ZMP

LOC557823

Ensembl ID:

ENSDARG00000078355

Human Orthologue:

ZC3H4

Human Description:

zinc finger CCCH-type containing 4 [Source:HGNC Symbol;Acc:17808]

Mouse Orthologue:

Zc3h4

Mouse Description:

zinc finger CCCH-type containing 4 Gene [Source:MGI Symbol;Acc:MGI:2682314]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22642	Essential Splice Site	Available for shipment	Available now
sa35886	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa22642

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109318	Essential Splice Site	452	1340	10	14
ENSDART00000109318	Essential Splice Site	452	1340	10	14

Genomic Location (Zv9):

Chromosome 15 (position 23067665)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	23778852
GRCz11	15	23714117

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTCTCTCATGACTCCCTAACAGAAGATACTCAAGAGTTGCTCGATAAGG[T/G]AATCTTAACATATATGTTGAAAAATATAGCTGATGCTTTGTAATTGTTGT

Long Flanking Sequence:

ATGACTTGTTGACAACGAGGAATTAATTCTGTTTTAATTTCTGTCAATTTATCTTCAGGGTGACCACTGTAATTTCAGCCATGACATTGAGTTGCCTAAGAAGAAAGAACTATGCAAGTTCTACATCACTGGCTTCTGTGCACGAGCAGAAAATTGTCCCTACATGCATGATATCCTTTGGTCATTTTGCTTGCTGAGTCTGACATTATCATTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGATACACACACATTTTAATGATACATATGGTTGCAGTCTTATGCTGCAAAAGAGTAAGAGTTTCCAATTGTGTTAATAACTTCTTGACTTCACTGCACGTGATTTCCCTTGCAAGCTGTTCCATACCACAGGGAACTGTGTGAATGGCGAGGAGTGCATGTTCTCTCATGACTCCCTAACAGAAGATACTCAAGAGTTGCTCGATAAGG[T/A]AATCTTAACATATATGTTGAAAAATATAGCTGATGCTTTGTAATTGTTGTTTCTGTACACCACTGGTGTGTGTGTGTGAATGTATGTATGTGTGTTATAATATATAATTTTTCTTTAATTATTTTATAAAGATGCTGGCAGAGGATGCAGAAGCTGGTGCAGAAGATGAGAAAGAGGTTGAGGAACTGAAAAAGCAAGGCATTAACCCTCTTCCTAAACCACCCCCTGGTGTTGGCCTTCTCCCAACTCCACCAAGACCTTCCCCAGGGGATTCTTCAACGCCCATGGAGTTTGGAATGCCTAGTGCCCCACATGGTAACATCCCTCCAAGTGGTCCACCGGCCCCAGGCCCTGGTGTTGGGCCTGTTCCTGGACCTGGACCTGGACCTGGTCCTGGTCCTGGAATTGGGCCCTGCCCAGTTCCCCCTCCTCCCTGCACTGATGGAGGCACCTTCCAAGGGCCTCCTCCAACTGGCCCTCCACCCCCTATGGGCCCACCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35886

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109318	Nonsense	1089	1340	14	14

Genomic Location (Zv9):

Chromosome 15 (position 23064912)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	23776099
GRCz11	15	23711364

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATCACCTCCGTCCGTCTCATCTGAAAAGCCCATTGACCCTCGTATGGCA[C/T]GAAAAACCCCTGCTGACCCCCGATTACAGCCTCAAAAATCTGCCCTTAAG

Long Flanking Sequence:

ATGAGGAAGAGGAGGGTGAAAGGATGCTGAGGGACAAGCCTGTGCCCATCCCTCTTGACCCTTTAATGGGCATGGCTTTACGCGATCCCCGCTCACAACTACAGCAGTTCAGCCACATCAAAAAGGATGTAGTTCTTCAAAAGCCTTCATTTTCTAAGGCGGTGCTGTGGAGTCCAGAAGACCTCATCCCTATCCCCATCCCTAAACAAGACTTGCTCCCACTACCCCCTGGCATCCCACCAGTCACTACCATTGACCCCCGCCTATCCCGCACACAGCCCCCTCATCACTCCTCTATTCTCCCACCTACTGTTGTTCCTCCTCCTGCTCCTGTTGAGCAATCGAATCAGTCCTCCTCTTCCCTACCAGACTTTGAGCTACTCTCCCGTATCCTTAAAACTGTTAACGCCTCTTCATCAAGCCCTGTTCAAGGCGCTTCTACGGGAATCTCATCACCTCCGTCCGTCTCATCTGAAAAGCCCATTGACCCTCGTATGGCA[C/T]GAAAAACCCCTGCTGACCCCCGATTACAGCCTCAAAAATCTGCCCTTAAGACCACCTCAGAGCCACTTGTTCCTCAAGGATCTCCCCCTACTAGTTCCTTATCTCCACCATCCTCCAGTCCCACCATTGCACCATATGATCCTCGGCTGCTATCAGCAGGAGGCTCGGTTCGAAGTGTGGGATCTGCCAGTGTAGGTAGTAGCAGCGGTGGCACCAGTGTGCTGAGCGGCATCAGTTTATACGACCCTCGGAGTCAAGGCGCAGACAAGACAGAGGGTTCAGTGGCCACTAGAAACAGTAGTCCTCCTCCTGAGCCCAAATCAAGCGAAAGTACAACTGCTTCAGCTAAGCCTAAGTCTAAAGAGCCACTGTTTGTGCGCAAGTCAGCACTGGACCAGCCTGAACCAGAGAAGAGCTCGACTGAGCAAACTACAGATCGCTACAATAGCTACAACCGCCCCCGACCCAAACCTTCACCCTCACCCAATGCAGGGACTGCC

Associated Phenotype:

Not determined