ZMP

KIAA0182 (2 of 2)

Ensembl ID:

ENSDARG00000062199

Description:

KIAA0182 [Source:HGNC Symbol;Acc:28979]

Human Orthologues:

AC011317.1, KIAA0182

Human Description:

KIAA0182 [Source:HGNC Symbol;Acc:28979]

Mouse Orthologues:

Gm11027, Gse1

Mouse Descriptions:

genetic suppressor element 1 Gene [Source:MGI Symbol;Acc:MGI:1098275]
predicted gene 11027 Gene [Source:MGI Symbol;Acc:MGI:3779250]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24678	Nonsense	Available for shipment	Available now
sa5998	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24678

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089652	Nonsense	52	1048	1	15

Genomic Location (Zv9):

Chromosome 25 (position 22761952)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	21941065
GRCz11	25	22038613

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCGCTGCCAGCGGGAGTCCTGCATCTCAATCCGGCTTCGCAGCAGCCCTC[C/T]GAAAGTTGGCCAAACAGGCTGAAGAGCCCAGAGGTCAGTGTTGAGCTTTC

Long Flanking Sequence:

CACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAAGTTAACTAGGCAGGTTATGGGAATTAGGCAAGTTTTTGTATAACAGTGGTTTGTTCTGTAGATTATCGAGAAAAAAATATAATTTAAAGGGGCTAGTAATTTTGTCCCTAAAATGGTTCATAAAAAAAATCAAAACTGCTTTTATTCTAGCCAAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAATTTTATCAGCCATACTGTGAAAATGTCTTTGCTTTGTTAAACATCATAATGAATGTAAACATGTAAACAGCAATAATAAACGTCTCTCTTTTCTCTCTTTCTGCAGGAATGAGCCTGGAGCCGAAGTCTCTGTCATTGGGAATGATCTCTGCGGCTCCGTGCACTATGGCCACTGTGAGTCCCCTCACTGCTTCACCCATCAGCGGATCAATCGCTGCCAGCGGGAGTCCTGCATCTCAATCCGGCTTCGCAGCAGCCCTC[C/T]GAAAGTTGGCCAAACAGGCTGAAGAGCCCAGAGGTCAGTGTTGAGCTTTCACATTTGAGCTCCAAATACTCCTCCTTACCTTAATGAGGAAAAGTATAATGGTCAATATGGGGAATGAAGCCACACCTTCTAGTACAGGAGCCAATCATCAATCGTTATAGACTGGCGATTCTTTGCGAGAGAGGCTCGGTCCAGACGTGAGTGAAGGAAAAAGTAGAATTTTCCTTCTACTTTTCGAAAACTAGCCAAACATGCTGAAGCATTTCTGTTTTGTTGTGCTGTTTGTTTGCCATTTTGTTTTGCTTTTTTGTTTTCTGATATCTGCATTTGTTAAATTTTAATTATTTGAGTTTTTTGTTTTTGTTTGTTTATTTCCTTTTTTTACACTTTATTTTTATTTTTTTTTTCAGATTTTTAATTGTTCGTCAATTTTGCATTTTCCTTCCACTTTTCGAAAACTACCCAAATATGTTGAAGCCTTTCTTTTTTGTTGTGTTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5998

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
ENSDART00000089652	Nonsense	889	1048	13	15

Genomic Location (Zv9):

Chromosome 25 (position 22814025)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	21993138
GRCz11	25	22090686

KASP Assay ID:

554-3841.1 (used for ordering genotyping assays)

KASP Sequence:

AATGAATCTGCCATTTTATATCCCTGTATATTTCAGCAGGAGTGAATGAG[C/T]AGGTTGACCCCGYAGCACATCCTTCTCCAGGCCTYCAGAGGGCARYGAAC

Long Flanking Sequence:

CTTGTGCAATATCTAGTGTATCTATGGTTTCGACCAATTGAACCAAACTACAGATGTGAAAGCACCCTACGTATGTAAAGAAGCATTTCAGATAAAATGGCACATTCTTATTGTAAAAACAAAGCTTCTTTTATTTGGAATTTGAAGAAATGTCATCAGTCGTTTACAGAATAAAGAATCACGTTTTACTCAAACACAAAACAATAAATTATGAATCCAGTAGAACTGAGAATTTTAAAGTGCTCTTTCAATTTTTTCATAGCTTCTGTATAAAAGAAGCTAATACTATGCATATTTATTGTGCATGAAATAGAAAAAAAAAATAAAAAATGTAAATAATTTTAAAAAATACAATTATTAGAAGTAAAAAGTGTGTTTCTTGTTCATAAATACACTCAAGTTGATTAATTAAAGTAAAGTACAATTCTGCAAAAATAACACTTCAACTAAAATGAATCTGCCATTTTATATCCCTGTATATTTCAGCAGGAGTGAATGAG[C/T]AGGTTGACCCCGTAGCACATCCTTCTCCAGGCCTTCAGAGGGCAGTGAACAAACTCCCTATCAGACAGACAAATGGCCACTCCTGGCCGGTATCAGCCCACCGTGACTCTCCGGTCGTAAGCAATGACCTTTCAGCTGGAGAGGGCATCAGTTCGGATGAAGACGAGGAAGAGGAGTCCTTTAGTCCCAGGTGGAAAGGCATCGAATCTATATTCACGGCCTATGAAGAGTACATAGAAGGTGAGCTTACTGTACATAAACCAATCAGACCTTTGCATTTCTTGCGTTACATGCTAACAAAATTTCGTGAACTGTCAGGTGATGTTTGAAATACACTCACTGGCCATTTTATTAGGGACATCTTGATAGTACCGGGTTGGAACCCCTTTGCCTTCAGAACTTCCTTAATCTTTCATGGAATAGATTCAGCAGGTTACTGGAAATAATCCTCAGAAATTCTGGTCTATTTAAACATGATAACATCACTCAGTTGCTGCAGA

Associated Phenotype:

Not determined