ZMP

ftr55

Ensembl ID:

ENSDARG00000009161

ZFIN ID:

ZDB-GENE-070424-161

Description:

Novel protein containing a B-box zinc finger domain [Source:UniProtKB/TrEMBL;Acc:Q1LXL5]

Human Orthologue:

TRIM65

Human Description:

tripartite motif-containing 65 [Source:HGNC Symbol;Acc:27316]

Mouse Orthologue:

Trim65

Mouse Description:

tripartite motif-containing 65 Gene [Source:MGI Symbol;Acc:MGI:2442815]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11517	Essential Splice Site, Missense	Available for shipment	Available now
sa36802	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11517

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:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019843	Essential Splice Site	192	537	None	6
ENSDART00000121858	Essential Splice Site	182	529	None	7
ENSDART00000136370	Missense	193	199	1	1

Genomic Location (Zv9):

Chromosome 19 (position 14866270)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	15529874
GRCz11	19	15434236

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TAGAAACCATCACACTGTATCAGCTGTTGCAAAGATRGCAGAGAATGAGG[T/A]ATGTACTGAAACAATACATTAACATTTTGAGGAGCTCATACSTACACTAT

Long Flanking Sequence:

TCCATGTGGACACAGTTACTGTATGAGCTGTATTACAGAATTCTGGGATCAGAAGAGCATCTACAGCTGCCCTCAGTGCAGACAGACCTACAAGCCAAGACCAGTTTTAGGTAAAAACACAATGCTGGCTGAAGTGGTGGAGCAGCTGAAGAAGACAAGACTCCAAACTGATGTTCCTGCTGTAAGTTTCATTACACCTGGAGACGTGAAGTGTGACGTCTGTACTGGAAAGAAATCAAAAGCGGTCAAGTCCTGTCTGGTGTGTCTGGAATCGTATTGCCTAACTCATTTTGAGCATCATGAGGAATTTCACTCAGGAAAGCGACACAAAGTGACTGACGCCATTGGTCATTTGCAGCAGATGATGTGCCGTGAGCATAATAAGATTCTGGAGGTTTTTTGTAACACTGATCAGCAGTACATTTGCGTGCTTTGTGTAATGGATAAACATAGAAACCATCACACTGTATCAGCTGTTGCAAAGATGGCAGAGAATGAGG[T/A]ATGTACTGAAACAATACATTAACATTTTGAGGAGCTCATACGTACACTATAAAACAATTATATGACGAATTAGCCTTAACAGCATATGTTTTTAGGTCATTGTATTATTAAGTGAAGTTTATTTATACATTTTGAGAGGAGCACATACTTATGATTGCATGCGGCAGGCCCCGCATTATTGAATTTATGATTCACCAATCACACGATTCCTAAGCCACAATAAATACCCTAAGTTCCATATAACCGCCATCTTTCATTTTGAAGAATCCCCCCTTCCACCCCTACTCCTCCTGCTTTCCTATGGGTGGCACAGTGGCTTAGTGGTAAGCACTGTTGCCTAAGAGCAAGAACATCACTTGTTCTAGTACTTACCAAGTCAGACAACGTTTCTGTGCAGAGTTTACATGTTCTCCCTGTGCTCACGTGGGTTCCCCCGGGTTCCCCGGTTTCCTCCCACCGTCTAAAAACATGCGACTTAAGTTAATTGACTAATCAAAATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36802

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000019843	Nonsense	198	537	2	6
ENSDART00000121858	Nonsense	188	529	3	7
ENSDART00000136370	None	None	199	None	1

Genomic Location (Zv9):

Chromosome 19 (position 14860421)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	15524025
GRCz11	19	15428387

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGACAGCTCATGTTTGACCATATTTGTCTAACAGAGTCGTTTAAAGGAG[A/T]AACAGAGAGCAATCAAAGAAAGAACTGAGCAGAAACAGAAAGCCATTAAG

Long Flanking Sequence:

CATTTAAAAGAGAAACAGAGAGCAATCAGAGTCATTTAAAGGAGAAACGGCAAGTTTGAAAAAATTGACTGGCCTGCAGAGAGTCCTGAGCTCAACTCAATAGAACAAATTTAGGATGAATCGTCTCGCATCAGTGTCTGTCTTCACAAATGCACCTCTAGAGGAGTGGTCAAACACACTCCTAAACCTTGTGGAGAGAATTTCCAGAAGAGTTGAAGCTGTTATGTCAAAAAAAATTAAAAAAATAAAAAAAAAATAAAAAATTGTGGGTCAACTGCATGAAACCCTCAGGACTAAGATTGTAATGTCATTAAAGTTTATGTTCATAAAGGCGGATGTCTCAAAACATTAGGTAATAGTGTAAGTTGTGGTTCATATTTACAATTCATGTGTAACACTGTTCAATCACTATACATCAAACTTACCTGGTGTGCTGTAAGAATATTAAAACAGACAGCTCATGTTTGACCATATTTGTCTAACAGAGTCGTTTAAAGGAG[A/T]AACAGAGAGCAATCAAAGAAAGAACTGAGCAGAAACAGAAAGCCATTAAGCAGCTGAGAGAAGCTATTGAGTCTCATAAGGTGAGTTTGGACAGAAGTTTGAACGCCTCTTCAGAGCTGAAGATATTCCAATCTCACTGAAGCTCACTATAGCTCACAGTAAGTGTGAATATGATGTGTGTCTTAACAGCGTTCTACACAGACAACAGTGGAGGACTGTACAAGGGTCTTCACAGAACTGATCTGCTTTATTAAGAGAAGTTGTTCAGAGTTGACAGAGCAGATCCGAGATCAAGAAAGGGCTGCAGTGAGTCGAGCTGAAGGACTTATGGAGCGATTGAAGCAAGAGATTGATCATCTGAAGCGGACAAACACTGAATTAGAGCAGCTTTCACACACTGACTGCAATCATATCCGTTTTCTTCAGGTATTAGTTCATATTCAGTTTATTAGGTACAGGTAATGTCAGGAATAATGGGTCGTAATGTCATTTTTATTGTC

Associated Phenotype:

Not determined