ZMP

ankrd44

Ensembl ID:

ENSDARG00000026028

ZFIN ID:

ZDB-GENE-070912-605

Human Orthologue:

ANKRD44

Human Description:

ankyrin repeat domain 44 [Source:HGNC Symbol;Acc:25259]

Mouse Orthologues:

Ankrd44, E230028L10Rik

Mouse Descriptions:

RIKEN cDNA E230028L10 gene Gene [Source:MGI Symbol;Acc:MGI:2685285]
ankyrin repeat domain 44 Gene [Source:MGI Symbol;Acc:MGI:3045243]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25429	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa15884	Essential Splice Site	Available for shipment	Available now
sa34678	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa6117	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25429

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000037182	Essential Splice Site	9	1050	1	28
ENSDART00000142768	None	None	1037	None	26

Genomic Location (Zv9):

Chromosome 9 (position 33191569)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	32347515
GRCz11	9	32158261

KASP Assay ID:

554-7435.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGGATGTCCAGTTTCACATGATATGGCTGTTCTCAAACTAGTCGACCAG[G/A]TAATTTACTAAGATTTTTTAAAATGTTTATAAAAATGAAGTTGACTTGTG

Long Flanking Sequence:

GTAGTAGGATTCCGAAATTAGCGAGGGGGGAAGCGTACAAAAACGCTGACTTCCTGTATTTTATTATAACGAATGAATACATTACGCAGAGCGTAAAGCAGTGGGGTTTCAAATCTAAAAATCGTTATCGTTTTGGATGCCACTGCTGTAAATGCGGATTGTTTACAGCACCCCTCGCATCCTTTCCTCCCTCCCCTTTTCCTCTTTCCCGGAGCGCCGGAGCGCTGGTGGTGAGGCAGCGGCTGCAGCTGCTCCCGCTGACCGAAGATAGCGCCTGCAGAACCGGCCACGGCCGTCACATCACCCCGGGCCCTTGGAGAGGGCGAACCACAGCAAAGCAGGAAGCAAGCTTTTGACGCCACATCATTGTGCAGCATCATCCTTCCGTAAAAAAAGCGCACGGCTCCTTCTGGATTTGATTAATCTACACCTTCAGGTCTTTTCAGGAGTTTGGATGTCCAGTTTCACATGATATGGCTGTTCTCAAACTAGTCGACCAG[G/A]TAATTTACTAAGATTTTTTAAAATGTTTATAAAAATGAAGTTGACTTGTGTGAAGATGAAACTGAGGAGTTACGTGAAATTAAATGTAATTTTCTGTTAATATGCTAATGATTATTGTGATGCTCCATATGCAGTATGCAACTGCAGAAACTAGCTATATTTGCAGCATATGCGTTACATGTTAAAAATGCATGAGACCACATACAAGTTTAATTTGCATAAGTCTGTTTCTGGTGTCTTGCATTTAGCAACGACATAAAAAAAAATAATAATTTTTTAGCAACGACATAATAGTCCTTGTTGGGAGACATTGGTCTTCCTGAAAACCAAAGAGCAGCAAACTGCTATTACTGATGTACAGAGTAGTGAATCAAATACTTAAATGTGCTTGAATTTACAAGTCAAATAGTTATGTGTGATAGTGTACCATTAATGATAGTAAGTCTATGATTAATAATGTGATTTACCCACACTGTTGTGTTTAGGGTAAGATAAATGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15884

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000037182	None	None	1050	None	28
ENSDART00000142768	Essential Splice Site	386	1037	11	26

Genomic Location (Zv9):

Chromosome 9 (position 33166590)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	32322536
GRCz11	9	32133282

KASP Assay ID:

2260-2022.1 (used for ordering genotyping assays)

KASP Sequence:

TCCTCTTCTGTGCACTGTATCCTTCCTCCTCATCCTTCCATTCCTCTACA[G/A]GACGGAGGTATAGCATAATGTGYCCTCTCAGTAATGACTCGGTCCTGTCT

Long Flanking Sequence:

