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Previous release (v1)
2024-04-28 07:12:57, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_137639 557 bp RNA linear PRI 13-SEP-2020
DEFINITION Homo sapiens translation machinery associated 7 homolog (TMA7),
transcript variant 3, non-coding RNA.
ACCESSION NR_137639
VERSION NR_137639.2
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 557)
AUTHORS Song Z, Zhou C, Wang J, Yang W and Hao F.
TITLE Effect of HSPC016 gene expression on the aggregative growth of
dermal papillae cells
JOURNAL Australas. J. Dermatol. 53 (2), e26-e29 (2012)
PUBMED 22571579
REMARK GeneRIF: Dermal papillae cells (DPC) lose aggregate behavior and
grow much slower after HSPC016 gene inhibition. Recombinant HSPC016
protein promoted the proliferation of high-passage DPC and induced
aggregative behaviour.
REFERENCE 2 (bases 1 to 557)
AUTHORS Zhiqiang S, Jiwen W, Fei H, Weibin Y, Feng Z, Xichuan Y and Chunlan
L.
TITLE Identification of differentially expressed genes HSPC016 in dermal
papilla cells with aggregative behavior
JOURNAL Arch. Dermatol. Res. 297 (3), 114-120 (2005)
PUBMED 16096800
REMARK GeneRIF: HSPC016 was was differentially expressed in dermal papilla
cells with aggregative behavior.
REFERENCE 3 (bases 1 to 557)
AUTHORS Yang WB, Hao F, Song ZQ, Yang XC and Ni B.
TITLE Apoptosis of the dermal papilla cells of hair follicle associated
with the expression of gene HSPCO16 in vitro
JOURNAL Exp. Dermatol. 14 (3), 209-214 (2005)
PUBMED 15740594
REMARK GeneRIF: Expression of gene HSPCO16 resulted in the apoptosis of
these cells, which suggested that the apoptosis of dermal papilla
cells might be associated with the expression of gene HSPC016 in
vitro.
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BU536461.1, AL712164.1 and AA149268.1.
On Jun 1, 2019 this sequence version replaced NR_137639.1.
Transcript Variant: This variant (3) uses an alternate splice
junction compared to variant 1. This variant is represented as
non-coding because the predicted protein does not meet RefSeq
quality criteria.
##Evidence-Data-START##
Transcript exon combination :: SRR1803616.450699.1,
SRR7410570.218571.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMEA1965299, SAMEA1966682
[ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-21 BU536461.1 28-48
22-554 AL712164.1 1-533
555-557 AA149268.1 1-3 c
FEATURES Location/Qualifiers
source 1..557
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="3"
/map="3p21.31"
gene 1..557
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/note="translation machinery associated 7 homolog"
/db_xref="GeneID:51372"
/db_xref="HGNC:HGNC:26932"
/db_xref="MIM:615808"
misc_RNA 1..557
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/product="translation machinery associated 7 homolog,
transcript variant 3"
/db_xref="GeneID:51372"
/db_xref="HGNC:HGNC:26932"
/db_xref="MIM:615808"
exon 1..56
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1455876878"
variation 2
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:766502736"
variation 4
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:751624442"
variation 5
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039521091"
variation 6
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:201530127"
variation 8
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165510592"
variation 9
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:781252946"
variation 10..36
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="ggcagggtctggggaagcggcggcagg"
/replace="ggcagggtctggggaagcggcggcagggtctggggaagcggcggcagg
"
/db_xref="dbSNP:1560095441"
variation 10
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:748439562"
variation 11
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1412173127"
variation 12
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275080613"
variation 13
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1482717530"
variation 14
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039521752"
variation 15
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:755896347"
variation 17
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:749164847"
variation 18
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473782185"
variation 19
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039522145"
variation 20..23
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="ggg"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:769956200"
variation 20
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:561847670"
variation 24
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773871244"
variation 25
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:200628256"
variation 26..33
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="gcggcggc"
/replace="gcggcggcggc"
/db_xref="dbSNP:777873183"
variation 26
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:374017589"
variation 27
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:368160492"
variation 28
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039522664"
variation 29
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765641351"
variation 30
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:773719062"
variation 31
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371673403"
variation 33
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754977247"
variation 34
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767698039"
variation 35
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:911440499"
variation 36
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1230136043"
variation 37
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace=""
/replace="c"
/db_xref="dbSNP:1384476244"
variation 37
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376665779"
variation 38
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:756339808"
variation 39
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163502495"
variation 40
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:777476469"
misc_feature 41..166
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/inference="COORDINATES: ab initio prediction:ORF Finder"
/note="predicted ORF does not meet quality criteria for
protein coding locus with longer protein data"
/db_xref="GeneID:51372"
variation 41
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:749111503"
variation 42
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:762935347"
variation 45
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:2107158968"
variation 46
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778692219"
variation 47
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745885023"
variation 48
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460187754"
variation 49
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1058384"
variation 50
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:746595421"
variation 52
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768458123"
variation 53
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1058391"
variation 54
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:773665734"
variation 55
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763391359"
variation 56
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:771370569"
exon 57..112
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/inference="alignment:Splign:2.1.0"
variation 57
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039528652"
variation 58
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:755792161"
variation 61
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:779105036"
variation 64
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:746265014"
variation 67
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:772371288"
variation 68
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039528976"
variation 69..74
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace=""
/replace="agccac"
/db_xref="dbSNP:1282921309"
variation 70
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1410444706"
variation 71
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301045969"
variation 76
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:766241443"
variation 81
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:1410321831"
variation 82
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:775944077"
variation 83..85
