ZMP

fam78a

Ensembl ID:

ENSDARG00000088222

ZFIN ID:

ZDB-GENE-080220-25

Description:

hypothetical protein LOC100002878 [Source:RefSeq peptide;Acc:NP_001107947]

Human Orthologue:

FAM78A

Human Description:

family with sequence similarity 78, member A [Source:HGNC Symbol;Acc:25465]

Mouse Orthologue:

Fam78a

Mouse Description:

family with sequence similarity 78, member A Gene [Source:MGI Symbol;Acc:MGI:2443569]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40613	Nonsense	Mutation detected in F1 DNA	Not yet available
sa40612	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa40613

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124587	Nonsense	70	262	1	2

Genomic Location (Zv9):

Chromosome 5 (position 75109044)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	71210286
GRCz11	5	71994792

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGGTGCTGGTGCCGCCGGTTGCCGGCAAGGAGAGCTGGACGGTCGGCTG[G/A]ATCCAGGCGTGCAACCACATGGAGTTCTACAACAAATACGGATCCAAAGG

Long Flanking Sequence:

TAGGGTCATCTCTTCTAAAGTGTGCATACTTCTAAGGGTTATCCCTTGTCTAGTGTACATTATGGGTCATCCCTTGTCAAGTGTGCACTAATTCTACAGTGTCTAGTGTGCATGATTCTGGGGGGTCATCCCTTCTGTTGTGTGCACTCATTCTAAGGAGTGTAGTGTGCATTATTGTGAGGGTCATCGTCAAGTGTGAGGGCTCGTCTAGTGCGCGCTCTTCTGAGGGTCCGGCTGTAGTGCGCGCTCCGCCGCGGGTTGATGTTCTTGTGGCCGCGGGTGCTGCTTGTGATGGGCTGCATTCAGAGCATCAGATGCAAACCCAAGAGTTTTCGGGACAGCATCATGGTTCTGGAGGTCAACTCCTCCATCGACTCGAACCCCACCAGCATCGACGAGTCCTCCAGCGTGGTGCTGCGCTACCGCACGCCGTACTTCCGCGCCTCCGCCCGGGTGCTGGTGCCGCCGGTTGCCGGCAAGGAGAGCTGGACGGTCGGCTG[G/A]ATCCAGGCGTGCAACCACATGGAGTTCTACAACAAATACGGATCCAAAGGGATGTGAGTAGATCTGAACAATGTAAGAGTGTGCGGTGTGTGCGGTGTGTCAGGGGCGAAGACGAGACGAGGAGAGTGTGCTGATGTGGTGTGCTTCACTCTGCATTCAGATCAGCCATCGACACTACAGTTATACTGTATACAATAATGGATTAAGTCATAATTTAGGGGAAAACTGATTCATTTAATGGCTTATTAAAGGTGCAAATACTCAGATTGCAAAATATACCATAGACATTTATATTAAACACTGTAGTAAACTCAGTGTTCATCAACTATAGCCTATATTATACTGCAATACACCACAGTAAAGTACACTATTACAGCTGATCAGTGCACTACAGTTTATTCTACAGTATGCTGGAGTGTTCATTAATGAAGAGTTGAAGATAATATAATGTGTACAGTGTAGTTTACTATAGTATAGTTCAAAAACAGTTGTAGTAACTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40612

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
ENSDART00000124587	Nonsense	97	262	2	2

Genomic Location (Zv9):

Chromosome 5 (position 75098382)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	71199624
GRCz11	5	71984130

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATCTCATGCTTTATATCCCTGCAGGTCCAGCTGGGAGCTTCCAGACCTG[C/T]GAGATGGTAAAATCCAGGCCATCAGCGACTCCGACGGCGTCAACTACCCG

Long Flanking Sequence:

ACAACAATAACAATAATAATAATGTATATATATATATATATATATATATAAGTTGCGTGGTTTAAGTGATGGATCAGCGAGAGAGAAACTATGGGTTTTGGAAAACACTCGTCACTACATTGTTCTTTTCCCAAACGATGCATCGTACTATGATAGTTCAGCTGTGAGATACGTCGTTGTTTGGGAAACGCACCCCTGACCAGCACTGACAACACACACATAGTGCTGTTTTACATCTGTCTCACTATGGTGACGTTTGTAGCTCCGCCCTCTTCTGAATACAGCTCAATCTCATTTGCATTTAAAGTGACAGACACCAAAACGCCACAATCAGGATCAAAGCCTGAAGGGGTCAGTTTCAGAGAGATCTATAGAGAACATCATCTGTGTGCCACTCTCAGCTCAAACACACACACACTCACACACACACTAGACACAGCTTTCACAGCTCATCTCATGCTTTATATCCCTGCAGGTCCAGCTGGGAGCTTCCAGACCTG[C/T]GAGATGGTAAAATCCAGGCCATCAGCGACTCCGACGGCGTCAACTACCCGTGGTACGGCAACACCACCGAGACCTGCACCATCACCGGCCCCACCAAAAAAGACACGCGCTTCACCGTCAGCATGAACGATAACTTCTACCCGAGCGTGACGTGGGGCGTCCCGGTGAGCGACAGCAGCGTCCCGCAGCTCAGCAGCATCTGGAGGGACCAGAGCTTCAGCACGTGGCTGGTGGCCATCAGTCAGAGCACAGGCGAGGTGCTGGTGCTGCAGACGGTGCGCTGGCGGATGCGTCTGCACATCGCCGTCGACCCAGAGAAACCGCTGGGTCAGAGAGCAGCACTGTGTGAACCCACAGCACAGGAGCCGCCGCAGATCCTGGGAAAAAACGAAGCCATTCCTGCGAACGCTTTGGTCAAACCCAACGCTAATGATGCGCAGGTGCTGATGTGGCGCCCTCGTGTGGGAGAGCCGGTGGTGGTCATCCCACCCAAACACTGA

Associated Phenotype:

Not determined