ZMP

NFATC2 (1 of 2)

Ensembl ID:

ENSDARG00000076640

Description:

nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 [Source:HGNC Symbol;Acc:77

Human Orthologue:

NFATC2

Human Description:

nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 [Source:HGNC Symbol;Acc:77

Mouse Orthologue:

Nfatc2

Mouse Description:

nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 Gene [Source:MGI Symbol;Ac

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12686	Nonsense	Available for shipment	Available now
sa45812	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12686

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112656	Nonsense	187	894	2	10

Genomic Location (Zv9):

Chromosome 23 (position 39198278)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	39086641
GRCz11	23	39093740

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGCCCTGCGTTTCGCCCAGTAACAGCCAGCTTTCTGGAGACCTCTGTCCA[C/T]GACTGCAGGGCGTCCATACGGGGTCTCCAAGAACCAGTCCGGGCACTTCT

Long Flanking Sequence:

AACAAACAACATGCTTGACTATTTTGCACACTTAACTACATCATTTCTTTTTTCTCTGTTTTACAGATGAGCAAGGCATCTCCTCACACAGCTCTCCTCCGAGCCTCTCCTATCCTCCAGAGGGCGTTGCCCCGTACGCCATCAAGCCGTGTGCGTCCTCCTATGTTGACGTCCACACTGAAGGCTTTTCTGCGTACGAGCAACTGGAGGCCAAGGGCTACCTGGAGCACGCCCGACCCAACAACCAGGCCTTGAGCCCCAGAATCGAAATCACACCTTCACGTGAGCTCTACAATCATGGTCAAAACCAGCTCATAAACACCAGCCCCAGTCCTGGACTCACCGTGCCAGGTCAAGATCCGTTAGCCTATCGGGAGCCACAATGCTTGAGTCCCGCCAGTAGCAATTCATCCACTTCCTGGCATTCAGAAAACCTCTCACCCTGGGCATCGCCCTGCGTTTCGCCCAGTAACAGCCAGCTTTCTGGAGACCTCTGTCCA[C/T]GACTGCAGGGCGTCCATACGGGGTCTCCAAGAACCAGTCCGGGCACTTCTCCACAGACCACCAGTCTGTCTGAGGACGCTTGCATTGGCCCGCGCTCTCCCTCCCCCCGACCTGGATCGCGTTCAACCTCCCCTCTATGCAAACGCACCTACGAGATGTACACAAACCCAAACCTTGTGCCTGTGGCCCGTTCTCGCAGCCCGTCGCCCCACGGTGGCCACAAGGAGCATCACGTCAATCATTACATCTCAAATAATGGCGTAAATGGCTTTAGTGTTGGCCAGGCGGCTTCTGTTCCTACTAAAATCGTAAAGACCAACCAGCAGGGCTACCCCCTTTATTCAGACAACCACACTGAGGGTTACCTGCTGTCCTGTGAGCAGGATATGAAGGGCAAACCTGGCCCCGAGCCTTTCTTCGTCATCCCTCAAATCTGGCCCAAACAGCTGGTACCTGGCATGTGCAGGTAAATATTTGCTTTTTTTTTCTTGTGTCTTTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45812

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112656	Essential Splice Site	633	894	8	10

Genomic Location (Zv9):

Chromosome 23 (position 39238209)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	39046710
GRCz11	23	39133671

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAAACGGAAGCGCAGTCAACCTCAGCATTTCACCTACACACCTCTACCAG[G/A]TACGCAAAGCGGTTTTTCTATATATTTTTGCTCCTGTACATCTAAGGATG

Long Flanking Sequence:

ACTGTTTTCTCATTTAATACTCCGTTTCTCTGGGAACTGAATCACAATATGGGAAAAAAAATGGTCGCAGCTTCCAGTTCATGTGCACTTACCATTGAGAAGCAGTAGATCAGTCATTTACTGATGAATAATGAGAGCTTTGGAATATGCATTACTTTAATTATGTGTATTCAACTTTTCTCTCTTTCTGTTTCCAGATGGACAGCAAATTTGGGAACTGGAAGCAACAGTTGACAAAGACAAAAGTCAAGCAGTAAGTATAAAGCATGCGTTATGCCAACGCTTGCACTTCCTGAAGGTCTATATTTAGTTCTCCTCCTGAAAAGTGACTGTAGATGCTGCAAATAAACAATTATCTCATTCACAGAGCATGCTGTTCATTGAGGTTCCTCCATATAGAGATCCGTCCATTTGCCATGCTGTCAAGGTCAATTTCTATGTAATAAATGGGAAACGGAAGCGCAGTCAACCTCAGCATTTCACCTACACACCTCTACCAG[G/A]TACGCAAAGCGGTTTTTCTATATATTTTTGCTCCTGTACATCTAAGGATGTGTTCACAATTATTGTTCAGTTCTTTTGCGCCAAACCACAAACTGCAAAGGATACAAATTTAAAACCAAACCTAAACCTGAAATGGCTTTGGTCAATGCATATTTTGTAATGGAACTTGCAGGTCATCCTAAACAATGTTATATGCTGAGATAAATCCACTCATTTGTGCTACATGTGATTGTAGTTTTATCAGCTTAAGACTTAAAGACTCCATATAAAGCATAAATTCCTTGGTTGTGCACAAACATGCCTTTACTGAATTGTAACAGGTAACATAGCTCTTATGAAAGAAAAAAAACAGCTATGCTTGAGCACACTGTCACATGCTGTTTTTATTATTGGTCCATGTTGCATAATTCATATTTCTGTTGAGTTGAGCTTGTTTGTAAGCAGAACAAGACCCATCATTATGCAGGTCTTGGTGTATATACTTGGCGTGCACAAGGTCT

Associated Phenotype:

Not determined