ZMP

si:dkey-33c12.4

Ensembl ID:

ENSDARG00000057890

ZFIN ID:

ZDB-GENE-030131-2527

Description:

si:dkey-33c12.4 [Source:RefSeq peptide;Acc:NP_001155071]

Human Orthologue:

TTC31

Human Description:

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

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35424	Nonsense	Mutation detected in F1 DNA	Not yet available
sa42140	Nonsense	Mutation detected in F1 DNA	Not yet available
sa22229	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa35424

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000083362	Nonsense	4	631	1	18
ENSDART00000144146	None	None	170	None	6

The following transcripts of ENSDARG00000057890 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 8732848)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	9035468
GRCz11	13	9367491

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATAATACAGTATTATATCAAATATAAATATATTCGTGATAATGTCAATAT[C/A]AAAAAAGCATACCATAGGACCAGGTGAGTGTTGTTAGGCTCTTTTCATGA

Long Flanking Sequence:

CACTTCTGTGAACTGTAAAGTTTCAAAATTATTTCATTATGCTGCTAGCTTGAATGGTTGCATCCTATCCTACGTAAAATCTGAACAAAATAAAAATAATATGTTATAAACGCACTCATTTTATGCAGATAGAAGACATTAAAATAAAAACCTTAAAGTATAATCGTTTTGGAAAACAAATAATAATCAGATTACGTTATAAATACGTTATAAATGTTTTTATATTTATCTTATTTAACATGTTTATCTTTAATATTACTTATTTCTTTAACCTATTTACATTTTCAAAAACCACATCACGTGGTTCGACGCGTTCATGTTGCACGCTGATGCGCATGCGTGCTGCTGTGAGTGAGCGCTGTGTGGTGTGTGCAAAGGTGGGGAAGAATCTCGAGAAAAGAGTGCGACTGAAAGGCATGTTAGACCATTAAGAAGATACGTAAATATTTAATAATACAGTATTATATCAAATATAAATATATTCGTGATAATGTCAATAT[C/A]AAAAAAGCATACCATAGGACCAGGTGAGTGTTGTTAGGCTCTTTTCATGATGTCTACCAAAACTTCGTCAGCTTATGCGAACATGTAGCTCTCCTGACAATAGAAAACCGTGTTGCTCTTGAACTCTAACCACAGTAACGTTATCTTAGACAAGTATCTTGTACTAATCTTTTTACCCTATTGGTAATTTAAATTATAATAAATTATGCAGTGTAAGGTTAAATTTAACAATGTAAGAAAGAGACAATATGTTTTTGTTTGGGTGGTGTAGGATCAAACCTCAGATTTCACTGTACACGTGTGTTTATATGAGATCTGTTCAAACCTTAAAAATATGTTTTTTTTTTCTCTTATTCTTCCAGACTACTTCCTGCTGCAAAATGATGAGCGCCTCATGCGGACCCACGTGAGTCGTTACGTTTTTGTCTGACGTGTCTTCGTTAAACGGAATAATCGATAAATTGGAGTACGCATTGTCTGCGTTTGTTTGTTGTGCTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42140

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000083362	Nonsense	263	631	8	18
ENSDART00000144146	None	None	170	None	6

The following transcripts of ENSDARG00000057890 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 8721438)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	9024058
GRCz11	13	9356081

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACAGAAACCTAAACCTGACAAGAAGCCTGCTCAAGCAAACCCAAAAAAA[C/T]AACACGAATCCCAGCAGAAAGCCACTGTGATGCCTCAAAAGCAGGTGGGC

Long Flanking Sequence:

ATGAGAATTGATGAAAATACAGTTACTAAACTCGCAGTGTTTTATTTTATGTTAACAAGTACATCTTTGGATTTTAATATTGCATTGATTTATTGTTTAACTATGATTTGATATATTCTGTATTGTTCATGTTAGTAAGTCCATAAATCGGCATTAACTAATAAAACCGTATTGTCAAGTGTGACCAATATTGGGATGTGCATTTATATATACATAACAAATATACACAGTGCAAACAAAGGTATGTAAACATTAACTTTTATTTTAGAATCGATGAGCTGTAATTGTTTCAGTGGCATTAGATATGACTCCTGTGACATTTTCCAAACTTGACCGAGCCATTCATTCCTTGCAAATGGTTGTAGTGACTTTTATTTTGTGTGTTTCAGGAGCTCGACATGAATAGCTGCTTTGTGTCAAACGCAGCTGCTATTGCCAAACGCAAACTGGAACAGAAACCTAAACCTGACAAGAAGCCTGCTCAAGCAAACCCAAAAAAA[C/T]AACACGAATCCCAGCAGAAAGCCACTGTGATGCCTCAAAAGCAGGTGGGCGGAGTTAAAAAGATAAATGTGTAAACTCTGAGGGTTTTTATAAGACATTTAAGAGGAGGTGCCTGGAAGAATTAAAACGGTCTCGTTCTCATGACTTTTCTTGTATAAGAGATTGGGTGTCTCTGAAACTGTAATCAGCTTAGTGAGTCAGTGTTGTGCAGTCATTTTAATCTTAATTTTAATCTACTTTAATCCTTTATATACAGAAATGGATAAAATTGTTGGTAGTCTTTGTTACTTTGCTGTTTTTAATGCTTCTGTTCAACCATCATTTGGAAGTAATATCTAATTTTCATTAGTTTACTTTTAGCAGGTCTTGATTAATTACTACTTTTTCAGTTTCAAGTTATTTCAGTTAACTCTGCAGCGTTTCTTCAATAGATGGCTACCAACAATATTGCCTATGTCTATAGGTATTTGGAGTTTTATTTAATAGATGCGGGGAATTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22229

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
ENSDART00000083362	Essential Splice Site	497	631	14	18
ENSDART00000144146	None	None	170	None	6

The following transcripts of ENSDARG00000057890 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 13 (position 8710533)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	9013153
GRCz11	13	9345176

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCCTCGACCCAGCATGCCAACCGCTGCTCCACTTCCCCCTCATTCCCCG[T/C]AAGGCGCACACACATATCCCAGCAATCATGGTACATAACCATTTACCCCA

Long Flanking Sequence:

TGTTTTTGAATGTGTAATTAACTACAGTATTTTTTTTTGTGAGATAATGTATAAGATCATGTTATCCGGAAGTGTATGAAAACAGCAACATGCTGTGATGAATGTGTCTGATGTCTAAACTCAAAGCGCTTTGTGGTGGCCTTTTTAACTTAATAAATTGGTATTTTTGGAGCATTGTTGTTGCCGCGTTGTTTATATATATTCTTCTTTTTGAATCAAATAAAAAAGCAGTTTTTTTTTAGCATTTCAACACTGATTTACATAAATATAAGTAAACAAATCGTAAGTGTGGCAAATTTAAAACAAGTAATTGGTTTGCACTAATAACACTCTAATTCTTTTCAGGTTTAGCCCCTGTCCTTGTGCCCAAAGAAAACGAGTTTAAATCAGTACAGTACAAACACCCTCAACCTCCAGCTAAATTCCCTCTCATGCCTCTTCCTCAAAACCAGCCTCGACCCAGCATGCCAACCGCTGCTCCACTTCCCCCTCATTCCCCG[T/C]AAGGCGCACACACATATCCCAGCAATCATGGTACATAACCATTTACCCCAAAAACACCTCAGTCTTAATGTCTCTTTCACCCCTAAACAGAGAGCTGTTCCCCATCTGGGTCGGAGACTTGGTGAGTTCTATAACCGGGAGCAAGCTTTATGACCTATTCAAATCGTAAGTGACCTGCTTGGTTTTCTAAAAGTGTTCTTCCAACCATTGGTGTGATTTGAACTCATTTTAAGCTATTGAAAACTATTTGTCTCTGTAAAACAGTGTTGGGAATATCCATAATGTAAGAGTGTTGCCTGACAGATACTGCGCATTTGTTAACTACACCAGCAAGGACAGCTGTGAGAAAGCCATACAAATGTTCAATGTGAGTATGTTTGCTTTCAGTTCAACGTTCAAAAGAAACCTTTAGTGCTAAGATGTTTTATGGCCTAATATTGTGTAAATCTTATCTCTTATGGAAATGTGTAAAAGTTTTGCGCTATTTTAAAGTTGCATTT

Associated Phenotype:

Not determined