ZMP

ZC3H7B (1 of 3)

Ensembl ID:

ENSDARG00000055930

Description:

zinc finger CCCH-type containing 7B [Source:HGNC Symbol;Acc:30869]

Human Orthologue:

ZC3H7B

Human Description:

zinc finger CCCH-type containing 7B [Source:HGNC Symbol;Acc:30869]

Mouse Orthologue:

Zc3h7b

Mouse Description:

zinc finger CCCH type containing 7B Gene [Source:MGI Symbol;Acc:MGI:1328310]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13447	Nonsense	Available for shipment	Available now
sa35262	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa13447

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078337	Nonsense	31	904	2	21

Genomic Location (Zv9):

Chromosome 12 (position 20280701)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	19062545
GRCz11	12	19184419

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTTTCTTTTTGCCACAGGTCATCTTTGCCTTTTCCCGAACCTGAAGGTTA[T/A]GAGGTATGACTTACTTGTATTATCCCTTAAGAAAAAATGCCCCACCTAGA

Long Flanking Sequence:

TTAGTATTTTTGCATACAGTTATAATTTAGTTGCCATGATTGTGTTTAATTAAGTGTATACAACTTTTCATCTTTAGTTTTCTTCTTGACTAATTACTGCCATTACGTTTTCCACCCCAGTATTCAACATCGTTTGCTTGCTAGGAAAAAAACACACAACTCAAATGTTTTCATGTAGAATGTTATATATTTTACTTTTATTATAAACCATTTGTAGTAATTGCTTGTTTTTTGTTGTTATTTTTTTTCATGATTGATGCATGTTGTAAATTGTTGTGATATGTTGCAGCTATGGATCTAGAACGACAAAAGCGCAAGGAAGAAATACAAAAAGCTTTGGGCTTCATCCAGTAAGTTTGTAGTTTTCTTTCCACAATACAGATATGATGTTAACAGACTCTCCTCCGCTCTCTCTTTATGTGGAATAATCCAAATATTGCTTGATGTACTTTTTCTTTTTGCCACAGGTCATCTTTGCCTTTTCCCGAACCTGAAGGTTA[T/A]GAGGTATGACTTACTTGTATTATCCCTTAAGAAAAAATGCCCCACCTAGATAATCCATTGTGATTGTATTTTGCTAGCGTAATTTTGAATGGAAACACTCTTTCTTTCTTTTCCCAGGCATTCCTGACTCAGCTGGTCTGTAATTTGCTGGATGAAGGTAATGCAGTGTATCGTGATGGAGAATGGAGACAGGCAGCAGTCCATTACAGCGAGGGTGTGAATGTTGCTCGCTACGCTCAGTCAGAAGCTCTGGTCATTCCTCCTGAGCTGTTAGAGAGCCTTTATGTAAACCGGGCAGCTGCACATTATAGTCTGGTGAGCTTGATTTTCATTGGTTGACGTGTAAATCTGTCATGTAAACTGAGAAGTTCATTGTACGGAAATGACAAGAACAGTTACATGTTGTATATGTGTTATTTTGTATATGTGTTATTTGCAAATCAGATTTGTTTTGTGTTGTGTGCTTAGGGCGAGTATGAGCGGGGAGTGCAGGACTGTGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35262

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
ENSDART00000078337	Nonsense	895	904	21	21

Genomic Location (Zv9):

Chromosome 12 (position 20255836)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	19037680
GRCz11	12	19159554

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCGACATGTCTAATGGTTAAATTTATCTTCGTTCTTTCTGACAGGTTGGA[C/T]GACGGATGTCTGGTGGTGGAGGAGACCTGTGACCAGTCCAAAAGTGTGTG

Long Flanking Sequence:

TTTCGTTATTTTTAAAGCATGATGGTAAAACACGAACGCGATTATGAATAAATTAAAACGTGTTTGTTTGTCATAAAAATTCGTAATAATGACAAAAAATACTAATTTGTGGATCTCCTTACTTCCGGGTTCAGCAATACTGCTGCTGTGGTTGGTGTATTCTGGAAAATTTTCTTAACCCTTGGTTTCGAGTGTGGTCCTAAAAAATCTTTGATCGAAGGCTATTCATCCCCTCCCCTTAGCCCTACGCCTTAAAGCTAAAGAGAATTGGGACACCTCTACCCCTTGGCGTGCATGCTCAAAACGAGGGGTAAGGGGAAGGGCTAAGGGGTAGAATTGGGATTGGGCCTAAATAATAAATAATTATTCACAGTATTTTGAAGTGCCCATGATATCACTGTTGTACTATTACTATATGTTCATTATCACATTATGTTGTAATATTGAATATCGACATGTCTAATGGTTAAATTTATCTTCGTTCTTTCTGACAGGTTGGA[C/T]GACGGATGTCTGGTGGTGGAGGAGACCTGTGACCAGTCCAAAAGTGTGTGGTCTGGATGAGTCTTCCTTTTCAAATGTCAATTTCGAAGGCCCTTCTCCACTCTTTCAGTGCCACTCTGGGAAGTAACAGGCTCTTCTGCCCTTCAGGGCAGAGTGTCTGACTTTAGGACTAACACACACTGATTGTTACCACATACACACACACACACACACACCACATGCTTTTTTCATTTATTATCAAACAAAATCTTGTGCACTCACCGACATGACACTTGGCACAGGCTCATAGTGTGGTGTATGTGAATGCACACTGGTACTTTTACAGCTAACTCAAATAAGGGCAGTTTCTTCCATTTGTACAATTCAGAGGAGTTGAATTGAGTTCAACCTTTTCCCACCGTGCTCTTCAAACTTAAACCCAAAACAGGCTGGTTCTCCCTGTATCAAATTAAAGCACCCGCCGTGAAGACCACGCATTCCTCAGTCATGTATGTGGTGTC

Associated Phenotype:

Not determined