GGAACTGTGTATAAAGAACTGCAAGTTCTAAAGAGTTTTACCGTAACCTGCTCTTAACACAAATAAAACTTTCTCACCAGCATATTTGCTTGAGCATTTAGCCTTCGACGTTCCCTGTTTAGGTCTGGCATGCCCTTATCTGCTATTTTAACTCTGACTCTTGATTGTGGGTTTGCTGCTGTATGAAATCATAGACTGTAGATCTGTTCTTTTTAAGTTGTTCTGCTTAGTTGCACACATTTTTGTTCTCACCTCTGTAAGTGATGGGTGTTTGTCTTGTCTTTCCTGTGTGCACTGTCTTTGTTTTTCCTGCACTAACATCCTTTCTCTCTCTGTGTCTCTCTTTCTCTCACACCGTCTCTTTCTTGGACTTCTTTTTCCTCCATTTCACACTTTCCCCCTACTGCGGTCTGACACTGTGGCTGTCTGCGTCTGGTTGTGGGGACACTTTCCTCTTCTGTGCACTGTATCCTTCCTCCTCATCCTTCCATTCCTCTACA[G/A]GACGGAGGTATAGCATAATGTGCCCTCTCAGTAATGACTCGGTCCTGTCTGCAGGCTTCCAAATCGATACGCCTGATGACCTGGGGAGGACATGTCTGCACGCTGCAGCCGCAGGAGGGTGAGTCTGTCAATCTGCAGATCTGATTTTTACTTGTTGAGCTGCAGAGTCAGATGGGATTGTATATAAGATGTGTGCTATATTAGAACAACTAAAGCTGGTCTGTGAACACTTGATTACTCAATTTAAATATATGTTTTTATAACTAGAGTTATAAAACTTTTTGTTTTTTCATTGTGGCTGTGGGTAATTTATAGGAATGTCAAGATCTGTTTTTTGGCCCTAGAGTCTGACTCAGTTGATTTTGAGTATCTACCGAAACCCGATCCGATACTTCTAGAGTACATAAGTTAGGTTTATTTATAAACTTATTTCGAGAGGATCACATGGCCATGATTGTTCTCAGCTGTTCCCGCATCAGCTCGCGATTGATTGTGCAATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34678

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000037182	Essential Splice Site	486	1050	14	28
ENSDART00000142768	Essential Splice Site	495	1037	13	26

Genomic Location (Zv9):

Chromosome 9 (position 33163946)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	32319892
GRCz11	9	32130638

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGGGGCGCACTGCTGTTCACTACGCTGCTGCTTCCGACCTGGACAGAAG[G/A]TACGTGCATCATTAAACAAGGATTACTCTCATAATTGGTAAAAATAAAGA

Long Flanking Sequence:

