ZMP

zgc:123010

Ensembl ID:

ENSDARG00000039082

ZFIN ID:

ZDB-GENE-051120-15

Description:

tetratricopeptide repeat protein 31 [Source:RefSeq peptide;Acc:NP_001139026]

Human Orthologue:

TTC31

Human Description:

tetratricopeptide repeat domain 31 [Source:HGNC Symbol;Acc:25759]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42276	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa17718	Essential Splice Site	Available for shipment	Available now
sa9064	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42276

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000057073	Essential Splice Site	328	501	10	16
ENSDART00000059443	None	None	342	None	12
ENSDART00000140875	Essential Splice Site	301	474	10	16

Genomic Location (Zv9):

Chromosome 13 (position 40606985)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	40133431
GRCz11	13	40259321

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAAGAAGCTGTCAATGACCTCTTGTACTGTAAAGTGCAACAACTTACGG[T/G]AAAGATAGTGCTGTCTTTGGCTCTTTCTGTTCAAATAATTTAGTGCACAT

Long Flanking Sequence:

CATGTTAATATAGCCCAAAATCTCTCCAATGAATTTTTTCCAGGACATTCTTGACTCAATGAGGGTTCAATGTAATACTACCAAGGTGTACCTAATAAAGTGGCCAGTTATGTTTGCACAATCTTTGTTGTTTTTATTTATTCTCTTATTATTCTGATTACAGGTTTTTTGGGAATCGCTCTTACTGCTACTGTTGTCTGGAGCAGTATGCTCTGGCTCTTGCTGATGCTGAGAAATCTATCCAGATGGCTCCTGATTGGCCCAAAGGATATTACCGTAGGGGAAGTGCACTAATGGGGCTTAAGGTACGACCCCGCGGCATTTTATACAGCTTTTTCTTCTTATTTATTGGGTGAATTTTTGCAGTGTATCAATTGAGGTTTGTTTTTAATAGAGGTACAGTGAAGCTGAGAAAGCCATGGAACAGGTGCTAAAACTGGATGGAGATTGTGAAGAAGCTGTCAATGACCTCTTGTACTGTAAAGTGCAACAACTTACGG[T/G]AAAGATAGTGCTGTCTTTGGCTCTTTCTGTTCAAATAATTTAGTGCACATTTTTTGACATAAAAATAAATTCTGTATGGAAACACTAAGATGTGCATAAGATTGAGTGCATAGTCAAGCACTTTGCAAAAGAAAAGCATCTTATACCAAAAACGGAAATAAGGGCAGTATTAATAGCTTAAAATGTGGGAGAGCATTGATGTTATGTGATTGTATTCTACTGCAATATGGAACAATTAAATGTTGATGTTAAATCAAAAGTAATTCACAAATAATTGAAAATGAGATGATTCAATGACAATAATTCTCTATGTTACAACTGAATTATAAAATGGCAAAATATGAAATGATAAAACATGATATAAATTGTACCCAGCTTAAATGTAAAATTAAAGTTACCAGAGGTAAAGGAGAGACAAAGGAGGAGGGAGAGCGATGCAAAGAGAGCAGGCCCAGAAGTTAGCCTGATTGCAGTAGAGTCCGAGAAGATAGAATCCAGAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17718

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000057073	Essential Splice Site	355	501	11	16
ENSDART00000059443	None	None	342	None	12
ENSDART00000140875	Essential Splice Site	328	474	11	16

Genomic Location (Zv9):

Chromosome 13 (position 40603892)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	40130338
GRCz11	13	40256228

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGTTGCTGGAAAAATATAATACAGTGCAGGCCGTTGTTGCAGCCAAGGG[T/C]AAGAGTTYATTTMTTTTCTCGATTGAAGYRAACCACTTGAGGGTGCTATT

Long Flanking Sequence:

