ZMP

LOC556392

Ensembl ID:

ENSDARG00000059003

Human Orthologue:

FAM40B

Human Description:

family with sequence similarity 40, member B [Source:HGNC Symbol;Acc:22209]

Mouse Orthologue:

Fam40b

Mouse Description:

family with sequence similarity 40, member B Gene [Source:MGI Symbol;Acc:MGI:2444363]

Alleles

There are 6 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20192	Essential Splice Site	Available for shipment	Available now
sa20191	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa20192

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
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Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081990	Essential Splice Site	423	810	13	22

Genomic Location (Zv9):

Chromosome 4 (position 4857558)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	4975739
GRCz11	4	4984309

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCTTCATCATCATTAAATCAATATACAGTTTTCTTTCTGATCTTATTTC[A/T]GTGACATCGACACTCTGGTTGGGTTGCCCAGACCTATACACGAGAGTGTC

Long Flanking Sequence:

TTTACACACGCATGCTCGTTCGCTCGAGAGTCGGAAGCAATATTGTTAGACCGCCCTCTCCCGTCCAAAATTACACCAGTTACTGATCGCTCCCGCACTTTATTCTGAAATTTATTCCCGCGCCGCAAGAAATCCGGTCGGGTCCCACGGAATCCAGACCTCTAGATGGTGGTTCATTCCCTAATAAATAAGGGACTAAGCCGAAGGAAAATAAATGAATAAATGTTCTGACCTCAATTGTTCACGTTTGTTTACTTTGCATATTAGAATCTATTGTTGTTGACTACAGTGGGTTATCGATTTCCTTCTTCCTGCAGAGAGAAAGACATCGAGCACTTTCTGGAGACCAGCAGAAACAAATTCATCGGCTTCACCTTGGGAAAGTGAGTCTCTGATCAATTCTCCCAGGCCACTAAGCTTATGAATCCATGATAAACTATTATAAAGGTCTCCTTCATCATCATTAAATCAATATACAGTTTTCTTTCTGATCTTATTTC[A/T]GTGACATCGACACTCTGGTTGGGTTGCCCAGACCTATACACGAGAGTGTCAAGACTCTGAAACTGGTGAGCATGGAAATACTTTTATTTTTTTATATTTTCGTATTTTACTAAACGTCAGAGGTTTATCCATGGCACATCATTATTAGTAGGAAACTCTACTGAAATAAATGAGGTGGTGATGTAAAATTGATGAACTCATGAATGCACTGTGAAGACATCACTGATGCGACATCAAACGACAGAGATAGCATTTGTTGTGAATGCTGCTATTATACATGTGTGTTTTTTGAAAGAAATGAATGTTTATGTTCATGAAGAACGCATTTGAGTGGATGGAAAGTGACAGAGGAGGCATTCGTGATGTAGATTTGTTGAAGTCAGAATTATTAGGCAAGTTAGGGTAATTATGCAAGTCTTTGTATGATGATGGTTTGTTCAGTAGACAATTGAAAAGAAAATATTGCAGAAGGGGACTTATAATATTGAGCTTAAAATGGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20191

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081990	Nonsense	716	810	21	22

Genomic Location (Zv9):

Chromosome 4 (position 4846745)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	4964926
GRCz11	4	4973496

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTGGAGAAAGAGTAACATGAAAACCATGTCTGCCATCTACCAGAAAGTC[A/T]GACATCGACTCAATGACGACTGGGCATATGGAAACGGTAAAAGTCTGAGT

Long Flanking Sequence:

ACCTTCTTGCTGTGAGGCAAAAGCACTGCCTACTGCGCCACTGCGTCGCCCTATTGACTTTCATAGTAGACAAAAAAACACACAATAGAAGTCAATGGTTACAGTTTTCTAGCTTTCTTCAAAATATAAAAAGAAAGAAACTCAAACTGGACCAATGAAAGGATGAGTAAACAATGACAGCATGTTCAGTTCTGGGTTTATTATCGCTTTAACGTTTTCTGATTGATGTTAGTATAGTAATGTACACCTTTTTTTTAATGCTGCTTTGAAACCGCAGTTGTGAGAGTGCTGTACAAATAAATAAGAACTGAATTGATTTATTTCGTTTGCAGATGCTTGTGGTGTTCAAGTCTGCTCCTATCCTGAAAAGGGCGCTCAAGGTCAAACAGGCCATGATGCAGCTCTATGTCCTCAAACTACTCAAGATCCAGACCAAGTATTTGGGACGACAGTGGAGAAAGAGTAACATGAAAACCATGTCTGCCATCTACCAGAAAGTC[A/T]GACATCGACTCAATGACGACTGGGCATATGGAAACGGTAAAAGTCTGAGTTTTGTCTTGTCAGGGGTGTTGAGGAAAACACTTTAAGTTGGTATTAAACAAAAGTTGCTGTATTTTTCGATCTTGGTTTGAGCCCAGAATTTTTATTTCCATGCATCTGTATTTGAACATTTCTAAATGTTTCTTTGATTAAGCTAAAGTTATTCTGATTATTCCTGTACACAATGCATTCTTTCAAATAATTCTACATTCCTCCTACCAGATATTGACGCTCGACCATGGGACTTCCAGGCGGAGGAGTGTGCGTTACGCGAGAGCATCGAGAAATTCAACACACGGCGCTATGATAAGAATCAGAACAGTGAGTTTGCACCAGTGGACAATTGCCTTCAAAGTGTTTTAGGTCAGCGCGTGGACCTGCCCGAAGACTTCCATTACAGCTACGAGATGTGGCTCGAAAGAGAGGTTTTCTCCCAGCCCATTCAGTGGGAAGGTCTGCTG

Associated Phenotype:

Not determined