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2039529501"
variation 83
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:747573501"
variation 84
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1237163472"
variation 85
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:375769495"
variation 86
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039529709"
variation 88
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:974347480"
variation 92
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219312291"
variation 94
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:776697669"
variation 95
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222306443"
variation 96
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027261461"
variation 97
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:761903507"
variation 98..99
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1031473549"
variation 100
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484352758"
variation 101
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:765521122"
variation 103
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1249244421"
variation 104
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:773359470"
variation 107
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189201905"
variation 109
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:762781672"
variation 110
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443626455"
exon 113..196
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/inference="alignment:Splign:2.1.0"
variation 113
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756907803"
variation 117
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:780358282"
variation 118
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:751946046"
variation 119
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469210976"
variation 121
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368919538"
variation 123
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:375346878"
variation 124
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:947286875"
variation 126
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1042930666"
variation 128
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039534877"
variation 132
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039534936"
variation 135
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:755387356"
variation 141
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039535056"
variation 142
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:781704300"
variation 143
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039535201"
variation 146
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039535264"
variation 149
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:748673790"
variation 150
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1174346418"
variation 151
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:769908733"
variation 153
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:777724168"
variation 154
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288705407"
variation 156
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1193047806"
variation 157..162
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:761139732"
variation 159
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:934455217"
variation 163
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749451817"
variation 164
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039535961"
variation 170
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052073226"
variation 173
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039536093"
variation 174
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:774236200"
variation 175
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1221226556"
variation 176
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243335311"
variation 177
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:759380856"
variation 179
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:557810359"
variation 185
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1214575338"
variation 186
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258778650"
variation 189
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489303101"
variation 190
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775492653"
variation 192
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:760587663"
variation 196
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479411229"
exon 197..557
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/inference="alignment:Splign:2.1.0"
variation 200
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:578066508"
variation 201
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356956100"
variation 202
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:375127083"
variation 203
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039621062"
variation 215
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039621099"
variation 216
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:367740188"
variation 217
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039621203"
variation 218
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039621245"
variation 219
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:753039055"
variation 221
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1203966172"
variation 225
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039621400"
variation 228
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756598367"
variation 229
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226977369"
variation 231
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:764488429"
variation 237
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039621608"
variation 239
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297910804"
variation 242
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:539074977"
variation 245
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:757410281"
variation 248..253
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="gag"
/replace="gaggag"
/db_xref="dbSNP:753435629"
variation 248
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:779953483"
variation 250
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:746030257"
variation 255
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:758578739"
variation 257
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241791348"
variation 258
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039622029"
variation 259
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:779848119"
variation 260
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:1575432509"
variation 262
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039622145"
variation 263
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469930387"
variation 268..270
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:761586507"
variation 272
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452956655"
variation 276
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746756668"
variation 284
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:1575432519"
variation 285
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:375880978"
variation 286..291
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="ct"
/replace="ctct"
/replace="ctctct"
/db_xref="dbSNP:2039622517"
variation 286
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1046532006"
variation 288
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:554268815"
variation 290
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039622598"
variation 291
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1319215785"
variation 293
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:906687216"
variation 294
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575432534"
variation 295
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298121859"
variation 297
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:572507761"
variation 299
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039622828"
variation 300
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2107173635"
variation 301
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454500460"
variation 303
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284780725"
