ZMP

fam46c

Ensembl ID:

ENSDARG00000010437

ZFIN ID:

ZDB-GENE-030131-5365

Description:

Protein FAM46C [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUP1]

Human Orthologue:

FAM46C

Human Description:

family with sequence similarity 46, member C [Source:HGNC Symbol;Acc:24712]

Mouse Orthologue:

Fam46c

Mouse Description:

family with sequence similarity 46, member C Gene [Source:MGI Symbol;Acc:MGI:1921895]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44703	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38733	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa44703

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
ENSDART00000023572	Nonsense	373	388	2	2
ENSDART00000032307	None	None	107	None	3
ENSDART00000139174	Nonsense	376	391	2	2
ENSDART00000142787	None	None	278	None	2

Genomic Location (Zv9):

Chromosome 9 (position 21816877)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	20972663
GRCz11	9	20783532

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACTACCAGCCGGCTCCGTATGTCAAAGACCTGAACTTCAACAACTACTA[T/A]GTGGCCTCTTGTAACCAGTCCATTCCAACTTGGTTGCCGTGTAACTAAGA

Long Flanking Sequence:

TTCCACCCTACGGTGGTAGGGGAGAGCATGTATGGTGACTTTGTTGAGGCTCTGGGCCACCTCACGAATAAGACCATTGCCACCAAACGCCCAGAGGAAATCCGTGGTGGTGGTTTACTCAAATACTGCAACCTCCTGGTGAGAGAATTCAAGCCTACAGATCCAGATGAATTTAAGGCTCTGGAACGCTACATGTGCTCCCGTTTCTTCATTGACTTTCCCGACATTGTTGAACAACAGCGCAAACTGGAGGCTTATCTTCAAAGCCACTTTATTGGTGAGGAGAGGAACAAGTACAACTACCTCATGATCCTGCGGCGGGTGGTGAACGAGAGCACTGTGTGTCTCATGGGACACGAGAGACGGCAGACGCTGAACCTCATCTCACTGACTGCGTTCAGGGTGCTCGCTGAGCAGAACGCTATACCTGATGTGTCCAGCGTCACCTGCTACTACCAGCCGGCTCCGTATGTCAAAGACCTGAACTTCAACAACTACTA[T/A]GTGGCCTCTTGTAACCAGTCCATTCCAACTTGGTTGCCGTGTAACTAAGACACAAAGGATGCTTATTTGAAGACTAAATCCATCAGTTGGTCAGAACGCCAGATAATTGGCCATAAGGGAAGTTTCCCTCTGTAGACATAAAGGATGTTTAAAATATCAAAGTTTTTTTTTCTTTTTTTCTTTTCTTTTTAATTCCTTCTCTGCAGAGGTGCCAAGACATTTCTAATTCAAAGTGATATATTTTAGGGATTTGAATTAATTTTTTTCCCTTTTTTTACTTTAATAAGAAGTTTCAGATTTGTTTGTTGCTCTCATCTGTCCCTTATCTGAGAGATTTATTTTCCATATTGAAGAGAAACAATTCCCATAGTGCCTTATTAGATTCTAACCCCAAAAGTAAAGCGTATTGGGACAAATTTATATATTTCCTGTGTGTTACAAAATATAAATGCCAAAAAAATATAATAATGTTCTTAGAAATTTGGAGAAAAAAAATACAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38733

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
ENSDART00000023572	Nonsense	387	388	2	2
ENSDART00000032307	None	None	107	None	3
ENSDART00000139174	Nonsense	390	391	2	2
ENSDART00000142787	None	None	278	None	2

Genomic Location (Zv9):

Chromosome 9 (position 21816919)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	20972705
GRCz11	9	20783574

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTACTATGTGGCCTCTTGTAACCAGTCCATTCCAACTTGGTTGCCGTG[T/A]AACTAAGACACAAAGGATGCTTATTTGAAGACTAAATCCATCAGTTGGTC

Long Flanking Sequence:

GTTGAGGCTCTGGGCCACCTCACGAATAAGACCATTGCCACCAAACGCCCAGAGGAAATCCGTGGTGGTGGTTTACTCAAATACTGCAACCTCCTGGTGAGAGAATTCAAGCCTACAGATCCAGATGAATTTAAGGCTCTGGAACGCTACATGTGCTCCCGTTTCTTCATTGACTTTCCCGACATTGTTGAACAACAGCGCAAACTGGAGGCTTATCTTCAAAGCCACTTTATTGGTGAGGAGAGGAACAAGTACAACTACCTCATGATCCTGCGGCGGGTGGTGAACGAGAGCACTGTGTGTCTCATGGGACACGAGAGACGGCAGACGCTGAACCTCATCTCACTGACTGCGTTCAGGGTGCTCGCTGAGCAGAACGCTATACCTGATGTGTCCAGCGTCACCTGCTACTACCAGCCGGCTCCGTATGTCAAAGACCTGAACTTCAACAACTACTATGTGGCCTCTTGTAACCAGTCCATTCCAACTTGGTTGCCGTG[T/A]AACTAAGACACAAAGGATGCTTATTTGAAGACTAAATCCATCAGTTGGTCAGAACGCCAGATAATTGGCCATAAGGGAAGTTTCCCTCTGTAGACATAAAGGATGTTTAAAATATCAAAGTTTTTTTTTCTTTTTTTCTTTTCTTTTTAATTCCTTCTCTGCAGAGGTGCCAAGACATTTCTAATTCAAAGTGATATATTTTAGGGATTTGAATTAATTTTTTTCCCTTTTTTTACTTTAATAAGAAGTTTCAGATTTGTTTGTTGCTCTCATCTGTCCCTTATCTGAGAGATTTATTTTCCATATTGAAGAGAAACAATTCCCATAGTGCCTTATTAGATTCTAACCCCAAAAGTAAAGCGTATTGGGACAAATTTATATATTTCCTGTGTGTTACAAAATATAAATGCCAAAAAAATATAATAATGTTCTTAGAAATTTGGAGAAAAAAAATACAAAAAAAAAATTAGAAAGAAAAAGATGAAAAATGTGAGCACAGG

Associated Phenotype:

Not determined