ZMP

ZNFX1

Ensembl ID:

ENSDARG00000074028

Description:

zinc finger, NFX1-type containing 1 [Source:HGNC Symbol;Acc:29271]

Human Orthologue:

ZNFX1

Human Description:

zinc finger, NFX1-type containing 1 [Source:HGNC Symbol;Acc:29271]

Mouse Orthologue:

Znfx1

Mouse Description:

zinc finger, NFX1-type containing 1 Gene [Source:MGI Symbol;Acc:MGI:2138982]

Alleles

There are 8 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15482	Nonsense	Available for shipment	Available now
sa17929	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa15482

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108597	Nonsense	179	1643	1	13

Genomic Location (Zv9):

Chromosome 6 (position 57375407)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	57428469
GRCz11	6	57425333

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTTTTTCTTAGCATTCTGCCACATCATGTAACTGGAAYGATGWCAGATTA[C/A]ATGCCAGCCCGAAGAGATCAGTATCCCCAGCATTTGARCAACATCATYAG

Long Flanking Sequence:

GGGAAATTTGGGAGATCTCTTCCTGGGTTGATGCAATTAAACCTGACCCCATCTTCAATGCAACAACCCATGAATTCAAGACACGACCTTGAAGGCATGAGTCTCCAAAGAACAAGTGGAGGCATGAGTGATTTAAGAGCCAGTCCACAAGGTGAAGCACGAACAGAATCTCAAAGAGGTAGAGGTGGTCATTGGAGAGGAAGAGGGAGAGATGGCCCCCCTGAGGTACGCACACTTGGGTATAAAACACTTGAAGGTCTGCTTGAGAAAGAAGCATCCGAGGTGGCCATCACTCTTTCATCTAGCACTGGACTTAGGAATCTGCTTGAGGAAAAGGTGATGAGAAATGACTTGGTGCAGCTGGTCTGTCAGGTTCTCTGCAAGGCCTTCCAGTCTCGAATTGATCGTAATACAGTGATGCACTTGGCTCGTGTCGTCAAGGACTCTCAGTTTTTTCTTAGCATTCTGCCACATCATGTAACTGGAATGATGTCAGATTA[C/A]ATGCCAGCCCGAAGAGATCAGTATCCCCAGCATTTGAGCAACATCATCAGCCTTGTCTCTGATGTTCTCAACATGTTTCCACAAAGTTCTGTGCATTCCGTCTCCATGTTGGTGACTCTTTTGAAACCAACCATCAATCAATTGCGTGCCTCTGGTGTGGATGTTCTCGCCAATACTGATCAGGACTTGGAGAGGGTGCAAGGTTTGGTAAACCATCTCCAAGAGAAATCAAGGGAAGGCACCTTGCGCTCAGATAAATACTCATTCCTAACAGCTGATGAAGATGCCCCACCTGGGGAGGAAGACTTCAGGATGATGAGCATTTATCCCTCGTTTGAGGAGTTCCACCTTGATCAGAAGCCTTTCTTGAGGCCGAACATAATCTCTCAAAGTTTCCCTAATGCTCGGATTTATTTAGACACACACTTTCGACTTCTGCGTGAAGATTTTGTGAGGCCACTGCGGGAGGGTGTCAAGGAGCTTTTGAGGATACACCATAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17929

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108597	Essential Splice Site	1048	1643	12	13
ENSDART00000108597	Essential Splice Site	1048	1643	12	13

Genomic Location (Zv9):

Chromosome 6 (position 57353813)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	57406875
GRCz11	6	57403739

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTCATCTCTGGAAAACCATCCCTCTGTGCTGAAGTATGACAATGWCAAGG[T/G]AAATCAATTAMGCACAAAGAACTTATGAAGATACTACTCACAGTAATTTG

Long Flanking Sequence:

TGAGATAATAACATACATTTTTTTATGAAATATGTTTTATTGATTTATTATTAATATTTTTTATTATTAAGTGGTAAAGAAAAATTGATAGCAAGTCTTAATTTATATTATTAATTAAAATAGCTTTCTGCTTCTGATTTACTGTGTTGCTTACATGTGTTAACATGTGTTAATGCACTTCAATCTTCGCAGCTGAGGCCTAGTGCAACAGTGTATGAACTTGCCAAGAATTTCAGTCTGGAAGTGTCCATGTTTGAGAGACTTGTCAGAGTGAACTTCCCATTCGTGCGCCTCAACTACCAGGTTAGTTTTTATATCAGTACCTCGGTTGACAAGTCAATAATCATTGACAATACCTAGTGAATACCTTGTTAACTTTTTTTTTTTTGCAATGCATTTTTAGCATCGCATGAGGCCAAGTATCGCTCGCCTGTTGACTCCTCATATATACTCATCTCTGGAAAACCATCCCTCTGTGCTGAAGTATGACAATGTCAAGG[T/G]AAATCAATTACGCACAAAGAACTTATGAAGATACTACTCACAGTAATTTGTGTACTATAATATACTTAACTCCTGCCTATGTTGGTCTACAGGGAGTTCTTACAAATCTCTTTTTCGTGGATCACATTCAACCTGAAGAAGAGATTAAAGATGGACGGAGCCACCAGAACCCACACGAAGCTCGTTTTGTGGTCGAGCTTTGTCAGTATTTGCTGTTCCAGGACTATAAGCCTTCCCAGATTACCATTCTGACTACATACACCGGACAGCTTCACTGTCTGCGTAAGCTCATGCCCTCTCCAAAGTTCTCTGGCGTCAAGGTCCATGTTGTTGACAAGTATCAAGGAGAGGAGAACGATATTATTATATTGTCCCTAGTGCGCAGCAATCCTCAAAGGAGGGTGGGCTTCCTGAACATACCCAACCGTGTCTGCGTTGCGCTTTCTCGAGCTAAAATGGGTCTGTATTGTATTGGAAATATGGACATGCTCAGCTCGGTT

Associated Phenotype:

Not determined