ZMP

LOC571865

Ensembl ID:

ENSDARG00000079972

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
sa20827	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa40804	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20827

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113805	Essential Splice Site	439	792	4	10

Genomic Location (Zv9):

Chromosome 6 (position 55215483)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	55231796
GRCz11	6	55241609

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAAGATCCTTGAGGTGCCGATGGAACCCAAGGAGAACATGAGAGCTGTG[T/A]AAGAACATTATTATTATCACATTCAGTTCAATTCAGGTTTATTTGTAAAG

Long Flanking Sequence:

TGAGAATTTAACTCAAAACAAACAGGAAGTGCATTTTCAGATTTCAATTTTAGATTACAAGGGCAAACCTTTTTTTAATGACACTGACAGATGAATTGTTCACCACAAAACTAGCAATTCATCCATTCATTCATTCATTTATTCATTCATTTCTTTTTTTTTTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGTAGTGCCTAAACTTGCAATGAGAGCAAACAAAATCAACAGGGTTAGGCTTGATGTCATGTGAATTTTAACTGTGTTTTGGGCTGTCTCAGTTGCGAGGGTACACCGGGACGGAGCCGCTGGTTCTCCAGATCTTTATTGGCACGGCTGATGACAGGAACCTTAGGCCTCACGCCTTTTACCAGGTCCACCGAATCACCGGCAAGACCGTCACCACCAACAGCCAAGACCGAATGCTGAACGGAACCAAGATCCTTGAGGTGCCGATGGAACCCAAGGAGAACATGAGAGCTGTG[T/A]AAGAACATTATTATTATCACATTCAGTTCAATTCAGGTTTATTTGTAAAGGGCTTTTCACAGTAATTATCCTTACACATGAAGAAGATCGGGTAGCACGGTGGCTCAGTGTTTAGCACTGTCGGCTCATAGCAAGAAGGTTGCGGGTCCCAACGGGTCCAGTTGGCATTTCTGTGGGGAGTTTGCATGTTCTCCCGTGTTGGTGTGGGTTTCCTCCAGGTACTCCGGTTTCCCCCACAGTCCAAACATATGCACTATAGGTAAATTGGATAAACAAAATTGGCCATAGTGTAAAGTATGATTGTGTGTGTGTTTGAATGAGTGTGTATGGATGTTTTCCAGTAGTGGGTTGTGGCTGGAAGGGCATCCGCTGCATAAACATATGCCTGAATAGTTGGTGGTTCAGTCCGCTGTGGCAACCCCTGATTAATAAGGGACTGAGCCAGAATGGTATATGCCAGAAATAAATTAAAGAAGCCCCAGAATAGAGATCTGCGCGGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40804

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
ENSDART00000113805	Nonsense	483	792	5	10

Genomic Location (Zv9):

Chromosome 6 (position 55214239)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	55230552
GRCz11	6	55240365

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACACCCGTGTGAGATTGGTCTTCCGTGTCCATATTCCTCAACCTGGAGGA[C/T]AGTGGCTTTCTCTCCAAGTGGCCTCGCAGACCATTGAATGCTGTATGCAT

Long Flanking Sequence:

ACACACACATTGACAGCGTCTCCCTCTCTCTTTCATTCACACACACACACACACACACACACACACACAGAGAGAGCACAAAGCTCACACAGACAGCAACAAACAAGCTAAACGGAGCATCATGCTGTCTCTTTCACACATATACATGCGCGTGCTTGCTTGCTCGGGAGTGGGGAGCTAGGAGCGATATTGTGGAACCGCCCGCTTCTGTCCAAAATTAAACCTGTTACCGTCCGCTCCCACGCTTAATTGGAAATTTATTCCCGCGCTACAGAAATGTGGTCGGGTCCTCTCCCCCAGAAAGAATGAAACATGAACAGCATGTGATAAAAGGAAGGTTTACTTGTTAAAAGTCTGTTTTTGTTTATAGAATTGACTGTGCCGGTATTCTGAAGCTGAGGAATGCTGACATCGAGCTGAAGAAAGGAGAGACGGATGTGGGACGGAAAAACACCCGTGTGAGATTGGTCTTCCGTGTCCATATTCCTCAACCTGGAGGA[C/T]AGTGGCTTTCTCTCCAAGTGGCCTCGCAGACCATTGAATGCTGTATGCATTTACATTTTTCAATTAAATCTTACTTAACTCATTGGCCCACATTTTATTGCACTTACTTTTGCATGGAAAGCTTTATAATATTAATGCTCTTATATGTGAATTTTAGATATTTAAATGTAATTATTACATTTAAATAAGTATATAAAGAGTTCAGATGCAAAAACCTCTAAGGCTACGTTCTGAATCAGATTTTTTTTTCTCAGATCAGATTTTTTTGCATGGCTGTTCACATTGTTGACATAAATGTGGCCAATATCAGATTTGCTGTGTGAACAGATCATGGTCCTAAACTGACCCGCATGCGCAAAAGTACAATTACGGACAGCACAAAATGTCTAATTATGCACACAGTGTGTATACAGTATGAAGTAAGCATGTTGTCGGATTATGCTTAATATGATTATTGCCCTTTTCACAGACAGCCGTGGTGTATTTCACGAACTGTGATA

Associated Phenotype:

Not determined