ZMP

LOC100001603

Ensembl ID:

ENSDARG00000061051

Human Orthologue:

FAM5C

Human Description:

family with sequence similarity 5, member C [Source:HGNC Symbol;Acc:22393]

Mouse Orthologue:

Fam5c

Mouse Description:

family with sequence similarity 5, member C Gene [Source:MGI Symbol;Acc:MGI:2443035]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20744	Nonsense	Available for shipment	Available now
sa17402	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa20744

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086627	Nonsense	314	766	5	7

Genomic Location (Zv9):

Chromosome 6 (position 35920149)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	36163683
GRCz11	6	36141577

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCATGGAGGAAAGCCTTTTGCGAATCTCTGAATCCTGGGCTCTTACCTA[C/A]AAAGAGTTTGAAGATTCAGGTAGGAGACTGAATTCAGTCATGTTTCACAC

Long Flanking Sequence:

CTGCTTAATATTTTGGAAGAAATTGTAATTTATGACTATTAACACTCTTGTGTATTTATAGTAAAAGCAAATTATACATTGTAATACAGAACTAATAACTTACTTTCACAATATGTTTCTTCACTTGGAACAAAAATGTATTTGAAGACATTCTTGTTATTTGATTGGCATGTACTGCATTCTCATTTGTTGAATAGAAAATGTATGCACCTGGTGGCAGTTTTTGTTATCAAACCACTTTGTTCAGGTAACACAGTATTCTCTCTTTTCTCTGTAACTGAAGGCTTGCAGGTCATTTTGCCAGATTATCTCAGAGACACATTCGTCCAAGCAGCTTTAAGTTACATTGCCTGCAATGGAGAGGGAACTTTTGTCTGCCGAGGGAATGACTGCTGGTGCAAGTGTGACCCTAAGTTTCCAGAGTGCAACTGCCCCTACATGGATATCCAGGCCATGGAGGAAAGCCTTTTGCGAATCTCTGAATCCTGGGCTCTTACCTA[C/A]AAAGAGTTTGAAGATTCAGGTAGGAGACTGAATTCAGTCATGTTTCACACTTTTTTTCAGGTTCATTTGTCCTCCTGGAGAGATTTTTCAAGTATCACTACACGGTCTAGGACAAAGAAATGTTTCCTTTTTTTGGTTCACTCTTCATCCATACTTGCAAAATCTCCAAGGTCATGTCATGTCTACTTGAATAATAAAATCTGAAAATCCCAAAAATAAAATATTTAAAATCAGCAGCACAATCTGACATGAACTGTCCTATAAAGGTTGTTTATTAGGCCCCACTTTACTTTGATGGTCTGTTTGTTAAATTTAAGTTACATTGCATCTACATGCCAACTAATTTTCATTAGATTGTAAGTAGACTGTTAGAGTTATGGTTAGTGTAAGTTGACATGTACTTGCAAAGTTTCTTATAGTCAGTTAAATGTCTGTTGAAGGAGCATATCAACAGATATTAAGCAGGCAGTCTACTAATGCTCAAATGGACCATCGTAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17402

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086627	Nonsense	556	766	7	7

Genomic Location (Zv9):

Chromosome 6 (position 35910238)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	36153772
GRCz11	6	36131666

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTAATAAATACAAATCCAACCTAGTCCATATGCTTTTAGGCATCTCTCTT[C/T]AAATCTGCCTTACAAAAAACAGCACTCTGGAACCCGCTCTCACCCTSTTT

Long Flanking Sequence:

TATCTATCCTCAAATACAGGCCACAGTCGTATTGGCTGAACTACTTCCAGTCTTTGCTATACTGCTCTGAAAACAACCAGCTGGGATCCTTCTCGGAAGAACTTCACACCTGCATTTGTGCATACGACCACAGCACCTGCCAGGTTCCCACACCATGCTCCGTTGGCGAAGGTGCCGCCTGTGCTGTGTGTGCCAGCGACAACCACACTCGCTGCGGCAGCTGCAACATCGGCTACATGCTAAGTCAAGGAGCCTGTCGACCAATGGTGGCAGATTCCACCGAGAACTACCTGGGCTTTGAAACTGATCTTCAAGACCTGGAGCTTCGCTATCTCCTCCAAAGAGCTGATCGGCGCTTGGAGGTCCACGCTATCTTTATAAGCAATGACATGCGCTTGAATAGCTGGTTCGATCCTTCATGGAGGAAGAGGATGTTGCTTACGCTAAAGAGTAATAAATACAAATCCAACCTAGTCCATATGCTTTTAGGCATCTCTCTT[C/T]AAATCTGCCTTACAAAAAACAGCACTCTGGAACCCGCTCTCACCCTCTTTATCAATCCCTTCGGAGGCAGCCACTCTGAAAGCTGGCTAATTCCTGTAAATGAGAACGGTTTTCCAGATTGGAAGTCGACTAAGCTGGATCTTCCACTGGAGTGCTTTAACTGGACTTTGACTTTTGGGAACAAGTGGAAGACTTTCTTTGAAACCATCCATATTTATTTGAGAAGCCGCATTAAAACTTCTGGAGCCGGGGGTAATGAGAGCATTTACCTGGAGCCTTTGGAAATGGCTGACCCTACTAGAAACCTGGGGTATATGAAGATTAACAGCATTCAAGTGTTCGGCTACAGTATGCATTTTGACCCGGAAGCGATCCGGGACTTGATCCTGCAGCTGGACTATCCATACACGCAGGGCTCGCAGGACTCGGCCTTGCTCCAGCTGCTGGAGATCCGAGACCGGGTCAACCGTCTCTCTCCGCCAGGTCAACAACCTCTGGAT

Associated Phenotype:

Not determined