AGAATTGCACTATTTGTAGCTCAATCTTATTGCAAATGATTTGTCAGATTAAATGGAAATTCCCTAAACTAGAAGTGTCACTCACAATTCAAAACCGTTCACTCAATGGGAATAAAAGAATACTTATTAACCATGACTCATCCGTATTCAATCTAATTTTAGCCTGAATAGAAGCTCAGACATGCCAAGCATCTCCTTTTGTTTGTTTCAGGGGAAAAAAAGTCAGTCTGACAGGCTTTAAATATGAACAGGTTGAGTAACTATGCAATTTTCTAAAATTATGGATTAGAATGGAGTCAGCTTTGGAAATATTACATTGGAAGGAAAATTACGCAATTCTGGAATGATGCACAAACTACAATGTATGCATAATATTTTCAGATCTTTAATGGATAAAGGTTTATACTTCCTCCTCTTTAGGAGCTTGGATATGATGAGGAGCAGAGTATTCAGTTGCTGGAAAAATATAATACAGTGCAGGCCGTTGTTGCAGCCAAGGG[T/C]AAGAGTTCATTTATTTTCTCGATTGAAGCGAACCACTTGAGGGTGCTATTGCTACACTCCATGATAGAGACTTAAAATTTGAATAAATATTGAGCATTGTGACTATAATCATTACTCAGTCACAATACAAGTTATTTTATTGTGTGCTTTTCAGCAGGAAAGGCAGTATTATGAAATATTCCTAGTTCTGTCAAATGATTAATCACACCCAAAATAAAAAAAAATTATTTAAATAAGGTACTTACTGTGTGTAAATATTGTGTGTATATAATTTGTATTGGATATAAGTATTAATAAAATGAATAAACATTCTCTCATTTTTTATCATTTATTTAGGCTAGAATAAAAGCTGTTATATTTTTCATAAACCATTTTTAGGTCAATATTTTGGTCAATATTTTGAAAGCATTTTTTTTTTTCAGTGGTCTACAGCAGTGGTTCCCAAAGTGGGGGTCGAGAGACATTAAAGGAGGGGTCGCCTGGTGATTTCAAAAAATCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9064

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
ENSDART00000057073	Nonsense	486	501	16	16
ENSDART00000059443	None	None	342	None	12
ENSDART00000140875	Nonsense	459	474	16	16

Genomic Location (Zv9):

Chromosome 13 (position 40598025)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	40124471
GRCz11	13	40250361

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GATGAGTGTTACTTCTGGAGGACCACCGGCTGTCATTTTGGAGATAGGTG[T/A]CGCTATAAGCACATTCCMGATCACAGAGGCAAAGACTGGCAACCTTGAAT

Long Flanking Sequence:

ATTTTAATAATAAATAAAAAAAATGTAAGTTTTTAATTTGTCAACTCTCATTATTTTCTATATAGAGCTTTTGTGCTTTTATAAAATGAGAGCTGGTAAACATTCAAGGGCGTGCACAGATGGGTAGCATTTTGATTGATGTAGTGGGCCGCTCTGTCCCAAAATGCCAGGGCCGATTAAAAAAAAATAAAATAAAAATACAAAAAATATATTATATTTTTCCCCTCTTCTCCTCCAGTCCAGCCCTGATAGCGAAACTGAATTATAGTCTACAACAGAAGGTTTTGAGCTCCACTTTAAATGCATAAAAAGATAACAAATGCACAGCGTGAAGGGTTTTTACTTATTTTACAACTGTACATTCAAATAAGTATTCTTTTGAAATGATTGCAAATGTCCAAATAAATCTTCGTCTCTTTCAGACCAAGACGCAGAGGTCCTGTCAACGGAGATGAGTGTTACTTCTGGAGGACCACCGGCTGTCATTTTGGAGATAGGTG[T/A]CGCTATAAGCACATTCCCGATCACAGAGGCAAAGACTGGCAACCTTGAATCAACACTAGCCTTACTTTCTCCCCCTAGGAACTCGACCGCATGACTGTAGGGGACTGTAATCTTCACTTTGATTAGCTGTAGGTCAGGACCAGTATTGTGGATCAGAGTCTTGAGGTCAGAGATCCCCCCCCACCCCCCTCCTCGAGTGAATTCACTGTCAGACTCTGAACCTCATGGGGATTCAAAGCAGACGGCTCCCTGGGAAAAAGTGTCTTTTGAGGTGGGGTTTGGGTGGTGCAGAGTGCCAGAGCATCGCTGTACCGCATGGCCGTCTGCTGAGGTTTAACACGGCCTCTCATATCCAATGCTCTCTTCTTTTTTCCTGTGCCAACACCACCAATCCAACCAATCCAAAGAAGAGTTGCAGAGCTTGTCTGACATTTGAGTTAATCTCGAGAGAAGAGAATGACTCTCAATATATATATATTTTTTTGCGTGTGAGGTTGCAG

Associated Phenotype:

Not determined