Busch Lab

ZMP

tcf12

Ensembl ID:
ENSDARG00000004714
ZFIN ID:
ZDB-GENE-040516-11
Description:
transcription factor 12 [Source:RefSeq peptide;Acc:NP_999981]
Human Orthologue:
TCF12
Human Description:
transcription factor 12 [Source:HGNC Symbol;Acc:11623]
Mouse Orthologue:
Tcf12
Mouse Description:
transcription factor 12 Gene [Source:MGI Symbol;Acc:MGI:101877]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa14175 Nonsense Available for shipment Available now
sa31600 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa14175
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009938 Nonsense 22 533 2 13
ENSDART00000073766 Nonsense 191 336 9 13
ENSDART00000127387 Nonsense 86 591 4 14
ENSDART00000131282 Nonsense 191 702 9 19
ENSDART00000136745 None None 54 None 4
ENSDART00000138263 Nonsense 22 177 2 6

The following transcripts of ENSDARG00000004714 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 54006676)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52276526
GRCz11 7 52551596
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTCTCAGTAGTAATRCTTTTTTTTNATTTATGTGTGTCTGCAGGTGTA[T/A]GCACCATCTCCCAGCTCAGAGGACTWCAACAGAGACTCTCCGTCTTATCC
Long Flanking Sequence:
GGCCGTAGCCTCATGCCTTTGATCCTCCTCTACTGGAATGGGCATTTCTGCAGCTGTAACCACTGCTCTGCTGGCCCGACCCCATCCAACCCCAAAGCTCCTAAAATACACATGCAGAAACACAAACACATGCACCCCCAACGCTCTTGCTTATTAATCCATTTGTTTCGATGCTTTGTTCCTGCATGTCGTCATCATTATACTACAATTAAGCACCGAAGCACACACACTCTATGTCGCAGATAATCCTCCGCTTTCTTATTATACGACTTCTAAATTAGCCATCTGCTTCATCAAAGACTTTGTAATTTGCCATGTGTGTTGCGTTGTGTTGTTTGTGCTCTATTATGCAGTCAGGTTTCATGGTATGTGTGTGTTAGACCGAGGGGTATGAGGATAGCTTAATGACGATGGTCGCTGTGGTTTATATTTGGTACAGAAACACCTGTCGGTTCTCAGTAGTAATGCTTTTTTTTTATTTATGTGTGTCTGCAGGTGTA[T/A]GCACCATCTCCCAGCTCAGAGGACTTCAACAGAGACTCTCCGTCTTATCCGTCTCCAAAACCCCCCGGCAGTATGTTCGCAAGCACTTTCTTTGGTCAGTCATCAGCATTTTATTCATTTATATTTAATTCTTTGTTTGATTGTCATATTTTTTTGGAGGGTGGGGGGTGTTGACTTTCTTTGAAAGGTTGTGTTTTTTGTAAACAGCAAAAGTCAGTCCAAGGCACTCAAAAATGTGGAAAAAATATTAAAAAGCCTTTATTGACATGGCTATTACTTAAAACTGCATTTCGGCAAACAACTGCCATCGTCAGGGTAGTGAAGACAATGTGCATCTGGAGTTTCTTTTGAACACTATGATCTCATGACTCATTAGAATATCTAAACAATACTAAAATAATATATTGAACACAATGTCAACTTAATTGTTATTAATTCAGCATTTCAGAATGGAAAAAACTCTTAATGGAAAAAAAAGATCATGCGTTATGCAACATTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31600
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000009938 Essential Splice Site 54 533 2 13
ENSDART00000073766 Essential Splice Site 223 336 9 13
ENSDART00000127387 Essential Splice Site 118 591 4 14
ENSDART00000131282 Essential Splice Site 223 702 9 19
ENSDART00000136745 None None 54 None 4
ENSDART00000138263 Essential Splice Site 54 177 2 6

The following transcripts of ENSDARG00000004714 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 54006580)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 52276430
GRCz11 7 52551500
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCGTCTCCAAAACCCCCCGGCAGTATGTTCGCAAGCACTTTCTTTGG[T/G]CAGTCATCAGCATTTTATTCATTTATATTTAATTCTTTGTTTGATTGTCA
Long Flanking Sequence:
GCTCCTAAAATACACATGCAGAAACACAAACACATGCACCCCCAACGCTCTTGCTTATTAATCCATTTGTTTCGATGCTTTGTTCCTGCATGTCGTCATCATTATACTACAATTAAGCACCGAAGCACACACACTCTATGTCGCAGATAATCCTCCGCTTTCTTATTATACGACTTCTAAATTAGCCATCTGCTTCATCAAAGACTTTGTAATTTGCCATGTGTGTTGCGTTGTGTTGTTTGTGCTCTATTATGCAGTCAGGTTTCATGGTATGTGTGTGTTAGACCGAGGGGTATGAGGATAGCTTAATGACGATGGTCGCTGTGGTTTATATTTGGTACAGAAACACCTGTCGGTTCTCAGTAGTAATGCTTTTTTTTTATTTATGTGTGTCTGCAGGTGTATGCACCATCTCCCAGCTCAGAGGACTTCAACAGAGACTCTCCGTCTTATCCGTCTCCAAAACCCCCCGGCAGTATGTTCGCAAGCACTTTCTTTGG[T/G]CAGTCATCAGCATTTTATTCATTTATATTTAATTCTTTGTTTGATTGTCATATTTTTTTGGAGGGTGGGGGGTGTTGACTTTCTTTGAAAGGTTGTGTTTTTTGTAAACAGCAAAAGTCAGTCCAAGGCACTCAAAAATGTGGAAAAAATATTAAAAAGCCTTTATTGACATGGCTATTACTTAAAACTGCATTTCGGCAAACAACTGCCATCGTCAGGGTAGTGAAGACAATGTGCATCTGGAGTTTCTTTTGAACACTATGATCTCATGACTCATTAGAATATCTAAACAATACTAAAATAATATATTGAACACAATGTCAACTTAATTGTTATTAATTCAGCATTTCAGAATGGAAAAAACTCTTAATGGAAAAAAAAGATCATGCGTTATGCAACATTTCTTAAATAACATTATCTTTTTTATTCTTAATTTTAAAATTTTAATATTGTTTAGATATTTTATCATAGATCATAGTGTTGAAAAGAAACTCCAGACA
Associated Phenotype:
Not determined