ZMP

Q5U400_DANRE

Ensembl ID:

ENSDARG00000045921

Description:

Zc3hdc1l protein [Source:UniProtKB/TrEMBL;Acc:Q5U400]

Human Orthologue:

ZC3HAV1

Human Description:

zinc finger CCCH-type, antiviral 1 [Source:HGNC Symbol;Acc:23721]

Mouse Orthologue:

Zc3hav1

Mouse Description:

zinc finger CCCH type, antiviral 1 Gene [Source:MGI Symbol;Acc:MGI:1926031]

Alleles

There are 7 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43346	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23600	Essential Splice Site	Available for shipment	Available now
sa8545	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43346

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067497	Essential Splice Site	419	782	7	12

Genomic Location (Zv9):

Chromosome 19 (position 46832144)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	22922
GRCz11	4	274775

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACAGGCCTGGTGTTCAGGACTAATATATAGTGAATCTGTCCTTCTCCTC[A/T]GACATGATCCAAACAAACAAGCAGTACAAAACCAAAAAAGTGATCAGACG

Long Flanking Sequence:

CTCCTTCATCCTGACCACCGAGTGGCTCTGGTTCTGGGAGGACGAGTTTGGAAACTGGATCCAGTACGCCAGCGCGGACGGCGGCCATAAGATATCCTCCATCACCAGTGCAGAGCTGGAGCAGAAATATCAGGCGGACCAGAGCGCAGTGCTGGAGTTCAGCGCCGGGTCACAGACGTACACGCTCAGCTTCCAGGGTAAACACACACATCTCATCATCACACTGGCACACTTACTGTCCTCCAAAAATCCTCCAATAATCTCATATCCGGATAGTGATATATAGCATGTATATATAGCCAGATCTGTCCGTTCACCTGAATGAATGGTCTATCTAAATTGGACACCTGTACAGGACTGCATCTTAATATAAAGTGCATAAACACTACAGCGTAATATCAAACGGCAGACTCTTTAATTCATCCACACGACACATATATCATCATATTGCACAGGCCTGGTGTTCAGGACTAATATATAGTGAATCTGTCCTTCTCCTC[A/T]GACATGATCCAAACAAACAAGCAGTACAAAACCAAAAAAGTGATCAGACGCCGCCCCAAATTCGTCTCCGCCGCAGATGTGAAGACGATCAAGAGCACGTGAGGATGACTGCACACTCCTTCTCTCTGTCAGACTCTATGAATGCTGATTAATCTCTGATATCTCCTCCTGTGCTCTCAGGAAACGAGCACCAATCAGCTTCAAGACTCTGCCGGAGCACTGGGACAAAGCGCTGACTCCTGAAACGGGATGCAAGGTTTGAGGACTATAAAGACTCTCGTTCACAACAAACACCATCACTATAAAGATATAGGTGTAATAATGTGTGACAGTGTTTACCAGCTGAGGAAGAATGAAACACTGACAGCCAATTAGAATCCAGTAAAACACTGACAGCCAATCAGCAGATTAAAGACAGGAGCAGAGAAGAGAGCGCTCTTTCATTATCACAGCTGTCTATCAATGCCAACGTGTGCAGTGTAAATGCAAATATACAGTCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23600

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

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067497	Essential Splice Site	477	782	9	12

Genomic Location (Zv9):

Chromosome 19 (position 46832733)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	23511
GRCz11	4	274186

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATATATATAGTGATGAGTTTGGTATATAACTCTATATGTGTGTTGACGC[A/G]GAGAGTGCAGCTGACAAAAACCACAGCCGAATTCATCAAAATACAGGAGC

Long Flanking Sequence:

