Busch Lab

ZMP

taf7

Ensembl ID:
ENSDARG00000019572
ZFIN ID:
ZDB-GENE-020419-18
Description:
transcription initiation factor TFIID subunit 7 [Source:RefSeq peptide;Acc:NP_775367]
Human Orthologue:
TAF7
Human Description:
TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 55kDa [Source:HGNC Symbol;
Mouse Orthologue:
Taf7
Mouse Description:
TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor Gene [Source:MGI Symbol;Acc

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa30678 Nonsense Mutation detected in F1 DNA Not yet available
sa7395 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30678
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
ENSDART00000074498 Nonsense 174 290 8 10
ENSDART00000128588 Nonsense 174 362 8 13
ENSDART00000139397 Nonsense 174 222 8 9

The following transcripts of ENSDARG00000019572 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 42181318)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 40492643
GRCz11 14 40859897
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTAACCTGATTTATCCTGCAGTACATCGAGTCTCCTGATGTGGAAAAA[G/T]AGGTGAAGAGACTCTTGAGCACAGATGCAGAAGCCGTCAGCGTTCGTATC
Long Flanking Sequence:
AGAAAGAGGCGGTTCAGGAAGACAGCGAAGAAGAAGGTAACCTCATTTGCTTTTCCTTAACTATGAGGTTTTTATTTCTGATGATTCAGCAATTCTTTATCAGTCCTAGATGGACTACAATTGTTTGCTCTTGCGGGAAAAGAGAATCGAGTTAATGGTAAAAGCTAAGATTTACATATAAATAAAGCATTCCATCTTCATTTGCCATAAAAGTATGCAGTAAAGGCTGCTCTTCTGATTGAAATGACAGCAGGCCAGTTAGCGGCTGGTTCTTCTCTCTGACTCCTGAATAAATCACCACTGCATTCCAGCTTGCTATTGACTTGGCTTCTTTTTTTAATCGCTAATGTGTTCTCTGGCCTACATCCAACCTCTACTGTTAGTACTGTGTGTGCATTTGAATGCATGCGTGCATTTTTTTTTTTTTACAACGTGTTCCTTGGGGGTAAATTCTAACCTGATTTATCCTGCAGTACATCGAGTCTCCTGATGTGGAAAAA[G/T]AGGTGAAGAGACTCTTGAGCACAGATGCAGAAGCCGTCAGCGTTCGTATCCTTTAATTCTTGCTTTTGTTTCCCTCGCTGTCATGTTTTGTTGAAACTGTGTCACAACAAATCTACATGAAAATGTCATTACTAATGGATTGAGCTTTCGTTATACTTGGCCTCGCCACCAGGTGGCAGACTTGCTCACAAGTTAAGCAGAGCGATTGGGCAAGAAGCAGTCAGTTAAGCTCAGTATTACAGGAAAAGGTGGCATGAGTCACATATAAATTTGTGTAGCTCAGCAGCAGTGATACAACCACAGCAAAATGTCCTGGTGCCAAAACTGAGAGGATGAAAAGATAACAGGATTATTGAAATGAACCTTGACCCTGCGGTCAGGATGGGAGGTGATTGCTGAAGATGAATCTAAAGAACCTGACAACAGCTTATCTCTTTCCAACCTGGAGTCTTCACCCGGAACCTCTGGACACAAGGGTCATGGCTCTTCAGGTAAATGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7395
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 > G
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000074498 Missense 228 290 10 10
ENSDART00000128588 Missense 228 362 10 13
ENSDART00000139397 None None 222 None 9

The following transcripts of ENSDARG00000019572 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 42184430)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 40495755
GRCz11 14 40863009
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCATGTAWAAAGTRTTCACACGTTTTTTTTNCCCCTAATTTAGTCCAA[C/G]ATGAYGAGCTTCGCGAGATCTTCAACGACATCAGCAGCAGCAGTGAGGAT
Long Flanking Sequence:
TGTTAATTGCGTGTCAGCATTGTTTTCGGAGGTGCAAGTCATTTATTAAATAAGTAAAAGATTGACGCAGCATCTCCTACCACAGCAAATTCCGTCTTCACTGTTGATATTTGGCACCAGTTAATCAGGAAGTCATGATTTTGGATGGAATTGCTGCTTTATTCGCACATCTGTTATGCGATATTCCAGTTTTCTGCATACATTTCATTCTTTGGATGCAAACAGCTATAGTGGTTATTAAAATCATGCTAAAAGATACTGATGCTGAAACTATTTTGATATTATTTGAAAAGTATTTTTTCATAGAAGAGTATTTTTATTATGTACTACTATTATATAAGCACAATAGCCGCCTGTTTTTTCTGTTTATTAGATGTCATGGAAAATCAGCTTTTTATTATTAATTTAATATTTGGCTTTTAGTGGGAAGTTGAGAATCCTGTACTTTGTACCCATGTATAAAGTGTTCACACGTTTTTTTTCCCCCTAATTTAGTCCAA[C/G]ATGATGAGCTTCGCGAGATCTTCAACGACATCAGCAGCAGCAGTGAGGATGAAGACGAAGAGGGCGATCGACATGATGATGAAGATCTAAACATCATGGACACTGAAGATGACATGGTCAGGCAGCTCCACGAGAAACTGAACGAGTCAGATGGAGGCAGAGATGAAAATGACCGGAACAGTCAGATCGGTAGGATGTTGCCACACTGGTTGTCTGATCAATTACAGCGCATCCTCAGCAGCTCAGACCCAACTTAAACCGCAATTCAGTATCACAGGCAGGCAGACCGGCAAACAAACAACAGCCGACCTAGATTAGCATTTGAATGATGAGTCTGCTGCAGTATTTAGGTCAGATGGGTGTACCGGTTGTCTGCTGGTGTTTCTACCCATGCTGATGAGTGACAGACGTGCCTGACCTTGGCATCAACTAGCCTTCAACGCCACACTGGCACTTAACCTGCAGAAATGAGCCATGCCGCTCAGAGCTGTGCCGTTGTG
Associated Phenotype:
Not determined