variation 306
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002334913"
variation 308
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033684753"
variation 309
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039623037"
variation 310..313
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:2039623065"
variation 311..312
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace=""
/replace="g"
/db_xref="dbSNP:1287993692"
variation 312
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440991908"
variation 313
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:1360626185"
variation 316
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:542826372"
variation 318
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:945114276"
variation 319
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212346096"
variation 320
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323317851"
variation 322
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:140064569"
variation 328
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039623435"
variation 330
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039623476"
variation 338..339
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1318088233"
variation 338
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202650492"
variation 347
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373592646"
variation 348
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039623640"
variation 352
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039623668"
variation 357
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576596946"
variation 366
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261642735"
variation 367
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426558643"
variation 371
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1011316178"
variation 372
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:11552877"
variation 374
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:369760515"
variation 378..384
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="aaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:565737200"
variation 379
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:373553505"
variation 384
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242095269"
variation 385
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1485191457"
variation 391
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039624163"
variation 394
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039624192"
variation 395
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2039624241"
variation 396
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039624282"
variation 397
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:748450207"
variation 400
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1188317268"
variation 401
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039624411"
variation 402
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039624442"
variation 403..410
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="tcatc"
/replace="tcatcatc"
/db_xref="dbSNP:1424435341"
variation 404
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039624540"
variation 408
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1458590171"
variation 409..413
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="tct"
/replace="tctct"
/db_xref="dbSNP:2039624648"
variation 409
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253639195"
variation 410..411
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace=""
/replace="aga"
/db_xref="dbSNP:2039624787"
variation 410
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:1202862698"
variation 412
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:1480200184"
variation 415
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039624885"
variation 420
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039624923"
variation 421
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:2039624970"
variation 433
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039625004"
variation 434
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:7126"
variation 435
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039625143"
variation 436
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1575432606"
variation 441
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039625221"
variation 442
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039625277"
variation 443
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:531938710"
variation 446
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039625445"
variation 447
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372767963"
variation 448..451
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:754291844"
variation 457
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:900381063"
variation 460..461
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:2039625640"
variation 463
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:138163950"
variation 469
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:558992283"
variation 471
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:1460264466"
variation 473
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:141110854"
variation 474
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039625940"
variation 476
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174033756"
variation 482
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039626012"
variation 483
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039626044"
variation 484..487
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1455715264"
variation 486
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:1575432632"
variation 488..504
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="tctgttctttggtcctt"
/replace="tctgttctttggtccttctgttctttggtcctt"
/db_xref="dbSNP:2039626290"
variation 494
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1393556780"
variation 497..498
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace=""
/replace="tg"
/db_xref="dbSNP:2039626367"
variation 498
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112430504"
variation 499
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:548012930"
variation 502
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:1193054614"
variation 504
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:909631628"
variation 512
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039626590"
variation 513
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:2039626624"
variation 518
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:879653506"
variation 521..523
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1290052300"
variation 522
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:569810524"
variation 523
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:941155193"
variation 528
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/db_xref="dbSNP:2039626838"
variation 541
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:772007260"
variation 542
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2039626911"
variation 543
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039627368"
variation 546
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="g"
/db_xref="dbSNP:2039627423"
variation 547
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="t"
/db_xref="dbSNP:1480596237"
variation 549
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004296182"
variation 550
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015718913"
variation 551
/gene="TMA7"
/gene_synonym="CCDC72; HSPC016"
/replace="a"
/replace="g"
/db_xref="dbSNP:2039627725"
ORIGIN
gtttccggtggcagggtctggggaagcggcggcaggcgccatgtccggccgcgaaggtggcaagaagaagccactgaaacagcccaagaagcaggccaaggagatggacgagataaggctttcaagcagaaacaaaaagaggagcagaagaaactcgaggagctaaaagcgaaggccgcggggaaggggcccttggccacaggtggaattaagaaatctggcaaaaagtaagctgttccttgtgcctgaggagatggtgaccctttatttcatctgtatttaaacctctctattccctgccataacatcttttgccacgtatagctggaattaagtgttgtcttggagctgttgtacatttaagaataaacttttgtaaaaaaagaaaaatcttacagtggctcatcatctctttagttgttttcactaagtcgttcctaccataactgtgaatttaaagtaaaaccagctcagaatcttgccagagtctgttctttggtccttgttctaccctaaactttgtatcacctgaaattaaaccaactcatttgaaagga
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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