TCAAGAGCACGTGAGGATGACTGCACACTCCTTCTCTCTGTCAGACTCTATGAATGCTGATTAATCTCTGATATCTCCTCCTGTGCTCTCAGGAAACGAGCACCAATCAGCTTCAAGACTCTGCCGGAGCACTGGGACAAAGCGCTGACTCCTGAAACGGGATGCAAGGTTTGAGGACTATAAAGACTCTCGTTCACAACAAACACCATCACTATAAAGATATAGGTGTAATAATGTGTGACAGTGTTTACCAGCTGAGGAAGAATGAAACACTGACAGCCAATTAGAATCCAGTAAAACACTGACAGCCAATCAGCAGATTAAAGACAGGAGCAGAGAAGAGAGCGCTCTTTCATTATCACAGCTGTCTATCAATGCCAACGTGTGCAGTGTAAATGCAAATATACAGTCACAAACAATCAGATGTGCAGGTTATGAGTGATATATATATATATATATAGTGATGAGTTTGGTATATAACTCTATATGTGTGTTGACGC[A/G]GAGAGTGCAGCTGACAAAAACCACAGCCGAATTCATCAAAATACAGGAGCTGTTCAACCGCACCATGCGGGGATTCACCATCCAGAATATCGAGAGGATCCAGAACAAAGCATTGTGGGAGGTGTTCCAGTGGTGAGTCCATCACAGCACTGACTTATATAACATCCTGAAAGTTGTGTGCACCTGCTTTGAAGACATTTTGACTGCGTAACAGGAGCGTAACAGTGTCCTGTTGCATAGTTCCGTGTCCTGTCAATCATCTCAACACACCATTCACATTTCTGTCATGTTTAAAGTCATCGTGAACTCAAAATAAAGGGATATAAATGTTAGTTTTAAGGATATATATAATCTAGTGTGCTCAAATTCCCATTAGGATGAAATAAACCTGATATAAACGTCTTAATCATGCAGTTTTTCTCTTCCTTCTAAATCATGAATGCTTTATTTTGATGTTGTCTTATAGTAGATCTTCTGACCAATCAGATGCTCTCTAGTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8545

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000067497	Splice Site, Nonsense	520	782	9	12

Genomic Location (Zv9):

Chromosome 19 (position 46832865)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	23643
GRCz11	4	274054

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCAGAWKATCGAGAGGATCCAGAACAAAGCATTGTGGGAGGTGTTCCAGT[G/A]GTGAGTCCATCACAGCACTGACTTRTATWACATCCTGAAAGNTRTGTGCA

Long Flanking Sequence:

TGGGACAAAGCGCTGACTCCTGAAACGGGATGCAAGGTTTGAGGACTATAAAGACTCTCGTTCACAACAAACACCATCACTATAAAGATATAGGTGTAATAATGTGTGACAGTGTTTACCAGCTGAGGAAGAATGAAACACTGACAGCCAATTAGAATCCAGTAAAACACTGACAGCCAATCAGCAGATTAAAGACAGGAGCAGAGAAGAGAGCGCTCTTTCATTATCACAGCTGTCTATCAATGCCAACGTGTGCAGTGTAAATGCAAATATACAGTCACAAACAATCAGATGTGCAGGTTATGAGTGATATATATATATATATATAGTGATGAGTTTGGTATATAACTCTATATGTGTGTTGACGCAGAGAGTGCAGCTGACAAAAACCACAGCCGAATTCATCAAAATACAGGAGCTGTTCAACCGCACCATGCGGGGATTCACCATCCAGAATATCGAGAGGATCCAGAACAAAGCATTGTGGGAGGTGTTCCAGT[G/A]GTGAGTCCATCACAGCACTGACTTATATAACATCCTGAAAGTTGTGTGCACCTGCTTTGAAGACATTTTGACTGCGTAACAGGAGCGTAACAGTGTCCTGTTGCATAGTTCCGTGTCCTGTCAATCATCTCAACACACCATTCACATTTCTGTCATGTTTAAAGTCATCGTGAACTCAAAATAAAGGGATATAAATGTTAGTTTTAAGGATATATATAATCTAGTGTGCTCAAATTCCCATTAGGATGAAATAAACCTGATATAAACGTCTTAATCATGCAGTTTTTCTCTTCCTTCTAAATCATGAATGCTTTATTTTGATGTTGTCTTATAGTAGATCTTCTGACCAATCAGATGCTCTCTAGTGTCTGGAATGCCCCGCCCCTTTTTTATCATTGGCTGTTCATTTGATGTGCTTGAGCTTAACCTCTCGTTGGCAGAGCTGGGAGTAAAAACAGCACGCTATTGGCTGATTTTTAAAAAGGGGAGGAGCTACACTG

Associated Phenotype:

Not determined