Busch Lab

ZMP

tcp1

Ensembl ID:
ENSDARG00000017891
ZFIN ID:
ZDB-GENE-990714-24
Description:
T-complex protein 1 subunit alpha [Source:RefSeq peptide;Acc:NP_571305]
Human Orthologue:
TCP1
Human Description:
t-complex 1 [Source:HGNC Symbol;Acc:11655]
Mouse Orthologue:
Tcp1
Mouse Description:
t-complex protein 1 Gene [Source:MGI Symbol;Acc:MGI:98535]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa7506 Missense Mutation detected in F1 DNA Not yet available
sa12092 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa7506
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:
T > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126038 Missense 65 558 3 12
Genomic Location (Zv9):
Chromosome 23 (position 2440140)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 2487008
GRCz11 23 2426387
KASP Assay ID:
554-4282.1 (used for ordering genotyping assays)
KASP Sequence:
TKCTTGTGTGTTTCAGGACGTGACCATCACCAATGACGGGGCCACCATCC[T/C]GAAGCTGCTGGAGGTCGAACACCCGGCTGCTAAAGTCCTCTGTGAGCTGG
Long Flanking Sequence:
ATGTGACTATTGCAGATTTGCACATTGCATTATCGATGCCGATATTGTGCAGCCCTTGTTTGAAACCCTTTAACATTTACATCCTACTGGTTATAGTATAAATGTGGTAAGGATAAAAAGGGAAACCTTTAAGTATCTGCTTTTTGTTTTTTCGCCCTGCAAATTTTTTTTGGGGTCAGAACCAAGAGTCAATAAACTGATTTGTTTTGAGCAATTGGAATTGCTAAAATTAAAATGACACCCTTTCCCAGAGATGGGTTGCGCCTGGAAGGGCATCCGCTGCAAAAAAAACTTGCTGGATAAGTTGGTGGTTCATTCCACTGTGGCGACACCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAAAATGACACCCAACCCTAGTGCTTGTCTTCACCCGTTGGAGTAACTAGTATCCAAGTTTTTAAGACCATTTGCTTGTGTGTTTCAGGACGTGACCATCACCAATGACGGGGCCACCATCC[T/C]GAAGCTGCTGGAGGTCGAACACCCGGCTGCTAAAGTCCTCTGTGAGCTGGCAGAGCTGCAGGACAAGGAGGTTGGAGACGGCACTACATCAGTGGTGAGCTGAAGCTGTGCATTAGCAGATTTTCCTGTTATAGTACCATCCATCTGAGCTGCGTCGGTGTGTGTGGCTATGCTAACAGGATACAGAAACCCTCTCGGAACCTTCAGGAAATGCAGAGCTTCTGCTGCAGCTTCCACAAGGTTGAGAGCACATTGAGTTTTCAGTCCCTGGACACTTTTCACGTTTCTGGGTTTCTCAGTAGTGGACATGATTGGGTAAACTCAGAGCGCAGTGAGAGTATAACAAATATTGTTTACAATACTGTTTGCTGAAATAAGAAAAACTTGATGGGGTTATCAAGTCTTTCAGAAGGACAAAAATGGTCTGAGACTGATGACGGCAATAATGTAAATCTACTAGGGGTGTCAATTAATCGTTTCTTCGGTGCATCGCGATGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12092
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
ENSDART00000126038 Essential Splice Site 328 558 8 12
Genomic Location (Zv9):
Chromosome 23 (position 2452272)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 2499140
GRCz11 23 2438517
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGAGTCCTGAAGAAAGACCTCAARCGCATYGCTAAAGCTACTGGAGG[T/C]CTGCTKAATTAACCTGCTCGCTTTACTCTGGTGTGTGCATTAGTGATYGA
Long Flanking Sequence:
CGGACCCCAGGTTAGCTTTTACCCTATAAATCTGATATGTTTACTCTACCATTGCTGTTTTTAAAATTAATGCACACAAACATTTTGCACCCATTTTAACATTAGAATCTATTGATGATCACTTGTGACAATGATCTTCATAACCATGTAAATATGACCTGTTACATGTGAGCATCTTATGAAGAATAAAAAATAAAAATGGGTAGAATATATCATTTTACCTGAGATGGTTTCAGGATTCGTTTGTAAGATTAGGCATGCTTTTTCCATATAGTTATAATTTTGTTTCTCTATTAATTTTTTTCCTCACTCTTGTTTTTCAGGGAATCGGACATCACAAAGGAACGTGTTCAGAAGATCCTGGCATCAGGGGCGAATGTGGTTTTGACCACAGGAGGAATCGACGACATGTGTCTGAAGTATTTCGTGGACGTGGGGGCCATGGCGGTGAGAAGAGTCCTGAAGAAAGACCTCAAGCGCATCGCTAAAGCTACTGGAGG[T/C]CTGCTGAATTAACCTGCTCGCTTTACTCTGGTGTGTGCATTAGTGATTGAGTTCTGATCATGAGTGTTTTTCCTTCACAGCCACGGTTTGCTCTTCTCTGTCCAACCTGGAGGGCGAGGAGACATTCGAGCCGTCCATGTTGGGTCAGGCAGAGGAGGTGGTGCAGGAGAGAGTGTGTGACGACGAGCTCATCCTCATCAAGAAGTGAGACTGAGATACTTTCATTTAAAACAAACTGAGAAGTCACGTTGAGCTTTATTGTCATCATGCTACATGTGTGGACATTAGGGCTGCACAATTAATCGAAGAAAGTTCACGATCTCGATTCGACCCTACACAGGATCTTAATTCAGCTTTTCTACGATTAAGCCAATTATATTTTCAAGGTCAGGAGGGAAGCTTAAAGGTTCAGGACACCCTGGAGAACTTTTTATATTAACAGATGTGTGTGTGTTGAGCATCAGTTAAGACAATGTTAGCACCTGTCAGCTGTATTTGTG
Associated Phenotype:
Not determined