ZMP

C14orf166B

Ensembl ID:

ENSDARG00000060062

Description:

chromosome 14 open reading frame 166B [Source:HGNC Symbol;Acc:23346]

Human Orthologue:

C14orf166B

Human Description:

chromosome 14 open reading frame 166B [Source:HGNC Symbol;Acc:23346]

Mouse Orthologue:

Gm6772

Mouse Description:

predicted gene 6772 Gene [Source:MGI Symbol;Acc:MGI:3646959]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36546	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39181	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa15338	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa36546

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
ENSDART00000084252	Nonsense	3	405	1	12
ENSDART00000103572	Nonsense	6	413	1	11

Genomic Location (Zv9):

Chromosome 17 (position 53137845)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	52523412
GRCz11	17	52609712

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCAGTATCAGGGGTGAAGCTGATCAGGAAGGATTTGTCGACTGAAGAAT[T/A]GTACCTGCAGGCCTGTAAACTGGTGGGAGTCATTCCTGTCAGATACTTCA

Long Flanking Sequence:

TTCAGGGACCACTGAATTGGGTTTACAGTGAGACTCAGAGGGAGTATAGTCTCAGGTCTCTCAGAGGGGTCTTTGGATGTGTGTTTGGGAAAGAGCATTGGCCTTAACATTGTTTGTCCCTGGACAACAGGCAATGGAGGAATTTTAGGACTTCTTTAAGAAATTAAAGAAGTGGGTTCACCTGATCTGCCTGGGATCCAGCTACTTTGTGTCTCTGAGATACTCATAAAGTTATGAGCACAAGGAAAGGGGAACGAGCCTGACTAGCCAGTGCCTCAGTTCTTCCAGTTCAAGCCTGAGGGGCAGTAACTCTCGGATGTCAGAATTCTGCTCTGGCAGGGGTCATTTATAGATCTATTACAGATGGGGAGCGTTTTTCCTGAGTTTGTCCTCTATATGCATTACTTTATTACATTATGTAAATCAGATGAAAGATGCGCTTGTGTTTTCTCCAGTATCAGGGGTGAAGCTGATCAGGAAGGATTTGTCGACTGAAGAAT[T/A]GTACCTGCAGGCCTGTAAACTGGTGGGAGTCATTCCTGTCAGATACTTCATCAGGAACCTGGGCTGTGCCACCATTAACCTCAACCACCACGGCCTCGGTCCACTGGGAGGAAAAGCCCTGGCCATCGCTCTAGTGGTGAGACTCATGCAGCACCATCTACAGGCTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTAAATTACACTATACTAAATTATAATAGACTAAACAATATCAGATTGAAGTAAACTATACTATATTATATTATACCAGACTATACTATAGAAAACTATACCGGACTATACTGTACTGTACTGTACTATACTACACTAAAATATACTTTACTTTACTAGACTAGACAACAATACACTAAACTAAAAGGTACTAGACTAAAGTAAACTATACTATATTATATTATACCAGCCTATACTATAGAAAACTACACCAGACTTAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39181

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000084252	Essential Splice Site	48	405	1	12
ENSDART00000103572	Essential Splice Site	51	413	1	11

Genomic Location (Zv9):

Chromosome 17 (position 53137708)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	52523275
GRCz11	17	52609575

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCACGGCCTCGGTCCACTGGGAGGAAAAGCCCTGGCCATCGCTCTAGTG[G/A]TGAGACTCATGCAGCACCATCTACAGGCTATACTATACTATACTATACTA

Long Flanking Sequence:

