ZMP

zgc:113068

Ensembl ID:

ENSDARG00000053082

ZFIN ID:

ZDB-GENE-050320-49

Description:

hypothetical protein LOC541356 [Source:RefSeq peptide;Acc:NP_001013501]

Human Orthologue:

THADA

Human Description:

thyroid adenoma associated [Source:HGNC Symbol;Acc:19217]

Mouse Orthologue:

Thada

Mouse Description:

thyroid adenoma associated Gene [Source:MGI Symbol;Acc:MGI:3039623]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31907	Essential Splice Site	Available for shipment	Available now
sa24927	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa31907

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075054	Essential Splice Site	None	364	1	10
ENSDART00000143705	None	None	959	None	17
ENSDART00000147371	None	None	636	None	9

The following transcripts of ENSDARG00000053082 do not overlap with this mutation:

ENSDART00000135848

Genomic Location (Zv9):

Chromosome 13 (position 8258347)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	8560867
GRCz11	13	8892890

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTATCTACACGCAGTATTGAACTTTTTTCCATAGGTACTTTGTTACACGG[G/A]TAAGGCAATGTGTTGTACATCAAATTGCAATTAATCTACAATAAAACAAT

Long Flanking Sequence:

CGCTTTTCACTTTTTCACCATGAAACAAAATTAAACATTTTAGATAACATTTAAAAACTATCCTTACCTGACAATAAGCGTAACTGTGCTAAAGACTGCGCTTCACAACGTAATTAAAATAATATTCCGTGATATCCAAGTTGCTATTTCAAATAAGGCTATGAAGAGCGACCGTCTCCCAGTTCATATTTTTCAATCCAGCAGAATCCTGTGGAAGTGGGCTGGCTGGAGGGAGGTTTATTTTTTTTTACAAGCACGTACAATCAAAGCATTGAAGTTGTTGTAAAGACGCATTTAGAGAGCGGCGGTGTCGTAAATGACTGACTGTCCCCAGGACCAATCACATATCGTAACGGTTTTGCCTGGACTAATCATGCTTTTCCTGGGCGGTCTTCCAGCGCGATACCGGAATTGACGTGGTTTACACGTGTTTGCTACTGTGGAAATACTCTATCTACACGCAGTATTGAACTTTTTTCCATAGGTACTTTGTTACACGG[G/A]TAAGGCAATGTGTTGTACATCAAATTGCAATTAATCTACAATAAAACAATAAGAGTATACTCTTTGGAAGAAAACGTTTGTTTACGTTACATGTCAGCAGAAAACAGTAATGTAACTAGCACTAGCTCTTGTGCTTTTTCATTGAGGTAAAGTTGGGTTTATATTGGCACATTCTGACTTTCCCCTAAATAAAATTAGTTTCTGAAAAGTATTATTTGCACATTCTAAACACTGGAATCATATTAGCAGCCAATCACTATAAAAGTACTACGTTGTTCACAGTCAATTAACGTTAAATAGTGCTAATGTTATTTTGTTGTAACTTGTGTTTGATTTCAGAGCGAATATTCAAAGTACTATGGTAAACATTATAGGAACCATGTCACAAGTTGTCCCATAACGATTGTGCAAAAATAAAACCAACTTTACCTCAATTGTTTATTTTATAGTTTAACTGAGAGCTGTTACAACTTTCAAAAGATAATCTTCTATGTATGTAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24927

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075054	Nonsense	121	364	5	10
ENSDART00000143705	Nonsense	97	959	3	17
ENSDART00000147371	None	None	636	None	9

The following transcripts of ENSDARG00000053082 do not overlap with this mutation:

ENSDART00000135848

Genomic Location (Zv9):

Chromosome 13 (position 8260570)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	8563090
GRCz11	13	8895113

KASP Assay ID:

554-7577.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTGCATTGGGTAGTGGTCCAGATTGGCTACAGGAGCAAATGGTTAGATG[T/A]CTGTCTGAGGGTCTGTCTGCTGCTTTCTCCTCTGCAAGCACAGATCAATT

Long Flanking Sequence:

CAATATAACTTATCTCTAAAACAACAACAAACTCTGTACTACATCTGATGTCATTCTCTCGCTATAAATGCTAGCGCTCCTGTTTTTTTTCTGCAACCTAGTTTTGCGGGCATCCTGAATGTTTACAAACCGGACAATTTACAAGTATGTGATGTTCAGTATAAAACACAAATACTTTGTATGTTGATTGCAGGCAGGCTGCATGCTGGAGCAGCTGATAGAGGATGAGTCTCCGTCGAGTCCTTTATTGGAGGCATGTCTGCATACCCTATCATTCCTGTATATCACACTGCCAGCTAAGAACCCGTTGAAAAGAGCTGTATCAAGGTTAAAATAACTTTTAATTCAAGTGTGATTAGACATCATCAACTTTATCTTAAAATTAATGATTTCTGGAGTATCTGTTTACAAATACTTACTTGTTCATTTTGTTCATCCATGTCTCCCCTCAGTGCATTGGGTAGTGGTCCAGATTGGCTACAGGAGCAAATGGTTAGATG[T/A]CTGTCTGAGGGTCTGTCTGCTGCTTTCTCCTCTGCAAGCACAGATCAATTCTCAAACCTAACGGATAGCATCACTTCCTGTCTGAGTGGCTTTGTAATCGGTATGAATGGTGATGTAGTTATATTCAATTGAGTCATAATATCAGATATACATTACTGCTATGTTTTGGTCATTTAGGTTATATTTGCTAGACATTCATATTTAGCACAGGTGTTAAAGGAGCATCCCACTTAATTGGAAAAAGGCTCTTATAGTTGAACAGTTGACTTGAACCATTTTTTTAACCTGTTCAGTTGATTCCCTGTTCTGGTAGGTTCACTCTTAGAATTTTGTTAAAAAAATATGCACAGCTACATTTTACCCCTATTGTTAAATTACATTTTATTGAGTATTTTGAGAACTTTTGTGTAAAACAAATAAACAGGATACACTATGTTGTGCGGGAAAAATGTTTTTACATTTAAGATTGTATAATTGTTAGTATTTGATGTTTGAAATCC

Associated Phenotype:

Not determined