCACTTGACTTCAGGTGAAAAATTGACTTCCTATTGTTTAAAACCACAGTTTCCATTTGTTGAGTGAGGAGCGGATGTTTCTGGTTTTAGAGCCTCATCAAATCAATTGAAATGCAAACACACCTGTCCAAGCAACTCTTACACCTGGCAACACTCAAACTATTATTAAAAGAATGGCTCTTTTGTGTCTCTTTCTAGCTCCTAAATCTCCAGGAGAACGCACCCGTTACGATACATCCCTTGGCCTGCTGACTAAGAAGTTTGTGGGCTTGCTGAGTGAATCTGCTGATGGGGTTCTGGATCTAAACTGGGCCTCAGAGGTTCTGGAGGTTCAGAAG[A/T]GACGCATCTATGACATCACCAATGTTCTGGAAGGAGTGCAGCTCATCCGCAAGAAATCCAAAAACAATATCCAGTGGCTGTAAGTGTGCCTGACTGAATGCTTTTTAAACAAGCTACTATATATTGAAATTTGATTAGATTTTTGAAACGCATGACACAAACAAGGTGGTGTTGTATTCCATTATAAAAGTCCCTTGTTCTTACTGTGTTTCCTAACATAGTTTTCTCTTACATCTGGCCAAGTACTGAATGATACTTCTGTTTTGTTTAAACATTATTAGATGATTTCTCCATAATAACTTTTTTTTTGTTGCTTTTTTTTCCATGTGAGAAAAATTACAGAAAACTTTTAAATGTTTGGGGCCAGTAAGATTGTTTAGAAAATAAGCAGTCTACACTTATATTAAGGATTATATAAATAAAAAGAGGCTTTAAAAGCATTTTAAGTGTTACAAAAGAATCCTGAAAGTATAATACAATTTCCACAAAAATATTTCTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36429

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110903	Nonsense	239	438	4	7

Genomic Location (Zv9):

Chromosome 17 (position 27090400)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	27230319
GRCz11	17	27248710

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGACAGACAGGAGAAAGCTCTGGACGATCTCATTCAGTCCAGCTCAACA[C/T]GACTACGAGAAATGACGGAGAGCAAGGACAACCAAAGATATCCTTTCATC

Long Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTGTGCTGTGTAAATAGTCCTTGTAATCAGTCCTCGACAGTCCTCCGGCTTTGTGTGTGCAATCAATGGCGATCTGAAACAGTTGTGTGCGAGGTGCATGACAGGATTTGTAGTTTGATAGTGTGGTATGTGTGTAGCTCTCCGGCGATCTACAGTCACTGTATCACTGGTGCTTGTGACAGTATACTCTGTGTACATTTAAGCACTTTTATAATTTAACATGGTCATCAAAATGTGGCCTTTCATCTATGACCCACATGTATATACAGTATAAGACATGTTTTGTTTGTTTGTGTTAAATTTTGTGCTGTCATCAGTTTAATCAAAGCATATTCTGTACATATGTTGTGTTCTCTAGGATCAGTGGTGTATTTGAAGGTTCGTCCAGCAACTCGGAGAAAGCCAGCGCTCTCAATAAAGAGCTCTCTGAACTGGACAGACAGGAGAAAGCTCTGGACGATCTCATTCAGTCCAGCTCAACA[C/T]GACTACGAGAAATGACGGAGAGCAAGGACAACCAAAGATATCCTTTCATCGTGTTCTTGATATTTGTGAGCTTGTTTAGACATGCTGTTCAACAGTATACATCCCCGCAGCCAAACACATGTGGACTCTAATTTTTGTAAGTTTTTAAAGAATACTTGATGTTAAATGCTCTGCTTTTCCTGCATTTGAGTTGGCAATCATTTTTTAATGCTTAAATGTTTTAGTCCTTAACTCGGTTTAACATTAGGGTATGTGACGTATCAGGACATTCGTACCATAACCAGCTTGAAAGATCAAACTGTGATTGCTGTCAAAGCACCATCTGAAACCAAACTGGAAGTTCCAGAAGCGTCCGAGGTATATTTGTCAAAACCAACATTCTTGAAATCCACTGTTATTCTGAGCTTGTTTATTTTAATTGCTGTTAAAGCTTGTGAACCATGATATCTTCCTAAAGTAAATAGCTGTCAGAAATATTTCTTTCTCCCATTTATCATGTG

Associated Phenotype:

Not determined