ZMP

C17orf63 (1 of 2)

Ensembl ID:

ENSDARG00000078578

Description:

chromosome 17 open reading frame 63 [Source:HGNC Symbol;Acc:25563]

Human Orthologue:

C17orf63

Human Description:

chromosome 17 open reading frame 63 [Source:HGNC Symbol;Acc:25563]

Mouse Orthologue:

BC017647

Mouse Description:

cDNA sequence BC017647 Gene [Source:MGI Symbol;Acc:MGI:2384939]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35839	Nonsense	Available for shipment	Available now
sa28422	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35839

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111228	Nonsense	209	596	2	2

Genomic Location (Zv9):

Chromosome 15 (position 15400567)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	16445530
GRCz11	15	16381552

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAGCCAGGCTCACCAACCGCCAGTACCACACCACACCCTAAACCACCAA[C/T]AGACTCTCATGCAGCAGCAGTTGTCCGCTCCACAAGGACTACGGCATTTG

Long Flanking Sequence:

CAGAATTGGATGCCTATGCTAAGAAAGTTGCCAATAACCCACTGACTATAAAAATCTTCCCCAATAGTGTAAAAGTACCTCAGAGGAAACACATTCGCCGCACTGTCAACGGTCTCGACACCTCCAGTCAGCGCTACAGCCCCTACCCACCTCAGGTCAACACCCGGACGGGCCTCTTGGCCATAGTCAAAGTTCCTGTCAAAGGGATCCTCAAGGACATTGAAGGCGGCCGAGCCCGTTTTCTCCCCAAGCTCATCATGAACCCGCACAGTGGGCTTTACGCCAATCCCAGCACTTTAAATGTTCCTCACACTGTTCCACATCTTCAGACTCCTTTAGGCCAGAAGAGTCTCGGTCACTCTCAGGCCTTGCAGGCCCATCCACAATCCCTGCAGCAGAAGAGCAGTTTACAACCACAGCAGAGCCTGGCCCATCAGGAGGCTTTACATCAGAGCCAGGCTCACCAACCGCCAGTACCACACCACACCCTAAACCACCAA[C/T]AGACTCTCATGCAGCAGCAGTTGTCCGCTCCACAAGGACTACGGCATTTGCCTGATATGGCACAGTCGGTAAACCTGCAGCACTCCCAGGGCTTTTCTCAATCCCAACCCATTCCACAGGCCTCTTGTGCTGGCCCTCCAGCATCTGGGGTCTTGCAGCCACCCTTGGCAGGCTTACAGATGCCACGAAAGCTGCCTGATGCCGATGCTCCTCCCAATGTGACTGTGTCTACCTCAACCATCCCGCTGTCTATGGCTGCCAGCCTGCACCAGAACCGGCCCAGCGACTTGAACAGCATCGTCAATCAGATTAATCAGTTCTGCCAGGCTCGGGCTGGCATGGGCTCTACCTCTGTGTGTGAAGGACAGATCGCCAACCCCAGTCCCATTAGCCGCAACCAGCTAATCAACGCGAGCTCTCGAGTGTGCCCACATCCTACTGTGGGTCCTCCATCTTCTTGCATTCTTGGAAATTCTGACAAAGGCGGTCCTGCCTCTGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28422

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
ENSDART00000111228	Nonsense	362	596	2	2

Genomic Location (Zv9):

Chromosome 15 (position 15400106)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	16445069
GRCz11	15	16381091

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCGAGCTCTCGAGTGTGCCCACATCCTACTGTGGGTCCTCCATCTTCTTG[C/A]ATTCTTGGAAATTCTGACAAAGGCGGTCCTGCCTCTGCTCTGCCACTGCC

Long Flanking Sequence:

CACCAACCGCCAGTACCACACCACACCCTAAACCACCAACAGACTCTCATGCAGCAGCAGTTGTCCGCTCCACAAGGACTACGGCATTTGCCTGATATGGCACAGTCGGTAAACCTGCAGCACTCCCAGGGCTTTTCTCAATCCCAACCCATTCCACAGGCCTCTTGTGCTGGCCCTCCAGCATCTGGGGTCTTGCAGCCACCCTTGGCAGGCTTACAGATGCCACGAAAGCTGCCTGATGCCGATGCTCCTCCCAATGTGACTGTGTCTACCTCAACCATCCCGCTGTCTATGGCTGCCAGCCTGCACCAGAACCGGCCCAGCGACTTGAACAGCATCGTCAATCAGATTAATCAGTTCTGCCAGGCTCGGGCTGGCATGGGCTCTACCTCTGTGTGTGAAGGACAGATCGCCAACCCCAGTCCCATTAGCCGCAACCAGCTAATCAACGCGAGCTCTCGAGTGTGCCCACATCCTACTGTGGGTCCTCCATCTTCTTG[C/A]ATTCTTGGAAATTCTGACAAAGGCGGTCCTGCCTCTGCTCTGCCACTGCCTGACATTGCTGCTATGAACAGGATACCCCTTTACCACAATGAGATGAAGCAGCAGCAGTCCCAGCCACAGTTACCCCAGCAACAACGTCAGCAGGGCCCCTGGGGCCAACACCAGTTGGGACATCTTCAGCACCTTCCAGAGGGAGCAGCTCACCAGGGTAAGAATCTCCCTCGAGAAGGCCTAATGGGACCAGGGTTCCTTACAAAGAACATGGGCTACCCACAGGAGGTGTGCATGGCGCAGCCATTCAACTTGAAGCCACCTACCGATAAACCAACTCCATCTCCTCCGGTTAACGGGATGCCTGTGAGTTACAGCAACGGCCACTACATGCAGCCTCCATGGAGCAACATCCTCCCCACACCAAACAGTGACAGCTCAGGGTCTCAAGACCTGGTGGGGTCATTTCACGGTGGCCTCTCAGGGGCCTCCTTAGACTGCACCCCTGG

Associated Phenotype:

Not determined