ZMP

fam169b

Ensembl ID:

ENSDARG00000069321

ZFIN ID:

ZDB-GENE-050419-217

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LWJ5]

Human Orthologue:

FAM169B

Human Description:

family with sequence similarity 169, member B [Source:HGNC Symbol;Acc:26835]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23290	Nonsense	Available for shipment	Available now
sa11717	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa23290

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100776	Nonsense	148	344	5	9
ENSDART00000141739	Nonsense	89	220	3	5

Genomic Location (Zv9):

Chromosome 18 (position 20842385)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	21072608
GRCz11	18	21061674

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTATTCCTGCTCAGCCAAGTTATATTTGGGATTCTGGAAAGGCCTCTT[G/T]AAGATGACCTATATTTTTCTGCCTATTCTTTGAGGGAACATGGCAAAATC

Long Flanking Sequence:

TAATTTAAATTCCTCATTAAAGAGTAATATTTGTGTTTACAGGTGAAAGTAAGCAGTGAGAACATTGGTCAGCTCTTGTTTCTGAATGATGGTGATTTATCACATTTTATTCTTGCTCTTCACACACCCGAGGATGAATCTCAAGGTCTGACTCCACACAATATAACACTATCCTTCCTATGCCACTTTTGAGTCATACGGTCTATTTAGATAATAATATAAACCCTGTTATTTTAGTGGTTGCCATGTTCCTGCAAGGCAAATGGTGGCCTGTTGGTGATGTTTTAAAGACGTCAAACAAATCCAGATGTGGACTTTTGTTAGTGAGTAACACAGTCTGACAGACTACATTTTAGTCTGCAATGTTTTGAGCAGAAATAAAATCATCATTTCCACGATAGCCATGACAGATATTGTCATCCCAGGTGGAGTCTCTGATGGAGAGAGTCGTGCTATTCCTGCTCAGCCAAGTTATATTTGGGATTCTGGAAAGGCCTCTT[G/T]AAGATGACCTATATTTTTCTGCCTATTCTTTGAGGGAACATGGCAAAATCCTGTGGCAAGATGGTGAAGCTGTTGGGTTTTATACTGTCAAGAAAAAGGGTAATGTGTTTGGAAATAAGGTTGTAGTATTTTTAGAAATTTATGGTGGATTTAAAAAATTGTTTTCATTATTTTTCTGTTTTTTATAGGCAGTCTGTGTAATGGCAGCACTGGCCAGAGTTATCGGCTCCCTGTGTTGGATACTGTGTTTGTTCGCCCTCGCTGGAGAAGGACTGGACTTGCTTTACAGATGCTGGAAGATTTCTGCTCATCTCAGCCTTTTGAGTGCATTCTGGGAATTAGCTTTCCTATGTCTCCTAGCATGTATGGAGGTAGGTGTACATTAGGATTAAAAATATGCTGATTTTGTGCTCAAGAACCTTTTTTTTTGTATCATCAGTGTTGAAAACAGTTGTTCAAGATGTTTTTGTGGAAAATATGATATGTTTTTTAGTATTATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11717

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:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000100776	Nonsense	258	344	7	9
ENSDART00000141739	Nonsense	199	220	5	5

Genomic Location (Zv9):

Chromosome 18 (position 20844027)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	21074250
GRCz11	18	21063316

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTGCAAGAAGTATCTTGAGSTCCATGAAAAAGAAARAGAGCGTCTCTA[T/G]GAAGTGGAAGCCCCTGGTGAATGGCCTCAGAGAYGTAATGTGTGGTTGAA

Long Flanking Sequence:

GGTGGGACAATGAGGCGCACGCCTCCCACCAGTGCCGATATACAGCCATATCGCACTGCTACTCATGTGATATTGCTCATATATTGCTATATCTCTTTAATGAATAGAAACAAACATTTATCTGACATGAAAATCTATTTTAACATTATAAATGTCTTAATTTTTGATCAATGTAATGCATAATTTCTGAATAAAAAATATAAATTTCTTTAGAAAACAGATTCAATATAATATGTCATAGTACAAGGTTTAGGAGTGATGACACCATTTAAGTATCAGAATAAATCCTTTAAATGATTATACCATATGTGTGCAGAAAACACAAACCACTCCTATTTCCCTCATTGGTTTACATTGACTGTTTATTAAACAACTCTTATCTGTTATTATAAGTGCAATGAAGGCCTGTGACCACAAGGTTTACACGACTTGTTAAAATAATGGTTTACAGTGTGCAAGAAGTATCTTGAGGTCCATGAAAAAGAAAGAGAGCGTCTCTA[T/G]GAAGTGGAAGCCCCTGGTGAATGGCCTCAGAGACGTAATGTGTGGTTGAATATCCAGCTTCGGGACCTCCCAAAACACTGTAAGATTAATATAGCAACATACTCATAGCACGTGAGCAAGGAGCTCTGATTAGAATAGCTTACTGCACTTGTGTTTTATTGCACCATATAGGACAGTTTATCTCTGAGGTGTTGTTTTTTATAGGTGGAAACTCAGAGCAAGGTCCACACTGCTCATCTAGTCACGAAAGAAGCCATGCTGATTTAAAAGAGGAGGTATGACATTTATTATCTTGCATTTATTTAAGCTTATCTAGAAACTGTTTACTGCCTATTACCGTAAGTTTGTCTTGGTATGTCATGCTTGTATCTGTAAAATTTTACATAATGAATTACAGTTGAAGTCAGAATTATTAGCCGCCCTGAATTATTCGCCCCCCTGTTTATTTTTTTCCAAATTTCTGTTTAATGGAGAAAAGATTGTTTCAACACATTTATATA

Associated Phenotype:

Not determined