ZMP

znf207b

Ensembl ID:

ENSDARG00000015572

ZFIN ID:

ZDB-GENE-030131-7377

Description:

zinc finger protein 207 [Source:RefSeq peptide;Acc:NP_955959]

Human Orthologue:

ZNF207

Human Description:

zinc finger protein 207 [Source:HGNC Symbol;Acc:12998]

Mouse Orthologue:

Zfp207

Mouse Description:

zinc finger protein 207 Gene [Source:MGI Symbol;Acc:MGI:1340045]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12303	Nonsense	Available for shipment	Available now
sa40666	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12303

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027464	Nonsense	171	435	5	12
ENSDART00000073740	Nonsense	171	436	5	10

Genomic Location (Zv9):

Chromosome 6 (position 19298258)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	22140813
GRCz11	6	18612134

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AAGTGTACCTTAACGCATCGTGTGTGTTTTTAAAGGCATGCCACCCATGT[T/A]GACTGGTGTMCCACCAATGATTCCAGGAATGCCCCCAGTAATGCCAGTTA

Long Flanking Sequence:

GATTTAATACCGGTACATACCGGTTACCAAGGGTTTCAGTACCCATATTTCTCAATCCATATGCACAACGCTTTGGCTTGTTTTCCTCGCTTGAAAGGTTTACAGACCTCCAGCACGTAGCTACAGTTGCTAAGCCACGATTGTTATGTGGCGGTCTTAGGGTGTGGCTTAGCGAAGGGTCAATTAAAACATCATTATAAACTTGTTCACTCCCAACAGAGAGTCAGAAAAAGAAACAGAATCAAGATGATTCTGATGAAGATGACGACGATGATGAGGACGAAGCTGGACCTTCATCATTTCAGCAGCCTACTGCTCAACCTCAGGCTGCCTACATGGCTCCAATGACTCAGACAGGCATCCATCTTGGACCTCAGGCTCAGGGCATGCCGTCTGCTGGTTATGCAGGTGGGTATGCCAGTATTTTGCTGAGTGCAGCTTAAATAAAAAAAGTGTACCTTAACGCATCGTGTGTGTTTTTAAAGGCATGCCACCCATGT[T/A]GACTGGTGTACCACCAATGATTCCAGGAATGCCCCCAGTAATGCCAGTTATGCCACCAGGGTATGTCTTTAATGTGTGCTTGTGTTGGTTAAAAGTGCATATTATGGTCCAATGTGATTTATATTTGTTTTTCTTGTTCATAGCATGATGCCAATGAGAGGGATGATGCCCCCTGGCCCAGCAATGCCTCCAATGATGCCTGGTATGCTACCAGGTCAGTTTTGTGCCTAGTTCCTGCTGATACATTATTTTAAAAGCCCAGGGCATATTAGTAAGGAAGTTTCTATTTTAAGTGATGTACTGAAATAATTTTTTTTCTGTAAAAAAAAAGTTGCATTGTAAAGATTTTATTAGATGTATTTGACAAATTGGATGGTTAAGGATGATATTGCTTGATCATAAAGTTGTAGTAAAAAATGTTGTTTTTTTGTAGGAATGCCACATCATGTTGGCAGACCTGGCATGCCTTCTATGGCACCTGCAGCCCCCGTCACAGTTCC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40666

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027464	Nonsense	329	435	10	12
ENSDART00000073740	Nonsense	330	436	8	10

Genomic Location (Zv9):

Chromosome 6 (position 19302938)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	22136133
GRCz11	6	18607454

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCCACCCTCACCACCTTGAGTGCTACCAGTAAGTTGATGCACCCTGAT[G/T]AGGATATCTCGCTGGTGAGTGCTTGAGTTTTGCTCTGACAACTTTTTTTG

Long Flanking Sequence:

TCAGTTGCAGCCCTGATATAAAACTTGATGTTAAGCTGGTTGTTTATTTATTTTAGTTGTAGATGCATGCATGCATAGGATTTTTTTTTAAAGTACATCACAAGTCTTTTTTTAAAACAAAGCTTTTGCGTTCTTTTTATACCAGTTTGCCCTAAATTATGAAGTTAGCAGGCTTATTTTAAATAGTCTGAAACGGCTATATTTGACCTTAATTTCACTTTTGTGCCATTGTTTGCTGTGAATAGGCAAAATCTCTTTTATTGCGAGCATGTTGTCAAAATATCAGTCTTGGTTTTCAGGCGCAGCAGACAGTATCAGGACCATCATCAACCAGCTCTGATTCTCCCAAGGTGACATTCCCAGCCTACACCCAGCCTCCTTCCACTTCCTCTGTGGTGCCTGCCTCCTCCAGCACTGTGGCCAAGCCCCCTGCCACAGTCACAAGTAAGCCAGCCACCCTCACCACCTTGAGTGCTACCAGTAAGTTGATGCACCCTGAT[G/T]AGGATATCTCGCTGGTGAGTGCTTGAGTTTTGCTCTGACAACTTTTTTTGACCGTAAGTAATGTGAATGCATAAACTGCTGAAATAAAATACGAATTTATTCTAGTTAAAAGTAGTGCTAGTTAAAGTATGAAGTTGTGCTATGAGAATGCGTACAGTCCAAATGGGTTTTTGTTACTGTAGTTGCCTGATTGCATTGTTATTGTCTTGGCTCTAATTCAGGAAGAGAGACGAGCTCAGCTGCCTAGGTATCAGAGGCTAATCCCTCGTCCTGGGCAGACTGCAGCCACGGCTGCCTCAGCTCCCCCTAGTGGAGCAGTGGGAGGAATGATGCCTCCTCAGCAGCCTGGAATGAGACATCCCATACATGGTAAGATGTGTGTGTAGATCATTCTCCTTTTAGAAGGTTAGTCACCATTAAATCCAAACAAATTAAAATGACTTATGTTGTAATTTAATGTTAGACACAGTACTGATGTTGAGTATTTGTTTTCAACACTT

Associated Phenotype:

Not determined