ATTGCTCAGCAGTGGAGCCGATCATAACCGCAGGGACAAACATGGAAGGTGAGTTCTTGAGTTCCTGGTAAACATTTATGTCAAGGCATTTATCCAACTAATTGCTGAGTTGTCCAGTTCATCACAGACAGTATACATATCTGTGCAATTGTGTGCAGTTTTGTGCTATTCTTGGTCAGTGCTATGAAATGTAATGCAAATGGCAGCTTTTTTCAGATGTTTTCACAGCTGTTTATAGAACCACCGATCAGCACTTATTACTGCATACATTAAATGAAATCATCCCTTCTGTAGTAGTTTGTTCTATCATGCTTATATTTGTCATATTATTTCCTGTCTTTTGTTATGGATGTCGACAGGACCCCTCTTCATTATGCGGCAGCTAGTCGTCACTTTCAGTGCCTGGAGACTTTGGTGTCCTGCGGTACCTGCATTAACGCCACTGACCAGTGGGGGCGCACTGCTGTTCACTACGCTGCTGCTTCCGACCTGGACAGAAG[G/A]TACGTGCATCATTAAACAAGGATTACTCTCATAATTGGTAAAAATAAAGATACATATAAAAAAAATATTGCGCTTTAAGCTTTTTAGACTAAATATTATGACGGATTTAAAGTACACATGAAATCAAAACTAACCATACTGATTTTATTTTTATTTTAGAAAAAAATGGCTGCGTTCAAAAACCGCCTACTACTCAGTAGGTACTGCATTTGAATTTACATGTACTACTCGGCCGTTAGAAAAGTACATTCCATACAGTTTAATTGTGAGAAGTATGAATGAAATTCGGGCATACTACATCCGCCATGCGTTAGTTGCGTCGCTTCATTCCCATTCATAAATTCTCTCGCAGAGCATCATGGGATAGCGCAGCATGCATGGGATGCGCACTTCAGAATCTCGCCGGAACGAGTAAGTCATTCAGGTACTTCTCGCAATCTGATTTTTGAATTCTATGAATTCGAATGTACTACTTGGCTCACGCACTGATTTTAGCTTAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6117

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
ENSDART00000037182	Nonsense	590	1050	18	28
ENSDART00000142768	Nonsense	577	1037	16	26

Genomic Location (Zv9):

Chromosome 9 (position 33153234)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	32309180
GRCz11	9	32119926

KASP Assay ID:

554-3656.1 (used for ordering genotyping assays)

KASP Sequence:

GGCACGCGCAGGCTCTAGAAGTGCTCTTGGAGGGTCACTGTGAGGTGGAT[C/T]AGGGGGATGAAGTTGRTCGGACTCCACTGGCCCTTGCTGCTCTCAGGGGC

Long Flanking Sequence:

AGACAACACCTATGATTCCACACTTACACTATCATCAAACTTTGCCTTTGTTTGTTGTGAATATGTTCCCTCTAATGGCAAAATTACATAGTGAGCCTTTTAAATGTACACACACACACACACATAGTAGTAGCACATTTTTGAAAAACGTCTTTTATTCTAACTAAGAGTACATTTATTTGATGGAAATGCATTAAAACTGTATATTAAGAAATGTTTTTACACTTTAACTGTCATATCATTCTTTTAAACACGCTAAAATCAATCATAGTACCTTTAGAAACGGCTGAGCACTGTTATCTACTACCTAATGCCACATTTTTCACAGAAAAACAGAGCTTAATAGGTTTGATCACCACAGATTACTTGCTTAAATAGGAGTAATATTTGAGAACACGTTTAGAATTTGTACACCTTTCAATGTGTGTATGTGTGTCTAGGCATATCACGGGCACGCGCAGGCTCTAGAAGTGCTCTTGGAGGGTCACTGTGAGGTGGAT[C/T]AGGGGGATGAAGTTGATCGGACTCCACTGGCCCTTGCTGCTCTCAGGGGCCACACTGACTGTGCTCTCACACTTCTGAACCACGGGGCTTCCCCGAGAAGCAGAGATACTGTCAGAGGACGTACGCCCATCCACCTTGCAGGTGTGGTGGAAACTATTCTGCACTTTTTTTAATGCATTATTGTTTGTGATTGTTACGTGTTTAATTTATGTTGGATGAGATGTAACATTCAGTCTCTAATGGTGCTGGGTGAAAATGAGAAAATGTTGAGCGAGAAGATGGATAAGTGAAACAAAAATTATCAATTTATTAAACTGAGAATATCAAACAATGAATATAGAAATTTAGATTTGTACTTTTTTTGTAATTTAATCAAAAACAGGACTGTTGCCAAAACAAAGTAATAAATATATAACAAAACAATCTAACTAAACTCCAATCCACTAAACTTACCAAAGAAAAATGCAGAAACAAACCCGTAATCTTCCGCGTATGCGATG

Associated Phenotype:

Not determined