Busch Lab

ZMP

nfatc1

Ensembl ID:
ENSDARG00000036168
ZFIN ID:
ZDB-GENE-060503-677
Description:
nuclear factor of activated T-cells, cytoplasmic 1 [Source:RefSeq peptide;Acc:NP_001038624]
Human Orthologue:
NFATC1
Human Description:
nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1 [Source:HGNC Symbol;Acc:77
Mouse Orthologue:
Nfatc1
Mouse Description:
nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1 Gene [Source:MGI Symbol;Ac

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa36826 Nonsense Mutation detected in F1 DNA Not yet available
sa39244 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36826
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052521 Nonsense 283 867 2 10
ENSDART00000134749 Nonsense 277 633 1 7
Genomic Location (Zv9):
Chromosome 19 (position 22706077)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 22637457
GRCz11 19 22221780
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGCCCTCACCACAGATGGATTAACAGATCTTGCAGAGGGGATTCCTT[T/A]GAAGTCCCGCAAGACCAGTCTGGAACACAGTGCTTCAATGAACCTGAAAG
Long Flanking Sequence:
TCGTGACCCTACCTGCCTCAGTCCGGCAAGCAGCGTGTCCTCTCGTAGCTGCCATTCAGATGCTTCTTCATACGAATCTGGCTTCTCCTACAACTACGACAACTCTCCGCAGAACTCGCCTTGGCAGTCCCCTTGCGTCTCCCCAAAAGGTTCCTCCTCTCTGCAGTCCTGCACTCTTGGTGCTTCTCCACGCCATTCTCCATCCGGTTCTCCTCGAACCAGTATCACTGATGACAACTGGATAGGCAATCGGGGTTCCCGTCCAAATTCTCCTTGTGGCGGTAAACGGAAGTACAGCTTCAATGGTGGGCCATCGCACAAGTACCATCCGTACTCGCCAAATCAATCTCCTGGGCCGTCGCCACAAACTTCACCTCGCCTCAGTGTGACGGAGGACAGTTGGTTGCCCAATACCAATCAATACACCAACTCTGCCATTGTTGCCGCCATCAATGCCCTCACCACAGATGGATTAACAGATCTTGCAGAGGGGATTCCTT[T/A]GAAGTCCCGCAAGACCAGTCTGGAACACAGTGCTTCAATGAACCTGAAAGTAGAACCAGGTGGAGACGAGACAGGGTCCCTGGAGCTTTGCCAGGATGACTTCTCCTCAGTACGCCTACCCTTCAAGAAGGAGACCTACTGCAGTGGCTTTTTGGACGTGCCCCAACACCCATATTGGTCTAAGCCTAAGCCTTACATCAGGTAGGATAAACATTAAGAGTTTTTTTTCACAATCACAGTTGAATAGTTTCTTTATCTACATTAACAAATGCTCTTTCTCATGTTCTTGTAGTCCATCACTGCCTGCTCTTGATTGGCAGTTGCCTTCGAGCTCAGGGCCGTACAGCCTACAGATTGATGTCCAACCCAAGTCTCATCACCGTGCTCATTATGAGACTGAAGGCAGCAGAGGAGCTGTGAAAGCACTAGCGGGAGGTCATCCAGTGGTCCAGGTATCAGTTCACAATCTCTCACAAACAGGCTTTTGCACTTAGTGAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39244
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052521 Nonsense 534 867 6 10
ENSDART00000134749 Nonsense 528 633 5 7
Genomic Location (Zv9):
Chromosome 19 (position 22722107)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 22653487
GRCz11 19 22237810
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTTCCTCACTTTCCTTCTGTGTCCTTCTTGCAGCCCAGCGCTCAGCA[C/T]AGGAGTTGCCCCTCGTGGATAAACAGAGCATGGAAAGCTGTGCCGCCTCA
Long Flanking Sequence:
TAGACTTCTACAACTGTATAACTGCAGGTTATGTTTATGTGTAATAACTTTAGCTGTTAAAAGCTATTAGTTACTAGCTAATTAGTTAAAGTTATTAGTAACTAATAAAGCTATGCCAGCTAATTAGTTAAAGTTATTAGTAACAAACAAGCTATGGTAAATAATAACCTCAAATTTTCAGAATTTGATTGAAATGCTTTAGTGAAGCTGCTTTGAAACAGTAATCATAGTTTAAAAGCACTATACAAATAAAGTTGAATTGAATTGAATTTACCTTACAGTCATGTAGTAATAAATTACAACCTGCAGATTGTTTCAATCATTACAGTTGTTGCTGTATTGTGATCAAAATTAATGCAACTTTAATGAGCACTGACATTTACATTCCCTTTAAAGCCATGTAGTAAACAATACAACAATAAATATGCATAGATTTGACAGGTTTTGTACGTCTTTCCTCACTTTCCTTCTGTGTCCTTCTTGCAGCCCAGCGCTCAGCA[C/T]AGGAGTTGCCCCTCGTGGATAAACAGAGCATGGAAAGCTGTGCCGCCTCAGGGGGGGAACAGATGCTTCTCAGCGGGCACAACTTCCAGCCCGATTCCAAGGTGGTGTTTGTGGAGCGAGCACAAGGTAGGGAACACACTCGAAGTTCTGACTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGAGTGAGCAATAAGGAATTGTTTTGAAATTGCATCTCATTTGGGAGGTTTCTGAGGATAAAGCTGTAGGGACAAACGCTGGATCCCAAATCACATGCTTTCCCCAAGTACTAGGAAATACGTAAGGTGCTGACGATAGTAAATAGCATACTTTTAAGTATGATGTAAACCTGTTGGTTTATAATTAGGCCCTAGAGGAATCTCTTCGTCATTTGCAAAGTATATCCCCCATCTCATATATGGTAATTGATTAATTTGGCTTATTAATTATGTTTTTGGTTACCGGTGCATATTGAAATGTCA
Associated Phenotype:
Not determined