ZMP

zgc:113056

Ensembl ID:

ENSDARG00000053474

ZFIN ID:

ZDB-GENE-050327-81

Description:

tudor and KH domain-containing protein [Source:RefSeq peptide;Acc:NP_001014377]

Human Orthologue:

TDRKH

Human Description:

tudor and KH domain containing [Source:HGNC Symbol;Acc:11713]

Mouse Orthologue:

Tdrkh

Mouse Description:

tudor and KH domain containing protein Gene [Source:MGI Symbol;Acc:MGI:1919884]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42071	Nonsense	Mutation detected in F1 DNA	Not yet available
sa16677	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa42071

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
ENSDART00000009794	Nonsense	39	573	3	15
ENSDART00000075511	None	None	460	3	16
ENSDART00000136617	Nonsense	7	211	2	6
ENSDART00000142329	None	None	445	None	7

Genomic Location (Zv9):

Chromosome 12 (position 35074030)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33478139
GRCz11	12	33579122

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGTGGAGTTTACCGGTTACTCCCACCCAAGTGATGGCTGCGGTGCAGGAT[G/T]GACCATGGAAGAGCCTGAGCTCTGGAAAGAAAGTGGCGTTGGCTGCTGGT

Long Flanking Sequence:

TGACACTATTGGGAGTGCATTATTGTGGTCTTCTATTGTGCTTGAACTTTAACATGTAATTTAATATAGTTGGATCATGTATGAAATGTTCCAGAAAAGTTCTCCACAGGCTGTAATGTCCAAAATCTAATTACTGAGGCATTAAAGTCTCAGTGTTTTGTGATCTTTGTTCTCTTTATTAAGCCAATTAGGTAACAAAAATAGGCTAACTAATCTCATAAATGAGTGCTCTAATATTAACAGTTGATTCTGTAGATTTTCTGGCTACATTTGGAGTTTGTTCTGAGATTGAAAGGCAACCTGAAAACTCATACTTGCTGTGATCATCAATCAATCAATCATTCATTCATGCTGCATGGCGCTACCACTATGGCCCATGTAAAGTCATACATGGTGCTGCAGACTAAACTTTGGGAGTTAACCTGTCTTACAGTTTATTTTGCATCTCTAGGTGGAGTTTACCGGTTACTCCCACCCAAGTGATGGCTGCGGTGCAGGAT[G/T]GACCATGGAAGAGCCTGAGCTCTGGAAAGAAAGTGGCGTTGGCTGCTGGTATCTCGGTTGGAGCAACAGTTGGATACCTTATTTATCGTCACATTCGAAACAGCACTGGTGAGTTTTAACGTTTAATTGCTTTTTAATAACAGCCCTGCTATAAACTTCAAAGTGCATGATATTTCACTGTCTTCCAAAAGAAAGAAGTAAATCTGAACTGCCTGAAATGTGTCTTTAGTGATTGCAATCTTAGGTTAGCAACAAATGTGTATAATGCCAGCCAACGGTCTTCATTAGCTACACATACATGTTAGCATTTCTTCTTTTGTGTAACACTTCTGAAACAATGGAAGGCGGTGGGTTCTCTATGATCAACTGTGTTTGGTTTCTTTGCCTGTGCTTTGGGTTAATGCCAGAAATGGATGCAGTATCACAATTAGGGTTGTAACAATATACCGGTATGACGGTTTACCACGATTTGAACGTGCACGATTATCATACCATGAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16677

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

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000009794	Essential Splice Site	75	573	None	15
ENSDART00000075511	Essential Splice Site	None	460	None	16
ENSDART00000136617	Essential Splice Site	43	211	None	6
ENSDART00000142329	None	None	445	None	7

Genomic Location (Zv9):

Chromosome 12 (position 35073920)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	33478029
GRCz11	12	33579012

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGAGCAACAGTTGGATACCTTRTTTATCGTCACATTCGAAACAGCASTGG[T/A]GAGTTTTAACGTTTAATKGCTTTTTAATAACAGCCCTGCTATAAACTTYA

Long Flanking Sequence:

CTGTAATGTCCAAAATCTAATTACTGAGGCATTAAAGTCTCAGTGTTTTGTGATCTTTGTTCTCTTTATTAAGCCAATTAGGTAACAAAAATAGGCTAACTAATCTCATAAATGAGTGCTCTAATATTAACAGTTGATTCTGTAGATTTTCTGGCTACATTTGGAGTTTGTTCTGAGATTGAAAGGCAACCTGAAAACTCATACTTGCTGTGATCATCAATCAATCAATCATTCATTCATGCTGCATGGCGCTACCACTATGGCCCATGTAAAGTCATACATGGTGCTGCAGACTAAACTTTGGGAGTTAACCTGTCTTACAGTTTATTTTGCATCTCTAGGTGGAGTTTACCGGTTACTCCCACCCAAGTGATGGCTGCGGTGCAGGATGGACCATGGAAGAGCCTGAGCTCTGGAAAGAAAGTGGCGTTGGCTGCTGGTATCTCGGTTGGAGCAACAGTTGGATACCTTATTTATCGTCACATTCGAAACAGCACTGG[T/A]GAGTTTTAACGTTTAATTGCTTTTTAATAACAGCCCTGCTATAAACTTCAAAGTGCATGATATTTCACTGTCTTCCAAAAGAAAGAAGTAAATCTGAACTGCCTGAAATGTGTCTTTAGTGATTGCAATCTTAGGTTAGCAACAAATGTGTATAATGCCAGCCAACGGTCTTCATTAGCTACACATACATGTTAGCATTTCTTCTTTTGTGTAACACTTCTGAAACAATGGAAGGCGGTGGGTTCTCTATGATCAACTGTGTTTGGTTTCTTTGCCTGTGCTTTGGGTTAATGCCAGAAATGGATGCAGTATCACAATTAGGGTTGTAACAATATACCGGTATGACGGTTTACCACGATTTGAACGTGCACGATTATCATACCATGAACAATTGCATATCAACGGTTTTAACCCTTAAAGACCGAGACAGCCGCCCGCGGCTAAAAATAAGTATTGCTCTTAAATGTTTAATAACTTTTGATCCGCTGATCCGATTCATA

Associated Phenotype:

Not determined