AGGAATTTTAGGACTTCTTTAAGAAATTAAAGAAGTGGGTTCACCTGATCTGCCTGGGATCCAGCTACTTTGTGTCTCTGAGATACTCATAAAGTTATGAGCACAAGGAAAGGGGAACGAGCCTGACTAGCCAGTGCCTCAGTTCTTCCAGTTCAAGCCTGAGGGGCAGTAACTCTCGGATGTCAGAATTCTGCTCTGGCAGGGGTCATTTATAGATCTATTACAGATGGGGAGCGTTTTTCCTGAGTTTGTCCTCTATATGCATTACTTTATTACATTATGTAAATCAGATGAAAGATGCGCTTGTGTTTTCTCCAGTATCAGGGGTGAAGCTGATCAGGAAGGATTTGTCGACTGAAGAATTGTACCTGCAGGCCTGTAAACTGGTGGGAGTCATTCCTGTCAGATACTTCATCAGGAACCTGGGCTGTGCCACCATTAACCTCAACCACCACGGCCTCGGTCCACTGGGAGGAAAAGCCCTGGCCATCGCTCTAGTG[G/A]TGAGACTCATGCAGCACCATCTACAGGCTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTATACTAAATTACACTATACTAAATTATAATAGACTAAACAATATCAGATTGAAGTAAACTATACTATATTATATTATACCAGACTATACTATAGAAAACTATACCGGACTATACTGTACTGTACTGTACTATACTACACTAAAATATACTTTACTTTACTAGACTAGACAACAATACACTAAACTAAAAGGTACTAGACTAAAGTAAACTATACTATATTATATTATACCAGCCTATACTATAGAAAACTACACCAGACTTAACTATACTAGAATACACTATACTACACCAGACCTTACTATACTATACTGTACTATCCTATCCTATCCTATCCTATCCTATACTATACTATACTATACTATAGTACACTACACTATATTATACTATACTACACTATCCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15338

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000084252	Essential Splice Site	133	405	5	12
ENSDART00000103572	Essential Splice Site	136	413	5	11

Genomic Location (Zv9):

Chromosome 17 (position 53133705)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	52519272
GRCz11	17	52605572

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

YAAACATCKCTCWGATTTTCAAGAGATGAAGGAYCTGATTTTGTTTCTTC[A/T]GAGCAACTACAGGGTGAAGGAGCTGGATTTAAGCCACAACGAGTTCAGCG

Long Flanking Sequence:

TCTGTAAGTCAAAGGGTTAGTTCAGCCAAAAATGAAACTCAACCACATGTCATCCACCAGACTGCAGTCGCACATGCACTGAAAACTGTTTGGCCACACTGTGGATTAAAGCTATGATACTTTAAATAATGTTAGGTTTCTTACTTGGAACGATCGTTAAACTTCACAAGACCTCAGCATGTCATCAGGAGTCGTGAATATTGATTGGGACTCGTTTCTGTGTGTTTGTTTTCAATCTAATAAGCCTGTCACCATTCACTGCCATTATATGCAGCAACAAACACCACAGATTCAGCTCAAAATCTGCTTTAATGTTCTGCTGAAGGAAAAAGAGTCAACTCTTGGGTGACCTGTGGGTGAGTAAATCAACAGGAGATTTTCATTGTTGAGTGAACTAACCCTTTAAAGTCTACTCCATGTTCCCTTGTGTCCACAAATGCCGAGAATAAACAAACATCTCTCTGATTTTCAAGAGATGAAGGACCTGATTTTGTTTCTTC[A/T]GAGCAACTACAGGGTGAAGGAGCTGGATTTAAGCCACAACGAGTTCAGCGGCAGAGGTGGAGAACATCTGGGCCAGATGATCGGTGAATAAAATAAACTGTGAGAATCAAACTTAGCAACACACAGACCAAAATCACAGTAATGAAATGTTTGTTCATGCAGCAAATAACGATGGTTTAGAAGTTCTTGATCTGAGCTGGAATCACCTGCGCATGAAAGGAGCCGTCGCTTTCTGTGCGGGACTGAAGGTGAAGACACAATAAATAATAATAATACCGTATATTTTGTCAAATATTTGTAGCATTATTATAGTTTGTACAATTTACTAGCATTGATAGTTTTTTGCTGTGTTTGCAGGTGAACACGACTCTGAAACACCTGGATCTGTCGTGGAATGGCTTTGGAAATGAAGGTGCTCTGGCTCTGGGTGAAGCGTTAAAGTTCAACAACACACTGCAGCACCTGGACCTCAATAACAACCGCATCACTGATGAAGGAGC

Associated Phenotype:

Not determined