ZMP

FAM190B (1 of 2)

Ensembl ID:

ENSDARG00000087749

Description:

family with sequence similarity 190, member B [Source:HGNC Symbol;Acc:29197]

Human Orthologue:

FAM190B

Human Description:

family with sequence similarity 190, member B [Source:HGNC Symbol;Acc:29197]

Mouse Orthologue:

Gcap14

Mouse Description:

granule cell antiserum positive 14 Gene [Source:MGI Symbol;Acc:MGI:101859]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa28865	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36424	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa28865

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
ENSDART00000122366	Nonsense	465	802	3	11

Genomic Location (Zv9):

Chromosome 17 (position 26358593)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26498512
GRCz11	17	26516903

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCATGTAGATCCTGATGTGTGTTTAATTTTTAGGTGGTAAGGCAGATTTA[C/T]AGAGTGCTCCACTACGTGGTCCACCGCTCATGTCTCCTGAAGTGGACCGT

Long Flanking Sequence:

CACTGATTCCCCAGAGGAGGTTGTGACAGAGCCGAGTCTGAATGGGACCCTTCACTACACTGGGGAGGGTGCGGAGGATATGTCTCTCTCCTCTGCATCTTCTCTGGAGAGGAATGACACCAGTGAGGAGTTCCTAGATGACTTTGAAAACCTAGGGGACCAGTCCCAGAATGGCATCCAGCAGAACAAAAATCCTGTTGCCACAGCCACCCGGATACGCATGCAGAGCTTTTTGAATGAGACCATGGACTGGGCTGGGATTGGGCTGGCAGGTATTGCTAAACATAACTTTCATTTCTGCCATTTATCAGGGTCAACCAGTTCAATGTCATGTAAACATTTAAATCTTAAGTGAAGCATGGCAGAAAAGGGTGTTCTGATTCTTTATTATTGGAATTCATGCTTTCAGTGGTCCATTTGAGATATAGTGGCTGATAACCCTTGTGGTAAGCATGTAGATCCTGATGTGTGTTTAATTTTTAGGTGGTAAGGCAGATTTA[C/T]AGAGTGCTCCACTACGTGGTCCACCGCTCATGTCTCCTGAAGTGGACCGTCATGCAGTCTCTTCTTTGGAGCTCTCACCCTCTAATAGCTCTGGAGGGACATACATGTGGGATGAGGAGGGCATGGAGCCACTGGGACACAACACACACATGCACCACTGCAGCAGTTTTGAGTCAGACCTCAACAGCGTCGTGAGTACACACATACATCCAAAATAAGATTGCAGAGTGTTGAGGTTATGTACAACAAAATAAAAAGCAGTACTTATTGACATGAGATGCATTGATCTGAAAGCTTCAAAGTACAGTGAACATATTAAATAAAAAAAAGAAATGATATAGTGAATCTGGAAAGACAGGTTATAACAGTTGAAATTATAAATGATACTAATGAATAACAATAATAATTGTTATGATAATGTTAATGTACATACTCGTATAATAGTAACATTTTGAGTAATAGCAACAATATTGTTAGCAAGAAAAAAACCCCCCCATAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36424

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
ENSDART00000122366	Nonsense	785	802	11	11

Genomic Location (Zv9):

Chromosome 17 (position 26323528)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26463447
GRCz11	17	26481838

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTCATCTTCCACAGCCTCAAATACTTCAGCCCATCAGTCGCATCCCCAA[C/T]GAGCCCCTCATCCAGGGAAAACTAGCAAGAACAGTCCCAATCGGGGGCCG

Long Flanking Sequence:

ACTATAGTGAACAAAGACTGCTCTCAGTAAAAATGCTGCTCTTAATTAATACTGTATTTGATTTGAATTTTCAGTTGGAAAATTCCAACATAAATTGGTCAAAACTCTAGCATGGGTCTCTAACTTGATTACTGGAGGGCCGCAGCTCTGCACGGTTTTGCTCCAACCCTAATCAAATACAGCTGATCCAAATAATCAAGTTTTTTAAGACTAATAGAAACTAGCATGTGTGAGTTGGAGGTGGTTGGAGATAAACTATGCAGAGCTGTGGCCCTCCAGGAATTGAGTTTGAGACCATTACTCTGCAGTATTTTTCTCATTCTCTGACATAATGAGATGCATACTTCGAAAGCTAATACCTTTTGTAAATAGAGATTTCAGTTCAAAATGCTGATCCCCTGATCGCAGATCATTGATTCCACTATTTTTTATTGTGTAATTAATCTTCTGTTTCATCTTCCACAGCCTCAAATACTTCAGCCCATCAGTCGCATCCCCAA[C/T]GAGCCCCTCATCCAGGGAAAACTAGCAAGAACAGTCCCAATCGGGGGCCGCAGTGATGCCTGCACCGGAGGTGAACAGCCACCCATGCCCTGTCCTCCATCCCCCTGTGCCCATCCAATTCTGCCTCCTGCTAGAGACCCTCGTCTAGAGTCGAAATCTTTACCTGACCCAGAGGAGATGAGTCGGTTGCTTAGCACCCACCTTCGCATACAAGACATCAATGAGTGTGACTCACCGGGGGCTGGAGAACAGATTGCGAGACCGACCCCAGAAAGCCATCAAAACAAACTGCTGCAAACACCTCACCCCCTGTCCCTCTTCAGCCCTCGTGTCCTGCAGCCTCCACGTCTACACAGACGGGTAACACTCTCTGCTCTGCCTGTAGGGGGCTGTAGTAGGTCAAATCCAAAATCTAGACTCTCAGTGAACTACAAGGCCCAGCAGCAGCAGCAGCAGCTTCCTCCTTCTCCGTCCAGAGGTTTGCCATGCTTCAGTGCTGA

Associated Phenotype:

Not determined