ZMP

ENSDARG00000088197

Ensembl ID:

Human Orthologues:

TAF4, TAF4B

Human Descriptions:

TAF4 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 135kDa [Source:HGNC Symbol
TAF4b RNA polymerase II, TATA box binding protein (TBP)-associated factor, 105kDa [Source:HGNC Symbo

Mouse Orthologues:

Taf4a, Taf4b

Mouse Descriptions:

TAF4A RNA polymerase II, TATA box binding protein (TBP)-associated factor Gene [Source:MGI Symbol;Ac
TAF4B RNA polymerase II, TATA box binding protein (TBP)-associated factor Gene [Source:MGI Symbol;Ac

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38975	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15594	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa38975

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126760	Nonsense	146	439	1	4

Genomic Location (Zv9):

Chromosome 13 (position 52366129)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	409600
GRCz11	18	298818

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAACAAAGGTGCGGACACCCGCAAGAAACACCCGACGCGCTCCCTGCGCT[C/A]AGCGGCATCACACAGTCTCAATGGCAACGGCGCGGCAGCATCAGCATCCG

Long Flanking Sequence:

CGCACCAGCAGACAGCCCATCACACACACACACAGAGAGAGAGAGAGAGTGAGAGAGAGCGAACATGGCGGGCGCCTCCGACCCTCTGGAAGACATGCTCTTCTCCGAGGTGGACGAGAAAGCCGTGAGCGATCTGGTGGGCTCTCTGGAGTCTCAGCTTGGGGGCCAGACCGACCCGTCCGCCGGGCAGCCCGAAAACACTCGCGGCAAGCAGCAGCAGGCAGGAGCAAGAGCGCAGCTGCCCGCTCATGACTCTCCATCACAACCACAACAACAAGCACAGCAGCAGCAGCAGAACGCGCGCAAAGCAACGCGCAACCCGGATCCAGACCCGAAAGATGTCAGCCCGGAAAAACACGCGAAAGCTCCGGAGAAGGAGAGCGCGCTCAAATCACATGGCAGCATCATTATCATCACCGCGGCTGCAGCATCCGACGCTCCTGCGCCGGGCAACAAAGGTGCGGACACCCGCAAGAAACACCCGACGCGCTCCCTGCGCT[C/A]AGCGGCATCACACAGTCTCAATGGCAACGGCGCGGCAGCATCAGCATCCGTCTCCAGCACCACCTTCACTGTGTCCAGCAACCCGCAGGCGATCGCGCTGGACCGCGGGACGCCCACCATCGCCCTGCACCGACTCCCGCGTCACATCATCGCCAGCATCGCGCAGAAGGGCAACGGCACGTCCGTGTCCGCGCTGGTCCAGCAGGGCGCGCGGGTCAACCACAGCAAAGCGCCCGCGGAGGCCAACGCGAAGCCCGCGCTGAGCTGCTCTCCGCCTCCGCCTGTCAAACCCGCGGTGGCTCCGGTCATCAGACCCGCGCAGACGCAGACGCAGAGGCTCGTGGCGCCGCAGCTGATTGTCAGACCTCCGCCGCCACAGCAGCAGCCGCAGCAGCAGACCACCATCCAGCTGCCACCCGGGTTCACCATCCCACCAGGTACCCAGAGCTTTCTCATTATTGCCCACTGCTGTCTGCTCTGACTGCAATGCACACACTGTC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15594

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126760	Essential Splice Site	292	439	1	4

Genomic Location (Zv9):

Chromosome 13 (position 52366568)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	409161
GRCz11	18	298379

KASP Assay ID:

2260-7045.1 (used for ordering genotyping assays)

KASP Sequence:

CAGCAGCAGACCACCAWCCAGCTGCCACCCGGGTTCACCATCCCACCAGG[T/C]ACCCAGAGCTTTCTCATTATTGCCCACTGCTGTCTGCTCTGACTGCAWTG

Long Flanking Sequence:

CCTGCGCCGGGCAACAAAGGTGCGGACACCCGCAAGAAACACCCGACGCGCTCCCTGCGCTCAGCGGCATCACACAGTCTCAATGGCAACGGCGCGGCAGCATCAGCATCCGTCTCCAGCACCACCTTCACTGTGTCCAGCAACCCGCAGGCGATCGCGCTGGACCGCGGGACGCCCACCATCGCCCTGCACCGACTCCCGCGTCACATCATCGCCAGCATCGCGCAGAAGGGCAACGGCACGTCCGTGTCCGCGCTGGTCCAGCAGGGCGCGCGGGTCAACCACAGCAAAGCGCCCGCGGAGGCCAACGCGAAGCCCGCGCTGAGCTGCTCTCCGCCTCCGCCTGTCAAACCCGCGGTGGCTCCGGTCATCAGACCCGCGCAGACGCAGACGCAGAGGCTCGTGGCGCCGCAGCTGATTGTCAGACCTCCGCCGCCACAGCAGCAGCCGCAGCAGCAGACCACCATCCAGCTGCCACCCGGGTTCACCATCCCACCAGG[T/C]ACCCAGAGCTTTCTCATTATTGCCCACTGCTGTCTGCTCTGACTGCAATGCACACACTGTCAAAGAGTAGACAACCAAGTCATGACAACTTTAGTTGTTATGCTAATTATAACATGTTAAACTCGGGTAATAACAAACTTTTTTTTTAAGTTAGCTGTTTTAAGATTAAATTCTGTGATCATTTGCTCACTGTTCACTATTTCCATACCCATTTCTTGTATTCTTTAAAAGGGTTATTTATCATTATTTTTCCAGCTCTTTCTCATTATTGCATTTACATTTACATTTAGTCATTTAGCAGACGCTTTTATCCAAAGCGACTTACAAATGAGGACAAGGAAGCAATTTACACAACCAAGAGCAACAATGAATAAGTGCTATAAGCAAGTTTCAGGTCTGTAAAGTCTAAGAAGGGAAGTATTAGTAGTATTAGTTTTTTTTTTTTTTTTTTTTGTACAGTTAGTGTGATATTCTGAGAGGCAATTGCAGATTAGGAAGTG

Associated Phenotype:

Not determined