ZMP

TTF2

Ensembl ID:

ENSDARG00000086795

Description:

transcription termination factor, RNA polymerase II [Source:HGNC Symbol;Acc:12398]

Human Orthologue:

TTF2

Human Description:

transcription termination factor, RNA polymerase II [Source:HGNC Symbol;Acc:12398]

Mouse Orthologue:

Ttf2

Mouse Description:

transcription termination factor, RNA polymerase II Gene [Source:MGI Symbol;Acc:MGI:1921294]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16912	Nonsense	Available for shipment	Available now
sa41360	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16912

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
Order Allele From EZRC

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126063	Nonsense	274	1149	5	25

Genomic Location (Zv9):

Chromosome 9 (position 10154902)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	9959077
GRCz11	9	9930450

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTCCTAGAAAAACCKSCGGCTCTGCACAAAGCCCTTCAAAAAGCTCACCT[G/T]GACTTGACAAGAAAACCTCAAACAAGCAAAGCAMTTCTAATTCAAAATCA

Long Flanking Sequence:

ATTTGTTGGAAAATCTTCAATCCTCAAGTTTGACTCTGGTCAGGAACCCTTTCAAGGTCAAGATAAAACAAGACAAGGCTTTAAAACTTAGAAGTGATCCAGATGCTGAAAAAGACAGAGGAGAGGTCAATGATGAAAATAAACATGCGAATGTGCAGGATAATGATAAAAAAAGAGATGAGCGAACTGGGACAACAGAAAGAGAAGGGAATAATAAGAAAGGGCCTGCTGTTCATAGTGACACAGAGAGAAGAGACTCTGCAGATTCAGAGTCCTGGAGAAACAAGACGCTTCCCACTGGGATGAAGATAAAGAAGAGAGTGTCTGATGATGAAAAACCAAAGAGCGCAGCAGAGGATGAGACATGTCCCGAGAGTTCAAACCCTGTGAAGGAAAATGATAAAGGGCAGACTGAATCTGAGAACAACCTCAAAGACCAGCAGGAGCAGAGTCCTAGAAAAACCGGCGGCTCTGCACAAAGCCCTTCAAAAAGCTCACCT[G/T]GACTTGACAAGAAAACCTCAAACAAGCAAAGCACTTCTAATTCAAAATCAGGTTCAGATAAAACTCAAAGCCAGTCACCCTCTTGCTCGACGTCACAGAACGGGACAGTTTCTGAAAAGCCCACAGCACTTGATGTTCAGAAGATAGAACCAAATCAGAGTAAGAATAAGGACCAGAGTGGAATAGCATGCTTCGGTGAGTGGAGCGATGAGGACGATGATGTTCTGGTGATTTCGGTACAGCCTCCATCACAGCAGAGTGCTCCAACTCCAGCTGTACCTGTTCAGAAAACAATCACTTCGTACCCTGGTTTTCAGATTGCTTCTAAAGTTCAGGGTCAGTCTGAAGACCCTAGAGCCCTCCACAGCCAGCTCAAAACCCAGCTCAAGCAGAAGAAGGTTACTTGCTCTTTAATGCTTTCTCATATTTCTCAACATTTAGACTGAACTAGTTATTTTTAACTCTATGTGGGTGCTTTATCCTCCAGGCCACTCTTTCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41360

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
ENSDART00000126063	Essential Splice Site	998	1149	22	25

Genomic Location (Zv9):

Chromosome 9 (position 10172730)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	9976678
GRCz11	9	9948051

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTAATGCTTGAGATTCTCTGAGTGGGTTTTTGTAATTTCTTGTTTGGCA[G/A]TGTGATTGTGTCTCAGTGGACCAGCATGCTGAAAATTGTTGCCGTTCACT

Long Flanking Sequence:

AATATGTTGGTTGTAGAACATGACCGATTTCCACTGAGAAAAAGTTATCAAAAGAACGTTCCTCACTACACTGTAAAAACAGATTTTTTTATTAGAGGCTTTGTCTCGTTTCTAGTCCAAATTAAACAAACAAACAGCAACAGCTGATTACAATTAGGTACGTTTCTCCTTAGAACAAACTAAATAATTGCCAATTGGGGTAAGCAAAATAATTTTTCTTACCCCACTAGCAGATTATTTAGCTTATTCTAATGAGAAACTTACTTATTTTGGCCTTTTTTTCTGAAAACAAGACAAAATAATTTAGCTTGTCTAGAAAAGTTTTCTTGATTTGAAAGTTTGAGATATTTGGACTGGAAGCAAGACAAAACCATATTTTAGAAAGAAAATACTGTCAAAAATCCTTGTATGTCATTAATTGGATTATTTCAGTCTTTCTTCAAACAATATTGTAATGCTTGAGATTCTCTGAGTGGGTTTTTGTAATTTCTTGTTTGGCA[G/A]TGTGATTGTGTCTCAGTGGACCAGCATGCTGAAAATTGTTGCCGTTCACTTAGAGAAAATGGGTCTGAAGTTTGCAGTAATTGATGGCACCGTCAATCCCAAACGCAGAATGGATCTAGTAGAGGAGTTCAACACAAACCCTAAAGGACCTCAGGTGTGTGGATTGTTCCTTTGCATTGTGAAGGTCAAAAATTTTGATTTATTGGTCAAACATTTTGATTTATTGAATGGCTTCAATCTCACAGATGGCTAAAGATCAATAGCTAATATTAGCAATTGTTATTTATGCTGTAGGTGATGCTGGTGTCTCTGTGTGCTGGAGGTGTAGGAATCAATCTGATTGGCGGAAATCATCTGTTTTTAATCGACATGCACTGGTGAGACACTTCACAAGAAAGATGCTTAATGAGCATTTTTACATAATTTCAGCGCTGCACAGAAGAACTTAATATTAGCAATTTCTGTCACTTGTTTAAATGTTTGAATTGTGTTTAAAACTG

Associated Phenotype:

Not determined